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Figure 8 in Biological characterization of the obligate symbiosis between Acropyga sauteri Forel (Hymenoptera: Formicidae) and Eumyrmococcus smithii Silvestri (Hemiptera: Pseudococcidae: Rhizoecinae) on Okinawa Island, southern Japan
Figure 8. Distribution of the numbers of alate female ants (a) and alate male ants (b) per colony of Acropyga sauteri. A plot represents the variable for a colony or the average for multiple colonies in the vicinity. When multiple queens were sampled from certain clods in the vicinity, we estimated the average numbers of the reproductives by dividing the total number of queens into the total numbers of the reproductives. Numerals above the solid circles indicate the number of colonies used for the average estimation.
Figure 5 in Biological characterization of the obligate symbiosis between Acropyga sauteri Forel (Hymenoptera: Formicidae) and Eumyrmococcus smithii Silvestri (Hemiptera: Pseudococcidae: Rhizoecinae) on Okinawa Island, southern Japan
Figure 5. Percentage of clods containing more than five workers of Acropyga sauteri across depths. Numerals above the bars indicate the sample size (number of cubic clods).
Figure 11 in Biological characterization of the obligate symbiosis between Acropyga sauteri Forel (Hymenoptera: Formicidae) and Eumyrmococcus smithii Silvestri (Hemiptera: Pseudococcidae: Rhizoecinae) on Okinawa Island, southern Japan
Figure 11. Adult male, right side shows venter of the adult male; left side shows dorsum of the adult male. (a) Lateral view of genitalia of the adult male; (b) ventral view of genitalia of the adult male. Scale bar: 0.1 mm.
Figure 2 in Biological characterization of the obligate symbiosis between Acropyga sauteri Forel (Hymenoptera: Formicidae) and Eumyrmococcus smithii Silvestri (Hemiptera: Pseudococcidae: Rhizoecinae) on Okinawa Island, southern Japan
Figure 2. Schematic illustration of the method used to determine colony identity. (a) Distance (D) between two particular ant aggregations was defined as the distance between the centre of the two clods containing the two aggregations; (b) five workers were placed in a plastic cup covered with black paper; (c) an ant worker was introduced into another cup (of recipient workers); (d) the contact behaviour of recipient and introduced workers was observed; (e) the trial ended after contact had occurred two or three times, after which the introduced worker was returned to the original cup. In a match between two aggregations, the method described from (c) to (e) was repeated five times.
Figure 3 in Biology and life cycle of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae), a scavenging amphipod from the continental slope of the Mediterranean
Figure 3. Size to weight ratios of males and females collected on 11 June 1990. L, length in mm; W, weight in mg.
Figure 4 in Biology and life cycle of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae), a scavenging amphipod from the continental slope of the Mediterranean
Figure 4. Maximum and minimum number of eggs per female, depending on the size. L, length in mm; N, number of eggs.
Figure 2 in Biology and life cycle of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae), a scavenging amphipod from the continental slope of the Mediterranean
Figure 2. Size distribution of the animals collected in the whole population, juveniles, males, and females.
Figure 6 in Biology and life cycle of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae), a scavenging amphipod from the continental slope of the Mediterranean
Figure 6. Size distribution of Tmetonyx similis in Toulon Canyon, in 1990. Lines show the development of one cohort in the various generations of males and females.
Figure 2 in Reproductive biology of Scinax fuscomarginatus (Anura, Hylidae) in south-eastern Brazil
Figure 2. Summary of the agonistic interactions between adult males of Scinax fuscomarginatus at Estação Ecológica de Itirapina, State of São Paulo, south-eastern Brazil.
Figure 1 in Reproductive biology of Scinax fuscomarginatus (Anura, Hylidae) in south-eastern Brazil
Figure 1. Distance between Scinax fuscomarginatus nearest males at Estação Ecológica de Itirapina during the calling activity. White bars represent distances where satellite males or agonistic interactions were observed; grey bars represent the distances when solitary males were observed calling without occurrence of agonistic interactions (Ntotal556).
Figure 1 in Reproductive biology and strategies of nine meloid beetles from Central Europe (Coleoptera: Meloidae)
Figure 1. Correlation between mean egg number per oviposition and female and the beetle's size (expressed as pronotum length), determined separately for each species (*not applicable for Meloe rufiventris, since four out of seven females had the same pronotum length).
Figure 2 in Reproductive biology and strategies of nine meloid beetles from Central Europe (Coleoptera: Meloidae)
Figure 2. Correlation between mean egg weight per oviposition and female and the beetle's size (expressed as pronotum length), determined separately for each species (*not applicable for Meloe rufiventris, since three out of four females had the same pronotum length).
Figure 2 in Breeding biology of Physalaemus centralis Bokermann, 1962 (Anura: Leptodactylidae) in southeastern Brazil
Figure 2. Monthly average number of calling males of Physalaemus centralis from January 1996 to February 1997 (bars) and total monthly precipitation (lines) at the study site, municipality of Pirassununga, São Paulo State, Brazil.
Figure 1 in Breeding biology of Physalaemus centralis Bokermann, 1962 (Anura: Leptodactylidae) in southeastern Brazil
Figure 1. Aspects of the life cycle of Physalaemus centralis: adult male (upper left); axillary amplexus (upper right); foam nest (bottom left); tadpole (bottom right).
Figure 3 in Breeding biology of Physalaemus centralis Bokermann, 1962 (Anura: Leptodactylidae) in southeastern Brazil
Figure 3. Average number of calling males during the nights at the study site, municipality of Pirassununga, São Paulo State, Brazil.
Figure 15 in Biology of Lissoderes Champion (Coleoptera, Curculionidae) in Cecropia saplings inhabited by Azteca ants
Figure 15. (a) Diagram of larva in normal position (head and thorax area); (b) diagram of larva in feeding position (arrow showing direction of head movement). H, head; V, ventral side; D, dorsal side.
Figures 8–14 in Biology of Lissoderes Champion (Coleoptera, Curculionidae) in Cecropia saplings inhabited by Azteca ants
Figures 8–14. Biology of Lissoderes pusillus. (8) Prepupa in situ, attached to upper node (note head is completely exposed). (9) Pupa in situ, hanging freely inside the internode. (10) Close-up view of shed exuvia of last larval instar and last abdominal segments of pupa (arrow pointing at the connection). (11) Pupa (several days old), ventral view. (12) Teneral adult male (note shape of male rostrum). (13) Adult female displaying thanatosis (note shape of female rostrum). (14) Pupa of parasitoid wasp, Neocatolaccus sp. in situ, hanging from internode chamber wall (arrow pointing at the connection).
Figure 1 in Biology of Lissoderes Champion (Coleoptera, Curculionidae) in Cecropia saplings inhabited by Azteca ants
Figure 1. Number of internodes per sapling occupied by Azteca ants and Lissoderes pusillus in Cecropia obtusifolia (n544) (A) and C. insignis (n535) (B). Saplings are ranked by increasing number of internodes.
Figures 2–7 in Biology of Lissoderes Champion (Coleoptera, Curculionidae) in Cecropia saplings inhabited by Azteca ants
Figures 2–7. Biology of Lissoderes pusillus. (2) Egg in situ. Arrow pointing at ovipositional perforation. (3) Ovipositional perforation (solid arrows) and prostoma (dashed arrow). (4) First instar larva feeding on underside of upper node. Grooves or holes indicate where the larva has consumed tissue (arrow pointing at the larva). (5) Second instar larva, lateral view (note the upside-down position). (6) Second instar larva, ventral view, feeding on spongy parenchyma tissue. (7) Mature third instar larva, ventral view (connected fecal pellets are seen on and near the larva).
Figure 1. A, B, solitary A. pacificus web, a in Notes on the biology of Anelosimus pacificus Levi, 1963 (Theridiidae, Araneae)-evidence for an evolutionary reversal to a less social state
Figure 1. A, B, solitary A. pacificus web, a flimsy tangle of silk lines with conspicuous globules of glue throughout; C, web of the subsocial A. may Agnarsson, 2005, a typical Anelosimus 'basket' web with dense silk sheet containing living and dead leaves, and aerial threads above, without visible glue; D, the bright white A. pacificus egg sac. All webs have been dusted with corn starch to enhance the visibility of the silk lines.
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.