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Figure 11 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 11. Lectotype female of Ichneumon cursorius Smith, 1874 (= Fileanta caterythra Townes, Momoi & Townes, 1965): (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) metasoma, dorsal view (g) mesoscutum, dorsal view (h) scutellum and propodeum, dorsal view (i) mesosoma, lateral view (j) fore wing (k) hind wing.
Figure 10 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 10. Lectotype male of Ichneumon cognatorius Smith, 1874 (= Amblyjoppa cognatoria (Smith, 1874)): (a) labels (b) lateral habitus (c) metasoma, dorsal view (d) head, frontal view (e) head, dorsal view (f) head, lateral view (g) mesoscutum, dorsal view (h) scutellum and propodeum, dorsal view (i) mesosoma, lateral view (j) fore wing (k) hind wing.
Figure 7 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 7. Holotype female of Cryptus maculipes Smith, 1874 (= Stenaoplus maculipes (Smith, 1874)): (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum, dorsal view (g) scutellum and propodeum, dorsal view (h) metasoma, dorsal view (i) mesosoma, lateral view (j) fore wing (k) hind wing.
Figure 35 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 35. Holotype female of Cryptus variator Walker, 1874 (= Hoplocryptus variator (Walker, 1874) comb. nov.): (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum and scutellum, dorsolateral view (g) propodeum, dorsolateral view (h) mesosoma, lateral view (i) wings (j) metasoma, dorsal view.
Figure 2 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 2. Holotype of Anomalon flavifrons Smith, 1874 (= Agrypon flavifrontatum (Dalla Torre, 1901)): label; first line handwriting (a) labels (b) lateral habitus (c) head, frontal view (D) head, dorsal view (e) head, lateral view (f) mesoscutum, dorsal view (g) scutellum and propodeum, dorsal view (h) mesosoma, lateral view (i) fore wing (j) hind wing.
Figure 1 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 1. Holotype female of Agathis atricornis Smith, 1874 (= Cremnops desertor (Linnaeus, 1758)): (a) labels (b) attached antenna and leg (c) lateral habitus (d) head, frontal view (e) head, dorsal view (f) head, lateral view (g) mesoscutum, dorsal view (h) scutellum and propodeum, dorsal view (i) metasoma, dorsal view (j) mesosoma, lateral view (k) wings.
Figure 24 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 24. Holotype male of Ophion pungens Smith, 1874 (= Enicospilus pungens (Smith, 1874)): (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum and scutellum, dorsal view (g) propodeum, dorsal view (h) mesosoma, lateral view (i) fore wing (j) hind wing.
Figure 22 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 22. Holotype female of Ichneumon virulentus Smith, 1874 (= Melanichneumon virulentus (Smith, 1874)): (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum, dorsal view (g) scutellum and propodeum, dorsal view (h) mesosoma, lateral view (i) wings (j) metasoma, dorsal view.
Figure 21 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 21. Holotype female of Ichneumon vexator Smith, 1874 (= Barichneumon tosaensis (Uchida, 1935)): (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum, dorsal view (g) scutellum and propodeum, dorsal view (h) mesosoma, lateral view (i) fore wing (j) hind wing (k) metasoma, dorsal view.
Figure 20 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 20. Holotype female of Ichneumon rufitarsis Smith, 1874: (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum and scutellum, dorsal view (g) propodeum, dorsal view (h) mesosoma, lateral view (i) metasoma, dorsal view (j) wings.
Figure 28 in Photographic catalogue of the oldest primary types of Japanese Ichneumonoidea (Hymenoptera), those described by Frederick Smith and Francis Walker in 1874
Figure 28. Holotype female of Pimpla luctuosa Smith, 1874: (a) labels (b) lateral habitus (c) head, frontal view (d) head, dorsal view (e) head, lateral view (f) mesoscutum, dorsal view (g) scutellum and propodeum, dorsal view (h) mesosoma, lateral view (i) fore wing (j) hind wing (k) metasoma, dorsal view.
FIGURE 3. Isotomurus graminis from Iran. A in Isotomurus graminis Fjellberg (Collembola: Isotomidae) new for Iran, key to Iranian species in genus with comment on the validity of photographic records
FIGURE 3. Isotomurus graminis from Iran. A, habitus of specimen fixed in alcohol (lateral view); B, post antennal organ in head indicate with arrow (40x); C, trichobothria present on abdomen IV, arrow indicates two trichobothria (40x); D, tibiotarsus distally and empodial complex of hind leg (posterior view)(40x).
FIGURES 1. A & B in Isotomurus graminis Fjellberg (Collembola: Isotomidae) new for Iran, key to Iranian species in genus with comment on the validity of photographic records
FIGURES 1. A & B: Different views of grassland sites on which Isotomurus graminis was found showing varied vegetation found on the Golil-Sarany protected rangelands in North Khorasan, Iran.
FIGURE 2 in Isotomurus graminis Fjellberg (Collembola: Isotomidae) new for Iran, key to Iranian species in genus with comment on the validity of photographic records
FIGURE 2. Location of protected area in Iran and IRS-P6 LISS III satellite image of Golil-Sarany protected rangelands.
Data from: Can terrestrial laser scanners (TLSs) and hemispherical photographs predict tropical dry forest succession with liana abundance?
Tropical dry forests (TDFs) are ecosystems with long drought periods, a mean temperature of 25 °C, a mean annual precipitation that ranges from 900 to 2000 mm, and that possess a high abundance of deciduous species (trees and lianas). What remains of the original extent of TDFs in the Americas remains highly fragmented and at different levels of ecological succession. It is estimated that one of the main fingerprints left by global environmental and climate change in tropical environments is an increase in liana coverage. Lianas are non-structural elements of the forest canopy that eventually kill their host trees. In this paper we evaluate the use of a terrestrial laser scanner (TLS) in combination with hemispherical photographs (HPs) to characterize changes in forest structure as a function of ecological succession and liana abundance. We deployed a TLS and HP system in 28 plots throughout secondary forests of different ages and with different levels of liana abundance. Using a canonical correlation analysis (CCA), we addressed how the VEGNET, a terrestrial laser scanner, and HPs could predict TDF structure. Likewise, using univariate analyses of correlations, we show how the liana abundance could affect the prediction of the forest structure. Our results suggest that TLSs and HPs can predict the differences in the forest structure at different successional stages but that these differences disappear as liana abundance increases. Therefore, in well known ecosystems such as the tropical dry forest of Costa Rica, these biases of prediction could be considered as structural effects of liana presence. This research contributes to the understanding of the potential effects of lianas in secondary dry forests and highlights the role of TLSs combined with HPs in monitoring structural changes in secondary TDFs.
Data from: Does my posterior look big in this? The effect of photographic distortion on morphometric analyses
Most geometric morphometric studies are underpinned by sets of photographs of specimens. The camera lens distorts the images it takes, and the extent of the distortion will depend on factors such as the make and model of the lens and camera and user-controlled variation such as the zoom of the lens. Any study that uses populations of geometric data digitized from photographs will have shape variation introduced into the data set simply by the photographic process. We illustrate the nature and magnitude of this error using a 30-specimen data set of Recent New Zealand Mactridae (Mollusca: Bivalvia), using only a single camera and camera lens with four different photographic setups. We then illustrate the use of retrodeformation in Adobe Photoshop and test the magnitude of the variation in the data set using multivariate Procrustes analysis of variance. The effect of photographic method on the variance in the data set is significant, systematic, and predictable and, if not accounted for, could lead to misleading results, suggest clustering of specimens in ordinations that has no biological basis, or induce artificial oversplitting of taxa. Recommendations to minimize and quantify distortion include: (1) that studies avoid mixing data sets from different cameras, lenses, or photographic setups; (2) that studies avoid placing specimens or scale bars near the edges of the photographs; (3) that the same camera settings are maintained (as much as practical) for every image in a data set; (4) that care is taken when using full-frame cameras; and (5) that a reference grid is used to correct for or quantify distortion.
FIGURE 19. Abyssianira argentenensis Menzies, 1962. SEM photographs. Adult male. A in On the Atlantic species of the genus Abyssianira Menzies, 1956 (Isopoda: Asellota: Paramunnidae)
FIGURE 19. Abyssianira argentenensis Menzies, 1962. SEM photographs. Adult male. A, habitus in lateral view. Brooding female: B, habitus in lateral view; C, head in dorsal view; D, anterior margin of frontal plate magnified. Scales = 0.2 mm (A, B), 0.1 mm (C), 0.05 mm (D).
FIGURE 2. A photographic illustration comparing D in A new species of Dendrobates (Anura: Dendrobatidae) from the Amazonian lowlands in Perú
FIGURE 2. A photographic illustration comparing D. uakarii, sp. nov. to similar species. D. uakarii, sp. nov. (holotype) from TamashiyacuTahauyo Communal Reserve (A. Dorsum B. Venter). Near Rio Yarapa, south of Rio Tahuayo, populations have thinner dorsolateral and vertebral lines with brighter red stripes (C. photo: Devon Graham). D. D. duellmani, Yasuni, Ecuador (photo: Petra Bartelds). E. D. ventrimaculatus sp. aff. Solimoes, Amazonas, Brazil (photo: Janalee P. Caldwell). F. D. ventrimaculatus sensu lato, TamashiyacuTahauyo Communal Reserve, Peru. G. D. reticulatus, Iquitos, Peru (photo: Evan Twomey).
FIGURE 7. Anterior SEM photographs showing frons. A. Hippeutister californicus. B. H. solisi, C. H. castaneus. D. H in A review of Hippeutister Reichensperger with new species from California and Costa Rica (Coleoptera: Histeridae: Hetaeriinae)
FIGURE 7. Anterior SEM photographs showing frons. A. Hippeutister californicus. B. H. solisi, C. H. castaneus. D. H. manicatus.
FIGURE 4. Dorsal SEM photographs showing elytra. A. Hippeutister californicus. B. H. solisi, C. H. castaneus. D. H in A review of Hippeutister Reichensperger with new species from California and Costa Rica (Coleoptera: Histeridae: Hetaeriinae)
FIGURE 4. Dorsal SEM photographs showing elytra. A. Hippeutister californicus. B. H. solisi, C. H. castaneus. D. H. manicatus.
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.