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Can environmental tolerances explain convergent patterns of distribution in endemic spring snails from opposite sides of the Australian arid zone?

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Abstract

Patterns of distribution are influenced by species environmental requirements and limits, but experimental tests are needed to discern whether correlates of abundance directly affect survival and success. Springs in Australia’s arid interior support a wide diversity of gastropods only found in springs, and these species show dichotomous patterns of distribution. “Amphibious” species are broadly distributed across many springs and microhabitats, and “aquatic” species confined to the deepest pool areas within large springs. This pattern appears to be driven by the interaction between different environmental conditions in different microhabitats and the environmental tolerances of each endemic snail species. Factorial experiments were used to test whether conditions in the environmentally extreme and variable tail area of springs (considering pH, conductivity, temperature and desiccation potential, alone and in synergistic scenarios) elicited lethal or sub-lethal responses in spring snails endemic to springs on opposite sides of the Australian arid zone. All species restricted to spring pools were able to endure 24 h exposed to the average tail conditions, alone and in combination, but most suffered mortalities when subjected to extremes, and mortalities occurred sooner in the most restricted species when elevated pH and conductivity were experienced in combination. Responses of species from different locations are similar, but pattern of distribution in the field were not correlated with tolerance of environmental extremes—with the “amphibious” species from the sub-tropics being far more sensitive than its arid counterpart. These findings suggest that environmental variance within springs can influence patterns of distribution and abundance, particularly when extremes are experienced simultaneously over sustained time periods. But despite similarities in responses across species from these two spring complexes, no simple generalisations linking distribution and tolerance were discernible.

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References

  • Benke M, Brandle M, Albrecht C, Wilke T (2011) Patterns of freshwater biodiversity in Europe: lessons from the spring snail genus Bythinella. J Biogeogr 38:2021–2032

    Article  Google Scholar 

  • Blinn DW (2008) The extreme environment, trophic structure, and ecosystem dynamics of a large fishless desert spring (Montezuma Well, Arizona). In: Stevens LE, Meretsky VJ (eds) Aridland springs in North America; ecology and conservation. The University of Arizona Press, Tucson, pp 98–126

    Google Scholar 

  • Borcard D, Gillet F, Legendre P (2011) Numerical ecology with R. Springer, Berlin

    Book  Google Scholar 

  • Boulton AJ (2005) Chances and challenges in the conservation of groundwaters and their dependent ecosystems. Aquat Conserv 15:319–323

    Article  Google Scholar 

  • Brown DS (2001) Freshwater snails of the genus Gyraulus (Planorbidae) in Australia: taxa of the mainland. Molluscan Res 21:17–107

    Article  Google Scholar 

  • Cañedo-Argüelles M, Hawkins CP, Kefford BJ, Schäfer RB, Dyack BJ, Brucet S, Buchwalter D, Dunlop J, Frör O, Lazorchak J, Coring E (2016) Saving freshwater from salts. Science 351:914–916

    Article  PubMed  Google Scholar 

  • Cantonati M, Fureder L, Gerecke R, Juttner I, Cox EJ (2012) Crenic habitats, hotspots for freshwater biodiversity conservation: toward an understanding of their ecology. Freshw Sci 31:463–480

    Article  Google Scholar 

  • Cantonati M, Segadelli S, Ogata K, Tran H, Sanders D, Gerecke R, Celico F (2016) A global review on ambient limestone-precipitating springs (LPS): hydrogeological setting, ecology, and conservation. Sci Total Environ 568:624–637

    Article  CAS  PubMed  Google Scholar 

  • Cardoso P, Erwin TL, Borges PAV, New TR (2011) The seven impediments in invertebrate conservation and how to overcome them. Biol Cons 144:2647–2655

    Article  Google Scholar 

  • Cloudsley-Thompson JL (1975) Adaptations of Arthropoda to arid environments. Annu Rev Entomol 20:261–283

    Article  CAS  PubMed  Google Scholar 

  • Côté IM, Darling ES, Brown CJ (2016) Interactions among ecosystem stressors and their importance in conservation. Proc R Soc B Biol Sci 283:1824

    Article  Google Scholar 

  • Danielopol DL, Griebler C, Gunatilaka A, Notenboom J (2003) Present state and future prospects for groundwater ecosystems. Environ Conserv 30:104–130

    Article  CAS  Google Scholar 

  • Davis JA, Kerezsy A, Nicol S (2017) Springs: conserving perennial water is critical in arid landscapes. Biol Cons 211:30–35

    Article  Google Scholar 

  • Dowd WW, King FA, Denny MW (2015) Thermal variation, thermal extremes and the physiological performance of individuals. J Exp Biol 218:1956–1967

    Article  PubMed  Google Scholar 

  • DSITIA (2015) Lake eyre basin springs assessment project: groundwater dependent ecosystem mapping report. Department of Science, I.T.a.I.A. (ed), Department of Science, Information Technology and Innovation, Brisbane

  • Dudgeon D, Arthington AH, Gessner MO, Kawabata ZI, Knowler DJ, Leveque C, Naiman RJ, Prieur-Richard AH, Soto D, Stiassny MLJ, Sullivan CA (2006) Freshwater biodiversity: importance, threats, status and conservation challenges. Biol Rev 81:163–182

    Article  PubMed  Google Scholar 

  • Dussart GBJ (1979) Life cycles and distribution of the aquatic gastropod molluscs Bithynia tentaculata (L.), Gyraulus albus (Muller), Planorbis planorbis (L.) and Lymnaea peregra (Muller) in relation to water chemistry. Hydrobiologia 67:223–239

    Article  Google Scholar 

  • Fairfax RJ, Fensham RJ (2002) In the footsteps of J. Alfred Griffiths: a cataclysmic history of Great Artesian Basin springs in Queensland. Aust Geogr Stud 40:210–230

    Article  Google Scholar 

  • Fairfax RJ, Fensham RJ (2003) Great Artesian Basin springs in Southern Queensland 1911–2000. Mem Queensl Mus 49:285–293

    Google Scholar 

  • Fairfax RJ, Fensham RJ, Wager R, Brooks S, Webb A, Unmack P (2007) Recovery of the red-finned blue-eye: an endangered fish from springs of the Great Artesian Basin. Wildl Res 34:156–166

    Article  Google Scholar 

  • Fensham RJ, Fairfax RJ (2003) Spring wetlands of the Great Artesian Basin, Queensland, Australia. Wetlands Ecol Manage 11:343–362

    Article  Google Scholar 

  • Fensham RJ, Silcock JL, Kerezsy A, Ponder WF (2011) Four desert waters: setting arid zone wetland conservation priorities through understanding patterns of endemism. Biol Conserv 144:2459–2467

    Article  Google Scholar 

  • Fleishman E, Murphy DD, Sada DW (2006) Effects of environmental heterogeneity and disturbance on the native and non-native flora of desert springs. Biol Invasions 8:1091–1101

    Article  Google Scholar 

  • Gaston KJ, Blackburn TM, Lawton JH (1997) Interspecific abundance-range size relationships: an appraisal of mechanisms. J Anim Ecol 66:579–601

    Article  Google Scholar 

  • Glover CJM (1982) Adaptations of fishes in arid Australia. In: Barker WR, Greenslade PJM (eds) Evolution of the Flora and Fauna of Arid Australia. Peacock Publications, Frewville, South Australia, pp 241–246

    Google Scholar 

  • Guisan A, Thuiller W (2005) Predicting species distribution: offering more than simple habitat models. Ecol Lett 8:993–1009

    Article  Google Scholar 

  • Habermehl M (1982) Springs in the Great Artesian Basin, Australia: their origin and nature. Canberra, Australia, Australian Government Publishing Service for the Bureau of Mineral Resources, Geology and Geophysics

  • Hart BT, Bailey P, Edwards R, Hortle K, James K, McMahon A, Meredith C, Swadling K (1991) A review of the salt sensitivity of the Australian freshwater biota. Hydrobiologia 210:105–144

    Article  Google Scholar 

  • Havas M, Rosseland BO (1995) Response of zooplankton, benthos, and fish to acidification: an overview. Water Air Soil Pollut 85:51–62

    Article  CAS  Google Scholar 

  • Hengeveld R (1993) Ecological biogeography. Prog Phys Geogr 17:448–460

    Article  Google Scholar 

  • Hengeveld R, Haeck J (1981) The distribution of abundance 2. Models and implications. Proc Koninklijke Nederlandse Akademie Van Wetenschappen Ser C Biol Med Sci 84:257–284

    Google Scholar 

  • Hengeveld R, Haeck J (1982) The distribution of abundance 1. Measurements. J Biogeogr 9:303–316

    Article  Google Scholar 

  • Hershler R, Liu HP, Howard J (2014) Springsnails: a new conservation focus in Western North America. Bioscience 64:693–700

    Article  Google Scholar 

  • Jackson MC, Loewen CJG, Vinebrooke RD, Chimimba CT (2016) Net effects of multiple stressors in freshwater ecosystems: a meta-analysis. Glob Change Biol 22:180–189

    Article  Google Scholar 

  • Kearney M (2006) Habitat, environment and niche: what are we modelling? Oikos 115:186–191

    Article  Google Scholar 

  • Kefford BJ, Nugegoda D (2005) No evidence for a critical salinity threshold for growth and reproduction in the freshwater snail Physa acuta. Environ Pollut 134:377–383

    Article  CAS  PubMed  Google Scholar 

  • Kefford BJ, Nugegoda D, Zalizniak L, Fields EJ, Hassell KL (2007) The salinity tolerance of freshwater macroinvertebrate eggs and hatchlings in comparison to their older life-stages: a diversity of responses. Aquat Ecol 41:335–348

    Article  CAS  Google Scholar 

  • Klockmann M, Scharre M, Haase M, Fischer K (2016) Does narrow niche space in a ‘cold-stenothermic’ spring snail indicate high vulnerability to environmental change? Hydrobiologia 765:71–83

    Article  Google Scholar 

  • Kodric-Brown A, Brown IH (1993) Highly structured fish communities in Australian desert springs. Ecology 74:1847–1855

    Article  Google Scholar 

  • Küry D, Lubini V, Stucki P (2017) Temperature patterns and factors governing thermal response in high elevation springs of the Swiss Central Alps. Hydrobiologia 793:185–197

    Article  Google Scholar 

  • Layman CA, Smith DE, Herod JD (2000) Seasonally varying importance of abiotic and biotic factors in marsh-pond fish communities. Mar Ecol Prog Ser 207:155–169

    Article  Google Scholar 

  • Leblanc M, Tweed S, Lyon B, Bailey J, Franklin C, Harrington G, Suckow A (2015) On the hydrology of the bauxite oases, Cape York Peninsula, Australia. J Hydrol 528:668–682

    Article  CAS  Google Scholar 

  • Losos JB (2008) Phylogenetic niche conservatism, phylogenetic signal and the relationship between phylogenetic relatedness and ecological similarity among species. Ecol Lett 11:995–1003

    Article  PubMed  Google Scholar 

  • McMahon T, Murphy R, Little P, Costelloe J, Peel M, Chiew F, Hayes S, Nathan R, Kandel D (2005) Hydrology of Lake Eyre Basin. The University of Melbourne, Melbourne

    Google Scholar 

  • Mitchell R (1974) The evolution of thermophily in hot springs. Q Rev Biol 49:229–242

    Article  Google Scholar 

  • Mitchell SC (2005) How useful is the concept of habitat? A critique. Oikos 110:634–638

    Article  Google Scholar 

  • Murphy NP, Guzik MT, Cooper SJB, Austin AD (2015) Desert spring refugia: museums of diversity or evolutionary cradles? Zoolog Scr 6:693–701

    Article  Google Scholar 

  • Nevill JC, Hancock PJ, Murray BR, Ponder WF, Humphreys WF, Phillips ML (2010) Groundwater-dependent ecosystems and the dangers of groundwater overdraft: a review and an Australian perspective. Pac Conserv Biol 16:187–208

    Article  Google Scholar 

  • Oksanen J, Blanchet FG, Kindt R, Legendre P, Minchin PR, O’Hara RB, Simpson GL, Solymos P, Stevens MHH, Wagner H (2015) Vegan: community ecology package. R package version 2.2-1

  • Pallarés S, Arribas P, Bilton DT, Millán A, Velasco J (2015) The comparative osmoregulatory ability of two water beetle genera whose species span the fresh-hypersaline gradient in inland waters (Coleoptera: Dytiscidae, Hydrophilidae). PLoS ONE 10:e0124299

    Article  PubMed  PubMed Central  Google Scholar 

  • Perez KE, Ponder WF, Colgan DJ, Clark SA, Lydeard C (2005) Molecular phylogeny and biogeography of spring-associated hydrobild snails of the Great Artesian Basin, Australia. Mol Phylogenet Evol 34:545–556

    Article  CAS  PubMed  Google Scholar 

  • Piggott JJ, Lange K, Townsend CR, Matthaei CD (2012) Multiple stressors in agricultural streams: a mesocosm study of interactions among raised water temperature, sediment addition and nutrient enrichment. PLoS ONE 7:49873

    Article  Google Scholar 

  • Piggott JJ, Townsend CR, Matthaei CD (2015) Reconceptualizing synergism and antagonism among multiple stressors. Ecol Evol 5:1538–1547

    Article  PubMed  PubMed Central  Google Scholar 

  • Pineda MC, McQuaid CD, Turon X, López-Legentil S, Ordóñez V, Rius M (2012) Tough adults, frail babies: an analysis of stress sensitivity across early life-history stages of widely introduced marine invertebrates. PLoS ONE 7:e46672

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ponder WF (1995) Mound spring snails of the Australian Great Artesian Basin. The IUCN Species Survival Commission on the Conservation Biology of Molluscs, Edinburgh, Scotland, IUCN/SSC Mollusc Specialist Group

  • Ponder WF (2003) Monograph of the Australian Bithyniidae (Caenogastropoda: Rissooidea). Zootaxa 230:1–126

    Article  Google Scholar 

  • Ponder WF, Clark GA (1990) A radiation of hydrobiid Snails in threatened artesian springs in western Queensland. Rec Aust Mus 42:301–363

    Article  Google Scholar 

  • Ponder WF, Slatyer C (2010) Freshwater molluscs in the Australian arid zone. In: Dickman C, Lunney D, Burgin S (eds) Animals of Arid Australia: out on their own. Royal Zoological Society of New South Wales, Mosman, pp 1–13

    Google Scholar 

  • Ponder WF, Hershler R, Jenkins B (1989) An endemic radiation of hydrobiid snails from artesian springs in Northern South Australia—their taxonomy, physiology, distribution and anatomy. Malacologia 31:1–140

    Google Scholar 

  • Ponder WF, Vial M, Jefferys E (2010) The aquatic macroinvertebrates in the springs on Edgbaston Station, Queensland. Queensland Museum, Brisbane

    Google Scholar 

  • Powell O, Fensham RJ (2016) The history and fate of the Nubian Sandstone Aquifer springs in the oasis depressions of the Western Desert, Egypt. Hydrogeol J 24:395–406

    Article  CAS  Google Scholar 

  • Powell O, Silcock J, Fensham RJ (2015) Oases to oblivion: the rapid demise of springs in the South-Eastern Great Artesian Basin, Australia. Groundwater 53:171–178

    Article  CAS  Google Scholar 

  • Pritchard G (1991) Insects in thermal springs. Mem Entomol Soc Can 123:89–106

    Article  Google Scholar 

  • R Studio Team (2015) RStudio: integrated development for R. RStudio, Inc., Boston. http://www.rstudio.com/

  • Richey AS, Thomas BF, Lo MH, Reager JT, Famiglietti JS, Voss K, Swenson S, Rodell M (2015) Quantifying renewable groundwater stress with GRACE. Water Resour Res 51:5217–5238

    Article  PubMed  PubMed Central  Google Scholar 

  • Rosati M, Cantonati M, Primicerio R, Rossetti G (2014) Biogeography and relevant ecological drivers in spring habitats: a review on ostracods of the Western Palearctic. Int Rev Hydrobiol 99:409–424

    Article  Google Scholar 

  • Rossini RA, Fensham RJ, Walter GH (2017) Spatiotemporal variance in environmental conditions of Australian artesian springs affects the abundance and distribution of six endemic snail species. Aquat Ecol. doi:10.1007/s10452-017-9633-4

    Google Scholar 

  • Shah AA, Gill BA, Encalada AC, Flecker AS, Funk CW, Guayasamin JM, Ghalambor CK (2017) Climate variability predicts thermal limits of aquatic insects across elevation and latitude. Funct Ecol. doi:10.1111/1365-2435.12906

    Google Scholar 

  • Shepard WD (1993) Desert springs—both rare and endangered. Aquat Conserv 3:351–359

    Article  Google Scholar 

  • Slatyer RA, Hirst M, Sexton JP (2013) Niche breadth predicts geographical range size: a general ecological pattern. Ecol Lett 16:1104–1114

    Article  PubMed  Google Scholar 

  • Smith H, Wood PJ, Gunn J (2003) The influence of habitat structure and flow permanence on invertebrate communities in karst spring systems. Hydrobiologia 510:53–66

    Article  Google Scholar 

  • Spitale D, Leira M, Angeli N, Cantonati M (2012) Environmental classification of springs of the Italian Alps and its consistency across multiple taxonomic groups. Freshw Sci 31:563–574

    Article  Google Scholar 

  • Stendera S, Adrian R, Bonada N, Cañedo-Argüelles M, Hugueny B, Januschke K, Pletterbauer F, Hering D (2012) Drivers and stressors of freshwater biodiversity patterns across different ecosystems and scales: a review. Hydrobiologia 696:1–28

    Article  Google Scholar 

  • Stomp M, Huisman J, Mittelbach GG, Litchman E, Klausmeier CA (2011) Large-scale biodiversity patterns in freshwater phytoplankton. Ecology 92:2096–2107

    Article  PubMed  Google Scholar 

  • Strayer DL (2006) Challenges for freshwater invertebrate conservation. J N Am Benthol Soc 25:271–287

    Article  Google Scholar 

  • Sultan SE (2015) Organism and environment: ecological development, niche construction, and adaptation. Oxford University Press, Oxford

    Book  Google Scholar 

  • Underwood A, Chapman M, Connell S (2000) Observations in ecology: you can’t make progress on processes without understanding the patterns. J Exp Mar Biol Ecol 250:97–115

    Article  CAS  PubMed  Google Scholar 

  • Unmack P, Minckley WL (2008) The demise of desert springs. Aridland Springs in North America; Ecology and Conservation. LE Stevens and VJ Meretsky. The University of Arizona Press, Tucson, pp 11–34

  • Vanhorne B (1983) Density as a midleading indicator of habitat quality. J Wildl Manage 47:893–901

    Article  Google Scholar 

  • Vera CL, Hyne RV, Patra R, Ramasamy S, Pablo F, Julli M, Kefford BJ (2014) Bicarbonate toxicity to Ceriodaphnia dubia and the freshwater shrimp Paratya australiensis and its influence on zinc toxicity. Environ Toxicol Chem 33:1179–1186

    Article  CAS  PubMed  Google Scholar 

  • von Fumetti S, Blattner L (2017) Faunistic assemblages of natural springs in different areas in the Swiss National Park: a small-scale comparison. Hydrobiologia 793:175–184

    Article  Google Scholar 

  • Walter GH, Hengeveld R (2014) Autecology: organisms, interactions and environmental dynamics. CRC Press, Boca Raton

    Book  Google Scholar 

  • Wiegert RG, Mitchell R (1973) Ecology of yellowstone thermal effluent systems: intersects of blue-green algae, grazing flies (Paracoenia, Ephydridae) and water mites (Partnuniella, Hydrachnellae). Hydrobiologia 41:251–271

    Article  Google Scholar 

  • Williams WD (1985) Biotic adaptations in temporary lentic waters, with special reference to those in semi-arid and arid regions. Hydrobiologia 125:85–110

    Article  Google Scholar 

  • Zalizniak L, Kefford BJ, Nugegoda D (2006) Is all salinity the same? I. The effect of ionic compositions on the salinity tolerance of five species of freshwater invertebrates. Mar Freshw Res 57:75–82

    Article  CAS  Google Scholar 

  • Zalizniak L, Kefford BJ, Nugegoda D (2009) Effects of pH on salinity tolerance of selected freshwater invertebrates. Aquat Ecol 43:135–144

    Article  CAS  Google Scholar 

  • Zullini A, Gatti F, Ambrosini R (2011) Microhabitat preferences in springs, as shown by a survey of nematode communities of Trentino (south-eastern Alps, Italy). J Limnol 70:93–105

    Article  Google Scholar 

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Acknowledgements

We would like to acknowledge the traditional owners of the land on which we work: the Jagera and Turrbal (Brisbane) and the Iningai and Bidjara people (Edgbaston and surrounds). We thank Bush Heritage Australia and their supporters for guaranteeing the conservation of Edgbaston, allowing us access and providing on-ground support. We are grateful for the advice of Prof Craig Franklin and Dr Rebecca Cramp and for the voluntary assistance of Sasha Jooste, Karlee Taylor and Ian Rossini. RAR was funded by an Australian Postgraduate Award Scholarship and a top-up scholarship from the Great Artesian Basin Coordinating Committee. A Student Research Grant awarded to RAR and HLT by the Ecological Society of Australia financially supported the construction of the experimental aquaria system.

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Rossini, R.A., Tibbetts, H.L., Fensham, R.J. et al. Can environmental tolerances explain convergent patterns of distribution in endemic spring snails from opposite sides of the Australian arid zone?. Aquat Ecol 51, 605–624 (2017). https://doi.org/10.1007/s10452-017-9639-y

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