
Family Dytiscidae.
Hydaticus litigiosus Régimbart, 1887. (Text-fig. 8.)
Table 6 gives the results of feeding experiments carried out with imagines of this diving beetle, which was usually encountered in some numbers in permanent pools in the neighbourhood of Palmalmal.
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| Experiment number. | 1 | 2 | 3 | 4 | |
|---|---|---|---|---|---|
| Mosquito species supplied to the predator as food. | Anopheles farauti. | Culex pullns | Anopheles farauti. | Culex pullus. | Mixture of both species. |
| Developmental stage supplied. | 3rd and 4th instar larvae. | 3rd and 4th instar larvae. | 3rd and 4th instar larvae. | 3rd and 4th instar larvae. | Pupae. |
| Number of larvae or pupae eaten by 2 adults of H. litigosus in 5 days. | 13 | 352 | 7 | 316 | 114 |
| Average number of larvae or pupae eaten by a single predator each day. | 1.3 | 35.2 | 0.7 | 31.6 | 11.4 |
It is evident from the above table that H. litigiosus destroyed about thirty times more larvae of C. pullus than of A. farauti when supplied with either pure or mixed cultures of these species. This

apparent preference for culicine larvae as food is brought about by the head-downwards attitude assumed by the diving beetle when near the water surface. In this attitude it can detect larvae of Culex, but not those of the surface-dwelling Anopheles. Although anopheline larvae are normally protected from the attacks of H. litigiosus by virtue of their surface-dwelling habit, they are seized by the predator without discrimination when caused to leave the water surface.
Two dytiscids, a male and a female, were kept in a vessel containing 8 cm. (250 cc.) of boiled and filtered water. The water in this container was changed each week, but no animals other than larvae of A. farauti were admitted. Any anopheline pupae were removed as soon as their presence was noticed, and they were replaced with early instar larvae of the same species. At the end of three weeks the female Hydaticus died, its body being promptly eviscerated by the male. During all this time only thirty-five of the anopheline larvae in the beaker had been consumed by both beetles. After a further week fifty larvae of C. pullus were introduced into the beaker. The surviving water beetle immediately began to attack these larvae, eating eleven within the first five minutes. All the larvae had been consumed at the end of an hour.
It was found that an average of 11.4 pupae were consumed by a single Hydaticus adult each day. Like the predators already discussed, this diving beetle was often seen to be eluded by pupae, although larvae were seldom observed to avoid capture.
In feeding, H. litigiosus captures its prey with a sudden lunge of its forelegs, then rises slowly to the surface while guiding the victim to its mouthparts with its fore and middle legs. Usually both larvae and pupae are eaten bodily, but sometimes the more heavily chitinized parts are discarded.
Hargreaves (1932) records that an Italian dytiscid devoured larvae and pupae of all mosquito species fed to it, at the rate of twenty a day. Howard (1912) quotes Galli-Valerio and Rochaz de Jongh as stating that an adult of Dytiscus marginalis Linnaeus, although previously fed with meat, devoured great numbers of mosquito larvae and pupae. No observations on the predacity of water beetle larvae were made at Palmalmal, although many authors have referred to the voracity of dytiscid and hydrophilid larvae as mosquito destroyers.
Anopheline larvae were often present in large numbers in pools inhabited by H. litigiosus, although species of Culex were seldom found in any numbers in association with the beetle. From this circumstance, and the results of the laboratory-feeding experiments outlined above, it appears that while H. litigiosus plays a significant part in the natural control of culieine mosquito breeding at Palmalmal, this beetle is of little importance as a factor in anopheline control.
Copelatus sp. (Text-fig. 9.)
This little dytiscid is a new species as yet undescribed, but for which Balfour-Browne proposes the name of Copelatus lairdii. It was commonly encountered in permanent pools throughout the Jacquinot Bay area. The results of feeding experiments with imagines of this water beetle are tabulated below.

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| Experiment number. | 1 | 2 | 3 | 4 | |
|---|---|---|---|---|---|
| Mosquito species supplied to the predator as food. | Anopheles farauti. | Culew pullus. | Anopheles farauti. | Culex pullus. | Mixture of both species. |
| Developmental stage supplied. | 3rd and 4th instar larvae. | 3rd and 4th instar larvae. | 3rd and 4th instar larvae. | 3rd and 4th instar larvae. | Pupae. |
| Number of larvae or pupae eaten by 2 adults of Copelatus sp. in 5 days. | 46 | 58 | 29 | 37 | 1 |
| Average number of larvae or pupae eaten by a single predator each day. | 4.6 | 5.8 | 2.9 | 3.7 | 0.1 |
It will be seen that Copelatus sp., in contrast to H. litigiosus, devoured very nearly the same number of Anopheles and Culex larvae. The reason for this is that Copelatus sp., unlike H. litigiosus, spends
much of its time in hunting prey near the water surface and thus has an equal chance of encountering larvae of both genera. Only a single pupa was destroyed by one of these predators during the investigation. The small size of this diving beetle makes the capturing of such vigorous and heavily-chitinized prey a difficult matter.
Although a single adult of Copelatus sp. was unable to account for any great number of mosquito larvae each day, the species was often present in natural pools in such numbers as to act as an important check on mosquito breeding.

