| Taxon Attribute Profiles 
         
          |  Cybister tripunctatus
 |  Family Dytiscidae Predaceous Water Beetles    Introduction 	Dytiscidae (predaceous water beetles) is one of the largest and most 
        commonly encountered groups of aquatic beetles. Both adults and larvae 
        are predaceous, and will attack a wide variety of small aquatic organisms. 
        Although most species are small to medium sized, some adults can attain 
        a length of 35 mm.  Taxonomy and Ecology Synopsis of included taxa	Australia has a rich fauna of Dytiscidae, with 226 species in 42 
        genera (Gooderham & Tsyrlin, 2002). Watts (1978) supplied a revision 
        of Australian Dytiscidae; and Pederzani (1995) provided keys to all dytiscid 
        genera and subgenera for the world. Watts (2002) provided a series of 
        easy to use keys to the genera of both adult and larval dytiscids. A checklist 
        of Australian Dytiscidae is available on the Australian Biodiversity Information 
        Facility website (Lawrence et al., 2002). 	General overviews of Australian Dytiscidae, including biological 
        and ecological information, are provided by Lawrence et al. (1991) 
        and Gooderham & Tsyrlin (2002).  Life Form	Dytiscids have a characteristic appearance, and can generally be 
        recognized by having a hard, smooth, oval body, without any ventral spine, 
        having the hind legs flattened and with a fringe of hairs so that it can 
        act like a paddle, and having long, thin antennae. In the water, dytiscids 
        swim by moving their hind legs simultaneously, like oars, while the similar 
        appearing Hydrophilidae alternate the movement of their hind legs. 
         
          |  Eretes australis
 |  Lancetes lanciolatus
 |   
          |  Megaporus howitti
 |  Sternopriscus hansardii
 |    
         
          |  Click to enlarge map
 |  Distribution	Dytiscidae are all aquatic, and are common throughout the continent, 
        with the greatest number of species found in the south-east. Adults are 
        capable of flying to isolated habitats, which has allowed their spread 
        to aquatic habitats throughout Australia.  Habitat	Dytiscids generally prefer slow moving or stagnant water, such as 
        ponds, lakes, billabongs, dams, and pools at the edges of streams. They 
        require atmospheric air, and the adult beetles go to the surface to gather 
        air which they store in a chamber underneath their elytra (wing covers) 
        to enable them to increase the time they can be submerged. Larvae lack 
        this ability, but many species use a siphon in the form of long filaments 
        at the end of the abdomen. Status in Community	Both adults and larvae are predaceous. The adults are capable of 
        eating through a normal mouth opening. Most larvae do not have a mouth 
        opening, but have long, sickle like jaws which enable them to suck fluids 
        out of their prey items. The larvae will attack animals much larger than 
        themselves, and have been known to feed on other insects, crustaceans, 
        worms, leeches, mollusks, tadpoles and small fish.   Reproduction and Establishment Reproduction	A variety of mating behaviours occur in the Dytiscidae, and many 
        of them reflect the fact that females are more selective in choosing a 
        mate than males (Miller, 2003). Males have a variety of methods to achieve 
        mating, and in some cases females have behaviours to resist mating, such 
        as swift and erratic swimming when approached by a male. Some males have 
        even developed sucker-shaped setae on the legs which allow them to grab 
        females and prevent them from escaping during mating. Dispersability	Adult dytiscids are capable of sustained flight, and often travel 
        some distance to disperse and find new habitats. They generally fly in 
        the evening or at night, and they use reflected light from a water surface 
        as a method of finding a new habitat. They can be confused by artificial 
        reflected surfaces (e.g. glass) or lights, and are often attracted to 
        these sources rather than water. Juvenile period	Adults generally lay eggs in the underwater stems of plants, using 
        their ovipositor to cut the stem to deposit the eggs. Dytiscid larvae 
        are very aggressive predators which attack a variety of prey. Pupation 
        takes place out of the water. The larva forms a cell in damp soil near 
        the water, and the adults return to the water after emerging. 
         
          |  Hyderodes sp. larva
 |  Hyphydrus sp. larva
 |  
 
         
          |  Rhantus sp. larva
 |  Hydrology and Salinity Salinity Tolerance	Gooderham & Tsyrlin (2002) and Chessman (2003) reported that 
        Dytiscidae as a family are quite tolerant of high levels of salinity. 
        However, Bailey et al. (2003) list several examples of specific 
        dytiscids which have very narrow ranges of salinity tolerance and could 
        be eliminated with minor rises in salinity levels. Flooding RegimesAlternating periods of flooding and drought could affect dytiscid populations, 
        which need water for survival. The strong flying ability of adults will 
        allow recolonization of aquatic habitats after periods of drought.   Conservation Status 	As with most invertebrates, there is insufficient data on Dytiscidae 
        to discuss conservation status in any intelligent manner. Many species 
        are known from only a few specimens, but whether this reflects insufficient 
        collecting or declining population numbers can not even be guessed at.  Uses	There are no records of Aboriginal use of dytiscids as food, although 
        many insect species were eaten by Aborigines (Tindale, 1966). The large 
        dytiscid Cybister explanatus is used as food in Mexico, where they 
        are eaten roasted with salt and in tacos (Ramos-Elorduy & Pino, 1989). 
        
        Summary 	Dytiscidae share the characteristics of macroinvertebrates that could 
        make them suitable species for including in programs for monitoring water 
        quality (Water and Rivers Commission, 1996; Chessman, 2003; Minnesota 
        Pollution Control Agency, 2004). As of yet, we lack specific examples 
        of their use in such programs.   List of MDB Species Table 1. Dytiscidae recorded from the Murray Darling Basin (50 species 
        in 19 genera). 
         
          | DYTISCIDAE  
           |   
          | Allodessus 
           |   
          | Allodessus bistrigatus (Clark) 
           |   
          | Antiporus 
           |   
          | Antiporus interrogationis (Clark) 
           |   
          | Antiporus balkei (Clark) 
           |   
          | Antiporus femoralis (Boheman) 
           |   
          | Antiporus gilberti (Clark) 
           |   
          | Chostonectes 
           |   
          | Chostonectes gigas (Boheman) 
           |   
          | Chostonectes johnsoni (Clark) 
           |   
          | Chostonectes nebulosus (Macleay) 
           |   
          | Chostonectes sharpi Sharp 
           |   
          | Copelatus 
           |   
          | Copelatus australiae Clark 
           |   
          | Copelatus australis (Clark) 
           |   
          | Copelatus ferrugineus Sharp 
           |   
          | Cybister 
           |   
          | Cybister tripunctatus (Olivier) 
           |   
          | Eretes 
           |   
          | Eretes australis (Erichson) 
           |   
          | Hydaticus 
           |   
          | Hydaticus parallelus Clark 
           |   
          | Hydaticus pulcher Clark 
           |   
          | Hyderodes 
           |   
          | Hyderodes schuckardi Hope 
           |   
          | Hydrovatus 
           |   
          | Hydrovatus armstrongi Watts 
           |   
          | Hydrovatus opacus Sharp 
           |   
          | Hydroglyphus 
           |   
          | Hydroglyphus godeffroyi (Sharp) 
           |   
          | Hyphydrus 
           |   
          | Hyphydrus elegans (Montrouzier) 
           |   
          | Lancetes 
           |   
          | Lancetes lanceolatus (Clark) 
           |   
          | Limbodessus 
           |   
          | Limbodessus amabilis (Clark) 
           |   
          | Limbodessus compactus (Clark) 
           |   
          | Limbodessus gemellus (Clark) 
           |   
          | Limbodessus shuckardii (Clark) 
           |   
          | Limbodessus praelargus (Lea) 
           |   
          | Megaporus 
           |   
          | Megaporus gardeneri Clark) 
           |   
          | Megaporus hamatus (Clark) 
           |   
          | Megaporus howittii (Clark) 
           |   
          | Megaporus wilsoni Mouchamps 
           |   
          | Necterosoma 
           |   
          | Necterosoma dispar (Germar) 
           |   
          | Necterosoma penicillatum (Clark) 
           |   
          | Necterosoma undecimlineatum Babington) 
           |   
          | Necterosoma aphrodite Watts 
           |   
          | Necterosoma susanna Zwick 
           |   
          | Onychohydrus 
           |   
          | Onychohydrus scutellaris (Germar) 
           |   
          | Platynectes 
           |   
          | Platynectes octodecimmaculatus (Macleay) 
           |   
          | Platynectes decempunctatus (Fabricius) 
           |   
          | Platynectes darlingtoni Gueorguiev 
           |   
          | Platynectes reticulosus (Clark) 
           |   
          | Platynectes ocularis (Lea) 
           |   
          | Rhantus 
           |   
          | Rhantus suturalis Macleay 
           |   
          | Sternopriscus 
           |   
          | Sternopriscus alpinus Hendrich & Watts 
           |   
          | Sternopriscus hansardi (Sharp) 
           |   
          | Sternopriscus tarsalis tarsalis Sharp 
           |   
          | Sternopriscus multimaculatus (Clark) 
           |   
          | Sternopriscus meadfootii (Clark) 
           |   
          | Sternopriscus mundanus Watts 
           |   
          | Sternopriscus wehnckei Sharp 
           |     References Bailey, P., Boon, P. & Morris, K. (2002) Australian Biodiversity 
          Salt Sensitivity Database. Land & Water Australia. http://www.rivers.gov.au/research/contaminants/saltsen.htm Chessman B. (2003) SIGNAL 2 - A Scoring System for Macroinvertebrate 
          ('Water Bugs') in Australian Rivers, Monitoring River Heath Initiative 
          Technical Report no 31, Commonwealth of Australia, Canberra. http://www.deh.gov.au/water/rivers/nrhp/signal/ Gooderham, J. & Tsyrlin, E. (2002) The Waterbug Book: a guide to 
          the freshwater macroinvertebrates of temperate Australia. CSIRO Publishing. Kefford, B.J., Papas, P.J., Nugegoda, D. (2003) Relative salinity tolerance 
          of macroinvertebrates from the Barwon River, Victoria, Australia. Marine 
          and Freshwater Research, 54: 755-765. Lawrence, J.F. & Britton, E.B. (1991) Coleoptera (Beetles). Pp. 
          543-683, in Insects of Australia: A textbook for students and research 
          workers. CSIRO. 2nd Edition. Lawrence, J.F., Weir, T.A. & Pyke, J.E. (2002) Australian Faunal 
          Directory: Checklist for Coleoptera: Adephaga: Dytiscidae. Australian 
          Biological Resources Survey, Department of the Environment and Heritage. 
          http://www.deh.gov.au/cgi-bin/abrs/abif-fauna/tree.pl?pstrVol=ADEPHAGA&pintMode=1 Miller, K. (2003) The phylogeny of diving beetles (Coleoptera: Dytiscidae) 
          and the evolution of sexual conflict. Biological Journal of the Linnean 
          Society, 79: 359-388.   Minnesota Pollution Control Agency (2004). Wetlands: Monitoring Aquatic 
          Invertebrates. http://www.pca.state.mn.us/water/biomonitoring/bio-wetlands-invert.html Pederzani, F. (1995) Keys to the identification of the genera and subgenera 
          of adult Dytiscidae (sensu lato) of the world (Coleoptera Dytiscidae). 
          Atti della Accademia Roveretana degli Agiati, Serie 7 B, 4: 5-83.   Ramos-Elorduy, J. & Pino M. (1990). Caloric content of some edible 
          insects of Mexico. Revista de la Sociedad Quimica de Mexico 34(2): 56-68. 
         Tindale, N.B. (1966) Insects as food for the Australian Aborigines. 
          Australian Natural History, 15(6), p. 179-183. Water and Rivers Commission (1996). Macroinvertebrates & Water 
          Quality. Water Facts 2. http://www.wrc.wa.gov.au/public/waterfacts/2_macro/WF2.pdf Watts, C.H.S. (1978) A revision of the Australian Dytiscidae (Coleoptera). 
          Australian Journal of Zoology, Supplementary Series no 57: 1-166. Watts, C.H.S. (2002) Checklists & Guides to the Identification, 
          to Genus, of Adult & Larval Australian Water Beetles of the Families 
          Dytiscidae, Noteridae, Hygrobiidae, Haliplidae, Gyrinidae, Hydraenidae 
          and the Superfamily Hydrophiloidea (Insecta: Coleoptera). Identification 
          and Ecology Guide no 43. Cooperative Research Centre for Freshwater 
          Ecology.  |