| Taxon Attribute Profiles 
         
          |    Hemianax papuensis
 |   
          |  Brachydiplax denticauda
 |   
          |  Rhyothemis graphiptera
 |   
          |  Indolestes obiri
 
 |   
          |  Nososticta coelestina
 |  Order ODONATA  Dragonflies and Damselflies    Introduction 	Dragonflies and damselflies are large, strong flying insects which 
        have fascinated watchers throughout time. They are among the best known 
        insects, and because of their large size (usually 30-90 mm, but some species 
        are known up to 150 mm), captivating behaviour, and ease of identification 
        by the non-specialist, they have been referred to as "bird-watchers" insects. 
        Many species are territorial, and they can display complex and intriguing 
        behaviour. Dragonflies and damselflies are components of most riparian 
        ecosystems. Both adult and larval stages are predaceous, and mostly prey 
        upon other invertebrate species.  Taxonomy and Ecology Synopsis of included taxa	The Odonata includes two suborders: Dragonflies (Anisoptera) and 
        Damselflies (Zygoptera). Damselflies are smaller and more delicate, and 
        have the forewing and hindwing similar in shape; dragonflies tend to be 
        larger and stouter, and have the forewing and hindwing different in shape, 
        with the base of the hindwing being wider than that of the forewing. In 
        living specimens, the dragonflies generally rest with their wings extended, 
        while the damselflies rest with wings folded together over their back. 
        The larvae live underwater and breathe through gills. Damselfly larvae 
        have the gills in the form of three long appendages extending from the 
        tail end of their abdomen; dragonflies lack these appendages, and have 
        internal rectal gills. Dragonfly larvae 
         
          |  Notoaeschna sagittata
 |   
          |  Synthemis macrostigma
 |  Damselfly larvae 
         
          |  Austroargiolestes icteromelas
 |   
          |  Austrolestes annulosus
 |  The classification of Odonata is not settled. Watson & O'Farrell 
        (1991) and Watson et al., (1991) list 11 families of damselflies 
        and 6 families of dragonflies, while the ABIF Fauna List shows 12 families 
        of damselflies and 18 families of dragonflies. Despite discrepancies concerning 
        the number of families, authors do agree that there are just over 300 
        species of Odonata in Australia (302 in Watson & O'Farrell, 1991; 
        320 in ABIF).  	General overviews of Australian Odonata, including morphology, biology 
        and keys to the suborders and families are provided by Watson et al. 
        (1991) and Watson & O'Farrell (1991).  Life Form	Dragonflies and damselflies are among the best known and recognized 
        insects. Adults are generally large and elongate, with two pairs of large, 
        membranous wings which have a dense network of veins. The compound eyes 
        are quite large, and often occupy most of the head. Many species are quite 
        beautiful, with bright metallic markings on the body, or various banded 
        patterns on the wings. Adults are strong flyers, and are among the fastest 
        of all insects. The larvae are aquatic, and have elongate, prehensile 
        mouthparts which they use to capture their prey. 
         
          |  click to enlarge map
 |  Distribution	Dragonflies and damselflies are widely distributed and common. Within 
        Australia, they are most diverse in the tropical regions of north-eastern 
        Queensland and Cape York. The aquatic habit of the larvae restricts reproduction 
        to water sources, but lone adults may be found throughout Australia, often 
        many kilometers from the nearest water source.   Habitat	Dragonflies and damselflies are tied to aquatic habitats. Although 
        the adults are free living and capable of strong flight, the other life 
        stages require a riparian habitat. Dragonfly and damselfly eggs are laid 
        in water. Most commonly, the hovering females dip their abdomens into 
        the water to deposit their eggs, and they can frequently be seen doing 
        this, either singly or still coupled to the male. Larvae spend their entire 
        life submerged in water, where they are predators on other small aquatic 
        organisms. Various species can occupy most freshwater habitats, including 
        waterfalls, torrents, streams, lakes, ponds, swamps, bogs and estuaries. 
        
 
         
          |  Cast skins of Hemicordulia tau
 |  Adult emergence takes place when the larva crawls up out of the water 
        onto a rock or branch, firmly grasps the substrate with its legs, and 
        the adult emerges from the cast larval skin. Adults are strong flyers. 
        Males are often territorial, and can be observed returning to a favourite 
        perch where they observe their territory and are ready to fly out to capture 
        food or guard against other males.    Status in Community 	Both adults and larvae are predaceous, and will be responsible for 
        removing numerous prey items during their life. Adults catch other invertebrates 
        which they eat during flight. Larval prey items are generally other invertebrates, 
        but larger species can take small fish and tadpoles.   
  Reproduction and Establishment Reproduction	The Odonata are unusual in that the male has secondary genitalia 
        at the base of the abdomen, to which he transfers sperm prior to mating. 
        This produces a very characteristic coupling pose, where the male grasps 
        the female behind the head with claspers at the end of his abdomen, and 
        the female places the tip of her abdomen up to the base of the male abdomen. 
        Elaborate courtship rituals are often precede mating. 
         
          |  Coenagrion lyelli
 |  Eusynthemis virgula
 |  Dispersability	Animals which inhabit standing, often temporary, water sources often 
        display the ability for dispersal and migration over great distances. 
        Adult dragonflies are strong fliers, and even though their larvae require 
        water, lone adults are often seen great distances from water. This enables 
        them to recolonize patches of standing water that are either unsuitable 
        or non-existent during parts of the year. Juvenile period	Larvae vary in habit, but all are aquatic. They can moult up to 15 
        times before they reach the final instar and are ready to emerge. All 
        larvae are predaceous, and they are generally ambush predators which remain 
        concealed in silt, or under rocks and plants, waiting for slow-moving 
        prey. Odonata larvae are unusual in having hinged, prehensile mouthparts 
        with strong teeth which they can shoot out to capture their prey.   Hydrology and Salinity Salinity Tolerance	Kefford et al. (2003) reported Odonata to be more tolerant 
        to salinity than many other aquatic macroinvertebrates; however, Bailey 
        et al. (2002), Gooderham & Tsyrlin (2002) and Chessman (2003) showed 
        a wide range of tolerance within the group. For example, on the SIGNAL 
        2 grades of 1-10 (1 being least sensitive and 10 being most sensitive), 
        Odonata families ranged from 1 (Lestidae) to 10 (Austrocorduliidae) (Chessman, 
        2003).  Flooding RegimesAlternating periods of flooding and drought could affect dragonfly and 
        damselfly larvae, which need water for survival. The strong flying ability 
        of adults will allow recolonization of aquatic habitats after periods 
        of drought. Several species of Australian Odonata have larvae that are 
        drought resistant, and can survive temporarily in an inactive state if 
        free water is withdrawn (Watson, 1982).  Conservation Status 	Hawking (1999) reviewed the conservation status of 314 Australian 
        dragonflies and damselflies. Of the 314 known Australian species, 1 was 
        listed as Critically Endangered, 12 Endangered, 24 Vulnerable, 39 Near 
        Threatened, 84 Data Deficient, and the remaining 154 Least Concern. 	The critically endangered species, Adams emerald dragonfly (Archaeophya 
        adamsi), is one of Australia's rarest dragonflies, with only 5 adults 
        having been captured. The species is known only from the greater Sydney 
        region, and some remaining habitats are under threat from development. 
       	Hawking (1999) pointed out three major concerns: 1) the large number 
        of endangered species, 2) the large number of species which deserve priority 
        conservation action; 3) the number of species where there is insufficient 
        data to make a proper assessment.  Uses	Although there are no records of Aboriginal use of dragonflies or 
        damselflies as food, it is not unlikely that certain species were eaten. 
        It is well known that many insect species were eaten by Aborigines (Tindale, 
        1966); and the use of dragonflies and damselflies as food items in Asia 
        and elsewhere in the world is well documented (Pemberton, 1995; Ramos-Elorduy, 
        1998; Menzel & D'Alusio, 1998).    Summary 	Several authors have suggested that macroinvertebrates, including 
        Odonata, can be effectively included in programs for monitoring water 
        quality (Watson, 1982; Water and Rivers Commission, 1996; Chessman, 2003; 
        Minnesota Pollution Control Agency, 2004). Due to the variability of response 
        to environmental factors within the order, certain groups may be much 
        more suitable as bioindicator species than others. The fact remains that 
        they are large, easy to observe, and can be recognized by non-specialists, 
        making them a very suitable group for a variety of monitoring purposes.  List of MDB Species Table 1. Odonata recorded from the Murray Darling Basin (Classification from Houston et al., 1999). 
         
          | DAMSELFLIES  
           | DRAGONFLIES 
           |   
          |  |  |   
          | Coenagrionidae 
           | Aeshnidae	 
           |   
          | 	Austroagrion watsoni Lieftinck, 1982 
           | 	Aeshna brevistyla (Rambur) 
           |   
          | 	Austrocnemis splendida (Martin, 1901) 
           | 	Aeshna brevistyla (Rambur) 
           |   
          | 	Caliagrion billinghursti (Martin, 1901) 
           | 	Austrogynacantha heterogena Tillyard, 1908 
           |   
          | 	Coenagrion lyelli (Tillyard, 1913) 
           | 	Hemianax papuensis (Burmeister, 1839) 
           |   
          | 	Ischnura aurora aurora (Brauer, 1865) 
           |  |   
          | 	Ischnura heterosticta (Burmeister, 1839) 
           | Austrocorduliidae 
           |   
          | 	Pseudagrion aureofrons Tillyard, 1906 
           | 	Apocordulia macrops Watson, 1980 
           |   
          | 	Pseudagrion ignifer Tillyard, 1906 
           | 	Austrocordulia refracta Tillyard, 1909 
           |   
          | 	Xanthagrion erythroneurum (Selys, 1876) 
           |  |   
          |  | Austropetaliidae	 
           |   
          | Diphlebiidae	 
           | 	Austropetalia patricia (Tillyard, 1909) 
           |   
          | 	Diphlebia lestoides lestoides (Selys, 1853) 
           |  |   
          | 	Diphlebia lestoides tillyardi Fraser, 1956 
           | Cordulephyidae	 
           |   
          | 	Diphlebia nymphoides Tillyard, 1912 
           | 	Cordulephya pygmaea Selys, 1870 
           |   
          |  |  |   
          | Hemiphlebiidae 
           | Gomphidae	 
           |   
          | 	Hemiphlebia mirabilis Selys, 1869 
           | 	Antipodogomphus acolythus (Martin, 1901) 
           |   
          |  | 	Austrogomphus amphiclitus (Selys, 1873) 
           |   
          | Isostictidae	 
           | 	Austrogomphus angeli Tillyard, 1913 
           |   
          | 	Rhadinosticta simplex (Martin, 1901) 
           | 	Austrogomphus australis Dale, 1854 
           |   
          |  | 	Austrogomphus cornutus Watson, 1991 
           |   
          | Lestidae	 
           | 	Austrogomphus divaricatus Watson, 1991 
           |   
          | 	Austrolestes analis (Rambur, 1842) 
           | 	Austrogomphus guerini (Rambur, 1842) 
           |   
          | 	Austrolestes annulosus (Selys, 1862) 
           | 	Austrogomphus melaleucae Tillyard, 1909 
           |   
          | 	Austrolestes aridus (Tillyard, 1908) 
           | 	Austrogomphus ochraceus (Selys, 1869) 
           |   
          | 	Austrolestes cingulatus (Burmeister, 1839) 
           | 	Hemigomphus gouldii (Selys, 1854) 
           |   
          | 	Austrolestes io (Selys, 1862) 
           | 	Hemigomphus heteroclytus Selys, 1854 
           |   
          | 	Austrolestes leda (Selys, 1862) 
           |  |   
          | 	Austrolestes psyche (Hagen, 1862) 
           | Hemicorduliidae	 
           |   
          |  | 	Hemicordulia australiae (Rambur, 1842) 
           |   
          | Megapodagrionidae	 
           | 	Hemicordulia intermedia (Selys, 1871) 
           |   
          | 	Austroargiolestes amabilis (Forster, 1899) 
           | 	Hemicordulia superba Tillyard, 1911 
           |   
          | 	Austroargiolestes brookhousei Theischinger & O'Farrell, 
              1986 
           | 	Hemicordulia tau (Selys, 1871) 
           |   
          | 	Austroargiolestes calcaris (Fraser, 1958) 
           | 	Procordulia jacksoniensis (Rambur, 1842) 
           |   
          | 	Austroargiolestes christine Theischinger & O'Farrell, 1986 
           |  |   
          | 	Austroargiolestes icteromelas (Selys, 1862) 
           | Libellulidae	 
           |   
          | 	Austroargiolestes isabellae Theischinger & O'Farrell, 1986 
           | 	Austrothemis nigrescens (Martin, 1901) 
           |   
          | 	Griseargiolestes eboracus (Tillyard, 1913) 
           | 	Crocothemis nigrifrons (Kirby, 1894) 
           |   
          | 	Griseargiolestes griseus (Hagen, 1862) 
           | 	Diplacodes bipunctata (Brauer, 1865) 
           |   
          | 	Griseargiolestes intermedius (Tillyard, 1913) 
           | 	Diplacodes haematodes (Burmeister, 1839) 
           |   
          |  | 	Nannophlebia risi Tillyard, 1913 
           |   
          |  | 	Nannophya dalei (Tillyard, 1908) 
           |   
          | Protoneuridae	 
           | 	Orthetrum caledonicum (Brauer, 1865) 
           |   
          | 	Nososticta solida (Hagen, 1860) 
           | 	Orthretrum villosovittatum villosovittatum (Brauer, 1868) 
           |   
          |  | 	Pantala flavescens (Fabricius, 1898) 
           |   
          | Synlestidae	 
           | 	Trapezostigma loewii (Kaup, 1866) 
           |   
          | 	Synlestes selysi Tillyard, 1917 
           |  |   
          | 	Synlestes weyersii tillyardi Fraser, 1948 
           | Synthemistidae	 
           |   
          |  | 	Archaeosynthemis orientalis (Tillyard, 1910) 
           |   
          |  | 	Choristhemis flavoterminata (Martin, 1901) 
           |   
          |  | 	Eusynthemis aurolineata (Tillyard, 1913) 
           |   
          |  | 	Eusynthemis brevistyla (Selys, 1871) 
           |   
          |  | 	Eusynthemis guttata (Selys, 1871) 
           |   
          |  | 	Eusynthemis tillyardi Theischinger, 1995 
           |   
          |  | 	Eusynthemis virgula (Selys, 1874) 
           |   
          |  | 	Parasynthemis regina (Selys, 1874) 
           |   
          |  | 	Synthemis eustalacta (Burmeister, 1839) 
           |   
          |  |  |   
          |  | Telephlebiidae	 
           |   
          |  | 	Austroaeschna atrata Martin, 1909 
           |   
          |  | 	Austroaeschna flavomaculata Tillyard, 1916 
           |   
          |  | 	Austroaeschna inermis Martin, 1901 
           |   
          |  | 	Austroaeschna multipunctata (Martin, 1901) 
           |   
          |  | 	Austroaeschna obscura Theischinger, 1982 
           |   
          |  | 	Austroaeschna parvistigma (Selys, 1883) 
           |   
          |  | 	Austroaeschna pulchra Tillyard, 1909 
           |   
          |  | 	Austroaeschna sigma Theischinger, 1982 
           |   
          |  | 	Austroaeschna subapicalis Theischinger, 1982 
           |   
          |  | 	Austroaeschna unicornis unicornis (Martin,1901) 
           |   
          |  | 	Notoaeschna geminata Theischinger, 1982 
           |   
          |  | 	Notoaeschna sagittata (Martin, 1901) 
           |   
          |  | 	Spinaeschna tripunctata (Martin, 1901) 
           |   
          |  | 	Telephlebia brevicauda Tillyard, 1916 
           |   
          |  | 	Telephlebia cyclops Tillyard, 1916 
           |   
          |  | 	Telephlebia godeffroyi Selys, 1883 
           |   
          |  | 	Telephlebia tillyardi Campion, 1916 
           |   
          |  |  |   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. Hawking, J.H. (1999) An evaluation of the current conservation status 
          of Australian dragonflies (Odonata). Pp 354-360, in: W. Ponder & 
          D. Lunney (eds), The Other 99%. The Conservation and Biodiversity 
          of Invertebrates. Transactions of the Royal Zoological Society of 
          New South Wales, Mosman. Houston, W.W.K., Watson, J.A.L. & Calder, A.A. (1999) Australian 
          Faunal Directory: Checklist for Odonata. Australian Biological Resources 
          Survey, Department of the Environment and Heritage. http://www.deh.gov.au/cgi-bin/abrs/abif-fauna/tree.pl?pstrVol=ODONATA&pintMode=1 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. Menzel, P. & D'Alusio, F. (1998) Man Eating Bugs: The Art and Science 
          of Eating Insects. Ten Speed Press, Hong Kong. Minnesota Pollution Control Agency (2004). Wetlands: Monitoring Aquatic 
          Invertebrates. http://www.pca.state.mn.us/water/biomonitoring/bio-wetlands-invert.html Pemberton, R. W. (1995) Catching and eating dragonflies in Bali and 
          elsewhere in Asia. American Entomologist, 41: 97-102 Ramos-Elorduy, J. (1998) Creepy Crawly Cuisine: The Gourmet Guide to 
          Edible Insects. Park Street Press, Rochester, Vermont. 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 Watson, J.A.L. (1982) Dragonflies in the Australian environment: taxonomy, 
          biology and conservation. Adv. Odonatol., 1: 293-302. Watson, J.A.L. & O'Farrell, A.F. (1991) Odonata (dragonflies and 
          damselflies). Pp. 294-310, in Insects of Australia: A textbook for students 
          and research workers. CSIRO. 2nd Edition. Watson, J.A.L., Theischinger, G. & Abbey, H.M. (1991) The Australian 
          Dragonflies: A Guide to the Identification, Distributions and Habitats 
          of Australian Odonata. CSIRO.
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