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Figure 84 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 84. Rayforstia vulgaris (Forster) from Lake Te Au, New Zealand (MCZ): A male habitus, dorsal view B female habitus, dorsal view C male cephalothorax, antero-dorsal view D female abdomen, ventral view.
Figure 69 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 69. Scanning electron micrographs of female Epigastrina fulva (Hickman) from Mount Wellington, Tasmania (WAM T77728): A leg I tarsal organ B leg I lyriform organ C leg I tibial trichobothrium D leg IV claws, showing elongate inferior claw.
Figure 68 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 68. Scanning electron micrographs of Epigastrina fulva (Hickman) from Mount Wellington, Tasmania (WAM T77728): A female chelicerae, frontal view B female cheliceral promargin C female pedipalp, antero-lateral view D tip of female pedipalp E male right chelicera (left removed), frontal view F male cheliceral promargin.
Figure 66 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 66. Epigastrina typhlops sp. n., holotype male from the Mole Creek karst, Tasmania (AMS KS29793): A left pedipalp, ventral view B left pedipalp, retrolateral view. Scale bar = 0.065 mm (65 µm).
Figure 65 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 65. Epigastrina typhlops sp. n. from the Mole Creek karst, Tasmania. A, C holotype male (AMS KS29793): A habitus, dorsal view C cephalothorax and right pedipalp (left removed), antero-dorsal view. B, D allotype female (QVM 13:12765): B habitus, dorsal view D abdomen, ventral view. Note the pale body colouration and complete absence of eyes.
Figure 30 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 30. Austropholcomma florentine sp. n. from the Florentine Valley, Tasmania. A, C holotype male (TMAG): A habitus, dorsal view C abdomen, ventral view. B, D allotype female (TMAG): B habitus, dorsal view D abdomen, ventral view.
Figure 32 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 32. Austropholcomma florentine sp. n., paratype male from the Florentine Valley, Tasmania (FMC): A left pedipalp, ventral view B left pedipalp, retrolateral view. Scale bar = 0.065 mm (65 µm). Note that the distal, intertwined embolus has been omitted in (A) for clarity.
Figure 6 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 6. Scanning electron micrographs of 'Inflaticrus' sp. from the Langeberg Range, Western Cape province, South Africa (TM 15228): A male pedipalp, pro-ventral view B male bulb, pro-ventral view C detail of (B), showing basal conductor and embolus D tip of male pedipalpal patella, pro-ventral view E female sternum, ventro-lateral view, showing sternal pits F female posterior median and posterior lateral spinnerets, ventral view. Note the enlarged bCY gland spigot base on the PLS, the single cylindrical gland spigot on the PMS, and the absence of any posterior minor ampullate gland spigot or nubbin on the PMS (arrow denotes the anterior, mesal direction).
Figure 2 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 2. Strict consensus cladogram resulting from an equal weights parsimony analysis of the 'expanded' matrix of Griswold et al. (1998) and Lopardo and Hormiga (2008) (see Appendix I), showing common clades recovered in 6 equally parsimonious trees (length = 225; CI = 0.52; RI = 0.77). Unambiguous character optimisations and clade support indices are shown for each node (Bremer support/ Jackknife frequencies> 50). The symphytognathidan "EbCY clade" is highlighted, including all anapid, symphytognathid, micropholcommatid and 'teutoniellid' taxa; an implied weights analysis (K=1–6) did not affect the monophyly or composition of this clade.
Figure 5 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 5. Scanning electron micrographs of Teutoniella cekalovici Platnick & Forster from Mirador Alemán, Chile (WAM T94536): A male pedipalp, pro-ventral view B male bulb, ventral view C detail of (B), showing basal conductor straddling embolus D male pedipalpal tibia and patella, pro-ventral view E male sternum, antero-ventral view, showing sternal pits F female left posterior median spinneret, antero-ventral view, showing single cylindrical gland spigot and absence of any posterior minor ampullate gland spigot or nubbin (arrow denotes the anterior, mesal direction).
Figure 4 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 4. Optimal cladogram for the Micropholcommatidae under equal and implied weights, and one of six equally parsimonious trees recovered from an equal weights analysis of the 'new' matrix (length = 135; see Appendix II). With the exception of the highlighted (*) node 'Patelliella adusta + Micropholcommatini', all clades shown were recovered in all iterations of an implied weights analysis (K=1–6); the phylogenetic position of P. adusta changed to 'P. adusta + Textricellini' under K-values 1–5. Unambiguous character optimisations are shown for each node, and bold species are newly described, with generic type species highlighted (*).
Figure 3 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 3. Strict consensus cladogram resulting from an equal weights parsimony analysis of the 'new' matrix (see Appendix II), showing common clades recovered in six equally parsimonious trees (length = 135; CI = 0.58; RI = 0.78). Unambiguous character optimisations and clade support indices are shown for each node (Bremer support/Jackknife frequencies> 50). Bold species are newly described, with generic type species highlighted (*).
Figure 7 in The spider family Micropholcommatidae (Arachnida: Araneae: Araneoidea): a relimitation and revision at the generic level
Figure 7. The genera of Micropholcommatidae, illustrated with habitus photographs of representative male specimens. A–D tribe Micropholcommatini: A Micropholcomma caeligenum Crosby & Bishop B Pua novaezealandiae Forster C Austropholcomma florentine sp. n. D Tricellina gertschi (Forster & Platnick). E–M tribe Textricellini: E Eterosonycha aquilina sp. n. F Epigastrina fulva (Hickman) G Raveniella peckorum sp. n. H Rayforstia vulgaris (Forster) I Normplatnicka lamingtonensis (Forster)] Eperiella alsophila sp. n. K Algidiella aucklandica (Forster) L Taliniella nigra (Forster) M Tinytrella pusilla (Forster). N Patelliella adusta sp. n., tribe Patelliellini. O–P subfamily Taphiassinae: O Olgania excavata Hickman P Taphiassa robertsi sp. n. Q–R subfamily Gigiellinae: Q Gigiella milledgei sp. n. R Gigiella platnicki sp. n. Note that Guiniella tropica (Forster) is not illustrated.
Figure 6 in First record of the family Pseudocerotidae (Platyhelminthes, Polycladida, Cotylea) from the Persian Gulf, Iran
Figure 6. Sagittal section of Tytthosoceros lizardensis: A male copulatory system B female copulatory system C pharynx: ma male antrum s stylet sv seminal vesicle p prostate fa female antrum fg female gonopore ce cement gland ph pharynx mo mouth.
Figure 3 in First record of the family Pseudocerotidae (Platyhelminthes, Polycladida, Cotylea) from the Persian Gulf, Iran
Figure 3. Ear-like pseudotentacle in Tytthosoceros lizardensis: te pseudotentacular eyes ce cerebral eyes.
Figure 7 in First record of the family Pseudocerotidae (Platyhelminthes, Polycladida, Cotylea) from the Persian Gulf, Iran
Figure 7. Sagittal reconstruction of Tytthosoceros lizardensis: ma male antrum mg male gonopore s stylet sv seminal vesicle p prostate fa female antrum fg female gonopore ce cement gland ph pharynx mo mouth
Fig. 16 in Contributions to the knowledge of Formicidae (Hymenoptera, Aculeata): a new diagnosis of the family, the first global male-based key to subfamilies, and a treatment of early branching lineages
Fig. 16. Male representatives of three subfamilies. A–B. Formica wheeleri, Formicinae (U.S.A., CASENT0173024, A. Nobile). C–D. Rhytidoponera, Ectatomminae, ectaheteromorph clade (Australia, CASENT0004610, A. Nobile). E–F. Pogonomyrmex rastratus (Argentina, CASENT0172673, A. Nobile). Scale bars: A, C = 0.5 mm, B, D, F = 1.0 mm, E = 0.2 mm.
Fig. 9 in Contributions to the knowledge of Formicidae (Hymenoptera, Aculeata): a new diagnosis of the family, the first global male-based key to subfamilies, and a treatment of early branching lineages
Fig. 9. Apomyrma CD01, male, photomicrographs. A. Forewing. B. Hindwing. C. Abdominal sternum IX, ventral view. D. Genital capsule, dorsal view. E. Genital valves, slightly splayed and without cupula, ventral view. F. Genital capsule, lateral view. G. Volsella and paramere, mesal view. H. Penisvalva in situ, mesal view. Scale bars: A–B = 0.5 mm, C–H = 0.1 mm. Abbreviations: see Material and Methods.
Fig. 10 in Contributions to the knowledge of Formicidae (Hymenoptera, Aculeata): a new diagnosis of the family, the first global male-based key to subfamilies, and a treatment of early branching lineages
Fig. 10. Representative males of Leptanillinae, lateral view A. Protanilla "TH01" (Thailand, CASENT0119776, A. Nobile), arrow indicates loss of abdominal segment II petiolation. B. Protanilla "TH03" (Thailand, CASENT0119791, E. Prado). C. Leptanilla swani (Australia, CASENT0172318, A. Nobile). D. Protanilla sp. (Indonesia, CASENT0178838, A. Nobile), arrow indicates basolateral basimeral process. E. Scyphodon sp. (Indonesia, MCZ155112w, A. Nobile). F. Noonilla sp., used with permission from Petersen (1968). Scale bars: A, C, E–F = 0.2 mm, D = 0.5 mm, B = 1.0 mm.
Fig. 12 in Contributions to the knowledge of Formicidae (Hymenoptera, Aculeata): a new diagnosis of the family, the first global male-based key to subfamilies, and a treatment of early branching lineages
Fig. 12. Martialis heureka Rabeling & Verhaagh, 2008, male, wing photomicrographs and genitalia illustrations, genital membranes not shown. A. Forewing. B. Hindwing. C. Abdominal sternum IX, ventral view. D. Genital capsule, dorsal view. E. Genital capsule, ventral view. F. Genital capsule, lateral view. G. Volsella and paramere, mesal view. H. Penisvalva in situ, mesal view. Scale bars: A–B = 0.5 mm, C–H = 0.1 mm. Abbreviations: see Material and Methods.
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.