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FIG. 1. True colour Landsat 7 in Development of a Geographical Information System for the marine resources of Rodrigues
FIG. 1. True colour Landsat 7 ETMz satellite image of Rodrigues as a raster image in TIF file format to form the base layer for the GIS. The island of Rodrigues is about 18 km in length.
FIG. 2 in Development of a Geographical Information System for the marine resources of Rodrigues
FIG. 2. Hierarchical biotope classification for the reef-fringed lagoon of Rodrigues. The colour bar indicates the colour used to illustrate the habitat group of biotopes in the biotope map (see figure 4).
FIG. 9 in Development of a Geographical Information System for the marine resources of Rodrigues
FIG. 9. Thematic map from the GIS to show the existing Fisheries Reserves (blue boundaries) Fisheries Act 75 (1984) and proposed Marine Reserves (yellow boundaries) and Core Areas (pink boundaries) suggested by Pearson (1988). The underlay shows the major habitat types of Coral (red); Consolidated limestone (orange); Lagoon muds (brown); Sand and rubble with moderate to dense vegetation (dark green) and with sparse vegetation (light green).
FIG. 7 in Oostegite development during the sexual maturation of females of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae)
FIG. 7. Tmetonyx similis female: the spreading of the induction process (arrows) from a single induction centre in segment 3. The predicted subsequent stages in the arrival and development of the oostegites are based on the observation data on Tmetonyx similis female. Stages A and B are generally merged. Cx, coxa; Segt, segment.
FIG. 6 in Oostegite development during the sexual maturation of females of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae)
FIG. 6. Distribution of the setae on the oostegites at St 5C (right coxae). (A) Oostegite on coxa 3. The setae are mainly on the distal part of the oostegite. (B) Oostegite on coxa 2. The setae are on the distal part and on the internal side of the oostegite.
FIG. 1 in Oostegite development during the sexual maturation of females of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae)
FIG. 1. Stages of development of the oostegites on coxae 2–5 in a Tmetonyx similis female. The sequence of the coxae is arbitrary, depending on the spreading of the induction process. The arrows indicate the 'bud' at St 2(-). PL, pigmented line on coxa 5; oost, oostegite; scale 1 gives St 2(-); scale 2 gives St 4 and St 4A; scale 3 gives St 2, St 2A, St 3 and St 3A. Scale bars: 1 mm.
FIG. 2 in Oostegite development during the sexual maturation of females of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae)
FIG. 2. St 2(-) on a right pereopod 4. (A) General view of the bud on coxa 4 (arrow) (the gill was separated); (B) enlargement of the bud.
FIG. 4 in Oostegite development during the sexual maturation of females of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae)
FIG. 4. Organization of a seta (oostegite on a right coxa 2). (A) general view. Note the cone at the base of the seta (arrow). (B) Enlargement of the distal part of the seta with the longitudinal rows of digitations. (C) Distal part of the seta. Note the presence of a pore (arrow).
FIG. 3 in Oostegite development during the sexual maturation of females of Tmetonyx similis (G. O. Sars, 1891) (Amphipoda, Lysianassidae)
FIG. 3. (A, B) Development of the setae (oostegite St 3A on a left coxa 3). (A) Distal part of the oostegite with a depression containing a small seta; (B) enlargement of the small seta. (C–F) Setae on the distal part of the oostegite (St 4A on a right coxa 5) (C) Distal part of the oostegite with the setae; (D) enlargement of the right side of the previous oostegite, showing the seta with a swollen base; (E) enlargement of left side of the previous oostegite, setae at a different stage of development; (F) development of a cone at the base of the seta on the distal part of the oostegite on a right coxa 4.
Fig. 2 in Survival and Time of Development forCreophilus maxillosus(L.) (Coleoptera: Staphylinidae) at Three Constant Temperatures
Fig. 2. Mortality (%) per life stage of Creophilus maxillosus reared at three constant temperatures, 16 (n = 323),
Fig. 1 in Survival and Time of Development forCreophilus maxillosus(L.) (Coleoptera: Staphylinidae) at Three Constant Temperatures
Fig. 1. Comparison of egg eclosion rates for Creophilus maxillosus reared at A) 16°C (n = 135), B) 24°C (n = 333), and C) 32°C (n = 659), 50% RH, and 12:12 hour L:D photoperiod. Seven outliers were removed for graphing purposes, including: 16°C (291 hours), 24°C (148 hours), and 32°C (114–121 hours).
Fig. 3. Creophilus maxillosus pupae. A in Survival and Time of Development forCreophilus maxillosus(L.) (Coleoptera: Staphylinidae) at Three Constant Temperatures
Fig. 3. Creophilus maxillosus pupae. A) Reared at 32°C, third-instar exuvia partially attached ventrally, lateral view, B) Reared at 24°C, ventral view.
Figs. 1–3. Eubulus parochus. 1 in Observations on the Natural History, Development, Range, and Future of Eubulusparochus(Herbst) (Coleoptera: Curculionidae)
Figs. 1–3. Eubulus parochus. 1) adult and grazed upon fungal hyphal pegs of Sirococcus clavigignenti-juglandacearum on a branch of butternut (Juglans cinerea); 2) adult with legs folded, ruler shows 1 mm markings; 3) adult feeding (arrow) on bark of butternut branch.
Figs. 9–10. Sirococcus clavigignenti-juglandacearum. 9 in Observations on the Natural History, Development, Range, and Future of Eubulusparochus(Herbst) (Coleoptera: Curculionidae)
Figs. 9–10. Sirococcus clavigignenti-juglandacearum. 9) black hyphal pegs and masses of spores (arrows) beneath split bark of dead branch of butternut (Juglans cinerea); 10) adult Eubulus parochus feeding on spores (arrow) on an excised butternut branch.
Fig. 4 in Observations on the Natural History, Development, Range, and Future of Eubulusparochus(Herbst) (Coleoptera: Curculionidae)
Fig. 4. Numbers of Eubulus parochus adults collected by date from Chittenden and Washington Counties of Vermont in 1997, 1998, and 1999. Dashed lines mark first day of the month for June, July, August, and September.
Fig. 1 in The Morphology and Temperature-dependent Development of Mylabris phalerata Pallas (Coleoptera: Meloidae)
Fig. 1. Developmental stages of Mylabris phalerata. A: Egg (2.4 mm); B: L1 (2.6 mm); C: L2 (5.1 mm); D: L3 (13.7 mm); E: L4 (22.4 mm); F: L5 (29.2 mm); G: Pupa (30.1 mm); H: Adult (31.2 mm).
Fig. 1 in Trigonopeltastes delta (Coleoptera: Scarabaeidae: Cetoniinae) Larva Developing in a Bromeliad Terrarium
Fig. 1. Developmental stages of Mylabris phalerata. A: Egg (2.4 mm); B: L1 (2.6 mm); C: L2 (5.1 mm); D: L3 (13.7 mm); E: L4 (22.4 mm); F: L5 (29.2 mm); G: Pupa (30.1 mm); H: Adult (31.2 mm).
Fig. 2 in Reproductive Development Of The Tasmanian Eucalypt-Defoliating Beetles Chrysophtharta Agricola (Chapuis) And C. Bimaculata (Olivier) (Coleoptera: Chrysomelidae: Paropsini)
Fig. 2. Diagrammatic representation of the female reproductive system of Chrysophtharta bimaculata, where F = filament, O = ovariole, C = calyx, LO = lateral oviduct, CO = common oviduct, S = spermatheca, BC = bursa copulatrix, and the scale bar represents approximately 1 mm. Morphological differences between the reproductive systems of C. bimaculata and C. agricola are described in the text.
Fig. 3 in Reproductive Development Of The Tasmanian Eucalypt-Defoliating Beetles Chrysophtharta Agricola (Chapuis) And C. Bimaculata (Olivier) (Coleoptera: Chrysomelidae: Paropsini)
Fig. 3. Days at 21°C, 16L:8D for 100% of Chrysophtharta agricola males (dashed lines) and females (solid lines) to obtain clearyellow haemolymph (l) and small fat body (v) and for females to attain mature ovarioles (M).
Fig. 1 in Effect Of Parental Care On The Duration Of Larval Development And Offspring Survival In Nicrophorus Mexicanus Matthews (Coleoptera: Silphidae)
Fig. 1. Differences in time development among the three experimental groups in N. mexicanus Mattews. 1.—Control group; 2.—Broodmass present and parents removed; 3.—Without parental care (brood mass not present and parents removed).
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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.