Authors:
R. Kędzior Department of Ecology Climatology and Air Protection, University of Agriculture, Krakow, Poland

Search for other papers by R. Kędzior in
Current site
Google Scholar
PubMed
Close
,
A. Kosewska Department of Entomology, Phytopathology and Molecular Diagnostic, University of Warmia and Mazury in Olsztyn, Prawochenskiego 17, 10-687 Olsztyn, Poland

Search for other papers by A. Kosewska in
Current site
Google Scholar
PubMed
Close
, and
T. Skalski Institute of Biology, Jan Kochanowski University of Kielce, Poland

Search for other papers by T. Skalski in
Current site
Google Scholar
PubMed
Close
Restricted access

Over the last 30 years there has been a great deal of interest in investigating patterns of species co-occurrence across space and time, which may be shaped by interspecific competition for shared resources. A good model of co-occurrence mechanisms is developed among predatory animals along a pollution gradient, where shared resources become more limited in more contaminated areas and the energy budget for detoxification is much higher. Community disassembly by heavy metal pollution may occur when the presence of toxic elements shifts patterns of species co-occurrence from structured to random. On the other hand, limited resources on a pollution gradient should lead to higher competition between dominant species. Disassembly may entail the loss of existing co-evolved interactions among species, which has ramifications for community dynamics and the quality of the functioning of polluted ecosystems. We expect an assemblage dominated by competitive species interactions to exhibit a significant segregation of taxa, whereas one dominated by mutualistic or syntrophic interactions would exhibit an aggregation of taxa. Responses of Carabidae co-occurrence patterns and changes in body size measures to heavy metal concentrations were investigated in a zinc contamination gradient in a Scots pine forest in the vicinity of Olkusz (southern Poland), at 12 study sites. The zinc concentration in the humus layer varied between 108 mg kg-1 dw to 6150 mg kg-1 dw. We used the C-score index, between all possible species pairs in a matrix. The ground beetle assemblages from the reference sites showed a significant segregation pattern. Community disassembly occurred only among assemblages in heavily polluted sites. The average value of skewness and kurtosis were significantly higher in the highly contaminated sites, indicating the greater proportion of small-bodied species in contaminated areas. The Gini coefficient was highest in the low contaminated sites, indicating the body-size inequality of carabid assemblages was greatest in the uncontaminated areas. Our data suggest that increased pollution contributes to the extinction of sensitive forest specialists with large body size and higher competitive abilities, leading to replacement by less sensitive generalists, with smaller body size and that the co-occurrence of species on heavily polluted sites is a result of unstable interactions between species in communities.

  • Aleksandrowicz, O.R. 2004. Biegaczowate (Carabidae). In: Bogdanowicz, W., E. Chudzińska, I. Pilipiuk, and E. Skibińska (eds.), Fauna Polski – charakterystyka i wykaz gatunków. Muzeum i Instytut Zoologii PAN. Warszawa. I: 2842 [In Polish].

    • Search Google Scholar
    • Export Citation
  • Azeria, E.T., J. Ibarzabal and C. Hébert. 2012. Effects of habitat characteristics and interspecific interactions on co-occurence patterns of saproxylic beetles breeding in tree boles after forest fire: null model analyses. Oecologia 168:11231135.

    • Search Google Scholar
    • Export Citation
  • Banado, E.I., H.A. Regidor, H.A. Nú̉nez, R. Acosta and E. Gianoli. 2005. Species richness and structure of ants communities in a dynamic archipelago: effects of island area and age. J. Biogeogr. 32:221227.

    • Search Google Scholar
    • Export Citation
  • Bayley, M., E. Baatrup, U. Heimbach and P. Bjerregaard. 1995. Elevated Cooper Levels during larval development cause altered locomotor behavior in the adult carabid beetle Pterostichus cupreus L. (Coleoptera: Carabidae). Ecotoxicol. Environ.Safety 32:166170.

    • Search Google Scholar
    • Export Citation
  • Bednarska, A.J., I. Portka, P.E. Kramarz and R. Laskowski. 2009. Combined effect of environmental pollutants (nickel, chlorpyrifos) and temperature on the ground beetle, Pterostichus oblongopunctatus (Coleoptera: Carabidae). Environ. Toxicol. Chem. 28:864872.

    • Search Google Scholar
    • Export Citation
  • Bednarska, A.J. and R. Laskowski. 2009. Environmental conditions enhance toxicant effects in larvae of the ground beetle Pterostichus oblongopunctatus (Coleoptera: Carabidae). Environ. Pollution 157:15971602.

    • Search Google Scholar
    • Export Citation
  • Blick, R.A.J. and K.C. Burns. 2011. Liana co-occurrence patterns in a temperate rainforest. J. Veg. Sci. 22:868877.

  • Bonari, G., M. Migliorini, M. Landi, G. Protano, P.P. Fanciulli and C. Angiolini. 2017. Concordance between plant species, oribatid mites and soil in Mediterranean stone pine forest. Arthropod-Plant Interaction 11:6169.

    • Search Google Scholar
    • Export Citation
  • Brandl R. and W. Topp. 1985. Size structure of Pterostichus spp. (Carabidae): aspects of competition. Oikos 44:234238.

  • Butovsky, R.O. 2011. Heavy metals in carabids (Coleoptera, Carabidae). In: Kotze DJ, Assmann T, Noordijk J, Turin H, Vermeulen R (eds.), Carabid beetles as bioindicators: biogeographical, ecological and environmental studies. ZooKeys 100:215222.

    • Search Google Scholar
    • Export Citation
  • Chase, J.M. and M.A. Leibold. 2003. Ecological Niches. Linking Classical and Contemporary Approaches. University of Chicago Press, Chicago, IL.

    • Search Google Scholar
    • Export Citation
  • Clarke, K.R. 1993. Non-parametric multivariate analysis of changes in community structure. Aust. J. Ecol. 18:117143.

  • Cody, M.L. and J.M. Diamond (eds). 1975. Ecology and Evolution of Communities. Harvard University Press, Cambridge., New York.

  • Diamond, J. M. 1975. Assembly of species communities. In: M. L. Cody and J.M. Diamond (eds), Ecology and Evolution of Communities. Harvard University Press, Cambridge, MA, USA, pp. 342444.

    • Search Google Scholar
    • Export Citation
  • Fountain, M.T. and S.P. Hopkins. 2004. A comparative study of the effects of metal contamination in Collembola in the field and in the laboratory. Ecotoxicology 13:573587.

    • Search Google Scholar
    • Export Citation
  • Gadd, G. M. 2010. Metals, minerals and microbes: geomicrobiology and bioremediation. Microbiology 156:609643.

  • Gall J.E. , R.S. Boyd and N. Rajakaruna. 2015. Transfer of heavy metals through terrestrial food webs: a review. Environ. Monit. Assess. 187:201222.

    • Search Google Scholar
    • Export Citation
  • Gallagher, F., I. Pechmann, J.E. Bogden, J. Grabosky and P. Weis. 2008. Soil metal concentartions and productivity of Betula populifolia (gray birch) as measured by field spectometry and incremental annula growth in an abandoned urban Brownfield in New Jersey. Environ. Pollut. 156:699706.

    • Search Google Scholar
    • Export Citation
  • Gotelli, N.J. 2000. Null model analysis of species co-occurence patterns. Ecology 81:26062621.

  • Grześ, I.M. 2010. Zinc tolerance in the ant species Myrmica rubra originating from a metal pollution gradient. Eur. J. Soil Biol. 46:8790.

    • Search Google Scholar
    • Export Citation
  • Hammer, Ø., D.A.T. Harper and P.D. Ryan. 2001. Past: Paleontological Statistics Software Package for Education and Data Analysis. Palaeontologia Electronica 4:9.

    • Search Google Scholar
    • Export Citation
  • Hedde, M., F. van Oort and I. Lamy. 2012. Functional traits of soil invertebrates as indicators for exposure to soil disturbance. Environ. Pollut. 164:5965.

    • Search Google Scholar
    • Export Citation
  • Heino, J. 2009. Species co-occurence, nestedness and guild- environment relationships in stream macroinvertebrates. Freshw.Biol. 54:19471959.

    • Search Google Scholar
    • Export Citation
  • Holmstrup, M., A.M. Bindesbøl, G.J. Oostingh, A. Duschl, V. Scheil, H.R. Köhler, S. Loureiro, A.M. Soares, A.L. Ferreira, C. Kienle, A. Gerhardt, R. Laskowski, P. Kramarz, M. Bayley, C. Svendsen and D.J. Spurgeon. 2010. Interactions between effects of environmental chemicals and natural stressors: a review. Sci. Total Environ. 408(18):374662.

    • Search Google Scholar
    • Export Citation
  • Hurka, K. 1996. Carabidae of the Czech and Slowak Republics.

  • Kabourek, Zlin. Koivula, M. 2011. Useful model organisms, indicators, or both? Ground beetles (Coleoptera, Carabidae) reflecting environmental conditions. ZooKeys 100:287317.

    • Search Google Scholar
    • Export Citation
  • Magura, T., B. Tóthmérész and G. Lövei. 2006. Body size inequality of carabids along an urbanisation gradient. Basic Appl. Ecol. 7:472482.

    • Search Google Scholar
    • Export Citation
  • Maryański, M., P. Kramarz, R. Laskowski and M. Niklińska. 2002. Decreased energetic reserves, morphological changes and accumulation of metals in Carabid Beetles (Poecilus cupreus L.) exposed to Zinc- or Cadmium-contaminated Food. Ecotoxicology 11:127139.

    • Search Google Scholar
    • Export Citation
  • Migliorini, M., A. Petroli and F. Bernini. 2002. Comparative analysis of two edaphic zoocoenoses (Oribatid mites and Carabid Beetles) in five habitats of the 'Pietraporciana' and 'Lucciolabella' Nature Reserves (Orcia Valley, cenral Italy). Acta Oecol. 23:361374.

    • Search Google Scholar
    • Export Citation
  • Migliorini, M., G. Pigino, T. Caruso, P.P. Fanciulli, C. Leonzio and F. Bernini. 2005. Soil communities (Acari Oribatida; Hexapoda Collembola) in a clay pigeon shooting range. Pedobiologia 49:113.

    • Search Google Scholar
    • Export Citation
  • Minor, M.A. 2011. Spatianl patterns and local diversity in soil oribatid mites (Acari: Oribatida) in three pine plantation forest. Eur. J. Soil Biol. 47:122128.

    • Search Google Scholar
    • Export Citation
  • Możdżer, J.T., P. Kramarz, A. Piśkiewicz and M. Niklińska. 2003. Effects of cadmium and zinc on larval growth and survival in the ground beetle, Pterostichus oblongopunctatus. Environ. Int. 28:737742.

    • Search Google Scholar
    • Export Citation
  • Niemelä, J. and D.J. Kotze. 2009. Carabid beetle assemblages along urban to rural gradients: A review. Landsc. Urban Plan. 92:6571.

  • Pitzalis, M., L. Luiselli and M.A. Bologna. 2010. Co-occurence analyses show that non-random community structure is disrupted by fire in two groups of soil arthropods (Isopoda Oniscidea and Collembola). Acta Oceol. 36:100106.

    • Search Google Scholar
    • Export Citation
  • Ribera, I., S. Doledec, I.S. Downie and G.N. Foster. 2001. Effect of land disturbance and stress on species traits of ground beetles assemblages. Ecology 82:11121129.

    • Search Google Scholar
    • Export Citation
  • Sanders, N.J., N.J. Gotelli, N.E. Heller and D.M. Gordon. 2003. Community disassembly by an invasive species. Proc. Nat. Acad. Sci. USA 100:24742477.

    • Search Google Scholar
    • Export Citation
  • Sanders, N.J., N.J., Gotelli, S.E. Wittman, J.S. Ratchford, A.M. Ellison and E.S. Jules. 2007. Assembly rules for ant communities across spatial scales and habitats. J. Biogeogr. 34:16321641.

    • Search Google Scholar
    • Export Citation
  • Šerić Jelaska L. and P. Durbešić. 2009. Comparison of the body size and wing form of carabid species (Coleoptera: Carabidae) between isolated and continuous forest habitats. Ann. soc. entomol. Fr. (n.s.). 45 (3):327338.

    • Search Google Scholar
    • Export Citation
  • Skalski, T., D. Stone, P. Kramarz and R. Laskowski. 2010. Ground beetle community responses to heavy metal contamination. Baltic J. Coleopterol. 10(1):112.

    • Search Google Scholar
    • Export Citation
  • Skalski, T., K. Gargasz and R. Laskowski. 2011. Does of mixed diffuse pollution degrease ground beetle diversity? Baltic J. Coleopterol. 11(1):115.

    • Search Google Scholar
    • Export Citation
  • Skalski, T., R. Kędzior, D. Kolbe and S. Knutelski. 2015a. Ground beetles as indicators of heavy metal pollution in forests. Sylwan 159:905911.

  • Skalski, T., R. Kędzior, D. Kolbe and S. Knutelski. 2015b. Different responses of epigeic beetles to heavy metal contamination depending on functional traits at the family level. Baltic J. Coleopterol. 15(2):8190.

    • Search Google Scholar
    • Export Citation
  • Skłodowski, J. 2014. Consequence of the transformation of a primeval forest into a managed forest for carabid beetles (Coleoptera: Carabidae) - a case study from Białowieża (Poland). Eur. J. Entomolo. 111(5):639648.

    • Search Google Scholar
    • Export Citation
  • Sota, T. 1987. Mortality pattern and age structure in two carabid populations with different seasonal life cycles. Res. Popul. Ecol. 29:237254.

    • Search Google Scholar
    • Export Citation
  • Spurgeon, D.J. and S.P. Hopkin. 1996. Effects of metal-contaminated soils on the growth, sexual development and early cocoon production of the earthworm Eisenia fetida with particular reference to zinc. Ecotoxicol. Environ. Safety 35:8695.

    • Search Google Scholar
    • Export Citation
  • StatSoft. 2012. STATISTICA (data analysis software system), version 12.0. www.statsoft.com.

  • Stefanowicz, A.M., M. Niklińska and R. Laskowski. 2008. Metals affect soil bacterial and fungal functional diversity differently. Environ. Toxicol. Chem. 27:591598.

    • Search Google Scholar
    • Export Citation
  • Stone, L. and A. Roberts. 1990. The checkerboard score and species distributions. Oecologia 85:7479.

  • Stone, D., P. Jepson, P. Kramarz and R. Laskowski. 2001. Time to death response in carabid beetles exposed to multiple stressors along a gradient of heavy metal pollution. Environ. Pollut. 113:239244.

    • Search Google Scholar
    • Export Citation
  • Szafer, W. and K. Zarzycki. 1972. Szata roślinna Polski. Tom II, PWN, Warszawa.

  • Szyszko, J. 1983. Methods of macrofauna investigations. In: Szujecki A, Szyszko J, Mazur S, Perliński S (eds). The Process of Forest Soil Macrofauna Formation after Afforestation of Farmland. Warsaw Agricultural University Press, Warsaw. pp. 1016.

    • Search Google Scholar
    • Export Citation
  • Thiele, H.U. 1977. Carabid Beetles in their Environments: A Study on Habitat Selection by Adaptations in Physiology and Behavior. Springer, Stuttgart.

    • Search Google Scholar
    • Export Citation
  • Ulrich, W. and H.J. Gotelli. 2007. Null model analysis of species nestedness patterns. Ecology 88:18241831.

  • Ulrich, W., K. Komosiński and M. Zalewski. 2008. Body size and biomass distributions of carrion visiting beetles: do cities host smaller species? Ecol. Res. 23:241248.

    • Search Google Scholar
    • Export Citation
  • Żmudzki, S. and R. Laskowski. 2012. Biodiversity and structure of spider communities along a metal pollution gradient. Ecotoxicology 21:15231532.

    • Search Google Scholar
    • Export Citation
  • Collapse
  • Expand

To see the editorial board, please visit the website of Springer Nature.

Manuscript Submission: HERE

For subscription options, please visit the website of Springer Nature.

Community Ecology
Language English
Size A4
Year of
Foundation
2000
Volumes
per Year
1
Issues
per Year
3
Founder Akadémiai Kiadó
Founder's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245
Publisher Akadémiai Kiadó
Springer Nature Switzerland AG
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
CH-6330 Cham, Switzerland Gewerbestrasse 11.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 1585-8553 (Print)
ISSN 1588-2756 (Online)