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Fig. 2 in Hamatospiculum flagellispiculosum (Nematoda: Diplotriaenidae) causing severe disease in a new host from Argentine Patagonia: Campephilus magellanicus (Aves: Picidae)
Fig. 2. Scanning electron micrograph (SEM) of female Hamatospiculum flagellispiculosum: (A) Detail of epaulette in anterior end (frontal view): a: amphid, b: cephalic papilla in inner circle, c: cephalic papilla in outer circle, d: tooth. (B) Anterior end with vulva (ventral view), Bar = 100 μm. (C) Anterior end (lateral view), Bar = 20 μm. (D) Detail of anal region (caudal view) with atrophied anus, Bar = 200 μm.
Fig. 1 in Hamatospiculum flagellispiculosum (Nematoda: Diplotriaenidae) causing severe disease in a new host from Argentine Patagonia: Campephilus magellanicus (Aves: Picidae)
Fig. 1. Parasitic infections at joints of a necropsied Magellanic woodpecker (Campephilus magellanicus) adult female from Argentine Patagonia: (A) Dissected distocranial extremity of the left tibiotarsus. (B) Urogygial gland area increased in size. Arrows show roundworms present in the tissues extracted from the affected locations.
Fig. 5 in Hamatospiculum flagellispiculosum (Nematoda: Diplotriaenidae) causing severe disease in a new host from Argentine Patagonia: Campephilus magellanicus (Aves: Picidae)
Fig. 5. Hamatospiculum flagellispiculosum, optical microscope micrograph of eggs: (A) Egg with first-stage larvae (L1), Bar = 15 μm. (B) Larvae hatching, Bar = 15 μm.
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).
F I G U R E 2 Fitted logistic curves with 95 in Circadian and seasonal flight activity differences between the sexes of the biocontrol agent Eadya daenerys (Hymenoptera: Braconidae) and the impact of host size on adult emergence
F I G U R E 2 Fitted logistic curves with 95% confidence intervals for the effect of Paropsisterna agricola beetle prepupal weight (mg) for three post-beetle prepupal outcomes (dead beetle prepupa, beetle or E. daenerys wasp).
F I G U R E 3 in Circadian and seasonal flight activity differences between the sexes of the biocontrol agent Eadya daenerys (Hymenoptera: Braconidae) and the impact of host size on adult emergence
F I G U R E 3 Host beetle prepupal weight (mg) (using both Paropsisterna agricola <80 mg and Paropsis charybdis>80 mg) and the head capsule width (mm) of laboratory-reared Eadya daenerys across both host species (n = 96).
F I G U R E 1 in Circadian and seasonal flight activity differences between the sexes of the biocontrol agent Eadya daenerys (Hymenoptera: Braconidae) and the impact of host size on adult emergence
F I G U R E 1 Weekly adult total malaise trap counts for three paropsine leaf beetle hosts of E. daenerys at Runnymede for the 2015/2016 season.
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.
F I G U R E 4 in Circadian and seasonal flight activity differences between the sexes of the biocontrol agent Eadya daenerys (Hymenoptera: Braconidae) and the impact of host size on adult emergence
F I G U R E 4 Head capsule width (mm) of adult Eadya daenerys (left) reared in the laboratory on Paropsisterna agricola (n = 179) or (right) collected in the field (n = 253).
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 2 in Assessing predation parameters of the predatory mite Typhlodromus bagdasarjani (Acari: Phytoseiidae) on different host plants
Figure 2. Age-stage-specific predation rate (cxj) of predatory mite Typhlodromus bagdasarjani fed on immature stages of Tetranychus urticae on different host plants.
Figure 1 in Assessing predation parameters of the predatory mite Typhlodromus bagdasarjani (Acari: Phytoseiidae) on different host plants
Figure 1. The age-specific survival rate (lx), age-specific predation rate (kx), age-specific net predation rate (qx) of predatory mite Typhlodromus bagdasarjani fed on immature stages of Tetranychus urticae reared on different host plants.
Figure 17 Periglischrus torrealbai, female. A in DNA barcoding, visual-guide resource, new localities and host associations of genus Periglischrus Oudemans, 1902 (Acari: Mesostigmata, Spinturnicidae) from Minas Gerais, Brazil
Figure 17 Periglischrus torrealbai, female. A – General view; B – Mediodistal lobe of palpal tibia indicated in red arrow; C – Dorsal plate with proteronotal setae (Pn1–Pn5) and poststigmal seta (Pst) indicated; D – Dorsal opisthosoma with hysteronotal setae (Op3–Op6) indicated
Figure 13 Periglischrus iheringi, protonymph. A in DNA barcoding, visual-guide resource, new localities and host associations of genus Periglischrus Oudemans, 1902 (Acari: Mesostigmata, Spinturnicidae) from Minas Gerais, Brazil
Figure 13 Periglischrus iheringi, protonymph. A – General view; B – Dorsal view; C – Ventral view; D – Ventral setae on legs I and II with details; E – Details ventral setae on leg I; F – Details ventral setae on leg II; G – Coxa I withpv anddvsetae, indicated; H – Femur–tibia I with proximal adsetae, indicated; I – Coxa II with posterolateral setapl () indicated; J – Femur II, proximaladandpdsetae, indicated; K – Proximal adandpd on tarsus III, indicated; L – Femur IV, proximaladandpd setae, indicated; M – Genu IV, proximaladandpd setae, indicated; N – Proximal adandpd on tarsus IV, indicated. Scale bars: A = 200 µm, B–D = 100 µm, E–N = 50 µm.
Figure 10 Periglischrus herrerai, protonymph. A in DNA barcoding, visual-guide resource, new localities and host associations of genus Periglischrus Oudemans, 1902 (Acari: Mesostigmata, Spinturnicidae) from Minas Gerais, Brazil
Figure 10 Periglischrus herrerai, protonymph. A – General view; B – Dorsal view; C – Ventral view; D – Ventral setae on legs I and II with details; E – Details ventral setae on leg I; F – Details ventral setae on leg II; G – Coxa I withpv anddvsetae, indicated; H – Femur–tibia I with proximal adsetae, indicated; I – Coxa II with posterolateral setapl () indicated; J – Femur II, proximaladandpdsetae, indicated; K – Proximal adandpd on tarsus III, indicated; L – Femur IV, proximaladandpd setae, indicated; M – Genu IV, proximaladandpd setae, indicated; N – Proximal adandpd on tarsus IV, indicated. Scale bars: A–N = 50 µm.
Figure 9 Periglischrus herrerai, male. A in DNA barcoding, visual-guide resource, new localities and host associations of genus Periglischrus Oudemans, 1902 (Acari: Mesostigmata, Spinturnicidae) from Minas Gerais, Brazil
Figure 9 Periglischrus herrerai, male. A – General view; B – Dorsal view with proteronotal setae (Pn1–Pn5) and poststigmal seta (Pst) indicated; C – Ventral view with sternogenital setaeSt(1–St4) and genital seta (Sg) indicated; D – Ventral setae on legs I and II with details; E Details ventral setae on leg I; F – Details ventral setae on leg II; G – Coxa I with pv anddvsetae, indicated in red arrow; H – Femur–tibia I with proximal adsetae, indicated; I – Coxa II with posterolateral setapl () indicated; J – Femur II, proximaladandpdsetae, indicated; K – Proximal adandpd on tarsus III, indicated; L – Femur IV, proximaladandpd setae, indicated; M – Genu IV, proximaladandpd setae, indicated; N – Proximal adandpd on tarsus IV, indicated. Scale bars: A =200 µm, B–C, E–M = 50 µm, D and N = 100 µm.
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.