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1,271 results for “Tropical forests”
Fig. 5 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 5. Neophyllobius tepoztlanensis sp. nov., ♀, holotype. A. Palp. B. Subcapitulum. C. Dorsal idiosoma. D. Ventral idiosoma. E. Trochanter–tibia of leg I. F. Tarsus I.
Fig. 4 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 4. Schematic tarsal setations of Neophyllobius cibyci sp. nov. A–D. ♀, holotype. A. Tarsus I. B. Tarsus II. C. Tarsus III. D. Tarsus IV. E–H. ♁, paratype (CNAC009238). E. Tarsus I. F. Tarsus II. G. Tarsus III. H. Tarsus IV. I–L. Protonymph, paratype (CNAC009241). I. Tarsus I. J. Tarsus II. K. Tarsus III. L. Tarsus IV. M–O. Larva, paratype (CNAC009242). M. Tarsus I. N. Tarsus II. O. Tarsus III.
Fig. 1 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 1. Neophyllobius cibyci sp. nov., ♀, holotype. A. Palp. B. Subcapitulum. C. Dorsal idiosoma. D. Ventral idiosoma. E. Trochanter–tibia of leg I. F. Tarsus I.
Fig. 2 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 2. Neophyllobius cibyci sp. nov. A–B. ♁, paratype (CNAC009238). A. Dorsal idiosoma. B. Ventral idiosoma. C–D. Protonymph, paratype (CNAC009241). C. Dorsal idiosoma. D. Ventral idiosoma. E–F. Larva, paratype (CNAC009242). E. Dorsal idiosoma. F. Ventral idiosoma.
Data from: A new approach to map landscape variation in forest restoration success in tropical and temperate forest biomes
1. A high level of variation of biodiversity recovery within a landscape during forest restoration presents obstacles to ensure large scale, cost-effective, and long-lasting ecological restoration. There is an urgent need to predict landscape variation in forest restoration success at a global scale. 2. We conducted a meta-analysis comprising 135 study landscapes to predict and map landscape variation in forest restoration success in tropical and temperate forest biomes. Our analysis was based on the amount of forest cover within a landscape – a key driver of forest restoration success. We contrasted 17 generalized linear models measuring forest cover at different landscape sizes (with buffers varying from 5 to 200 km radii). We identified the most plausible model to predict and map landscape variation in forest restoration success. We then weighted landscape variation by the amount of potentially restorable areas (agriculture and pasture land areas) within the same landscape. Finally, we estimated restoration costs of implementing Bonn Challenge commitments in three specific temperate and tropical forest biome types in USA, Brazil and Uganda. 3. Landscape variation decreased exponentially as the amount of forest cover increased in the landscape, with stronger effects within a 5 km radius. Thirty-eight percent of forest biomes have landscapes with more than 27% of forest cover and showed levels of landscape variation below 10%. Landscapes with less than 6% of forest cover showed levels of variation in forest restoration success above 50%. 4. At the biome level, Tropical and Subtropical Moist Broadleaf Forests had the lowest (12.6%), while Tropical and Subtropical Dry Broadleaf Forests had the highest (22.9%) average of weighted landscape variation in forest restoration success. Our approach can lead to a reduction in implementation costs for each Bonn Challenge commitment between US$ 973 Mi and 9.9 Bi. 5. Policy implications. Our approach identifies landscape characteristics that increase the likelihood of biodiversity recovery during forest restoration – and potentially the chances of natural regeneration and long-term ecological sustainability and functionality. Identifying areas with low levels of landscape variation can help to reduce the risks and financial costs associated with implementing ambitious restoration commitments.
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).
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.
Dataset on light measuments in the understory of a Tropical forest restoration submitted to four thinning intensities through chemical management
<p>The lack of information on the management of light in tropical forests causes a technical constraint for timber production in restoration sites, especially given the light restrictions for timber production. This issue could be amended with the development of methods to easily manage and estimate light availability, targeting practices that balance restoration success and productivity. We conducted the study that gathered this data in an area within the Atlantic Forest, Brazil, where we tested the efficiency of chemical thinning fast-growing species to increase light availability in the understory of a five-year-old restoration planting. Our goal was to increase the growth rates of desirable timber species in the understory of the restoration site. <br>Moreover, we tested the viability of using hemispherical photography taken with a smartphone to assess light incidence and assist restoration management practices. We calculated the percentage of photosynthetically active radiation (PAR) using a ceptometer in four different thinning intensities and compared them to the smartphone measures using correlation analysis and generalized mixed models. Chemical thinning increased light incidence in the understory Light management through PAR and canopy opening were highly correlated overall, especially after three months of management and above 60% of the basal area thinned. Data demonstrates the potential of chemical thinning as a management practice to enhance light availability in the understory of tropical forest restoration sites and highlights the value of using smartphones and fisheye clips for the indirect assessment of light conditions. </p>
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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.