A rockling's choice:The trade-off between thermal preference and physical structure in the five bearded rockling, Ciliata mustela

Changes in the environment can alter the suitability of habitats for organisms. In marine systems, fish species have their own specific requirements in terms of temperature and other habitat features. Behavioral responses such as thermoregulatory behavior in ectothermic species allow mobile organisms to respond to detrimental changes and search for more suitable habitats. However, for many species, limited information exists on the ecological requirements to help explain species abundance in a changing habitat. An example of a quickly changing habitat is the Wadden Sea, where five bearded rockling (Ciliata mustela) abundance has increased, unlike other Wadden Sea species. The increasing abundance of rockling has coincided with increasing average sea water temperatures and the recovery of mussel and Pacific oyster beds. Warming waters and increased structural habitat may have provided rockling with a more desirable habitat. Therefore, to better understand why rockling abundance is increasing within a changing Wadden Sea, a water temperature preference chamber was used to determine rockling's preferred temperature range. In addition, rockling's affinity for structural habitat and the trade-off between preferred temperature was examined by following their response to the systematic removal of artificial physical structures within the preferred temperature conditions. The preferred temperature range of rockling was found to be 10.4–15.7 °C. Following structure removals, rockling repeatedly moved away from their chosen temperatures to adjacent compartments with different temperatures but containing physical structure, indicating that the presence of physical structure was more important than preferred temperature until 18.6 °C. These novel findings provide insight and experimental support for the hypothesis explaining rockling's increase in the Wadden Sea: 1) mean annual temperatures have been steadily increasing towards rockling's preferred thermal range and 2) increasing mussel and Pacific oyster beds are plausibly providing structural habitat, an important habitat requirement for rockling. When fish display a strong association with physical structure it is necessary to link physiological and habitat preferences to better understand climate change related responses

A rockling's choice:The trade-off between thermal preference and physical structure in the five bearded rockling, Ciliata mustela

Changes in the environment can alter the suitability of habitats for organisms. In marine systems, fish species have their own specific requirements in terms of temperature and other habitat features. Behavioral responses such as thermoregulatory behavior in ectothermic species allow mobile organisms to respond to detrimental changes and search for more suitable habitats. However, for many species, limited information exists on the ecological requirements to help explain species abundance in a changing habitat. An example of a quickly changing habitat is the Wadden Sea, where five bearded rockling (Ciliata mustela) abundance has increased, unlike other Wadden Sea species. The increasing abundance of rockling has coincided with increasing average sea water temperatures and the recovery of mussel and Pacific oyster beds. Warming waters and increased structural habitat may have provided rockling with a more desirable habitat. Therefore, to better understand why rockling abundance is increasing within a changing Wadden Sea, a water temperature preference chamber was used to determine rockling's preferred temperature range. In addition, rockling's affinity for structural habitat and the trade-off between preferred temperature was examined by following their response to the systematic removal of artificial physical structures within the preferred temperature conditions. The preferred temperature range of rockling was found to be 10.4–15.7 °C. Following structure removals, rockling repeatedly moved away from their chosen temperatures to adjacent compartments with different temperatures but containing physical structure, indicating that the presence of physical structure was more important than preferred temperature until 18.6 °C. These novel findings provide insight and experimental support for the hypothesis explaining rockling's increase in the Wadden Sea: 1) mean annual temperatures have been steadily increasing towards rockling's preferred thermal range and 2) increasing mussel and Pacific oyster beds are plausibly providing structural habitat, an important habitat requirement for rockling. When fish display a strong association with physical structure it is necessary to link physiological and habitat preferences to better understand climate change related responses

Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation.

Resources are a core currency of species interactions and ecology in general (e.g., think of food webs or competition). Within parasite-infected hosts, resources are divided among the competing demands of host immunity and growth as well as parasite reproduction and growth. Effects of resources on immune responses are increasingly understood at the cellular level (e.g., metabolic predictors of effector function), but there has been limited consideration of how these effects scale up to affect individual energetic regimes (e.g., allocation trade-offs), susceptibility to infection, and feeding behavior (e.g., responses to local resource quality and quantity). We experimentally rewilded laboratory mice (strain C57BL/6) in semi-natural enclosures to investigate the effects of dietary protein and gastrointestinal nematode (Trichuris muris) infection on individual-level immunity, activity, and behavior. The scale and realism of this field experiment, as well as the multiple physiological assays developed for laboratory mice, enabled us to detect costs, trade-offs, and potential compensatory mechanisms that mice employ to battle infection under different resource conditions. We found that mice on a low-protein diet spent more time feeding, which led to higher body fat stores (i.e., concentration of a satiety hormone, leptin) and altered metabolite profiles, but which did not fully compensate for the effects of poor nutrition on albumin or immune defenses. Specifically, immune defenses measured as interleukin 13 (IL13) (a primary cytokine coordinating defense against T. muris) and as T. muris-specific IgG1 titers were lower in mice on the low-protein diet. However, these reduced defenses did not result in higher worm counts in mice with poorer diets. The lab mice, living outside for the first time in thousands of generations, also consumed at least 26 wild plant species occurring in the enclosures, and DNA metabarcoding revealed that the consumption of different wild foods may be associated with differences in leptin concentrations. When individual foraging behavior was accounted for, worm infection significantly reduced rates of host weight gain. Housing laboratory mice in outdoor enclosures provided new insights into the resource costs of immune defense to helminth infection and how hosts modify their behavior to compensate for those costs

Feeding immunity: Physiological and Behavioral responses to infection and resource limitation

Resources are a core currency of species interactions and ecology in general (e.g., think of food webs or competition). Within parasite-infected hosts, resources are divided among the competing demands of host immunity and growth as well as parasite reproduction and growth. Effects of resources on immune responses are increasingly understood at the cellular level (e.g., metabolic predictors of effector function), but there has been limited consideration of how these effects scale up to affect individual energetic regimes (e.g., allocation trade-offs), susceptibility to infection, and feeding behavior (e.g., responses to local resource quality and quantity). We experimentally rewilded laboratory mice (strain C57BL/6) in semi-natural enclosures to investigate the effects of dietary protein and gastrointestinal nematode (Trichuris muris) infection on individual-level immunity, activity, and behavior. The scale and realism of this field experiment, as well as the multiple physiological assays developed for laboratory mice, enabled us to detect costs, trade-offs, and potential compensatory mechanisms that mice employ to battle infection under different resource conditions. We found that mice on a low-protein diet spent more time feeding, which led to higher body fat stores (i.e., concentration of a satiety hormone, leptin) and altered metabolite profiles, but which did not fully compensate for the effects of poor nutrition on albumin or immune defenses. Specifically, immune defenses measured as interleukin 13 (IL13) (a primary cytokine coordinating defense against T. muris) and as T. muris-specific IgG1 titers were lower in mice on the low-protein diet. However, these reduced defenses did not result in higher worm counts in mice with poorer diets. The lab mice, living outside for the first time in thousands of generations, also consumed at least 26 wild plant species occurring in the enclosures, and DNA metabarcoding revealed that the consumption of different wild foods may be associated with differences in leptin concentrations. When individual foraging behavior was accounted for, worm infection significantly reduced rates of host weight gain. Housing laboratory mice in outdoor enclosures provided new insights into the resource costs of immune defense to helminth infection and how hosts modify their behavior to compensate for those costs

Twenty years of monitoring reveal overfishing of bony fish stocks in the coastal national park Banc d’Arguin, in Mauritania

Along Africa’s western coast, many local communities rely on the ocean for their livelihood. Over the last decades, introductions of new fishing techniques along with globalizing trade have strongly changed local fishing practices. The Parc National du Banc d’Arguin (PNBA) in Mauritania had for centuries been subjected to an artisanal, low-impact, fishery. This fishing was exclusively oriented towards migratory bony fish species, mullet (Mugil cephalus) and meagre (Argyrosomus regius). Since the 1980s, these species have been replaced by illegal catches of internationally traded elasmobranchs (sharks and rays) and by non-migratory and relict species (resident) such as tilapias (Sarotherodon melanotheron) and catfishes (Arius sp.). To date, most monitoring and management efforts have been dedicated to evaluating changes in elasmobranch populations and less focus has been on bony fish species. Data from a fishery monitoring programme are used to analyse the trends in effort, catch and catch per unit of effort of bony fish species by fitting non-parametric generalized additive models to capture changes in the fish community over the last 20 years. Mullet and meagre became overfished early on, and the contribution of resident species (tilapias and catfishes) increased in the catches. Together with a pattern of increased effort on the traditionally targeted species, such a change in the catch could reflect a change in the fish community. These results call for the implementation of sustainable fishing practices within PNBA. We propose the need to implement closures of fisheries during the species’ breeding periods as well as the use of biological reference points such as the size at first capture and maximum sustainable yield targets for resident species.</p

Feeding immunity: Physiological and Behavioral responses to infection and resource limitation

Resources are a core currency of species interactions and ecology in general (e.g., think of food webs or competition). Within parasite-infected hosts, resources are divided among the competing demands of host immunity and growth as well as parasite reproduction and growth. Effects of resources on immune responses are increasingly understood at the cellular level (e.g., metabolic predictors of effector function), but there has been limited consideration of how these effects scale up to affect individual energetic regimes (e.g., allocation trade-offs), susceptibility to infection, and feeding behavior (e.g., responses to local resource quality and quantity). We experimentally rewilded laboratory mice (strain C57BL/6) in semi-natural enclosures to investigate the effects of dietary protein and gastrointestinal nematode (Trichuris muris) infection on individual-level immunity, activity, and behavior. The scale and realism of this field experiment, as well as the multiple physiological assays developed for laboratory mice, enabled us to detect costs, trade-offs, and potential compensatory mechanisms that mice employ to battle infection under different resource conditions. We found that mice on a low-protein diet spent more time feeding, which led to higher body fat stores (i.e., concentration of a satiety hormone, leptin) and altered metabolite profiles, but which did not fully compensate for the effects of poor nutrition on albumin or immune defenses. Specifically, immune defenses measured as interleukin 13 (IL13) (a primary cytokine coordinating defense against T. muris) and as T. muris-specific IgG1 titers were lower in mice on the low-protein diet. However, these reduced defenses did not result in higher worm counts in mice with poorer diets. The lab mice, living outside for the first time in thousands of generations, also consumed at least 26 wild plant species occurring in the enclosures, and DNA metabarcoding revealed that the consumption of different wild foods may be associated with differences in leptin concentrations. When individual foraging behavior was accounted for, worm infection significantly reduced rates of host weight gain. Housing laboratory mice in outdoor enclosures provided new insights into the resource costs of immune defense to helminth infection and how hosts modify their behavior to compensate for those costs

When less is more: positive population-level effects of mortality

Experimental and theoretical studies show that mortality imposed on a population can counter-intuitively increase the density of a specific life-history stage or total population density. Understanding positive population-level effects of mortality is advancing, illuminating implications for population, community, and applied ecology. Reconciling theory and data, we found that the mathematical models used to study mortality effects vary in the effects predicted and mechanisms proposed. Experiments predominantly demonstrate stage-specific density increases in response to mortality. We argue that the empirical evidence supports theory based on stage-structured population models but not on unstructured models. We conclude that stage-specific positive mortality effects are likely to be common in nature and that accounting for within-population individual variation is essential for developing ecological theory

Top predator status and trends: ecological implications, monitoring and mitigation strategies to promote ecosystem-based management

The conservation and management of marine ecosystems hinge on a comprehensive understanding of the status and trends of top predators. This review delves into the ecological significance of marine top predators, examining their roles in maintaining ecosystem stability and functioning through an integrated analysis of current scientific literature. We first assess the efficacy of various monitoring methods, ranging from traditional field observations to cutting-edge technologies like satellite tracking and environmental DNA (eDNA) analysis and evaluating their strengths and limitations in terms of accuracy, spatial coverage, and cost-effectiveness, providing resource managers with essential insights for informed decision-making. Then, by synthesizing data from diverse marine ecosystems, this study offers a comprehensive overview of the trends affecting top predator populations worldwide. We explore the multifaceted impacts of human activities, climate change, and habitat degradation on the abundance and distribution of these key species. In doing so, we shed light on the broader implications of declining top predator populations, such as trophic cascades and altered community structures. Following a thorough assessment of successful strategies for reversing the decline of top predators, a compilation of recommendations is presented, encompassing effective governance interventions. A crucial aspect of effective ecosystem-based management is the implementation of robust monitoring strategies. Mitigation measures are imperative to reverse the adverse impacts on marine top predators. We present a comprehensive array of mitigation options based on successful case studies. These include the establishment of marine protected areas, the enforcement of fisheries regulations, and the promotion of sustainable fishing practices. We deepen the synergies between these strategies and their potential to mitigate human-induced stressors on top predator populations to safeguard their pivotal role in maintaining marine ecosystem structure and function. By examining marine top predators’ ecological significance, analyzing population trends, discussing monitoring techniques, and outlining effective mitigation strategies, we provide a comprehensive resource for researchers, policymakers, and stakeholders engaged in fostering ecosystem-based management approaches. We conclude that integrating these insights into current management frameworks will be essential to safeguard both top predators and the broader marine environment for future generations