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20 results for “invertebrate predators”
Data from: Changes in Invertebrate Food Web Structure Between High- and Low-productivity Environments are Driven by Intermediate but Not Top Predator Diet Shifts
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Data from: Predator-prey Interactions of Terrestrial Invertebrates are Determined by Predator Body Size and Species Identity
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Predation shapes invertebrate diversity in tropical but not temperate seagrass communities
<p>1. The hypothesis that biotic interactions are stronger at lower relative to higher latitudes has a rich history, drawing from ecological and evolutionary theory. While this hypothesis suggests that stronger interactions at lower latitudes may contribute to the maintenance of contemporary patterns of diversity, there remain few standardized biogeographic comparisons of community effects of species interactions. 2. Using marine seagrasses as a focal ecosystem of conservation importance and sessile marine invertebrates as model prey, we tested the hypothesis that predation is stronger at lower latitudes and can shape contemporary patterns of prey diversity. To further advance understanding beyond prior studies, we also explored mechanisms that likely underlie a change in interaction outcomes with latitude. 3. Multiple observational and experimental approaches were employed to test for effects of predators, and the mechanisms that may underlie these effects, in seagrass ecosystems of the western Atlantic Ocean spanning 30 degrees of latitude from the temperate zone to the tropics. 4. In predator exclusion experiments conducted in a temperate and a tropical region, predation decreased sessile invertebrate abundance, richness, and diversity on both natural and standardized artificial seagrass at tropical but not temperate sites. Further, predation reduced invertebrate richness at both local and regional scales in the tropics. Additional experiments demonstrated that predation reduced invertebrate recruitment in the tropics but not the temperate zone. Finally, direct observations of predators showed higher but variable consumption rates on invertebrates at subtropical and tropical relative to temperate latitudes. 5. Together, these results demonstrate that strong predation in the tropics can have consequential impacts on prey communities through discrete effects on early life stages as well as longer-term cumulative effects on community structure and diversity. Our detailed experiments also provide some of the first data linking large-scale biogeographic patterns, community-scale interaction outcomes, and direct observation of predators in the temperate zone and tropics. Therefore, our results support the hypothesis that predation is stronger in the tropics, but also elucidate some of the causes and consequences of this variation in shaping contemporary patterns of diversity. 16-Sep-2019</p>
Linking agri-environment scheme habitat area, predation and the abundance of chick invertebrate prey to the nesting success of a declining farmland bird
<p>Across Europe, farmland bird populations have continued to decline since the 1970s owing to the intensification of farming practices. Studies of such declines have tended to focus specifically on either the impacts of habitats (nesting and foraging), nest predators or prey availability on bird demographics. The study presented here provides new insights into the relative effects of each of these factors on Yellowhammer nest survival. The Yellowhammer was selected for this study as it is a UK red-listed bird species whose population is in decline across much of Europe. We use a long-term dataset of 147 nests, monitored between 1995 and 2007, to provide an insight into how Yellowhammer nest survival is influenced by nesting habitat (nest concealment and nest height), foraging habitats (habitat coverage within 100 m of nests), the removal of nest predators (Magpie Pica pica abundance as an inverse measure of avian predator removal through gamekeeping) and food availability (measured with a D-vac invertebrate suction sampler). Our results indicated that Yellowhammer hatching success was negatively related to the coverage of spring agri-environment scheme habitats, a group which represents invertebrate-rich agri-environment habitats, but hatching success increased with nest height. Fledging success was positively related to the coverage of the seed-rich habitat Wild Bird Seed mixture. The farm-level abundance of Yellowhammer chick-food invertebrates declined over the study period. Our results highlight the importance of simultaneously considering multiple agents that shape avian breeding success, i.e. their ability to produce offspring, to inform conservation management. Our key finding for land managers relates to the positive relationship between the proportion seed rich foraging habitat within the Yellowhammer's average foraging range and Yellowhammer fledging success, which shows that a habitat intended primarily to provide winter food resources is also important to breeding birds. Chick food abundance in this habitat was, however, similar to broadleaf and cereal crops. We recommend that this habitat should be provided near to potential Yellowhammer nesting sites and adjacent to invertebrate-rich agri-environment scheme habitats such as beetle banks and conservation headlands to further boost invertebrate resources for a declining farmland bird.</p>
Observations of invertebrate predation on Xenopus mellotropicalis frogs.
<p>We report here for the first time our observations of predation events on <em>Xenopus mellotropicalis</em> frogs that illustrate the diversity of predators for that species.</p>
Data from: Plant functional traits affect invertebrate predator diversity via bottom-up effects in a deadwood-based food web
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Predation shapes invertebrate diversity in tropical but not temperate seagrass communities
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Linking agri-environment scheme habitat area, predation and the abundance of chick invertebrate prey to the nesting success of a declining farmland bird
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Data from: Gape-limited predators as agents of selection on the defensive morphology of an invasive invertebrate
Invasive species have widespread and pronounced effects on ecosystems and adaptive evolution of invaders is often considered responsible for their success. Despite the potential importance of adaptation to invasion, we still have limited knowledge of the agents of natural selection on invasive species. Bythotrephes longimanus, a cladoceran zooplankton, invaded multiple Canadian Shield lakes over the past several decades. Bythotrephes have a conspicuous caudal process (tail spine) that provides a morphological defense against fish predation. We measured viability selection on the longest component of the Bythotrephes spine, the distal spine segment, through a comparison of the lengths of first and second instar Bythotrephes collected from lakes differing in the dominance of gape-limited predation (GLP) and non-gape-limited predation (NGLP) by fish. We found that natural selection varied by predator gape-limitation, with strong selection (selection intensity: 0.20-0.79) for increased distal spine length in lakes dominated by GLP, and no significant selection in lakes dominated by NGLP. Further, distal spine length was 17% longer in lakes dominated by GLP, suggesting the possibility of local adaptation. As all study lakes were invaded less than twenty years prior to our collections, our results suggest rapid divergence in defensive morphology in response to selection from fish predators.
Heatwave induced invertebrate predation reshapes the plankton community
<p>Climate change stressors including warming and heatwaves can alter zooplankton composition and dominance patterns in shallow lakes, which can disrupt ecosystem function and curtail ecosystem services. To understand such changes, we performed a mesocosm experiment with controls reflecting the present temperature conditions and a treatment reflecting a future climate change scenario, including heatwaves of 0-8°C. In the future climate scenario, the predatory invertebrate, <em>Mesostoma</em> exerted a strong top-down control particularly on <em>Daphnia</em>, resulting in a switch in the herbivore dominance to <em>Ceriodaphnia</em>. Cyclopoid copepods were the least affected taxa but showed tendencies to sustain longer into the winter at elevated temperatures. A complementary predation experiment revealed that <em>Mesostoma</em> feed at a higher rate on <em>Daphnia</em> than on <em>Ceriodaphnia</em> and cyclopoid copepods. In addition to the food-chain alterations, the algal biomass and cyanobacteria increased with warming which has considerable implications for management of shallow lakes.</p>
Indirect control of decomposition by an invertebrate predator
<p>Datasets and R scripts for the above article.</p>
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Data from: Viability selection by invertebrate predators in the polyphenic scavenger fly Sepsis thoracica
Predation is a major factor influencing the fitness and life history of animals. Two key traits affecting prey survival are body size and coloration. Sepsis thoracica males display a sigmoid relationship between these two traits, defining a size threshold above which investment in melanin drastically drops, producing small melanic (black) or large amber morphs. In trying to understand the evolution of this rare dimorphism, we performed laboratory predation experiments to estimate the intensity of adult viability selection exerted by various arthropod predators (bugs, flies, spiders) on male body size and coloration. Selection was performed against two different backgrounds mimicking the natural habitat (dung and grass) in which the camouflage and/or warning effect of the morphs should vary. Body size was mainly under positive selection (larger survived better), which overpowered selection on coloration and varied somewhat among predator species but not backgrounds. No disruptive selection was found, nor did selection change the sigmoid relationship between the two traits. We conclude that, for this fly, predator evasion and escaping skills determined by body size are more effective against invertebrate predators than its conspicuousness determined by coloration, contrasting what has been found for vertebrate predators, where prey coloration is important and negative selection on size dominates. Because arthropod predators have strong effects on insect populations, the positive directional selection imposed by invertebrate predators is likely an important force driving the evolution of body size in S. thoracica and insects in general.
Data from: Top-down control by an aquatic invertebrate predator increases with temperature but does not depend on individual behavioural type
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Assisted colonization of a regionally native predator impacts benthic invertebrates in fishless mountain lakes
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Data from: Gape-limited predators as agents of selection on the defensive morphology of an invasive invertebrate
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Data from: Viability selection by invertebrate predators in the polyphenic scavenger fly Sepsis thoracica
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Heatwave induced invertebrate predation reshapes the plankton community
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Number of drifting and emerging invertebrates under control and predator exposure conditions in an outdoor mesocosm experiment
<p>Predator-prey interactions drive adaptation in aquatic communities, shaping invertebrate behaviour. In response to predation risk, invertebrates may exhibit behavioral changes, such as drifting with the downstream current or altering the timing of emergence to avoid predators. To investigate predator-induced drift behaviour and emergence patterns, we collected drifting and emerging invertebrates from an outdoor mesocosm system (<em>ExStream</em> system) between March and April 2022. The study examined the effects of indirect and direct predation pressure on drift and emergence by recording the number, lowest possible taxonomic resolution, and size of invertebrates. Drift nets attached to the outflow and emergence nets placed over the mesocosms were collected every 24 hours at 4 PM over nine days. Mesocosms were maintained under either control or predator exposure conditions. In the predator exposure treatment, invertebrates were first exposed to elevated chemical cues from fish (<em>Gasterosteus aculeatus</em> and <em>Cottus rhenanus</em>) to simulate indirect predation. On the fifth day after sampling, one <em>Cottus rhenanus</em> was introduced into each predator-treated mesocosm to simulate direct predation.</p>
Managing island-invasive ants: invertebrate predation, targeted suppression and subsequent endemic insect recovery
<p>These two datasets accompany the manuscript of the same title.</p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
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