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7,883 results for “tropics.”
Fig. 21 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 21 (opposite page). Phylogenetic hypothesis for the Aglaopheniidae Marktanner-Turneretscher, 1890. Species discussed in this study are highlighted in yellow. Newly produced sequences are in bold. Numbers at nodes represent Bayesian posterior probabilities (BPP) and maximum likelihood bootstrap supports (BS), respectively, and are shown only when both BPP Ż 0.9 and BS Ż 75.
Fig. 10 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 10 (opposite page). A. Schizoplumularia elegans Ansín Agís et al., 2016, monosiphonic portion of a branch with proximal part of a cladium, from sample MNHN-IK-2015-548. — B–K. Schizoplumularia helicoidalis sp. nov., portion of stem showing fate of component tubes (B); portion of branch with five successive cladial apophyses and proximal part of a cladium (C); portions of cladia from material other than the holotype (D–E); detail of cladial apophysis (F); cladial internode with hydrotheca and its associated nematothecae (G); nematothecae of stem (H) and of cladial intersegment in adaxial (I) and lateral (J) views; gonotheca from material not belonging to the type (K); B–C, F–J from the holotype, MNHN-IK-2015-610; D–E, K from sample MNHN-IK-2015-596. Scale bars: A, C–E = 300 µm; B = 1 mm; F–K = 100 µm
Fig. 20 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 20 (opposite page). Thamnopteros uniserius Galea gen. et sp. nov., portion of fascicled stem giving rise laterally to a Halopteris-like branch, of which only the proximalmost part, showing the prosegment, is depicted (A); more distal portion of another branch, note slight change in the hydrothecal shape (the arrow indicates a cladial apophysis) (B); two cauline hydrothecae seen laterally, to show variation in the length of the lateral nematothecae (C–D); cladial hydrothecae seen laterally (E) and frontally (F), note differences in the size of the lateral nematothecae belonging to each pair; detail of the hydrothecal axil (G); nematothecae: mesial (H), of the component tubes of the fascicled stem (I), and from above the cauline hydrothecae (J); gonotheca (K); all from sample MNHN-IK-2015-611. Scale bars: A–B = 500 µm; C–F = 200 µm; G–J = 100 µm; K = 300 µm.
Figs 128–131 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 128–131. Male genitalia of Tischeriidae from Las Cuevas, Belize (NHMUK). 128. Paratischeria neotropicana (Diškus & Stonis, 2015), capsule with phallus removed (genitalia slide no. 010316205). 129. Same, phallus. 130–131. Dishkeya gouaniae (Diškus & Stonis, 2007), paratype (genitalia slide no. 010316202).
Figs 83–89 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 83–89. Male genitalia of Astrotischeria spp. (NHMUK). 83. A. selvica Diškus, Carvalho-Filho & Stonis, 2018, capsule with phallus removed, holotype (genitalia slide no. AD920). 84. Same, phallus, paratype (genitalia slide no. AD919). 85. A. casila Diškus & Stonis, 2018, capsule with phallus removed, holotype (genitalia slide no. AD939). 86. Same, phallus. 87. A. furcata Diškus & Stonis, 2018, capsule with phallus removed, holotype (genitalia slide no. AD925). 88. Same, lateral view of capsule. 89. Same, phallus.
Figs 70–77 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 70–77. Male genitalia of Astrotischeria basilobata Remeikis & Stonis sp. nov. (NHMUK). 70. Capsule, with phallus inside, holotype (genitalia slide no. 010316194). 71. Capsule, with phallus removed, paratype (genitalia slide no. 010316198). 72. Phallus, paratype (genitalia slide no. 010316196). 73–74. Main element and dorsal lobe of valva, with anellus broken, paratype (genitalia slide no. 010316197). 75. Same, uncus and tegumen. 76. Same, chitinized ring of anellus. 77. Same, apex of phallus.
Figs 65–69 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 65–69. Female genitalia of Astrotischeria scutifera Diškus & Stonis, sp. nov., paratype (genitalia slide no. 010316179, NHMUK). 65. Papillae of ovipositor. 66–68. Details of prela and apophyses. 69. Corpus bursae and coils of ductus spermathecae.
Figs 118–123 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 118–123. Female genitalia of Paratischeria tubifex Diškus & Stonis sp. nov., paratype (genitalia slide no. 010316173, NHMUK). 118. General view. 119–122. Details. 123. Ovipositor lobes.
Figs 132–138 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 132–138. Male genitalia of Tischeriidae from Las Cuevas, Belize (NHMUK). 132. Coptotriche pulverea (Walsingham, 1897), capsule with phallus removed (genitalia slide no. 010316203). 133–134. Same, phallus. 135. C. forsteroniae Stonis & Diškus, 2008, capsule with phallus removed, paratype (genitalia slide no. 010316201). 136–138. Same, phallus.
Figs 21–34 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 21–34. Tischeriidae collected in Las Cuevas, Belize. 21. Paratischeria tubifex sp. nov., holotype (NHMUK 010289272). 22. Same, paratype (010289282). 23. Same, paratype (010289276). 24–25. P. belizensis sp. nov., holotype (010289283). 26–28. P. neotropicana (010289285). 29. Dishkeya gouaniae, paratype (010289320). 30. Coptotriche pulverea (010289324). 31. Same (010289322). 32–34. C. forsteroniae, paratype (010289330).
Figs 35–46 in Exceptional diversity of Tischeriidae (Lepidoptera) from a single tropical forest site in Belize, Central America
Figs 35–46. Male genitalia of Astrotischeria papilloma Diškus & Stonis sp. nov. (NHMUK). 35–36. Dorsal and ventral lobes of uncus, paratype (genitalia slide no. 010316184). 37. Ventral lobes of uncus, paratype (genitalia slide no. 010316185). 38. Dorsal lobes of uncus, holotype (genitalia slide no. 010316182). 39. General view, uncus, holotype (genitalia slide no. 010316182). 40–41. Same, valva. 42. Dorsal lobe of valva, paratype (genitalia slide no. 010316185). 43–44. Anellus and dorsal lobe of valva, holotype (genitalia slide no. 010316182). 45–46. Phallus, paratype (genitalia slide no. 010316185).
Data for GRL "Tropical Stratospheric Circulation and Ozone Coupled to Pacific Multi-Decadal Variability" paper
<p>Data of the CESM-WACCM sensitivity simulations. These simulations follow the REFC1 configuration from the Chemistry-Climate Model Initiative (CCMI), but for: fixed long-lived halogenated substances at year 1955 (REFC1-fODS); fixed long-lived halogens and nitrogen oxide emissions at year 1955 (REFC1-fODS-N2O); fixed stratospheric aerosol averaged over 1998–1999 (REFC1-fSAD); climatological sea surface temperatures (SSTs) and sea-ice concentrations (SICs) for the 1960–2010 period (REFC1-fSST); climatological SSTs and SICs for the 1960–2010 period, including a 28-months cyclical QBO (REFC1-fSST-QBO).</p>
Geo-referenced crop-nutrient response function dataset for Tropical Africa
The profit potential for a given investment in fertilizer use can be estimated using representative crop nutrient response functions. Where response data is scarce, determination of representative response functions can be strengthened by using results from homologous crop growing conditions. Maize (Zea mays L.) nutrient response functions were selected from the Optimization of Fertilizer Recommendations in Africa (OFRA) database of 5500 georeferenced response functions determined from field research conducted in Sub-Saharan Africa. Three methods for defining inference domains for selection of response functions were compared. Use of the OFRA Inference Tool (OFRA-IT; http://agronomy.unl.edu/OFRA) resulted in greater specificity of maize N, P, and K response functions with higher R2 values indicating superiority compared with using the Harvest Choice Agroecological Zones (HC-AEZ) and the recommendation domains of the Global Yield Gap Atlas project (GYGA-RD). The OFRA-IT queries three soil properties in addition to climate-related properties while the latter two options use climate properties only. The OFRA-IT was generally insensitive to changes in criteria ranges of 20–25% used in queries suggesting value in using wider criteria ranges compared with the default for information scarce crop nutrient response functions.
Fig. 1 in A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
Fig. 1. Xim trenzado gen. et sp. nov. A–C, G. ♁ (ECOTAAR-004950). D–F, H. ♀ (ECOTAAR-005063). A–F. Habitus. A, D. Dorsal view. B, E. Lateral view. C, F. Ventral view. G, H. Carapace in frontal view. Scale bars: A–F = 0.25 mm.
Fig. 4 in A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
Fig. 4. Xim trenzado gen. et sp. nov. A–B. ECOTAAR-004950. C–F, H–I. ECOTAAR-004962. G. ECOTAAR-004952. A–G. Male left femur I. D–G. Details of macrosetae. A, D. Dorsal view. B, E. Prolateral view. C, F. Ventral view. G. Apical view. H. Tarsal organ of leg I. I. Trichobothrium of retrolateral palpal tibia. Scale bars: A–C = 70 μm; D–F = 30 μm; H = 5 μm; I = 10 μm.
Fig. 2 in A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
Fig. 2. Xim trenzado gen. et sp. nov., male left palpus. A–C. ECOTAAR-004974. D–E, G–I. ECOTAAR-004950. F. ECOTAAR-004952. A, D. Mesal view. B, E. Ventral view. C, F. Ectal view. G. Dorsal view. H. Apical view. I. Detail of E showing radix and embolus. Scale bars: A–E = 50 μm; F = 20 μm.
Fig. 7 in A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
Fig. 7. Strict consensus tree of the eight most parsimonious trees, showing only the distal clades where Xim trenzado gen. et sp. nov. is situated. Tree with unambiguous character optimization; character and character-state numbers given above and below marks, respectively; color of marks denotes homoplasious (white) or non-homoplasious (black) character-state changes.
Fig. 5 in A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
Fig. 5. Xim trenzado gen. et sp. nov., ♀, epigynum. A–B. ECOTAAR-005063. C–F. ECOTAAR-005183. A, G. Ventral view. B. Posterior view. C–D, H. Dorsal view. D. Detail of C showing left copulatory duct and spermatheca. E. Antero-dorsal view. F. Detail of E showing left copulatory duct and spermatheca. Scale bars: A–C, E, G–H = 40 μm; D, F = 20 μm.
Fig. 6 in A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
Fig. 6. Strict consensus tree of the eight most parsimonious trees, showing only the distal clades where Xim trenzado gen. et sp. nov. is situated. Tree with Bremer support values noted beside nodes.
Figs 20–23. Raunolina spp. 20–22 – R in First record of the genus Raunolina (Hemiptera: Fulgoroidea: Caliscelidae) from tropical Africa with description of two new species from Sudan and Saudi Arabia
Figs 20–23. Raunolina spp. 20–22 – R. circularis (Linnavuori, 1952), holotype. 23 – R. arabica (Gnezdilov & Wilson, 2006). 20 – left wing; 21 – right wing; 22, 23 – head, pro- and mesonotum, dorsal view.
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.