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Figs 27-29 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 27-29. Oosagitta melanopicta sp. nov. 27. Habitus, semi-schematic dorsal view. 28. Basal four antennomeres of 2 ♂♂ and 2 ♀♀. 29. Median lobe. A. Dorsal. B. Lateral. Scale bars: 1 mm.
Figs 23-25 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 23-25. Oosagitta thomasi sp. nov. 23. Habitus, semi-schematic dorsal view. 24. Basal four antennomeres of 2 ♂♂ and 2 ♀♀. 25. Median lobe. A. Dorsal. B. Lateral. Scale bars: 1 mm.
Figs 15-17. O in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 15-17. O. anningae sp. nov. 15. Habitus, semi-schematic dorsal view. 16. Basal four antennomeres of 2 ♂♂ and 2 ♀♀. 17. Median lobe. A. Dorsal. B. Detail: apex of endophallus. C. Lateral. Scale bars: 1 mm.
Figs 10-12. Oosagitta minuta comb. nov. 10 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 10-12. Oosagitta minuta comb. nov. 10. Habitus, semi-schematic dorsal view. 11. Basal four antennomeres of 2 ♂♂ and 2 ♀♀. 12. Median lobe: A. Dorsal. B. Detail: apex of endophallus. C. Lateral. Scale bars = 1 mm.
Fig. 9 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Fig. 9. Holotype of Oosagitta angolensis comb. nov. A. Overview with labels. B. Close-up of specimen.
Figs 5-7. Oosagitta angolensis comb. nov. 5 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 5-7. Oosagitta angolensis comb. nov. 5. Basal four antennomeres of 2 ♂♂ and 2 ♀♀. 6. Spermathecae of 3 ♀♀. 7. Median lobe: A. Dorsal. B. Detail: apex of endophallus. C. Lateral. Scale bars = 1 mm.
Figs 19-21 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 19-21. Oosagitta geescheae sp. nov. 19. Habitus, semi-schematic dorsal view. 20. Basal four antennomeres of 2 ♂♂ and 2 ♀♀. 21. Median lobe. A. Dorsal. B. Lateral. Scale bars: 1 mm.
Fig. 1 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Fig. 1. Measurements taken. Absolute measurements: TL = total length from apex of labrum to apex of elytron; PL = pronotal length; PW = maximum pronotal width; EL = elytral length; EW = maximum width of elytra combined. Relative measurements: 2, 3, 4 = length of second, third and fourth antennomeres; DE = minimum distance between eyes; WE = maximum width of eye; TA = length of basimetatarsus; TI = length of metatibia.
Figs 2-4. Oosagitta angolensis comb. nov. 2 in Oosagitta gen. nov. from tropical Africa, with revision of two species and description of four new species (Coleoptera: Chrysomelidae, Galerucinae)
Figs 2-4. Oosagitta angolensis comb. nov. 2. Habitus, semi-schematic dorsal view, ♀. 3. Habitus, lateral view, ♀. 4. Legs: A. Prothoracic leg. B. Mesothoracic leg. C. Metathoracic leg. Scale bars = 1 mm.
Fig. 4. ― A. Gonaxia crassicaulis Vervoort, 1993 in Notes on some sertulariid hydroids (Cnidaria: Hydrozoa) from the tropical western Pacific, with descriptions of nine new species
Fig. 4. ― A. Gonaxia crassicaulis Vervoort, 1993 (MUSORSTOM 4, Stn. DW205), portion of cladium. ― B–D. Gonaxia elegans Vervoort, 1993 (BATHUS 3, Stn. DW809). B. Portion of stem and basal part of a cladium. C. Two consecutive internodes with their hydrothecae. D. Portion of stem with male gonothecae. ― E–F. Gonaxia cf. errans Vervoort, 1993 (BATHUS 2, Stn. CP737). E. Distalmost portion of stem with basal parts of four hydrocladia. F. Two consecutive cladial internodes with their hydrothecae. ― G–J. Gonaxia plumularioides sp. nov. (BIOCAL, Stn. CP34). G. Distalmost part of a stem, showing the structure of internodes. H. Two consecutive cladial internodes with their hydrothecae. I. Stem hydrotheca. J. Axillar hydrotheca. Scale bars: A–B, D–E, G = 1 mm; C, F, H–J = 300 µm.
Fig. 2. ― A. Gonaxia amphorifera Vervoort, 1993 in Notes on some sertulariid hydroids (Cnidaria: Hydrozoa) from the tropical western Pacific, with descriptions of nine new species
Fig. 2. ― A. Gonaxia amphorifera Vervoort, 1993 (SMIB 6, Stn. DW127), portion of stem with cladium. ― B. Gonaxia ampullacea Vervoort, 1993 (BATHUS 4, Stn. DW914), portion of stem with cladia. ― C. Gonaxia compacta Vervoort, 1993 (BATHUS 4, Stn. DW923), portion of stem with cladium. ― D. Gonaxia intermedia Vervoort, 1993 (BATHUS 4, Stn. CP906), portion of stem with cladium. ― E. Gonaxia sinuosa Vervoort, 1993 (SMIB 4, Stn. DW40), portion of stem with cladia. Scale bar: A–E = 1 mm.
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.
Fig. 23. Phylogenetic hypothesis for the Halopterididae Millard, 1962 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 23. Phylogenetic hypothesis for the Halopterididae Millard, 1962. The species discussed in this study is highlighted in yellow, and the newly-produced sequence is in bold. Numbers at nodes represent BPP and BS, respectively, and are shown only when both BPP Ż 0.9 and BS Ż 75.
Fig. 18. Monostaechas fisheri Nutting, 1905 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 18. Monostaechas fisheri Nutting, 1905, morphotype with shallower hydrothecae and longer lateral nematothecae: patterns of branching. Slender lines represent cladia, thicker lines show primary, secondary or tertiary stems; dots correspond to the hydrothecae.
Fig. 15. A–B in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 15. A–B. Halopteris campanula (Busk, 1852), female (A) and male (B) gonothecae from samples MNHN-IK-2015-598 and MNHN-IK-2015-597, respectively. — C. Halopteris infundibulum Vervoort, 1966, possible female gonotheca, from sample MNHN-IK-2015-608. — D–E. Halopteris peculiaris Billard, 1913, female (D) and male (E) gonothecae, both from sample MNHN-IK-2015-609. Scale bar: 300 µm.
Fig. 14 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 14 (opposite page). A–D. Corhiza patula Galea sp. nov., from holotype MNHN-IK-2015-602, proximal portion of cladium (A); nematothecae: mesial (B), lateral (C), and from ahydrothecate internode (D). — E–J. Corhiza pauciarmata Ansín Agís et al., 2009, from sample MNHN-IK-2015-604, portion of cladium (E); nematothecae: mesial (F), lateral (G) and from ahydrothecate internode in lateral (H) and adaxial (I) aspects; cnidome (J). — K. Halopteris campanula (Busk, 1852), portion of cladium from sample MNHN-IK-2015-597. — L–M. Halopteris infundibulum Vervoort, 1966, cladial hydrotheca in lateral (L) and frontal (M) aspects, both from sample MNHN-IK-2015-608. — N–P. Halopteris peculiaris Billard, 1913, proximal portion of cladium seen laterally (N); single (O) or paired (P) lateral nematothecae associated to cauline hydrothecae; all from sample MNHN-IK-2015-609. Scale bars: A, E = 500 µm; B–D, F–I, O–P = 100 µm; J = 10 µm; K–N = 300 µm
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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.