Structure of litter macrofauna communities in poplar plantations in an urban ecosystem in Ukraine

Keywords: forest ecosystems, biological diversity, litter invertebrates, dominance structure, trophic structure, size structure


The litter macrofauna of 8 plantations of Populus italica (Du Roi) Moench, P. deltoides Marsh. and P. alba L. was studied in the city of Dnipro. The invertebrates were taken by manual sifting of litter from experimental plots of 8 m2. The total number of litter macrofauna in the poplar plantations varied from 8 to 187 specimen/m2, on average 53 specimen/m2. The greatest variety of species was obtained from a white poplar plantation with common hop and an elm-poplar plantation with bare soil and Amorpha fruticosa L. bushes (15 and 9 species correspondingly). The ma ximum readings on the Shannon–Weaver diversity index come from the abovementioned areas (3.2 and 2.9 bits respectively). The highest number of zoophages (40%) was obtained from the white poplar plantation with common hop. There was great consistency in the species composition across the plots, with the same 60 species (more than 50% of the total number of species of litter macrofauna recorded in the study) being found in 7 out of the 8 study plots. The share of species rare for any given ecosystem exceeded 10% in only 2 out of the 8 plantations studied. The dominant group in the size structure of the litter macrofauna of the poplar plantations (44–96%) was invertebrates of 4–7 mm length. In 5 out of 8 poplar plantations no species over 15 mm in length were found. This indicates the degraded size structures of the litter macrofauna communities. In taxonomic structure the dominant groups were Formicidae, Pulmonata, Porcellionidae, Lygaeidae, Julidae, Silphidae, Araneae, Carabidae, Staphylinidae. The results obtained indicate the low variety and degradation of the trophic and size structure of the litter macrofauna of these urban poplar plantations, which are subject to lack of moisture. 


Brockerhoff, E. G., Jactel, H., Parrotta, J. A., Quine, C. P., & Sayer, J. (2008). Plantation forests and biodiversity: oxymoron or opportunity? Biodiversity and Conservation, 17(5), 925–951. >>
Brygadyrenko, V. V. (2014). The influence of moisture conditions on the structure of litter invertebrate communities in shelterbelt and plantation forests in southern Ukraine. Journal of Bio-Science, 22, 77–88. >>
Brygadyrenko, V. V. (2015a). Community structure of litter invertebrates of forest belt ecosystems in the Ukrainian steppe zone. International Journal of Environmental Research, 9(4), 1183–1192.
Brygadyrenko, V. V. (2015b). Parameters of ecological niches of Badister, Licinus and Panagaeus (Coleoptera, Carabidae) species measured against eight ecological factors. Baltic Journal of Coleopterology, 15, 137–154.
Brygadyrenko, V. V. (2015c). Vplyv umov zvolozhennja ta mineralizacii’ grunto¬vogo rozchynu na strukturu pidstylkovoi’ mezofauny shyrokolystjanyh lisiv stepovoi’ zony Ukrai’ny [Influence of moisture conditions and soil salinity on structure of litter macrofauna of the deciduous forests of Ukraine’s steppe zone]. Visnyk of Dnipropetrovsk University. Biology, Ecology, 23(1), 50–65 (in Ukrainian). >>
Brygadyrenko, V. V. (2016a). Vplyv potuzhnosti pidstylky na strukturu pidstyl¬kovoi’ mezofauny shyrokolystjanyh lisiv stepovoi’ zony Ukrai’ny [Influence of litter thickness on the structure of litter macrofauna of deciduous forests of Ukraine’s steppe zone]. Visnyk of Dnipropetrovsk University. Biology, Ecology, 24(1), 240–248 (in Ukrainian). >>
Brygadyrenko, V. V. (2016b). Evaluation of ecological niches of abundant species of Poecilus and Pterostichus (Coleoptera: Carabidae) in forests of the steppe zone of Ukraine. Entomologica Fennica, 27(2), 81–100.
Brygadyrenko, V. V., & Ivanyshin, V. М. (2014). Vlijanie soli zheleza na massu tela Megaphyllum kievense (Diplopoda, Julidae) i granulometricheskij sostav podstilki v laboratornom jeksperimente [Impact of ferric salt on body weight of Megaphyllum kievense (Diplopoda, Julidae) and litter granulometric composition in the laboratory experiment]. Visnyk of Dnipropetrovsk University. Biology, Ecology, 22(1), 83–87 (in Russian). >>
Brygadyrenko, V. V., & Nazimov, S. S. (2015). Trophic relations of Opat¬rum sabulosum (Coleoptera, Tenebrionidae) with leaves of cultivated and uncultivated species of herbaceous plants under laboratory conditions. Zookeys, 481, 57–68. >>
Butterfield, J., & Malvido, J. B. (1992). Effect of mixed-species tree planting on the distribution of soil invertebrates. In: Cannell, M. G. R., Malcolm, D. C., & Robertson, P. A. (Eds.) The ecology of mixed-species stands of trees, Spec. Publ. № 11. British Ecological Society, Blackwell, Oxford, 255–265.
Cameron, K. H., & Leather, S. R. (2012). How good are carabid beetles (Coleoptera, Carabidae) as indicators of invertebrate abundance and order richness? Biodiversity and Conservation, 21(3), 763–779. >>
Christian, E., & Szeptycki, A. (2004). Distribution of Protura along an urban gradient in Vienna. Pedobiologia, 48(5–6), 445–452. >>
Cmoluch, Z. (1972). Weevils (Coleoptera, Curculionidae) of town plants associations of Lublin. Polskie Pismo Entomologiczne, 42, 545–562.
Crouau, Y., Gisclard, C., & Perotti, P. (2002). The use of Folsomia candida (Collembola, Isotomidae) in bioassays of waste. Applied Soil Ecology, 19(1), 65–70. >>
Czechowski, W. (1982). Occurrence of carabids (Coleoptera, Carabidae) in the urban greenery of Warsaw according to the land utilization and cultivation. Memorabilia Zoologica, 39, 3–108.
Dlussky, G. M. (2001). Structure of ant community (Hymenoptera, For¬micidae) from an oligotrophic peat bog. Zoologicheskii Zhurnal, 80(8), 984–985.
Faly, L., & Brygadyrenko, V. (2014). Patterns in the horizontal structure of litter invertebrate communities in windbreak plantations in the steppe zone of the Ukraine. Journal of Plant Protection Research, 54(4), 414–420. >>
Ferguson, S. H., & Berube, D. K. A. (2004). Invertebrate diversity under artificial cover in relation to boreal forest habitat characteristics. The Canadian Field-Naturalist, 118(3), 386–394. >>
Halaj, J., Halpern, C. B., & Yi, H. (2008). Responses of litter-dwelling spiders and carabid beetles to varying levels and patterns of green-tree retention. Forest Ecology and Management, 255, 887–900. >>
Kubicka, A. (1981). Scarabaeids (Coleoptera, Scarabaeidae) of Warsaw and Mazovia. Memorabilia Zoologica, 34, 145–164.
Kul’bachko, Y. L., Didur, O. O., Loza, I. M., Pakhomov, O. E., & Bezrodnova, O. V. (2015). Environmental aspects of the effect of earthworm (Lumbri¬cidae, Oligochaeta) tropho-metabolic activity on the pH buffering capacity of remediated soil (steppe zone, Ukraine). Biology Bulletin, 42, 899–904. >>
Maleque, M. A., Maeto, K., & Ishii, H. T. (2009). Arthropods as bioindicators of sustainable forest management, with a focus on plantation forests. Applied Entomology and Zoology, 44(1), 1–11. >>
Moroz, K. O., Lygun, A. V., & Brygadyrenko, V. V. (2011). Sezonna dynamika pidstylkovoi’ mezofauny antropogenno transformovanyh ekosystem m. Dniprodzerzhyns’k [Litter mesofauna seasonal dynamics of anthropogenically transformed ecosystems in Dniprodzerzhinsk city]. Visnyk of Dnipropetrovsk University. Biology, Ecology, 19(2), 93–102. >>
O’Grady, A., Breen, J., Harrington, T. J., & Courtney, R. (2013). The seed bank in soil from the nests of grassland ants in a unique limestone grassland community in Ireland. Ecological Engineering, 61, 58–64. >>
Oxbrough, A., French, V., Irwin, S., Kelly, T. C., Smiddy, P., & O’Halloran, J. (2012). Can mixed species stands enhance arthropod diversity in plantation forests? Forest Ecology and Management, 270, 11–18. >>
Oxbrough, A. G., Gittings, T., O’Halloran, J., Giller, P. S., & Smith, G. F. (2005). Structural indicators of spider communities across the forest plantation cycle. Forest Ecology and Management, 212(1–3), 171–183. >>
Pearce, J. L., & Venier, L. A. (2006). The use of ground beetles (Coleoptera: Carabidae) and spiders (Araneae) as bioindicators of sustainable forest management: A review. Ecological Indicators, 6(4), 780–793. >>
Pielou, E. (1977). Mathematical Ecology. John Wiley & Sons, New York.
Polchaninova, N. Y., & Prokopenko, E. V. (2013). Catalogue of the spiders (Arachnida, Aranei) of Left-Bank Ukraine. Arthropoda Selecta. Supplement No. 2. КMК Scientific Press. Moscow.
Reynolds, B. C., Crossley, D. A., & Hunter, M. D. (2003). Response of soil invertebrates to forest canopy inputs along a productivity gradient. Pedobiologia, 47(2), 127–139. >>
Schuldt, A., Fahrenholz, N., Brauns, M., Migge-Kleian, S., Platner, C., & Schaefer, M. (2008). Communities of ground-living spiders in deci¬duous forests: Does tree species diversity matter? Biodiversity and Conservation, 17(5), 1267–1284. >>
Shannon, C., & Weaver, W. (1949). The mathematical theory of communi¬cation. University of Illinois Press, Urbana.
Slipinski, P., Zmihorski, M., & Czechowski, W. (2012). Species diversity and nestedness of ant assemblages in an urban environment. European Journal of Entomology, 109(2), 197–206. >>
Sobek, S., Steffan-Dewenter, I., Scherber, C., & Tscharntke, T. (2009). Spatiotemporal changes of beetle communities across a tree diversity gradient. Diversity and Distributions, 15(4), 660–670. >>
Spitzer, L., Konvicka, M., Benes, J., Tropek, R., Tuf, I. H., & Tufova, J. (2008). Does closure of traditionally managed open woodlands threaten epigeic invertebrates? Effects of coppicing and high deer densities. Biological Conservation, 141(3), 827–837. >>
Taboada, A., Tarrega, R., Calvo, L., Marcos, E., Marcos, J. A., & Salgado, J. M. (2008). Plant and carabid beetle species diversity in relation to forest type and structural heterogeneity. European Journal of Forest Research, 129(1), 31–45. >>

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