1,721,094 research outputs found
Size- and sex-based habitat partitioning by Lepetodrilus fucensis near hydrothermal vents on the Juan de Fuca Ridge, Northeast Pacific
This study examines habitat partitioning by a hydrothermal vent limpet, Lepetodrilus fucensis, along environmental gradients and among vents with differing levels of flux. To test for spatial patterns in size structure, two distances from isolated vent flows were sampled (0–25 cm and 51–75 cm). Lepetodrilus fucensis displays a size gradient: juveniles are rare in flow (relative abundance < 5%, density = 56 ± 46 individuals·dm–2) and abundant peripherally (>95%, 2616 ± 2002 individuals·dm–2). Next, sex-based habitat partitioning was examined. High flux locations are female-biased (proportion male = 0.34 ± 0.07), whereas males are overrepresented peripherally and at waning vents (0.64 ± 0.08). The spatial mismatch between the sexes within a vent is driven by differential habitat occupation at decimetre scales. One hypothesis to explain this pattern is that females suffer a higher cost of reproduction and outcompete males for habitats with high food availability. Indeed, relatively higher percentages of females in waning vents had empty gonads in comparison with males (32%–78% vs. 0%–16%, respectively). Furthermore, females transplanted to the vent periphery for one year displayed much lower survivorship than males (2% vs. 27%). This finding suggests that differential survivorship between the sexes when food is limited can yield male-biased populations at waning vents
Persistence, morphology, and nutritional state of a gastropod hosted bacterial symbiosis in different levels of hydrothermal vent flux
The limpet, Lepetodrilus fucensis McLean, is found in prominent stacks around hydrothermal vents on the Juan de Fuca Ridge. L. fucensis hosts a filamentous episymbiont on its gill lamellae that may be ingested directly by the gill epithelium. To assess the persistence of this symbiosis I used microscopy to examine the gills of L. fucensis from sites representing its geographic range and different habitats. The symbiosis is present on all the specimens examined in this study, including both sexes and a range of juvenile and adult sizes. Next, I aimed to determine if patterns in bacterial abundance, host condition, and gill morphology support the hypotheses that the bacteria are chemoautotrophic and provide limpets with a food resource. To do so, I compared specimens from high and low flux locations at multiple vents. My results support the above hypotheses: (1) gill bacteria are significantly less abundant in low flux where the concentrations of reduced chemicals (for chemoautotrophy) are negligible, (2) low flux specimens have remarkably poor tissue condition, and (3) the lamellae of high flux limpets have greater surface area: the blood space and bacteria-hosting epithelium are deeper and have more folds than low flux lamellae, modifications that support higher symbiont abundances. I next asked if the morphology of the lamellae could change. To test this, I moved high flux limpets away from a vent and after 1 year the lamellar depth and shape of the transplanted specimens resembled low flux gills. Last, I was interested in whether bacterial digestion by the gill epithelium is a significant feeding mechanism. As bacteria-like cells are rarely apparent in lysosomes of the gill epithelium, I predicted that lysosome number would be unrelated to bacterial abundance. My data support this prediction, suggesting that digestion of bacteria by the gill epithelium probably contributes only minimally to the limpet’s nutrition. Overall, the persistence and morphology of the L. fucensis gill symbiosis relates to the intensity of vent flux and indicates that specimens from a variety of habitats may be necessary to characterize the morphological variability of gill-hosted symbioses in other molluscs
Influence of density-dependent food consumption, foraging and stacking behaviour on the growth rate of the Northern abalone, Haliotis kamtschatkana
Growth of abalone in the wild and hatchery is density-dependent in response to intraspecific competition for food and/or space. To determine if a candidate aquaculture species, Haliotis kamtschatkana, exhibits density-dependent growth we raised animals at three density levels and two food treatments: unlimited (ad libitum) and rationed (individual portions were the same among density treatments). We also tested for differences in food consumption, foraging patterns and stacking behaviour among the density levels. We observed density-dependent growth in the rationed treatments, indicating that relatively high growth rates at lower densities are driven, in part, by factors other than differences in food consumption. However, overall the quantity of food consumed related directly to growth; treatments fed ad libitum had higher growth rates. Furthermore, even when food was provided in excess, foraging was restricted to ~ 2 h after sunset in all treatments and the amount consumed per abalone was significantly lower at high densities. This is probably because high density animals could not access the food provided: fewer were observed foraging and they had to move from prominent stacks. Our results indicate that both temporal and spatial access to food are critical and that managers can observe foraging and stacking by abalone in tanks to determine if a specific design will limit food consumption, and ultimately growth
More rapid and severe disease outbreaks for aquaculture at the tropics: implications for food security
Aquaculture is replacing capture fisheries in supplying the world with dietary protein. Although disease is a major threat to aquaculture production, the underlying global epidemiological patterns are unknown.We analysed disease outbreak severity across different latitudes in a diverse range of aquaculture systems.Disease at lower latitudes progresses more rapidly and results in higher cumulative mortality, in particular at early stages of development and in shellfish.Tropical countries suffer proportionally greater losses in aquaculture during disease outbreaks and have less time to mitigate losses.Synthesis and applications. Disease can present a major problem for food production and security in equatorial regions where fish and shellfish provide a major source of dietary protein. As the incidences of some infectious diseases may increase with climate change, adaptation strategies must consider global patterns in disease vulnerability of aquaculture and develop options to minimize impacts on food production.<br/
Both rare and common species make unique contributions to functional diversity in an ecosystem unaffected by human activities
Aim Rare species typically contribute more to functional diversity than common species. However, humans have altered the occupancy and abundance patterns of many species - the basis upon which we define ‘rarity’. Here, we use a globally unique dataset from hydrothermal vents – an untouched ecosystem – to test whether rare species over-contribute to functional diversity. Location Juan de Fuca Ridge hydrothermal vent fields, Northeast Pacific Ocean.Methods We first conduct a comprehensive review to set up expectations for the relative contributions of rare and common species to functional diversity. We then quantify the rarity and commonness of 37 vent species with relevant trait information to assess the relationship between rarity and functional distinctiveness - a measure of the uniqueness of the traits of a species relative to traits of coexisting species. Next, we randomly assemble communities to test whether rare species over-contribute to functional diversity in artificial assemblages ranging in species richness. Then, we test whether biotic interactions influence functional diversity contributions by comparing the observed contribution of each species to a null expectation. Finally, we identify traits driving functional distinctiveness using a distance-based redundancy analysis.Results Across functional diversity metrics and species richness levels, we find that both rare and common species can contribute functional uniqueness. Some species always offer unique trait combinations, and these species host bacterial symbionts and provide habitat complexity. Moreover, we find that contributions of species to functional diversity may be influenced by biotic interactions. Main Conclusions Our findings show that many common species make persistent, unique contributions to functional diversity. Thus, it is key to consider whether the abundance and occupancy of species have been reduced, relative to historical baselines, when interpreting the contributions of rare species to functional diversity. Our work highlights the importance of testing ecological theory in ecosystems unaffected by human activities for the conservation of biodiversity
Impact of temperature on an emerging parasitic association between a sperm-feeding scuticociliate and Northeast Pacific sea stars
Global warming has important implications for the dynamics and ecological impacts of emerging diseases. We investigated temperature effects on scuticociliate, Orchitophrya cf. stellarum, infections in ripe testes of two Pacific northeast sea stars (Asterina miniata Brandt and Pisaster ochraceus Brandt) using laboratory and field approaches. We predicted that a small increase in temperature would result in higher ciliate growth rates and heightened infection intensities. To test this we (1) cultured free-living O. stellarum at 10 and 15 °C and quantified ciliate abundance after 3 days, and (2) housed sea stars of both species at 10 and 15 °C for durations varying from 4 to 21 days and then measured the infection intensity. Ciliate densities in cultures were two orders of magnitude higher in the warmer treatment. Infection intensity was also temperature sensitive: greater proportions of testes were infected and infection stage was more advanced at 15 versus 10 °C, leading to a reduction in spermatozoa and regression of the germinal layer within three weeks. In seven field populations surveyed, we found a tight linear correlation between infection prevalence (percent infected sea stars) and infection intensity (proportion of infected testes per individual and mean infection score). However, 45% of P. ochraceus testes exhibited heavy infections versus 8% of A. miniata testes, which may relate to the different thermal habitat of each species: P. ochraceus occurs higher on the shore and likely reaches higher body temperatures at low tide. While the sex ratio of A. miniata is unbiased, P. ochraceus populations are consistently female-biased and show no relationship to infection prevalence (ranged from 30 to 90%). O. cf. stellarum infections of testes of both sea stars are prevalent in field populations, are highly temperature sensitive, and lead to rapid loss of reproductive potential
Global trade-offs of functional redundancy and functional dispersion for birds and mammals
AimThe diversity of birds and mammals is typically described in separate analyses, but species may play similar roles. Here, we develop a comparative trait framework for birds and mammals to provide a global quantification of the similarity of species roles (functional redundancy) and the breadth of roles across taxa (functional dispersion). We predict different contributions of birds and mammals to redundancy and dispersion, and unique geographical patterns of redundancy and dispersion by including both taxa.LocationGlobal.Time periodContemporary.Major taxa studiedBirds and mammals.MethodsWe systematically select, compile and impute the same six traits (i.e., a common currency of traits) across 15,485 bird and mammal species from multiple databases. We use these six traits to compute functional redundancy and functional dispersion for birds and mammals across all 825 terrestrial ecoregions. We then calculate the standardized effect size (SES) of these observed values compared with null expectations, based on a randomization of species composition (i.e., independent of differences in species richness).ResultsWe find that species‐rich regions, such as the Neotropics, have high functional redundancy coupled with low functional dispersion, characterizing a global trade‐off. Thus, in general, as species richness increases, the similarity in species functional roles also increases. We therefore suggest that different processes generate species richness/functional redundancy and functional dispersion, leading to a novel, and generally non‐tropical, distribution of hotspots of high functional dispersion across Madagascar, Eastern Asia and Western USA.Main conclusionsWe recommend consideration of both the similarity and the breadth of functional roles across species pools, including taxa that may play similar roles. We therefore suggest that functional redundancy, as a means of insurance, and functional dispersion, as an indicator of response diversity, should be evaluated further as conservation objectives
Incorporating otolith-isotope inferred field metabolic rate into conservation strategies
Fluctuating ocean conditions are rearranging whole networks of marine communities - from individual-level physiological thresholds to ecosystem function. Physiological studies support predictions from individual-level responses (biochemical, cellular, tissue, respiratory potential) based on laboratory experiments. The otolith-isotope method of recovering field metabolic rate has recently filled a gap for the bony fishes, linking otolith stable isotope composition to in situ oxygen consumption and experienced temperature estimates. Here, we review the otolith-isotope method focusing on the biochemical and physiological processes that yield estimates of field metabolic rate. We identify a multidisciplinary pathway in the application of this method, providing concrete research goals (field, modeling) aimed at linking individual-level physiological data to higher levels of biological organization. We hope that this review will provide researchers with a transdisciplinary 'roadmap', guiding the use of the otolith-isotope method to bridge the gap between individual-level physiology, observational field studies, and modeling efforts, while ensuring that in situ data is central in marine policy-making aimed at mitigating climatic and anthropogenic threats.</p
Projected losses of global mammal and bird ecological strategies
Species, and their ecological strategies, are disappearing. Here we use species traits to quantify the current and projected future ecological strategy diversity for 15,484 land mammals and birds. We reveal an ecological strategy surface, structured by life-history (fast-slow) and body mass (small-large) as one major axis, and diet (invertivore-herbivore) and habitat breadth (generalist-specialist) as the other. We also find that of all possible trait combinations, only 9% are currently realized. Based on species’ extinction probabilities we predict this limited set of viable strategies will shrink further over the next 100 years, shifting the mammal and bird species pool towards small, fast-lived, highly fecund, insect-eating, generalists. In fact, our results show that this projected decline in ecological strategy diversity is much greater than if species were simply lost at random. Thus, halting the disproportionate loss of ecological strategies associated with highly threatened animals represents a key challenge for conservation
Ecological distinctiveness of birds and mammals at the global scale
Ecologically distinct species - species with distinct trait combinations - are not directly prioritized in current conservation frameworks. The consequence of this blind spot means species with the most distinct ecological strategies might be lost. Here, we quantify ecological distinctiveness, based on six traits, for 10,960 bird and 5,278 mammal species, summarizing species-level ecological irreplaceability. We find that threatened birds and mammals are, on average, more ecologically distinct. Specific examples of ecologically distinct and highly threatened species are Great Indian Bustard, Amsterdam Albatross, Asian Elephant and Sumatran Rhinoceros. These species have potentially irreplaceable ecological roles and their loss could undermine the integrity of ecological processes and functions. Yet, we also identify ecologically distinct widespread generalists, such as Lesser Black-backed Gull and Wild Boar. These generalist species have distinct ecological strategies that allow them to thrive across multiple environments. Thus, we suggest that high ecological distinctiveness is associated with either high extinction risk or successful hyper-generalism. We also find that ecologically distinct species are generally charismatic (using a previous measure of public perceptions of charisma). We thus highlight a conservation opportunity: capitalizing on public preferences for charismatic species could provide support for the conservation of the most ecologically distinct birds and mammals. Overall, our prioritization framework supports the conservation of species with irreplaceable ecological strategies, complementing existing frameworks that target extinction risk and evolutionary distinctiveness
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