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Fig. 3 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 3. (a) Example of trunk cages made from small Petri dishes (with an open bottom) that were used to isolate scale patches in Massachusetts. (b) Patches of beech scale initiated by delimiting groups (<50) of newly settled crawlers with top patch (defined by black circle marked on bark) lef uncaged, whereas lower patch was caged (caged removed here) from Oct 2011 to Oct 2012 (1 scale generation) at which time scales were a mixture of adults and crawlers of the next generation; done on American beech at Notchview Reservation (property of Trustees of Reservations), Windsor, Massachusetts, USA. Note the greater number of large white woolly dots (adults of the test generation) in the bottom circle, suggesting significant mortality due to factors, like generalist predators, that were excluded by the cages.
Fig. 1 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 1. Sites in Georgia where studies were conducted. Site 1 (Gulelebi Forest) was used in 2011 for the phenology observations, and sites 2 (Gombori) and 3 (Lagodekhi) were used for the cohort survival experiment in 2012.
Fig. 1 in An update on mealybugs and scale insects (Hemiptera) on native epiphytic orchids in South Florida, including a new record for Pseudococcus microcirculus (Pseudococcidae)
Fig. 1. (a) Debris deposited by ants around the base of Prosthechea cochleata where orchid mealybugs were concealed; (b) removal of an orchid leaf sheath on a new shoot reveals a large population of mealybugs on P. cochleata; and (c) 2 orchid mealybugs on the inflorescence of Polystachya concreta.
Figs. 24-39. Figs. 24-26 in Dorsal chaetotaxy of neotropical species supports a basal position for the genus Lepidonella among scaled Paronellidae (Collembola, Entomobryoidea)
Figs. 24-39. Figs. 24-26 Metathoracic claw complex; (24) L. marimuti, afer Mari Mutt 1987; (25) L. nigrofasciata; (26) L. oudemansi; Figs. 25-26 afer Yoshii 1983. Figs. 27-29 Mucro; (27) L. kei afer Yoshii and Suhardjono 1992a; (28) L. oudemansi afer Yoshii 1983; (29) L. tokiokai afer Yoshii 1960.Figs. 30-37 Color pattern; (30) L. kei, afer Yoshii and Suhardjono 1992a; (31) L. duodecimoculata afer Prabhoo 1971; (32) L. oudemansi afer Yoshii 1983; (33) L. nigrofasciata afer Handschin 1928; (35) L. ceylonica afer Yoshii 1966; (35-37) L. annulicornis afer Yoshii 1981; (38) L. subcarpenteri color pattern afer Denis 1948; (39) L. lecongkieti chaetotaxy of labial triangle afer Deharveng & Bedos 1995.
Figs. 15-21 in Dorsal chaetotaxy of neotropical species supports a basal position for the genus Lepidonella among scaled Paronellidae (Collembola, Entomobryoidea)
Figs. 15-21. Lepidonella marimuti; (15) complete dorsal chaetotaxy of head; (16) Detail of anterior chaetotaxy of head; (17) Apical bulb and subapical sense organ of antennal segment 4; (18-19) Sensilla of antennal segment 3 sense organ in different individuals; (20) Maxillary palp and sublobal plate; (21) Chaetotaxy of labial triangle and postlabium, 'v' symbols represent scales.
Figs. 1-8 in Dorsal chaetotaxy of neotropical species supports a basal position for the genus Lepidonella among scaled Paronellidae (Collembola, Entomobryoidea)
Figs. 1-8. Lepidonella zeppelinii sp. nov., arrows point anteriorly and outer sides, setae that may be present or absent are marked with a line; (1) Habitus; (2) Sense organ antennal segment 3 and associated setae and sensilla; (3) Dorsal chaetotaxy of head, open and closed circles are macro- and microsetae, respectively; (4) Eyepatch; (5) Chaetotaxy of postlabium, all setae are ciliate; (6) Labial palp and labial triangle; (7) Maxillary palp and sublobal plate; (8) Labial papilla E.
A Large-Scale Sensitivity Analysis on Latent Embeddings and Dimensionality Reductions for Text Spatializations
<p>Result Files for the Paper "A Large-Scale Sensitivity Analysis on Latent Embeddings and Dimensionality Reductions for Text Spatializations" to be published at IEEE Vis 2024</p>
Fig. 14 in Seasonal dynamics of small-scale fisheries in the Adriatic Sea
Fig. 14: Size-frequency distributions of gillnet landings. TL = total length; CL = carapace length; ML = mantle length. Vertical lines: minimum landing size.
Fig. 1 in Influence of environmental factors and sessile biota on vagile epibionts: The case of amphipods in marinas across a regional scale Abstract
Fig. 1: Composition (percentage of total abundance) of amphipod assemblages occurred on pontoons of each marina (CHI = Chipiona, AME = Puerto. América, BAR = Barbate, LIN= La Línea, FUE = Fuengirola, ALM = Almería. Numbers represents the three pontoons). Exotic species are represented by red textures.
Fig. 6 in Influence of environmental factors and sessile biota on vagile epibionts: The case of amphipods in marinas across a regional scale Abstract
Fig. 6: RDA graphic showing the similarity between the amphipod community present in each marina and its relationship with the physical-chemical parameters (CHI = Chipiona, AME = Puerto. América, BAR = Barbate, LIN= La Línea, FUE = Fuengirola, ALM = Almería; Green = Atlantic; Orange = Mediterranean)..
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main
◂Fig. 13 Crystallographic structure on the columellar lamellae of Dinaride Zospeum and Iberozospeum shells; (a) Zospeum spelaeum, (AJC 847), Betalov Spodmol jama, Slovenia (45.7922 14.1877), pattern of low, non-overlapping, wedges of crystallographic structure on the lamella; (b) Zospeum spelaeum, (MCBI CSR SASA 37049a), Velika Pasica, Slovenia (N45.9189 E14.4934), non-overlapping wedges of crystallographic structure on lamella in old shell; (c) Iberozospeum sp., (RMNH.MOL. 234,120), Cueva Refugio, Trucios, overview of dense, overlapping, scale-like wedges of localized, crystallographic structure on upper part of the lower lamella; (d) ibid., closeup view of c; (e) Iberozospeum sp., (RMNH.MOL. 234,104), Cueva del Comediante, Santander, upper part of the lamella of chemically treated shell showing dense, overlapping wedges of localized, crystallographic structure; (f) Iberozospeum sp., (RMNH. MOL. 234,141), Cueva a Sul, Oviedo, localized, overlapping wedges of crystallographic structure on lamella of chemically treated shell; (g) Iberozospeum vasconicum, (AJC 1849), Cueva Arrikrutz, overview of dense, localized, crystallographic structure on lower part of the lamella; h, ibid., closeup view of g. — Magnification varies for each perspective, see scale bars; Figs. a–b, g–h) imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main; Figs. c–f imaged by Dirk Vendermarel, Naturalis Biodiversity Center in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 13 Crystallographic structure on the columellar lamellae of Dinaride Zospeum and Iberozospeum shells; (a) Zospeum spelaeum, (AJC 847), Betalov Spodmol jama, Slovenia (45.7922 14.1877), pattern of low, non-overlapping, wedges of crystallographic structure on the lamella; (b) Zospeum spelaeum, (MCBI CSR SASA 37049a), Velika Pasica, Slovenia (N45.9189 E14.4934), non-overlapping wedges of crystallographic structure on lamella in old shell; (c) Iberozospeum sp., (RMNH.MOL. 234,120), Cueva Refugio, Trucios, overview of dense, overlapping, scale-like wedges of localized, crystallographic structure on upper part of the lower lamella; (d) ibid., closeup view of c; (e) Iberozospeum sp., (RMNH.MOL. 234,104), Cueva del Comediante, Santander, upper part of the lamella of chemically treated shell showing dense, overlapping wedges of localized, crystallographic structure; (f) Iberozospeum sp., (RMNH. MOL. 234,141), Cueva a Sul, Oviedo, localized, overlapping wedges of crystallographic structure on lamella of chemically treated shell; (g) Iberozospeum vasconicum, (AJC 1849), Cueva Arrikrutz, overview of dense, localized, crystallographic structure on lower part of the lamella; h, ibid., closeup view of g. — Magnification varies for each perspective, see scale bars; Figs. a–b, g–h) imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main; Figs. c–f imaged by Dirk Vendermarel, Naturalis Biodiversity Center
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main
◂Fig. 1 Morphology of thecate and coccoid cells, with labelled thecal plates. a–c, i, m Light microscopy, d–h, k–l scanning electron microscopy. a Ventral view of strain GeoM*788; b dorsal view of strain GeoM*793; c apical view of strain GeoK*044; d ventral view of strain GeoK*037; e dorsal view of strain GeoM*788; f apical view of strain GeoK*024, with the dehiscence of epithecal opening indicated by a blue line; g antapical view of strain GeoK*044; h leftlateral view of strain GeoM*866; i motile cell of strain GeoK*037; k–m coccoid cells showing variability in shape and size of strains k GeoM*866, l GeoM*793 and m GeoK*024. Abbreviations: n′: apical plate, n′′: precingular plate, n′′′: postcingular plate, n′′′′: antapical plate, na: anterior intercalary plate, nC: cingular plate, Sa: anterior sulcal plate, Sd: right sulcal plate, Sp: posterior sulcal plate. Ss: left sulcal plate. Scale bar: 10 µm. UA: 15 kV in Morphological and molecular variability of Peridinium volzii Lemmerm. (Peridiniaceae, Dinophyceae) and its relevance for infraspecific taxonomy
◂Fig. 1 Morphology of thecate and coccoid cells, with labelled thecal plates. a–c, i, m Light microscopy, d–h, k–l scanning electron microscopy. a Ventral view of strain GeoM*788; b dorsal view of strain GeoM*793; c apical view of strain GeoK*044; d ventral view of strain GeoK*037; e dorsal view of strain GeoM*788; f apical view of strain GeoK*024, with the dehiscence of epithecal opening indicated by a blue line; g antapical view of strain GeoK*044; h leftlateral view of strain GeoM*866; i motile cell of strain GeoK*037; k–m coccoid cells showing variability in shape and size of strains k GeoM*866, l GeoM*793 and m GeoK*024. Abbreviations: n′: apical plate, n′′: precingular plate, n′′′: postcingular plate, n′′′′: antapical plate, na: anterior intercalary plate, nC: cingular plate, Sa: anterior sulcal plate, Sd: right sulcal plate, Sp: posterior sulcal plate. Ss: left sulcal plate. Scale bar: 10 µm. UA: 15 kV
Рис. 1. Cyana guttifera (Walker, 1856) (A — самец, B — самка), Cyana adita (Moore, 1859) (C, D — самцы) и Cyana puella (Drury, 1773) (E — самец, F — самка) из Пакистана. Масштабная Λинейка = 5 мм Fig. 1. Cyana guttifera (Walker, 1856) (A — male, B — female), Cyana adita (Moore, 1859) (C, D — males) and Cyana puella (Drury, 1773) (E — male, F — female) from Pakistan. Scale bar = 5 mm in New records of Cyana Walker, 1854 from Pakistan (Lepidoptera: Erebiae: Arctiinae)
Рис. 1. Cyana guttifera (Walker, 1856) (A — самец, B — самка), Cyana adita (Moore, 1859) (C, D — самцы) и Cyana puella (Drury, 1773) (E — самец, F — самка) из Пакистана. Масштабная Λинейка = 5 мм Fig. 1. Cyana guttifera (Walker, 1856) (A — male, B — female), Cyana adita (Moore, 1859) (C, D — males) and Cyana puella (Drury, 1773) (E — male, F — female) from Pakistan. Scale bar = 5 mm
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm in New species of moths (Lepidoptera, Macroheterocera) in the fauna of Amur Oblast, Russian Far East
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm
Рис. 2. Philonthus nitidicollis: A — общий виΑ (размерная Λинейка 1 мм), B — среΑинная ΑоΛя эΑеагуса сбоку, С — парамера Fig. 2. Philonthus nitidicollis: A — habitus (scale bar 1 mm), B — median lobe of aedeagus in lateral view, C — paramere in New records of rove beetles (Coleoptera: Staphylinidae) for Orenburg Oblast
Рис. 2. Philonthus nitidicollis: A — общий виΑ (размерная Λинейка 1 мм), B — среΑинная ΑоΛя эΑеагуса сбоку, С — парамера Fig. 2. Philonthus nitidicollis: A — habitus (scale bar 1 mm), B — median lobe of aedeagus in lateral view, C — paramere
Рис. 1–8. Barsine pulchra (Butler, 1877): 1–2 — самцы; 3 — самка; 4 — генитаΛии самца; 5 — кокон; 6 — кукоΛка; 7–8 — гусеница. Масштабная Λинейка — 5 мм Figs. 1-8. Barsine pulchra (Butler, 1877): 1–2 — male; 3 — female; 4 — male genitalia; 5 — cocoon; 6 — pupa; 7–8 — larva. Scale bar — 5 mm in The first data on preimaginal stages of Barsine pulchra (Butler, 1877) (Erebidae: Arctiinae)
Рис. 1–8. Barsine pulchra (Butler, 1877): 1–2 — самцы; 3 — самка; 4 — генитаΛии самца; 5 — кокон; 6 — кукоΛка; 7–8 — гусеница. Масштабная Λинейка — 5 мм Figs. 1-8. Barsine pulchra (Butler, 1877): 1–2 — male; 3 — female; 4 — male genitalia; 5 — cocoon; 6 — pupa; 7–8 — larva. Scale bar — 5 mm
Рис. 1. Euplocia membliaria (Cramer, 1780) (A) и Asota javana (Cramer, 1780) (B) из Αаоса. Масштабная Λинейка = 10 мм Fig. 1. Euplocia membliaria (Cramer, 1780) (A) and Asota javana (Cramer, 1780) (B) from Laos. Scale bars = 10 mm in New records of Aganainae (Lepidoptera: Erebidae) from Laos
Рис. 1. Euplocia membliaria (Cramer, 1780) (A) и Asota javana (Cramer, 1780) (B) из Αаоса. Масштабная Λинейка = 10 мм Fig. 1. Euplocia membliaria (Cramer, 1780) (A) and Asota javana (Cramer, 1780) (B) from Laos. Scale bars = 10 mm
Рис. 23–31. Tonkinilla graminea, gen. et comb. nov., синтип: 23–25, общий виΔ; 26 — верхняя губа, наΛичник и чеΛюстные щупики; 27 — наΔкрыΛья сбоку; 28, 29 — простернаΛьный отросток (28 — сбоку; 29 — спереΔи); 30, 31 — парамеры и базаΛьная пΛастинка эΔеагуса (30 — виΔ сверху; 31 — виΔ снизу). Масштаб: 23–25 — 2,5 мм; 26, 27, 30, 31 — 1 мм; 28 — 0,5 мм; 29 — 0,3 мм (Λинейка общая ΔΛя 23–25 и ΔΛя 30 и 31) Figs. 23–31. Tonkinilla graminea, gen. et comb. nov., syntype: 23–25, habitus; 26 — labrum, clypeus and mandibular palpi; 27 — lateral view of elytron; 28, 29 — prosternal process (28 — lateral view; 29 — frontal view); 30, 31 — parameres and basal plate of aedeagus (30 — dorsal view; 31 — ventral view). Scale bars: 23–25 — 2.5 mm; 26, 27, 30, 31 — 1 mm; 28 — 0.5 mm; 29 —0.3 mm (common bar for 23–25 and for 30 and 31) in On the systematics of the Anomalina subtribe in Southeast Asia (Coleoptera: Scarabaeidae: Rutelinae: Anomalini)
Рис. 23–31. Tonkinilla graminea, gen. et comb. nov., синтип: 23–25, общий виΔ; 26 — верхняя губа, наΛичник и чеΛюстные щупики; 27 — наΔкрыΛья сбоку; 28, 29 — простернаΛьный отросток (28 — сбоку; 29 — спереΔи); 30, 31 — парамеры и базаΛьная пΛастинка эΔеагуса (30 — виΔ сверху; 31 — виΔ снизу). Масштаб: 23–25 — 2,5 мм; 26, 27, 30, 31 — 1 мм; 28 — 0,5 мм; 29 — 0,3 мм (Λинейка общая ΔΛя 23–25 и ΔΛя 30 и 31) Figs. 23–31. Tonkinilla graminea, gen. et comb. nov., syntype: 23–25, habitus; 26 — labrum, clypeus and mandibular palpi; 27 — lateral view of elytron; 28, 29 — prosternal process (28 — lateral view; 29 — frontal view); 30, 31 — parameres and basal plate of aedeagus (30 — dorsal view; 31 — ventral view). Scale bars: 23–25 — 2.5 mm; 26, 27, 30, 31 — 1 mm; 28 — 0.5 mm; 29 —0.3 mm (common bar for 23–25 and for 30 and 31)
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.