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Fig. 6 in Two new species of Scolopocryptops centipedes from southern Japan (Chilopoda: Scolopendromorpha: Scolopocryptopidae)
Fig. 6. Scolopocryptops miyosii sp. nov., holotype, ♂ (KUZ Z4375). Forcipules and coxosternite, ventral view. Abbreviations: am = anterior margin of forcipular coxosternite; bs = basal suture on forcipular trochanteroprefemoral process; md = median diastema; op = outer part of anterior margin of forcipular coxosternite; ptr = process of forcipular trochanteroprefemur; t = tooth on anterior margin of forcipular coxosternite. Scale bar = 1 mm.
Fig. 13 in Two new species of Scolopocryptops centipedes from southern Japan (Chilopoda: Scolopendromorpha: Scolopocryptopidae)
Fig. 13. Scolopocryptops brevisulcatus sp. nov. A–B, D–E. Holotype, ♂ (KUZ Z4390). C. Paratype, sex undetermined (KUZ Z4387). A. Cephalic plate and tergites 1–8, dorsal view. B. Sternites 10–17, ventral view. C. Sternite 23, ventral view. D. Right coxopleuron, lateral view. E. Tergite 23, dorsal view. Abbreviations: cxp = coxopleural process; dm = dorsal margin of ultimate pleuron; mds = minute dark spine on ultimate pleuron; tm = tergal margination; tps = tergal paramedian suture. Scale bars: A–B = 5 mm; C–E = 1 mm.
Fig. 12 in Two new species of Scolopocryptops centipedes from southern Japan (Chilopoda: Scolopendromorpha: Scolopocryptopidae)
Fig. 12. Scolopocryptops brevisulcatus sp. nov. A. Holotype, ♂ (KUZ Z4390). B. Paratype, subadult, sex undetermined (KUZ Z4386). Forcipules and forcipular coxosternite, ventral view. Abbreviations: am = anterior margin of forcipular coxosternite; bs = basal suture on forcipular trochanteroprefemoral process; md = median diastema; op = outer part of anterior margin of forcipular coxosternite; ptr = process of forcipular trochanteroprefemur; t = tooth on anterior margin of forcipular coxosternite. Scale bars: A = 1 mm; B = 0.2 mm.
Fig. 5 in Two new species of Scolopocryptops centipedes from southern Japan (Chilopoda: Scolopendromorpha: Scolopocryptopidae)
Fig. 5. Scolopocryptops miyosii sp. nov., holotype, ♂ (KUZ Z4375). A. Cephalic plate and tergite 1, dorsal view. B. Distal part of article 2, article 3, and pretarsus of left second maxilla, medial view. C. Article 3 and pretarsus of left second maxilla, lateral view. D. Head, ventral view. Abbreviations: am = anterior margin of forcipular coxosternite; bs = basal suture on forcipular trochanteroprefemoral process; db = dorsal brush on article 3 of second maxilla; ds = dorsal spur on article 2 of second maxilla; pt = pretarsus of second maxilla; ptr = process of forcipular trochanteroprefemur; t = tooth on anterior margin of forcipular coxosternite. Scale bars: A, D = 1 mm; B–C = 0.2 mm.
Fig. 9 in Two new species of Scolopocryptops centipedes from southern Japan (Chilopoda: Scolopendromorpha: Scolopocryptopidae)
Fig. 9. Scolopocryptops brevisulcatus sp. nov., holotype, ♂ (KUZ Z4390) and habitat at the type locality. A. Habitat (laurel tree forest) on Okinawa Island. B. Live specimen, dorsal view. Scale bar = 10 mm.
Fig. 3 in Two new species of Scolopocryptops centipedes from southern Japan (Chilopoda: Scolopendromorpha: Scolopocryptopidae)
Fig. 3. Scolopocryptops miyosii sp. nov., paratype, ♂ (KUZ Z4376) and habitat at the type locality. A. Habitat (laurel tree forest) in Kagoshima, Kyushu. B. Live specimen, dorsal view. Scale bar = 10 mm.
Fig. 11 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 11. Male genitalia of Viuria acadia sp. nov., paratype (DZ 47.183). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Right lateral view. D. Left lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 10 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 10. Male genitalia of Viuria acadia sp. nov., paratype (DZ 47.183). A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, dorsal view. F. Aedeagus, lateral view. Scale bar: 500 µm.
Fig. 9 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 9. Male genitalia of Viuria innana sp. nov., paratype (DZ 47.172). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 8 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 8. Male genitalia of Viuria innana sp. nov., paratype (DZ 47.172) A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, dorsal view. E. Aedeagus, lateral view. Scale bar: 500 µm.
Fig. 7 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 7. Male genitalia of Viuria lista (Evans, 1953) (OM 4.507). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. D. Right lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 13 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 13. Patches of modified scales in DHW of species of Viuria Grishin, 2019. A–D. Viuria lista (Evans, 1953). E–F. Viuria licisca (Plötz, 1882). A. Overall view. B. Detail of the modified greyish scales in the swollen vein Sc+R1. C. Details of the creamy scales near the base of the swollen veins Rs and M1. D–F. Same sequence with diaphanized wings.
Fig. 5 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 5. Male genitalia of Viuria licisca (Plötz, 1882) (OM 43.281). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. D. Right lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 4 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 4. Male genitalia of Viuria licisca (Plötz, 1882) (OM 43.776). A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, lateral view. F. Aedaegus, dorsal view. Scale bar: 500 µm.
Fig. 2 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 2. Male genitalia of Viuria herophile (Harward, 1914) (DZ 9.681). A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, dorsal view. F. Aedeagus lateral view. Scale bar: 500 µm.
Fig. 3 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 3. Male genitalia of Viuria herophile (Harward, 1914) (DZ 9.677). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. D. Right lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 1 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 1. Species of Viuria Grishin, 2019, dorsal and ventral views. A–D. V. herophile (Harward, 1914). A–B. ♂, Peru, Madre de Dios, Parque Manu, Pakitza (DZ 52.466). C–D. ♀, Brazil, Acre, 50 km NO of Bujari (DZ 47.221). E–H. V. licisca (Plötz, 1882). E–F. ♀, Costa Rica, San José, Ciudad Colón (OM 26.945). G–H. ♂, Mexico, Oaxaca, Candelaria Loxicha (DZ 47.162). I–L. V. lista (Evans, 1953). I–J. ♀, Brazil, Rondônia, 58 km W of Ariquemes (OM 14.507). K–L. ♀, Brazil, Rondônia, 58 km W of Ariquemes, (OM 14.504). M–P. V. inanna sp. nov. M–N. ♂, holotype (DZ 52.489), Brazil, Paraná, Fênix. O–P. ♀ (DZ 52.492), Brazil, Paraná, Fênix. Q–T. V. acadia sp. nov. Q–R. ♂, holotype (DZ 52.520), Brazil, Mato Grosso, 31 km NO of Barra do Bugres. S–T. ♀ (DZ 52.517), Brazil, Mato Grosso, 31–35 km NO of Barra do Bugres.
Climate and vegetation change in a coastal marsh: two snapshots of groundwater dynamics and tidal flooding at Piermont Marsh, NY spanning 20 years
<p>Groundwater hydrology plays an important role in coastal marsh biogeochemical function, in part because groundwater dynamics drive the zonation of macrophyte community distribution. Changes that occur over time, such as sea level rise and shifts in habitat structure are likely altering groundwater dynamics and eco-hydrological zonation. We examined tidal flooding and marsh water table dynamics in 1999 and 2019 and mapped shifts in plant distributions over time, at Piermont Marsh, a brackish tidal marsh located along the Hudson River Estuary near New York City. We found evidence that the marsh surface was flooded more frequently in 2019 than in 1999, and that tides were propagating further into the marsh in 2019, although marsh surface elevation gains were largely matching that of sea level rise. The changes in groundwater hydrology that we observed are likely due to the high tide rising at a rate that is greater than that of mean sea level. In addition, we reported on changes in plant cover by <em>P. australis</em>, which has displaced native marsh vegetation at Piermont Marsh. Although <em>P. australis</em> has increased in cover, wrack deposition and plant die off associated Superstorm Sandy allowed for native vegetation to rebound in part of our focus area. These results suggest that climate change and plant community composition may interact to shape ecohydrologic zonation. Considering these results, we recommend that habitat models consider tidal range expansion and groundwater hydrology as metrics when predicting the impact of sea level rise on marsh resilience.</p>
Figure 1. A in Evaluate the efficiency of releasing two predatory species at their optimal temperature for controlling Tetranychus urticae (Acari: Tetranychidae) in a croton greenhouse
Figure 1. A timeline representing the release of predatory species P. persimilis and S. punctillum to control the twospotted mite T. urticae in a croton greenhouse.
Figure 3 in Evaluate the efficiency of releasing two predatory species at their optimal temperature for controlling Tetranychus urticae (Acari: Tetranychidae) in a croton greenhouse
Figure 3. The comparison between the population of T. urticae in predators' greenhouse and control greenhouse.
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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.