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Data: Flower visiting insects of kiwifruit within New Zealand commercial orchard blocks sampled over two years in the Bay of Plenty, New Zealand
<p>These data are total counts of individual bee and non–bee insects observed visiting the flowers of kiwifruit (<em>Actinidia chinensis</em> var.deliciosa) (‘Hayward’) vines in three commercial orchards located in the Bay of Plenty Region of New Zealand (37° 46' 56" S; 176° 19' 10" E). Each block was located on a different farm and each separated by a distance of at least two kilometres and surveyed twice in two consecutive years. A total of 1181 insects were observed, 741 in the 2014 season and 460 in the 2015 season. Insects from four orders were recorded. The most abundant species were honey bees <em>Apis mellifera</em> (n= 1068; 90.4%), flower longhorn beetles <em>Zorion guttigerum</em> (n= 52; 4.4%), the native bee <em>Lasioglossum</em> <em>sordidum</em>/c<em>ognatum</em> (n= 12; 1.0%) and the hover fly <em>Melanostoma fasciatum</em> (n= 11; 0.9%) Others insects represented 3.2% of individuals observed (n=38). We present a table of counts of the insects observed.</p>
Figs 29‒32. Living individuals and habitats. 29 in Two new species of the genus Cryptostemma from Japan (Hemiptera: Heteroptera: Dipsocoridae)
Figs 29‒32. Living individuals and habitats. 29 – Cryptostemma miyamotoi sp. nov., male; 30 – C. pavelstysi sp. nov., male; 31 – habitat of C. miyamotoi, Sonosegawa Riv., Sanagouchi-son, Tokushima Pref.; 32 – habitat of C. pavelstysi, near Nagura Dam, Ishigaki Is.
Figs 11‒19 in Two new species of the genus Cryptostemma from Japan (Hemiptera: Heteroptera: Dipsocoridae)
Figs 11‒19. Morphological details of Cryptostemma miyamotoi sp. nov., male (11‒18) and female (19). 11‒12 – abdomen (mediotergite II and sternite II omitted), dorsal (11) and lateral (12) views; 13 – left side of sternite VII, laterodorsal view; 14 – left laterotergite VIII, laterodorsal view; 15 – right laterotergite VIII, laterodorsal view; 16‒17 – left paramere, dorsal and anterior views; 18 – right paramere, dorsal view; 19 – spermatheca.Abbreviations: adpp = anterodorsal projection of pygophore; an = anophore; app = apical process of paramere; bpp = basal process of paramere; g = spermathecal gland; lp = left paramere; lt4‒8 = laterotergite IV‒VIII; mt8 = mediotergite VIII; py = pygophore; rp = right paramere; sc = seminal capsule; st4, 7, 8 = sternite IV, VII, VIII. Scale bars = 0.2 mm for 11‒12; 0.1 mm for 13‒18; 0.05 mm for 19.
Figs 9‒10 in Two new species of the genus Cryptostemma from Japan (Hemiptera: Heteroptera: Dipsocoridae)
Figs 9‒10. Right forewings of Japanese Cryptostemma spp. 9 – Cryptostemma miyamotoi sp. nov., male; 10 – C. pavelstysi sp. nov., male. Abbreviations: cf = costal fracture; clf = claval fracture. Scale bars = 0.2 mm.
Figs 20‒28 in Two new species of the genus Cryptostemma from Japan (Hemiptera: Heteroptera: Dipsocoridae)
Figs 20‒28. Morphological details of Cryptostemma pavelstysi sp. nov., male (20‒27) and female (28). 20‒21 – abdomen, dorsal (20) and lateral (21) views; 22 – left side of sternite VII, laterodorsal view; 23 – left laterotergite VIII, laterodorsal view; 24 – right laterotergite VIII, laterodorsal view; 25‒26 – left paramere, dorsal and anterior views; 27 – right paramere, dorsal view; 28 – spermatheca. Abbreviations: adpp = anterodorsal projection of pygophore; an = anophore; app = apical process of paramere; bpp = basal process of paramere; dag = dorsal abdominal gland scars; g = spermathecal gland; lp = left paramere; lt4–8 = laterotergite IV–VIII; mt8 = mediotergite VIII; py = pygophore; rp = right paramere; sc = seminal capsule; st4, 5, 7, 8 = sternite IV, V, VII, VIII. Scale bars = 0.2 mm for 20‒21; 0.1 mm for 22‒27; 0.05 mm for 28.
Figs 1‒8 in Two new species of the genus Cryptostemma from Japan (Hemiptera: Heteroptera: Dipsocoridae)
Figs 1‒8. Habitus of Japanese Cryptostemma spp., dorsal (1, 3, 5, 7) and lateral (2, 4, 6, 8) views. 1‒4 – Cryptostemma miyamotoi sp. nov., holotype, male (1‒2) and female (3‒4); 5‒8 – C. pavelstysi sp. nov., holotype, male (5‒6) and female (7‒8). Scale bars = 0.5 mm.
Figs 28–32. Male genitalia. 28–29 in Two new species of Rohdendorfia (Diptera: Syrphidae) from Central Asia
Figs 28–32. Male genitalia. 28–29 – Rohdendorfia dimorpha Smirnov, 1924 (adapted from BARKALOV & NIELSEN 2010). 28 – epandrium, dorsal view; 29 – epandrium, lateral view. 30–32 – R. montivaga Violovitsh, 1984 (adapted from BARKALOV & NIELSEN 2010). 30 – epandrium, dorsal view; 31 – epandrium, lateral view; 32 – hypandrium, lateral view.
Figs 18–24 in Two new species of Rohdendorfia (Diptera: Syrphidae) from Central Asia
Figs 18–24. Rohdendorfia khakimovi Barkalov, sp. nov. 18–19 – paratype male (ZFMK-DIP-00055236): 18 – dorsal view; 19 – lateral view. 20–21 – paratype female (ZFMK-DIP-00055237): 20 – dorsal view; 21 – lateral view. 22 – paratype male (ZFMK-DIP-00055236), frontal view. 23 – paratype female (ZFMK- DIP-00055237), frontal view. 24 – paratype male (ZFMK-DIP-00055236), metaleg and sterna, lateral view. Scale bars: 18–21 – 1 mm, 22–24 – 0.5 mm.
Figs 9–17. Male genitalia. 9–11 in Two new species of Rohdendorfia (Diptera: Syrphidae) from Central Asia
Figs 9–17. Male genitalia. 9–11 – Rohdendorfia bella Mengual, sp. nov. 9 – epandrium, dorsal view; 10 – epandrium, lateral view; 11 – hypandrium, lateral view. 12–14 – Rohdendorfia khakimovi Barkalov, sp. nov. 12 – epandrium, dorsal view; 13 – epandrium, lateral view; 14 – hypandrium, lateral view. 15–17 – Rohdendorfia alpina Sack, 1938 (adapted from CLAUSSEN 1988). 15 – epandrium, dorsal view; 16 – epandrium, lateral view; 17 – hypandrium, lateral view. Scale bars = 0.2 mm.
Figs 2–8 in Two new species of Rohdendorfia (Diptera: Syrphidae) from Central Asia
Figs 2–8. Rohdendorfia bella Mengual, sp. nov. 2–3 – holotype male (ZFMK-DIP-00027140). 2 – dorsal view; 3 – lateral view. 4–5 – paratype female (ZFMK-DIP-00027194); 4 – dorsal view; 5 – lateral view. 6 – holotype male, frontal view. 7 – paratype female (ZFMK-DIP-00027194), frontal view. 8 – holotype male, metaleg, lateral view. Scale bars: 2–5 – 1 mm, 6–8 – 0.5 mm..
Fig 1 in Two new species of Rohdendorfia (Diptera: Syrphidae) from Central Asia
Fig 1. Type locality of Rohdendorfia khakimovi Barkalov, sp. nov. in Tajikistan (37°29′ N 72°47′ E).
Fig. 5. A in Two new species and ten new records of Heteroptera from Turkey, including the first record of the potential alien Campylomma miyamotoi in the Western Palaearctic
Fig. 5. A ‒ Phytocoris (Exophytocoris) carapezzai sp. nov., alive female attracted to UV light; B‒C ‒ Campylomma miyamotoi Yasunaga, 2001 (B ‒ male; C ‒ female). D ‒ Hallodapus concolor (Reuter, 1890), male; E ‒ Zanchius breviceps (Wagner, 1951), alive male on Ficus sp.; F ‒ Montandoniola moraguesi (Puton, 1896), alive male attracted to UV light; G ‒ Temnostethus (Temnostethus) gracilis Horváth, 1907, male; H ‒ Plinthisus (Isioscytus) minutissimus Fieber, 1864, female.
Fig. 2 in Two new species and ten new records of Heteroptera from Turkey, including the first record of the potential alien Campylomma miyamotoi in the Western Palaearctic
Fig. 2. Phytocoris (Exophytocoris) carapezzai sp. nov.: A ‒ male; B ‒ posterior leg; C‒D ‒ vesica in two different views; E ‒ left paramere; F ‒ right paramere. Scale bars: A, B ‒ 1 mm; C, D ‒ 0.1 mm; E, F ‒ 0.1 mm.
Fig. 1 in Two new species and ten new records of Heteroptera from Turkey, including the first record of the potential alien Campylomma miyamotoi in the Western Palaearctic
Fig. 1. Adelphophylus oenderi sp. nov.: A ‒ male; B ‒ female; C ‒ vesica; D ‒ bursa copulatrix. Abbreviation: SR ‒ sclerotized recess. Scale bars: A, B ‒ 1 mm; C ‒ 0.5 mm; D ‒ 0.1 mm.
Fig. 4. A‒B ‒ Maurodactylus kukuensis V. G. Putshkov, 1978 in Two new species and ten new records of Heteroptera from Turkey, including the first record of the potential alien Campylomma miyamotoi in the Western Palaearctic
Fig. 4. A‒B ‒ Maurodactylus kukuensis V. G. Putshkov, 1978: A ‒ male; B ‒ female. C ‒ Pinalitus viscicola (Puton, 1888), male. D ‒ Platycranus (Genistocapsus) alkestis Linnavuori, 1999, male. Scale bars: 1 mm.
Fig. 3. A‒B in Two new species and ten new records of Heteroptera from Turkey, including the first record of the potential alien Campylomma miyamotoi in the Western Palaearctic
Fig. 3. A‒B ‒ Campylomma miyamotoi Yasunaga, 2001: A ‒ male, B ‒ vesica. C ‒ Compsidolon (Compsidolon) elegantulum Reuter, 1899, male. Scale bars: A, C ‒ 1 mm; B ‒ 0.1 mm.
Figure 17 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 17 Caleremaeus nasutusn. sp., transmitted-light micrographs of adult: A – legs I-IV, abaxial view (trochanter II not shown); B – femur II (cerotegument mostly separated; insert = seta d of femur I); C – tibia and tarsus I; D – chelicera, abaxial view. Scale bars: 20 µm (A); 10 µm (B-D).
Figure 18 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 18 Transmitted-light micrographs of C. monilipes,(A-D) and Caleremaeus'retractus' group from New York (E-G): A – adult (from Sweden), rostral bulge, deep focus to show embossed pattern; B – adult (from Spain), setah2 and nearby cerotegument; C – deutonymph (from Sweden), pygidial region, ventral view of flattened specimen; D – same, leg I and rostral region, dorsal view (lower left insert: tibia II coupled seta d and solenidion); E – anterior part of coxisternum; F – anterior third, ventrolateral view; G – deutonymph, hysterosoma, lateral view. Scale bars: 20 µm (C-G); 10 µm (A, B).
Figure 19 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 19 Food boluses and fecal pellets from within specimens of Caleremaeus retractus(A-E), C. arboricolus(F-H) and C. nasutus n. sp. (I-L): A – food bolus in adult; B – part of different bolus in same adult; C – fecal pellet in different adult; D – same, different adult; E – fecal pellet in tritonymph (arrow on spiral thickening of plant tracheid cell); F – food bolus in adult; G – food bolus in deutonymph; H – food bolus in protonymph; I – food bolus in adult; J, K, L – fecal pellet in three different adults. Scale bar: 10 µm (all to same scale).
Figure 14 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 14 Caleremaeus nasutusn. sp., scanning electron micrographs of adult: A – dorsal view cerotegument broken from central region of notogaster; B – ventral view, with enlargement of preanal region in upper right (* indicates location of C); C – fractured cerotegument on ventral plate; D – subcapitulum and surrounding region, ventral view; E – bothridial region, anterior view; F – proterosoma, anterior view. Scale bars: 50 µm (A, B); 10 µm (D-F); 2 µm (C).
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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.