
Studies on Australian and New Zealand Diatoms
II.—Normally Epontic and Benthic Genera
[Read before the Auckland Institute March 19, 1958, received by Editor December 20, 1957.]
Summary
This paper deals with the taxonomy of species of diatoms collected mainly from Zostera, Posidonia, and Ruppia washings, from fouling test plates, muds, and rocks on the Australasian coast. It will give an indicatoin of the epontic and benthic diatom flora of estuaries in this region and contains descriptions and illustrations of 195 species
In addition, information is given on the seasonal distributions of diatoms, their significance as indicators in the estuarine environment, their importance in the food cycle in this environment and their importance in marine fouling.
Introduction
Although most of the species described in this paper normally occur on plants, on rocks, or at the surface of muds in the photic zone (epontic), some planktonic species (e. g., Synedra spathulata, Nitzschia seriata) will be included in this section, while many normally epontic species listed here (e. g., Licmophora spp., Climacosphenia moniligera) will frequently be found in estuarine plankton.
Source of Material
The material described in this part has been largely obtained from (1) washings from the marine grasses Zostera and Posidonia; (2) scrapings from marine fouling test plates; (3) surface muds and sands; (4) tow nettings.
Stations at which collections of benthic and epontic species have been made to date include: Swan River (Western Australia), Port Phillip, Paynesville, Lakes Entrance, Betka River, and Mallacoota (Victoria), Lake Dobson (Tasmania), Eden, Merimbula, Tuross, Conjola, Coila, Ulladulla, George's Basin, Jervis Bay, Lake Illawarra, Port Hacking, Broken Bay, Port Jackson, Botany Bay, Lake Macquarie, Port Stephens, and Yamba (New South Wales); Moreton Bay, Heron Island, Townsville and Thursday Island (Queensland); Fly River (New Guinea); Auckland Harbour (New Zealand).
Methods of Preparation
Diatoms with weakly siliceous tests (this category includes the majority of planktonic forms) were examined directly in plankton catches (usually in water mounts), or concentrated by centrifugation if necessary. More detailed studies were made by pipetting the specimens onto slides, or cover clips, drying and mounting in a suitable medium. More strongly silicified forms (this category includes the majority of epontic and benthic species) were usually treated to remove cell contents and detritus so that the sculpture of the frustule could be properly seen.
The diatoms were first washed free from preservative by successive decantations with distilled water, centrifuged, and the sediment covered with an excess of concentrated hydrochloric acid, boiled for about 20 minutes and the contents sedimented. The acid treatment was repeated, using fresh acid, and nitric acid added drop by drop until red fumes ceased. The diatoms were then washed free from acid by repeated centrifugations with distilled water.

If this method did not clear the frustules, the sedimented diatoms were placed in an evaporating dish with 10 volumes of concentrated sulphuric acid, heated for one to two hours in a fume chamber, and, while the mix was still hot, small crystals of sodium nitrate were added until the black mass became colourless or pale yellow. The cooled sample was poured into an excess of distilled water and washed free from acid as above. The sample was then mounted on cover glasses, which were dried by heat and mounted with an appropriate medium (hyrax, styrax, and Canada balsam have been used).
Strewn mounts were usually made, as single specimens are too difficult to find for rapid microscopy.
Photographs were taken of diatoms which gave sufficient contrast, a Zeiss photomicrographic apparatus being used. The film was Ilford “Micro-neg” or Kodak “Microfile”, the paper Kodak Grade 5.
The Diatom Species
Sub-Order Araphidineae
Family Fragilariaceae
Genus Fragilaria Lyngbye 1819
Cells rectangular in girdle view, elliptical in valve view, in band-like chains. Valves flat, without raphe or septa, bilaterally symmetrical, with a row of puncta running perpendicular to apical axis and a narrow, clear field along apical axis of valve.
| Valves elliptic lanceolate | F. oceanica |
| Valves constricted | F. constricta |
| Valves narrow, lanceolate | F. striatula |
136 Fragilaria oceanica Cl. (Pl. 2, Fig. 1.)
Cleve 1873b, 22, 4, 25.
Gran 1905, 114, 54.
Cells rectangular in girdle view, forming a double cube, and arranged in band-like, spiral chains, elliptic-lanceolate in valve view; frustules striate only at margin, otherwise smooth, chromatophores 2, on either side of cell nucleus. Breadth 10–35μ.
Distribution. Australia: C. Moreton to Eden; New Zealand waters and sub-Antarctic.
137 Fragilaria constricta Ehr. (Pl. 2, Fig. 2.)
Ehr 1843b, 127, 1, 1, 21; 3, 6, 10.
Cleve-Euler 1953a, 50, 362.
Cells in ribbon-like or zig-zag chains, frustule in valve view constricted in the middle, drawn out or rostrate ends; pseudoraphe narrow; striae fine, parallel, slightly radial towards poles Length 30–50μ.
Distribution Fresh waters, Lake Dobson, Tasmania. Recorded from Australia by Ralfs (1861).
138. Fragilaria striatula Lyngbye (Pl. 1, Fig. 1.)
Lyngb. 1819, 183, 63.
Hend. 1937, 331.
Cleve-Euler 1953a, 367 a-c.
Cells in chains, seldom solitary; valves narrowly lanceolate, apices somewhat attenuate; narrow, median pseudoraphe; valve surface delicately striate, striae parallel to transverse axis; girdle zone plicate. Dimensions 30 × 5μ.
Distribution. Common in New Zealand waters and in sub-Antarctic and Antarctic waters south of New Zealand.
Also recorded are:
-
F. capucina Desm. (Ralfs in Pritch., 1861, 776). Australia.
-
F. diophthalma Ehr. (Ehr., 1869). New Zealand. = F. capucina Desm.
-
F. pinnata Ehr.? (Opephora pinnata (Jan. & Rab.) Petit) (Petit, 1877, Lvall Bay).

-
F. rhabdosoma Ehr. (Ehr., 1869). New Zealand. v. setacea Ehr. (Ehr., 1869). New Zealand. = F. capucina Desm.
Genus Fragilariopsis Hust.
Hust. in A.S. 1913.
Hend. 1937.
This genus differs from Fragilaria by having no median hyaline area or pseudoraphe, and the markings are interrupted, consisting of transverse lines of puncta alternating with hyaline ridges.
139. Fragilariopsis antarctica (Castr.) Hust. (Pl. 2, Fig. 3a, b.)
Hust. in A.S. 1913, 299, 9–14.
Fragilaria antarctica, Castr. 1886, 56, 25, 12.
Cells usually in chains, sometimes single; chains straight and ribbon-like; valves flat or slightly convex, elliptic-lanceolate, apices rounded; valve margin strong, connected by stout transverse ribs, separated by two parallel rows of puncta; girdle zone narrow, simple. 6–15 × 20–80μ.
Distribution. Antarctic, extending into sub-Antarctic water south of New Zealand.
Genus Thalassiothrix Cl. and Grun. 1880
Cells rod-shaped, straight or slightly curved, single or united into stellate or zig-zag colonies by mucilage pads; valves linear, without raphe, poles similar or slightly dissimilar; chromatophores small, numerous.
| 1. | Cells in zig-zag colonies | T. nitzschiodes. |
| Cells in stellate colonies | T. nitzschioides. | |
| Cells not in colonies | ||
| 2 | Cells sigmoid. | T. antarctica. |
| Cells not sigmoid | T. longissima. |
140. Thalassiothrix nitzschioides Grun. (Pl. 1 Fig. 2..)
Grun. in van H. 1880–1885, 43, 7.
Gran and Angst 1931, 496, 83.
Synedra nitzschioides Grun. 1862, 403, 5, 18.
T. curvata Castr. 1886, 55, 14, 6.
T. frauenfeldu Cl. 1894, 6.
Cells straight or slightly curved, forming irregularly star-shaped or zig-zag colonies; valves linear or slightly lanceolate, poles similar. Length, 10–80μ.
Distribution. Australia: Cape York to Eden; Gordon; Swan River, Rottnest, Timor Sea. New Zealand: Hauraki Gulf.
141. Thalassiothrix frauenfeldii Grun. (Pl. 1, Fig. 3.)
Grun. in Cl & Grun. 1880, 109.
Cupp 1943, 184, 135.
Cells in stellate colonies, united near one pole of adjacent cells; valves narrow, linear, tapering slightly towards one end. Differs from T. nitzschioides in having dissimilar ends, and in the more stellate chains. Length, 60–80μ.
We agree with Cleve-Euler (1953a) pp. 74–75 that these differences do not warrant the transfer of T. nitzschioides to another genus (Thalassionema of Hustedt).
Distribution. Australia: North and east Australia, in plankton. New Zealand: Hauraki Gulf.
142. Thalassiothrix longissima Cl. and Grun. (Pl. 1, Fig. 4.)
Cl. and Grun. 1880, 108.
Gran. and Angst 1931, 496, 82.
Synedra thalassiothrix Cl. 1873b, 22, 4, 24.
Cells thread-like, solitary; valves very long (3–4 mm), slightly curved, poles dissimilar; chromatophores very small, numerous.

Distribution. Australia: Darwin to Eden. New Zealand waters from 30° S. to 65° S. in Antarctic. Dominant at times south of New Zealand.
143. Thalassiothrix antarctica Karsten (Pl. 1, Fig. 5.)
Karst. 1906, 173, 30.
Hend. 1937, 335.
Cells very long and thin, often sigmoid; valves with parallel sides and rounded apices; striations on valve margins very fine; chromatophores numerous. Length, 1–3 mm.
Distribution. Together with T. longissima and Synedra pelagica in Antarctic waters south of New Zealand.
Genus Asterionella Hassal 1850 ex W. Sm. 1886
Cells drumstick- or hammer-shaped, forming stellate or spiral colonies connected by larger ends of cells.
144. Asterionella japonica Cl. (Pl. 1, Fig. 6.)
Cl. in Cl. and Muller 1882, 307.
Gran and Angst 1931, 497, 84.
A. glacialis Castr. 1886, 50, 14, 1.
A. spatulifera Cl. 1897b, 101.
Cells spatulate, inner part three-cornered in girdle view, outer part hair-like; valves with mucilage pad at broad end; poles very dissimilar; chromatophores large, 2 per cell. Length, 50–80μ.
Distribution. Australia: Sandy Cape to Maria Island. Dominant at times, especially in estuaries.
145. Asterionella kariana Grun. (Pl. 1, Fig. 7.)
Grun. in Cl. and Gr. 1880.
Gran and Angst 1931, 497, 85.
Cells in wide spiral chains, in girdle view broad to base, constricted, then swollen, tapering to end; chromatophores several; Length, 60μ.
Distribution. New Zealand Milford: Sound.
Genus Plagiogramma Grev. 1859
Frustules quadrangular, free or in chains; valves costate, costae central, sometimes also terminal or absent; striae transverse; central space and ends usually hyaline.
| 1 | Pseudoraphe deep | P. vanheurckii. |
| Pseudoraphe not deep | ||
| 2. | Costae present | P. staurophorum. |
| Costae absent | P. decussatum. |
146. Plagiogramma vanheurckii Grun. (Pl. 2. Fig. 4.)
Grun. in Cl. and Grun. 1880, 119, 145.
Boden 1950, 405, 85.
Cells rectangular in girdle view but constricted near valve margins, lanceolate in valve view; single deep pseudoseptum at valve centre. Striae longitudinal and transapical. Size, 40 × 5μ.
Distribution. Cultured from phytoplankton tow off Port Hacking. Summer.
147. Plagiogramma staurophorum (Greg.) Heiberg (Pl. 2, Fig. 5.)
Heib. 1863, 55.
Boyer 1927(a), 178.
Denticella staurophora Greg. 1857, 21, 496.
P. gregorianum Grev. 1859, 7, 208.
Frustules quadrangular, free or in twos and threes; valves lanceolate or lanceolate-oblong, hyaline median space extending to margin, bounded by two costate lines slightly concave towards apices of valve; pseudoraphe narrow, indistinct; striae in transverse or slightly radiate lines of puncta; ends of valves hyaline. Length, 40μ.
Distribution. Australia: Port Hacking, Heron Island.

148. Plagiogramma decussatum Greville (Pl. 2, Fig. 6.)
Grev. 1866, 14, 1.
Boyer 1927, 181.
Valves oblong-elliptic; pseudoraphe not eviden; terminal costae absent, striae somewhat radiate.
Distribution. Port Hacking, Heron Island.
The following species of Plagiogramma have been recorded by previous authors:—
-
P. atomus Grev., 1863c (Grev., 1863, 36, 1, 9). Woodlark Island (type loc.).
-
P. constricticum Grev. 1863c var.? nancoorense Grun. (Gr. & St., 1887, 73). Oamaru. (Type loc., New Caledonia.)
-
P. costatum Grev. 1863c. (Grev., 1863c, 35, 1, 5–6.) New Caledonia.
-
P. neogradense Pant., 1886. (Gr. & St., 1887, 73.) Oamaru.
-
P. pulchellum Grev., 1859. (Petit, 1877.) Lyall Bay.
-
P. pygmaeum Grev., 1859. (Petit, 1877.) Lyall Bay.
-
P. robertsianum Grev., 1863 (A. S., 1893, 209, 33.) Port Stephens (type loc.), Thursday Island.
-
P. rutilarioides Cl., 1881 (Cl., 1881, 18.). Australia.
-
P. spectabile Grev., 1863c (Grev., 1863c, 35, 1, 7.) New Caledonia.
-
P. tenuistriatum Cl., 1881? (A.S., 1893, 209, 33). Thursday Island.
-
P. tesselatum Grev., 1859. (Gr. & St., 1887, 73.) Oamaru.
-
P validum Grev., 1859. (Petit, 1877.) Campbell Island.
Genus Synedra Ehr., 1830
Cells stipitate, single or adnate in small clusters, becoming free, or rarely not stipitate, in bundles; frustules elongate in valve view, linear or linear lanceolate; longitudinal median line well defined, pseudoraphe distinct; raphe absent; surface striate, punctate; plastids vary; pyrenoids may be present.
| 1. | Frustules very long and narrow, one end spatulate | S. pelagica.. |
| Frustules less than 800μ | ||
| 2. | Frustules undulate | S. undulata. |
| Frustules not undulate | ||
| 3. | Frustules more or less sigmoid in valve view | S. closteroides. |
| Frustules curved | S. gaillonii. | |
| Frustules linear | ||
| Frustules broadly linear | S. superba. | |
| 4. | Frustules with swollen, rounded apices | S. splendens. |
| Apices rounded but not swollen | S. frauenfeldii. | |
| Apices cuneate | ||
| 5. | Central area slightly inflated | S. fulgens. |
| Central area linear | S. ulna. |
149. Synedra pelagica Hendey, 1937 (Pl. 2, Fig. 7.)
Hend, 1937, 335.
S. spathulata Schimper in Karst 1905, 124, 17, 11.
non S. spathulata O'Meara 1875, 310, 28, 34.
Cells very long and narrow, often matted together in dense masses. Valves slightly inflated at centre and ends but not abruptly so; valve surface faintly striate, particularly at ends; chromatophores numerous Length, 800–1,500 × 5–9μ.
Distribution. Antarctic. South of New Zealand. Also recorded by Karsten, Hart and Hendey from Antarctic waters.
150. Synedra frauenfeldii Grun. (Pl. 2, Fig. 8.)
Grun 1863, vii, 26.
Cells stipitate; frustule in valve view linear-oblong with rounded extremities, in girdle view, with slightly raised centre and broadly rounded ends; surface transversely striate, with a clear axial area. Length, 100 to 500μ. This could be a variety of S. ulna, which shows great variation.
Distribution. Estuarine, occasionally marine. Epontic on Zostera, algae, and marine fouling test plates; not common in plankton hauls; Australia. Moreton Bay to Port Phillip.

151. Synedra undulata (Bail.) Greg. (Pl. 2, Fig. 9.)
Greg. 1857, 531, 14, 107.
Cupp 1943, 181.
Toxarium undulatum Bail. 1854, 15, 24–25.
Synedra undulata Bail. in Grun. 1861, 74.
Cells stipitate, solitary; frustule very long and narrow, slightly inflated central portion and extremities; margins undulate; striae in valve view marked, perpendicular to margin; no central area; pseudoraphe indistinct. Length, 300μ.
Distribution. Estuarine-neritic, tropical, marine. Epontic; found on fouling test plates. Australia: Heron Island, Moreton Bay. New Zealand: Dunedin.
152. Synedra fulgens (Grev.) W. Sm. (Pl. 2, Fig. 10.)
W. Sm. 1853, 74, 12, 103.
Boyer, 1927(a), 208.
Exilaria fulgens Grev. 1827, Pl. 291.
Licmophora fulgens Kütz. 1844, 123, 13 5.
Ardissonia fulgens (Grev.) Grun., in Cl & Grun. 1880, II, 17, 108.
Cells solitary, usually attached by a mucous pad, forming irregular, tufted colonies; valves linear, with slightly inflated central area, apices cuneate; valve surface with fine transverse striae, median line indistinct. Length, 100–750μ, breadth, up to 35μ.
Distribution. Estuarine-neritic; marine. Epontic on rocks and plants, and on fouling test plates. Rare in plankton hauls. Australia: abundant in Moreton Bay, Port Stephens, Port Jackson, Botany Bay, Port Hacking, Eden. New Zealand: Hauraki Gulf and Auckland Harbour.
153. Synedra ulna (Nitzsch) Ehr. (Pl. 2, Fig. 11a, b.)
Ehr. 1838, 211.
Boyer, 1927 (a), 198.
Cleve-Euler, 1953a, 60.
Bacillaria ulna, Nitzsch, 1817, 99.
Cells stipitate, colonial; frustules in valve view linear, suddenly constricted towards extremities; pseudoraphe distinct; striae transverse, median area quadrangular. Length, 280–320μ.
Distribution. Fresh to brackish water. Epontic. Australia: Head of Port Hacking, Lake Macquarie, Conjola, Lakes Entrance, Nepean River. Previously recorded from Australia by Ralfs. (1861), Boyer (1927a). New Zealand: Auckland Harbour, Wellington (Wainui), Wellington Harbour.
154. Synedra splendens Kütz. (Pl. 2, Fig. 12a, b.)
Kütz. 1844, 66.
Boyer 1927(a), 199.
Valves linear, elongate, swollen and rounded at ends; differs from S. ulna in the rounded apices.
Distribution. Australia: Heron Island.
155. Synedra closteroides Grunow var. jährnefelti Mölder, 1939. (Pl. 2, Fig. 13.)
In Cleve-Euler, 1953a, 60.
Cells attached by a mucous pad, forming clustered colonies; frustules in valve view more or less sigmoid, with inflated centre and gently tapering apices; striae transverse, longitudinal median line very fine; a very small species; Length 35μ.
Distribution. Estuarine, stenohaline, brackish (up to 2.5 per cent salt). Epontic. Australia. Lake Macquarie.
156. Synedra gaillonii (Bory) Ehr. (Pl. 2, Fig. 14.)
Ehr. 1838, 17.
Grun. 1862, 87.
Boyer. 1927(a), 204.
Cleve-Euler 1953(a), 60, 281.
Synedra gallionii W. Sm. 1853, 74, 30, 265.
Synedra gaillionii Hend. 1951, 36, 3.
Navicula gailloni Bory, 1822, 24.
Cells colonial, stipitate; frustules in valve view linear-oblong, gently curved and tapering slightly; the curvature is characteristic of New South Wales specimens; pseudoraphe distinct; valve surface with transverse, marginal, moniliform striae. Length, 100 to 150μ.
Distribution. Estuarine; marine. Epontic on algae, Zostera, Posidonia,, etc., and from fouling test plates; very common, occurring in large numbers. Australia: Heron

Island, Conjola, Port Hacking, Botany Bay. New Zealand: Hauraki Gulf, Lyall Bay (Petit 1877).
157. Synedra superba Kütz. (Pl. 2, Fig. 15.)
Kütz. 1844, 69.
Cl. & Grun. 1880, 108.
Boyer 1927(a), 209.
Valves broadly linear, slightly contracted towards the rounded ends; striae marked, transverse, punctate, traversed by three longitudinal lines. Length, 300μ.
Distribution. Australia: Lake Conjola. New Zealand: Lyall Bay (Petit 1877).
The following species of Synedra have been recorded by previous authors:—
-
S. acuta Ehr., 1839. (Ralfs in Pritch., 1861, 788.) Australia = S. ulna.
-
S. crystallina (Agh.) Kütz., 1844. (Hardy, 1910.) Kew, Victoria.
-
S. dissipata Kütz., 1844. (is Nitzschia dissipata (Kütz.) Grun. in Cl. & Grun., 1880). (Ralfs in Pritch., 1861). Australia.
-
S. pulchella (Ralfs) Kütz., 1944. (Hardy, 1910.) Kew, Victoria.
-
S. salina W. Sm., 1853. (Petit, 1877, 31.) Lyall Bay. = S. ulna.
Genus Grammatophora Ehr., 1839
Cells adnate or in zig-zag chains, usually free; frustules quadrangular, with rounded corners, divided by two nearly straight or sinuate, perforate septa; valves with straight, convex, or sinuous sides Pseudoraphe present; surface with transverse, punctate striae; chromatophores granular or in bands; pyrenoids may be present.
| 1. | Septa straight | |
| Septa undulate | G. serpentina | |
| 2. | Septa with knobbed ends | |
| Ends of septa not knobbed | G. marina. | |
| 3. | Septa h-shaped at margin | G. oceanica. |
| Septa slightly sigmoid at margin. | G. macilenta. |
158. Grammatophora marina (Lyngb) Kütz (Pl. 2, Fig. 16.)
Kütz. 1844, 17, 24.
W. Sm. 1856, ii, 42, 42, 314.
Boyer 1927 (a), 156.
Diatoma marinum Lyngb. 1819, 180, 62.
Cells forming a zig-zag chain or solitary; frustules in girdle view quadrangular, with rounded ends; in valve view, linear or linear elliptic; internal septa straight, with a semicircular curve near ends; valve surface striate. Length, 50–70μ.
Distribution. Estuarine-neritic; marine; free or epontic on algae, sea-grasses, rocks, fouling test plates, etc., planktonic. Australia: Moreton Bay, Port Stevens, Port Jackson, Botany Bay, Port Hacking, Lake Macquarie, Eden; Port Phillip, as epontic form; planktonic in Port Hacking. New Zealand: Auckland Harbour; Campbell Island; Lyall Bay and Foveaux Strait (Petit, 1877).
159. Grammatophora serpentina Ehr (Pl; 2,.Fig. 17.)
Ehr. 1844, 203.
Kutz. 1844, 129, 29, 82.
W Sm. 1856, 42, 43, 315.
Hend 1951, 38
G. pusilla Grev., 1863c, 181, 4, 15.
Cells united to form zig-zag chains, or solitary; frustule in girdle view quadrangular, in valve view linear-elliptic; septa robust, strongly undulate, hooked at ends, valve surface faintly striate. Length, 20–50μ.
Distribution. Estuarine; marine; epontic on algae. Australia: Port Phillip, Eden; Curtis Island by Grev., 1863c as G. pusilla. New Zealand: Campbell Island and Lyall Bay (Petit 1877).

160. Grammatophora oceanica Ehr. var. subtilissima (Pl. 2, Fig. 18.)
de Toni, 1894, 755.
Grammatophora subtilissima Bail. in Bail. 1854, 15.
G. subtilissima Bail. in Pritch. 1861.
Hend. 1951, 38, 12, 8–10.
Cells in zig-zag chains; frustules in girdle view linear-oblong; septa in girdle view appear h-shaped near margin, later straight, with knobbed ends; valve striae, very difficult to see. Length, 50–80μ.
Distribution. Estuarine neritic; marine. Usually planktonic. Australia: Port Hacking, Port Jackson, Sussex Inlet. New Zealand: Auckland Harbour: Oamaru (Gr. and St., 1886).
161. Grammatophora macilenta W. Sm. (Pl. 2, Fig. 19.)
W. Sm. 1856, 43, 41, 382.
Cleve-Euler 1953a, 12, 307.
Cells solitary or in zig-zag chains; rectangular in girdle view, lanceolate in valve view with slightly swollen central portion; septa straight, slightly sigmoid near margin, knobbed. Width, 35–40μ.
Distribution. New Zealand: Auckland Harbour.
The following species of Grammatophora have previously been recorded from this region:—
-
G. angulosa Ehr., 1839. (Petit, 1877, 33.) Lyall Bay.
-
G. arcuata Ehr., 1854 (Petit, 1877, 34.) Lyall Bay.
-
G. arnottii Grun in v H., 1885. (Boyer, 1927.) New Zealand (type loc.).
-
G. gibberula Kütz., 1844. (Petit, 1877, 33.) Lyall Bay.
-
G. longissima Petit, 1877. (Petit, 1877, 34) Lyall Bay.
-
G. undulosa Ehr., 1839. (Petit, 1877, 34.) Lyall Bay.
Genus Rhabdonema Kütz., 1844
Cells in ribbon-like chains, shortly stipitate. Frustules quadrangular, composed of numerous septate compartments, in valve view elliptical or linear-lanceolate; septa with one or more foramina; pseudoraphe present; costae transverse in valve and girdle views; puncta usually present.
162. Rhabdonema adriaticum Kütz. (Pl. 1, Fig. 20a, b, c.)
Kütz. 1844, 126, 18, 7.
Boyer 1927(a), 150.
Hend. 1937, 339; 1951, 39.
Cells in ribbon-like chains, shortly stipitate; frustules oblong to square, abruptly rounded: multiseptate, septa with three foramina in valve view; surface in valve view with marked transverse striae and hyaline areas at each end; in girdle view, costate, costae united by cross ribs. Length, 40–60μ.
Distribution. Estuarine, epontic, occurred on ship fouling test plates. Australia: Moreton Bay, Port Jackson, Botany Bay, Port Hacking, Corner Inlet, Port Phillip. New Zealand: Auckland Harbour, Campbell Island and Lyall Bay (Petit 1877).
The following additional species of Rhabdonema are recorded:—
-
R. arcuatum (Lyngb.) Kütz., 1844. (Petit, 1877, 34.) Campbell Island.
-
R. crozieri (Ehr.?) Fricke in A. S., 1900, 220 (= R. ehrenbergi Fr.?) (Petit, 1877, 35). Lyall Bay. = R. arcuatum.
-
R. hamuliferum Kitt. in Petit, 1877. (Petit, 1877, 35.) Lyall Bay on coralline algae.
-
R. minutum Kütz., 1844. (Petit, 1877, 34.) Campbell Island.
Genus Diatomella Grev. 1855
Frustules quadrangular, divided longitudinally by two septa each with a central and two terminal lacunae; valves oblong, or elliptic-lanceolate, slightly swollen in middle, ends rounded; differs from Grammatophora in having straight septa, and from Tabellaria in having perforate septa.

163. Diatomella balfouriana Grev. (Pl. 2. Fig. 21.)
Grev. 1855, 259.
Boyer 1927(a), 153.
Valve finely striate, punctate. Length, 40μ.
Distribution. Auckland Harbour: Disiphonia australis v. seelandica Ehr., 1869, recorded from New Zealand, is probably Diatomella balfouriana, though Ehrenberg's diagram is not clear.
Genus Terpsinoe Ehr., 1843
Cells free or in chains; frustules elliptical or quadrangular, constricted or crenate; septate, septa prominent in girdle view, either straight or curved at ends.
164. Terpsinoe musica Ehr. (Pl. 2, Fig. 22.)
Ehr. 1843,3, 4, 1, 7, 30.
Kütz. 1844, 128, 30, 72, 29, 94.
Boyer 1927(a), 144.
Rhabdonema musica (Ehr.) A. S. 1875.
Cells in ribbon-like chains, stipitate; frustules oblong in girdle view, with four septa resembling notes of music; in valve view with crenate margin and globose ends. Length, 60μ.
Distribution. Estuarine; brackish to marine; collected from a fouling test plate from Dunwich, Moreton Bay.
Terpsinoe americana (Bail.) Ralfs in Pritch., 1861. (Gr. & St., 1887, 77; A. S., 1893, 9, 10). Oamaru.
Genus Licmophora Ag., 1827 em. Roper, 1863
Cells flabellate, in clusters of two or more, on short or long stipes; frustules in girdle view cuneate, with apical corners slightly rounded, intercalary bands present; septa are more or less superficial and appear as lines penetrating from broad end of cell; valve view cuneate-lanceolate, pseudoraphe present; plastids granular or as plates.
| 1. | Valves with linear basal portion | L. gracilis. |
| Basal portion of valve not linear | ||
| 2. | Septa difficult to see | L. grandis v. divisa. |
| Septa obvious as lines in girdle view | ||
| 3. | Valves short, with broad, rounded base | L. abbreviata. |
| Valves narrow, lanceolate-cuneate, slightly inflated at base | L. flabellata. |
165. Licmophora flabellata (Carmichael) Ag. (Pl. 2, Fig. 23a, b.)
Ag. 1830–1832, 41.
Boyer 1927(a), 165.
Hendey, 1951, 39, 16, 1, 2, 12.
Echinella flabellata Carm, 1826 Mss. ex Roper, 1863.
Cells stipitate, arranged in flabellate manner from stipes which are frequently branched, up to 20 cells per stipe; frustule in valve view cuneate-lanceolate to clavate, faintly striate, base slightly swollen; in girdle view cuneate with numerous septa penetrating from upper part of cell; chromatophores give a double-banded effect. Length, 70–120μ.
Distribution. Estuarine-neritic; marine. Epontic, frequently but adventitiously planktonic. Very common, usually attached to algae, sea grasses, rocks, etc., and common on fouling test plates and in fish stomachs, frequently collected in estuarine and coastal phytoplankton samples. Australia: Heron Island, Moreton Bay, Clarence River, Port Stephens, Lake Macquarie, Port Jackson, Port Hacking, Jervis Bay, Eden, Port Phillip. New Zealand: Auckland Harbour.
166. Licmophora abbreviata Ag. (Pl. 2, Fig. 24.)
Ag. 1830–1832, 42.
Cleve-Euler, 1953, 17.
L. lyngbyei (Kütz.) Grun. 1867, 35.
Lebour 1930, 203, 165.
Hend. 1937, 337. 1951, 40.
Podosphenia lyngbyei Kütz. 1844, 121.
Cells stipitate, flabellate, when planktonic often solitary; frustules clavate in valve view, cuneate in girdle view with hardly rounded ends; septa visible as lines in girdle view; pseudoraphe very narrow but distinct; marginal striae in girdle view transverse. Length, 50–70μ.

Distribution. Estuarine-neritic, marine; epontic on algae, Zostera, rock, fouling test plates, in fish stomachs and planktonic; common. Australia: Moreton Bay, Port Stephens, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking, Eden. New Zealand: Auckland Harbour.
167. Licmophora grandis (Kütz.) Grun. var. divisa (Pl. 3, Fig. 25.)
Rhipidophora grandis Kütz. 1844, 122, 9, 8.
Licmophora divisa Kütz. 1844, 123, 11, 5.
Cells stipitate, usually solitary or in pairs; frustules in girdle view cuneate, in valve view clavate; septa difficult to define. Length 50–70μ.
Distribution. Estuarine, marine; epontic; from algal and seagrass washings. Australia: Port Hacking, Lake Macquarie; not common.
168. Licmophora gracilis (Ehr.) Grun. (Pl. 3 (a), Fig. 26a & b.)
Grun. 1867, 6, 34.
Boyer, 1927, 167.
Podosphenia gracilis Ehr. 1838, 17.
Frustules cuneate in valve view, narrow, septa not very deep; in valve view, clavate or obovate, linear towards base; pseudoraphe distinct. Length, 40–60μ.
Distribution. Lake Conjola.
Also Licmophora tincta (Ag.) Grun., 1867 (Podospheina) (Petit, 1877). Lyall Bay.
Genus Climacosphenia Ehr., 1841
Cells usually two or three, flabellate on short or long stipes; frustule in valve view clavate, in girdle view cuneate with intercalary bands, and two septa with numerous round foramina giving the cells a characteristic appearance in valve view; valve surface with fine transverse striae; chromatophores granular, numerous.
169. Climacosphenia moniligera Ehr. (Pl. 3 Fig. 27.a—d.)
Ehr. 1843, 411, 11, 6.
Kütz. 1844, 123, 29, 80.
Cells on very short stipes, frustules in girdle view cuneate, in valve view clavate; septa two with large foramina at apex, diminishing towards base; very fine moniliform striae. Length, from 187μ.
Distribution. Estuarine-neritic; marine. Algal washings and plankton tows: on fouling test plates. Australia: Port Hacking and other eastern estuaries and offshore on continental shelf. New Zealand: Lyall Bay, (Petit 1877).
Also C. australis Kütz., 1844. Type loc. Australia on Polysiphonia and other algae. Referred to by Ralfs, 1861; may = C. moniligera.
Genus Striatella Ag., 1832
Cells tabulate, cohering by opposite ends to form zig-zag chains, stipitate; frustules rectangular in girdle view, linear-elliptic in valve view, with many intercalary bands, septate; chromatophores granular or stellate; pyrenoids present.
| Septa apparently interrupted in pervalvar axis | S. interrupta. |
| Septa not interrupted in pervalvar axis | S. unipunctata. |
170. Striatella unipunctata (Lyngb.) Ag. (Pl. 3, Fig. 28.)
Ag. 1830–32, iii, 61.
Kütz. 1844, 125, 18, 1–4.
Boyer 1916, 38, 8, 22, 23.
Fragilaria unipunctata Lyngb. 1819, 62.
Cells stipitate, in zig-zag chains; frustules in girdle view rectangular, in valve view lanceolate, finely punctate; septa not interrupted in pervalvar axis; pseudoraphe distinct; plastids stellate in centre of cell. Length, 60–75μ.
Distribution. Estuarine-neritic, marine; planktonic and epontic usually epiphytic, also in fish stomachs; very common Australia: Moreton Bay, Clarence River, Port Hacking, Lake Macquarie, Eden, Port Phillip. New Zealand: Wellington Harbour.

171. Striatella interrupta (Ehr.) Heiberg (Pl. 3, Fig. 29.)
Heib. 1863, 202 (73), 5, 15.
Boyer 1916, 38, 8, 24.
Cleve-Euler, 1952a, 8, 297.
Tessella interrupta Ehr. 1838, 202.
Cells usually in ribbons, stipitate; frustules in girdle view quadrangular, with rounded corners, in valve view linear elliptic with distinct pseudoraphe; septa in girdle view apparently interrupted in pervalvar axis; plastids granular. Length, 30–40μ.
Distribution. Brackish water form, epiphytic, rarely planktonic. Australia: Moreton Bay, Lake Macquarie, Botany Bay, Port Hacking, Lake Illawarra, Lake Conjola, Lake Tuross.
Sub-order Raphidioidineae
Family Eunotiaceae
Genus Eunotia Ehr., 1837
Cells usually in ribbons, stipitate; frustules in girdle view quadrangular, with rounded transverse; pseudoraphe absent, narrow or indistinct; chromatophores one per cell.
| 1. | Dorsal side of valve biarcuate | 2. | |
| Dorsal side of valve crenate | 4. | ||
| Dorsal side of valve straight or slightly arcuate | E. gracilis. | ||
| 2. | Ends inflated dorsally | E. sarekensis. | |
| Ends not inflated | 3. | ||
| 3. | Ventral side straight or nearly so | E. bidentula. | |
| Ventral side concave | E. pectinalis var. undulata. | ||
| 4. | Valve elongate | 5. | |
| Valve not elongate | 6 | ||
| 5. | Valve with slight median swelling in ventral side | E. pectinalis var. ventralis. | |
| No ventral swelling | E. pectinalis var. undulata. | ||
| 6. | Striae branched | E. diadema. | |
| Striae unbranched | E. crista galli. |
172. Eunotia diadema Ehr. (Pl. 3, Fig. 30.)
Ehr. 1838, 193, 22.
Cleve-Euler 1953a, 125, 464.
Cells not elongate; valves crenate on dorsal, concave on ventral margin; striae coarse, often branched. Length, 25–40μ.
Distribution. Australia: Lake Dobson, Tasmania; fresh water.
173. Eunotia crista galli Cl. (Pl. 3, Fig. 31.)
Cl. 1891, 57.
Hust. in A. S. 1933, 382.
Cells not elongate; valves crenate on dorsal, concave on ventral margin; striae coarse, unbranched Length 40–50μ.
Distribution. Lake Dobson, Tasmania; fresh water.
174. Eunotia bidentula W. Sm. (Pl. 2, Fig. 32.)
W. Sm. 1856, 83.
Boyer 1927, 223.
Cleve-Euler 1953a, 128, 69.
Cells not elongate; valves straight or almost so on ventral, biarcuate on dorsal margin; apices rounded, somewhat produced; striae moderately marked, unbranched. Length, 40–50μ.
Distribution. Fresh water. Australia: Lake Dobson, Tasmania.
175. Eunotia pectinalis (Dillwyn) Rab.
Rab. 1864, 73.
Boyer 1927(a), 218.
Himantidium pectinale Kütz.
Conferva pectinalis Dillw., 1809.
Cells may be elongate, if so linear, slightly arcuate; striae light to moderately marked, punctate; ends not inflated.

var. undulata Ralfs in v H. 1885. (Pl. 3, Fig. 33a.)
van. H. 1885, 33, 17.
Boyer 1927(a), 218.
Hust. in A. S. 1924, 289.
Himantidium undulatum W. Sm. 1856, 33, 281.
Valves with dorsal margin biarcuate to crenate, and if crenate elongate, ends rounded; ventral margin concave, without median swelling. Length, 40 to 150μ.
Distribution. Fresh water. Australia: Lake Dobson, Tasmania.
var. ventralis (Ehr.) Hust. (Pl. 3, Fig. 33b.)
Hust. in A.S. 1911, 271, 9–12.
E. ventralis Ehr. 1843, 6–126.
Valves with dorsal margin evenly or unevenly convex and ventral margin with median swelling; striae not well marked. Length, 100–150μ.
Distribution. In brackish water. Australia: Port Hacking.
176. Eunotia sarekensis Cleve-Euler (Pl. 3, Fig. 34.)
Cleve-Euler 1953a, 117, 454.
Cells small, relatively broad; valves with concave ventral biarcuate dorsal margin, ends blunt, swollen ventrally; striae coarse, branched towards ventral margin. Length, 20–40μ.
Distribution. Fresh water. Australia: Lake Dobson, Tasmania.
177. Eunotia gracilis (Ehr.) Rab. (Pl. 3, Fig. 35.)
Rab. 1864, 1, 72.
Boyer 1927(a), 217.
Himantidium gracilis Ehr. 1843a, 129.
Valves slightly arcuate, narrow, sides parallel, apices slightly capitate, striae fine, lineate. Length up to 150μ.
Distribution. Fresh water. Australia: Lake Dobson.
The following additional Eunotias have been recorded:—
-
E. amphioxys (is Hantzschia amphioxys q. v.).
-
E. arcus (Himantidium) Ehr., 1838. Ehr., 1869. New Zealand.
-
E. cistula (Ehr., 1869). New Zealand. (Epithemia ?)
-
E. depressa (Ehr., 1869). New Zealand. (= E. pectinalis).
-
E. dianae (Ehr., 1869). New Zealand (is Hantzschia amphioxys v. elongata).
-
E. diodon Ehr., 1838. (Ehr., 1869.) New Zealand.
-
E. formica Ehr., 1854. (Ralfs in Pritch., 1861). Australia.
-
E. (Eunotiogramma?) lunaris (Ehr.) Grun. in vH., 1885. (Gr. & St., 1887, 77.) Oamaru.
-
E. monodon Ehr., 1838. (Ehr., 1869.) New Zealand.
-
E. praerupta Ehr., 1841. (Ehr., 1869). New Zealand.
-
E. rostrata (Ehr., 1869). New Zealand. (Nomen nudum.)
In addition, Ehrenberg (1869) has recorded from New Zealand two genera, Heterocampa and Ophidocampa, which appear to be identical with Eunotia eruca, differing in the number of crenations along the valves; E. eruca is also reported from New Zealand in A. S., 1913, 290, 8, and from Melbourne (Brightw., 1859, 179, 9 1, 1a).
Sub-order Monoraphidineae
Family Achnanthaceae
Genus Achnanthes Bory, 1822
Cells stipitate or free, single or in fasciae, arranged in palisade formation, stipe often long and curved; frustules in valve view linear-elliptic, often constricted in the middle; in girdle view arcuate; raphe present on lower valve, pseudoraphe on upper.
| Puncta in 2 rows between costae | A. longipes. |
| Single row of puncta between costae | A. brevipes. |
178. Achnanthes longipes Ag. (Pl. 3, Fig. 36a—c.)
Ag. 1824, 1.
Hend. 1951, 42, 1, 1–9, 2, 1–12, 3, 1–12, 16, 6, 7, 18, 2–5.
Cells solitary or more usually in ribbons, attached by a very strong and at times long, usually curved stipe; frustules in valve view linear-elliptic, often constricted in the middle.

in girdle view chevron-shaped; valve surface punctate; puncta in double rows separated by strong costae. Girdle with finely punctate parallel striations; pseudoraphe central on upper valve, strong raphe on lower. Length 75–85μ.
Distribution. Estuarine-neritic, marine; epontic, epiphytic and on fouling test plates, planktonic at times. Australia: Moreton Bay, Port Stephens, Port Jackson, Botany Bay, Port Hacking, Eden. New Zealand: Auckland Harbour, Hauraki Gulf, Lyall Bay, N. Z. (Petit 1877). This form is regarded by Hendey (1951) as extremely tolerant of copper, and is therefore important in studies of ship fouling.
179. Achnanthes brevipes Ag. (Pl. 3, Fig. 37a, b.)
Ag., 1824, 1; 1832, 59.
Schönfeldt, 1907, 122.
Boyer, 1916, 59, 16, 3; 1927, 232.
Hend., 1951, 41, 16, 9, 10.
Cells usually in short filaments, supported on short stipe; frustules in valve view linear-elliptic, with rounded extremities, slightly constricted towards the middle; in girdle view arcuate; valve surface punctate in transverse and longitudinal rows; pseudoraphe eccentric on upper valve; raphe supported by a stout costa dilated at central nodule to form a transverse stauros. Length, 85–120μ.
Distribution. Estuarine; brackish water. Australia: Lake Conjola. New Zealand: Auckland Harbour; Lyall Bay (Petit 1877).
The following species of Achanthes have been previously recorded:—
-
A. glabrata Grun., 1863. (Petit, 1877, 16; Cl. & Grun., 1880.) Lyall Bay.
-
A. inflata (Kütz.) Grun., 1880 (as A. ventricosa, Ehr., 1869). New Zealand.
-
A. subsessilis Kütz. 1844 (= A. brevipes) (Petit, 1877, 16). Lyall Bay.
-
A. trinodis (W. Sm.) Grun., in v H. 1881. (Ehr., 1869.) New Zealand.
Genus Cocconeis Ehr., 1838, em. Grun., 1868
Cells solitary, epontic, attached by a lower valve; frustules in valve view elliptic-oval, in girdle view arcuate, usually with a loculiferous annulus on the margin; upper valve with a pseudoraphe, and transverse or radiating punctate striae; lower valve with true raphe, and central nodule, sometimes with a marginal line; plastids may be present.
| Upper valve with coarse radial puncta | C. scutellum. |
| Upper valve with fine, radial to transverse striae | C. heteroidea. |
180. Cocconeis heteroidea Hantzsch (Pl. 3 Fig. 38.)
Hantz., 1863, 1; 21.
Boyer, 1927(b), 248.
Hust., 1931–33, 356, 811 (synonymy).
Cells solitary, usually attached; frustule elliptic to almost circular; upper valve with fine radial to transverse striae, interrupted by hyaline areas and crossed by curved longitudinal lines; lower valve with strongly marked radial striae, central nodule indistinct, raphe sigmoid, margin hyaline. Length, 40μ.
Distribution. Estuarine, marine; epiphytic or benthic. Occasionally on algae or sea grasses; often on fouling test plates. Australia: Lake Macquarie, Moreton Bay, Botany Bay, Port Hacking, Port Albert. New Zealand: Auckland Harbour, Lyall Bay (Petit 1877).
181. Cocconeis scutellum Ehr. (Pl. 3, Fig. 39a, b.)
Ehr., 1838, 194.
Hust., 1931–33, 337, 790 (synonymy).
Hend., 1951, 44, 10, 9.
Cleve-Euler, 1953b, 6, 489.
Cells epiphytic, attached, solitary; frustule in valve view broadly elliptical; valves dissimilar; upper valve with coarse radial puncta, and marked pseudoraphe, finely punctate at margin, with puncta in rows; lower valve with median line, raphe and small central area; finely radiately striate with broad marginal loculiferous rim. Length, 20–40μ.
Distribution. Estuarine; brackish water form, usually epontic on algae, sea grasses and fouling test plates; moderately common. Australia: Lake Conjola, Port

Hacking; recorded by Østrup, 1910, in A. S., 192, 36; 189, 21 (as C. paniformis Brun.) and from Lyall Bay, Foveaux Strait, and Campbell Island (Petit 1877).
The following species of Cocconeis have been recorded previously:—
-
C. adriatica Kütz. (Petit, 1877, 12.) Lyall Bay (= C. scutellum v. major Grun.)
-
C. australicum A. S. (A. S, 1876, 10, 34–35.) Australia.
-
C. australis Petit (Petit, 1877, 11). Lyall Bay.
-
C. barbadensis Grev., 1857. (Gr. & St., 1886, 322.) Oamaru.
-
C. caelata Arnott, 1868. (Petit, 1877, 12; A.S., 1893, 193, 53.) Lyall Bay, New New Zealand (= Diploneis campylodiscus Grun.)
-
C. costata Greg., 1855 (Gr. & St., fig. in A. S., 1894, 189, 8 = C. britannica Naeg. in Kütz. 1849 fide Hust. 1933, 333.) Oamaru.
-
C. crux Ehr. (Petit, 1877, 11.) Lyall Bay (= C. interrupta Greg.)
-
C. cyclophora Grun. (A.S., 1893, 197, 20, 28). S. Australia, Oamaru.
-
C. decipiens? Cl., 1873. (Petit, 1877, 11.) Campbell Island.
-
C. dirupta Greg., 1857. (Petit, 1877, 11.) Lyall Bay.
-
var.? (as C. hospes) (A.S., 1893, 198, 4–6.) Australia.
-
C. distans Greg., 1857. (Petit, 1877, 13.) Lyall Bay.
-
C. hospes A. S., 1893 v. C. dirupta var.
-
C. illustris A. S. (A. S., 1893, 192, 32.) Port Lincoln. (? = Mastogloia horvathiana qv).
-
C. lineata Ehr.=C. placentula v. lineata. (Ehr., 1869; Petit, 1877, 11.) Lyall Bay.
-
C. major Grev., 1857. (Petit, 1877, 12.) Lyall Bay, Campbell Island.
-
C. marginata Kütz. (prob. = C. scutellum var.) Petit, 1877). Lyall Bay.
-
C. maxima (Grun.) Perag. (A. S., 1894, 191, 44–46.) Oamaru.
-
C. mediterranea Kütz., 1844 = C. scutellum (Petit, 1877). Lyall Bay.
-
C. naviculoides Grev., 1857. (Gr. & St., 1887, 72.) Oamaru.
-
C. nodulifer Gr. & St., 1887 is Rhaphoneis nodulifera.
-
C. notata Petit, 1877. (Petit, 1877.) Lyall Bay.
-
C. pacifica Grun, in v H., 1880–1885. (Petit, 1877, 12.) Lyall Bay (= C. costata v. pacifica (Grun.) Cl.)
-
C. pediculus Ehr., 1838. (Ehr., 1869.) New Zealand.
-
C. pellucida Grun. in Rab., 1862. (Petit, 1877, 11; A. S., 1894, 191, 48.) Lyall Bay, Campbell Island; Oamaru.
-
C. placentula v. euglypta Ehr., 1838. (Østrup, 1910.) Australia.
-
v. lineata (Ehr.) (Ehr., 1869.) New Zealand.
-
C. pseudo-marginata Greg. 1857 non Rab. v. intermedia Petit. (Petit, 1877, 12: Gr. & St., 1886, 322.) Lyall Bay, Oamaru (= C. britannica Naeg.)
-
C. punctata Ehr. = (C. placentula Ehr., 1838). Ralfs in Pritch., 1861 Australia.
-
C. wrightii O'Meara. (Petit, 1877, 12.) Lyall Bay.
Sub-Order Biraphidineae
Family Naviculaceae
Genus Navicula Bory 1894
Cells solitary or colonial in mucous sheaths; frustules in valve view linear-elliptic or oblong, with rounded, capitate or rostrate ends; raphe present on each valve; axial and central areas usually distinct; striae parallel or radiate, finely or coarsely punctate, lineate or apparently smooth; plastids vary; pyrenoids usually absent.
| 1. | Frustules in valve view elliptical | 2. | |
| Frustules in valve view elliptic-lanceolate | 5. | ||
| Frustules in valve view lanceolate | 10. | ||
| Frustules in valve view rhombic-lanceolate | N. cuspidata. | ||
| 2. | Two hyaline lateral areas constricted at central area | 3. | |
| Axial area narrow, linear, central area rounded to stellate | N. clementis. | ||
| Axial area narrow, with dilated central area | N. tuscula. |

| 3. | Lateral areas convergent at apices | N. forcipata. | |
| Lateral areas not convergent at ends | 4. | ||
| 4. | Axis elevated in girdle view | N. subcarinata. | |
| Axis not elevated | 14. | ||
| 5. | Cells in gelatinous matrix | 6. | |
| Cells solitary | 7. | ||
| 6. | Apices rounded in valve view | N. grevillei. | |
| Apices obtuse, constricted | N. viridula. | ||
| 7. | Central area slightly produced on one side, giving an irregular appearance | N. peregrina. | |
| Central area not markedly asymmetrical | 8. | ||
| 8. | Valve coarsely punctate | 11. | |
| Valve not coarsely punctate | 9. | ||
| 9. | Axial area narrow, linear | 13. | |
| Axial area broad (half valve width) | N. americana. | ||
| Axial area lanceolate, indented centrally | N. yarrensis. | ||
| 10. | Surface striate | N. gracilis. | |
| Surface costate | 12. | ||
| 11. | Central area narrow, straight; puncta irregular near central area | N. brasiliensis. | |
| Central area wider between central and terminal nodules; puncta regular | N. granulata. | ||
| 12. | Apices produced | N. cyprinus. | |
| Apices sub-acute | N. radiosa. | ||
| 13. | Valve centrally depressed | N. meniscula. | |
| Valve not centrally depressed | N. clementis. | ||
| 14. | Lateral areas of more or less even width | N. lyra. | |
| Lateral area wide in the middle, tapering to apices | N. spectabilis. |
182. Navicula cyprinus (W. Sm.) Boyer (Pl. 4, Fig. 40.)
Boyer, 1916, 95, 26, 21.
Hend., 1951, 47, 9.9.
Pinnularia cyprinus Ehr., 1844, 7, i, 11, 7.
Navicula cyprinus Kütz., 1844, 99, 29, 35.
Pinnularia cyprinus Ehr. in W. Sm. 1853, 57, 18, 176.
Cells solitary; frustules in valve view lanceolate, in girdle view linear with produced apices: surface costate, costae transverse at extremities, radiating near centre, and somewhat sigmoid. Length, 70–85μ.
Distribution. Estuarine; euryhaline, benthic, occasionally epontic on weeds and fouling test plates. Australia: Heron Island, Lake Macquarie, Port Hacking; freshwater, Lake Conjola. New Zealand: Wainui (Wellington).
183. Navicula brasiliensis Grün. (Pl. 3, Fig. 41.)
Grün., 1863, 152, 14, 10.
Hend., 1953, 157, 1, 3.
Cells solitary; frustules in valve view elliptic-lanceolate, apex rounded; striae coarsely punctate, puncta irregular near central area; central area narrow, almost uniform in width Length, 72–90μ. Hendey (1.c.) examined type specimens and separated this species from other closely allied forms.
Distribution. Estuarine; euryhaline; benthic as a rule but also epontic on weeds and fouling test plates. Australia: Lake Macquarie, Port Hacking. New Zealand: Oamaru (Gr. and St., 1887).
184. Navicula grevillei (Ag.) Cl. (Pl. 3, Fig. 42a; Pl. 4, Fig. 42b.)
Cl., 1894, 152.
Boyer, 1916, 99, 31, 3–4; 1927, 376.
Hend., 1951, 46, 4, 1–6, 5, 1–4, 6, 1–13, 7, 1–5.
Schizonema grevillei Ag., 1830, 19.
W. Sm, 1856, 77, 68, 364.
Cells usually colonial, enclosed in a gelatinous tube, much branched and tufted, usually uniseriate, one end of each cell overlapping its neighbours; frustules in girdle view oblong, with rounded corners, in valve view elliptic-lanceolate; valve surface with transverse and slightly, radiate striae, girdle longitudinally striate; axial area narrow and linear Length 28–40μ.
Distribution. Estuarine; euryhaline; benthic; forms slime on rocks and sand, and acts as shore binding agent; also epipytic slime on algae and marine grasses, and

epontic on fouling test plates; common; widely distributed on shores in Australia and New Zealand.
185. Navicula lyra Ehr. (Pl. 4, Fig. 43a.)
Ehr., 1843b, 131.
Kütz., 1844, 94, 28, 55.
Hend., 1951, 50, 10, 1.
Cells solitary; frustules in valve view elliptical, apices gently rounded; this species group is characterized by two hyaline lateral areas constricted in the central area, and accounting for the specific name; striae transverse, punctate. Length, 60–150μ.
Distribution. Estuarine; euryhaline; benthic. Australia: Port Hacking, found on a few occasions on surface of muds.
N. lyra v. australica is recorded by Schmidt (1875), from Port Lincoln, v. atlantica by Petit (1877) from Foveaux Strait, and v. bullata by Norman from Shark Bay (type loc.).
Navicula lyra var. elliptica A. S. (Pl. 4. Fig. 44b, c, d.)
A.S., 1874, 1, 39.
Hend., 1951, 50, 10, 4–5.
Cells solitary; frustules in valve view elliptical with gently rounded ends; lateral areas converging towards the ends; surface transversely striate; striae reduced to one or two puncta in the central area and towards the apices. Length, 50–150μ.
Distribution. Estuarine; euryhaline; benthic; sometimes epiphytic, and epontic. on fouling test plates. Australia: Heron Island, Moreton Bay, Lake Macquarie, Botany Bay, Port Hacking.
186. Navicula subcarinata, Hendey (Pl. 4, Fig. 44.)
Hend., 1951, 50, 10, 2–3.
N. lyra var. subcarinata Grun., in A. S., 1875, 2, 5.
Cells solitary; frustule in valve view elliptical with slightly rounded or produced extremities; in girdle view the axial area appears elevated, particularly at the extremities; this may be a variety of N. lyra, as Grunow suggests, but the central area seems characteristic. Length 72–100μ.
Distribution. Estuarine; euryhaline; benthic, but occasionally epontic on weeds and fouling test plates. Australia: Heron Island, Moreton Bay, Lake Macquarie, Botany Bay and Port Hacking. New Zealand: Auckland Harbour.
187. Navicula peregrina (Ehr.) Kütz. (Pl. 4, Fig. 45.)
Kütz., 1844, 97, 28, 52.
Boyer 1916, 94 26, 20; 1927, 339.
Hend., 1951, 52, 16, 5, 17, 12.
Pinnularia peregrina Ehr., 1844, 133.
Cells solitary; frustules in valve view linear-elliptic with abruptly rounded ends; valves with narrow axial area central area clear, oval or rectangular, slightly produced on one side giving a very uneven appearance; surface striate, striae transverse, radiating towards ends. Length 100–150μ.
Distribution. Estuarine; euryhaline, benthic, occasionally epontic on algae and marine fouling test plates. Australia: Port Hacking, Lake Macquarie; not very common. New Zealand. As Pinn. peregrina form by Ehr., 1869.
188. Navicula gracilis Ehr. (Pl. 4, Fig. 46.)
Ehr., 1838, 176, 13, 11.
Kütz. 1844, 91, 3, 48.
Boyer, 1927(b), 385.
Cleve-Euler, 1953b, 130, 756, a-d.
Cells colonial in gelatinous tube; frustules in valve view lanceolate with obtuse extremities: striae transverse, short in central area radial, then more or less transverse. Length, 30–50μ.
Distribution. Fresh water form; found in brackish water at Lake Conjola, Australia.
189. Navicula viridula Kütz. (Pl. 3, Fig. 47.)
Kütz., 1844, 91, 30, 47; 4, 10, 15.
Boyer, 1927, 388.
Schizonema thwaitesi Grun. in van H., 1880–85, 15, 38.
Cleve-Euler, 1953b, 150, 805a.

Cells usually colonial in sheath; frustules enclosed in gelatinous tube forming dense, crowded colonies; in valve view lanceolate-elliptic, with obtuse, constricted apices; striae transverse to radial; central area large, oval. Length, 50–18μ.
Distribution. From brackish water at Lake Conjola, Australia.
190. Navicula americana Ehr. (Pl. 4, Fig. 48.)
Ehr., 1843, 129.
Boyer, 1916, 98, 26, 8; 1927, 372.
Cleve-Euler, 1953b, 183, 887.
Cells solitary; frustules linear-elliptic with broadly rounded ends; axial area broad, about half width of valve, dilated centrally; striae parallel with the middle, radiate near extremities. Length, 180μ.
Distribution. Brackish water at Lake Conjola; recorded from Australia by Østrup (1910).
191. Navicula forcipata Grev. (Pl. 4, Fig. 49.)
Grev., 1859, 83, 6, 10–11.
Hend., 1951, 48, 12, 1.
Cleve-Euler, 1953b, 105, 709 a, b.
Cells solitary; frustules in valve view elliptical; surface striate, striae transverse, punctate; striae interrupted by two hyaline areas constricted in the middle and convergent at the ends, resembling Navicula lyra. Length, 50μ.
Distribution. Estuarine; brackish water. Australia: Lake Conjola, uncommon.
192. Navicula yarrensis Grun. (Pl. 4 Fig. 50.)
Grun. in A. S., 1876, 46.
Boyer, 1927(b), 418.
Valves elliptic-lanceolate with obtuse ends; axial area lanceolate, widened centrally; striae radiate in middle, slightly convergent and closer at ends. Length, 60–90μ.
Distribution. Brackish water. Australia: Lake Macquarie, Lake Illawarra, Conjola, Mallacoota, Betka River; type locality Yarra Yarra, Victoria (fossil). A. S. (1876).
193. Navicula cuspidata Kütz. (Pl. 4, Fig. 51.)
Kütz, 1844, 94.
Boyer, 1927(b), 366.
Valves rhombic-lanceolate with acute ends; axial area narrow, not widened centrally; striae transverse, parallel, finely punctate. Some valves have a strongly costate inner stratum. Length, 80–150μ.
Distribution. Lake Conjola. Recorded from Australia by Ralfs (1861).
194. Navicula tuscula (Ehr.) van H. (Pl. 4, Fig. 52.)
van H., 1885, 95.
Boyer, 1927(b), 385.
Pinnularia tuscula Ehr., 1840, 21.
Stauroptera tuscula Ehr., 1854, 6.
Stauroneis punctata Kütz., 1844, 106.
Navicula punctata (Kütz.) Donk., 1871, 36.
N. amphibola Cl.? in Cleve-Euler, 1953b.
Valves elliptical, with rostrate-capitate ends; axial area narrow; central area dilated into large, irregularly divided transverse area; striae coarsely lineate, usually interrupted by several longitudinal blank lines, radiate in curved lines. Length, 40–70μ.
Distribution. Lake Conjola.
195. Navicula clementis Grun. (Pl. 4, Fig. 53.)
Grun., 1882, Cleve-Euler, 1953b, 148.
Valves broad-lanceolate to elliptic with rostrate to swollen, rarely produced ends; axial area narrow, linear, central area irregularly rounded to almost stellate with 1–4 isolated puncta near the central nodule; striae radial, fine, closer at ends. Length, 30–60μ.
var. rhombica Brockmann, 148.
In Cleve-Euler, 1953b, 148.
Broadly rhombic-lanceolate with slightly produced, blunt ends. Length, 35–40μ.
Distribution. Australia: Lake Conjola.
196. Navicula granulata Bail. (Pl. 4, Fig. 54a, b.)
Bail., 1853, 7, 10.
Boyer, 1927b, 404.
Hend, 1953.

This species differs from N. brasiliensis in that the central area is wider, slightly panduri-form, while the puncta are regular near the central area; intergrades occur between the two species (Pl. 4, Fig. 54b), and it seems doubtful whether they can be maintained. Length. 80–90μ.
Distribution. Australia: Port Hacking, Lake Macquarie, Gippsland Lakes. New Zealand: Auckland Harbour. Recorded from Australia by Østrup (1910).
197. Navicula radiosa Kütz. (Pl. 5. Fig. 55.)
Kütz., 1844, 91.
Boyer. 1927b, 3, 97.
Cleve-Euler, 1953b, 816.
Cells solitary; valves lanceolate, narrow, with sub-acute ends; axial area very narrow, indistinct; central area small; costae radiate in the middle, convergent at ends. Length, 80–120μ.
Distribution. Fresh to brackish water Australia: Lake Dobson, Port Hacking. Recorded from Australia by Østrup (1910).
198. Navicula meniscula Schumann (Pl. 5, Fig. 56.)
Schumann, 1864–9.
Hust in A.S., 1934, 399, 30–33.
Hohn, 1951, 16, 34, 129.
Cells solitary, valves elliptic-lanceolate with acute ends; costate, punctate, somewhat irregular near central nodule. Length, 50μ.
Distribution. Fresh water. Australia: Lake Dobson, Tasmania.
199. Navicula spectabilis Greg. (Pl. 5, Fig. 57.)
Greg, 1857, 481.
Boyer 1927, 412.
Cleve-Euler 1953b, 107, 712.
Valves elliptic; lateral areas broad, constricted in middle, and tapering sharply at apices, with faint striae in middle of area; a row of punctate striae on each side of axial area; differs from N. lyra and N. hennedyi in shape of axial area. Striae radiate, coarse, parallel to transverse axis Length 70–110μ.
Distribution. Australia: Port Hacking.
The following forms have been recorded previously as Naviculas; their generic affiliations will be indicated.
-
N. affinis Ehr. var. undulata Grun. is Neidium affine var. undulatum (Petit, 1877). Lyall Bay.
-
N. amphilepta Ehr. (Ehr., 1869). New Zealand. (= N. affinis).
-
N. amphirhynchus v. Neidium amphirhynchus (Ehr.) Boyer. (Ralfs in Pritch. 1361). Australia.
-
N. amphisbaena (is Caloneis amphisbaena. Ehr., 1869). New Zealand.
-
N. apis Ehr. (is Diploneis adonis var. Oamaruensis Cl.). (Gr. & St., 1886. 322: A.S. 1890, 172, 7.) Oamaru.
-
N. atomas (Naegeli) Grun., 1860. (Synedra atomas Nag. in Kütz., 1849.) (Østrup, 1910, 68.) Australia.
-
N. (stauroneis) Australis (Grev.) (Grev. 1863c) type loc. Harvey Bay. (? = N. biformis Grun.)
-
N. bacilliformis Grun. in Cl. & Grun., 1880. (Østrup, 1910; Boyer, 1927, 369.) Australia, New Britain.
-
N. bacillum Ehr., 1854. (Østrup, 1910, 40.) Australia.
-
N. biconstricta Gr. & St., 1887, 132 is a Diploneis. Oamaru.
-
N. biseriata Petit, 1877 (non. Diploneis biseriata Cl.) (Petit, 1877.) Foveaux Strait (= Caloneis biseriata (Pet.) Cl.)
-
N. campbellu Petit, 1877 (non N. campbellu Perag., 1915). (Petit, 1877, 22.) Campbell Island (Caloneis campbellu (Pet. Cl.)
-
N. cancellata Donk., 1871. (Petit, 1877.) Foveaux Strait.
-
N. capitata Ehr. (Ralfs in Pritch., 1861, 900). Australia.
-
N. cardinalis Ehr. (Ralfs in Pritch., 1861.) Australia.
-
N. cari? (Ehr., 1869). New Zealand (=N. cincta v. cari (Ehr.) Cl.)

-
N. chilensis (Ehr.) Kütz., 1844 (Ralfs in Pritch., 1861, 907). Australia. (= Pinn. borealis v. brevistriata Aust.)
-
N. cincta (Ehr.) vH., 1885 (Pinnularia cincta Ehr., 1854.) (Navicula Kützingiana H. L. Sm., 1878.) (Østrup, 1910, 75.) Australia.
-
N. clancula A.S., 1875 (is Diploneis interrupta var. clancula (A.S.) Cl. (Ralfs in Pritch, 1861.) Australia.
-
N. crabro Ehr. (is Diploneis crabro Ehr., 1854.) (Petit, 1877.) Lyall Bay.
-
N. decora Gr. & St., 1887. (Gr. & St., 1887, 133; A.S., 1890.) Oamaru.
-
N. decussata Erh.? (Petit, 1877, 23). Lyall Bay.
-
N. diversa Grev. 1863c. Curtis Island (type loc.) (= Diploneis weissflogn A.S.?).
-
N. definita Gr. & St. (Gr. & St., 1887, 73). Oamaru.
-
N. diconstricta Gr. & St. (Gr. & St., 1887, 132). Oamaru. (? Diploneis.)
-
N. dispersa Gr. & St. (Gr. & St., 1887, 132) Oamaru.
-
N. disphenia (Ehr.) Kütz., 1844 (Pinnularia disphenia Ehr., 1843). Ralfs in Pritch., 1861, 908. Australia (Ehr., 1869). New Zealand.
-
N. distans W. Sm., 1853. var. (Petit, 1877, 26). Foveaux Strait.
-
N. dubia (Ehr.) (v. Neidium dubium (Ehr.) Cl., 1894). (Ralfs in Pritch., 1861.) Australia.
-
N. entomon Ehr. in Kütz., 1844 (is Diploneis gemmatula (Grun.) Cl., 1894; Petit, 1877.) Lyall Bay.
-
N. esox Kütz., 1844 (is Pinnularia esox Kütz.) Cl., 1891. (Petit, 1877.) Campbell Island.
-
N. firma Kütz., 1844 (is Neidium iridis (Ehr.) Cl., 1894). (Petit, 1877; Boyer, 1927, 321.) Foveaux Strait; Australia.
-
N. fortis (Greg.) Donk, 1871. (Petit, 1877, 22.) Foveaux Strait.
-
N. fusca Ralfs in Pritch., 1861 (is Diploneis fusca (Greg.) Cl., 1894). (Petit, 1877, 25.) Foveaux Strait.
-
N. gastrum exigua (Greg.) Grun., 1880. (Østrup, 1910, 78.) Australia.
-
N. gemmata and v. mediterranea Grun. (are Diploneis gemmata (Grev.) Cl. 1894. (Petit, 1877; Gr. & St., 1886.) Foveaux Strait, Oamaru.
-
N. gracilis Ehr., 1838 (Ehr., 1869). New Zealand.
-
N. graeffii Grun. in A.S., 1875 (is Diploneis graeffii (Grun.) Cl. 1894.) (Petit, 1877, 24.) Lyall Bay.
-
N. gotlandica Grun., 1880. (Østrup, 1910, 78.) Australia.
-
N. gruendleri A.S., 1873 (is Diploneis gruendleri (A.S.,) Cl., 1894). (Cl. & Grun., 1880.) Oamaru.
-
N. hennedyi W. Sm., 1856. (Petit, 1877.) Foveaux Strait.
-
N. hochstetteri Grun. in A.S., 1875. (Petit, 1877.) Foveaux Strait.
-
N. incurvata Greg., 1856 (is Diploneis incurvata (Greg.) Cl., 1894). (Petit, 1877.) Lyall Bay.
-
N. inelegans Gr. & St. (Gr. & St., 1887, 132; A.S., 1934, 393, 12, 13.) Oamaru.
-
N. inflexa (Greg.) Donk., 1871. (Petit, 1877, 22.) Lyall Bay.
-
N. inhalata A.S., 1875 (Petit, 1877, 24.) Lyall Bay.
-
N. interlineata Gr. & St. (Gr. & St., 1886). Oamaru. (N. lyra gp.)
-
N. interlinedia Gr. & St. (A.S., 1893, 204, 11.) Oamaru.
-
N. johnsoniana Grev., 1861. Harvey Bay; New Zealand. (= Trachyneis johnsoniana (Grev.) Cl.)
-
N. lanceolata (Agh.) Kütz., 1844. (Østrup, 1910, 80.) Australia.
-
N. liber W. Sm., 1853. (Is Caloneis liber (W. Sm.) Cl. 1894.) (Petit, 1877, 21.) Lyall Bay.
-
N. linearis Grun., 1860 (is Caloneis linearis (Grun.) Boyer, 1927).
-
N. lobata Gr. & St. (Gr. & St., 1887, 133.) Oamaru.
-
N. longa (Greg.) Ralfs, 1861. (Petit, 1877, 26.) Foveaux Strait.

-
N. luxuriosa Grev., 1863. Type loc. N.S. Wales, Australia.
-
N. margino-lineata Gr. & St. (Gr & St., 1887, 132). Oamaru. (= Caloneis musca v. marginolineata.
-
N. margino-punctata Gr. & St. (Gr.& St., 1887, 132). Oamaru. (= Caloneis musca v. marginolineata.)
-
N. maxima Greg., 1857. (Is Caloneis liber (W. Sm.) Cl., 1894.) (Petit, 1877, 21.) Foveaux Strait.
-
N. mediopartita Gr. (A.S., 1893, 204, 6). Oamaru.
-
N. microsoma Kütz., 1844. (Petit, 1877, 20.) Campbell Island.
-
N. nitescens Ralfs in Pritch., 1861. (Is Diploneis nitescens (Greg.) Cl., 1894.) (Petit, 1877, 24.) Foveaux Strait.
-
N. nivalis Ehr. (Østrup, 1910, 37.) Australia. (= N. mutica v. nivalis (Ehr.) Aust.)
-
N. nobilis (Ehr.) Kütz., 1844. (Boyer, 1927, 445.) Port Lincoln.
-
N. notabilis A.S., 1875 (Petit, 1877, 25). Foveaux Strait.
-
N. oamaruensis Grun. (Is Diploneis adonis (Grun.) Cl. var. oamaruensis Cl., 1894.) (A.S., 1893, 204, 13.) Oamaru.
-
N. ovulum Grun., 1860. (Petit, 1877, 21.) Lyall Bay. (= Diploneis litoralis (Donk.) Cl.).
-
N. oxyptera Kütz., 1844. (Ralfs in Pritch., 1861, 906.) Australia.
-
N. pachyptera (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia. (= Pinn. lata v. costata.)
-
N. placentula Ehr., 1843. (Østrup, 1910, 82.) Australia.
-
N. placita Gr. & St. (Gr. & St., 1887, 133.) Oamaru. (= N hochstetteri v. placita.)
-
N. praetexta Ehr., 1840 (Petit, 1877, 24; Gr. & St., 1886, 323). Lyall Bay, Foveaux Strait, Oamaru.
-
N. quarnerensis Grun., 1860 var. dilatata Petit, 1877. (Is Mastogloia jelineckii Grun.) (Petit, 1877, 21.) Campbell Island.
-
N. radiosa Kütz., 1844. (Østrup, 1910, 82.) Australia.
-
N. retusa Breb. in Cl., 1895. (Is Pinnularia ambigua Cl., 1895.) (Petit, 1877, 22.) Lyall Bay.
-
N. rhomboides Ehr. (Is Frustulia rhomboides.) (Ralfs in Pritch., 1861.) Australia.
-
N. rhombus Petit, 1877. (Is Mastogloia rhombus (Petit) Cl., 1895.) (Petit, 1877 23.) Lyall Bay.
-
N. roteana (Rab.). vH., 1880. (Østrup, 1910, 323). Australia.
-
N. salicula Ehr. (Ralfs in Pritch., 1861). Australia.
-
N. salandriana Grun. (Gr. & St., 1887, 73.) Oamaru.
-
N. serians Breb. (Is Anomoeoneis serians (Breb.) Cl., 1894. (Ralfs in Pritch. 1861.) Australia.
-
N. smithii Breb. (Is Diploneis smithii (Breb.) Cl., 1894. A.S., 1875, 7, 18; Petit. 1877.) Australia; Foveaux Strait; v. minor Petit, 1877; non West, 1812. (Is D. smithii) (Petit, 1877; Gr. & St., 1886, 322.) Lyall Bay, Oamaru.
-
N. spathifera (Gr. & St., = N. lobata Gr. & St., 1887).
-
N. sparsipunctata Gr. & St. (Gr. & St., 1886) Oamaru.
-
N. splendida Greg., 1856. (Is Diploneis splendida (Greg.) Cl., 1894.) (Petit, 1877, 26.) Lyall Bay.
-
N. styliformis Ehr. (Ralfs in Pritch., 1861, 907). Australia. (= Pinn. streptoraphe.)
-
N. trilineata Gr. & St. (Gr. & St., 1887, 132.) Oamaru.
-
N. variolata Cl. (A.S., 1890, 174, 26). Oamaru.
-
N. weissflogii A.S., 1875. (Is Diploneis weissflogii (A.S.) (Cl., 1894.) (Petit, 1877. 26.) Lyall Bay.

Genus Frustulia Ag. 1824
Cells free or in mucous sheaths; valves linear-elliptic to rhombic-lanceolate; median line between two siliceous ribs; central and terminal nodules more or less elongated.
200. Frustulia rhomboides (Ehr.) de Toni (Pl. 6, Fig. 58a, b.)
de Toni, 1891, 2, 277.
Navicula rhomboides Ehr., 1843, 3, 15.
Valves lanceolate or rhombic-lanceolate, obtuse; central and terminal nodules short; striae transverse, punctate, puncta in longitudinal rows. Length, 70–140μ.
Distribution. Freshwater; Lake Conjola, Lake Dobson, Nepean River. Previously recorded from Australia (Pritchard 1861, 903, and Østrup 1910, 33). New Zealand: Dunedin.
Also Frustulia lanceolata (Agh.) Kütz., 1844. (Østrup, 1910, 80.) Australia.
Genus Neidium Pfitzer 1871
Valves linear, linear-lanceolate or elliptical, with obtuse, acute, produced, sub-rostrate or sub-capitate ends; striae usually oblique, finely punctate, crossed by one or more blank lines on each side; axial area usually narrow or indistinct; median line with central pores in opposite directions; terminal fissures appearing trifurcate.
| 1. | Ends rostrate or protracted | N. affine. | |
| Ends cuneate | N. amphigomphus. | ||
| Ends not rostrate, rounded | 2. | ||
| 2. | Valves linear | N. bisulcatum. | |
| Valves linear-elliptic | N. iridis. |
201. Neidium bisulcatum (Lagerstet) Cleve (Pl. 5, Fig. 59.)
Cl., 1894, 26, 68.
Boyer, 1927b, 323.
Navicula bisulcata Lager., 1873, 1, 31.
Valves linear with rounded ends; central area dilated transversely. Length, 55μ.
Distribution. Fresh-brackish water. Australia: Lake Conjola.
202. Neidium affine (Ehr.) Pfitzer (Pl. 5, Fig. 60a.)
Pfitz., 1871, 2, 39.
Boyer, 1916, 83, Navicula affine Ehr., 1843, 129.
Cells in valve view linear with protracted, sub-rostrate or capitate ends; striae oblique in middle, convergent at ends. Length very variable.
Distribution. Fresh water; Lake Dobson, Tasmania; recorded from Australia by Østrup (1910); New Zealand (Ehr., 1869, Lyall Bay; Petit, 1877).
var amphirhynchus (Ehr.) Cl. (Pl. 5, Fig. 60b.)
Cl., 1894, 26, 68.
Hohn, 1951, 77.
N. amphirhynchus Ehr., 1843.
Boyer, 1927b, 321.
Valve linear-elliptic with broad, rostrate ends.
Distribution. Fresh to brackish water; Lake Dobson, Port Hacking; recorded from Australia by Ralfs, 1861.
203. Neidium amphigomphus (Ehr.) Pfitz. (Pl. 5, Fig. 61.)
Pfitz., 1871, 2, 39.
Boyer, 1927b, 322.
Navicula amphigomphus Ehr., 1843, 129.
Valves linear, with straight sides and cuneate ends; striae slightly oblique, punctate; central area large, dilated transversely. Length, 100–120μ.
Distribution. Fresh to brackish water. Australia: Lake Dobson, Port Hacking.
204. Neidium iridis (Ehr.) Cl. (Pl. 5. Fig. 62.)
Cl., 1894, 26, 39.
Boyer, 1927b, 321.
Navicula iridis Ehr., 1843, 130.
Valves linear-elliptic with rounded ends; striae slightly oblique. Length, 100–150μ.
Distribution. Fresh to brackish water. Australia: Lake Dobson, Port Hacking. New Zealand Foveaux Strait (Petit, 1877).

N. dubium (Ehr.) Cl., 1894 (as Navicula dubium) (Ralfs, 1861, Østrup, 1910). Australia.
Genus Trachyneis Cl. 1894
Cells solitary; valves elliptic-lanceolate, lanceolate or rhomboid Axial area linear or lanceolate, frequently asymmetrical; central area asymmetrical, or widened into a fascia; the valve has a threefold structure, an inner, coarsely punctate stratum, an outer, finely punctate layer; and an intermediate network of anastomosing costae, forming rectangular or rhomboid alveoli.
205. Trachyneis aspera (Ehr.) Cl. (Pl. 5, Fig. 63.)
Cl., 1894, 191.
Pinnularia aspera Ehr., 1840, 213.
Navicula aspera Ehr., 1854, 35.
Frustule rectangular in girdle view, with rounded angles and a median constriction; girdle broad, finely punctate; valves elliptical to rhomboid with obtuse ends; axial area narrow, unilateral; central area transversely dilated, widened outward; alveoli radiate in oblique rows. Length, 100–200μ.
Distribution. Common on Heron Island, in east coast estuaries and Auckland Harbour. Previously recorded from Australia by Østrup (1910) and New Zealand by A.S. (1875).
Genus Pinnularia Ehr., 1843
Cells single, valves linear or nearly so; axial area broad; central and terminal areas large; costae smooth, differentiating this genus from Navicula; chromatophores two.
| 1. | Ends acute | P. splendida. | |
| Ends subcapitate | 2. | ||
| Ends rounded, not subcapitate | 3. | ||
| Ends slightly gibbous | P. major. | ||
| 2. | Striae convergent at ends | P. gibba. | |
| Striae not convergent at ends | P. stauroplera. | ||
| 3. | Striae short, almost marginal | P. brevicostata. | |
| Striae long | P. borealis. |
206. Pinnularia major W. Sm. (Pl. 5, Fig. 64.)
W. Sm., 1853, 1, 54.
Boyer, 1916, 102, 28, 4.
Navicula major Kütz., 1844, 97, 4, 19–20.
Cells solitary; valves linear, usually slightly swollen centrally, ends slightly gibbous; raphe oblique; axial area less than ⅓ width of valve, convergent at ends; striate, striae radiate in middle, convergent at ends, crossed by a narrow band. Length, 200μ.
Distribution. Usually from Zostera washings and bottom samples. Australia: Lake Macquarie, Botany Bay, Port Hacking.
207. Pinnularia borealis Ehr. (Pl. 5, Fig. 65.)
Ehr., 1843b, 1.
Boyer, 1927b, 437; 1916, 22.
Valves linear, with rounded ends; axial area about ¼ width of valve, widened in middle: raphe with large hook-shaped terminal fissures; striae slightly radiate in middle, convergent ends. Length, 40–65μ.
Distribution. Fresh water. Australia: Lake Dobson. New Zealand: Near Auckland (Ehr., 1869).
208. Pinnularia brevicostata Cl. (Pl. 5, Fig. 66.)
Cl., 1891, 25, 1, 5.
A.S., 1875, 43, 26–27 (Nav. hemiptera Kütz)
Valves linear, ends rounded; striate almost marginal, short; axial area very large, more than half valve; raphe almost straight. Length, 120μ.
Distribution. Brackish water. Australia: Port Hacking. New Zealand: Wellington (Wainui).
209 Pinnularia gibba Ehr. (Pl. 5, Fig. 67.)
Ehr., 1843b, 1, 11.
P. gibba (vH.) Boyer, in Boyer, 1927b.
Valves linear, tapering to subcapitate ends; axial area dilated in middle; striae divergent in middle, convergent at ends. Length, 80–90μ.

Fig. 1—I Fragilaria striatula. Fig. 2–Thalassiothrix nitzschioides. Fig. 3–T. frauenfeldii. Fig. 4–I. longissima. Fig. 5–7. antarctica. Fig. 6—Asterionella japonica. Fig. 7–A. kariana. Fig. 8—Amphipleura micans. Fig. 9—Mastogloia strigilis. Fig. 10—M. gracilis. Fig. 11—M. smithu. Fig. 12—M. cocconeiformis. Fig. 13—M. horrathiana. Fig. 14—M. rostellata. Fig. 15–Amphoia hyalina. Fig. 16—Nitzschia longissima longissima. Fig. 17—N. closterium. Fig. 18—N. Seriata. Fig. 19—N. sigma. Fig. 20—N. angularis. Fig. 21—N. brebissonii. Fig. 22—N. plana. Fig. 23—N. pacifica. Fig. 24—N. maritima. Fig. 25—Chaetoceros aequatorialis.

Fig. 1—Fragilaria oceanica. Fig. 2—F. constucta. Fig. 3a. and b—Fragilariopsis antarctica. Fig. 4—Plagiogiamma vanheurckii. Fig.—5 P stausophoium. Fig. 6—P. dicussatum. Fig. 7—Synidia pelagica. Fig. 8—S. fiaucufeldii. Fig. 9—S. undulata. Fig. 10—S. fulgens. Fig. 11—S. ulug, Fig. 12—S. splendens.. Fig. 13—S. closteroides. Fig. 14—S gaillonii. Fig. 15—S. supeiba. Fig. 16—Grammatophoia maiina. Fig. 17—G. serpentina. Fig. 18—G. ocianica v. subtilissma. Fig. 20 a-c—Rhabonima adiiaticum. Fig. 21—Dithomella balfouriana.. Fig. 22—Terpsinoe musica. Fig. 23a.b—Licmophora ilabellata..

Fig. 24—Licmophora abbreviata. Fig. 25a, b—L. grandis v. divisa.. Fig. 26—L. giacilis. Fig. 27 a-c—clima-cosphenia moniligera. Fig. 28—Striatella unipunctata. Fig. 29—S. interrupta. Fig. 30—Eunolia diadema. Fig. 31—E. crosta galli. Fig. 32—E. bidentula. Fig. 33a—E. pectinalis v. undlata; 33b—v. centralis. Fig. 34—E. sarekensis.. Fig. 35—E. gracilis. Fig. 36 a-c—Achnanthes longipes. Fig. 37a b—A. brevipes.. Fig. 38—Cocconeis heteroidea. Fig. 39a, b—C. scutellum.. Fig. 47—Navicula viridula. Fig. 41 a-d—V. brasiliensis. Fig. 42a—N. grevillei..

Fig. 42b—Navicula grevillei. Fig. 43a—N. lyra; 43b-e—v. eilliptica. Fig. 44a, b—N. subcarinata.. Fig. 45—N. peregiina. Fig. 46—N. gracilis. Fig. 48—N. americana. Fig. 49—N. jorcipata. Fig. 50—N. yarrensis.. Fig. 51—N. cuspidata. Fig. 52—N. climentis. Fig. 54a—N. gianulata. 54b—N. gianulatabrasilunsis intergrade.

Fig. 55—Navicula radiosa. Fig. 56—N. minusculus. Fig. 57—N. spectabilis. Fig. 58a, b—Fiustulia thomboides. Fig. 59—Neidium bisulcatum. Fig. 60a—Neid affine 60b—N. amphiihynchus. Fig. 61—Neid amphigomplius. Fig. 62—Neid iridis. Fig. 63a b—Trachyneis aspera. Fig. 64—Pinnulana major. Fig. 65—P. borealis. Fig. 66—P. brevicostata. Fig. 67 a b—P. gibba. Fig. 68—P. splendidu. Fig. 69—P. stauioplera. Fig. 70a—Diploneis ciabo; 70—v. pandura. Fig. 71a—D. smithu 71b—v. rhombica.

Fig. 72—D. constricta. Fig. 73a—D. justa; 73b—v. aestiva. Fig. 74—D. vacillans. Fig. 75—D. chersonensis. Fig. 76—D. weissflogii. Fig. 77—D. flaetfoimis. Fig. 78—Pleurosigma naviculaceum. Fig. 79a b—P. angulatum. Fig. 80a b—P. balticum. Fig. 81—P. fasctola. Fig. 82a b—P. formosum. Fig. 83—Stauioniss ancips. Fig. 87—S. phoinicciiteron. Fig. 85—Anomoeonesis seroams. Fig. 86—A. sphaerophora. Fig. 87—Mastogloia cribrosa. Fig. 88a-b—M. quinquicostata. Fig. 89—M. horvathiana. Fig. 90—M. cocconeiformis.

Fig. 88c—M. quinquicostat. Fig. 91a, b—Amphipioia alata. Fig. 92—I ropidoneis lepidopiera. Fig. 93—Amphoia robusta. Fig. 94—A. proteus. Fig. 95—A. egregia. Fig. 96—A. linceolata. Fig. 97—A. osticaria. Fig. 98a, b—A. gigantea. Fig. 99a, b—A. angusta Fig. 100—A. granulata. Fig. 101—A. mexicana. Fig. 102—A. spectabilis. Fig. 103—A. rhombica. Fig. 104—A. hendeyi. Fig. 105—A. arcta. Fig. 106—Epithemia westermannu. Fig. 107a, b—E. argus. Fig. 108a b—Rhopalodia gibba. Fig. 109a b—R. culricosa. Fig. 110—Cymbella affinis. Fig. 111—C. aspera.

Fig. 112—Cymbilla subtuigida. Fig. 113—C. cistula. Fig. 114—Gomphonema acuminatum v. turris. Fig. 115a, b—G. exiguum. Fig. 116a, b—G. olivaceum. Fig. 117—Nitzschia hungarica. Fig. 118—N. plana. Fig. 119—Bacillaiia paiadoia. Fig. 120—Hantzschia amphioxus. Fig. 121a, b—Surirella fastuosa. Fig. 122—S. gimma. Fig. 123a, b—S. tenera. Fig. 124a, b—S. ja antia. Fig. 125—S. ovalis. Fig. 126—S. elogata. Fig. 127—Campylodiscus ornatus. Fig. 128a, b—C. adriaticus.

Fig. 129a—Camphylodiscus undulatus; 129b—v. leudigeri. Fig. 130—C. biangulatus. Fig. 131—C. samoensis. Fig. 132—C. crebrecostatus. Fig. 134—Coscinodiscus argus. Fig. 135—C.argis. Fig. 136—C.dibilis. Fig. 137—Cyclotella menenghiniana. Fig. 123c—Surirella tenera var. Fig. 138—Amphipleura micans. Fig. 139—Campylodiscus daemelianus.

Distribution. Brackish water Australia: Port Hacking. New Zealand: Near Auckland (Ehr., 1869).
210. Pinnularia splendida Hust. (Pl. 5, Fig. 68.)
Hust. in A.S., 1934, 391, 5–6.
Valves broad-linear, tapering to ends; axial area dilated on one side in middle; striae divergent; raphe curved at ends and in middle. Length, 45μ.
Distribution. Brackish water. Australia: Port Hacking.
211 Pinnularia stauroptera (Grun.) Cl. (Pl. 5, Fig. 69.)
Cl., 1891, 26.
Navicula stauroptera Grun., 1860, 14.
Valves linear, tapering to subcapitate ends; axial area more than ⅓ valve width, widened in middle, striae short, divergent, continuous or interrupted on one or both sides of central nodule. Length, 95–150μ.
Distribution. Brackish water. Australia: Port Hacking.
The following species of Pinnularia have been previously recorded:—
-
P. ambigua Cl., 1895, as Nav. retusa (by Petit, 1877). Lyall Bay.
-
P. cruciformis (Donk.) Cl., 1895 (Østrup, 1910, 108.)
-
P. dactylus Ehr. (Ehr., 1869) New Zealand.
-
P. decurrens Ehr. (Ehr., 1869). New Zealand.
-
P. divergens W. Sm., 1853. (Østrup, 1910, 98.) Australia.
-
P. divergenttissima (Grun.) Cl., 1895 (Østrup, 1910, 103.) Australia.
-
P. esox (Kütz.) Cl. as Nav. esox (by Petit, 1877). Campbell Island.
-
P. hemiptera (Kütz). W. Sm., 1856. (Østrup, 1910, 103.) Australia.
-
P. intermedia Lager., 1873 (Østrup, 1910, 100.) Australia.
-
P. interrupta W. Sm. f. biceps, W. Sm., 1853. (Østrup, 1910, 95.) Australia.
-
P. macilenta Ehr. (Ehr., 1869) New Zealand.
-
P. mesogongyla Ehr, 18 (Ehr., 1869). New Zealand.
-
P. microstauron (Ehr.) Cl., 1895 (Østrup, 1910, 95.) Australia.
-
P. molaris (Grun.) Cl., 1895. (Østrup, 1910, 95.) Australia
-
P. quadratarea (A.S) Cl., 1895. (Østrup, 1910, 109.) Australia.
-
P. stomatophora Grun. in A.S., 1876. (Østrup, 1910, 102.) Australia.
-
P. subsolaris (Grun.) Cl., 1895. (Østrup, 1910, 102) Australia.
-
P. tabellaria Ehr. (Ehr., 1869). New Zealand.
-
P. viridis (Nitzsch) Ehr., 1838. (Østrup, 1910, 107.) Australia.
-
v. leptogongyla (Ehr.?) Grun. (as P. leptygongyla) (Ehr., 1869). New Zealand.
-
v. comutata (A.S., 1875, 45, 35–37). Australia.
-
v. fallax Cl. Australia.
-
v. intermedia Cl. (A.S., 1875, 42, 9, 10). Australia.
-
v. rupestris Hantzsch. (A.S., 1875, 44, 42.) Australia.
Genus Diploneis Ehr., 1840
Cells solitary; frustules in valve view elliptical or panduriform. Dividing bands and septa absent; central area enclosed in strongly siliceous horns corresponding to the lyre-shaped areas of Navicula lyra; central nodule quadrate; valves costate, striate or both; outside siliceous horns are depressions (sulci) and, in some species, are narrow spaces called lunulae; poroids (areolae) between the transapical costae in single or multiple rows (usually double); plastids two.
| 1. | Transapical ribs not crossed by longitudinal lines | 2. | |
| Transapical ribs crossed by longitudinal lines | 6. | ||
| 2. | Outer wall smooth or faintly poroid | 3. | |
| Outer wall strongly poroid | 4. | ||
| 3. | Valves linear or elliptic | D. coffaeiformis. | |
| Valves constricted in transapical plane | D. constricta | ||
| 4. | Inner side of lunulae with 1 or more pores | D. crabro. | |
| Inner side of lunulae otherwise | |||
| 5. | Poroids of the outer side in almost straight longitudinal rows, fine throughout, double rows not visible | D. vacillans. | 5. |
| Poroids of outer side in a criss-cross arrangement, irregular |

| double rows evident | D. smithii. | ||
| 6. | Valves with true longitudinal ribs, lunulae separated therefrom | 7. | |
| Valves without true longitudinal ribs, lunulae not separated | D. fusca. | ||
| 7 | Apical nodule quadrate | D. chersonensis. | |
| Apical nodule constricted in the middle | D. weissflogii. |
212 Diploneis crabro Ehr. var. pandura (Breb.) Cl. (Pl. 5 Fig. 70.)
Ehr., 1844, 85.
Cl., 1894, 100.
Hust., 1927–33, 622, 1034B.
Cleve-Euler, 1953b, 86, 660c.
Navicula pandura Breb., 1854, 4.
Cells solitary; frustules in valve view panduriform, ends abruptly rounded to acute; median nodule large, horns narrow, nearly parallel with a row of large puncta; costae strongly marked, radiating, curved at central and distal areas with two rows of areolae between costae; lunulae broad, usually linear. Length, 60–100μ.
Distribution. Estuarine; euryhaline; benthic, occasionally epontic on weeds and fouling test plates. Australia: Heron Island, Moreton Bay, Yamba, Lake Macquarie, Botany Bay, Port Hacking, Weber Deep at 7,400 m (Galathea). New Zealand: Hauraki Gulf; Lyall Bay (Petit 1877).
213. Diploneis smithii (Breb.) Cl. (Pl. 5, Fig. 71a.)
Cl., 1894, 96.
Hust., 1937, 647, 1051.
Cleve-Euler, 1953b, 81, 654a (synonymy).
Navicula smithii Breb. in W. Sm., 1856, 92.
Cells solitary; frustules in valve view elliptical; central nodule more or less elliptical with truncate ends; horns parallel on inner, evenly curved on outer edge; costae transverse, radial towards extremities, separated by two rows of areolae decreasing in size from margin. Length, 60–100μ.
Distribution. Estuarine; mesohaline, benthic and epontic on weeds and fouling test plates; common. Australia: Port Hacking, Lake Macquarie, Botany Bay. Previously recorded from Australia (Schmidt, 1875). New Zealand: Lyall Bay (Petit 1877).
214. Diploneis smithii f. rhombica Mereschkowsky (Pl. 5, Fig. 71b.)
Mereschkowsky 1902, 12.
Hust., 1937, 649, 1952a.
Cells solitary; frustules in valve view elliptic-rhomboid, with obtuse apices; costae strong radial; two sets of areolae between each rib. Length, 50–80μ.
Distribution. Estuarine; marine; benthic and epontic on algae, sea grasses and fouling test plates. Fly River (New Guinea). Australia: Moreton Bay, Clarence River, Port Stephens, Port Jackson, Lake Macquarie, Botany Bay, Port Hacking, Eden, Port Phillip, Fremantle, Macquarie Island Very common throughout Australia.
215. Diploneis constricta (Grun.) Cl. (Pl. 6, Fig. 72.)
Cl., 1894, 1, 83.
Hust., 1937, 594, 102a (synonymy).
Cleve-Euler, 1953b, 70, 630b.
Navicula constricta Grun., 1860, 535, 3, 18.
Cells solitary; frustules in valve view panduriform with bluntly rounded or acute apices: median area simple, large, quadrate; horns strong, converging at apices; costae wide, heavily marked, transverse, radial towards extremities; lunulae broad, with a single row of delicate pores, linear; lunulae without obvious pores on the inside. Length, 40–60μ.
Distribution. Estuarine; benthic. Australia: Port Hacking. Uncommon.
216. Diploneis fusca (Greg.) Cl. (Pl. 6, Fig. 73a.)
Cl., 1894, 93.
Hust., 1933, 654, 1053.
Cleve-Euler, 1953b, 81.
Valves elliptic to linear-elliptic; central nodule large, sub-quadrate: horns strongly marked, tapering towards apices, expanded near central nodule; costae transverse, strong, radial to parallel, with numerous longitudinal ribs; areolae adjacent to horns in tetrads or in quincunx. Length, 80–150μ.
Distribution. Australia: Lake Macquarie. Recorded as Navicula fusca from Foveaux Strait by Petit (1877).

var. aestiva (Donkin) Hust. (Pl. 6, Fig. 73b.)
Hust., 1933, 657, 1059.
Navtcula aestiva Donk., 1858, 32, 3, 18.
Diploneis aestiva Cl., 1894, 94.
Differs from type in the strongly elongated central nodule. Length, 40–100μ.
Distribution. Australia: Port Hacking.
217. Diploneis vacillans (A.S.) Cl. (Pl. 6, Fig. 74.)
Cl., 1894, 95.
Hust., 1927, 1933, 662.
Navicula vacillans A.S., 1875, 8, 34, 36, 37.
Valves elliptic to linear, with broad to blunt-cuneiform apices and slightly convex to parallel sides; central nodule rather small, almost quadrate or elongate; horns strong, parallel; transapical costae radial, almost perpendicular to midline in centre; longitudinal lines delicate. closer together than costae. Puncta in double row between ribs, difficult to see. Length, 20–50μ.
Distribution. Brackish water. Australia: Lake Conjola.
218. Diploneis chersonensis (Giun.) Cl. (Pl. 6 Fig. 75.)
Cl., 1891, 91.
Hust., 1933, 709, 1088.
Navicula chersonensis Grun. in A.S., 1876, 69, 21.
Valves panduriform, with constricted middle and bluntly cuneate apices; central nodule small, quadrate; horns strong, parallel. Sulci broad to narrow, linear; transapical costae strong. parallel to radial, with one to several longitudinal ribs, straight or slightly bent; one row of poroids on lunulae. Length, 30–100μ.
Distribution.. Australia: Lake Macquarie, Port Hacking, Conjola.
219. Diploneis weissflogi (A.S.) Cl. (Pl. 6, Fig. 76.)
Cl., 1894, 91.
Hust., 1933, 703, 1085.
Navicula weissflogi A.S., 1875, 12, 26–32.
Frustule in valve view linear-elliptic with more or less sharply narrowed sides and elliptic to tongue-shaped halves; central nodule small, elongated, constricted in the middle; horns almost parallel, approaching slightly at ends; transapical costae well defined, strongly marked and elongated in middle, somewhat radial, crossed by several almost straight or slightly irregular longitudinal ribs, broken on either side of central nodule. Length, 30μ.
Distribution. Brackish water. Australia: Lake Conjola. New Zealand: Auckland Harbour. Recorded from Australasia by Petit (1877) (Lyall Bay); and Boyer (1927b).
220. Diploneis coffaeiformis (A.S.) Cl. (Pl. 6, Fig. 77)
Cl., 1894, 81.
Hust., 1937, 611, 1025 (synonymy).
Cleve-Euler, 1953, 69.
Cells elliptic, nearly circular; central nodule large; costae transverse to radial; longitudinal rows of poroids adjacent to raphe. Length, 60–80μ.
Distribution. Estuarine; marine. Epontic. Australia: Port Hacking; Heron Island.
The following additional species of Diploneis have been recorded:—
-
D. adonis (Brun.) Cl., 1894. v. oamaruensis Cl., 1894. (Gr. & St., 1887 (as Nav apis); A.S., 1890, 174, 3). Oamaru.
-
D. gemmata (Grev.) Cl., 1894 (as Navicula gemmata & v. mediterranea Grun.) (Petit, 1877; Gr. & St., 1886, 322) Foveaux Strait, Oamaru.
-
D. gemmatula (Grun.) Cl., 1894 (as Nav. entomon Ehr.) (Petit, 1877.) Lyall Bay.
-
D. graeffii (Grun.) Cl., 1894. As Nav. graeffii Grun. (Petit, 1877). Lyall Bay.
-
D. gruendlerii (A.S.) Cl., 1894. (As Nav. gruendlerii A.S). (Gr. & St., 1886.) Oamaru.
-
D. incurvata (Greg.). Cl., 1894. (as Nav. incurvata Greg.) (Petit, 1877.) Lyall Bay.
-
D. interrupta (Kütz.) Cl., 1894 v. clancula (A.S.) Cl., 1894. (Nav. clancula A.S.) (A.S., 1875) Australia.
-
D. lobata (Gr & St.) 1877. (As Nav. lobata Gr. & St.) Oamaru. Probably D. novae zeelandiae.

-
D. nitescens (Greg.) Cl., 1894. (As Nav. nitescens). (Petit, 1877.) Foveaux Strait.
-
D. novae zeelandiae (A.S.) Hust., 1933. (As Nav. interrupta v. novae zeelandiae A.S.) (Petit, 1877.) Lyall Bay.
-
D. smithii (Breb.) Cl., 1894. (As Nav. smithii.) (A.S., 1875, 7, 8, 18.) Australia.
-
v. nitescens (Greg.) (Gr. & St., 1886). Oamaru.
-
v. minor Petit (Petit, 1877.) Lyall Bay.
-
D. splendens (Greg.) Cl., 1894. (As Nav. splendida Greg.) (Petit, 1877.) Lyall Bay.
Genus Pleurosigma W. Sm., 1853
Cells solitary, free; frustules in valve view sigmoid. Valves with central and terminal nodules; raphe usually sigmoid, often more so than valve margin; cell surface delicately marked by longitudinal or oblique and transverse striae; some authors maintain two genera, Pleurosigma wtih oblique, Gyrosigma with longitudinal and transverse striae.
| 1. | Frustules with definite angle on margins on transapical axis. | P. angulatum. | |
| Margin evenly curved | 2. | ||
| 2. | Raphe straight in central portion | P. fasciola. | |
| Raphe sigmoid, central portion curved | 3. | ||
| 3. | Frustules evenly sigmoid | P. formosum. | |
| Frustules sigmoid towards extremities | 4. | ||
| 4. | Raphe evenly sigmoid | P. balticum. | |
| Raphe more strongly sigmoid at apices | P. naviculaceum. |
221. Pleurosigma naviculaceum Breb. (Pl. 6, Fig. 78.)
Breb., 1867, 17.
Boyer, 1916, 74, 22, 6; 1927, 471.
Valves lanceolate, slightly sigmoid at the subacute ends. Raphe nearly central, sigmoid near ends. Striae transverse and oblique, the latter closer at the ends. Central nodule dilated transversely. Length, 80μ.
Distribution. Australia: Heron Island, Lake Conjola. New Zealand: Hauraki Gulf, Wellington Harbour.
222. Pleurosigma angulatum (Queckett) W. Sm. (Pl. 6 Fig. 79a, b.)
W. Sm., 1853, 65, 21, 205.
Boyer, 1916, 74, 22, 3; 1927, 471.
Hend., 1951, 61, 11, 8 (synonymy).
Navicula angulata Queckett, 1848, 438, 7, 4–7.
Cells solitary; frustules in valve view sigmoid-rhomboid, with at times a definite angle on valve margin adjacent to central nodule; raphe sigmoid, central; central nodule small, more or less rhombic; valve surface obliquely and transversely striated. Length, 80–120μ. This form is often smaller than specimens of P. angulatum received from Hendey from Great Britain, and Hendey (in litt.) considers the Australasian form is a distinct species. However, because of considerable variation in form we hesitate at this time to separate our form from P. angulatum.
Distribution. Estuarine-nertic; marine, benthic, epontic, and planktonic, found in algal and Zostera washings, and on fouling test plates. Australia: Moreton Bay, Port Stephens, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking, and from coastal plankton stations of New South Wales. In mud at 135 in off Jibbon Cape (living form). New Zealand: Wellington Harbour.
223. Pleurosigma balticum (Ehr.) W. Sm. (Pl. 6, Fig. 80a, b.)
W. Sm., 1853, 66; 22; 207.
Hend., 1951, 61, 11, 9.
Gyrosigma balticum (Ehr.) Cl., 1894, 118.
Boyer, 1916, 75, 23, 2; 1927. 456.
Cells solitary; frustules in valve view sigmoid towards extremities. Raphe sigmoid and slightly curved close to central nodule; striae longitudinal and transverse. Length 80–182μ × up to 27μ wide.
Distribution. Estuarine. neritic, common in plankton on fouling plates, algae and sea grasses and as a benthic form. Australia: Moreton Bay, Lake Macquarie, Port

Stephens, Port Jackson, Botany Bay, Port Hacking, Eden, Port Philip. New Zealand: Hauraki Gulf. From Australia by Østrup (1910).
224. Pleurosigma fasciola (Ehr.) W. Sm. (Pl. 6, Fig. 81.)
W. Sm., 1853, 67, 21, 211.
Hend., 1951, 62.
Gyrosigma fasciola (Ehr.) Cl., 1894, 116.
Boyer, 1927, 463.
Cells solitary, sigmoid, extremities drawn out into long, curving beaks; raphe central, straight except at the beaks, where it is sigmoid; striae very fine, transverse and oblique. Length, 60μ.
Distribution. Neritic, marine, epiphytic. Australia: Port Hacking; rare.
225. Pleurosigma formosum W. Sm., 1853 (Pl. 6, Fig. 82a, b.)
W. Sm., 1853, 63, 20, 195.
Boyer, 1916, 73, 22, 5; 1927, 467.
Hend., 1951, 62, 11, 6.
Cells solitary; frustule in valve view sigmoid; raphe strongly sigmoid, sweeping from the central nodule towards the valve margin, giving a very twisted appearance; striae transverse and oblique. Length, 100–180μ × up to 20μ.
Distribution. Estuarine-neritic; epontic on weeds and fouling test plates, common, frequently benthic, and occasionally planktonic. Australia: Heron Island, Moreton Bay, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking. New Zealand: Hauraki Gulf, Lyall Bay (Petit 1877).
The following additional species of Pleurosigma have been recorded previously:—
-
P. compactum Grev., 1857 (Gyrosigma) (Østrup, 1910, 31). Australia. (As Donkinia compacta) (Gr. & St., 1887, 133). Oamaru.
-
P. cuspidatum Cl., 1894. (As P. lanceolatum cuspidatum Cl., 1881.) Type loc. Port Jackson.
-
P. elongatum W. Sm., 1853 (Hardy, 1910). Kew, Victoria.
-
P. kuetzingii Grun., 1860 (Gyrosigma) (Østrup, 1910, 31). Australia.
-
P. nubecula W. Sm., 1853 (as P. intermedium Sm., 1853) (Petit, 1877, 28). Lyall Bay.
-
P. marinum Donk., 1858. (Petit, 1877, 28.) Lyall Bay.
-
P. reticulatum (as Donkinia) Norman in Pritch., 1861, 921.
-
P. validum Shadb., 1854. (Petit, 1877, 28.) Lyall Bay, Foveaux Strait. (= P. rigidum.)
-
P. vitraeum Cl., in Cl. & Grun., 1880 is Navicula vitraea Cl., 1894. (Cl. & Grun., 1880, 60.) Australia.
Genus Amphipleura Kütz. 1844
Cells solitary or embedded in a gelatinous matrix; frustules delicately silicified; valves fusiform, more rarely linear; central nodule narrow, extending half the valve-length or more. then forking at the end; terminal nodules elongate.
226. Amphipleura micans (Lyngb.) Cl. (Pl. 1, Fig. 8; Pl. 9, Fig. 13a.)
Cl., 1894, 126.
Hust, 1933, 723, 1094.
Bangia micans Lyngb, 1819b, 84, 29 (apud Cl.).
Berkeleya adriatica Grun., 1867 in Grun., 1877, 180.
Cells in gelatinous matrix forming a branched sheath; frustules elongate, valves linear with bluntly rounded ends, and tapering only slightly; central nodule not obviously curved; transapical ribs parallel to transverse axis, converging towards the poles near the ends of the valves.
Distribution. Australia: East coast estuaries, including Lake Macquarie, Port Jackson, Botany Bay, Port Hacking; var fragilis (Berkeleya) fragilis is recorded from Lyall Bay, N.Z., by Petit (1877).
Genus Stauroneis Ehr., 1843
Valves more or less lanceolate, with slightly radiate, fine punctate striae; central nodule dilated into a transverse stauros.

| Valves with produced ends | S. anceps. |
| Valves lanceolate. | S. phoenicenteron. |
227. Stauroneis anceps Ehr. (Pl. 6, Fig. 83.)
In Kütz., 1844, 105.
Boyer, 1927b, 422.
Valves lanceolate with produced, subcapitate ends; axial area narrow or indistinct; stauros not reaching margin; striae radiate. Length, 40–80μ.
Distribution. Fresh water; Lake Dobson. From Australia by Østrup (1910).
228. Stauroneis phoenicenteron (Nitzsch) Ehr. (Pl. 6, Fig. 84.)
Ehr., 1843, 134.
Boyer, 1927b, 421.
Bacillaria phoenicenteron Nitzsch, 1817, 92, 4.
Valves lanceolate with obtuse ends, axial area linear, with transverse stauros; striae radiate, punctate, puncta in longitudinal rows. Length, 80–180μ.
Distribution. Fresh water; Lake Dobson. Recorded from Australia by Østrup (1910), from New Zealand, near Auckland (Ehr., 1869).
The following species of Stauroneis have been recorded previously:—
-
S. (Stauroptera) acus Ehr. (Ehr., 1869). New Zealand.
-
S. acuta W. Sm., 1853. (Petit, 1877; Østrup, 1910.) Foveaux Strait, Australia.
-
S. (Stauroptera) cardinalis Ehr. (Ehr., 1869). New Zealand.
-
S. constricta Ehr., 1843 non W. Sm. (Ralfs in Pritch., 1861). Australia.
-
S. dilatata Ehr., 1843. (Ralfs in Pritch, 1861.) Australia.
-
S. frauenfeldiana Grun., in A. S. (A. S., 1903, 242, 2) Talbot, N. Z.
-
S. fulmen Brightw. (in A. S., 1903, 241, 1). Yarra River.
-
S. hochstetteri Ehr. (Ehr., 1869). New Zealand.
-
S. inflata A. S., 1893 non Kütz., non H. L. Sm. (A. S., 1903, 241, 2). Yarra River.
-
S. salina W. Sm., 1853. (Østrup, 1910, 323.) Australia.
-
S. vibrio Ehr., 1869 (Ehr., 1869). New Zealand.
Genus Anomoeoneis Pfitz. 1871
Cells solitary, frustules in valve view lanceolate; central nodule small; raphe central, axial area narrow, enlarging at the central area, and dilated on one side; valve surface with transverse striae, puncta in longitudinal rows interrupted by clear lines.
| Apices acute in valve view | A. serians. |
| Apices swollen and rounded | A. sphaerophora. |
229. Anomoeoneis serians (Brebisson) Cleve (Pl. 6, Fig. 85.)
Cl., 1895, 11, 7.
Boyer, 1916, 80, 17, 13.
Cleve-Euler, 1953b. 197, 918
Navicula serians Kütz., 1844, 92, 30, 23.
Frustulia serians Breb. in Kütz., 1844, 92, 30, 23.
Cells solitary; frustules in valve view lanceolate, acute; central nodule small, raphe central, axial area lanceolate, narrow, enlarged central area, dilated on one side; valve surface with transverse striae, interrupted by clear lines. Length, 85μ.
Distribution. Estuarine, benthic. Australia: Port Hacking, rare; Heron Island. Previously reported from Australia as Navicula serians by Cl. (1895) and Ralfs (1861).
230. Anomoeoneis sphaerophora (Kütz.) Pfitzer (Pl. 6, Fig. 86.)
Pfitz. 1871, 77, 3, 10.
Boyer 1927b, 324.
Cleve-Euler 1953b, 202.
A. sphaerophora (Kütz.) Cl. in Boyer, 1916, 80 40, 2.
Navicula sphaerophora Kütz. 1844, 95, 4, 17.
Cells solitary. Frustules in valve view elliptic-lanceolate with swollen, rounded apices. Axial area linear, central area asymmetric, elongated transversely, almost reaching margin at one side. Striae transverse with faint longitudinal lines. Length, 45μ.

Distribution. Estuarine, benthic. Australia: Port Hacking. Very rare.
Genus Mastogloia Thwaites in W. Sm., 1856, 63
Valves similar, orbicular, linear, elliptical, lanceolate or rhombic, with obtuse, acute or ostrate ends; axial area narrow or indistinct; central area usually small; median line straight or undulate; striae punctate, the puncta usually in longitudinal or decussate lines; a septate plate divided into loculi is found between the connective zone and the valve, next to the margin; plastids two, each consisting of a band with its centre at the apex, and extending on both valves toward the centre, with a sinus on the middle of the band at its upper part; a pyrenoid between the folds of each band.
| 1. | Valves typically elliptic, with broadly rounded, rarely constricted ends | 2. | |
| Valves more or less lanceolate, or elliptic with rostrate or acute ends | 4. | ||
| 2. | Frustules radially punctate | M. cribrosa. | 3. |
| Frustules with a network of areolae | |||
| 3. | Areolae in strongly radial rows, in the middle alternately long and short | M. cocconeiformis. | |
| Areolae almost parallel to the transapical axis, those in the middle of even length | M. horvathiana. | ||
| 4. | Valves slightly constricted on transapical axis | M. rostellata. | |
| Valves rhombic-lanceolate, loculi small, numerous (38–40) | M. strigilis. | ||
| Valves ovate to ovate-lanceolate with acute apices, loculi large and few (18–20) | M. quinquecostata. | ||
| Valves rostrate or at least constricted near apices | 5. | ||
| 5. | Transapical ribs light, longitudinal lines weak | M. smithii. | |
| Transapical ribs marked, longitudinal lines evident | M. gracilis. |
231. Mastogloia cribrosa Grun. (Pl. 6, Fig. 87.)
Grun., 1860, 577, 7, 10c.
Hust., 1931–33, 468, 887.
Cells solitary, often enclosed in a gelatinous sheath, frustule in valve view broadly elliptic, with usually twelve loculi; central nodule small. Raphe straight or very slightly curved; striae radial, areolate or coarsely punctate. Length, 30μ.
Distribution. Estuarine; marine; epontic. Frequent from algae, sea grasses, and fouling test plates. Australia: Heron Island. Botany Bay, Port Hacking, Conjola, Mallacoota. New Zealand: Lake Ellesmer.
232. Mastogloia strigilis Hust. (Pl. 1, Fig. 9.)
Hust., 1937, 541, 974.
Cells solitary; frustule in valve view rhombic-lanceolate with bluntly rounded ends, depressed on either side of the mid-line, with from 38 to 40 loculi; raphe straight, central area very narrow; surface with transverse moniliform striae of interrupted puncta. Length, 60–75μ.
Distribution. Estuarine, mesohaline, epiphytic, found on Zostera. Frequent but not abundant. Australia: Lake Macquarie.
233. Mastogloia quinquecostata Grun. (Pl. 6, Fig. 88a. b; Pl. 7, Fig. 88c.)
Grun., 1860, 578, 7, 8.
Hust., 1931–33, 556, 989 (synonymy).
Cells solitary; frustule in valve view linear-elliptic, with acute ends, with 18 to 20 loculi reaching practically to the apices. Raphe somewhat undulate; valve surface with transverse striae, puncta forming longitudinal striae, usually farther apart than the transverse striae; on each side of the median line are several longitudinal depressions which lack longitudinal striae. Length, 55–80μ.
Distribution. Estuarine; euryhaline; benthic, epontic on algae, sea grasses, and fouling test plates Australia: Heron Island, Moreton Bay, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking, Lake Conjola, Lake Coila, Eden, Mallacoota. Port Phillip. The most common member of this genus. New Zealand: Wellington (Wainui).

234. Mastogloia gracilis Hust. (Pl. 1, Fig. 10.)
Hust., 1931–33, 507, 933.
Cells solitary; frustules in valve view elliptic-lanceolate with constricted apices; raphe slightly undulate, well defined; loculi 24 to 28; surface with strong transverse striae, crossed by faint longitudinal striae, which are usually somewhat undulate. Length, 40–50μ.
Distribution. Estuarine; mesohaline, epontic on Zostera. Australia: Port Hacking, Lake Macquarie. Infrequent.
235. Mastogloia smithii Thwaites (Pl. 1, Fig. 11..)
Thwaites in W. Sm., 1856, 65, 54, 341.
Boyer, 1916, 87, 17, 19.
Hust., 1931–33, 502, 928, a.
Cells solitary; frustules in valve view elliptic-lanceolate, subrostrate; raphe straight; loculi usually 6 to 9 ending some distances from the apices; central area more or less oval; surface striate, striae transverse, punctate; puncta forming longitudinal rows. Length, 30–60μ.
Distribution. Estuarine, euryhaline; benthic. Australia: Port Hacking, Lake Conjola, Lake Macquarie, Botany Bay.
236. Mastogloia cocconeiformis Grun. (Pl. 6, Fig. 90; Pl. 1, Fig. 12.)
Grun., 1860, 578, 7, 14.
Hust., 1931–33, 469, 888
Cells elliptical, almost circular; raphe slightly curved; axial area very narrow, central area small, circular to elliptic; valves evenly areolate, areolae hexagonal, forming a net in a three-directional system; loculi narrow, rectangular, reaching apices. Length, 25–60μ.
Distribution. Australia: Lake Macquarie and Lake Conjola.
237. Mastigloia horvathiana Grun. (Pl. 6, Fig. 89; Pl. 1, Fig. 13.)
Grun., 1860, 578, 7, 13.
Hust., 1933, 471, 890.
Valves broadly elliptic with cuneate ends; raphe curved, gap varying in width; axial area very narrow, central area small, rounded; valve surface evenly areolate, irregularly hexagonal forming two-directional system, areolate nearest raphe transversely elongate; loculi radially elongate, reaching apices. Length, 50μ.
Distribution. Australia: Heron Island.
238. Mastogoloia rostellata Grun. (Pl. 1, Fig. 14.)
Grun., 1877, 174, 195, 2.
Hust., 1931–33, 485, 907.
Cells broadly linear-lanceolate, constricted near apices and centrally; raphe straight, areas narrow; valve surface evenly areolate, areolae elongated transapically, arranged in a three-directional system; loculi narrow, varying in size, elongated apically, inner border convex. Length. 40–60μ.
Distribution. Australia: Port Hacking.
The following species of Mastogloia have been recorded previously:—
-
M. elliptica (Agh.) Cl., 1895 (A. S., 1893, 185, 5–7). Australia.
-
M. exigua Lewis, 1861 (Petit, 1877, 26.) Lyall Bay.
-
M. inaequalis Cl., 1895. (Boyer, 1927, 334.) Australia.
-
M. jelineckii Grun., 1867 (Navicula quarnerensis Grun. v dilatata Petit. (Petit, 1877.) Foveaux Strait.
-
M. macdonaldii Grev., 1865. Type loc., Australia.
-
M. marginulata Grun., 1868. (A.S., 1893, 186, 30; Boyer, 1927, 335). New Zealand.
-
M. rhombus (Petit) Cl., 1894 (as Navicula rhombus Petit, 1877). (Petit, 1877.) New Zealand.
-
M. splendida (Greg.) Cl., 1895. (As Orthoneis.) (Gr. & St., 1887.) Oamaru.
-
Navicula trilineata of Gr. & St., 1887, may also be a species of Mastogloia.
Genus Amphiprora Ehr., 1843
Cells single or in ribbon-like chains of 2–3 cells; frustules lanceolate, acute, convex, twisted in longitudinal axis, constricted centrally; raphe confined within a central keel which is twisted into an S, with central terminal nodules separated by a line from other parts of the valve; girdle zone complex with numerous longitudinal rows of transverse striae; valve surface punctate with transverse striae.

239. Amphiprora alata (Ehr.) Kütz. (Pl. 7, Figs. 91a, b.)
Kütz., 1844, 107, 3, 63.
Boyer, 1916, 68, 14, 3.
Hend., 1951, 66, 15, 1–3.
Navicula alata Ehr., 1840, 18.
Cells solitary or in short chains; frustules in valve view linear with acute apices; in girdle view panduriform, twisted in the middle; axial area raised to form a sigmoid keel bearing the raphe; valves striate, keel coarsely punctate; girdle bands multiple, striate. Length, 50μ.
Distribution. Estuarine-neritic, marine, planktonic, benthic and epontic on fouling test plates. Australia: Moreton Bay, Lake Macquarie, Botany Bay, Port Hacking Western Bass Strait, Lake Conjola. Was maintained in culture for several months.
The following Amphiprora have been recorded. Many of them, however, are not Amphiprora, some being obviously Tropidoneis, others Amphora.
-
A. brebissoniana Grev., 1863c. Curtis Island (type loc.).
-
A. ? clepsydra Grev., 1863c. Curtis Island (type loc.).
-
A. ? cornuta Chase (not Amphiprora) (Gr. & St., 1887, 73.) Oamaru.
-
A. delicatula Grev., 1863c. Woodlark Island (type loc.) prob. = Tropidoneis lepidoptera.
-
A. eximia Grev., 1863c. Curtis Island (type loc.) prob. = T. lepidoptera.
-
A. jolisiana Grev., 1863c. Curtis Island (type loc.).
-
A. lineata Grev., 1863c. Woodlark Island (type loc.).
-
A. menenghiniana Grev., 1863c. Curtis Island (type loc.).
-
A. nitida Grev., 1863c. Curtis Island (type loc.) is an Amphora.
-
A. ? paradoxa Grev., 1863c. Curtis Island (type loc.).
-
A. pulchra Bail. (Petit, 1877.) Campbell Island.
-
A. oblonga Grev., 1861, Hervey Bay (type loc.).
-
A. ? rabenhorstiana Grev., 1863c. Curtis Island (type loc.).
-
A. rectangularis Grev., 1863c. Woodlark Island (type loc.).
-
A. rugosa Petit, 1877. Campbell Island (type loc.). (Gr. & St., 1887.) Oamaru.
-
A. ? superba Grev., 1863c. New Caledonia (type loc.) prob. an Amphora.
-
A. thwaitesiana Grev., 1863c. Curtis Island (type loc.).
-
A. ? undulata Grev., 1863c. Curtis Island (type loc.).
Tropidoneis Cleve, 1891
Cells solitary; frustules in valve view very convex, lanceolate, acute, usually with a wing or longitudinal band on one or both sides; raphe straight, not sigmoid, borne on a central or excentric keel; valve striae transverse, puncta in longitudinal rows; girdle zone simple, not folded; plastids 2 or 4 plates.
240. Tropidoneis lepidoptera (Greg.) Cl., 1894 (Pl. 7, Fig. 92.)
Cl., 1894,25.
Boyer, 1916, 69, 14, 8, 9.
Hend., 1951, 66.
Amphiprora lepidoptera Greg., 1857, 505, 4, 59.
Cells solitary; frustules in valve view ovate-lanceolate; in girdle view strongly depressed centrally, forming a figure of 8; lateral area more or less hyaline; striae transverse, reaching lateral longitudinal line. Length, 65–100μ.
Distribution. Estuarine-neritic; marine; benthic, epontic on fouling test plates, occurs in plankton. Australia: Moreton Bay, Port Stephens, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking, Eden, Port Phillip, Mallacoota, Gippsland Lakes, Woodlark Island?., Curtis Island? New. Zealand: Dunedin.
Family Cymbellaceae
Genus Amphora Ehr., 1840
Cells solitary; frustules in valve view arcuate to reniform, in girdle view broadly elliptical with truncate apices; valves asymmetrical along the longitudinal axis, but with the planes passing through the dorsal and ventral sides of one valve at an angle with that of the other; raphe evident, usually nearer the ventral side of the valve; girdle composed of several bands, punctate; central nodule may be dilated to a stauros. Plastids usually single.

| 1 | Linear-elliptic, ends slightly rostrate | A. granulata. | |
| Elliptic with rounded ends | 2. | ||
| Elliptic, ends truncate | 3. | ||
| Elliptic, ends rostrate | A. lineolata. | ||
| Sub-rectangular, ends rounded | 4. | ||
| Rhombic, triangular in valve view | A. rhombica. | ||
| 2. | Striae of fine puncta | A. proteus. | |
| Heavily striate | A. gigantea. | ||
| 3. | Faintly striate | A. robusta. | |
| Heavily striate | A. egregia. | ||
| 4. | In valve view, ventral margin undulate. | ||
| In valve view, ventral margin arcuate | A. ostrearia. | ||
| Ventral margin straight in middle, concave near ends | A. mexicana. | ||
| Ventral margin straight | 5. | ||
| 5. | Longitudinal lines of striae present | A. hyalina. | |
| Longitudinal lines absent | A. angusta. | ||
| 6. | Striae strong, frequently furcate | A. spectabilis. | |
| Striae rather faint, not furcate | A. hendeyi. |
241. Amphora hyalina Kütz. (Pl. 1, Fig. 15.)
Kütz., 1844, 108, 30, 18.
Boyer, 1927b, 264.
Hend., 1951, 70, xv, 5.
Cleve-Euler, 1953b, 100, 693.
Cells solitary; frustules in girdle view sub-rectangular, with rounded corners; valves with convex dorsal margin; ventral margin nearly straight; fine longitudinal striae. Length, 50μ.
Distribution. Estuarine-neritic; marine; epontic on algae and sea grasses, and on fouling test plates, also planktonic, rarely benthic (probably adventitious). Australia: Moreton Bay, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking. New Zealand: Wellington.
242. Amphora robusta Greg. (Pl. 7, Fig. 93.)
Greg., 1857, 516, 79.
Boyer, 1916, 65, 15, 1.
Cleve-Euler, 1953b, 92, 672.
Cells solitary; frustule in girdle view broad by oval with truncate extremities; valves arcuate, ventral margin straight or concave; raphe biarcuate; surface striate, striae transverse, moniliform; ventral side with broad band of striae along median line. Length, 50–70μ.
Distribution. Estuarine; marine; benthic and epontic, chiefly on fouling test plates, less commonly on weeds. Australia: Port Hacking, Botany Bay. New Zealand: Lyall Bay (Petit 1877).
243. Amphora proteus Greg. (Pl. 7, Fig. 94.)
Greg., 1857, 518, 81.
Boyer, 1916, 65, 15, 5, 6, 19.
Cleve-Euler, 1953b, 92, 673.
Cells solitary; frustules variable—in girdle view elliptic to oblong, bairel-shaped, broad, long and narrow, etc., with rounded ends; valves lunate, acute, sometimes arcuate, with straight ventral margin; raphe biarcuate, no central area in our specimens; striae transverse, moniliform, radial towards extremities; ventral side striate towards ends. Length, 40–95μ.
Distribution. Estuarine; epiphytic and benthic. Australia: Moreton Bay, Port Hacking. Recorded from Australia by A. S. (1875, 39) and from Lyall Bay, New Zealand, by Petit (1877).
244. Amphora egregia A. S. (Pl. 7, Fig. 95.)
A. S., 1875, 28, 13–15.
Boyer, 1927b, 257.
Cleve-Euler, 1953b, 95.
Cells solitary; in girdle view elliptic with truncate ends; valves lunate with rounded ends, ventral margin biarcuate, swollen at central area; raphe biarcuate; surface with series of marked transverse striae, ventral side with a row of strong radial ribs without puncta in between; girdle with 2 to 4 longitudinal rows of rounded areolae. Length, 50μ.
Distribution. Estuarine, epiphytic. Australia: Port Hacking; rare.

245. Amphora lineolata (Ehr.) Kütz. (Pl. 7, Fig. 96.)
Kütz., 1844, 107, 5, 36.
Boyer, 1916, 66, 15, 9, 10.
Cleve-Euler, 1953b, 100, 694.
Navicula lineolata Ehr., 1838, 14, 4.
Cells solitary; frustules lightly siliceous, in girdle view linear-elliptic with rostrate extremities, in valve view slender sickle-shaped without central area or central nodule; intercalary bands numerous, girdle zone finely striate. Length, 40–60μ.
Distribution. Fresh and brackish water; benthic. Australia: Port Hacking; rare.
246. Amphora ostrearia Breb. (Pl. 7, Fig. 97.)
In Kütz., 1849, 94.
Boyer, 1927, 265.
Amphora quadrata Breb. in Kütz., fide Boyer, 1927b, 265.
Amphora membranacea W. Sm., 20, 1853, fide Boyer, 1927, 265.
Cells solitary; frustules very thin-walled, and lightly silicified, elliptical-oblong with rounded ends in girdle view; in valve view with arcuate dorsal and straight ventral margin and acute ends; girdle zone with numerous longitudinal striac; central nodule dilated to a transverse stauros; chromatophores numerous, rounded. Length, 50–70μ.
Distribution. Estuarine; mesohaline; benthic; epontic on fouling test plates, and algae and sea grasses. Australia: Moreton Bay, Lake Macquarie, Botany Bay, Port Hacking, Port Phillip.
247. Amphora gigantea Grun. in A.S. (Pl. 7, Fig. 98a, b.)
A. S., 1875, 27, 16, 46.
Boyer, 1927b, 255.
Cleve-Euler, 1953b, 102, 699.
Cells solitary, epiphytic; frustule in girdle view broadly elliptic with rounded extremities; in valve view lunate with straight ventral margin and transverse moniliform striae; dorsally with fine longitudinal lines, ventrally hyaline except along median line and at ends, which are obliquely striate. Length, 80–120μ.
Distribution. Estuarine, marine; epontic and benthic; very common from algae and Zostera, fouling test plates, rocks and surface muds. Australia: Moreton Bay, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking.
248. Amphora angusta Greg. var. typica Cl. (Pl. 7, Fig. 99a, b.)
Greg., 1857, 510, 12, 66.
Cleve, 1894–5, 135.
Cleve-Euler, 1953b, 103, 705a, b.
Cells solitary; frustules in girdle view, linear-elliptic, in valve view semi-elliptic with more or less straight raphe nearer to ventral wall, and clear axial area; striae transverse, marginal striae more distinct. Length, 40–60μ.
Distribution. Estuarine, brackish water. Australia: Lake Conjola, Lake Coila; common in these localities, but has not been found elsewhere.
249. Amphora granulata Greg. (Pl. 7, Fig. 100.)
Greg., 1857, 21, 525.
Boyer, 1927, 263.
Cells solitary; frustules in girdle view linear-elliptic, with broad, rostrate, truncate ends; in valve view, arcuate on dorsal side, straight or slightly concave on ventral side; median line straight, close to ventral margin. Length, 50μ.
Distribution. Australia: Lake Macquarie and east coast estuaries.
250. Amphora mexicana A.S. (Pl. 7, Fig. 101.)
A. S., 1875, 27, 46, 48.
Boyer, 1927, 255.
Cells solitary; frustules elliptical, truncate in girdle view; in valve view lunate with straight ventral margin; median line biarcuate; axial area not distinct; longitudinal line near dorsal margin on dorsal side. Length, 150μ.
Distribution. Australia: Lake Conjola, Mallacoota. New Zealand: Lyall Bay (Petit 1877).
251. Amphora spectabilis Greg. (Pl. 7, Fig. 102.)
Greg., 1857, 516.
Boyer, 1927, 269.

Cells solitary; frustules in girdle view oblong with rounded ends, girdle zone with numerous striated divisions; in valve view, arcuate, ends rounded on dorsal side, margin sinuate on ventral side. Median line biarcuate; striate frequently furcate, finer on ventral side, curved. Length, 80–100μ.
Distribution. Australia: Heron Island and east coast estuaries.
252. Amphora rhombi Kitton. (Pl. 7, Fig. 103).
Kitt. in A. S., 1875, 40, 39.
Boyer, 1927b, 266.
Cells solitary; frustules semi-rhombic with sharply acute, slightly incurved ends, in valve view obtusely triangular, ventral margin slightly incurved near apices and in centre; median line biarcuate; striae fine; puncta in undulating, longitudinal lines. Length, 200–250μ.
Distribution. Australia: Port Hacking.
253. Amphora hendeyi n. sp. (Pl. 7, Fig. 104).
Valves with slightly undulate ventral margin; dorsal margin almost straight in middle, then sharply and evenly curved at ends; large apical nodules, and characteristically large central nodule; raphe arcuate at each side of, and closely approaching or reaching, ventral margin of central nodule; striae fine, parallel to transverse axis. Length, 35–40μ.
Distribution. Fresh water. Australia: Lake Dobson; common.
254. Amphora arcta A. S. (Pl. 7, Fig. 105).
A. S., 1875, 26, 63.
Frustule elongate, tapering slightly from centre to poles, with rounded ends; valves with arcuate dorsal, almost straight ventral margins, narrow, elongate; raphe almost straight Length, 70–80μ.
Distribution Epontic, and on fouling plates. Australia: Port Hacking. New Zealand: Auckland Harbour; type locality, Port Lincoln, South Australia.
The following species of Amphora have been recorded previously:—
-
A. acuta Greg., 1857. (Petit, 1877, 18.) Foveaux Strait.
-
A. aponina Kütz., (is A. coffaeiformis) (Petit, 1877, 19.) Lyall Bay.
-
A. aspera Petit, 1877. (Petit, 1877, 19.) Lyall Bay, Foveaux Strait (type loc.), Campbell Is.
-
A. berggrenii Cleve, 1881. (Cleve, 1881.) Arthur's Pass. N.Z.
-
A. bigibba Grun. in A.S., 1875. (Petit, 1877, 17.) Lyall Bay.
-
A. cingulata Cl., 1878 (is A. ocellata Donk., 1861) (Gr. & St., 1886, 322.) Oamaru.
-
A. coffaeiformis (Agh.) Kütz., 1844. (Petit, 1877.) Lyall Bay.
-
A. contracta Grun. (is A. janischii A. S., 1875 (Gr. & St, 1887, 131.) Lyall Bay.
-
A. crass Greg., 1857. (Petit, 1877, 17; Gr. & St., 1886, 322.) Foveaux Strait, Oamaru.
-
A. cristat Petit (Petit, 1877, 18.) Foveaux Strait.
-
A. cymbifera Greg., 1857 (Petit, 1877, 19.) Lyall Bay.
-
A. eulensteinii Grun. var. A. S., 1875. (Petit, 1877, 18.) Foveaux Strait.
-
A. furcata Leud.-Fort. (is A. spectabilis Greg., 1857). (Gr. & St., 1887, 72.) Oamaru.
-
A. flexuosa Grev., 1863 c. (Curtis Island, type loc.)
-
A. gracilis Ehr. (Ralfs in Pritch., 1861.) Australia.
-
A. graeffei Grun. in A. S., 1875, 25. (Petit, 1877, 18.) Foveaux Strait.
-
A. interlineata Gr. & St. (Gr. & St., 1887, 131.) Oamaru.
-
A. janischi A.S., 1875. Recorded as A. contracta.
-
A. labuensis Cl., 1878. (Gr. & St., 1886.) Oamaru.
-
A. lineata Greg., 1857 (is A. coffaeiformis) (Petit, 1877)
. -
A. marina W. Sm., 1853. (Petit, 1877, 19.) Lyall Bay.
-
A. mexicana A.S, 1875, 27. (Petit, 1877. 16.) Lyall Bay.
-
A. obtusa Greg., 1857. (Gr. & St., 1887, 131.) Oamaru.
-
A. ocellata Donk, 1861. Recorded as A. cingulata.
-
A. proboscidea (Greg.?) Cl., 1894–5. (Petit, 1877, 18.) Foveaux Strait.
-
A. pulchra Grev., 1863 c. Curtis Island (type loc.).
-
A. schmidtii Grun. in A. S., 1875. (Petit, 1877, 17) Foveaux Strait.

-
A. sinuata Grev., 1869. (Petit, 1877, 17.) Foveaux Strait.
-
A. spectabilis Greg., 1857. (Petit, 1877, 16; Gr. & St., 1887, 72.) Foveaux Strait, Oamaru.
-
A. subpunctat Gr. & St. (Gr. & St., 1887, 131.) Oamaru.
-
A. tesselata Gr. & St. (Gr. & St., 1887, 131). Oamaru.
-
A turgida Greg., 1857. (Petit, 1877, 19.) Lyall Bay.
-
A undulata Grev., 1863 c. Curtis Island (type loc.).
-
A. weissflogii A. S., 1875 (Petit, 1877, 18). Foveaux Strait.
Genus Epithemia Breb., 1838
Frustules epiphytic, solitary, sometimes geminate, adherent on ventral side at ends; girdle view rectangular, elliptic or sub-orbicular; valves arcuate with interior stratum or transverse septa, extending to girdle, often detached, and an exterior valve surface with narrow bands of puncta between costae; central and terminal nodules not easy to see.
| Ends of valve constricted | E. argus. |
| Ends of valve not constricted | E. westermannii. |
255. Epithemia westermannii (Ehr.) Kütz. (Pl. 7, Fig. 106.)
Kütz., 1844, 33, 5, 12.
Eunotia westermanni Ehr., 1838, 190, 14, 6.
Frustules inflated in girdle view; valves strongly arcuate, ends rounded; costae radiate, strongly marked, alternating with double rows of puncta; raphe curved. Length, 40–80μ.
Distribution. Fresh to brackish water. Australia: Lake Conjola.
256. Epithemia argus (Ehrenberg) Küzing. (Pl. 7, Fig. 107 a, b.)
Kütz., 1844, 35.
A.S., 1904, 251, 11–19.
Eunotia argus Ehr., 1843, 125.
Frustules rectangular in girdle view, the thickened ends of the costae forming large nodules in a row along edge of valve next to girdle zone; in valve view, dorsal margin convex, ventral nearly straight, ends rounded, constricted; costae robust alternating with more than two rows of puncta. Length, 80–100μ.
Distribution. Fresh to brackish water; abundant in Lake Dobson and Port Hacking; recorded by Ralfs (1861) from Australia.
The following species of Epithemia have been recorded previously:—
-
E. gibberula (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia. (= Rhopalodia).
-
E. granulata Kütz., 1844. (Petit, 1877.) Lyall Bay. (= E. turgida v. granulata)
-
E. monilifera Petit, 1877. (Petit, 1877.) Lyall Bay.
-
E. musculus Kütz., 1844. (Petit, 1877.) Lyall Bay. (= Rhopalodia musculus.)
-
E. textricula (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia. (= R. gibberula.)
-
E. zebrina (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia. (E. turgida v. zebrina.)
Genus Rhopalodia O. Müller 1895
Frustule in girdle view linear, linear-elliptic or clavate; in valve view, reniform or lunate; raphe occurs along convex margin on keel; median and terminal nodules very small; differs from Epithemia in position of raphe.
| Frustule linear, elongate | R. gibba |
| Frustule oblong, elliptical | R. ventricosa |
257. Rhopalodia gibba (Ehr.) O. Müller. (Pl. 7, Fig. 108 a, b.)
Müller, 1895, 22, 65.
Boyer, 1927b, 491.
Eunotia gibba Ehr., 1843, 3.
Valves linear, arcuate on dorsal, straight on ventral side, reflexed at ends; costate, striate. Length, 150μ.
Distribution. Fresh water; Lake Dobson; by Ralfs (1861) from Australia.

258. Rhopalodia ventricosa (Kütz.) O. Müller. (Pl. 7, Fig. 109 a, b.)
Mull., 1895, 22, 65.
Boyer, 1916, 24, 31; 1927, 491.
Epithemia ventricosa Kütz., 1844, 35.
Valve swollen in middle on dorsal, straight on ventral margin, with reflexed ends; costate, striate; median nodule minute, depressed. Length. 80μ.
Distribution. Fresh to brackish water. Australia: Lake Dobson, Nepean River, upper Port Hacking.
Genus Cymbella Ag., 1830.
Frustules free, stipitate or in gelatinous tubes; valves more or less asymmetrical along longitudinal axis, linear, elliptic, cymbiform or arcuate; median line excentric, straight or curved; striae usually radiate and more or less distinctly punctate; chromatophore single.
| 1. | Ventral margin straight | C. affinis. | |
| Ventral margin convex or gibbous | 2. | ||
| 2. | Ends acute | C. subturgida. | |
| Ends rounded | 3. | ||
| 3. | Area dilated | C. cistula. | |
| Area broad | C. aspera. |
259. Cymbella affinis Kütz. 1844. (Pl. 7, Fig. 110.)
Kütz., 1844, 80.
Boyer, 1927b, 276.
Hust., in A.S., 1934, 376, 17–25.
Valves strongly convex on dorsal side, straight on ventral, with subobtuse or rostrate ends; median line arcuate, axial area narrow, not widened in middle; usually a punctum on ventral side of median line. Length, 35μ.
Distribution. Fresh water; Lake Dobson; from Australia by Ralfs (1861).
260. Cymbella aspera (Ehr.) Cl. (Pl. 7, Fig. 111.)
Cl., 1894, 26, 175.
Boyer, 1927b, 278.
Cocconema asperum Ehr., 1840, 12.
Valve cymbiform, arcuate on dorsal, swollen on ventral side, with rounded ends; central area linear, broad, slightly widened in middle; no row of puncta on ventral side; striae punctate, in long, curved lines. Length, 100–150μ.
Distribution. Fresh water; Lake Dobson; by Ralfs (1861) from Australia.
261. Cymbella subturgida Hust. (Pl. 8, Fig. 112.)
Hust., in A.S., 1934, 374, 4.
Valve strongly arcuate on dorsal, swollen on ventral side, with acute ends; central area narrow, slightly dilated on dorsal side at middle; striae punctate. Length, 80μ.
Distribution. Fresh water. Australia: Lake Dobson.
262. Cymbella cistula (Hempr.) v H. (Pl. 8, Fig. 113.)
v H., 1885, 64.
Boyer, 1927b, 280.
Cocconema cistula Hempr. in Ehr., 1838, 224.
Valves arcuate, ventral margin swollen, ends rounded or sub-truncate, terminal fissures reflexed; central area linear, dilated in middle on dorsal side; distinct row of puncta on ventral side of central nodule. Length, 100–160μ.
Distribution. Fresh water; Lake Dobson; from Australia by Østrup (1910).
The following species of Cymbella have been recorded previously:—
-
C. ehrenbergii Kütz., 1844. (Østrup, 1910, 55.) Australia
. -
C. lanceolata (Ehr.) Brun, 1880 (as Cocconema) (Ralfs in Pritch., 1861; Hardy, 1910). Kew; Australia.
-
C. leptoceras (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia
. -
C. (Cocconema) lunula Rab. (Ehr., 1869.) New Zealand. (Is C. ventricosa Kütz.)
-
C. naviculiformis Auersf. (Østrup, 1910.) Australia.
-
C. sinuata Greg., 1856 (Østrup, 1910, 59.) Australia.
-
C. ventricosa Kütz. Recorded as C. lunula..

Genus Gomphonema Ag., 1824
Cells sessile stipitate, or in mucous masses; frustules linear or slightly cuneate; valve asymmetrical to transverse axis, clavate or lanceolate; chromatophore single; Boyer (1927) points out that there is considerable variation in forms of this genus, and therefore poor agreement regarding the identification of species.
| 1. | Stigma present in central area | G. acuminatum. | ||
| Stigma absent | 2. | |||
| 2. | Naviculoid in valve view | G. exiguum. | ||
| Clavate in valve view | G. olivaceum. |
263. Gomphonema acuminatum Ehr.
Ehr., 1838, 217.
Boyer, 1927b, 290.
A.S., 1902, 239, 31, 33, 36.
Valves clavate to cuneate, apex apiculate, base narrow; frequently biconstricted; axial area narrow, central area small, unilateral; stigma on side opposite shorter striae; striae evident; outline of frustule variable. Length, 30–65μ.
Distribution. Australia: Nepean River. New Zealand: Wellington (Wainui). Recorded from Australia by Ralfs (1861), and from New Zealand (Auckland) by Ehr., 1869.
var. turris (Ehr.) Cl. (Pl. 8, Fig. 114.)
Cl., 1894, 26, 184.
Boyer, 1927b, 291.
G. turris Ehr., 1843, 128.
Valves with cuneate apiculate apex and narrow base; striae radiate in upper part, distant in middle.
Distribution. Fresh water. Australia: Lake Dobson.
264. Gomphonema exiguum Kütz. (Pl. 8, Fig. 115a, b.)
Kütz., 1844, 84.
Boyer, 1927b, 297.
A.S., 1902, 233, 28, 29.
Valves naviculoid, slightly clavate with acute apex; axial area narrow, not dilated in middle, and without stigma; striae fine. Length, 10–25μ.
Distribution. Brackish water. Australia: Port Hacking.
265. Gomphonema olivaceum (Lyngb.) Kütz. (Pl. 8, Fig. 116a, b.)
Kütz., 1844, 85.
Boyer, 1927b, 296.
A.S., 1902, 233, 9–24.
Echinella olivacea Lyngb., 1819, 209.
Frustule in girdle view clavate, in valve view clavate-lanceolate, apex broad, base narrow; axial area very narrow; central area irregular, no stigma; striae radiate, punctate. Length, 10–35μ.
Distribution. Fresh water. Australia: Lake Dobson.
The following species of Gomphonema have been recorded previously:—
-
G. abbreviatum Agh., 1824. (Ralfs in Pritch., 1861.) Australia.
-
G. angustatum Kütz., 1844 (G. commune Rab., 1864; Sphenella angustata Kütz., 1844). (Østrup, 1910, 62.) Australia.
-
v. obtusa (as G. obtusa) (Ehr., 1869.) New Zealand.
-
G. augur Ehr., 1854. (Ralfs in Pritch., 1861; Ehr., 1869.) Australia; New Zealand.
-
G. capitatum Ehr. (is G. constrictum v. capitatum). (Ehr., 1869.) New Zealand.
-
G. constrictum Ehr. Recorded as G. capitatum..
-
G. coronatum Ehr., 1838. (Ralfs in Pritch., 1861.) Australia. (G. acuminatum.)
-
G. gracile Ehr., 1838. (Østrup, 1910.) Australia; (Ehr., 1869). New Zealand.
-
G. intricatum Kütz., 1844. (Boyer, 1927, 295.) Australia.
-
v. vibrio (Ehr.) (as G. vibrio) (Ehr., 1869) New Zealand.

-
G. longiceps Ralfs, 1861. (Ralfs in Pritch., 1861) Australia; (Ehr., 1869.) New Zealand. (Is G. subclavatum v. montana).
-
G. subclavatum v. montana (Schumann) v H., 1881 Recorded as G. longiceps.
Family Bacillariaceae
Genus Nitzschia Hassall, 1845, em. Grunow, 1880
Cells single or united in colonies, sheathed as in Homoeocladia or in palisade formation as in Nitzschia seriata; frustules in valve view spindle-shaped; valves keeled, keels usually diagonally opposite and including a raphe which is partly concealed; raphe either central or excentric; keel puncta short or prolonged; striae transverse, punctate; plastids consist of two bands placed transversely.
| 1. | Cells in branched gelatinous matrix | N. martiana. | 2. | |
| Cells solitary | 3. | |||
| Cells in staggered chains | 4. | |||
| 2. | Cells spindle-shaped, with long awns | |||
| Cells linear | N. hungarica. | |||
| Cells lanceolate, inflated at centre | N. angularis. | |||
| Cells constricted in transapical axis | N. plana. | |||
| Cells slightly sigmoid | 5. | |||
| 3. | Cells with indistinct keel puncta | N. seriat. | ||
| Keels distinctly punctate | N. pacifica. | |||
| 4. | Cells up to 70μ | N. closterium. | ||
| Cells 150–800μ | N. longissima. | |||
| 5. | Cells truncate at ends | N. brebisonii. | ||
| Cells with sub-acute apices | N. sigma. |
266. Nitzschia longissima (Breb.) Ralfs. (Pl. 1, Fig. 16.)
Nitzschia longissima (Breb.) Ralfs in Pritch., 1861.
Ceratoneis longissima Breb. in Kütz., 1849, 891.
Cells solitary, spindle-shaped with a single chromatophore which extends into the awns of the frustule, similar to N. closterium. Length, 140–800μ.
Distribution. Marine; found on fouling test plates, or planktonic. Australia north and east Australia, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking, Eden, Port Phillip, Fremantle New Zealand Antarctic south of New Zealand.
267. Nitzschia closterium (Ehr.) W.S. (Pl. 1, Fig. 17.)
W. Sm., 1853, 42, 15, 120.
Boyer, 1927b, 526.
Hend., 1937, 352, 11, 1.
Ceratoneis closterium Ehr., 1840, 44.
Cells solitary but usually interlocked to form a network, or if attached, arranged parallel to each other, vertically to the substrate, frustules in valve view fusiform, with ends drawn out into long awns curved in the same or in opposite directions; striae distinct. Length, 54 to 64μ.
Distribution. Epontic, benthic, planktonic; euryhaline; the commonest diatom in the estuarine environment. Australia: found at all stations, Queensland to Eden.
268. Nitzschia seriata Cl. (Pl. 1, Fig. 18.)
Cl., 1883, 3, 478.
Boyer, 1927b, 526.
Lebour, 1930, 213, 78.
Cells colonial, in staggered formation, united near their ends, and moving in a sliding fashion relative to each other, frustules fusiform; keel puncta indistinct, obsolete or nearly so, about the same number as the striae. Length, 35–50μ.
Distribution. Estuarine-neritic, marine; planktonic and epontic on rocks, algae, sea grasses, and fouling test plates Australia: North Australia, Lake Macquarie, Port Jackson, Botany Bay, Port Hacking, Eden, Port Phillip, Derwent River, Fremantle Harbour, and in coastal plankton tows from Queensland, New South Wales, Victoria, Tasmania and Western Australia; winter form in plankton from Sandy Cape offshore station to Storm Bay New Zealand: frequent in phytoplankton tows from many stations, distribution appears general.

269. Nitzschia sigma (Kütz.) W. Sm. (Pl. 1, Fig. 19.)
W. Sm., 1853, 39, 13, 108.
Hend., 1951, 74, 16, 11.
Synedra sigma Kütz., 1844, 67.
Frustule in valve view linear, slightly sigmoid, with sub-acute apices; keel distinct, excentric; valves transversely striated. Length, 30–40μ.
Distribution. Estuarine, benthic; observed twice as dominant benthic form, but rare otherwise. Australia: Botany Bay and Lake Macquarie, North Queensland.
270. Nitzschia hungarica Grun. (Pl. 8, Fig. 114.)
Grun., 1862, 568, 12, 31.
Boyer, 1927b, 498.
Hend, 1951, 73, 15, 8.
Cells solitary, frustules in valve view linear, margins slightly concave, ends rounded to acute, keel puncta well defined, striae obvious, transverse Length, 80–120μ.
Distribution. Estuarine, epontic on fouling plates. Australia: Heron Island, Lake Macquarie, Port Hacking, Lake Conjola, North Queensland.
271. Nitzschia angularis W. Sm. (Pl. 1, Fig. 20.)
W. Sm., 1853, 40, 13, 117.
Boyer, 1927b, 511.
Hend., 1951, 74, 11, 5.
Cells usually free, solitary; valves lanceolate, inflated towards the centre; keel central, puncta large, prominent, unequal in size. Longitudinal, like on either side of keel; valve striae indistinct Length, 40μ.
Distribution. Estuarine, benthic Australia: Port Hacking on one occasion.
272. Nitzschia brebissonii W. Sm. (Pl. 1, Fig. 21.)
W. Sm., 1853, 38, 31, 266.
Pant., 1902, 88, 261.
Boyer, 1927b, 513.
Cells solitary; frustule sigmoid, truncate at ends; valves linear, straight, arcuate or sigmoid with produced, obtuse ends; keel puncta coarse, central; striae transverse, fine, filiform. Length, 150–200μ.
Distribution. Usually fresh water; uncommon generally, but numerous at Lake Conjola, Australia, in brackish water.
273. Nitzschia plana W. Sm. (Pl. 8, Fig. 118., Pl. 1, Fig. 22.)
W. Sm., 1853, 42, 15, 114.
Frustule in valve view linear-elliptic, with slight median constriction and rounded ends with acute apices; keel almost marginate and very heavily punctate; puncta oblong; valve surface faintly striate. Length, 70μ.
Distribution. Planktonic. Australia: Waterhouse Island, Bass Strait.
274. Nitzschia pacifica Cupp. (Pl. 1, Fig. 23.)
Cupp., 1943, 204, 157.
Cells spindle-shaped, slightly sigmoid, forming chains by overlapping ends; striations punctate, keel punctate, thus differing from N. seriata. Length, 30–40μ.
Distribution. Antarctic, south of New Zealand. Relatively common.
275. Nitzschia martiana (Ag.) Schütt. (Pl. 1, Fig. 24.)
Schütt, 1896, 144, 261.
Homoeocladia martiana Ag., 1830, 25.
Homoeocladia moniliformis Kütz., 1844, 110, 22, 10.
Cells in bundles within a tubular, sub-membranaceous branched filament; frustules linear, with obtuse ends; keel puncta faint; cell length, 50μ.
Distribution. Estuarine, marine; epontic, on fouling test plates from Port Jackson, Australia, in tufts up to ½ inch in length.
The following species of Nitzschia have been recorded previously:—
-
N. amphibia Grun. v. acutiuscula Cl. & Grun., 1880. (Østrup, 1910, 162.) Australia.
-
N. antiqua Gr. & St. (Gr. & St., 1887, 73.) Oamaru. (=N. groveana de Toni.)
-
N. distans Greg., v. australiensis Cl. & Grun. (Cl. & Grun. 1880.) Australia.
-
N. entomon Ehr. (Ralfs in Pritch., 1861.) Australia.
-
N. graeffii Grun. (In Cl. & Grun., 1880.) Australia.

-
N. granulata Grun. (In Cl. & Grun., 1880.) Australia.
-
N. grovei Grun. (In A.S., 1922, 351, 8.) Oamaru.
-
N. gruendleri Grun. in Cl., 1877. (Gr. & St., 1877.) Oamaru.
-
N. guineensis Hust., 1922 (in A.S., 1922, 346, 8). New Guinea.
-
N. lata Witt (Petit, 1877, 29). Campbell Island, Lyall Bay, Foveaux Strait. (N. panduriformis v. lata.)
-
N. marginulata Grun. v. subconstricta Cl. & Grun., 1880. (Østrup, 1910, 149.) Australia.
-
N. nicobarica Grun. (in Cl. & Grun., 1880). Australia.
-
N. novae-hollandiae Grun. (in Cl. & Grun., 1880). Type loc. Yarra.
-
N. panduriformis Greg., 1857. (Petit, 1877.) Lyall Bay, Campbell Island, Foveaux Strait.
-
N. spectabilis (Ehr.) Ralfs non W. Sm. (in Pritch., 1861). Australia.
-
N. subacuta Hust., 1921. (In A.S., 1922, 346, 24–26). New Guinea.
-
N. tenuistriata Hust., 1922 (in A.S., 1922, 348, 92–93). New Guinea.
-
N. tryblionella v. yarrensis Grun. (in Cl. & Grun., 1880). Java.
Bacillaria Gmelin
Cells linear-oblong, united into moveable colonies by its neighbouring cells; movement either as a group or by individual cells relative to one another; keel straight, median, punctate.
Many authors, including Boyer, unite Bacillaria and Nitzschia in which case Bacillaria antedates Nitzschia. Hendey considers the characters are distinctive enough for separation of the genera (see Hendey, 1951, pp. 74–75), and also for synonymy.
276. Bacillaria paxillifer (O. F. Muller) Nitzsch. (Pl. 8, Fig. 119.)
Nitzsch 1817, 75.
Hend 1851, 74.
Vibrio paxillifer O. F. Muller 1786, 54.
Bacillaria paradoxa Gmelin, 1788, 3903, ex Nitzsch 1817.
Cells in colonies arranged in palisade formation or free; frustules linear-lanceolate to lanceolate, with tapering, blunt extremities; keel puncta strong, central, striae transverse; cells in colonies actively motile with respect to each other. Length, 50–75μ.
Distribution. Estuarine-neritic, marine; planktonic, benthic, epontic on algae, sea grasses, fouling test plates, Queensland, New South Wales, Victoria, South Australia, Tasmania and Western Australia, New Zealand. Very widely distributed.
Genus Hantzschia Grun. in Cl. & Grun., 1880
Cells free; frustules in valve view arcuate with rostrate ends. dorsal margin concave, ventral straight or slightly convex with rostrate ends; keels opposite, excentric; keel puncta short, or prolonged into costae, extending over entire valve or part of it; median puncta distant with evidence of a pseudo-nodule, plastids, four.
277. Hantzschia amphioxys (Ehr.) Grun. (Pl. 8, Fig. 120.)
Grun. in Cl. & Grun., 1880, 103.
Boyer, 1927b, 528.
Eunotia amphioxys Ehr., 1843, 125.
Cells solitary, frustules linear-arcuate, ends rostrate; keel on concave margin, punctate; striae punctate, moniliform. Length, 35–60μ.
Distribution. Estuarine, brackish water, and occasionally in more marine waters; common. Australia: Moreton Bay, Lake Macquarie, Port Hacking. From New Zealand as Eunotia amphioxys by Ehr. (1869).
Suborder Surirellineae
Family Surirellaceae
Genus Surirella Turpin, 1828
Cells solitary; frustules in valve view linear-elliptic oval, or ovate sometimes constricted; valve surface nearly flat or spirally twisted; girdle view linear or cuneate; costae long or short, converging from margins towards central space; intermediate striae more or less evident; central space linear or lanceolate, often obscure; valves with longitudinal, central “pseudoraphe”.

(Hendey, in litt., does not consider this a pseudo-raphe), and marginal, more or less elevated, keels produced into wings (alae) containing the raphes on each side. Distinct canal pores usually visible.
| 1. | Frustules slightly constricted in the middle | S. javanica. | |
| Frustules broadly elliptic | S. fastuosa. | ||
| Frustules ovate, tapering | 2. | ||
| Frustules lanceolate, ovate | S. elongata. | ||
| Frustules broadly ovate | S. ovalis. | ||
| 2. | Striae well defined near centre | S. fastuosa. | |
| Striae faint | S. gemma. | ||
| Striae punctate | S. tenera. |
278. Surirella fastuosa (Ehr.) Kütz. (Pl. 8, Fig. 121a.)
Kütz., 1844, 62, 28, 19.
Boyer, 1916, 127, 35, 1.
Hend, 1951, 75, 9, 7.
Navicula fastuosa Ehr., 1841, 19.
Cells solitary; frustule in valve view ovate or broadly elliptic; valves with costae inflated at margins, tapering to central area which is broadly lanceolate and hyaline or very faintly striate; striae more evident at margins, and toward centre where they are well defined and parallel to the margins. Length, 65μ.
Distribution. Estuarine-neritic, marine; benthic and epontic, on weeds and fouling test plates. Australia: Heron Island, Moreton Bay, Lake Macquarie, Botany Bay, Port Hacking. New Zealand Hauraki Gulf, Lyall Bay (Petit, 1877). Frequent but never abundant. var.? (Pl. 8, Fig. 121b.)
Differs from type in narrower central area, and in having the ratio of the septa in the central area to those of margin of three to one.
Distribution. Brackish water; Port Hacking.
279. Surirella gemma (Ehr.) Kütz., 1844. (Pl. 8, Fig. 122.)
Kütz., 1844, 62, 7, 11.
Boyer, 1916, 125, 36, 4, 1927, 540.
Hend., 1951, 76, 8, 10.
Navicula gemma Ehr., 1840, 76, 4, 5.
Cells solitary; frustule in girdle view narrow-cuneate, valves ovate to elliptic-ovate; alae very reduced; axial area very narrow; surface faintly striate between unequally distant costae, which reach median line. Length, 75–80μ.
Distribution. Estuarine; benthic, mesohaline, epiphytic, infrequent. Australia: Lake Macquarie, Port Hacking, Botany Bay. New Zealand: Hauraki Gulf.
280. Surirella tenera Greg. (Pl. 8, Fig. 123a, b; Pl. 9, Fig. 123c.)
Greg., 1856, 4, 11.
Boyer, 1927b, 540.
Valves ovate, rounded at one end, acute at other; central space narrow, well defined; costae indistinct, striae punctate, evident near margin. Length, 100–150μ.
Distribution. Australia: Port Hacking, Lake Dobson.
var. ? (Pl. 8, Fig. 123b.)
Distribution. Australia: Lake Dobson.
281. Surirella javanica A.S. (Pl. 8, Fig. 124a, b.)
A.S., 1875, 4, 13.
Valves with rounded ends, slightly constricted in middle, girdle straight; central space lanceolate, well-defined; costae distinct, about 17 on each side; costae of central area alternating. Length, 70μ.
Distribution. Australia: Heron Island, Port Denison (Grun.).
282. Surirella ovalis Breb. (Pl. 8, Fig. 125.)
In Kütz., 1844, 61.
Boyer, 1916, 39, 11; 1927b, 541.
Valves ovate; costae short, marginal, radiate, often unequal; central space ovate, indistinctly costate; striae scarcely visible. Length, 40–80μ.
Distribution. Fresh later. Australia: Lake Dobson.

283. Surirella elongata (Pantocsek) nov. comb. (Pl. 8, Fig. 126.)
Surirella biseriata Breb. var. elongata Pant. 1902, 99, 12, 293.
Valves lanceolate-ovate, ends acute; costae marginal, central space represented by an irregular line; surface of valve punctate, puncta large, irregularly dispersed over valve surface. Length, 50–80μ.
Distribution. Fresh later. Australia Lake Dobson.
The following species of Surirella have been recorded previously:—
-
S. biseriata Breb., 1835. (Petit, 1877, 29.) Lyall Bay.
-
S. craticula Ehr. (is Navicula cuspidata Kütz., 1844)
-
S. filholii Petit. (Petit, 1877, 30.) Foveaux Strait.
-
S. hastata. A.S., 1875. (A.S., 1875, 21, 4.) Australia.
-
S. hochstetteri Ehr., 1869 (Ehr., 1869). New Zealand.
-
S. intermedia (Stenopterobia intermedia) Lewis, 1863. (Petit, 1877, 30.) Lyall Bay.
-
S. munda Hust., 1927 (in A.S., 1927, 366, 1). Bass Strait.
-
S. robusta Ehr., 1840. (Hardy, 1910.) Kew, Victoria.
Genus Campylodiscus Ehr., 1841
Cells solitary; frustules with two saddle-shaped valves at right angles to each other; valve surface costate, costae mostly converging from margin towards hyaline centre which sometimes appears like a pseudoraphe; plastids. 2.
| 1. | Costae continued across median space | C. undulatus. | |
| Costae not continued across median space | 2. | ||
| 2. | Median space linear | 4. | |
| Median space more or less rectangular | 3. | ||
| 3. | Costae forked towards margin | C. adriaticus. | |
| Costae paired | C. ornatus. | ||
| 4. | Area with transverse costate lines | C. crebrecostatus. | |
| Area clear | C. biangulatus. | ||
| Area finely striate | C. samoensis. |
284. Campylodiscus ornatus Grev., 1863. (Pl. 8, Fig. 127.)
Grev., 1863b, 13, 1, 3.
A.S., 1875, 51, 6, 17, 17.
Boyer, 1927b, 555.
Cells solitary; frustule discoid-saddle shaped; costae converging from margins towards hyaline centre, then tapering, paired; rows of parallel poroids between each rib; central area more or less rectangular, punctate. Diameter, 85μ.
Distribution. Estuarine. Epiphytic. Australia: Port Hacking, Lake Macquarie, v.mesoleia Grev., 1863. From Australia by A.S. (1875) 51.
285. Campylodiscus adriaticus Grun. (Pl. 8, Fig. 128a, b.)
Grun., 1862, 126, 11, 8.
A.S., 1875, 16, 13.
In valve view sub-orbicular, somewhat flexuous; costae radiate, forked near margin, with fine interstitial puncta; median area subquadrate, with two folds. Diameter, 70μ.
Distribution. Australia: Port Hacking.
286. Campylodiscus undulatus Grev. (Pl. 9, Fig. 129a.)
Grev., 1863b, 3, 229.
Boyer, 1927, 550.
Suborbicular in valve view; costae bifurcating, continued across median area but interrupted by lanceolate median space; very variable form Diameter, 100μ.
Distribution. East Australian estuaries, not uncommon.
v leudigeri Deby. (Pl. 9, Fig. 129b.)
Differs from type in narrow median space.
Distribution. Australia: Port Hacking.

287. Campylodiscus biangulatus Grev. (Pl. 9, Fig. 130.)
Grev., 1863, 4, 2.
Grun., 1862, 120.
A.S., 1875, 14, 18–22.
Valves heart-shaped, strong convolute; costae strong, bifurcate near margin, reaching linear-ovate median space; costae strong, very strong in valve view. Diameter, 60–80μ.
Distribution. Australia: West of Bass Strait.
288. Campylodiscus samoensis Grun. (Pl. 9, Fig. 131.)
In A.S., 1875, 15.
C. incertus A.S., 1875, 15.
Valves suborbicular; rays narrow, extending to about half radius; area elliptical, with narrow, linear median space from which extend transversely finely punctate striae. Diameter, 70μ.
Distribution. New Zealand: Auckland Harbour; Campbell Island (Petit, 1877).
289. Campylodiscus crebrecostatus Grev. (Pl. 9, Fig. 132.)
Grev., 1863b, 11, 14.
Boyer. 1927b, 550.
Valves sub-orbicular; costae extending to ⅓ of radius; area elliptical with transverse costate lines; median space narrow, linear. Diameter, 60μ.
Distribution. Australia: Heron Island. Described from Port Jackson, New South Wales, by Greville (type locality). St. Vincent Gulf (A.S., 1875, 15).
290. Campylodiscus daemelianus Grun. (Pl. 9, Fig. 138c.)
In A.S., 1878, 54, 1, 2.
Valves sub-circular, slightly curved; costae thin, extending inwards about ⅓ radius, with two irregular rows of puncta, one on each side of costae and in two orders with a space between, the large central area contains rows of irregularly-spaced puncta, almost parallel in the central portion of valve, radiate towards ends. Diameter, 80–100μ.
Distribution. Australia: Yamba, Gippsland Lakes. Type locality, Yarra Yarra, Victoria.
The following species of Campylodiscus have been recorded previously:—
-
C. diplostictus Norman. (In Pritchard, 1861.) Australia.
-
C. latus Shadb., 1854. (C. kittonianus Grev., 1860; C. ambiguus Grev., 1860; C. contiguus A.S., 1875; C. centralis Greg., 1857). (A.S, 1893, 207, 6.) Australia.
-
C. ornatus v. mesoleia Grev., 1863. (A.S., 1875, 51.) Australia.
-
C. ralfsi W. Sm., 1863. (Petit, 1877, 30.) Lyall Bay.
-
C. simulans Greg. (Petit, 1877, 31.) Campbell Island. (C. thuretii Breb.)
-
C. robertsianum Grev., 1861 Harvey Bay (=C. diplostictus Norm.)
Appendix to Descriptive Section
The following species of centric forms have been observed since Part 1 was prepared for press.
Genus Melosira
291. Melosira crenulata (Ehr.) Kütz. (Pl. 9, Fig. 133.)
Kütz., 1844, 55.
Boyer, 1927a, 29.
Gallionella crenulata Ehr., 1843, 2.
Cells in short chains; frustules cylindrical, two to three times longer than broad, denticulate at junction of cells with a narrow furrow on each side of suture; puncta irregular or transverse. Length, 25μ.
Distribution. Fresh water. Australia: Lake Dobson.
Genus Coscinodiscus
292. Coscinodiscus argus Ehr. (Pl. 9 Fig. 134, 135.)
Ehr., 1839. 129.
Kolbe, 1954, 28.
Coscinodiscus crassus Bail., 1856, 22, 4.
C. heteroporus Ehr., 1844.

Cells discoid, solitary; small angular central space present, valve markings larger near centre, angular, somewhat irregular, decreasing then increasing to large hexagonal cells, smaller at border. Diameter, 130μ.
Distribution. Australia: Port Hacking, Paynesville (Gippsland lakes), benthic. New Zealand: Auckland Harbour, Hauraki Gulf, planktonic; from Oamaru as C. heteroporus.
293. Coscinodiscus debilis Grove. (Pl. 9, Fig. 136.)
In A.S., 1890, 163, 5.
Cells large, discoid, solitary; valves flat, with no central area; areolae fine, even except near margin, almost radial.
Distribution. Brackish water, benthic Australia: Port Hacking; Lake Dobson. Recorded from Oamaru (type locality).
Genus Cyclotella (Kütz.) Breb. 1838
Frustules single or geminate, cylindrical, discoid; in girdle view rectangular with undulating sides; valves with central area and wide border; the centre bullate, hyaline or with fine radiating lines and scattered puncta; border striate or costate; chromatophores numerous.
294. Cyclotella menenghiniana Kütz. (Pl. 9, Fig. 137.)
Kütz., 1844, 50.
Boyer, 1927a, 38.
A.S., 1900, 222, 23, 24.
Frustules rectangular, slightly undulate in girdle view; central part of valve minutely punctate in radiating lines; margin well defined, wide, coarsely striate, striae transversely punctate. Diameter, 35–40μ.
Distribution. Australia: Clarence River, N.S.W. (near mouth).
The following genera, not listed in Part II, have been described by previous authors from the Australasian region:—
Genus Anaulus Ehr., 1844
-
A. mediterraneus Grun. (in A.S., 1893, 200, 22). Auckland.
-
Genus Caloneis Cleve, 1894
-
C. alpestris (Grun.) Cl., 1894. (Østrup, 1910, 10.) Australia.
-
C. amphisbaena (Ehr.) Cl., 1894. (As Navicula amphisbaena) (Ehr., 1869). New Zealand.
-
C. blanda (A.S.) Cl., 1894. (Østrup, 1910, 11.) Australia.
-
C. liber (W. Sm.) Cl., 1894. (Nav. maxima Greg., Nav. liber W. Sm.) (Petit, 1877.) Foveaux Strait.
-
C. linearis (Grun.) Boyer, 1927. (Nav. linearis Grun.) (Petit, 1877.) Foveaux Strait.
Genus Campyloneis Grun., 1862
-
C. grevillei W. Sm., 1856. (Petit, 1877.) Lyall Bay.
Genus Diatoma D.C., 1805
-
D. cretae Ralfs, 1861 (in Pritch., 1861). Australia.
-
D. hiemale (Lyngb.) Heib., 1865. (Ralfs in Pritch., 1861.) Australia.
-
D. pinnatum (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia.
-
D. striolatum (Ehr.) Kütz., 1844. (Ralfs in Pritch., 1861.) Australia.

Genus Dictyoneis Cl., 1890
-
D. marginatus (Lewis) Cl., 1890 v. janischi Cl., 1894. (A.S., 1893, 188, 50.) Oamaru.
Genus Dimerogramma Ralfs in Pritch., 1861
-
D. australe (Petit) Boyer, 1927, 194. (Petit, 1877.) Type loc. New Zealand. (=Rhaphoneis surirella.)
-
D. fulvum (Greg.) Ralfs, 1861. (Gr. & St., 1887.) Oamaru.
Genus Entopyla Ehr., 1848
-
E. australis Ehr., 1848. (Petit, 1877, 15.) Lyall Bay, Shark Bay. (As Gephyra incurvata Arn. by Gr. & St., 1886, 323.) Oamaru.
-
E. ocellata (Arn.) Grun., 1862 (A.S., 1902, 231, 5–6.) Australia
Genus Eunotogramma Weisse, 1854
-
E. weissii Ehr., 1854 v. producta Gr. & St. (Gr & St, 1886, 8). Oamaru.
Genus Glyphodesmis Grev.
-
G. marginata Gr. & St. (Gr. & St., 1886, 323.) Oamaru.
Genus Omphalopsis Grev., 1863c
-
O. australis Grev., 1863. (Grev., 1863c, 35.) Woodlark Island.
Genus Opephora Petit, 1888.
-
O. pinnata (Jan. & Rab., 1849–50). Petit, 1888. New Zealand.
Genus Podocystis Kütz, 1844.
-
P. adriatica Kütz., 1844. (Petit, 1877.) Lyall Bay.
Genus Rhaphoneis Ehr., 1844.
-
R. nodulifera (Gr. & St.) Brun, 1891 (As Cocconeis nodulifera) (Gr. & St., 1887, 131; A.S., 1893, 193, 12). Oamaru.
-
R. fasciolata Greg., 1857. (Petit, 1877.) Lyall Bay. v. australis Petit, 1877. (Petit, 1877.) Lyall Bal (=R. surirella v. australis).
-
R. rhombus Ehr. (Petit, 1877.) Lyall Bay (=R. amphiceras.)
Genus Rhoicosphenia Grun., 1860
-
R. curvata (Kütz.) Grun. in v H., 1885. (Gr. & St., 1886, 322.) Oamaru.
Genus Rutilaria Grev.
-
R. epsilon Grev., 1863. (Gr. & St., 1887, 74.) Oamaru.
-
R. lanceolata Gr. & St (Gr. & St., 1886, 323.) Oamaru.
-
R. (Pseudorutilaria) monile Gr. & St. (Gr. & St., 1886, 324.) Oamaru.
-
R. pulchra A.S, 1893 (A.S., 1893, 183, 20). Oamaru.
-
R. radiata Gr. & St. (Gr. & St., 1886, 323.) Oamaru.
Genus Stictodesmis Grev., 1863c
-
S. australis Grev., 1863c. (Grev., 1863c, 34.) Harvey Bay, Port of France, New Caledonia.
Genus Toxonidea Donk., 1858.
-
T. falcata Donk., 1858. (Petit, 1857.) Foveaux Strait.

Genus Trachysphenia Petit, 1877
-
T. aucklandica Grun. (Rhaphoneis australis H. L. Sm.) (Boyer, 1927.) Australia.
-
T. australis Petit, 1877. (Petit, 1877.) Campbell Island.
Seasonal Distribution of Epontic Diatoms
The data which have been accumulated in this laboratory on the seasonal distribution of epontic diatoms include information from Botany Bay (Text-fig. 1, Fig. 26) and Lake Macquarie. In each case, there appear to be three diatom maxima in these estuaries, in December-January, in April-May (sometimes May-June) and in August-September On most occasions, there are several species involved in the maximum, but on a particular occasion in Botany Bay (June, 1948) only one species (Nitzschia sigma) occurred, completely overgrowing and excluding most other species. At other times, N. sigma was an unimportant and infrequent member of the flora
A. diatom maximum, as depicted in a graph, usually represents a succession of dominants—i.e., there are several, superimposed peaks. As the species involved in these maxima may vary from season to season, it is difficult to make a detailed correlation of diatom maxima with hydrological conditions.
The Significance of Diatoms
(a) Diatoms As Indicators
The use of diatoms as indicators depends on the existence of species which are sensitive to changes in water conditions. This has been discussed in Part I, as most indicator forms are regarded as planktonic. However, the presence of epiphytic species (e.g., Rhabdonema, Licmophora) in the plankton is an indication of recent or present estuarine influence, and other species (e.g., Striatella irterrupta) indicate brackish water.
The writers have found that, in east Australian estuaries, at a given time, each Zostera flat can often be characterized by the diatom association thereon. Typical

examples are given in Tables I and II, taken from a series of monthly examinations at Lake Macquarie. Fourteen stations, each on a Zostera flat, were taken, and samples of epiphytes collected therefrom. It will be seen that the dominant species change from one station to another, while on some stations the diatom population is sparse and on others it is quite prolific. Table I is for April and Table II for May, 1954.
The same picture was given by a series of weekly stations in Port Hacking. The variability of samples from the same area were checked by taking 12 samples at 50 yard intervals. A pooled sample was made and it was found that the same species (except for occasional rare forms) could be obtained from any five samples as from the pooled sample, so that it was concluded that five sub-samples should be taken on a given flat to show the representative flora of that flat.
[The section below cannot be correctly rendered as it contains complex formatting. See the image of the page for a more accurate rendering.]
| Station. | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 |
| Species. | ||||||||||||||
| Synedra fulgens | *** | * | * | |||||||||||
| S. ulna | * | |||||||||||||
| S. frauenfeldii | * | * | * | * | ||||||||||
| Grammatophora marina | * | * | * | * | * | * | * | * | ||||||
| Melosira juergensii | * | * | ||||||||||||
| M. sulcata | * | * | ** | |||||||||||
| M. moniliformis | * | |||||||||||||
| Pleurosigma formosum | * | ** | * | |||||||||||
| P. angulatum | * | * | ** | * | * | * | ||||||||
| Surirella fastuosa | * | * | * | * | ||||||||||
| Amphora hyalina | * | * | * | |||||||||||
| A. javanica | * | ** | * | * | * | |||||||||
| Licmophora abbreviata | * | * | * | * | ||||||||||
| L. flabellata | * | |||||||||||||
| Terpsinoe musica | * | * | * | * | ||||||||||
| Trachyneis aspera | * | * | ||||||||||||
| Navicula subcarinata | * | * | ||||||||||||
| N. grevillei | ** | |||||||||||||
| Bacillaria paxillifer | * | * | * | |||||||||||
| Biddulphia turgida | * | |||||||||||||
| Cocconeis heteroidea | * | * | ||||||||||||
| Nitzschia longissima | * |

[The section below cannot be correctly rendered as it contains complex formatting. See the image of the page for a more accurate rendering.]
| Stations. | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 |
| Species. | ||||||||||||||
| Synedra fulgens | * | * | *** | * | *** | * | * | * | ||||||
| S. ulna | * | |||||||||||||
| S. frauenfeldii | * | * | * | * | * | |||||||||
| Grammatophora marina | * | * | * | |||||||||||
| Melosira juergensii | * | |||||||||||||
| M. sulcata | * | * | ||||||||||||
| M. moniliformis | * | ** | * | |||||||||||
| Pleurosigma formosum | * | * | ||||||||||||
| P. balticum | * | |||||||||||||
| Surirella fastuosa | * | |||||||||||||
| Amphora hyalina | * | * | ||||||||||||
| Licmophora abbreviata | * | * | ||||||||||||
| L. grandis v. divisa | *** | |||||||||||||
| Terpsinoe musica | *** | * | ||||||||||||
| Navicula subcarinata | * | * | * | * | ||||||||||
| Bacillaria paxillifer | * | ** | ||||||||||||
| Cocconeis heteroidea | * | * | ||||||||||||
| Nitzschia closterium | *** | |||||||||||||
| Mastogloia cribrosa | * | |||||||||||||
| Ma. quinquecostata | * | |||||||||||||
| Striatella unipunctata | * | *** | * | * | * | |||||||||
| Tropidoneis lepidoptera | * | ** | ||||||||||||
| Hantzschia amphioxys | * | |||||||||||||
| Biddulphia aurita | * | |||||||||||||
| Campylodiscus ornatus | * |

| Diatom Species. | Zostera | Mud Surface | Mullet Stomachs |
| Licmophora abbreviata | *** | * | *** |
| L. flabellata | * | ||
| Striatella unipunctata | * | ** | |
| Biddulphia aurita | * | * | |
| Achnanthes longipes | * | ||
| Synedra frauenfeldii | ** | ** | |
| Navicula grevillei | * | ||
| Navicula subcarinata | * | *** | |
| N. brasiliensis | * | ||
| Auliscus sculptus | * | * | |
| Amphora granulata | * | * | |
| A. hyalina | * | ||
| N. lyra v. elliptica | * | ||
| Tropidoneis lepidoptera | * | * | |
| Trachyneis aspera | * |
| Diatom Species | Zostera | Mud Surface | Mullet Stomachs |
| Striatella unipunctata | *** | ||
| Licmophora flabellata | ** | ||
| L. grandis v. divisa | ** | ||
| Achnanthes longipes | * | ||
| Navicula grevillei | * | * | |
| N. subcarinata | * | ** | |
| N. brasiliensis | * | * | |
| N. smithii | * | ||
| Amphora granulata | * | * | |
| A. hyalina | * | ||
| Tropidoneis lepidoptera | * | * | |
| Trachyneis aspera | * | ||
| Pleurosigma balticum | * | ||
| P. fasciola | * | ||
| Nitzschia closterium | * | ||
| N. longissima | * | ||
| Melosira sulcata | * | ||
| Triceratium robertsianum | * | ||
| Biddulphia pulchella | * | ||
| Bellerochea malleus | * |

(b) Diatoms in the Food Cycle
Because of their abundance in the sea, diatoms have been regarded as the chief food of plant-feeding fish, copepods, etc. (see Harvey, 1937, Clarke and Gellis, 1935). Recently, however, Atkins (1945) and others have suggested that the micro-flagellates rival the diatoms in importance, with blue-green algae, dinoflagellates, coccolithophores, Halosphaera and silicoflagellates of lesser importance. There is evidence that copepods and herring avoid large diatom blooms (Manteufel 1941), and in such a case it is probably the saprophytic bacteria and heterotrophic protozoa that afford food for the zooplankton. Marshall and Orr (1956) have shown that copepods can live and metamorphose when feeding on the diatom Skeletonema costatum, and Harvey (1937) suggested selective feeding on certain species by Calanus.
In estuaries, the relation between diatoms and fish is more direct. In the case of phytophagous fish such as the mullets, diatoms, often in large quantities, are found in the gut. Even in fish not normally regarded as plant feeders (e g., leather-jackets), large numbers of diatoms may occur. In one case, the gut contents of such a fish consisted of an almost pure culture of Melosira moniformis.
Although epiphytic diatoms are continually falling onto the mud of a sea-grass flat, the different ratio of species on the weeds and on the mud, enable the observer to separate the two communities. In this way, it has been possible to determine that mullet feed largely on the epiphytes and use the mud as a grinding paste in their stomach mills, to comminute the diatoms of which only fragments remain in the hindgut. Of course, the fish utilize any available material in the muds as well. Table III shows a case where the fish had been feeding on the epiphytes, and not on the mud. In Table IV the fish had obviously been feeding elsewhere than on the flat on which they were caught. Studies of the local diatom floras and of stomach contents of fish may be used to demonstrate the movements of fish in an estuary, since, as has been stated previously, the flora of an estuary changes from place to place.
(c) Diatoms in Marine Fouling
A number of authors have stressed the importance of primary film in marine fouling, and have shown that this film aids in the colonization of a surface by higher organisms (ZoBell 1946, Wood 1950, Hendey 1951, Wood 1953). ZoBell, working on the Californian coast, found that bacteria were the most important micro-organisms occurring in primary films, but Wood found that, in Sydney Harbour, algae and diatoms were more important than bacteria on non-toxic surfaces, though probably not on toxic ones. Hendey, while appreciating the importance of bacteria, gives reasons for the pie-eminence of diatoms “(1) they are the most numerous (apart from bacteria), (2) they are widely distributed throughout the world, (3) they are present at all seasons of the year, (4) they are oxygen producers and provide a rich source of nutriment for the bacterial flora, (5) they affect the hydrogen ion concentiation of the slime, and (6) they are highly resistant to copper and mercury”, the usual toxins used in antifouling paints.
Hendey gives a very useful discussion on the formation of diatom slimes and the resistance to poisons of the species occurring in Chichester Harbour.
The following species have been found on marine fouling test plates in Australian waters:—
| Melosira sulcata | N. lyra v. elliptica |
| M. nummuloides | N. subcarinata |
| M. moniliformis | N. peregrina |
| Biddulphia pulchella | Pleurosigma angulatum |
| B. aurita | P. balticum |
| Grammatophora marina | P. fasciola |
| G. serpentina | P. formosum |
| Striatella unipunctata | Nitzschia angularis |
| Achnanthes longipes | N. dosterium |

| Cocconeis heteroidea | N. longissima |
| Navicula cyprinus | N. sigma |
| N. granulata | N. martiana |
| N. grevillei | N. hungarica |
| N. lyra | Surirella fastuosa |
| Actinoptychus senarius | Surirella gemma |
| Auliscus sculptus | Diploneis crabro |
| Cerataulina pclagica | D. smithii |
| Synedra fulgens | M. cribrosa |
| S. undulata | M. strigilis |
| Rhabdonema adriaticum | Amphora alata |
| Licmophora flabellata | A. gigantea |
| L. abbreviata | A. hyalina |
| L. grandis v. divisa | A. javanica |
| L. grandis v. divisa | A. spectabilis |
| Pinnularia major | A. proteus |
| Trachyneis aspera | Hantschia amphioxys |
| Anomoeoneis serians | Bacillaria paxillifer |
| Tropidoneis lepidoptera | Campylodiscus ornatus |
This flora has much in common with that described by Hendey, though some northern species have been replaced by their southern hemisphere counterparts. It is obviously related to the flora of the estuaries, and there is no evidence of a specific fouling flora to correspond with the fauna that is often specific to fouling associations.
On toxic surfaces, selectivity occurs, as Hendey has pointed out, and this selectivity is due to a difference in the resistance of individual species to the poisons used to combat fouling. The resistance of some Australian species to copper and mercury is given in Table V.
Unfortunately, the actual concentrations of the poisons in the paints referred to in Table V is not known, but the mercury paint was more inhibitory than the copper. Stanbury, working at Plymouth, England, found that some species—e.g., Amphora exigua, Amphiprora paludina, Achnanthes longipes, Navicula grevillei, Nitzchia closterium and Cocconeis scutellum, resisted higher concentrations of mercury than of copper in in vitro experiments.
Diatoms can attach readily to moving surfaces, and Wood (1956) found that they assisted in forming a felt (primary film) on a disc the periphery of which was rotating at a continuous 11.2 knots. As the stationary controls, did not have a diatom felt, it would appear that the movement favoured growth of diatoms by inhibiting the attachment of other organisms, which failed at speeds above 2 knots.
| Non-toxic Controls | Mercury Paint | Cold Plastic MI. 143E | High Leaching Rate Copper |
| Nitzschia longissima | N. longissima | N. longissima† | |
| N. closterium | N. closterium | ||
| Amphora arcta | A. arcta | A. arcta | A. arcta† |
| Licmophora abbreviata | L. abbreviata | L. abbreviata† | |
| Climacosphenia moniligera | |||
| L. flabellata | L. flabellata | ||
| Grammatophora marina | G. marina | ||
| Cocconeis heteroidea | |||
| Melosira moniliformis | |||
| Coscinodiscus centralis | C. centralis |

IX. Acknowledgments
The writers have to acknowledge the very great help and encouragement that they received from Mr. N. Ingram Hendey, who gave freely of his experience, to Professor V. J. Chapman for his interest in publication of the papers, Dr. M. Cassie for supplying material from New Zealand, and to Mr. R. Breach for his able assistance with the microphotography.
Bibliography
Agardh, C., 1824–1832. Conspectus Criticus Diatomacearum. Parts 1–3. Lund.
Aleem, A. A., 1950. The diatom community inhabiting the mud-flats at Whitstable, Kent. New Phytol. 49: 174–188
Allen, W. E., and Cupp, Easter E., 1935. Plankton Diatoms of the Java Sea. Ann. Jard. Bot. Buitenz. 44: 101–174.
Atkins, W. R. G., 1945. Autotrophic flagellates as the major constituent of the oceanic phytoplankton. Nature, 156: 446–7.
Baas Becking, L. G. M., and Wood, E. J. F., 1955. Biological processes in the estuarine environment, 1 and 2. Ecology of the sulphur cycle. Proc. Kon. Ned. Akad. Wet. 58B: 160–181.
Bailey, J. W., 1851. Microscopical observations made in South Carolina, Georgia and Florida. Smithson. Contr. Knowl. 2: 8.
— 1853–54. Notes on new species and localities of microscopical organisms. Smithson. Contr. Knowl. 7: 1–16.
—1855. New species of the Diatomaceae. Quart. J. Micr. Sci. 3.
— 1856. On microscopic forms in the Sea of Kamchatka. Amer. J. Sci. Arts, 2: 22.
Bailey, L. W., 1862. Notes on new species of microscopical organisms chiefly from the Para River, South America. Bost. J. Nat. Hist. 7.
Bergon, P., 1903. Etudes sur la flore diatomique du Bassin d'Arcachon et des parages de l'Atlantique voisins de cette station. Bull. Soc. d'Arcachon Stat. Biol. 6.
Boden, B. P., 1950. Some marine plankton diatoms from the west coast of South Africa. Trans. Roy. Soc. S. Afr. 32: 321–434.
Boyer, C. S., 1900. The biddulphoid forms of North American Diatomaceae. Proc. Acad. Nat. Sci. Philad. 52: 685–748, 1900.
— 1916. The Diatomaceae of Philadelphia and Vicinity. (J. B. Lippincott: Philadelphia.)
— 1927a. Synopsis of North American Diatomaceae. Part 1. Coscinodiscatae, Rhizoselenatae, Biddulphiatae, Fragilariatae. Proc. Acad. Nat. Sci. Philad. 78: Suppl.: 1–228, 1926.
— 1927b. Synopsis of North American Diatomaceae. Part II. Naviculatae, Surirellatae. Proc. Acad. Nat. Sci. Philad. 79, Suppl. 229–582.
Bory de Saint Vincent, 1822. Dict. Class. Hist. Nat. 1: 79 (Paris).
Braarud, T., 1937. A quantitative method for the experimental study of plankton diatoms. J. Cons. int. Explor. Mer. 12: 321–32.
Brebisson, A. De, 1838. Considerations sur les diatomées et essai d'une classification des genres et des éspèces appartenant à cette famille. Falaise, 1838.
— (1854) 1867. Notes sur quelques diatomées marines, nouvelles ou rares du littoral de Cherbourg. Mem. Soc. Imp. Cherbourg, 1854.
Brightwell, T., 1856. On the filamentous, long-horned Diatomacea. Quart. J. Micr. Sci. 4.
— 1858a. Remarks on the genus Rhizosolenia of Ehrenberg. Quart. J. Micr. Sci. 6.
— 1858b. Further observations on the genera Triceratium and Chaietoceros. Quart. J. Micr. Sci. 6.
— 1859–60. On some of the rarer or undescribed species of Diatomacea. Parts 1 and 2. Quart. J. Mict. Sci. 7, 8.
Callame, B., and Debuyser, J., 1954. Observations sur les mouvements des diatomées à la surface des sédiments marins de la zone intercotidiale. Vie et Milieu 5: 243–249.
Castracane, A. F. de, 1886. Report on the Diatomaceae collected by H.M.S. Challenger during the years 1873–76. Rept. Challenger Exp. Botany, 2.
Clarke, G. L. and Gellis, S. S., 1935. The nutrition of copepods in relation to the food cycle of the sea. Biol. Bull. 68: 231–246.
Cleve, P. T., 1873a. Examination of diatoms found on the surface of the Sea of Java. Bih. svensk. Vetenskakad. Handl. 1 (11): 1–13.
— 1873b. On diatoms from the Arctic Sea. Bih. svensk. Vetenskakad. Handl. 1 (13): 1–28.

Cleve, P. T., 1878. Diatoms from the West Indian archipelago. Bih. svensk. Vetenskakad. Handl. 5 (8): 1–22.
— On some new and little-known diatoms. Bih. svensk. Vetenskakad. Handl. 18 (5): 1–28.
— 1883. Diatoms collected during the expedition of the Vega. Vega-Exped. Vetensk. Arbet. Iakttag. 3: 457–517.
— 1889. Pelagiske Diatomeer från Kattegat. Vidensk. Udbytte kanonbaaden. “Hauchs” Togter Danske Have. (1): 53–6.
— 1891. Diatoms of Finland. Acta. Soc. Fauna Flora Fenn. 8:
— 1894. Planktonunterskningar. Cilioflagellater og Diatomaceer. Bih. svensk. Vetenskakad. Handl. 20 (3), 2.
— 1894–5. Synopsis of the naviculoid diatoms. Parts 1 and 2. Bih. svensk. Vetenskakad. Handl. 26 (2): 1–194. 27 (3): 1–219.
— 1896. Planktonuntersokningar. Vegetabiliskt Plankton. Bih. svensk. Vetenskakad. Handl. 22 (3) 5.
— 1897a. A treatise on the phytoplankton of the Atlantic and its tributaries. Uppsala.
— 1897b. Report on the phytoplankton collected on the expedition of H.M.S. Research, 1896. 15th Ann. Rep. Fish. Bd. Scot. (3): 297–304.
— 1900a. Notes on seme Atlantic plankton organisms. Bih. svensk. Vetenskakad. Handl. 34 (1): 1–22.
— 1900b. Plankton from the Southern Atlantic and the Southern Indian Oceans. Ofver. svensk. Vetenskakad. Forh. 8.
— 1901. The seasonal distribution of Atlantic plankton organisms. K. Vet. och Vett. Samh. Handl. 17.
— and Grunow, A., 1880. Beitrage zur Kenntnis der arctischen Diatomeen. Bih. svensk. Vetenskakad. Handl. 17 (2): 1–121.
— and Moller, J. D., 1877–1882. Diatoms, Parts I-VI. Upsala u. Wedel.
Cleve-Euler, A., 1953a. Die Diatomeen von Schweden und Finnland. Teil II. Araphideae, Brachyraphideae. K. svenska Vetenskakad. Handl. (4) 4 (1): 1–158.
— 1953b. Die Diatomeen von Schweden und Finnland. Teil III. Monoraphideae, Biraphideae 1. K. svenska Vetenskakad. Handl. (4) 4 (5): 1–255.
Cupp, E. E., 1943. Marine plankton diatoms of the west coast of North America. Bull. Scripps Instn. Oceanogr. tech. 5 (1): 1–238.
Dakin, W. J. and Colefax, A. N., 1940. The plankton of the Australian coastal waters off New South Wales. 1. Publ. Univ. Dept. Zool. Monogr. 1.
De Toni, G. B., 1891–1894. “Sylloge Algarum Omnium Hucusque Cognitarum. 2. Sylloge Bacillariarum, sect. III.” (Typis Seminarii: Patavii.)
Dillwyn, L. W., 1809. British Confervae, London.
Donkin, A. S., 1858. On the marine diatomaccae of Northumberland, with a description of 18 new species. Trans. Micr. Soc. 6: 12–34.
— 1871. The natural history of the British Diatomaceae. 1.
Ehrenberg, C. G., 1828. Die geographische Verbreitung der Infusionsthierchen in Nord-Afrika und West-Asien, beobachtet auf Hemprich und Ehrenbergs Reisen.
— 1830. Beitrage zur Kenntnis der Organisation der Infusorien und ihrer geographischen Verbreitung, besonders in Sibirien. Abh. Kgl. Akad. dtsch. Wiss. Berl. 1830: 1–88.
— 1832. Zur Erkenntnis der Organisation in der Richtung des kleinsten Raumes. Zweiter Beitrag.” Abh. Kgl. Akad. dtsch. Wiss. Berl.
— 1836. Über das Massenverhaltnis der jetzt lebenden Kiesel-Infusorien und über neues Infusorien-Conglomerat als Polirschiefer von Jastraba in Ungarn. Abh. Kgl. Akad. dtsch. Wiss. Berl. 1836: 109–132.
— 1838. Die Infusionsthierchen als vollkommene Organismen. Ein Blick in das tiefere organische Leben der Natur. Leipzig. Leopold Voss.
— 1839. Die Bildung der europaischen, libyschen, und arabischen Kreidefelscn und des Kreidemergels aus mikroskopischen Organismen. (Abh. Kgl. Akad. dtsch. Wiss. Berl.) 56–147.
— 1840. Über noch zahlreich jetzt lebende Tierarten der Kreidebildung und den Organismus der Polythalamien. Abh. Kgl. Akad. dtsch. Wiss. Berl. 4: 81–174.
— 1843a. Neue Beobachtungen uber den sichtlichen Einfluss der mikroskopischen Meeres-Organismus auf den Boden des Elbbettes bis oberhalb Hamburg. Mon. Akad. Wiss. Berl.
— 1843b. Verbreitung und Einfluss des mikroskopischen Lebens in Sud-und Nord-Amerika. Abh. Kgl. Akad. dtsch. Wiss. Berl. 1841: 291–446.
— 1844. Einige vorlaufige Resultate seiner Undersuchungen der ihm von der Sudpolreise des Capitan Ross sowie von den Herre Schayer und Darwin zugekommen Materiel en. Mon. Akad. Wiss. Berl. 182–207.

Ehrenberg, C. G., 1845. Neue Untersuchungen über das kleinste Leben als geologisches Moment. Mon. Akad. Wiss. Berl. 53–88.
— 1849. Passatstaub und Blutregen. Ein grosses organisches unsichtbares Wirken und Leben in der Atmosphäre. Abh. Kgl. Akad. dtsch. Wiss. Berl. 1847. 269–460.
— 1854. Mikrogeologie. Leipzig.
— 1869. Über machtige Gebirgs-Schichten vorherrschend aus mikroskopischen Bacillarien unter und bei der Stadt Mexico. Abh. Kgl. Akad. dtsch. Wiss. Berlin.
— 1873. Mikrogeologische Studien uber das kleinste Leben der Meeres Tiefgrunde aller Zonen und dessen geologischen Einfluss. Abh. Kgl. Akad. dtsch. Wiss. Berl. 1872: 131–397.
Engler, A., 1883. über die pelagischen Diatomeen der Ostsee. Ber. deut. bot. Ges. 1. Berlin.
Gough, Lewis H., 1905. Report on the plankton of the English Channel, in 1903. Mar. Biol. Ass. Internat. Inv. Rept. 1. 325–77.
Gran, H. H., 1897. Protophyta; Diatomacea, Silico-flagellata and Cilioflagellata. Norske Nordhaus. Exped. 1876–78. 24: 1–36.
— 1900. Bermerkungen uber einige Planktondiatomeen. Nyt. Mag. Naturvidensk. 38: 103–6.
— 1904. Die Diatomeen der Arktischen Meere I. Die Diatomeen des Planktons. Fauna Antarctica 3: 511–54.
— 1905. Diatomeen. Nord. Plankt. 3 (19): 1–146.
— and Angst, E. C., 1931. Plankton diatoms of Puget Sound. Publ. Puget. Sd. Mar. (Biol.) Sta. 7: 417–519.
— and Thompson, T. G., 1930. The diatoms and the physical and chemical condition of the sea water of the San Juan archipelago. Publ. Puget Sd. Mar. (Biol.) Sta. 7: 169–204.
Gray, S. F., 1821. A natural arrangement of British plants.
Gregory, R. W., 1856. Notice on some new species of British freshwater diatoms. Quart. J. Micr. Sct. 4.
Gregory, W., 1857. On new forms of marine Diatomaceae found in the Firth of Clyde and in Loch Fyne. Trans. Roy. Soc. Edinb. 21: 473–542.
Greville, R. K., 1827. Scottish cryptogam flora.
— 1855. Report on a collection of Diatomaceae made by Prof Balfour and M. G. Lawson in the district of Braemar. Ann. Mag. Nat. Hist. Ser. 2, 15.
— 1859. Descriptions of diatomaceae observed in California guano. Quart. J. Micr. Sct. 7: 155–66.
— 1860. A monograph on the genus Asterolampra including Asteromphalus and Spatangidium. Trans. Micr. Soc. 8: 102–24.
— 1861. Descriptions of new and rare diatoms, 1–4. Trans. Micro. Soc., 9, 39–45, 67–87.
— 1862. Descriptions of new and rare diatoms. 5–6. Trans. Micro. Soc. 10, 18–29, 89–96. 7, Quart, J. Micr. Sci. n.s. 2, 231–236.
— 1863a. A monograph of the genus Auliscus. Trans. Micro. Soc. 11: 36–53.
— 1863b. Descriptions of new and rare diatoms 8–9. Trans. Micro. Soc. 11, 13–21, 63–76. 10, Quart. J. Micr. Sci. 3: 227–237.
— 1863c. Descriptions of new genera and species from the South Pacific. Edinburgh New Phil. J.. 18, 34–43, 181–187.
— 1864. Descriptions of new and rare diatoms. 11–13. Trans. Micr. Soc. 12: 8–14. 81–86, 86–94.
— 1865a. Descriptions of new and rare diatoms. 14–17. Trans. Micr. Soc. 13: 1–10: 24–34; 43–56; 97–105.
— 1865b. Descriptions of genera and species from Hong Kong. Ann. Mag. Nat. Hist. 16.
— 1866. Descriptions of new and rare diatoms. 18–20. Trans. Micr. Soc. 14: 1–9, 77–86, 121–130.
— and Arnot, 1857. See Gregory W., 1857.
Gross, F., and Zeuthen, F., 1948. The buoyancy of diatoms; a problem in cell physiology. Proc. Roy. Soc. Edinb. B135.
Grove, E., and Sturt, G., 1886–7. On a fossil marine diatomaceous deposit from Oamaru, Otago, New Zealand. Quart. J. Micr. Sci. 17: 321–330. 18: 7–12, 63–78, 131–148.
Grunow, A., 1860. über neue oder ungenugend gekannte Algen. Verh. Zool.-bot. Ges. Wien. 1860: 503–582.
— 1862. Die österreichischen Diatomaceen nebst anschluss einiger neuen Arten von andern Lokalitaten und einer kritischen übersicht der bisher bekannten Gattungen und Arten, 1 and 2. Verh. Zool.-bot. Ges. Wien. 12: 315–472, 544–588.
— 1863. Über einige neue ungenugend bekannte Arten und Gattungen von Diatomaceen. Verh. Zool.-bot. Ges. Wien. 13, 137–162.

Grunow, A., 1867. Nachtragliche Bermerkungen uber die von Herrn Lindig gesammelten Diatomeen von Honduras. Hedwigia 6, 33–37.
— 1868. Reise seiner Majestat Fregatte Novara um die Erde. Bot. Teil. 1: 1–104.
— 1877. Trans. of Grunow 1867 by F. Kitton. Trans. Micr. Soc. 18.
— 1878. Algen und Diatomaceen aus dem Kaspischen Meere. In Dr. Schneider, Naturw. Beit. zur Kauk auf Grunde sein Sammel. Dresden.
— 1884. Die Diatomeen von Franz Josefs-Land. Denkschr. Akad. Wiss. Math. Naturw. Klasse. 48: 53–112.
Hantzsch, C. A., 1862. Uber einige Diatomaceen aus dem Ostindischen Archipel. Rabenh Beitr. 1. 4.
Hart, T. M., 1937. Rhizosolenia curvata Zacharias, an indicator species of the Southern Ocean. “Discovery” Rep. 16: 413–446.
Harvey, H. W., 1937. Notes on selective feeding by Calanus. J. Mar. Biol. Ass. U. K. 22: 97–100.
— 1945. Recent advances in the chemistry and biology of sea water. (Univ. Press. Cambridge.)
Hassall, A. H., 1855. Diatomaceae in the water supplied to the inhabitants of London. Microscopic examination of the water. London.
Heiberg, P. H. C., 1863. Conspectus criticus Diatomacearum danicarum.
Henddy, N. I., 1937. The plankton diatoms of the southern seas. “Discovery” Rep. 16: 151–364.
— 1951. Littoral diatoms of Chichester Harbour with special reference to fouling. J. R. Micr. Soc. 71: 1–86.
— 1953. Taxonomic studies on some Naviculae punctatae. J. R. Micr. Soc. 73: 156–161.
Hensen, V., 1887. über die Bestimmung des Planktons. Ber. Wiss. Untersuch dtsch. Meere, Kiel. 1882. 6: 1–108.
Hohn, M. H., 1951. A study of the distribution of diatoms in western New York State. Mem. 308, Cornell agric. Exp. Sta.: 1–37.
Hooker, 1833. In Smith, J. E. English Flora 5.
Hustedt, F., 1924. Die Bacillariaceen-Vegetation. des Sarekgebirges. Naturw. Untersuch Sarekgeb. Bot. 3 (6): 525–626.
Hustedt, F., 1927–1937. Die Kieselalgen Deutschlands, Osterreichs und der Schweiz, mit berucksichtigung der ubrigen Lander Europas sowie der angrenzenden Meeresgebeite. in Rabenhorst, Kryptogamenflora. Part 1. 1–272 (1927), 273–464 (1928), 465–608 (1929), 609–784 (1930), 785–920 (1930). Part 2. 1–176 (1931), 177–320 (1932), 321–432 (1933), 433–576 (1933), 577–736 (1937).
Janisch, C., 1862. Zur Characteristik des Guanos von Verschiedenen Fundorten. Abh. Schles. Ges. Vatarl. Kult. Nat.-Med. Abt.
Jorgensen, E., 1901. Protistenplankton aus dem Nordmeere in den Jahren 1897–1900. Bergens Mus. Aarb. 1900. 6.
— 1905. Protistplankton and diatoms in bottom samples. Hydrographical and biological investigations in Norwegian fjords. Bergens Mus. Skr. 7: 49–148.
Karsten, G., 1905–7. Das phytoplankton des Antarktischen Meeres nach dem Materiel der Deutschen Tiefsee-Expedition, 1898–9. Wiss. Ergebn. dtsch. Tiefsee-Exped. 2: 1–136, 137–219, 223–544.
Kolbe, R. W., 1954. Diatoms from equatorial Pacific cores. Repts. Swedish Deep-Sea Exp. 1947–8. Goteborgs Kungl. Vetensk. och vitterh. samh. 6 (1), 1–49.
Kützing, F. T., 1834. Synopsis Diatomearum oder Versuch einer systematischen Zusammen-stelling der Diatomeen. Linnaea. 8: 529–620.
— 1844. Die Kieselschaligen Bacillarien oder Diatomeen. Kohne, 152 pp.
— 1849. Species algarum. Lipsiae, F. A. Brochaus. 922 pp.
Lagerstet, N. G. W., 1873. Solvattens-Diatomaceer fran Spetsbergen och Beeren Eiland. Akad. Afh. Vidtb. Filosof. Fakult. Uppsala Samt. 1–52.
Lauder, H. S., 1864. Remarks on the marine Diatomaceae found at Hong Kong, with descriptions of new species. Trans. Micr. Soc. 12: 75–9.
Lebour, Marie V., 1930. The Planktonic Diatoms of Northern Seas. (Ray Society: London.)
Leuduger-Fortmorel, G., 1898. Diatomes marines de la côte occidentale d'Afrique. Saint Brieuc.
Lewin, Joyce C., 1953. Heterotrophy in diatoms. J. Gen. Microbiol. 9: 305–13.
Lyngby, H. C., 1819. “Tentamen Hydrophytologiae Danicae.” (Copenhagen.)
Mangin, L., 1917. Sur le Chaetoceros criophilus Castr. espèce characteristique des mers antarctiques. C. R. Acad. Sci. 164: 704, 770.
Manguin, E., 1954. Diatomées marines provénant de L'ile Heard. Australian Nat. Antarctic Research Expedition. Rev. Algol. 1 (1): 14–24.
Mann, A., 1937. Diatoms. Aust. Antarctic Exp. Sci. Repts C. 1 (1): 1–82.

Manteufel, B. P., 1941. Plankton and herring in the Barents Sea. Trans. Knipovich Polar Sci. Inst. Sea Fish. Oceanogr. 7: 125–210.
Marshall, S. M. and Orr, A. P., 1955. Experimental feeding of the copepod Calanus finmarchicus (Gunner) on phytoplankton cultures labelled with radioactive carbon (14 C). Deep Sea Res. 3 (Supp): 110–114.
Mereschkowsky, C., 1902. Note sur quelques diatomées de la Mer Noir suivie d'une liste de formes obsérvées dans cette mer. J. Bot. Paris 16: 319–324, 358–360.
Meunier, A., 1910. Microplancton des Mers de Barents et de Kara. Duc. d'Orleans, Campagne Arctique de 1907. Brussels.
— 1913. Microplancton de la Mer Flamande. 1 er partie. Le genre Chaetoceros Ehrg. Mem. Mus. r. Hist. nat. Belg. 7: 1–55.
Muller, O., 1871. über den feineren Bau der Zellwand der Bacillariaceen insbesondere des Triceratium favus Ehrbg. und der Pleurosigma. Arch. Anal. Physiol. Wiss. Med. Lptz. 5–6: 619–643.
— 1895. Rhopalodia ein neues genus de Bacillariaceen. Engler's Bot. Jahrib. 22. Leipzig.
Muller, O. F., 1786. Animalia, infusoria et marina quae detexit etc. Hauniae in-4.
Nitzsch, C. L., 1817. Beitrag zur Infusorienkunde oder Naturbeschreibung der Zerkarien und Bacillarien. Neue Schr. Naturf. Ges. Halle, 3 (1): 1–128.
Norman, G., 1861. On some undescribed species of Diatomaceae. Trans. Micro. Soc. 9.
O'Meara, E., 1875–7. Report on the Irish Diatomaceae. Proc. R. Irish Acad. (2), 2: 235–425.
Ostenfeld, C. H., 1899. Plankton in 1898. Iagttagelser over Overfladevandets Temperatur, Saltholdighed og Plankton paa islandske og gronlandske Skibsrouter 1 1898 udgivne Martin Knudsen og C. Ostenfeld, Copenhagen.
— 1901. Iagttageler over Plankton-Diatomeer. Nyt. Mag. Naturvid. 39.
— 1902. Marine plankton diatoms in Johs Schmidt, Flora of Koh Chang. Part 7 (Repr. Bot Tidskr. 25) 219–45.
— 1908. The immigration of Biddulphia sinensis Greville and its occurrence in the North Sea during 1903–7. Medd. Kom. Hav S. Plankton. 1 (6) Copenhagen.
— 1915. A list of phytoplankton from Boeoton Strait, Celebes. Dansk. Bot. Ark. 2 (4). Note.
— and Schmidt, Johs., 1901. Plankton fia det Rode Hav og Adenbugten. Vidensk. Med. Naturh. For. Koybenhaven: 141–90.
Østrup, E., 1910. Danske Diatomeer. 323 pp. Reitzels. Copenhagen.
Pantocsdk, J., 1886. Fossilen Bacillarien Ungarns. 1.
— 1902. Kieselalgen oder Bacillarien des Balaton. Result. Wiss. Erg. Balatonsees 2 (2): 1–112. Wien.
Pavili Ard, J., 1913. Observations sur les Diatomées. 2. Bull. Soc. bot. Fr. 60: 126–133.
— 1925. Bacillariales. Rept. Danish Exp. (1908–10) to Mediterranean and adjacent seas. 2, Biol. J4: 1–72.
Peragallo, H., 1880. Diatomées de la baie de Villefranche (Alpes Maritimes). Bull. Soc. Hist. Nat. Toulouse. 22: 13–100.
— 1892. Monographie du genre Rhizosolenia et de quesques genres voisins. Le Diatomiste 1: 79–82, 99–117. Paris.
Peragallo, M., 1921. Diatomées d eau douce, et Diatomées d'eau salai 2-Exped. Antarct. franc. 1908–10.
Petersen, C. G. J.. 1918. The sea bottom and its production of fishfood: a survey of the work done in connection with valuation of the Danish waters from 1883–1917. Rep. Danish Biol. Sta. 1918: 1–62.
Petit, P., 1877. Catalogue des diatomées de l'ile Campbell et de la Nouvelle Zelande. Fonds de la Mer 3: 164–198.
Pfitzer. E. 1871. Untersuchungen uber Bau und Entwicklung der Bacillariaceen (Diatomaccen). Adolph Marcus: Bonn.
Pritchard. A., 1861. History of the Infusoria. 4th Ed. (Diatoms by J. Ralfs) (London).
Provasoli, L., and Pintner, I. F., 1953. Ecological implications of in vitro nutritional requirements of algal flagellates. Ann. N.Y. Acad. Sci. 56: 839–51.
Queckett, J., 1848. A Practical Treatise on the Microscope. (London.)
Rabenhorst, L., 1864. Flora europaea Algarum. 1. Algae, Diatomaceae.
Ralfs, J., 1843a. On the Diatomaceae. Ann. Mag. Nat. Hist. 11: 447–57. 12: 104–11, 270–6, 346–52.
— 1843b. On the British species of Meridion and Gomphonema. Ann. Mag. Nat. Hist. 12, Suppl.: 457–67.
— 1844a. On the British species of Grammonema and Eunotia. Ann. Mag. Nat. Hist. 13: 457–61.
— 1844b. On the British species Achnanthes. Ann. Mag. Nat. Hist. 13: Suppl.: 489–93.

Ralfs, J., 1845. On the British Diatomaceae. Ann. Mag. Nat. Hist. 16: 109–12.
— 1861. Diatoms in Pritchard's Infusoria. q. v.
— 1864. See Lauder, 1864, notes by Ralfs.
Rattray, J., 1888. A revision of the genus Auliscus and some allied genera. J. Roy. Micr. Soc. 8.
— 1890. A revision of the genus Cosinodiscus and some allied genera. Proc. Roy. Soc. Edinb. 16: 449–692.
Ropdr, F. C. S., 1858. Notes on some new species and varieties of British Marine Diatomaceae. Quart. J. Micr. Sci. 6: 17–25.
— 1859. On the genus Biddulphia and its affinities. Trans. Micr. Soc. 7.
— 1863. On the genus Licmophora (Agardh). Trans. Micr. Soc. 11: 53–62.
Schmidt, A., 1875–1934. Atlas der Diatomaceen-Kunde. (Ernst Schlegel: Aschersleben).
von Schonfeld, H., 1907. Diatomaceae Germania Die dcutschen Diatomeen des Susswasseis und des Brackwassers. (Theodor Oswald Weigel: Leipzig.)
Schroder, B., 1900. Das Phytoplankton des Golfes von Neapel. Mitt Zool. Sta. Neapel, 14.
— 1906. Beitrage zur Kenntnis der Phytoplanktons warmer Meere. Vjschr. naturf. Ges. Zurich, 51: 319–377.
Schultze, M. S., 1858. Innere Bewegungserscheinungen bei Diatomeen der Nordsee aus den Gattungen Coscinodiscus, Denticella, Rhizosolenia. Mullers Arch. 1858. (summ Quart. J. micr. Sci. 7: 3–21, 1859).
Schumann, J., 1864–1869. Preussische Diatomeen. Phys. Ok. Gesell. Konigsberg.
Schütt, F., 1889. über die Auxosporebildung der Gattung Chaetoceros. Ber. dtsch. bot. Ges.
— 1893. Des Pflanzenleben der Hochsee. Kiel u. Leipzig.
— 1895. Arten von Chaetoceras und Peragallia. Ein Beitrag zur Hochseeflora. Ber. dtsch. Bot. Ges. 13: 35–48.
— 1896. Bacillariales in Engler u. Prantl. Die naturlichen Pflanzenfamilien, 1 (1b): 31–150.
Shadbolt, G., 1854. A note on the proposed new genus Actiinosphenia. Trans Micr. Soc. 2.
Shrubsole, W. H., 1890. On a new diatom from the estuary of the Thames. J. Queckett micr. Club (Ser. 2) 4: 259–262.
Smith, J. E., 1807. English Botany. 23, 25, 27. Lond.
Smith, W., 1853–1856. A synopsis of the British Diatomaceae. Smith and Beck, London.
Stanbury, F. H., 1944. Experiments in the growth of marine plants with special reference to the effects of copper and mercury salts. Marine Corrosion Sub. Com. Rept. Iron & Steel Corr. Comm. M.S.
de Sousa e Silva Estdla, (1953) 1956. Diatomacees do plankton marinho de Angola. Trab. Miss. Biol. Marit. 1–56.
Subrahmanyan, R., 1946. A systematic acount of the marine plankton diatoms of the Madras coast. Proc. Ind. Acad. Sci. B.24: 85–197.
Sverdrup, H. U., Johnson, M. W. and Fleming, R. H., 1942. The Oceans. (Prentice-Hall, N.Y.).
van Hdurck, H., 1880–1895. Synopsis des Diatomées de Belgique. (Anvers.)
Vanhoffen, E., 1897. Die Fauna und Flora Groenlands. Groenland Exp. Ges. Erdkunde, 10: Bd. 2 Berlin.
Vdnkataraman, G., 1939. A systematic account of some South Indian Diatoms. Proc. Ind. Acad. Sci. B10: 293–368.
Wallich, G. C., 1858. On Triceratium and some new allied forms, with figures of same. Quart. J. Micr. Sci. 6: 242–253.
— 1860. On the siliceous organisms found in the digestive cavities of the Salpae. Trans. Micr. Soc. n.s. 8: 36–55.
West, Tuffen, 1860. Remarks on some Diatomaceae new or imperfectly described, and a new desmid. Trans. Micr. Soc. n.s. 8: 147–153.
Wood, E. J. F., 1950. Investigations in underwater fouling. 1. The role of bacteria in the early stages of fouling. Aust. J. Mar. Freshw. Res. 1. 85.
— 1953. Heterotrophic bacteria in marine environments of eastern Australia. Aust. J. Mar. Freshw. Res. 4: 160–200.
— 1954. Dinoflagellates in the Australian region. Aust. J. Mar. Freshw. Res. 5: 171–351.
— 1955. Effect of temperature and flow rate on some marine fouling organisms. Aust. J. Sci. 18: 33–4.
— 1956. Diatoms in the ocean deeps. Pac. Sci. 10: 377–381.
Zacharias, O., 1905. Rhizosolenia curvata mihi, eine neue marine Plankton diatomee. Arch. Hydrobiol v. Planktonkuade 1: 120–121.
Zobell, C. E., 1946. Marine Microbiology. Chronica Botanica Co., Waltham Mass.

List of Genera
-
Achnanthes
-
Amphipleura
-
Amphyroia
-
Amphora
-
Anaulus
-
Anomaeoneis
-
Asterionella
-
Bacillaria
-
Caloneis
-
Campylodiscus
-
Campyloneis
-
Climacospheria
-
Cocconeis
-
Coscinodiscus
-
Cyclotella
-
Cymbella
-
Diatoma
-
Diatomella
-
Dictyoneis
-
Dimerogramma
-
Diploneis
-
Entopyla
-
Epithemia
-
Eunatia
-
Eunotiogramma
-
Fragilaria
-
Fragilariopsis
-
Fruslutia
-
Glyphodesmis
-
Gomphonema
-
Grammatophora
-
Hantzschia
-
Lienophora
-
Mastogloia
-
Inclosira
-
Navicula
-
Neidium
-
Nityschia
-
Omphalopsis
-
Opephora
-
Pinnularia
-
Plagrogramma
-
Pleurosigma
-
Podocystis
-
Rhabdonema
-
Rhaphoneis
-
Rhoicosphenia
-
Rhopalodia
-
Rutilaria
-
Stauroneis
-
Stictodiscus
-
Striatella
-
Surriella
-
Synedra
-
Terpsinae
-
Thalassiathix
-
Toxonidia
-
Trachyneis
-
Trachyspheria
-
Tropidoneis
