Shell medium to large sized, oblong to oval or subcircular, valves thin, inflated, rarely winged, sculpture of growth lines, umbos without sculpture but are often eroded, olive brown to black periostracum, interior of valves nacreous bluish to bronze to white, hinge teeth with pseudocardinal teeth thin, rarely grooved, usually smooth; hinge sometimes reduced.
Anatomy: The gills (ctenidia) are eulamellibranch and the foot is a compressed, tongue-shaped foot lacking a byssal groove. Larvae are brooded in a marsupium that occupies about two thirds of the inner pair of demibranchs. Inhalant and exhalant siphons not prominent and formed by the mantle edge which is open ventrally, branchial 'siphon' larger than anal 'siphon' bearing up to five rows of papillae internally; often heavily pigmented. Labial palps of medium size, triangular to subtriangular in shape.
The species of Velesunio can be distinguished as follows:
V. ambiguus. Compressed to globose, ventral margin at least slightly rounded; width/length ratio 58-69%; shell length up to 105 mm; pseudocardinals usually smooth, sometimes grooved. Anterior adductor scar weak, except in old individuals.
V. moretonicus. Shell slightly swollen, anteriorly and posteriorly rounded, pseudocardinals grooved; shell length up to 105 mm; ventral margin straight over mid-section; anterior adductor scar usually deeply impressed.
V. wilsoni. Shell compressed, rather elongate for genus (height/length ratio less than 53%); shell length up to 125 mm; tapered and not winged or very slightly winged posteriorly, ventral margin slightly rounded in juveniles, straight in adults.
Hyridella. Beak of young specimens at least sculptured with V-shaped ridges; shell quadrate to elongate (ratio of maximum height of shell to its length >50%), not markedly winged. Hinge strong with grooved pseudocardinal teeth and simple 'lateral' teeth. Shell surface (other than beaks) more-or-less smooth except for concentric growth lines.
Velesunio. Beaks smooth, shell can be rather thick, rounded in outline (ratio of maximum height of shell to its length >50%), often inflated, hinge lamellar, usually simple (rarely serrated). Shell surface with concentric growth lines only.
Alathyria. Shell typically large, elongate-ovate (ratio of maximum height of shell to its length >50%), often distinctly winged, thick, hinge usually with heavy, pseudocardinal teeth grooved, 'lateral' teeth smooth. Shell surface more-or-less smooth, with concentric growth lines only.
Cucumerunio. Shell very elongate (ratio of maximum height of shell to its length <40%), beaks sculptured with V-shaped ridges; rest of shell surface with conspicuous nodules or ridges. Hinge strong, pseudocardinal teeth grooved.
Lortiella. Shell elongate (ratio of maximum height of shell to its length <45%), winged posteriorly, hinge simple, not well developed. Beaks smooth and shell surface with concentric growth lines only. Found in NW Australia.
Westralunio. Shell more or less oblong (ratio of maximum height of shell to its length >50%). Pseudocardinal teeth erect, strongly serrated, shell small (less than 70 mm in length). Beaks smooth, shell rather thick, with concentric growth lines only. Restricted to SW Australia.
Genus Velesunio Iredale, 1934
Type species: Unio balonnensis Conrad, 1850
Original reference: Iredale, T. (1934). The Freshwater mussels of Australia. Australian Zoologist 8: 57-78.
Type locality: Balonne River, New South Wales.
Synonyms: Centralhyria Iredale, 1934; Aparcthyria Iredale, 1934.
The last major taxonomic revision of Australian freshwater mussels was by McMichael and Hiscock (1958). Based on the available molecular results, Walker et al. (2014) pointed out that a re-assessment of Australian hyriids is needed.
Rivers, streams, lakes, billabongs and water catchment dams. Infaunal, living two thirds to almost fully buried in sand and sediment. Suspension feeders. Sexes separate. Females brood young in marsupia in the inner pair of demibranchs. Larvae parasitic, using fish as hosts and dispersal agents. Tends to favour still to sluggish streams, rivers and lakes.
Most of mainland Australia and Tasmania, except for the southwest corner of Western Australia. The genus also occurs in Papua New Guinea.
Baker, A. M., Bartlett, C., Bunn, S. E., Goudkamp, K., Sheldon, F. & Hughes, J. M. (2003). Cryptic species and morphological plasticity in longlived bivalves (Unionoida: Hyriidae) from inland Australia. Molecular Ecology 12:2707–2717.
Baker A. M, Sheldon F, Somerville, J., Walker, K.F. & Hughes J.M. 2004. Mitochondrial DNA phylogenetic structuring suggests similarity between two morphologically plastic genera of Australian freshwater mussels (Unionoida: Hyriidae) Molecular Phylogenetics and Evolution 32. 902–912
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Graf, D. L., Jones, H. A., Geneva, A. J., Pfeiffer, J. M. III & Klunzinger, M. W. (2015). Molecular phylogenetic analysis supports a Gondwanan origin of the Hyriidae (Mollusca: Bivalvia: Unionida) and the paraphyly of Australasian taxa. Molecular Phylogenetics and Evolution. 85: 1-9.
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Hughes, J. M., Baker A. M, Bartlett, C, Bunn, S. E, Goudkamp, K. & Somerville, J., 2004. Past and present patterns of connectivity among populations of four cryptic species of freshwater mussels Velesunio spp.(Hyriidae) in central Australia. Molecular Ecology 13, 3197–3212.
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Iredale, T. (1934). The freshwater mussels of Australia. Australian Zoologist 8: 57-78.
Iredale, T. (1943). A basic list of the fresh water Mollusca of Australia. Australian Zoologist 10: 188-230.
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Walker, K. F. (1981). The distribution of freshwater mussels (Mollusca: Pelecypoda) in the Australian zoogeographic region. Pp. 1233-1249 in A. Keast. Ecological Biogeography of Australia. The Hague, Dr W. Junk.
Walker, K. F., Byrne, M., Hickey, C. W. & Roper, D. S. (2001). Freshwater Mussels (Hyriidae) of Australasia. Pp. 5-31 in G. Bauer & Wächtler, K. Ecology and Evolution of the Freshwater Mussels Unionoida. Ecological Studies. Berlin, Springer-Verlag.
Walker, K. F., Jones, H. A. & Klunzinger, M. W. (2014). Bivalves in a bottleneck: taxonomy, phylogeography and conservation of freshwater mussels (Bivalvia: Unionoida) in Australasia. Hydrobiologia 735:61–79.
Zieritz, A., Sartori, A. F. & Klunzinger, M. W. (2013). Morphological evidence shows that not all Velesunioninae have smooth umbos. Journal of Molluscan Studies 79: 277–282.