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Fig. 10 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 10. Bisulcopsallus pallidus: Male genitalia (AMNH_PBI 00068621; entire vesica drawn at 50% scale of other structures).
Fig. 5 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 5. Angelopsallus gregalis (upper) (male genitalia: AMNH_PBI 00077130; female genitalia: AMNH_PBI 00077131). Arizonapsallus stonedahli (lower) (male genitalia: AMNH_PBI 00096983, right paramere only, AMNH_PBI 00063971; female genitalia: AMNH_PBI 00063971).
Fig. 4 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 4. Arizonapsallus stonedahli: A. Lateral view of head. B. Mesothoracic spiracle and metathoracic scent-efferent system. C. Setae on costal margin of wing. D. Ventral view of pretarsus.
Fig. 3 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 3. Habitus views of Phymatopsallus-group taxa: Cercocarpopsallus gracilis, Knightopsallus, Phymatopsallus, Salicopsallus, Stictopsallus, Schaffneropsallus (see appendix for specimens examined).
Fig. 2 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 2. Habitus views of Phymatopsallus-group taxa: Ceratopsallus croceus–Ceratopsallus vauqueliniae, Cercocarpopsallus bispinosus (see appendix for specimens examined).
Fig. 6 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 6. Bisulcopsallus fuscipunctatus: A. Lateral view of head. B. Mesothoracic spiracle and metathoracic scent-efferent system. C. Setae on costal margin of wing. D. Lateral view of pretarsus. E. Lateral view of pygophore. F. Bisulcopsallus huachucae: Confocal microscopic image, lateral view, showing in situ position of vesica in pygophore and abdomen.
Fig. 1 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 1. Habitus views of Phymatopsallus-group taxa: Angelopsallus, Arizonapsallus, Bisulcopsallus, Ceratopsallus aquilonius (see appendix for specimens examined).
Fig. 9 in Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae)
Fig. 9. Bisulcopsallus huachucae: Male genitalia (AMNH_PBI 00062967; entire vesica drawn at 50% scale of other structures).
Figure 3 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 3. Acmaeodera conoidea Fall, paralectotype ♂. a) Dorsal view. b) Ventral view. c) Lateral view. d) Broadly arcuate clypeus e) Third stria split near umbone. f) Protarsal claw.
Figure 2. Male genitalia, Acmaeodera tubulus species group. a in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 2. Male genitalia, Acmaeodera tubulus species group. a) A. natlovei new species. b) A. neoneglecta. c) A. tubulus. d) A. neglecta. e) A. opuntiae.
Figure 1. Acmaeodera natlovei new species. a in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 1. Acmaeodera natlovei new species. a) Holotype, dorsal view. b) Holotype, ventral view. c) Holotype, lateral view. d) Holotype, clypeus. e) Paratype protarsal claw ♂. f) Paratype protarsal claw ♀.
Data for: Biomechanical adaptations enable phoretic mite species to occupy distinct spatial niches on host burying beetles
<p>Niche theory predicts that ecologically similar species coexist by minimising interspecific competition through niche partitioning. Therefore understanding the mechanisms of niche partitioning is essential for predicting interactions and coexistence between competing organisms. Here we study two phoretic mite species, <em>Poecilochirus carabi, </em>and <em>Macrocheles nataliae</em> that coexist on the same host-burying beetle <em>Nicrophorus vespilloides </em>and use it to 'hitchhike' between reproductive sites. Field observations revealed clear spatial partitioning between species in distinct host body parts. <em>P. carabi</em> preferred the ventral side of the thorax, whereas <em>M. nataliae </em>were exclusively found ventrally at the hairy base of the abdomen. Experimental manipulations of mite density showed that each species preferred these body parts, largely regardless of the density of the other mite species on the host beetle. Force measurements indicated that this spatial distribution is mediated by biomechanical adaptations, because each mite species required more force to be removed from their preferred location on the beetle. While <em>P. carabi</em> attached with large adhesive pads to the smooth thorax cuticle, <em>M. nataliae</em> gripped abdominal setae with their chelicerae. Our results show that specialist biomechanical adaptations for attachment can mediate spatial niche partitioning among species sharing the same host.</p>
Fig. 1 in (macro-) Evolutionary ecology of parasite diversity: From determinants of parasite species richness to host diversification
Fig. 1. Expression of the basic transmission rate (R0) for the case of microparasites (i.e. viruses) and macroparasites (i.e. helminths with direct transmission) (for derivations of these expressions see Morand and Deter, 2008), emphasizing the importance of two host traits, longevity and density, as likely determinants of parasite invasion and then parasite species richness. In the right panel, relationships showing that both density and longevity are in allometry with host body mass (after Brown, 1995).
Fig. 2 in (macro-) Evolutionary ecology of parasite diversity: From determinants of parasite species richness to host diversification
Fig. 2. (A) Variability of ectoparasite species richness among 113 families of mammals (20 orders) (data from Kim, 1985;see Poulin and Morand, 2004). (B) Ectoparasite species richness is related to mammal diversification. The statistical analysis follows Nunn et al. (2004), where the change in the number of descendent clades is related to the change in the number of ectoparasite species, estimated using a modified version of the independent contrast method (Agapow and Isaac, 2002), for each node of the mammal phylogeny (from Binida-Emonds et al., 2007).
FIGURE 6 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form
FIGURE 6 The temperature inside nests of O. lunifer larvae compared with ambient over a 24 h cycle: (a) tree-hugger nests (n = 9) and (b) ground nests (n = 14). The data point for each nest is the mean of seven to eight consecutive days of measurement.
FIGURE 5 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form
FIGURE 5 Ochrogaster lunifer (a) pupa with cocoon cut open and (b) newly emerged adult female of the tree-hugger form.
FIGURE 1 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form
FIGURE 1 The egg masses and nests of the two forms of O. lunifer co-occurring at Gatton, QLD: (a) tree-hugger egg mass in the fork of a twig, (b) tree-hugger nest on the trunk of C. tessellaris, (c) three ground egg masses at base of an Acacia sp., and (d) a ground nest.
FIGURE 2 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form
FIGURE 2 The confirmed locations of the O. lunifer tree-hugger form and the range of C. tessellaris occurrence in Australia. C. tessellaris data from the Atlas of Living Australia.
FIGURE 3 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form
FIGURE 3 The orientation of egg masses and nests of O. lunifer: (a) tree-hugger egg masses, (b) ground-nester egg masses, (c) tree-hugger nests, and (d) ground nests. Dashed line is the mean orientation.
Figure 3 in A new species of Polypoetes Druce, 1885 (Lepidoptera: Notodontidae) from Colombia, with confirmation of a new host plant for the Dioptinae
Figure 3. Female genitalia of Polypoetes milleri spec. nov. A. Dorsolateral. B. Ventrolateral. C. Corpus bursae detail showing signum. Scale: 1 mm. / A. Dorsolateral. B. Ventrolateral. C. Detalle del corpus bursae mostrando el signum. Escala: 1 mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
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.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.