posted on 2024-11-02, 09:35authored byKatherine Jeppe, Jianghua Yang, Sara HoskinSara Hoskin, Melissa Carew, Xiaowei Zhang, Vincent Pettigrove, Ary Hoffmann
Sediments accumulate chemicals that can be toxic to biota and often contribute to aquatic ecosystem decline. Measuring mortality in laboratory-bred organisms is a common way to assess sediment toxicity. However, mortality-based responses of resilient laboratory organisms may not reflect indigenous macroinvertebrate responses, which can be relatively more sensitive to sediment toxicants. A possible solution is to also measure responses at the subindividual level. Several organism responses to sediment copper toxicity were assessed in a field-based microcosm. Responses of laboratory-bred chironomids and snails deployed in microcosms were compared at subindividual (metabolomic and gene expression), individual (survival and dry weight) and population (reproduction) levels, and contrasted to the abundance of colonizing macroinvertebrates in the microcosms. Colonizing macroinvertebrate abundance showed a range of sensitivities based on EC50 (effect dose 50% change). Chironomidae made up 94·5% of the microcosm macroinvertebrates, with Paratanytarsus the most sensitive genus (EC50: 89 mg kg-1copper) and Procladius the least sensitive (EC50: 681 mg kg-1). Survival of laboratory-bred organisms was the least sensitive response, comparable to decreased abundance of the least sensitive macroinvertebrate. Juvenile production in the snail, Potamopyrgus antipodarum, was the most sensitive population-level response (EC50: 121 mg kg-1), in contrast the snail Physella acuta was relatively more tolerant (EC50: 298 mg kg-1). Changes in subindividual responses (gene expression and metabolite abundance) in laboratory-bred chironomid, Chironomus tepperi, were evident at 60 mg kg-1. These changes likely reflect the direct effects of copper exposure and represent metal-specific responses. Synthesis and applications. We showed that copper toxicity in sediments could be readily detected through changes in gene exp