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Type: Article
Published: 2021-05-26
Page range: 561–573
Abstract views: 200
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Distribution of epi-endogeic and endogeic earthworm species (Oligochaeta: Lumbricidae) in the forest belt of the Northwest Caucasus

Center for Forest Ecology and Productivity Russian Academy of Sciences, Moscow, 117997, Russiа.
Center for Forest Ecology and Productivity Russian Academy of Sciences, Moscow, 117997, Russiа.
Annelida soil spatial modeling maxent potential area climatic parameters mountain forests peregrine species endemic native species

Abstract

The distribution of the often dominant in density and biomass epi-endogeic and endogeic earthworm species in forests of the Northwest Caucasus was estimated based on a large array of field data and GIS modeling of modern potential areas. Quantitative accountings of earthworms were conducted annually from 2014 to 2019 in different types of forests: sticky alder forest, small-leaved forests, broadleaf forests (hornbeam and beech forests), coniferous-deciduous forests, dark coniferous forests, and pine forests (792 geographic locations). It is shown that the native species of the Caucasian fauna dominate in the number and biomass from piedmont to high mountain forests. The most widespread species that is found in all types of forests from low to high mountains and makes the main contribution to the biomass of earthworms is the Crimean-Caucasian subendemic Dendrobaena schmidti. Peregrine species of epi-endogeic and endogeic earthworms inhabit sticky alder forest, small-leaved, broadleaf and pine forests in which they inhabit together with native species, while not dominating either in numbers or in biomass among other species. Dark coniferous forests are inhabited mainly by the native endogeic species D. schmidti and A. jassyensis. Maxent modeling shows that the species of the endogeic earthworm group have wider potential areas than epi-endogeic species. The most significant bioclimatic factors that make the greatest contribution to the distribution: amount of precipitation in the driest month, altitude above the sea level, isothermality.

 

References

  1. Ashwood, F., Vanguelova, E.I., Benham, S. & Butt, K.R. (2019) Developing a systematic sampling method for earthworms in and around deadwood. Forest Ecosystems, 6, 1–12.

    https://doi.org/10.1186/s40663-019-0193-z

    Baker, G., Carter, P., Barrett, V., Hirth, J., Mele, P. & Gourley, C. (2002) Does the deep-burrowing earthworm, Aporrectodea longa, compete with resident earthworm communities when introduced to pastures in south-eastern Australia? European Journal of Soil Biology, 38 (1), 39–42.

    https://doi.org/10.1016/S1164-5563(01)01121-9

    Bouche, M.B. (1977) Strategies lombriciennes. Ecological Bulletins, 25, 122–132. [in French]

    Callaham, M.A., Snyder, B.A., James, S.W. & Oberg, E.T. (2016) Evidence for ongoing introduction of non-native earthworms in the Washington, DC metropolitan area. Biological invasions, 18 (11), 3133–3136.

    https://doi.org/10.1007/s10530-016-1230-2

    Csuzdi, C. & Zicsi, A. (2003) Earthworms of Hungary (Annelida: Oligochaeta; Lumbricidae). Hungarian Natural History Museum, Budapest, 271 pp.

    Csuzdi, C., Zicsi, A. & Misirlioðlu, M. (2006) An annotated checklist of the earthworm fauna of Turkey (Oligochaeta: Lumbricidae). Zootaxa, 1175 (1), 1–29.

    https://doi.org/10.11646/zootaxa.1175.1.1

    De Wandeler, H., Sousa-Silva, R., Ampoorter, E., Bruelheide, H., Carnol, M Dawud, S. M., Danila, G., Finér, L., Hättenschwiler, St., Hermy, M., Jaroszewicz, B., Joly, Fr.-X., Müller, S., Pollastrini, M., Ratcliffe, S., Raulund-Rasmussen, K., Selvi, F., Valladares, F., Van Meerbeek, K., Verheyen, Kr., Vesterdal, L. & Muys, B. (2016) Drivers of earthworm incidence and abundance across European forests. Soil Biology and Biochemistry, 99, 167–178.

    https://doi.org/10.1016/j.soilbio.2016.05.003

    Didham, R.K., Tylianakis, J.M., Gemmell, N.J., Rand, T.A. & Ewers, R.M. (2007) Interactive effects of habitat modification and species invasion on native species decline. Trends in ecology & evolution, 22 (9), 489–496.

    https://doi.org/10.1016/j.tree.2007.07.001

    Fawcett, T. (2006) An introduction to ROC analysis. Pattern Recognition Letters, 27, 861–874.

    https://doi.org/10.1016/j.patrec.2005.10.010

    Ferlian, O., Eisenhauer, N., Aguirrebengoa, M., Camara, M., Ramirez‐Rojas, I., Santos, F., Tanalgo, K. & Thakur, M.P. (2018) Invasive earthworms erode soil biodiversity: A meta‐analysis. Journal of Animal Ecology, 87 (1), 162–172.

    https://doi.org/10.1111/1365-2656.12746

    Geraskina, A.P. (2016) Earthworms (Oligochaeta, Lumbricidae) near the township Dombay of Teberda Reserve (North-Western Caucasus, Karachay-Cherkessia). Proceedings of the Zoological Institute of Russian Academy of Sciences, 320 (4), 450–466. [in Russian]

    https://doi.org/10.31610/trudyzin/2016.320.4.450

    Geraskina, A. & Shevchenko, N. (2019a) Biotopic Association of Earthworms in Intact юForests of Teberda Nature Reserve. Contemporary Problems of Ecology, 12 (7), 731–742.

    https://doi.org/10.1134/S1995425519070047

    Geraskina, A. & Shevchenko, N. (2019b) Spatial distribution of the epigeic species of earthworms Dendrobaena octaedra and D. attemsi (Oligochaeta: Lumbricidae) in the forest belt of the northwestern Caucasus. Turkish Journal of Zoology, 43 (5), 480–489.

    https://doi.org/10.3906/zoo-1902-31

    Geraskina, A.P. (2019) Transformations of earthworm communities during post-logging successions in the forests of the Northwest Caucasus. Forest science issues, 2 (2), 1–11.

    https://doi.org/10.31509/2658-607x-2019-2-2-1-11

    Geraskina, A.P. (2020) Impact of earthworms of different morpho-ecological groups on carbon accumulation in forest soils. Forest science issues, 3 (2), 1–20. [in Russian]

    https://doi.org/10.31509/2658-607x-2020-3-2-1-20

    Golovanova, E.V., Knyazev, S.Yu. & Karaban, K. (2018) Are there advantages in an aboriginal earthworm species compared to invasive species in Western Siberia? Materials of the XVIII All-Russian Meeting on Soil Zoology. KMK, Moscow, pp. 60–61. [in Russian]

    Gonzalez, G., Huang, C.Y., Zou, X. & Rodriguez, C. (2006) Earthworm invasions in the tropics. Biological Invasions, 8, 1247–1256.

    https://doi.org/10.1007/s10530-006-9023-7

    Hale, C.M., Frelich, L.E. & Reich, P.B. (2005) Exotic European earthworm invasion dynamics in northern hardwood forests of Minnesota, USA. Ecological Applications, 15 (3), 848–860.

    https://doi.org/10.1007/s10021-005-0066-x

    Hale, C.M., Frelich, L.E. & Reich, P.B. (2006) Changes in hardwood forest understory plant communities in response to European earthworm invasions. Ecology, 87 (7), 1637–1649.

    https://doi.org/10.1890/0012-9658(2006)87[1637:CIHFUP]2.0.CO;2

    Hendrix, P.F. & Bohlen, P.J. (2002) Exotic earthworm invasions in North America: Ecological and policy implications. BioScience, 52, 801–811.

    https://doi.org/10.1641/0006-3568(2002)052[0801:EEIINA]2.0.CO;2

    Hendrix, P.F., Callaham, M.A., Drake, J.M., Huang, C.-Y., James, S.W., Snyder, B.A. & Zhang, W. (2008) Pandora’s Box contained bait: The global problem of introduced earthworms. Annual Review of Ecology, Evolution, and Systematics, 39, 593–613.

    https://doi.org/10.1146/annurev.ecolsys.39.110707.173426

    Hirth, J.R., Li, G.D., Chan, K.Y. & Cullis, B.R. (2009) Long-term effects of lime on earthworm abundance and biomass in an acidic soil on the south-western slopes of New South Wales, Australia. Applied Soil Ecology, 43 (1), 106–114.

    https://doi.org/10.1016/j.apsoil.2009.06.007

    Kalisz, P.J. & Dotson, D.B. (1989) Land-use history and the occurrence of exotic earthworms in the mountains of eastern Kentucky. American Midland Naturalist, 122, 288–297.

    https://doi.org/10.2307/2425915

    Lavelle, P., Blanchart, E., Martin, A., Spain, A.V. & Martin, S. (1992) Impact of soil fauna on the properties of soils in the humid tropics. Myths and Science of Soils of the Tropics, 29, 157–185.

    https://doi.org/10.2136/sssaspecpub29.c9

    McCay, T.S. & Scull, P. (2019) Invasive lumbricid earthworms in northeastern North American forests and consequences for leaf-litter fauna. Biological Invasions, 21 (6), 2081–2093.

    https://doi.org/10.1007/s10530-019-01959-1

    Migge-Kleian, S., McLean, M.A., Maerz, J.C. & Heneghan, L. (2006) The influence of invasive earthworms on indigenous fauna in ecosystems previously uninhabited by earthworms. Biological Invasions, 8 (6), 1275–1285.

    https://doi.org/10.1007/s10530-006-9021-9

    Moore, J.D., Ouimet, R. & Bohlen, P.J. (2013) Effects of liming on survival and reproduction of two potentially invasive earthworm species in nothern forest Podzol, Soil Biology and Biochemistry, 64, 174–180.

    https://doi.org/10.1016/j.soilbio.2013.04.013

    Omodeo, P (1952) Particolaritádella Zoogeografia dei Lombrichi. Bollettino di Zoologia, 19, 349–359. [in Italian]

    https://doi.org/10.1080/11250005209439182

    Omodeo, P. & Rota, E. (1989) Earthworms of Turkey. Bollettino di zoologia, 56, 167–199.

    https://doi.org/10.1080/11250008909355639

    Omodeo, P. & Rota, E. (1991) Earthworms of Turkey II. Bollettino di zoologia, 58, 171–181.

    https://doi.org/10.1080/11250009109355749.

    Perel, T.S. (1979) Range and regularities in the distribution of earthworms of the USSR fauna. Nauka, Moscow, 272 pp. [in Russian]

    Rapoport, I.B. (2009) Morpho-ecological forms of Dendrobaena schmidti Мichaelsen, 1907 (Oligochaeta, Lumbricidae) of North Caucasus. Fourth International Oligochaete Taxonomy Meetings: Book of Abstracts. Dicle University, Diyarbakir, pp. 39–39.

    Rapoport, I.B. (2014) Fauna, community structure and distribution of mountain-belt earthworms (Oligochaeta, Lumbricidae) the central part of the Kuban variant belts (North-Western Caucasus, the Republic of Adygea). Bulletin of Adyghe State University, 147 (4), 77–84. [in Russian]

    Rapoport, I.B. & Tsepkova, N.L. (2015) Population structure and topical preferendumy earthworms (Oligochaeta, Lumbricidae) in soils of forest formations river basins of the Teberda and the Big Zelenchuk (Teberda Reserve, North-Western Caucasus). News of the Samara Scientific Center of the Russian Academy of Sciences, 17 (6), 33–39. [in Russian]

    Rapoport, I.B., Zenkova, I.V. & Tsepkova, N.L. (2017) Earthworm (Oligochaeta, Lumbricidae) populations of the Karasu River basin (Central Caucasus). Biology Bulletin 44 (8), 941–951.

    https://doi.org/10.1134/S1062359017080131

    Sariyildiz, T. (2008) Effects of tree canopy on litter decomposition rates of Abies nordmanniana, Picea orientalis and Pinus sylvestris. Scandinavian journal of forest research, 23 (4), 330–338.

    https://doi.org/10.1080/02827580802275816

    Sariyildiz, T. & Küçük, M. (2008) Litter mass loss rates in deciduous and coniferous trees in Artvin, northeast Turkey: Relationships with litter quality, microclimate, and soil characteristic. Turkish journal of Agriculture and Forestry, 32 (6), 547–559.

    Scheldeman, X. & Zonneveld, M. (2010) Training manual on spatrial analysis of plant diversity and distribution. Bioversity International, Rome, 179 pp.

    Schwarz, B., Dietrich, C., Cesarz, S., Scherer-Lorenzen, M., Auge, H., Schulz, E. & Eisenhauer, N. (2015) Non-significant tree diversity but significant identity effects on earthworm communities in three tree diversity experiments. European Journal of Soil Biology, 67, 17–26.

    https://doi.org/10.1016/j.ejsobi.2015.01.001

    Shekhovtsov, S.V., Rapoport, I.B., Poluboyarova, T.V., Geraskina, A.P., Golovanova, E.V. & Peltek, S.E. (2020) Morphotypes and genetic diversity of Dendrobaena schmidti (Lumbricidae, Annelida). Vavilov Journal of Genetics and Breeding, 24 (1), 48–54.

    https://doi.org/10.18699/VJ20.594

    Shevchenko, N.E. & Geraskina, A.P. (2019) Northwest Caucasus forest spreading evaluation by GIS modeling and historical and geographic data analysis. Ecological Questions, 30 (2), 47–55.

    https://doi.org/10.12775/EQ.2019.011

    Singh, J., Cameron, E., Reitz, T., Schädler, M. & Eisenhauer, N. (2020) Grassland management effects on earthworm communities under ambient and future climatic conditions. European Journal of Soil Science, 20 (1), 1–13.

    https://doi.org/10.1111/ejss.12942

    Spirin, V.A. & Shirokov, A.I. (2002) The specific humification of wood felling in the virgin fir-pruce forests of Nizhny Novgorod oblast. Mycology and Phytopathology, 36 (3), 25–31. [in Russian]

    Szederjesi, T. (2017) The first combined checklist of earthworms of the Northeastern Mediterranean region (Clitellata: Megadrili). Opuscula Zoologica, 48 (2), 77–116.

    https://doi.org/10.18348/opzool.2017.2.77

    Taylor, A.R., Lenoir, L., Vegerfors, B. & Persson, T. (2019) Ant and earthworm bioturbation in cold-temperate ecosystems. Ecosystems, 22 (5), 981–994.

    https://doi.org/10.1007/s10021-018-0317-2

    Vsevolodova-Perel, T.S. (1997) Earthworms of the fauna of Russia: Cadastre and key. Nauka, Moscow, 101 pp. [in Russian]

    Vsevolodova-Perel, T.S. (2003) Supplement to the fauna of earthworms of Russian (Oligohaeta, Lumbricidae). Zoological journal, 62 (2), 275–280. [in Russian]

    Winsome, T., Epstein, L., Hendrix, P.F. & Horwath, W.R. (2006) Competitive interactions between native and exotic earthworm species as influenced by habitat quality in a California grassland. Applied Soil Ecology, 32 (1), 38–53.

    https://doi.org/10.1016/j.apsoil.2005.01.008

    Wisz, M.S., Hijmans, R.J., Li, J., Peterson, A.T., Graham, C.H., Guisan, A. & NCEAS Predicting Species Distributions Working Group (2008) Effects of sample size on the performance of species distribution models. Diversity and distributions, 14 (5), 763–773.

    https://doi.org/10.1111/j.1472-4642.2008.00482.x

    World Reference Base for Soil Resources (2015) International soil classification system for naming soils and creating legends for soil maps. World Soil Resources Reports. FAO, IUSS Working Group, Rome, 203 pp.