Articles | Volume 12, issue 23
https://doi.org/10.5194/bg-12-7209-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-12-7209-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Constant diversification rates of endemic gastropods in ancient Lake Ohrid: ecosystem resilience likely buffers environmental fluctuations
K. Föller
Department of Animal Ecology & Systematics, Justus Liebig University Giessen, Heinrich-Buff-Ring 26–32, 35392 Giessen, Germany
B. Stelbrink
CORRESPONDING AUTHOR
Department of Animal Ecology & Systematics, Justus Liebig University Giessen, Heinrich-Buff-Ring 26–32, 35392 Giessen, Germany
T. Hauffe
Department of Animal Ecology & Systematics, Justus Liebig University Giessen, Heinrich-Buff-Ring 26–32, 35392 Giessen, Germany
C. Albrecht
Department of Animal Ecology & Systematics, Justus Liebig University Giessen, Heinrich-Buff-Ring 26–32, 35392 Giessen, Germany
T. Wilke
Department of Animal Ecology & Systematics, Justus Liebig University Giessen, Heinrich-Buff-Ring 26–32, 35392 Giessen, Germany
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Lake Ohrid is considered to be the oldest existing lake in Europe. Moreover, it has a very high degree of endemic biodiversity. During a drilling campaign at Lake Ohrid in 2013, a 569 m long sediment sequence was recovered from Lake Ohrid. The ongoing studies of this record provide first important information on the environmental and evolutionary history of the lake and the reasons for its high endimic biodiversity.
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Preprint withdrawn
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Lake Ohrid is considered to be the oldest existing lake in Europe. Moreover, it has a very high degree of endemic biodiversity. During a drilling campaign at Lake Ohrid in 2013, a 569 m long sediment sequence was recovered from Lake Ohrid. The ongoing studies of this record provide first important information on the environmental and evolutionary history of the lake and the reasons for its high endimic biodiversity.
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Cited articles
Albrecht, C. and Wilke, T.: Ancient Lake Ohrid: biodiversity and evolution, Hydrobiologia, 615, 103–140, https://doi.org/10.1007/s10750-008-9558-y, 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, https://doi.org/10.1016/j.ode.2005.12.003, 2006.
Albrecht, C., Hauffe, T., Schreiber, K., Trajanovski, S., and Wilke, T.: Mollusc biodiversity and endemism in the potential ancient Lake Trichonis, Greece, Malacologia, 51, 357–375, https://doi.org/10.4002/040.051.0209, 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.
Albrecht, C., Föller, K., Clewing, C., Hauffe, T., and Wilke, T.: Invaders versus endemics: alien gastropod species in ancient Lake Ohrid, Hydrobiologia, 739, 163–174, https://doi.org/10.1007/s10750-013-1724-1, 2014.
Brooks, J. L.: Speciation in ancient lakes, Q. Rev. Biol., 25, 30–60, 131–176, 1950.
Cohen, A. S., Stone, J. R., Beuning, K. R. M., Park, L. E., Reinthal, 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 tropial Africa, Proc. Natl. Acad. Sci. USA, 104, 16422–16427, 2007.
Cristescu, M. E., Adamowicz, S. J., Vaillant, J. J., and Haffner, G. D.: Ancient lakes revisited: from the ecology to the genetics of speciation, Mol. Ecol., 19, 4837–4851, https://doi.org/10.1111/j.1365-294X.2010.04832.x, 2010.
Cvetkoska, A., Jovanovska, E., Francke, A., Tofilovska, S., Vogel, H., Levkov, Z., Donders, T. H., Wagner, B., and Wagner-Cremer, F.: Ecosystem regimes and responses in a coupled ancient lake system from MIS 5b to present: the diatom record of lakes Ohrid and Prespa, Biogeosciences Discuss., 12, 15051–15086, https://doi.org/10.5194/bgd-12-15051-2015, 2015.
Drummond, A. J. and Rambaut, A.: BEAST: Bayesian evolutionary analysis by sampling trees, BMC Evol. Biol., 7, 214, https://doi.org/10.1186/1471-2148-7-214, 2007.
Falniowski, A. and Szarowska, M.: The genus Daphniola Radoman, 1973 (Caenogastropoda: Hydrobiidae) in the Peloponnese, Greece, Folia Malacol., 19, 131–137, https://doi.org/10.2478/v10125-011-0020-9, 2011.
Falniowski, A., Szarowska, M., Glöer, P., and Pešic, V.: Molecules vs morphology in the taxonomy of the Radomaniola/Grossuana group of Balkan Rissooidea (Mollusca, Caenogastropoda), J. Conchol., 41, 19–36, 2012.
Folmer, O., Black, M., Hoeh, W., Lutz, R., and Vrijenhoek, R.: DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates, Mol. Mar. Biol. Biotechnol., 3, 294–299, 1994.
Francke, A., Wagner, B., Just, J., Leicher, N., Gromig, R., Baumgarten, H., Vogel, H., Lacey, J. H., Sadori, L., Wonik, T., Leng, M. J., Zanchetta, G., Sulpizio, R., and Giaccio, B.: Sedimentological processes and environmental variability at Lake Ohrid (Macedonia, Albania) between 640 ka and present day, Biogeosciences Discuss., 12, 15111–15156, https://doi.org/10.5194/bgd-12-15111-2015, 2015.
Gould, S. J. and Eldredge, N.: Punctuated equilibria: the tempo and mode of evolution reconsidered, Paleobiology, 3, 115–151, 1977.
Greenwood, P. H., Echelle, A. A., and Kornfield, I.: What is a species flock?, in Evolution of fish species flocks, edited by: Echelle, A. A. and Kornfield, I., Orono Press, University of Maine, 13–19, 1984.
Grummer, J. A., Bryson Jr., R. W., and Reeder, T. W.: Species delimitation using Bayes factors: simulations and application to the Sceloporus scalaris species group (Squamata: Phrynosomatidae), Syst. Biol., 63, 119–133, https://doi.org/10.1093/sysbio/syt069, 2014.
Hall, T. A.: BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT, Nucleic Acids Symp. Ser., 41, 95–98, 1999.
Hauffe, T., Albrecht, C., Schreiber, K., Birkhofer, K., Trajanovski, S., and Wilke, T.: Spatially explicit analysis of gastropod biodiversity in ancient Lake Ohrid, Biogeosciences, 8, 175–188, https://doi.org/10.5194/bg-8-175-2011, 2011.
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.
Hinderer, M. and Einsele, G.: The world's large lake basins as denudation-accumulation systems and implications for their lifetimes, J. Paleolimnol., 26, 355–372, https://doi.org/10.1023/A:1012651232541, 2001.
Ivanov, A. V., Gladkochub, D. P., Déverchère, J., and Ernst, R. E.: Introduction to special issue: geology of the Lake Baikal region, J. Asian Earth Sci., 62, 1–3, https://doi.org/10.1016/j.jseaes.2012.12.010, 2013.
Jovanovska, E., Cvetkoska, A., Hauffe, T., Levkov, Z., Wagner, B., Sulpizio, R., Francke, A., Albrecht, C., and Wilke, T.: Differential resilience of ancient sister lakes Ohrid and Prespa to environmental disturbances during the Late Pleistocene, Biogeosciences Discuss., 12, 16049–16079, https://doi.org/10.5194/bgd-12-16049-2015, 2015.
Kilikowska, A., Wysocka, A., Burzy\'nski, A., Kostoski, G., Rychli\'nska, J., and Sell, J.: Patterns of genetic differentiation and population history of endemic isopods (Asellidae) from ancient Lake Ohrid: combining allozyme and mtDNA data, Cent. Eur. J. Biol., 8, 854–875, https://doi.org/10.2478/s11535-013-0204-y, 2013.
Kroll, O., Hershler, R., Albrecht, C., Terrazas, E. M., Apaza, R., Fuentealba, C., Wolff, C., and Wilke, T.: The endemic gastropod fauna of Lake Titicaca: correlation between molecular evolution and hydrographic history, Ecol. Evol., 2, 1517–1530, https://doi.org/10.1002/ece3.280, 2012.
Lavenu, A.: Formation and geological evolution, in Lake Titicaca: a synthesis of limnological knowledge, edited by C. Dejoux and A. Iltis, pp. 3–15, Kluwer Academic Publishers, Dordrecht, 1992.
Leicher, N., Zanchetta, G., Sulpizio, R., Giaccio, B., Wagner, B., Nomade, S., Francke, A., and Del Carlo, P.: First tephrostratigraphic results of the DEEP site record from Lake Ohrid, Macedonia, Biogeosciences Discuss., 12, 15411–15460, https://doi.org/10.5194/bgd-12-15411-2015, 2015.
Levkov, Z. and Williams, D. M.: Checklist of diatoms (Bacillariophyta) from Lake Ohrid and Lake Prespa (Macedonia), and their watersheds, Phytotaxa, 45, 1–76, 2012.
Lézine, A. M., von Grafenstein, U., Andersen, N., Belmecheri, S., Bordon, A., Caron, B., Cazet, J. P., Erlenkeuser, H., Fouache, E., Grenier, C., Huntsman-Mapila, P., Hureau-Mazaudier, D., Manelli, D., Mazaud, A., Robert, C., Sulpizio, R., Tiercelin, J. J., Zanchetta, G., and Zeqollari, Z.: Lake Ohrid, Albania, provides an exceptional multi-proxy record of environmental changes during the last glacial-interglacial cycle, Palaeogeogr. Palaeoclimatol. Palaeoecol., 287, 116–127, https://doi.org/10.1016/j.palaeo.2010.01.016, 2010.
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.
Lindhorst, K., Krastel, S., Reicherter, K., Stipp, M., Wagner, B. and Schwenk, T.: Sedimentary and tectonic evolution of Lake Ohrid (Macedonia/Albania), Basin Res., 27, 84–101, https://doi.org/10.1111/bre.12063, 2015.
Martens, K.: Speciation in ancient lakes, Trends Ecol. Evol., 12, 177–182, https://doi.org/10.1016/S0169-5347(97)01039-2, 1997.
Martens, K., Goddeeris, B. and Coulter, G. (Eds.): Speciation in ancient lakes, E. Schweitzerbart'sche Verlagsbuchhandlung, Stuttgart, 1994.
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, https://doi.org/10.3394/0380-1330(2006)32[158:SOALOT]2.0.CO;2, 2006.
Morvan, C., Malard, F., Paradis, E., Lefébure, T., Konecny-Dupré, L., and Douady, C. J.: Timetree of Aselloidea reveals species diversification dynamics in groundwater, Syst. Biol., 62, 512–522, https://doi.org/10.1093/sysbio/syt015, 2013.
Newton, M. A. and Raftery, A. E.: Approximate Bayesian inference with the weighted likelihood bootstrap, J. R. Stat. Soc. B, 56, 3–48, 1994.
Pagel, M.: Inferring the historical patterns of biological evolution, Nature, 401, 877–884, 1999.
Palumbi, S. R., Martin, A., Romano, S., McMillan, W. O., Stice, L., and Grabowski, G.: The simple fool's guide to PCR, University of Hawaii, Honolulu, 1991.
Paradis, E., Claude, J., and Strimmer, K.: APE: analyses of phylogenetics and evolution in R language, Bioinformatics, 20, 289–290, https://doi.org/10.1093/bioinformatics/btg412, 2004.
Pennell, M. W., Harmon, L. J., and Uyeda, J. C.: Is there room for punctuated equilibrium in macroevolution?, Trends Ecol. Evol., 29, 23–32, https://doi.org/10.1016/j.tree.2013.07.004, 2014.
Pešić, V.: A new species of the water mite genus Hygrobates Koch, 1837 (Acari: Hydrachnidia: Hygrobatidae) from the ancient Lake Ohrid, Zootaxa, 3926, 287–295, https://doi.org/10.11646/zootaxa.3926.2.9, 2015.
Posada, D.: jModelTest: phylogenetic model averaging, Mol. Biol. Evol., 25, 1253–1256, https://doi.org/10.1093/molbev/msn083, 2008.
Purvis, A., Orme, C. D. L., Toomey, N. H., and Pearson, P. N.: Temporal patterns in diversification rates, in: Speciation and patterns of diversity, edited by: Butlin, R. K., Bridle, J. R., and Schulter, D., 278–300, Cambridge University Press, Cambridge, 2009.
Rabosky, D. L.: Extinction rates should not be estimated from molecular phylogenies, Evolution, 64, 1816–1824, https://doi.org/10.1111/j.1558-5646.2009.00926.x, 2010.
Radoman, P.: Hydrobioidea, a superfamily of Prosobranchia (Gastropoda). I. Systematics, Monographs Vol. 547, Department of Sciences No. 57, Serbian Academy of Sciences and Arts, Beograd, 1983.
Radoman, P.: Hydrobioidea, a superfamily of Prosobranchia (Gastropoda). II. Origin, zoogeography, evolution in the Balkans and Asia Minor, Monographs Vol. 1, Institute of Zoology No. 1, Faculty of Science – Department of Biology, Beograd, 1985.
Rambaut, A. and Drummond, A. J.: Tracer v. 1.5, available at: http://tree.bio.ed.ac.uk/software (last access: 7 December 2015), 2007.
R Core Team: R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria, available at: http://www.R-project.org (last access: 7 December 2015), 2015.
Reed, J. M., Cvetkoska, A., Levkov, Z., Vogel, H., and Wagner, B.: The last glacial-interglacial cycle in Lake Ohrid (Macedonia/Albania): testing diatom response to climate, Biogeosciences, 7, 3083–3094, https://doi.org/10.5194/bg-7-3083-2010, 2010.
Revell, L. J.: phytools: an R package for phylogenetic comparative biology (and other things), Methods Ecol. Evol., 3, 217–223, https://doi.org/10.1111/j.2041-210X.2011.00169.x, 2012.
Rossiter, A. and Kawanabe, H.: Ancient lakes: biodiversity, ecology and evolution, Academic Press, San Diego, 2000.
Salzburger, W., Mack, T., Verheyen, E., and Meyer, A.: Out of Tanganyika: genesis, explosive speciation, key-innovations and phylogeography of the haplochromine cichlid fishes, BMC Evol. Biol., 5, 17, https://doi.org/10.1186/1471-2148-5-17, 2005.
Salzburger, W., Van Bocxlaer, B., and Cohen, A. S.: Ecology and evolution of the African Great Lakes and their faunas, Annu. Rev. Ecol. Evol. Syst., 45, 519–545, https://doi.org/10.1146/annurev-ecolsys-120213-091804, 2014.
Scheffer, M. and Carpenter, S. R.: Catastrophic regime shifts in ecosystems: linking theory to observation, Trends Ecol. Evol., 18, 648–656, https://doi.org/10.1016/j.tree.2003.09.002, 2003.
Scheffer, M., Carpenter, S., Foley, J. A., Folke, C., and Walker, B.: Catastrophic shifts in ecosystems, Nature, 413, 591–596, https://doi.org/10.1038/35098000, 2001.
Schluter, D.: The ecology of adaptive radiation, edited by: May, R. M. and Harvey, P. H., Oxford University Press, Oxford, 2000.
Scholz, C. A., Johnson, T. C., Cohen, A. S., King, J. W., Peck, J. A., Overpeck, J. T., Talbot, M. R., Brown, E. T., Kalindekafe, L., Amoako, P. Y. O., Lyons, R. P., Shanahan, T. M., Castañeda, I. S., Heil, C. W., Forman, S. L., McHargue, L. R., Beuning, K. R., Gomez, J., and Pierson, J.: East African megadroughts between 135 and 75 thousand years ago and bearing on early-modern human origins, Proc. Natl. Acad. Sci. USA, 104, 16416–21, https://doi.org/10.1073/pnas.0703874104, 2007.
Schön, I. and Martens, K.: Adaptive, pre-adaptive and non-adaptive components of radiations in ancient lakes: a review, Org. Divers. Evol., 4, 137–156, https://doi.org/10.1016/j.ode.2004.03.001, 2004.
Schreiber, K., Hauffe, T., Albrecht, C., and Wilke, T.: The role of barriers and gradients in differentiation processes of pyrgulinid microgastropods of Lake Ohrid, Hydrobiologia, 682, 61–73, https://doi.org/10.1007/s10750-011-0864-4, 2012.
Schultheiß, R., Van Bocxlaer, B., Wilke, T., and Albrecht, C.: Old fossils–young species: evolutionary history of an endemic gastropod assemblage in Lake Malawi, Proc. R. Soc. London B, 276, 2837–2846, https://doi.org/10.1098/rspb.2009.0467, 2009.
Schultheiß, 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.
Sherbakov, D. Y.: Molecular phylogenetic studies on the origin of biodiversity in Lake Baikal, Trends Ecol. Evol., 14, 92–95, https://doi.org/10.1016/S0169-5347(98)01543-2, 1999.
Slager, D. L., Battey, C. J., Bryson, R. W., Voelker, G., and Klicka, J.: A multilocus phylogeny of a major New World avian radiation: the Vireonidae, Mol. Phylogenet. Evol., 80, 95–104, https://doi.org/10.1016/j.ympev.2014.07.021, 2014.
Stadler, T.: Mammalian phylogeny reveals recent diversification rate shifts, Proc. Natl. Acad. Sci. USA, 108, 6187–6192, 2011.
Stadler, T.: TreePar: Estimating birth and death rates based on phylogenies, R package version 3.3, available at: http://CRAN.R-project.org/package=TreePar (last access: 7 December 2015), 2015.
Stankovic, S.: The Balkan Lake Ohrid and its living world, Dr. W. Junk, The Hague, 1960.
Stocchino, G. A., Sluys, R., Deri, P., and Manconi, R.: Integrative taxonomy of a new species of planarian from the Lake Ohrid basin, including an analysis of biogeographical patterns in freshwater triclads from the Ohrid region (Platyhelminthes, Tricladida, Dugesiidae), Zookeys, 313, 25–43, https://doi.org/10.3897/zookeys.313.5363, 2013.
Suchard, M. A., Weiss, R. E., and Sinsheimer, J. S.: Bayesian selection of continuous-time Markov chain evolutionary models, Mol. Biol. Evol., 18, 1001–1013, https://doi.org/10.1093/oxfordjournals.molbev.a003872, 2001.
Sulpizio, R., Zanchetta, G., D'Orazio, M., Vogel, H., and Wagner, B.: Tephrostratigraphy and tephrochronology of lakes Ohrid and Prespa, Balkans, Biogeosciences, 7, 3273–3288, https://doi.org/10.5194/bg-7-3273-2010, 2010.
Szarowska, M.: Molecular phylogeny, systematics and morphological character evolution in the Balkan Rissooidea (Caenogastropoda), Folia Malacol., 14, 99–168, https://doi.org/10.12657/folmal.014.014, 2006.
Szarowska, M., Grzmil, P., Falniowski, A. and Sirbu, I.: Grossuana codreanui (Grossu, 1946) and the phylogenetic relationships of the East Balkan genus Grossuana (Radoman, 1973) (Gastropoda: Rissooidea), Hydrobiologia, 579, 379–391, https://doi.org/10.1007/s10750-006-0530-4, 2007.
Trajanovski, S., Albrecht, C., Schreiber, K., Schultheiß, 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.
Van Bocxlaer, B., Damme, D. V., and Feibel, C. S.: Gradual versus punctuated equilibrium evolution in the Turkana Basin molluscs: evolutionary events or biological invasions?, Evolution, 62, 511–520, https://doi.org/10.1111/j.1558-5646.2007.00296.x, 2008.
Wagner, B., Wilke, T., Krastel, S., Zanchetta, G., Sulpizio, R., Reicherter, K., Leng, M. J., Grazhdani, A., Trajanovski, S., Francke, A., Lindhorst, K., Levkov, Z., Cvetkoska, A., Reed, J. M., Zhang, X., Lacey, J. H., Wonik, T., Baumgarten, H., and Vogel, H.: The SCOPSCO drilling project recovers more than 1.2 million years of history from Lake Ohrid, Sci. Dril., 17, 19–29, https://doi.org/10.5194/sd-17-19-2014, 2014.
Wilke, T. and Davis, G. M.: Infraspecific mitochondrial sequence diversity in Hydrobia ulvae and Hydrobia ventrosa (Hydrobiidae: Rissooidea: Gastropoda): Do their different life histories affect biogeographic patterns and gene flow?, Biol. J. Linn. Soc., 70, 89–105, https://doi.org/10.1006/bijl.1999.0388, 2000.
Wilke, T., Davis, G. M., Falniowski, A., Giusti, F., Bodon, M., and Szarowska, M.: Molecular systematics of Hydrobiidae (Mollusca: Gastropoda: Rissooidea): testing monophyly and phylogenetic relationships, Proc. Acad. Nat. Sci. Philadelphia, 151, 1–21, https://doi.org/10.1635/0097-3157(2001)151[0001:MSOHMG]2.0.CO;2, 2001.
Wilke, T., Davis, G. M., Qiu, D., and Spear, R. C.: Extreme mitochondrial sequence diversity in the intermediate schistosomiasis host Oncomelania hupensis robertsoni: another case of ancestral polymorphism?, Malacologia, 48, 143–157, 2006.
Wilke, T., Albrecht, C., Anistratenko, V. V., Sahin, S. K., and Yildirim, Z.: Testing biogeographical hypotheses in space and time: faunal relationships of the putative ancient Lake Egirdir in Asia Minor, J. Biogeogr., 34, 1807–1821, https://doi.org/10.1111/j.1365-2699.2007.01727.x, 2007.
Wilke, T., Schultheiß, 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, https://doi.org/10.4003/006.027.0203, 2009.
Wilke, T., Haase, M., Hershler, R., Liu, H.-P., Misof, B., and Ponder, W.: Pushing short DNA fragments to the limit: phylogenetic relationships of "hydrobioid" gastropods (Caenogastropoda: Rissooidea), Mol. Phylogenet. Evol., 66, 715–736, https://doi.org/10.1016/j.ympev.2012.10.025, 2013.
Wilson, A. B., Glaubrecht, M., and Meyer, A.: Ancient lakes as evolutionary reservoirs: evidence from the thalassoid gastropods of Lake Tanganyika, Proc. R. Soc. London B, 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?, Fundam. Appl. Limnol. / Arch. für Hydrobiol., 172, 301–313, https://doi.org/10.1127/1863-9135/2008/0172-0301, 2008.
Wysocka, A., Grabowski, M., Sworobowicz, L., Burzy\'nski, A., Kilikowska, A., Kostoski, G.. and Sell, J.: A tale of time and depth: intralacustrine radiation in endemic Gammarus species flock from the ancient Lake Ohrid, Zool. J. Linn. Soc., 167, 345–359, https://doi.org/10.1111/j.1096-3642.2012.00878.x, 2013.
Wysocka, A., Grabowski, M., Sworobowicz, L., Mamos, T., Burzy\'nski, A., and Sell, J.: Origin of the Lake Ohrid gammarid species flock: ancient local phylogenetic lineage diversification, J. Biogeogr., 41, 1758–1768, https://doi.org/10.1111/jbi.12335, 2014.
Xia, X. and Xie, Z.: DAMBE: Data analysis in molecular biology and evolution, J. Hered., 92, 371–373, https://doi.org/10.1093/jhered/92.4.371, 2001.
Zhang, Z., Schwartz, S., Wagner, L.. and Miller, W.: A greedy algorithm for aligning DNA sequences, J. Comput. Biol., 7, 203–214, https://doi.org/10.1089/10665270050081478, 2000.
Short summary
Based on our molecular data and performed analyses we found that the gastropods studied represent a comparatively old group that most likely evolved with a constant rate of diversification. However, preliminary data of the SCOPSCO deep-drilling program indicate signatures of environmental/climatic perturbations in Lake Ohrid. We therefore propose that the constant rate observed has been caused by a potential lack of catastrophic environmental events and/or a high ecosystem resilience.
Based on our molecular data and performed analyses we found that the gastropods studied...
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