Effects of intra- and interspecific competition on the sensitivity of aquatic macroinvertebrates to carbendazim.

The Ecological Risk Assessment of pesticides and other potentially toxic chemicals is generally based on toxicity data obtained from single-species laboratory experiments. In the field, however, contaminant effects are ubiquitously co-occurring with ecological interactions such as species competition and predation, which might influence the sensitivity of the individuals exposed to toxicants. The present experimental study investigated how intra- and interspecific competition influence the response of sensitive aquatic organisms to a pesticide. For this, the effects of the fungicide carbendazim were assessed on the mortality and growth of the snail Bithynia tentaculata and the crustacean Gammarus pulex under different levels of intraspecific and interspecific competition for a food resource. Interspecific competition was created by adding individuals of Radix peregra and Asellus aquaticus, respectively. The interaction of competition and carbendazim exposure significantly influenced B. tentaculata growth, however, combined effects on survival and immobility were considered transient and were less easily demonstrated. Positive influence of competition on G. pulex survival was observed under low-medium carbendazim concentrations and under medium-high density pressures, being partly related to cannibalistic and predation compensatory mechanisms, enhanced under food limiting conditions. This study shows that intra- and interspecific competition pressure may influence the response of sensitive aquatic organisms in a more complex way (positive, non-significant and negative effects were observed) than just increasing the sensitivity of the studied species, as has generally been hypothesized.

[1]  P. Calow,et al.  Comparative ecology of Gammarus pulex (L.) and Asellus aquaticus (L.) II: fungal preferences , 1994, Hydrobiologia.

[2]  D. Hering,et al.  Drivers and stressors of freshwater biodiversity patterns across different ecosystems and scales: a review , 2012, Hydrobiologia.

[3]  J. Lajtner,et al.  The Contribution of Gastropod Biomass in Macrobenthic Communities of a Karstic River , 1995 .

[4]  D. Baird,et al.  Among‐ and within‐population variability in tolerance to cadmium stress in natural populations of Daphnia magna: Implications for ecological risk assessment , 2002, Environmental toxicology and chemistry.

[5]  M. Liess Population response to toxicants is altered by intraspecific interaction , 2002, Environmental toxicology and chemistry.

[6]  P. Gaskell,et al.  Importance of prey and predator feeding behaviors for trophic transfer and secondary poisoning. , 2009, Environmental science & technology.

[7]  R. Sibly,et al.  Density-dependent effects of a toxicant on life-history traits and population dynamics of a capitellid polychaete , 1999 .

[8]  I. Jones,et al.  The Influence of Fresh Water Pollutants and Interaction with Asellus aquaticus (L.) on the Feeding Activity of Gammarus pulex (L.) , 1998, Archives of environmental contamination and toxicology.

[9]  M. Liess,et al.  The influence of predation on the chronic response of Artemia sp. populations to a toxicant , 2006, The Journal of applied ecology.

[10]  S. Crum,et al.  Variability in the Dynamics of Mortality and Immobility Responses of Freshwater Arthropods Exposed to Chlorpyrifos , 2010, Archives of environmental contamination and toxicology.

[11]  D. Baird,et al.  Assessing structural and functional plankton responses to carbendazim toxicity , 2004, Environmental toxicology and chemistry.

[12]  J. V. Buskirk Influence of Size and Date of Emergence on Male Survival and Mating Success in a Dragonfly, Sympetrum rubicundulum , 1987 .

[13]  S. Crum,et al.  Toxicicity of derosal (active ingredient carbendazim) to aquatic invertebrates , 1998 .

[14]  Paul J. Van den Brink,et al.  Assessing aquatic population and community-level risks of pesticides. , 2013 .

[15]  Alastair Grant,et al.  Joint effects of density dependence and toxicant exposure on Drosophila melanogaster populations. , 2008, Ecotoxicology and environmental safety.

[16]  C. Gordon The coexistence of species La coexistencia de especies , 2000 .

[17]  P. J. Van den Brink,et al.  Impact of the fungicide carbendazim in freshwater microcosms. I. Water quality, breakdown of particulate organic matter and responses of macroinvertebrates. , 2000, Aquatic toxicology.

[18]  Matthias Liess,et al.  Environmental context determines community sensitivity of freshwater zooplankton to a pesticide. , 2011, Aquatic toxicology.

[19]  M. Liess,et al.  Automated Nanocosm test system to assess the effects of stressors on two interacting populations. , 2012, Aquatic toxicology.

[20]  P. Vanrolleghem,et al.  Do we have to incorporate ecological interactions in the sensitivity assessment of ecosystems? An examination of a theoretical assumption underlying species sensitivity distribution models. , 2008, Environment international.

[21]  M. Daam,et al.  Sensitivity of macroinvertebrates to carbendazim under semi-field conditions in Thailand: implications for the use of temperate toxicity data in a tropical risk assessment of fungicides. , 2009, Chemosphere.

[22]  R. Jiménez-Melero,et al.  Agricultural impacts on Mediterranean wetlands : the effect of pesticides on survival and hatching rates in copepods , 2005 .

[23]  R. Schulz,et al.  Effects of current-use fungicides and their mixtures on the feeding and survival of the key shredder Gammarus fossarum. , 2014, Aquatic toxicology.

[24]  P. Calow,et al.  Comparative ecology of Gammarus pulex (L.) and Asellus aquaticus (L.) I: population dynamics and microdistribution , 1994, Hydrobiologia.

[25]  Frederik De Laender,et al.  Brief communication: The ecosystem perspective in ecotoxicology as a way forward for the ecological risk assessment of chemicals , 2013, Integrated environmental assessment and management.