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Figure 2 in New records and hosts for three species of pseudionine bopyrids (Crustacea: Isopoda: Bopyridae) parasitizing munidid squat lobsters (Crustacea: Anomura: Munididae) in Philippine waters
Figure 2. Aporobopyrus retrorsa (Richardson, 1910) (CI1081y). Female, 8.58 mm (A–J): (A) dorsal view; (B) ventral view; (C) left antenna and antennule; (D) right side of barbula;; (E) right maxilliped, external view; (F) palp of maxilliped; (G) right oostegite 1, external view; (H) right oostegite 1, internal view; (I) right pereopod 1; (J) right pereopod 7. Male, 3.33 mm (K– Q): (K) dorsal view; (L) ventral view; (M) right antenna and antennule; (N) left pereopod 1; (O) right pereopod 2; (P) right pereopod 3; (Q) right pereopod 7. Scale bars = 1 mm (A, B), 0.14 mm (C, F, M–Q), 0.18 mm (D), 0.40 mm (E, G, H), 0.15 mm (I, J), 0.38 mm (K, L).
Figure 6 in Nesting habits of the Japanese foliage spider, Cheiracanthium japonicum (Araneae: Miturgidae): host plant preference based on the physical traits of plant leaves
Figure 6. Differences in the nest size among all types examined by the Tukey test. A solid line indicates a range of 95% confidence intervals. If the interval crosses zero, the difference between the nest types is not significant. On the contrary, if the interval does not cross zero, the difference is significant. The nest types are abbreviated as follows: S1, season's first nest; S2, season's second nest; S3, season's third nest; S4, season's fourth nest; S5, season's fifth nest; M, mating nest; B, breeding nest.
Figure 5 in Nesting habits of the Japanese foliage spider, Cheiracanthium japonicum (Araneae: Miturgidae): host plant preference based on the physical traits of plant leaves
Figure 5. Relationship between the nest size and the nest type (n = 167). The nest types are abbreviated as follows: S1, season's first nest; S2, season's second nest; S3, season's third nest; S4, season's fourth nest; S5, season's fifth nest; M, mating nest; B, breeding nest.
Figure 4 in Nesting habits of the Japanese foliage spider, Cheiracanthium japonicum (Araneae: Miturgidae): host plant preference based on the physical traits of plant leaves
Figure 4. Principal component analysis bi-plot of relationships between the four physical traits of a leaf and the nest type (n = 133). Physical traits are shown by vectors. Each plot represents a nest type: square: season's first nest; diamond: season's second nest; solid square: season's third nest; circle: season's fourth nest; solid circle: season's fifth nest; triangle: mating nest; solid triangle: breeding nest. Plots with similar physical traits are formed into three groups (A, B and C) surrounded by lines.
Figure 4 in A new species of the pseudoscorpion genus Megachernes (Pseudoscorpiones: Chernetidae) associated with a threatened Sri Lankan rainforest rodent, with a review of host associations of Megachernes
Figure 4. Megachernes kanneliyensis sp. nov., paratype female, unless stated otherwise. (A) Carapace, dorsal; (B) coxae III and IV, ventral; (C) right pedipalp, male holotype, dorsal; (D) right pedipalp, dorsal; (E) right chelicera, dorsal; (F) right rallum; (G) left leg IV, lateral; (H) left leg I, lateral; (I) left chela, lateral; (J) left chela, protonymph, dorsal. Scale bars = 1.0 mm (A, C, D, G, H), 0.5 mm (B, I), 0.2 mm (E, J), 0.1 mm (F).
Figure 3 in A new species of the pseudoscorpion genus Megachernes (Pseudoscorpiones: Chernetidae) associated with a threatened Sri Lankan rainforest rodent, with a review of host associations of Megachernes
Figure 3. Megachernes kanneliyensis sp. nov., paratype female, ventral showing detail of coxae and brood-sac.
Figure 2 in A new species of the pseudoscorpion genus Megachernes (Pseudoscorpiones: Chernetidae) associated with a threatened Sri Lankan rainforest rodent, with a review of host associations of Megachernes
Figure 2. Megachernes kanneliyensis sp. nov. (A) Holotype male, dorsal; (B) holotype male, ventral; (C) paratype female, dorsal; (D) paratype female, ventral.
Figure 2 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 2. Non-metric multi-dimensional scaling (MDS) ordination showing hemipteran composition for all sampling periods with selected plant species superimposed.
Figure 5 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 5. Annual cyclic pattern of the proportion of the effectively specialized fauna (squares) and singleton species (circles) for the total number of hemipteran species from each sampling period.
Figure 3 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 3. Mean number of individuals (from SIMPER analysis) of dominant hemipteran species, during each sampling period, for most plant species.
Figure 1 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 1. Interactions between plant species sampled and sampling period for (A) abundance (number of individuals) per plant and (B) species richness per plant (standard error bars are shown).
Figure 6 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 6. Relationship between the effectively specialized fauna (squares) and singleton species (circles) for the number of hemipteran species from each sampling period and for the entire collection. An exponential decay equation is fitted for effectively specialized fauna, y = 2.973∗ exp (−0.00575∗ x) + (−1.478), R2 = 0.7598, and for singleton species, y = 22.53∗exp (−0.08466∗x) + 0.2614, R2 = 0.9873.
Figure 5 in The host-plant range of twig-girdling beetles (Coleoptera: Cerambycidae: Lamiinae: Onciderini) of the Atlantic rainforest in southeastern Brazil
Figure 5. (A) Distribution of frequencies (%) of host-plant species girdled by Psyllotoxus griseocinctus from 2002 to 2006 in Serra do Japi. Asterisks indicate significant differences of the frequencies between girdled and available plant species (Bonferroni 95% confidence interval). (B) The preference for host plants was evaluated using the Manly's index. Values to the right of the dotted line indicate a preference for host plants; values to the left of the line indicate a preference for the alternate host.
Figure 2 in The host-plant range of twig-girdling beetles (Coleoptera: Cerambycidae: Lamiinae: Onciderini) of the Atlantic rainforest in southeastern Brazil
Figure 2. Host specificity of Onciderini beetles based on the percentage of girdled plant species from all taxa. (n = 35 native plant species). Different letters above bars indicate significant differences (Tukey-type multiple comparison test for the analysis of proportions, p <0.05)
Figure 1 in The host-plant range of twig-girdling beetles (Coleoptera: Cerambycidae: Lamiinae: Onciderini) of the Atlantic rainforest in southeastern Brazil
Figure 1. Distribution of frequencies (%) of native host-plant families used by Onciderini beetles from 2002 to 2006 along trails in Serra do Japi (see text for statistics).
Figure 3 in The host-plant range of twig-girdling beetles (Coleoptera: Cerambycidae: Lamiinae: Onciderini) of the Atlantic rainforest in southeastern Brazil
Figure 3. Percentage of host-plant families girdled by Onciderini beetles according to their degree of feeding specialization (n = 1436) (see text for statistics).
Figure 4 in The host-plant range of twig-girdling beetles (Coleoptera: Cerambycidae: Lamiinae: Onciderini) of the Atlantic rainforest in southeastern Brazil
Figure 4. Distribution of frequencies of both host-plant families (A) and species (C) girdled by Oncideres dejeani from 2002 to 2006 in Serra do Japi. Asterisks indicate significant differences of the frequencies between girdled and available plant species (Bonferroni 95% confidence interval). The preference for host-plant families (B) and species (D) was evaluated using the Manly's index. Values to the right of the dotted line indicate a preference for host plants; values to the left indicate a preference for an alternative host.
Figure 6 in The host-plant range of twig-girdling beetles (Coleoptera: Cerambycidae: Lamiinae: Onciderini) of the Atlantic rainforest in southeastern Brazil
Figure 6. (A) Distribution of frequencies (%) of host-plant species girdled by Oncideres saga from 2002 to 2006 in Serra do Japi. Asterisks indicate significant differences of the frequencies between girdled and available plant species (Bonferroni 95% confidence interval). (B) The preference for host plants was evaluated using the Manly's index. Values to the right of the dotted line indicate a preference for host plants; values to the left of the line indicate a preference for the alternate host.
Figure 6 in Life history and host utilization pattern of a strepsipteran parasite (Insecta: Strepsiptera) on the Blissine bugs (Hemiptera: Lygaeidae) living under dwarf bamboo leaf sheaths
Figure 6. Comparison of Macropes obnubilus body lengths between sexes and between stylopized and unstylopized bugs. Bar shows SD.
Figure 4 in Life history and host utilization pattern of a strepsipteran parasite (Insecta: Strepsiptera) on the Blissine bugs (Hemiptera: Lygaeidae) living under dwarf bamboo leaf sheaths
Figure 4. Seasonal changes in the number of strepsipterans per host bug compared among larva, male pupa (including exuvia), and female adult.
ScienceDex guides
Understand access before you commit
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.