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211 results for “Feeding habits”
Fig. 3 in Feeding habits and habitat of herbivorous mammals from the Early-Late Hemphillian (Miocene) of Costa Rica
Fig. 3. Comparative analysis of carbon and oxygen stable isotope values in dental enamel from fossil herbivorous mammals of the San Gerardo de Limoncito locality.
Fig. 1. A in Feeding habits and habitat of herbivorous mammals from the Early-Late Hemphillian (Miocene) of Costa Rica
Fig. 1. A. Geographic location of studied area. B. Geological map of the San Gerardo de Limoncito area, modified from Denyer and Alvarado (2007).
Fig. 3 in The hidden threat: Exploring the parasite burden and feeding habits of invasive raccoon dogs (Nyctereutes procyonoides) in central Europe
Fig. 3. Examples of ecto- and endoparasites and parasite eggs found in fecal investigation of the examined raccoon dogs, A-B ectoparasites, C-D endoparasites, E-F eggs from endoparasites found through MIFC. A: Chaetopsylla globiceps; B: Trichodectes canis; C: Isthmiophora melis; D: Echinococcus multilocularis; E: eggs from Alaria alata; F: Egg from Toxocara canis.
Fig. 2 in The hidden threat: Exploring the parasite burden and feeding habits of invasive raccoon dogs (Nyctereutes procyonoides) in central Europe
Fig. 2. Examples of different stomach contents of the examined raccoon dogs, A-F each from one stomach. A: mouse, plants, amphibian; B: grass, maize, feathers and bird foot; C: amphibian, insects; D: insects; E: opened stomach filled with grass; F: hair, plant material, feathers, bones and hair.
Fig. 1 in The hidden threat: Exploring the parasite burden and feeding habits of invasive raccoon dogs (Nyctereutes procyonoides) in central Europe
Fig. 1. Origin of the examined raccoon dogs in the different federal states of Germany, red areas show the sampling sites (N = 73). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in The hidden threat: Exploring the parasite burden and feeding habits of invasive raccoon dogs (Nyctereutes procyonoides) in central Europe
Fig. 4. Diet of the raccoon dog Nyctereutes procyonoides according to percentages of the individual components, components that cannot be further determined are summarized in the respective class, with * marked species are most likely to have been eaten as carrion. On the right side are listed the parasites, which are transmitted via a known intermediate host, which made up part of the food of the examined animals.
Fig. 1 in Diet composition and feeding habits of the eyespot skate, Atlantoraja cyclophora (Elasmobranchii: Arhynchobatidae), off Uruguay and northern Argentina
Fig. 1. Study area showing the location of trawl stations (black dots) and cells of the fishing grid (black rectangles) where individuals of Atlantoraja cyclophora were captured off North Argentina and Uruguay.
Fig. 4 in Diet composition and feeding habits of the eyespot skate, Atlantoraja cyclophora (Elasmobranchii: Arhynchobatidae), off Uruguay and northern Argentina
Fig. 4. Mean number of shrimps and teleosts consumed for Atlantoraja cyclophora from off Uruguay and northern Argentina by season and region, respectively.
Fig. 3 in Diet composition and feeding habits of the eyespot skate, Atlantoraja cyclophora (Elasmobranchii: Arhynchobatidae), off Uruguay and northern Argentina
Fig. 3. Changes in consumption of different prey with body size, maturity stage, season and region of Atlantoraja cyclophora from off Uruguay and northern Argentina estimated by generalized linear models for number of shrimps, crabs and teleosts. In shrimps: warm season with solid lines and open circles; cold season with dashed lines and solid circles. In teleosts: north region with solid lines and open circles; south region with dashed lines and solid circles.
Fig. 2 in Diet composition and feeding habits of the eyespot skate, Atlantoraja cyclophora (Elasmobranchii: Arhynchobatidae), off Uruguay and northern Argentina
Fig. 2. Cumulative mean Shannon diversity index as a function of sample size for prey of Atlantoraja cyclophora from off Uruguay and northern Argentina. Dashed lines indicate standard deviation.
Fig. 5 in Diet composition and feeding habits of the eyespot skate, Atlantoraja cyclophora (Elasmobranchii: Arhynchobatidae), off Uruguay and northern Argentina
Fig. 5. Quantile regressions of carapace width (CW) of crabs, cephalothorax length (CL) of shrimps and total length (TL) of teleosts and total length of Atlantoraja cyclophora. The solid, dashed and dotted lines are 5%, 50% and 95% quantile regressions, respectively.
Linked collectors and determiners for: Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits.
Natural history specimen data linked to collectors and determiners held within, "Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/726c8af4-e8a8-46cb-ab0b-0ef22e432dae">https://bionomia.net/dataset/726c8af4-e8a8-46cb-ab0b-0ef22e432dae</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/726c8af4-e8a8-46cb-ab0b-0ef22e432dae">https://gbif.org/dataset/726c8af4-e8a8-46cb-ab0b-0ef22e432dae</a>. Formatted as a Frictionless Data package.
Data from: Andriollo T., Michaux J.R., Ruedi M. (2021). Food for everyone: differential feeding habits of cryptic bat species inferred from DNA metabarcoding. Molecular Ecology
<p><strong>Supporting data for:</strong> Andriollo T., Michaux J.R., Ruedi M. (2021). Food for everyone: differential feeding habits of cryptic bat species inferred from DNA metabarcoding. Molecular Ecology. https://doi.org/ 10.1111/mec.16073</p> <p>Raw DNA sequences of prey of <em>Plecotus auritus</em>, <em>P. austriacus</em> and <em>P. macrobullaris</em> with complete sampling information and taxonomic assignations. Data separated by semicolums as follows:</p> <p>Sample name; Dataset; Colony; Bat species; Date; Season; Read numbers (Size); DNA sequence; Lowest taxonomic identification (ID_MOTU); Family; Order; Class; Is the sequence attributable to the diet or not (Diet)</p>
FIG. 2 in Feeding habits of the first European colobine, (Mammalia, Primates): evidence from a comparative dental microwear analysis with modern cercopithecids
FIG. 2. — Dental facets nine of second molars for extant and extinct cercopithecids displaying dental microwear scars: A, Nasalis larvatus (Wurmb, 1787) (ZSM-1907-4023); B, Lophocebus albigena (Gray, 1850) (RMCA-83-006-0276); C, Chlorocebus aethiops (Linnaeus, 1758) (MNHN-CG-1972-309); D, Papio hamadryas hamadryas Linnaeus, 1758 (SNG-15831); E, Mesopithecus delsoni/ pentelicus (HD-340); F, M. pentelicus (NHMW-1998z77-14). Scale bars: 300 μm.
Fig. 1 in Feeding habits and morphometry of Iheringichthys labrosus (Lütken, 1874) in the Uruguay River (Uruguay)
Fig. 1. Map of the study area. Samples sites are located on the Uruguay River: LC: Las Cañas, NB: Nuevo Berlín and Y: Yaguareté.
Fig. 2 in Feeding habits and morphometry of Iheringichthys labrosus (Lütken, 1874) in the Uruguay River (Uruguay)
Fig. 2. Amundsen diagrams for individuals of the size class 1(a-c) and 2 (b-d). Superior diagrams correspond to individual obtained in May and inferior to individual obtained in November. COP: Copepoda, TRIC: Trichoptera, OTH: others, HYD: Hydracharina, CLAD: Cladocera, GAS: Gastropoda, NEM: Nematoda, OST: Ostracoda, BIV: Bivalvia, DIP: Diptera, EPH: Ephemeroptera, IMM. BIV: immature bivalvia, ODO: Odonata, COL: Coleoptera, COLL: Collembola.
Fig. 4 in Feeding habits and morphometry of Iheringichthys labrosus (Lütken, 1874) in the Uruguay River (Uruguay)
Fig. 4. Correspondence analysis between prey items (circles) and studied months (squares). (a) Prey items of individuals of the size class 1 (b) Prey items of individuals of the size class 2. Note that the analysis resolved in only one dimension.
Fig. 3 in Feeding habits and morphometry of Iheringichthys labrosus (Lütken, 1874) in the Uruguay River (Uruguay)
Fig. 3. Correspondence analysis between prey items (circles) and fish size ranges (squares), 1 and 2. Note that the analysis resolved in only one dimension.
Fig. 5 in Temporal and ontogenetic variations in feeding habits of Hollandichthys multifasciatus (Teleostei: Characidae) in coastal Atlantic rainforest streams, southern Brazil
Fig. 5. Proportion of autochthonous and allochthonous food items in the diet of Hollandichthys multifasciatus according to the method proposed by Costello (1990).
Fig. 3 in Temporal and ontogenetic variations in feeding habits of Hollandichthys multifasciatus (Teleostei: Characidae) in coastal Atlantic rainforest streams, southern Brazil
Fig. 3. Monthly distribution of the environmental factors measured pH (a), water temperature (b) and water current (c) in the streams investigated.
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