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Temporal Changes in the Macroinvertebrate Fauna of Two Glacial Lakes, Cootapatamba and Albina, Snowy Mountains, New South Wales
Avondale College ResearchOnline@Avondale Science and Mathematics Papers and Journal Articles School of Science and Mathematics 7-29-2013 Temporal Changes in the Macroinvertebrate Fauna of Two Glacial Lakes, Cootapatamba and Albina, Snowy Mountains, New South Wales Brian Timms University of New South Wales Jason K. Morton Avondale College of Higher Education, [email protected] Ken Green National Parks and Wildlife Service Follow this and additional works at: https://research.avondale.edu.au/sci_math_papers Part of the Ecology and Evolutionary Biology Commons Recommended Citation Timms, B. V., Morton, J. & Green, K. (2013). Temporal changes in the Macroinvertebrate Fauna of two Glacial Lakes, Cootapatamba and Albina, Snowy Mountains, New South Wales. Proceedings of the Linnean Society of New South Wales, 135, 45-54. This Article is brought to you for free and open access by the School of Science and Mathematics at ResearchOnline@Avondale. It has been accepted for inclusion in Science and Mathematics Papers and Journal Articles by an authorized administrator of ResearchOnline@Avondale. For more information, please contact [email protected]. Temporal changes in the Macroinvertebrate Fauna of two Glacial Lakes, Cootapatamba and Albina, Snowy Mountains, New South Wales BRIAN V TIMMS1, JASON MORTON2 AND KEN GREEN3. 1Australian Wetlands, Rivers and Landscape Centre, School of Biology, Earth and Environmental Sciences, University of New South Wales, Kensington, NSW, 2052. 2School of Science and Mathematics, Avondale College of Higher Education, PO Box 19, Cooranbong, NSW, 2265. 3National Parks and Wildlife Service, Snowy Mountains Region, PO Box 2228, Jindabyne, NSW, 2627. Published on 29 July 2013 at http://escholarship.library.usyd.edu.au/journals/index.php/LIN Timms, B.V., Morton, J. -
Molecular Phylogeny and Biogeography of Spring-Associated Hydrobiid Snails of the Great Artesian Basin, Australia
Molecular Phylogenetics and Evolution 34 (2005) 545–556 www.elsevier.com/locate/ympev Molecular phylogeny and biogeography of spring-associated hydrobiid snails of the Great Artesian Basin, Australia Kathryn E. Pereza,¤, Winston F. Ponderb, Donald J. Colganb, Stephanie A. Clarkc,1, Charles Lydearda a Department of Biological Sciences, Biodiversity and Systematics, University of Alabama, Box 870345, Tuscaloosa, AL 35487-0345, USA b Australian Museum, Sydney, NSW 2010, Australia c Centre for Biostructural and Biomolecular Research, University of Western Sydney, Hawkesbury Campus, Locked Bag 1797 Penrith South DC, NSW 1797, Australia Received 6 July 2004; revised 15 November 2004 Available online 6 January 2005 Abstract The Great Artesian Basin (GAB) of Australia underlies some of the driest parts of South Australia and Queensland and feeds numerous freshwater springs. Prominent and endangered components of the GAB spring community are snails of the family Hydro- biidae. This paper examines the evolutionary relationships of the entire hydrobiid fauna associated with the GAB, and includes appropriate non-GAB species to place the GAB fauna in a broader phylogenetic context. The Queensland genus Jardinella is a focus of this paper, providing a Wne scale examination of relationships between spring supergroups in the northeastern regions of the GAB. Maximum parsimony and Bayesian analyses performed on 16S, CO1, and combined sequence data from 40 hydrobiid taxa found four major clades of Australian taxa. The analysis revealed that at least three separate colonization events of the GAB spring fauna have occurred. Two of these are represented by considerable radiations, (1) Jardinella to the north and east and (2) Caldicochlea, Fonscochlea, and possibly Trochidrobia in South Australia. -
Nudipleura Bathydorididae Bathydoris Clavigera AY165754 2064 AY427444 1383 AF249222 445 AF249808 599
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`);D8D-S-"Q"'("%)D:":/)U&55/B.&%)&I)_"5/&%:&5&1K)"%7)</&5&1K,)</&V(&)U/%:/')\AP,) M(BC"'7S>"1%/'SD:'=)+a,)Xa333)A9%BC/%,)</'H"%K`)?>/#:/'%)4$#:'"5("%)A$#/$H,)\&BR/7)-"1);b,)>/5#CG&&5)FU,)_/':C,) >4)YbXY,)4$#:'"5("=))U&''/#G&%7/%B/)"%7)'/c$/#:#)I&')H":/'("5#)#C&$57)V/)"77'/##/7):&)!=*=)d/H"(5e)R"%&f"&'(=$S :&RK&="B=gGh) 7&33'+8+#1-.9)"#:/.8-;/#<) =-*'+)7>?)8$B5/&.7/)#/c$/%B/#)&I)G'(H/'#)$#/7)I&')"HG5(iB".&%)"%7)#/c$/%B(%1 =-*'+)7@?)<"#:'&G&7)#G/B(/#)"%7)#/c$/%B/#)$#/7)(%):C/)GCK5&1/%/.B)'/B&%#:'$B.&%)&I)/$:CK%/$'"%)B5"7/#)(%B5$7(%1) M(%1(B$5&(7/" A"$&.+)7>?)M46A\):'//#)V"#/7)&%)I&$'S1/%/)7":"#/:)T(:C&$:)&%/)&I):T&)H"g&')%$7(G5/$'"%)#$VB5"7/#e)d"h)8$7(V'"%BC(") d!"#$%&'()*+"%7),-.)/)&"h)"%7)dVh)_5/$'&V'"%BC&(7/")d0.-1('2("34$1*+"%7)5'/#$'/6*'3)"h= A"$&.+)7@?)O(H/SB"5(V'":/7)-J4DO):'//#)T(:C&$:)&%/)&I)I&$')B"5(V'".&%)G'(&'#e)d"h)i'#:)#G5(:)T(:C(%)J$&G(#:C&V'"%BC(")"%7) dVh)#G5(:#)V/:T//%)7"(%4$)1/)"%7)8/-"9'.)"%7)dBh)V/:T//%):)39)41.'6*)*)"%7):C'//)&:C/')'(%1(B$5(7#= A"$&.+)7B?)A'-"K/#):'//)V"#/7)&%)I&$'S1/%/)7":"#/:= -
“Opisthobranchia”! a Review on the Contribution of Mesopsammic Sea Slugs to Euthyneuran Systematics
Thalassas, 27 (2): 101-112 An International Journal of Marine Sciences BYE BYE “OPISTHOBRANCHIA”! A REVIEW ON THE CONTRIBUTION OF MESOPSAMMIC SEA SLUGS TO EUTHYNEURAN SYSTEMATICS SCHRÖDL M(1), JÖRGER KM(1), KLUSSMANN-KOLB A(2) & WILSON NG(3) Key words: Mollusca, Heterobranchia, morphology, molecular phylogeny, classification, evolution. ABSTRACT of most mesopsammic “opisthobranchs” within a comprehensive euthyneuran taxon set. During the last decades, textbook concepts of “Opisthobranchia” have been challenged by The present study combines our published morphology-based and, more recently, molecular and unpublished topologies, and indicates that studies. It is no longer clear if any precise distinctions monophyletic Rhodopemorpha cluster outside of can be made between major opisthobranch and Euthyneura among shelled basal heterobranchs, acte- pulmonate clades. Worm-shaped, mesopsammic taxa onids are the sister to rissoellids, and Nudipleura such as Acochlidia, Platyhedylidae, Philinoglossidae are the basal offshoot of Euthyneura. Furthermore, and Rhodopemorpha were especially problematic in Pyramidellidae, Sacoglossa and Acochlidia cluster any morphology-based system. Previous molecular within paraphyletic Pulmonata, as sister to remaining phylogenetic studies contained a very limited sampling “opisthobranchs”. Worm-like mesopsammic hetero- of minute and elusive meiofaunal slugs. Our recent branch taxa have clear independent origins and thus multi-locus approaches of mitochondrial COI and 16S their similarities are the result of convergent evolu- rRNA genes and nuclear 18S and 28S rRNA genes tion. Classificatory and evolutionary implications (“standard markers”) thus included representatives from our tree hypothesis are quite dramatic, as shown by some examples, and need to be explored in more detail in future studies. (1) Bavarian State Collection of Zoology. Münchhausenstr. -
(Gastropoda: Hydrobiidae): a Morphostatic Radiation of Freshwater Gastropods in Southeastern Australia
© Copyright Australian Museum, 2003 Records of the Australian Museum, Supplement 28 (2003): 1–109 ISBN 0-7347-2313-X Revision of the Snail Genus Austropyrgus (Gastropoda: Hydrobiidae): A Morphostatic Radiation of Freshwater Gastropods in Southeastern Australia STEPHANIE A. CLARK1, ALISON C. MILLER AND WINSTON F. PONDER Australian Museum, 6 College Street, Sydney NSW 2010, Australia 1 current address: Department of Biological Sciences, Biodiversity & Systematics, University of Alabama, Box 870345, Tuscaloosa, AL 35487, Unites States of America [email protected] · [email protected] · [email protected] ABSTRACT. The species that comprise a morphostatic radiation in southeastern Australia of the hydrobiid genus Austropyrgus Cotton are described using shell, opercular, anatomical and radular characters, and the genus is redefined. The previously described taxa have been included under several generic names, including Fluvidona (now a separate genus), Rivisessor, Pupiphryx and Angrobia, which are now treated as synonyms of Austropyrgus. Seventy-four species are described from southeastern Australia, fifty- seven of them new. These are grouped into six informal morphological groups to aid identification. Two recently described outlying species, A. bunyaensis from Mt Bunya, southern Queensland and A. centralia from Dalhousie Springs, northern South Australia, are not included in this revision. Members of the genus are typically found in streams, although a few species live in springs, rivers or lakes. A large number of the species have restricted distributions and several are known only from single locations. In southern New South Wales, Victoria and South Australia Austropyrgus is the dominant native freshwater hydrobiid genus whereas in Tasmania it is often sympatric with the native freshwater hydrobiid genera Beddomeia and/or Phrantela. -
Austropyrgus Tathraensis Clark, Miller & Ponder, 2003
Austropyrgus tathraensis Clark, Miller & Ponder, 2003 Diagnostic features This is one of several species of Austropyrgus found in the southern half of New South Wales. They are all very similar, being separated on small differences in size and shape of the shells and Distribution of Austropyrgus tathraensis. Austropyrgus tathraensis (adult size 2.1-2.8 mm) in anatomical details. They have elongate-conic shells with adults having a slightly thickened aperture and the operculum bears several pegs. Like most species of Austropyrgus, it is geographically isolated and has a restricted range. This species is found around Bega and Tathra. Austropyrgus tathraensis is most similar to A. sparsus, A. wombeyanensis, A. buchanensis and A. abercrombiensis. t differs from A. sparsus in lacking a simple outer lip (i.e, it is not reflected). From A. wombeyanensis it differs in its slightly narrower shell and in some radular differences while A. buchanensis has a slightly broader shell and some anatomical differences. Classification Austropyrgus tathraensis Clark, Miller & Ponder, 2003 Class Gastropoda I nfraclass Caenogastropoda Order Littorinida Suborder Rissoidina Superfamily Truncatelloidea Family Tateidae Genus Austropyrgus Cotton, 1942 Original name: Austropyrgus tathraensis Clark, Miller & Ponder, 2003. Clark, S. A., Miller, A. C. and Ponder, W. F. (2003). Revision of the snail genus Austropyrgus (Gastropoda: Hydrobiidae): A morphostatic radiation of freshwater gastropods in southeastern Australia. Records of the Australian Museum Supplement 28: 1ĕ109. Type locality: Tributary of Wapengo Creek, on Tathra-Bermagui Road, New South Wales. Biology and ecology n small streams on water weeds, hard substrata (rocks etc.) and crawling on litter and sediment. Can be locally abundant. -
Caenogastropoda
13 Caenogastropoda Winston F. Ponder, Donald J. Colgan, John M. Healy, Alexander Nützel, Luiz R. L. Simone, and Ellen E. Strong Caenogastropods comprise about 60% of living Many caenogastropods are well-known gastropod species and include a large number marine snails and include the Littorinidae (peri- of ecologically and commercially important winkles), Cypraeidae (cowries), Cerithiidae (creep- marine families. They have undergone an ers), Calyptraeidae (slipper limpets), Tonnidae extraordinary adaptive radiation, resulting in (tuns), Cassidae (helmet shells), Ranellidae (tri- considerable morphological, ecological, physi- tons), Strombidae (strombs), Naticidae (moon ological, and behavioral diversity. There is a snails), Muricidae (rock shells, oyster drills, etc.), wide array of often convergent shell morpholo- Volutidae (balers, etc.), Mitridae (miters), Buccin- gies (Figure 13.1), with the typically coiled shell idae (whelks), Terebridae (augers), and Conidae being tall-spired to globose or fl attened, with (cones). There are also well-known freshwater some uncoiled or limpet-like and others with families such as the Viviparidae, Thiaridae, and the shells reduced or, rarely, lost. There are Hydrobiidae and a few terrestrial groups, nota- also considerable modifi cations to the head- bly the Cyclophoroidea. foot and mantle through the group (Figure 13.2) Although there are no reliable estimates and major dietary specializations. It is our aim of named species, living caenogastropods are in this chapter to review the phylogeny of this one of the most diverse metazoan clades. Most group, with emphasis on the areas of expertise families are marine, and many (e.g., Strombidae, of the authors. Cypraeidae, Ovulidae, Cerithiopsidae, Triphori- The fi rst records of undisputed caenogastro- dae, Olividae, Mitridae, Costellariidae, Tereb- pods are from the middle and upper Paleozoic, ridae, Turridae, Conidae) have large numbers and there were signifi cant radiations during the of tropical taxa. -
Glacidorbis Iredale, 1943
Glacidorbis Iredale, 1943 Diagnostic features Shell small to minute, dextral, orthostrophic, near planispiral with wide, shallow umbilicus. Protoconch terminated by abrupt change in sculpture, lacking varix; sculptured with pustules or pits over whole surface, or on initial portion only with remaining part smooth. Teleoconch whorls evenly convex or ridged or keeled near mid-dorsally and near mid ventrally, sculptured with orthocline axial growth lines or ridges, sometimes also with spiral sculpture. Operculum circular to oval, multispiral to paucispiral, with central, subcentral to eccentric nucleus, and surface covered with minute pustules. Headfoot with long cephalic tentacles, the snout is short and very broad and fused to the dorsal part of the anterior foot, the eyes are in the middle of the tentacle bases. Foot posteriorly bifid, anteriorly with lateral processes. Jaw with dorsal and ventral elements. Radula with large central teeth bearing several sharp cusps on a pointed mesocone, with broader, arched base lacking additional cusps. Lateral teeth vestigial or narrow and small; marginal teeth absent. Mantle cavity widely open, not modified as a lung, with ciliated ridge on right side. The kidney is in the mantle roof, and there is no gill. Protandrous, and several large embryos brooded in mantle cavity. Penis narrow and small, completely invaginated, with large sucker or knob-like glands in the large praeputium. Classification Class Gastropoda Infraclass Heterobranchia Infrasubcohort Panpulmonata Superorder Pyropulmonata Order Amphibolida Suborder Glacidorbina Superfamily Glacidorboidea Family Glacidorbidae Genus Glacidorbis redale, 1943 Type species: Glacidorbis hedleyi redale, 1943 Original reference: redale, T. (1943). A basic list of the freshwater Mollusca of Australia. Australian Zoologist 10(2): 188ĕ230. -
Striadorbis Ponder and Avern, 2000
Striadorbis Ponder and Avern, 2000 Diagnostic features Shell differs from Glacidorbis in being planispiral, and in having spiral microsculpture on the latter part of protoconch and (at least) the early teleoconch. A mid-dorsal and mid-ventral spiral keel may be present. Protoconch with pustules in initial part, teleoconch whorls keeled or evenly rounded. Operculum circular with overlapping whorls, a central nucleus and external pustules. Anatomy differs from Glacidorbis in that the mantle cavity is longer and narrower and the rectum longer; the mantle lobe is shorter; the vagina is large and contains a prominent internal fold; and the penis is narrower and the praeputium contains fewer glandular protuberances that are rounded distally, not disk- like as in G. hedleyi. Striadorbis apparently does not brood embyos. Classification Class Gastropoda Infraclass Heterobranchia Infrasubcohort Panpulmonata Superorder Pyropulmonata Order Amphibolida Suborder Glacidorbina Superfamily Glacidorboidea Family Glacidorbidae Genus Striadorbis Ponder and Avern, 2000 Type species: Valvata(?) pedderi B. J. Smith, 1973. Original reference: Ponder, W. F. and. Avern, G. J. (2000). The Glacidorbidae (Mollusca: Gastropoda: (Heterobranchia) of Australia. Records of the Australian Museum 52: 307ĕ353. Type locality: n small hole in plain just south of Lake Edgar (now drowned as part of Lake Pedder) Tasmania. Biology and ecology Lives in rivers, streams, lakes, seeps and bogs. Found amongst weed, sedges, rushes and roots, rocks, gravel and cobbles, and muddy, silty or sandy substrata. Feeding biology unknown, possibly carnivorous. Like Glacidorbis hedleyi, Striadorbis pedderi appears to be a protandrous hermaphrodite but, unlike G. hedleyi, there is no evidence that brooding occurs in S. pedderi. Distribution Striadorbis has an unusual disjunct range - two species are found in the western and northern half of the east coast of Tasmania and one species is found in western Victoria. -
Austropyrgus Centralia (Ponder, Colgan, Terzis, Clark & Miller, 1996)
Austropyrgus centralia (Ponder, Colgan, Terzis, Clark & Miller, 1996) Diagnostic features This species is distinguished from the similar and co-occurring Caldicochlea harrisi by its small, conical shell and more evenly conical spire outline. A. centralia also differs from both species Distribution of Austropyrgus centralia. Austropyrgus centralia (adult size 1.4-2.2 mm) of Caldicochlea in its prominent opercular pegs, multiple (not two) basal denticles on the central teeth, as well as considerable differences in the female genital system and penial morphology. Classification Austropyrgus centralia (Ponder, Colgan, Terzis, Clark & Miller, 1996) Class Gastropoda I nfraclass Caenogastropoda Order Littorinida Suborder Rissoidina Superfamily Truncatelloidea Family Tateidae Genus Austropyrgus Cotton, 1942 Original name: Fluvidona centralia Ponder, Colgan, Terzis, Clark & Miller, 1996. Ponder, W. F., Colgan, D. J, Terzis, T., Clark, S. A and Miller, A. C. (1996). Three new morphologically and genetically determined species of hydrobiid gastropods from Dalhousie Springs, northern South Australia, with the description of a new genus. Molluscan Research 17: 49ĕ106. Type locality: Spring Cd11, Dalhousie Springs, South Australia. Biology and ecology Found in a few small (cold) isolated seeps and in shallow lower cold outflows distant from the warm to hot water sources of large springs. Distribution Dalhousie Springs, northern South Australia. Notes This is one of two species of Austropyrgus occurring far outside the range of the majority of species, being found in Dalhousie Springs in the far north of South Australia, while the other (A. bunyaensis) is found in southern Queensland. Most species of Austropyrgus are geographically isolated and have restricted ranges, and this one is no exception. -
Stygofauna Diversity and Distribution in Eastern Australian Cave and Karst Areas
--- - ------------------------------ DOI: 10.18195/issn.0313-122x.64.2001.049-062 Records of the Western Australian Museum Supplement No. 64: 49-62 (2001). Stygofauna diversity and distribution in Eastern Australian cave and karst areas 1 2 3 Mia E. Thurgate *, Jane s. Gough , Arthur K. Clarke , Peter Serov4and Andy Spate! 1 Jenolan Caves Reserve Trust, Locked Bag, Jenolan Caves, New South Wales 2790, Australia e-mail: [email protected] 2 NSW National Parks and Wildlife Service, PO Box 2115, Queanbeyan, New South Wales 2620, Australia 3 School of Zoology, University of Tasmania, GPO Box 252-05, Hobart, Tasmania 7001, Australia 4 Centre for Natural Resources, Biodiversity and Conservation Unit, University of New England, PO Box U245, Armidale, New South Wales 2351, Australia * For correspondence Abstract - This paper reviews the diversity and distribution of the stygofauna of Eastern Australia on a regional basis. Most of the stygofauna is concentrated in the highland karsts of New South Wales and Tasmania. Two hundred and thirty-eight taxa are present and amphipods, syncarids and hydrobiid gastropods are the dominant and most widespread groups. Nearly half of the total fauna are stygobites (82 taxa) and stygophiles (34 taxa). Also present are taxa with Gondwanan and Pangaean affinities, taxa that are phylogenetic and distributional relicts, and locally endemic taxa. Diversity and distribution at the local karst scale is also discussed using a case study of Wombeyan Caves, one of the richest stygofauna sites in Eastern Australia. The paper concludes with suggestions for further research. INTRODUCTION surveys suggest this is also an important region of The presence of a diverse global stygofauna stygofauna diversity (Eberhard et al., 1991; (fauna inhabiting groundwater environments) has Eberhard and Spate, 1995). -
South, Tasmania
Biodiversity Summary for NRM Regions Guide to Users Background What is the summary for and where does it come from? This summary has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. It highlights important elements of the biodiversity of the region in two ways: • Listing species which may be significant for management because they are found only in the region, mainly in the region, or they have a conservation status such as endangered or vulnerable. • Comparing the region to other parts of Australia in terms of the composition and distribution of its species, to suggest components of its biodiversity which may be nationally significant. The summary was produced using the Australian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. The list of families covered in ANHAT is shown in Appendix 1. Groups notnot yet yet covered covered in inANHAT ANHAT are are not not included included in the in the summary. • The data used for this summary come from authoritative sources, but they are not perfect.