Description: Human-induced habitat destruction, overexploitation, introduction of alien species and climate change are causing species to go extinct at unprecedented rates, from local to global scales. There are growing concerns that these kinds of disturbances alter important functions of ecosystems. Our current understanding is that key parameters of a community (e.g. its functional diversity, species composition, and presence/absence of vulnerable species) reflect an ecological network’s ability to resist or rebound from change in response to pressures and disturbances, such as species loss. If the food web structure is relatively simple, we can analyse the roles of different species interactions in determining how environmental impacts translate into species loss. However, when ecosystems harbour species-rich communities, as is the case in most natural systems, then the complex network of ecological interactions makes it a far more challenging task to perceive how species’ functional roles influence the consequences of species loss. One approach to deal with such complexity is to focus on the functional traits of species in order to identify their respective roles: for instance, large species seem to be more susceptible to extinction than smaller species. Here, we introduce and analyse the marine food web from the high Antarctic Weddell Sea Shelf to illustrate the role of species traits in relation to network robustness of this complex food web. Our approach was threefold: firstly, we applied a new classification system to all species, grouping them by traits other than body size; secondly, we tested the relationship between body size and food web parameters within and across these groups and finally, we calculated food web robustness. We addressed questions regarding (i) patterns of species functional/trophic roles, (ii) relationships between species functional roles and body size and (iii) the role of species body size in terms of network robustness. Our results show that when analyzing relationships between trophic structure, body size and network structure, the diversity of predatory species types needs to be considered in future studies.

Description: Traditionally, the rationale for energy flow studies was found in the elucidation of energy transfers within ecosystems or within the practical context of the rational management of resources, but it is now widely recognised that its scope embodies almost all biology, including the field of population dynamics and evolutionary studies. Here, we first describe conceptual models of energy and mass budgets at the level of the individual, the population and the community. However, the emphasis is on the next part in which the practicalities of measuring the various components of these budgets in the marine zoobenthic community are described in detail. The measurement of, among other things, ingestion, absorption, defaecation, excretion, growth, reproduction and respiration is discussed. Finally, attention is paid to the estimation of secondary production of benthic populations and to community-level modelling methods.

Description: We compared primary production and respiration of temperate (Helgoland, North Sea) and subtidal Arctic (Kongsfjorden, Svalbard) microphytobenthic communities during summer. The diatom communities were generally characterized as cosmopolitan, displayed no site specificity, and had similar chl a and fucoxanthin concentrations. Their net and gross photosynthesis rates and light adaptation intensities, derived from laboratory microsensor measurements, were also similar, despite differences in water temperature. Daily oxygen fluxes across the sediment− water interface were estimated by combining laboratory microprofile and planar optode measurements with in situ data on oxygen penetration and light dynamics. During the study period, the Svalbard sediments were on average net heterotrophic,while the Helgoland sediments were net autotrophic (−22.4 vs. 9.2 mmol O2 m−2 d−1). This was due to high infaunal abundance in the Svalbard sediments that caused high oxygen uptake rates in the sediments and consumption below the sediment euphotic zone. Additionally, bioirrigation of the sediment due to infaunal burrow ventilation was reduced by light; thus, the sedimentary oxygen inventory was reduced with increasing light. Conversely, light-enhanced the oxygen inventory in the Helgoland sediments. Oxygen dynamics in the Svalbard sediments were therefore dominated by bioirrigation, whereas in the Helgoland sediments they were dominated by photosynthetic oxygen production.