Articles | Volume 8, issue 1
https://doi.org/10.5194/bg-8-175-2011
© Author(s) 2011. This work is distributed under
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the Creative Commons Attribution 3.0 License.
Special issue:
https://doi.org/10.5194/bg-8-175-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
26 Jan 2011
Research article |
| 26 Jan 2011
Spatially explicit analysis of gastropod biodiversity in ancient Lake Ohrid
T. Hauffe
Department of Animal Ecology and Systematics, Justus Liebig University, Giessen, Germany
C. Albrecht
Department of Animal Ecology and Systematics, Justus Liebig University, Giessen, Germany
K. Schreiber
Department of Animal Ecology and Systematics, Justus Liebig University, Giessen, Germany
K. Birkhofer
Department of Animal Ecology and Systematics, Justus Liebig University, Giessen, Germany
S. Trajanovski
Department of Zoobenthos, Hydrobiological Institute Ohrid, Ohrid, Macedonia
T. Wilke
Department of Animal Ecology and Systematics, Justus Liebig University, Giessen, Germany
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A. C. Kraberg, E. Druzhkova, B. Heim, M. J. G. Loeder, and K. H. Wiltshire
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D. Van Damme and A. Gautier
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I. Domaizon, O. Savichtcheva, D. Debroas, F. Arnaud, C. Villar, C. Pignol, B. Alric, and M. E. Perga
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E. W. Helbling, P. Carrillo, J. M. Medina-Sánchez, C. Durán, G. Herrera, M. Villar-Argaiz, and V. E. Villafañe
Biogeosciences, 10, 1037–1050, https://doi.org/10.5194/bg-10-1037-2013, https://doi.org/10.5194/bg-10-1037-2013, 2013
C. H. Hsieh, Y. Sakai, S. Ban, K. Ishikawa, T. Ishikawa, S. Ichise, N. Yamamura, and M. Kumagai
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G. Kostoski, C. Albrecht, S. Trajanovski, and T. Wilke
Biogeosciences, 7, 3999–4015, https://doi.org/10.5194/bg-7-3999-2010, https://doi.org/10.5194/bg-7-3999-2010, 2010
K. Lindhorst, H. Vogel, S. Krastel, B. Wagner, A. Hilgers, A. Zander, T. Schwenk, M. Wessels, and G. Daut
Biogeosciences, 7, 3531–3548, https://doi.org/10.5194/bg-7-3531-2010, https://doi.org/10.5194/bg-7-3531-2010, 2010
C. Albrecht, H. Vogel, T. Hauffe, and T. Wilke
Biogeosciences, 7, 3435–3446, https://doi.org/10.5194/bg-7-3435-2010, https://doi.org/10.5194/bg-7-3435-2010, 2010
S. Trajanovski, C. Albrecht, K. Schreiber, R. Schultheiß, T. Stadler, M. Benke, and T. Wilke
Biogeosciences, 7, 3387–3402, https://doi.org/10.5194/bg-7-3387-2010, https://doi.org/10.5194/bg-7-3387-2010, 2010
T. Wilke, R. Schultheiß, C. Albrecht, N. Bornmann, S. Trajanovski, and T. Kevrekidis
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Cited articles
Abell, R., Thieme, M. L., Revenga, C., Bryer, M., Kottelat, M., Bogutskaya, N., Coad, B., Mandrak, N., Balderas, S. C., Bussing, W., Stiassny, M. L. J., Skelton, P., Allen, G. R., Unmack, P., Naseka, A., Ng, R., Sindorf, N., Robertson, J., Armijo, G., Higgins, J. H., Heibel, T. J., Wikramanayake, E., Olson, D., López, H. L., Reis, R. E., Lundberg, J. G., Pérez, M. H. S., and Petry, P.: Freshwater ecoregions of the world: a new map of biogeographic units for freshwater biodiversity conservation, Bioscience, 58(5), 403–414, 2008.
Albert, C. H., Yoccoz, N. G., Edwards Jr., T. C., Graham, C. H., Zimmermann, N, E., and Thuiller, W.: Sampling in ecology and evolution – bridging the gap between theory and practice, Ecography, 33, 1028–1037, 2010.
Albrecht, C. and Wilke, T.: Ancient Lake Ohrid: biodiversity and evolution, Hydrobiologia, 615, 103–140, 2008.
Albrecht, C., Trajanovski, S., Kuhn, K., Streit, B., and Wilke, T.: Rapid evolution of an ancient lake species flock: Freshwater limpets (Gastropoda: Ancylidae) in the Balkan Lake Ohrid, Org. Divers. Evol., 6, 294–307, 2006.
Albrecht, C., Wolff, C., Glöer, P., and Wilke, T.: Concurrent evolution of ancient sister lakes and sister species: the freshwater gastropod genus Radix in lakes Ohrid and Prespa, Hydrobiologia, 615, 157–167, 2008.
Albrecht, C., Hauffe, T., Schreiber, K., Trajanovski, S., and Wilke, T.: Mollusc biodiversity and endemism in the potential ancient lake Trichonis, Greece, Malacologia, 51(2), 357–375, 2009.
Albrecht, C., Vogel, H., Hauffe, T., and Wilke, T.: Sediment core fossils in ancient Lake Ohrid: testing for faunal change since the Last Interglacial, Biogeosciences, 7, 3435–3446, https://doi.org/10.5194/bg-7-3435-2010, 2010.
Anderson, M. J.: A new method for non-parametric multivariate analysis of variance, Austral Ecol., 26, 32–46, 2001.
Baddeley, A. and Turner, R.: Spatstat: an R package for analyzing spatial point patterns, J. Stat. Softw., 12(6), 1–42, ISSN 1548-7660, www.jstatsoft.org, 2005.
Belmecheri, S., Namiotko, T., Robert, C., von Grafenstein, U., and Danielopol, D. L: Climate controlled ostracod preservation in Lake Ohrid (Albania, Macedonia), Palaeogeogr. Palaeocl., 277, 236–245, 2009.
Blanchet, F. G, Legendre, P., and Borcard, D.: Forward selection of explanatory variables, Ecology, 89(9), 2623–2632, 2008.
Bodon, M., Manganelli, G., and Giusti, F.: A survey of the European valvatiform hydrobiid genera with special reference to Hauffenia Pollonera, 1898 (Gastropoda: Hydrobiidae), Malacologia, 43(1–2), 103–215, 2001.
Borcard, D. and Legendre, P.: All-scale spatial analysis of ecological data by means of principal coordinates of neighbour matrices, Ecol. Model., 153, 1826–1832, 2002.
Boss, K. J.: On the evolution of gastropods in ancient lakes, in: Pulmonates, vol. 2a, Systematics, Evolution and Ecology, edited by: Fretter, V. and Peake, J., Academic Press, London, New York, San Francisco, 385–428, 1978.
Buckley, L. B. and Jetz, W.: Linking global turnover of species and environment, P. Natl. Acad. Sci. USA, 105(46), 17836–17841, https://doi.org/10.073/pnas.0803524105, 2008.
Cohen, A. S.: Extinction in ancient lakes: Biodiversity crises and conservation 40 years after J. L. Brooks, Arch. Hydrobiol., 44, 451–479, 1994.
Cohen, A. S., Stone, J. R., Beuning, K. R. M., Park, L. E., Reintal, P. N., Dettman, D., Scholz, C. A., Johnson, T. C., King J. W., Talbot, M. R., Brown, E. T., and Ivory, S. J.: Ecological consequences of early Late Pleistocene megadroughts in tropical Africa, P. Natl. Acad. Sci. USA, 104, 16422–16427, https://doi.org/10.1073/pnas.0703873104, 2007.
Cooper, N. and Purvis, A.: Body size evolution in mammals: complexity in tempo and mode, Am. Nat., 175(6), 727–738, 2010.
Dejoux, C.: The benthic populations: distribution and seasonal variations, in: Lake Titicaca a synthesis of limnological knowledge, edited by: Dejoux, C. and Iltis, A., Kluwer Academic Publishers, The Netherlands, 383–401, 1992.
Diniz-Filho, J. A. F. and Bini, L. M.: Modelling geographical patterns in species richness using eigenvector-based spatial filters, Global Ecol. Biogeogr., 14, 177–185, 2005.
European Soil Portal: European Commission Joint Research Centre, Institute for Environment and Sustainability, http://eusoils.jrc.ec.europa.eu, last access: 25 October 2008.
Gaston, K. J.: Global patterns of biodiversity, Nature, 405, 220–227, 2000.
Gaston, K. J. and Spicer J. I.: Biodiversity: an introduction, 2nd edn., Blackwell Science Ltd, Malden, 191 pp., 2005.
Genner, M. J., Michel, E., Erpenbeck, D., de Voogd, N., Witte, F., and Pointier, J. P.: Camouflaged invasion of Lake Malawi by an oriental gastropod, Mol. Ecol., 13, 2135–2141, https://doi.org/10.1111/j.1365-294x.2004.02222.x, 2004.
Glaubrecht, M. and von Rintelen, T.: The species flocks of lacustrine gastropods: Tylomelania on Sulawesi as models in speciation and adaptive radiation, Hydrobiologia, 615, 181–199, 2008.
Gotelli, N. J. and McGill, B. J.: Null versus neutral models: what's the difference?, Ecography, 29, 793–800, https://doi.org/10.1111/j.2006.0906-7590.04714.x, 2006.
Gotelli, N. J. and Ulrich, W.: The empirical Bayes approach as a tool to identify non-random species associations, Oecologia, 162, 463–477, https://doi.org/10.1007/s00442-009-1474-y, 2010.
Grigorovich, I. A., Therriaul, T., and Maclsaac, H. J.: History of aquatic invertebrate invasions in the Caspian Sea, Biol. Invasions, 5, 103–115, 2002.
Hadžišće, S.: II. Beitrag zur Kenntnis der Gastropodenfauna des Ohridsees. Beschreibung der bis jetzt unbekannten Schnecken und Beispiele der Speciation bei den Gastropoden des Ohridsees, Recueil des Traveaux, Station Hydrobiologique Ohrid, 4, 57–107, 1956.
Harzhauser, M. and Mandic, O.: Neogene lake systems of Central and South-Eastern Europe: faunal diversity, gradients and interrelations, Palaeogeogr. Palaeocl., 260, 417–434, 2008.
Hauswald, A. K., Albrecht, C., and Wilke, T.: Testing two contrasting evolutionary patterns in ancient lakes: species flock versus species scatter in valvatid gastropods of Lake Ohrid, Hydrobiologia, 615, 169–179, 2008.
Herder, F., Nolte, A. W., Pfaender, J., Schwarzer, J., Hadiaty, R. K., and Schliewen, K.: Adaptive radiation and hybridization in Wallace's dreamponds: evidence from sailfin silversides in the Malili Lakes of Sulawesi, P. Roy. Soc. Lond. B Bio., 273, 2209–2217, https://doi.org/10.1098/rspb.2006.3558, 2006.
Hof, C., Brändle, M., and Brandl, R.: Latitudinal variation of diversity in European freshwater animals is not concordant across habitat types, Global Ecol. Biogeogr., 17, 539–546, 2008.
Hoffmann, N., Reicherter, K., Fernández-Steeger, T., and Grützner, C.: Evolution of ancient Lake Ohrid: a tectonic perspective, Biogeosciences, 7, 3377–3386, https://doi.org/10.5194/bg-7-3377-2010, 2010.
Holtvoeth, J., Vogel, H., Wagner, B., and Wolff, G. A.: Lipid biomarkers in Holocene and glacial sediments from ancient Lake Ohrid (Macedonia, Albania), Biogeosciences, 7, 3473–3489, https://doi.org/10.5194/bg-7-3473-2010, 2010.
Hubendick, B. and Radoman, P.: Studies on the Gyraulus species of Lake Ochrid, Morphology, Ark. Zool., 12(16), 223–243, 1959.
Kashiwaya, K., Sakai, H., Ryugo, M., Horii, M., and Kawai, T.: Long-term climato-limnological cycles found in a 3.5-million-year continental record, J. Paleolimnol., 25(3), 271–278, https://doi.org/10.1023/A:1011122808544, 2001.
Kershner, M. W. and Lodge, D. M.: Effects of substrate architecture on aquatic gastropod-substrate associations, J. N. Am. Benthol. Soc., 9(4), 319–326, 1990.
Kostoski, G., Albrecht, C., Trajanovski, S., and Wilke, T.: A freshwater biodiversity hotspot under pressure - assessing threats and identifying conservation needs for ancient Lake Ohrid, Biogeosciences, 7, 3999–4015, https://doi.org/10.5194/bg-7-3999-2010, 2010.
Kruskal, J. B. and Wish, M.: Multidimensional scaling, Sage Publications, Beverly Hills, California, 93 pp., 1978.
Kunz, M.: Karst springs of Lake Ohrid, Master thesis, Swiss Federal Institute of Technology (ETH), Zürich, 2006.
Legendre, P. and Anderson, M. J.: Distance-based redundancy analysis: testing multispecies responses in multifactorial ecological experiments, Ecol. Monogr., 69, 1–24, 1999.
Legendre, P., Borcard, D., and Peres-Neto, P. R.: Analyzing beta diversity: partitioning the spatial variation of community composition data, Ecol. Monogr., 75, 435–450, 2005.
Lindhorst, K., Vogel, H., Krastel, S., Wagner, B., Hilgers, A., Zander, A., Schwenk, T., Wessels, M., and Daut, G.: Stratigraphic analysis of lake level fluctuations in Lake Ohrid: an integration of high resolution hydro-acoustic data and sediment cores, Biogeosciences, 7, 3531–3548, https://doi.org/10.5194/bg-7-3531-2010, 2010.
Marková, S., Šanda, R., Crivelli, A., Shumka, S., Wilson, I. F., Vukić, J., Berrebi, P., and Kotlík, P.: Nuclear and mitochondrial DNA sequence data reveal the evolutionary history of Barbus (Cyprinidae) in the ancient lake systems of the Balkans, Mol. Phylogenet. Evol., 55(2), 488–500, https://doi.org/10.1016/j.ympev.2010.01.030, 2010.
Martens, K.: Speciation in ancient lakes (review), Trends Ecol. Evol. (Amst), 12, 177–182, 1997.
Matzinger, A., Jordanoski, M., Veljanoska-Sarafiloska, E., Sturm, M., Müller, B., and Wüest, A.: Is Lake Prespa jeopardizing the ecosystem of ancient Lake Ohrid?, Hydrobiologia, 553, 89–109, 2006a.
Matzinger, A., Spirkovski, Z., Patceva, S., and Wüest, A.: Sensitivity of ancient Lake Ohrid to local anthropogenic impacts and global warming, J. Great Lakes Res., 32, 158–179, 2006b.
Michel, E.: Why snails radiate: a review of gastropod evolution in long-lived lakes, both recent and fossil, in: Speciation in Ancient Lakes, edited by: Martens, K., Godderis, B., and Coulter, G., Arch. Hydrobiol., 44, 285–317, 1994.
Mikulič, F. and Pljakic, M. A.: Die Merkmale der Qualitativen Distribution der endemischen Candonaarten im Ohridsee, Ekologija, 5(1), 101–115, 1970.
Oksanen, J., Blanchet, F. G., Kindt, R., Legendre, P., O'Hara, R. G., Simpson, G. L., Solymos, P., Stevens, M. H. H., and Wagner, H.: vegan: Community Ecology Package, R package version 1.18-20., http://R-Forge.R-project.org/projects/vegan/, last access: 4 January 2011.
Parr, T. D., Tait, R. D., Maxon, C. L., Newton III, F. C., and Hardin J. L.: A descriptive account of benthic macrofauna and sediment from an area of planned petroleum exploration in the southern Caspian Sea, Estuar. Coast. Schelf S., 71, 170–180, 2007.
Peres-Neto, P. R., Legendre, P., Dray, S., and Borcard, D.: Variation partitioning of species data matrices: estimation and comparison of fractions, Ecology, 87, 2614–2625, 2006.
Poli\'{n}ski, V.: Limnološka ispitivanja Balkanskog Poluostrva I. Reliktna fauna gasteropoda Ohridskog Jezera, Glas Srpska Kraljevske Akademije, Belgrade, 137, 129–182, 1929.
Popovska, C. and Bonacci, O.: Basic data on the hydrology of Lakes Ohrid, Hydrol. Process., 21, 658–664, 2007.
Prendergast, J. R., Quinn, R. M., Lawton, J. H., Eversham, B. C., and Gibbons, D. W.: Rare species, the coincidence of diversity hotspots and conservation strategies, Nature, 365, 335–337, 1993.
R Development Core Team: R: A language and environment for statistical computing, R Foundation for Statistical Computing, Vienna, Austria, ISBN 3-900051-07-0, http://www.r-project.org, 2009.
Radoman, P.: Hydrobioidea a superfamily of Prosobranchia (Gastropoda), I Systematics, Serbian Acadamy of Sciences and Arts, Belgrade, 256 pp., 1983.
Radoman, P: Hydrobioidea a superfamily of Prosobranchia (Gastropoda), II Origin, Zoogeography, Evolution in the Balkans and Asia Minor, Monographs Institute of Zoology1, Beograd, 180 pp., 1985.
Reid, D. F. and Orlova, M. I.: Geological and evolutionary underpinnings for the success of Ponto-Caspian species invasions in the Baltic Sea and North American Great Lakes, Can. J. Aquat. Sci., 59, 1144–1158, 2002.
Rohde, R. A. and Muller, R.: Cycles in fossil diversity, Nature, 434, 208–210, 2005.
Scholz, C. A.: East African megadroughts between 135 and 75 thousand years ago and bearing on early-modern human origins, P. Natl. Acad. Sci. USA, 104, 16416–16421, https://doi.org/10.1073/pnas.070387410, 2007.
Schulthei{ß}, R., Albrecht, C., Bö{ß}neck, U., and Wilke, T.: The neglected side of speciation in ancient lakes: phylogeography of an inconspicuous mollusk taxon in lakes Ohrid and Prespa, Hydrobiologia, 615, 141–156, 2008.
Schulthei{ß}, R., Van Bocxlaer, B., Wilke, T., and Albrecht, C.: Old fossils-young species: evolutionary history of an old endemic gastropod assemblage in Lake Malawi, P. Roy. Soc. B-Biol. Sci., 276, 2837–2846, https://doi.org/10.1098/rsb.2009.0467, 2009.
Schulthei{ß}, R., Wilke, T., Jørgensen, A., and Albrecht, C.: The birth of an endemic species flock: demographic history of the Bellamya group (Gastropoda, Viviparidae) in Lake Malawi, Biol. J. Linn. Soc., 102, 130–143, 2011.
Sell, J., Wysocka, A., Kostoski, G., and Trajanovski, S.: Genetic diversification of the endemic Ochridogammarus complex in Lake Ohrid explored with mtDNA sequencing, 1st Symposium for Protection of Natural Lakes in Republic of Macedonia, Ohrid, 72–73, 2007.
Smith, T. W. and Lundholm, J. T.: Variation partitioning as a tool to distinguish between nich and neutral processes, Ecography, 33, 648–655, https://doi.org/10.1111/j.1600-0587.2009.06105.x, 2010.
Sitnikova, T. Y.: Endemic gastropod distribution in Baikal, Hydrobiologia, 568(S), 207–211, 2006.
Stanković, S.: The Balkan Lake Ohrid and its living world, Monographiae biologicae, Vol. IX., edited by: Junk, W., Bodenheimer, F. S., and Weisbach, W. W., Den Haag, 358 pp., 1960.
Stone, L. and Roberts, A.: The checkerboard score and species distributions, Oecologia, 85, 74–79, 1990.
Strayer, D. L.: Challenges for freshwater invertebrate conservation, J. N. Am. Benthol. Soc., 25(2), 271–287, 2006.
Tocko, M. and Sapkarev, J.: Annual variations of the important zoobenthic populations in Lake Ohrid, Angew. Limnol., 20(2), 1090–1095, 1978.
Trajanovski, S., Albrecht, C., Schreiber, K., Schulthei{ß}, R., Stadler, T., Benke, M., and Wilke, T.: Testing the spatial and temporal framework of speciation in an ancient lake species flock: the leech genus Dina (Hirudinea: Erpobdellidae) in Lake Ohrid, Biogeosciences, 7, 3387–3402, https://doi.org/10.5194/bg-7-3387-2010, 2010.
Ulrich, W.: Pairs – a FORTRAN program for studying pair-wise species associations in ecological matrices, www.uni.torun.pl/ ulrichw, last access: 2 November 2010, 2008.
UNEP: Convention on biological diversity, UNEP, Nairobi, Kenya, 1992.
Van Bocxlaer, B., Van Damme, D., and Feibel, C. S.: Gradual versus punctuated equilibrium evolution in the Turkana Basin molluscs: evolutionary events or biological invasions?, Evolution, 62(3), 511–520, 2008.
Vogel, H., Wessels, M., Albrecht, C., Stich, H.-B., and Wagner, B.: Spatial variability of recent sedimentation in Lake Ohrid (Albania/Macedonia), Biogeosciences, 7, 3333–3342, https://doi.org/10.5194/bg-7-3333-2010, 2010.
Watzin, M. C., Puka, V., and Naumoski, T. B.: Lake Ohrid and its watershed, state of the environment report, Lake Ohrid Conservation Project, Tirana, Albania and Ohrid, Macedonia, edited by: Guseska, D., Hydrobiological Institute Ohrid, 134 pp., 2002.
Weir, J. T.: Divergent timing and patterns of species accumulation in lowland and highland neotropical birds, Evolution, 60(4), 842–855, 2006.
Whittaker, R. J.: Evolution and measurement of species diversity, Taxon, 21(2/3), 213–251, 1972.
Wilke, T. and Albrecht, C.: How to stop the creeping biodiversity crisis in Lake Ohrid? Suggestions for sustainable conservation strategies of biodiversity hotspots, in: Proceedings of the I Symposium for protection of the natural lakes in Republic of Macedonia, Ohrid, Republic of Macedonia, 31 May–3 June 2007, 44–45, 2007.
Wilke, T., Schulthei{ß}, R., and Albrecht, C.: As time goes by: a simple fool's guide to molecular clock approaches in invertebrates, Am. Malacol. Bull., 27, 25–45, 2009.
Wilke, T., Schulthei{ß}, R., Albrecht, C., Bornmann, N., Trajanovski, S., and Kevrekidis, T.: Native Dreissena freshwater mussels in the Balkans: in and out of ancient lakes, Biogeosciences, 7, 3051–3065, https://doi.org/10.5194/bg-7-3051-2010, 2010.
Williams, P., Gibbons, D., Margules, C., Rebelo, A., Humphries, C., and Pressey, R.: A comparison of richness hotspots, rarity hotspots and complementary areas for conserving diversity using British birds, Conserv. Biol., 10, 155–174, 1996.
Williamson, P. G.: Palaeontological documentation of speciation in Cenozoic molluscs from the Turkana Basin, Nature, 293, 437–443, 1981.
Wilson, A. B., Glaubrecht, M., and Meyer, A.: Ancient lakes as evolutionary reservoirs: Evidence from the thalassoid gastropods of Lake Tanganyika, P. Roy. Soc. Lond. B Bio., 271, 529–536, https://doi.org/10.1098/rspb.2003.2624, 2004.
Wysocka, A., Kostoski, G., Kilikowska, A., Wróbel, B., and Sell, J.: The Proasellus (Crustacea, Isopoda) species group, endemic to the Balkan Lake Ohrid: a case of ecological diversification?, Fund. Appl. Limnol., 172(4), 301–313, 2008.
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