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Dispersal of Two Species of Trichoptera from Desert Springs: Conservation Implications for Isolated vs Connected Populations

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Abstract

During the Pleistocene, when the climate was wetter and cooler, aquatic habitats in the Great Basin of western North America were much more extensive and connected. As the climate warmed over the last 10 000 years, many of these habitats dried but others remained as isolated springs and inland lakes. The isolation of desert springs and lack of dispersal between populations of non-vagile species (e.g. fish, spring snails) has led to genetic differentiation and speciation. However, the extent to which vagile species of aquatic insects disperse from spring to spring is unknown. We examined the population genetics of two caddisflies, Hesperophylax designatus (Limnephilidae) and Lepidostoma ojanum (Lepidostomatidae) that occur in isolated springs in Nevada and eastern California to determine the extent of their dispersal from spring to spring. Mitochondrial DNA sequences indicate that the populations of L. ojanum are isolated and that the populations represent management units. In contrast, H. designatus individuals are flying from spring to spring and their populations are connected by dispersal. Disturbance impacts (e.g. grazing by ungulates, water extraction) that eliminate poor dispersers (e.g. L. ojanum) locally may result in permanent losses of genetic diversity; this is less likely with broader dispersers such as H. designatus.

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References

  • Anderson, N.H. (1976) The distribution and biology of Oregon Trichoptera. Oregon Agric. Exp. Station Tech. Bull. 134, 1-160.

    Google Scholar 

  • Clary, D.O. and Wolstenholme, D.R. (1985) The mitochondrial DNA molecule of Drosophila yakuba: nucleotide sequence, gene organization, and genetic code. J. Mol. Evol. 22, 252-71.

    Google Scholar 

  • Colburn, E.A. (1984) Diapause in a salt-tolerant desert caddisfly: the life cycle of Limnephilus assimilis (Trichoptera) in Death Valley. Am. Midland Naturalist 111, 280-87.

    Google Scholar 

  • Cole, G.A. and Watkins, R.L. (1977) Hyallela montezuma, a new species (Crustacea: amphipoda) from Montezuma Well, Arizona. Hydrobiologia 52, 175-84.

    Google Scholar 

  • Crichton, M.I. (1971) A study of caddis flies (Trichoptera) of the family Limnephilidae, based on the Rothamsted Insect Survery, 1964-68. J. Zool., London 163, 533-63.

    Google Scholar 

  • Erman, N.A. and Erman, D.C. (1990) Biogeography of caddisfly (Trichoptera) assemblages in cold springs of the Sierra Nevada (California, USA). California Water Resources Center Contribution 200.

  • Erman, N.A. and Erman, D.C. (1995) Spring permanence, Trichoptera species richness, and the role of drought. J. Kansas Entomol. Soc. (Suppl.) 68, 50-64.

    Google Scholar 

  • Excoffier, L., Smouse, P. and Quattro, J. (1992) Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131, 479-91.

    Google Scholar 

  • Ferrington, L.C. (ed) (1995) Biodiversity of aquatic insects and other invertebrates in springs. J. Kansas Entomol. Soc. 68, 1-165.

    Google Scholar 

  • Griffith, M.B., Barrows, E.M. and Perry, S.A. (1998) Lateral dispersal of adult aquatic insects (Plecoptera, Trichoptera) following emergence from headwater streams in forested Appalachian catchments. Entomol. Soc. Am 91, 195-201.

    Google Scholar 

  • Hansen, T.A. (1980) Influence of larval dispersal and geographic distribution on species longevity in neogastropods. Paleobiology 6, 193-207.

    Google Scholar 

  • Hershler, R. (1989) Springsnails (Gastropoda: Hydrobiidae) of Owens and Amargosa River (Exclusive of Ash Meadows) drainages, Death Valley System, California-Nevada. Proc. Biol. Soc. Washington 102, 176-248.

    Google Scholar 

  • Hershler, R. (1998) A systematic review of the hydrobiid snails (Gastropoda: Rissooidea) of the Great Basin, Western United States, Part I. Genus Pyrgulopsis. Veliger 41, 1-132.

    Google Scholar 

  • Hogg, I.D., Eadie, J.M. and De Lafontaine, Y. (1998) Atmospheric change and the diversity of aquatic invertebrates: are we missing the boat? Environ. Monitor. Assessment 49, 291-301.

    Google Scholar 

  • Jackson, J.K. and Resh, V.H. (1989) Distribution and abundance of adult aquatic insects in the forest adjacent to a Northern California stream. Environ. Entomol. 18, 278-83.

    Google Scholar 

  • Kovats, Z.E., Ciborowski, J.J.H. and Corkum. L.D. (1996) Inland dispersal of adult aquatic insects. Freshwater Biol. 36, 265-76.

    Google Scholar 

  • La Rivers, I. (1953) New gelastocorid and naucorid records and miscellaneous notes, with a description of the new species, Ambrysus amargosus (Hemiptera: Naucoridae). Wassmann J. Biol. 11, 83-96

    Google Scholar 

  • Lefkovitch, L.P. and Fahrig, L. (1985) Spatial characteristics of habitat patches and population survival. Ecol. Model. 30, 297-308.

    Google Scholar 

  • Moritz, C. (1994) Defining ‘Evolutionarily Significant Units’ for conservation. Trends in Ecol. and Evol. 9, 373-75.

    Google Scholar 

  • Myers, M.J. (2000) Aquatic invertebrates in island habitats: dispersal, population genetics, and ecology. Ph.D. dissertation, University of California, Berkeley, California.

    Google Scholar 

  • Myers, M.J. and Resh, V.H. (1999a) Use of pan traps to collect adult Trichoptera in high desert spring habitats of California, USA. In Proceedings of the 9th International Symposium on Trichoptera. (H. Malicky and P. Chantaramongkol, eds), pp. 259-67. Faculty of Science, Chiang Mai University, Chiang Mai, Thailand.

    Google Scholar 

  • Myers, M.J. and Resh, V.H. (2000) Undercut banks: a habitat for more than just fish. Trans. Am. Fisheries Soc. 129, 594-97.

    Google Scholar 

  • Myers, M.J. and Resh, V.H. (2002) Trichoptera and other macroinvertebrates in springs of the Great Basin: species composition, richness, and distribution.Western North Am Naturalist (in press).

  • Myers, M.J., Meyer, C.P. and Resh, V.H. (2000) Neritid and thiarid gastropods from French Polynesian streams: how reproduction (sexual, parthenogenetic) and dispersal (active, passive) affect population structure. Freshwater Biol. 43, 1-11.

    Google Scholar 

  • Parker, C.R. and Wiggins, G.B. (1985) The Nearctic genus Hesperophylax Banks (Trichoptera: Limnephilidae). Can. J. Zool. 63, 2443-72.

    Google Scholar 

  • Polhemus, J.T. and Polhemus, D.A. (1994) A new species of Ambrysus Stål from Ash Meadows, Nevada (Heteroptera: Naucoridae). J. N.Y. Entomol. Soc. 102, 261-65

    Google Scholar 

  • Ross, H.H. (1944) The caddis flies, or Trichoptera, of Illinois. Bull. Illinois Nat. History Surv. 23, 1-326.

    Google Scholar 

  • Sada, D.W., Britten, H.B. and Brussard, P.F. (1995) Desert aquatic ecosystems and the genetic and morphological diversity of Death Valley system Speckled Dace. Am. Fisheries Soc. Symp. 17, 350-59

    Google Scholar 

  • Schneider, S., Kueffer, J-M, Roessli, D. and Excoffier, L. (1997) Arlequin ver 1.1: A software for population genetic data analysis. Genetics and Biometry Laboratory, University of Geneva, Switzerland.

    Google Scholar 

  • Shepard, W.D. (1990) Microcylloepus formicoideus (Coleoptera: Elmidae), a new riffle beetle from Death Valley National Monument, California. Entomol. News 101, 147-53.

    Google Scholar 

  • Shepard, W.D. (1992) Riffle beetles (Coleoptera: Elmidae) of Death Valley National Monument, California. Great Basin Naturalist 52, 378-81.

    Google Scholar 

  • Shepard, W.D. (1993) Desert springs-both rare and endangered. Aquatic Conservation: Mar. and Freshwater Ecosystems 3, 351-59.

    Google Scholar 

  • Simon, C., Frati, F., Beckenbach, A., Crespi, B., Liu, H. and Flook, P. (1994) Evolution, weighting, and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers. Ann. Entomol. Soc. Am. 87, 651-701.

    Google Scholar 

  • Sode, A. and Wiberg-Larsen, P. (1993) Dispersal of adult Trichoptera at a Danish forest brook. Freshwater Biol. 30, 439-46.

    Google Scholar 

  • Sokal, R.R. and Rohlf, F.J. (1995) Biometry.W.H. Freeman and Company, New York.

    Google Scholar 

  • Sperling, F.A.H., Raske, A.G. and Otvos, I.S. (1999) Mitochondrial DNA sequence variation among populations and host races of Lambdina fiscellaria (Gn.) (Lepidoptera: Geometridae). Insect Mol. Biol. 8, 97-106.

    Google Scholar 

  • Svensson, B.W. (1974) Population movements of adult Trichoptera at a south Swedish stream. Oikos 25, 157-75.

    Google Scholar 

  • Swofford, D.L. (1999) PAUP * : Phylogenetic Analysis Using Parsimony ver4.0b2a. Sinauer, Sunderland, Massachusetts.

    Google Scholar 

  • Thomas, E.P., Blinn, D.W. and Keim, P. (1997) Genetic and behavioural divergence among spring amphipod populations. Freshwater Biol. 38, 137-43.

    Google Scholar 

  • Weaver, J.S. III and Myers, M.J. (1998) Two new species of caddisflies of the genus Lepidostoma Rambur (Trichoptera: Lepidostomatidae) from the Great Basin. Aquatic Insects 20, 189-95.

    Google Scholar 

  • Wiggins, G.B. (1996) Larvae of the North American Caddisfly Genera (Trichoptera). University of Toronto Press, Toronto, Canada.

    Google Scholar 

Download references

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Correspondence to V.H. Resh.

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Myers, M.J., Sperling, F. & Resh, V. Dispersal of Two Species of Trichoptera from Desert Springs: Conservation Implications for Isolated vs Connected Populations. Journal of Insect Conservation 5, 207–215 (2001). https://doi.org/10.1023/A:1017998513721

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