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Fig. 1 in Diet composition and feeding strategy of the southern pipefish Syngnathus folletti in a Widgeon grass bed of the Patos Lagoon Estuary, RS, Brazil
Fig. 1. Relationship between mouth gape (a) and prey size (b) with total length (in mm) of female (open circles) and male (dots) individuals of the southern pipefish Syngnathus folletti.
Fig. 3 in Diet composition and feeding strategy of the southern pipefish Syngnathus folletti in a Widgeon grass bed of the Patos Lagoon Estuary, RS, Brazil
Fig. 3. Conceptual diagram showing the microhabitat distribution within the Widgeon grass bed of some benthic macroinvertebrates consumed by Syngnathus folletti. Gastropoda: 1. Heleobia australis; Tanaidacea: 2. Kalliapseudes schubartii, 3. Tanais stanfordi; Isopoda: 4. Dies fluminensis, 5. Uromunna peterseni; Amphipoda: 6. Mellita mangrovi.
Figure 3 in Do mites eat and run? A systematic review of feeding and dispersal strategies
Figure 3. Multivariate generalized linear mixed-effects model results showing correlations (see coloured scale for total range) of different dispersal modes among species.
Figure 2 in Do mites eat and run? A systematic review of feeding and dispersal strategies
Figure 2. Multivariate generalized linear mixed-effects model results showing joint effects of feeding strategies on dispersal modes in mites. Posterior means are given (dots), along with 50% (thick lines) and 95% (thin lines) credible intervals for Acariformes (orange) and Parasitiformes (violet). If the 95% credible intervals do not cover zero (intense colours), the particular dispersal mode is significantly more frequent or less frequent than expected by chance (at the α = 0.05 level).
Figure 4 in Do mites eat and run? A systematic review of feeding and dispersal strategies
Figure 4. Relationship between the number of studies carried out on the dispersal syndrome of a given mite species and the proportion of dispersal modes revealed. The shaded region depicts 95% confidential intervals around the fit. Points are observed data points. Note the logarithmic scale on both axes.
Figure 1 in Do mites eat and run? A systematic review of feeding and dispersal strategies
Figure 1. Database collection summary. PRISMA (preferred reporting items for systematic reviews and meta-analyses) diagram detailing the procedure for the identification and inclusion of relevant publications.
Fig. 5 in Feeding strategies and competition between terrestrial Haemadipsa leeches (Euhirudinea: Arhynchobdellida) in Danum Valley rainforest (Borneo, Sabah)
Fig. 5. Typical postures of haemadipsid leeches on the example of Haemadipsa picta Moore, 1929. A – in resting position; B – in at- tack position. Photo ©Ryszard Laskowski, used with permission.
Fig. 4 in Feeding strategies and competition between terrestrial Haemadipsa leeches (Euhirudinea: Arhynchobdellida) in Danum Valley rainforest (Borneo, Sabah)
Fig. 4. The dispersion plot depicting the correlation between the length and preferred altitude of attack of Haemadipsa picta Moore, 1929. The best-fitting logarithmic curve is drawn and the following equation of regression is assigned to this curve: y = 30.682 × log10(x) - 22.7252.
Fig. 3 in Feeding strategies and competition between terrestrial Haemadipsa leeches (Euhirudinea: Arhynchobdellida) in Danum Valley rainforest (Borneo, Sabah)
Fig. 3. An average body length (mm) of Haemadipsa picta Moore, 1929 individuals hunting during morning (M) and afternoon (A). The line segments indicate 95% confidence intervals.
Fig. 1. A in Feeding strategies and competition between terrestrial Haemadipsa leeches (Euhirudinea: Arhynchobdellida) in Danum Valley rainforest (Borneo, Sabah)
Fig. 1. A – Location of Danum Valley Conservation Area (DVCA) in Sabah (Malaysia); B – Danum Valley Field Centre (DVFC) vicinity. Grey circles signify sampling sites in the primary (P1–P5) and secondary (S1, S2) rainforest. Modified from Willott et al. (2000).
Fig. 2 in Feeding strategies and competition between terrestrial Haemadipsa leeches (Euhirudinea: Arhynchobdellida) in Danum Valley rainforest (Borneo, Sabah)
Fig. 2. An average number of individuals (found on 100 m2 plot) occurring in the particular type of habitat. A – Haemadipsa picta Moore, 1929; B – H. subagilis (Moore, 1929). The line segments indicate 95% confidence intervals.
Investigating Host Feeding Strategy as a Determinant of Insect Gut Microbial Community Profile at the Sevilleta National Wildlife Refuge, New Mexico
Diverse microbial communities live in the gut regions of animals. The precise ecological and evolutionary circumstances that govern relationships between hosts and their gut communities is unclear. In this study, we hypothesize that host feeding strategy shapes the microbial communities within the gut systems of insects. We collected five insect species from the Sevilleta National Wildlife Refuge that exhibited herbivorous, detritovorous and carnivorous diets. Using gut samples from the insects we measured if and how microbial communities are shaped based on any effect host feeding strategy might have. Preliminary analysis of bacterial communities using 16S rDNA sequences has thus far revealed that the sampled community profiles initially appear to show signs of being determined by host feeding type. Analysis has also shown that sequences from the phyla Firmicutes and Proteobacteria appear to contribute most significantly to the differences between communities of different feeding types. We expect that upon further data recovery, the extent of the effect host feeding type has on the communities will be clarified. Additionally we intend to incorporate bacterial community data from previous studies to further broaden our sample set. We expect our results to further define the ecological circumstances that shape the microbial populations within living systems.
Data from: Feeding strategies of brown howler monkeys in response to variations in food availability
Primates display varying degrees of behavioral flexibility that allow them to adjust their diet to temporal changes in food availability. This trait might be critical for the survival of folivorous-frugivorous species inhabiting small forest fragments, where the availability of food resources tends to be lower than in large fragments and continuous forests. However, the scarcity of studies addressing this issue hampers our understanding of the adaptive behaviors that favor the survival of these primates in low-quality habitats. We conducted a 36-mo study testing the hypothesis that brown howler monkeys (Alouatta guariba clamitans) are able to adjust their diet in response to local and seasonal changes in resource availability. We compared the diet of six free-ranging groups inhabiting three small (<10 ha) and three large (>90 ha) Atlantic forest fragments in southern Brazil and estimated the temporal availability of their top food species (i.e., those species that together contribute ≥80% of total feeding records). We found that brown howlers exploited similarly rich diets in small (45, 54, and 57 plant species) and large (48, 51, and 56 species) fragments. However, intermonth diet similarity was higher for groups in small fragments, where howlers also fed on plant items from nine alien species. Fruits and leaves were the most consumed plant items in both small (42% and 49% of feeding records, respectively) and large (51% and 41%, respectively) fragments. The consumption of young leaves was higher in small than in large fragments, whereas the consumption of other plant items did not show a pattern related to fragment size. Regarding the contribution of growth forms as food sources, only the exploitation of palms showed a pattern related to fragment size. Palms contributed more to the diet of groups inhabiting large fragments. The availability of seasonal food items–ripe fruits and young leaves–influenced their consumption in both habitat types. Therefore, brown howlers cope with local and seasonal fluctuations in food availability by opportunistically exploiting resources. We believe that this feeding flexibility is a key component of the phenotypic plasticity that enables howlers to thrive in disturbed habitat patches, where periods of scarcity of preferred foods shall be more common.
Dataset of: Deconvolving feeding niches and strategies of abyssal holothurians from their stable isotope, amino acid, and fatty acid composition
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Fig. 1 in Feeding strategy of the introduced Astronotus crassipinnis (Cichlidae) in upper Paraná river floodplain
Fig. 1. Upper Paraná River floodplain with Nupelia field laboratory in detail.
Termite trait data from: Continental-scale shifts in termite diversity and nesting and feeding strategies
<p>Typically, termites are treated as a single guild, which ignores important internal diversity, including diverse feeding and nesting traits. These termite traits are crucial for both ecosystem-level fluxes and trophic webs, with implications for vertebrate species. Despite their ecological importance, the large-scale distribution of termite feeding and nesting traits and the relationship with termite diversity is largely unknown. We investigated whether functional diversity, species richness, and feeding (wood, litter, grass, dung) and nesting trait (aboveground mound, belowground nest, inside tree or outside tree nest) distributions of termites were climatically control. To address this gap, we assembled a continental-scale database of termite traits and occurrence in Australia and modelled termite nesting and feeding traits in response to macroclimate. Functional richness and evenness increased primarily with temperature. Australia showed multiple hotspots of termite diversity with each hotspot showing a distinct guild composition. The large-scale distribution of nesting traits showed that aboveground nesting species were the most common nesting guild in the dry and wet tropics while belowground nesting dominated in seasonally cold arid environments, demonstrating a strong climatic control on nesting strategy. Given their large biomass and many interactions with other species, the macro-ecology of termite traits may be especially important in predicting shifts in other species' distributions at continental and global scales.</p>
Environmental data from: Feeding strategy and dietary preference shape the microbiome of epipelagic copepods in a warm nutrient-impoverished ecosystem
<p><span>Copepods provide a rich organic microenvironment allowing the settlement and proliferation of microorganisms, forming dynamic microbial hotspots in the oceans. Such symbiotic associations in the plankton were previously hypothesized to be especially developed in warm oligotrophic seas, as they may serve as alternative sources of nutrients in biologically-poor waters. Aiming to better understand how copepod microbiomes are shaped in an oligotrophic sea, we characterized microbiota associated with three dominant coastal epipelagic copepod species in the ultra-oligotrophic Eastern Mediterranean Sea using amplicon sequencing of the 16S rRNA gene</span><span>. Our results show that copepod-associated microbial communities were host-specific rather than determined by seasonal environmental changes. In the filter-feeding copepod with a tendency to herbivory, <em>Temora stylifera</em>, microbial diversity was low and relatively stable throughout the year. In contrast, omnivorous copepods, the ambush-feeding <em>Oithona nana</em>, and the mixed-feeding <em>Centropages ponticus</em> harbored more diverse microbiomes dominated by transient taxa. We suggest that filter-feeding strategy and narrow food spectrum can limit copepod-microbe interactions, while the ambush and mixed feeding strategies combined with omnivory confer higher microbial diversity. Filter feeders may reduce the recruitment of opportunistic microbes by maintaining high fidelity associations, as indicated by the large number of core taxa in <em>T. stylifera</em>. We underline the importance of the copepod-microbe associations in nutrient-impoverished ecosystems, based on predicted enrichment of nitrogen metabolism in the core micro</span>biome<span>, mostly during summer when the shallow coastal waters are nitrogen-depleted. </span></p>
Termite trait data from: Continental-scale shifts in termite diversity and nesting and feeding strategies
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Data from: Feeding strategies of the Pleistocene insular dwarf elephants <em>Palaeoloxodon falconeri</em> and <em>Palaeoloxodon mnaidriensis</em> from Sicily (Italy)
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Data from: Feeding strategies of brown howler monkeys in response to variations in food availability
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