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FIGURE 3 in Revision and phylogeny of the subaptera-group of Phyllodromica (Blattoptera: Blattellidae: Ectobiinae), including a parthenogenetic species and the evaluation of COI sequences for species identification (DNA barcoding)
FIGURE 3. Phyllodromica iberica morph #1, male (holotype). A Thoracal nota. B–F Abdominal tergites 5–9. (B) Tergite 5 and (C) tergite 6 with membranous glands in the lateral region of the anterior margin of tergites (black arrows); (D) tergite 7, white arrow heads point to the shallow pouches appearing as crescent–shaped black shadows; (E) tergite 8; (F) tergite 9 on glass rod. G Terminalia with tergite 10 (sa), cerci and paraprocts. H Hook of left phallomere with the posterior end on the top. I Subgenital plate with remaining genital sclerites (without hook). Abbreviations: ap anterior process, bf bristle field, c cercus, cm central mound, cp conelike process, ll lateral lobe, m mound, mes mesonotum, met metanotum, ml median lobe, mp medio-anterior process, pml posterior median lobe, pro pronotum, r ridge between bristle fields, rp right paraproct, sa supraanal plate, se sinusoidal edge, sp shallow pits, tm tegmen, tr transversal ridge, tt transversal trough. Same scale for (B, C, G) and (D, E, H). Identification: Sp 292b/M3 (holotype).
FIGURE 2 in Revision and phylogeny of the subaptera-group of Phyllodromica (Blattoptera: Blattellidae: Ectobiinae), including a parthenogenetic species and the evaluation of COI sequences for species identification (DNA barcoding)
FIGURE 2. Phyllodromica subaptera (female). A Thoracal nota. B Abdominal tergite 5. C Subgenital plate with two apodemal processes (a). D Dorsal complex of genitalia with additional sclerite (as): ventral view, posterior end on top. E Additional sclerite in higher enlargement (equivalent to "black frame" in D). F Ventral complex of genitalia: laterosternal shelf with intersternal folds between the arms. Abbreviations: as additional sclerite, a apodemal process, bd dorsal sclerite of basivalvula, bv ventral sclerite of basivalvula, c cercus, i intersternal fold, is intercalary sclerite, l laterosternal shelf, ls laterosternite IX, pl posterior lobe of valvifer II, pp paraproct, pt paratergites, T9 tergite 9, T10 tergite 10, v valves. Same scale for (B, C) and (D, F). Identification: Sp 203c/W4.
FIGURE 1. A–C P in Revision and phylogeny of the subaptera-group of Phyllodromica (Blattoptera: Blattellidae: Ectobiinae), including a parthenogenetic species and the evaluation of COI sequences for species identification (DNA barcoding)
FIGURE 1. A–C P. iberica morph #1, habitus. (A) Male in dorsal view; (B) female in dorsal and (C) ventral view. D Oothek of P. quadracantha (lateral view). Abbreviations: a antenna, c cercus, fl coxa of foreleg, h head, hl coxa of hindleg, mes mesonotum, met metanotum, ml coxa of midleg, pm palpus maxillaris, pro pronotum, sub subgenital plate, T2–T10 tergites 2–10, tm tegmen. Same scale in A and B. Localities: (A–C) Sp 449a, (D) Sp 500.
FIGURE 4 in Who's your daddy? On the identity and distribution of the paternal hybrid ancestor of the parthenogenetic gecko Lepidodactylus lugubris (Reptilia: Squamata: Gekkonidae)
FIGURE 4. Photos in life comparing putative members of Lepidodactylus pantai or Lepidodactylus woodfordi. (A) Lepidodactylus pantai from the type locality, Kei Kecil, Indonesia (photo by Luke M. Bloch). (B) Lepidodactylus cf. pantai from Opea Island, Papua New Guinea (photo by Fred Kraus). The dark coloration is the night-time coloration, whereas during the day (and in preservative) they show similar coloration as the other images. (C) Lepidodactylus pantai from Palmyra Atoll (photo by Robert Fisher). (D) Lepidodactylus pantai from Rangiroa Atoll (Tuamotu Archipelago) (photo by Ivan Ineich). (E) Lepidodactylus cf. woodfordi from Alu Island, Solomon Islands, adjacent to Fauro Island, the type locality of L. woodfordi (photo by Michael McCoy). Further comparison is needed to assess if L. woodfordi may be conspecific with L. pantai and would therefore have priority.
FIGURE 3 in Who's your daddy? On the identity and distribution of the paternal hybrid ancestor of the parthenogenetic gecko Lepidodactylus lugubris (Reptilia: Squamata: Gekkonidae)
FIGURE 3. Haplotype network for the Lepidodactylus pantai clade estimated for the mitochondrial ND2 gene. Circle sizes correspond to the number of individuals sharing a given haplotype and hash marks designate the number of nucleotide differences between haplotypes. Colors correspond to labeled locations.
FIGURE 1 in Who's your daddy? On the identity and distribution of the paternal hybrid ancestor of the parthenogenetic gecko Lepidodactylus lugubris (Reptilia: Squamata: Gekkonidae)
FIGURE 1. Map of the Pacific Basin displaying island populations of Lepidodactylus pantai. Red dots indicate populations with genetic sampling (*arno atoll based on cytochrome b sequences of Radtkey et al. [1995]). Yellow dots indicate populations identified by morphology either by field observations or examination of museum specimens. Stars indicate type localities of Lepidodactylus pantai (red) and Lepidodactylus woodfordi (green). Map data copyrighted OpenStreetMap contributors and available from https://www.openstreetmap.org.
Figure 2 in Parthenogenetic Darevskia lizards mate frequently if they have the chance: a quantitative analysis of copulation marks in a sympatric zone
Figure 2. Variation of snout–vent length (SVL, in mm) according to the number of copulation marks in parthenogenetic females of D. armeniaca from Kuchak (Armenia). Mean values and 0.95 confidence intervals are displayed as well as the raw data with symbols proportional to the number of individuals. Letters between parenthesis on the x-axis indicate the groups according to Duncan posthost tests (p <0.05) after significant ANOVA (see results).
Figure 1 in Parthenogenetic Darevskia lizards mate frequently if they have the chance: a quantitative analysis of copulation marks in a sympatric zone
Figure 1. Representative images of females of Darevskia sp. from Kuchak (Armenia). Left: dorsal view; right: ventral view and scar detail. (a) D. valentini (2n, bisexual); (b) D. armeniaca (2n, parthenogenetic); (c) D. unisexualis (2n, parthenogenetic); (d) D. valentini × D. armeniaca (3n, backcross); (e) D. valentini × D. unisexualis (3n, backcross). Identifications are all supported by genetic data (Freitas et al. in press)
Figure 1 in Feeding habits of the endemic tropical parthenogenetic lizard Cnemidophorus nativo (Teiidae) in a restinga area of northeastern Brazil
Figure 1. Monthly number of isopterans and larvae in relation to total number of consumed prey by Cnemidophorus nativo in the restinga of Guaratiba, Prado, BA, Brazil. Lizard sample sizes for each month are given above the bars.
FIGURE 3. Eurycercus macracanthus, parthenogenetic female from a in A revision of the subgenus Eurycercus (Eurycercus) Baird, 1843 emend. nov. (Cladocera: Eurycercidae) in the Holarctic with the description of a new species from Alaska
FIGURE 3. Eurycercus macracanthus, parthenogenetic female from a small lake covered by Stratiotes aloides, on left side of Sosnovka-Ahuny road, vicinities of Penza, Penza Area (A); small water bodies near Zeya Water Reservoir dam, Amur Area (B); Lake Bezymiannoje, near the Schugor River, Komi Autonomous Republic (C); Degtyarniy Zaton, a tributary of River Sura near village Sosnovka, vicinity of Penza, Penza Area (D, F, H, I); Lake Svetloe near River Chulym, Tomsk Area (G, E), all in Russia. A, lateral view. B, anterior view. C, head, lateral view. D, head pores. E, postabdomen. F, its distal portion. G, its basal portion. H, antenna I. I, antenna II. Scale bar denotes 1 mm (A–B); 0.1 mm (C–H).
FIGURES 285–293. Leydigia laevis, parthenogenetic female from unnamed lake 8 in A revision of Leydigia Kurz, 1875 (Anomopoda, Cladocera, Branchiopoda), and subgeneric differentiation within the genus
FIGURES 285–293. Leydigia laevis, parthenogenetic female from unnamed lake 8, SW of Cooma, Australia. 285–286. Dorsal head pores. 287–288. Postero-ventral and posterior margin of valve. 289. Postabdomen. 290. Base of postabdomen in dorsal view. 291–292. Preanal margin. 293. Distal portion of postabndomen. Scale bar denotes 100 µm for 285, 289–290, 293; 10 µm for 286–288, 291–292.
FIGURES 107–115. 107–111. Leydigia australis, parthenogenetic female from tube GOS F 18336a in A revision of Leydigia Kurz, 1875 (Anomopoda, Cladocera, Branchiopoda), and subgeneric differentiation within the genus
FIGURES 107–115. 107–111. Leydigia australis, parthenogenetic female from tube GOS F 18336a, possibly type material of G. O. Sars from unknown locality in Australia. 107–108. Adult and its antenna II. 109–111. Postabdomen and its preanal margin. 112–115 Leydigia macrodonta, lectotype, parthenogenetic female from slide GOS F9222, marked as "S.A.Mus. I", Republic of South Africa. 112–113. General view and head. 114–115. Distal and basal portion of postabdomen. Scale bar denotes 100 µm.
FIGURES 194–203. Leydigia macrodonta, parthenogenetic female from slide GOS F9222 in A revision of Leydigia Kurz, 1875 (Anomopoda, Cladocera, Branchiopoda), and subgeneric differentiation within the genus
FIGURES 194–203. Leydigia macrodonta, parthenogenetic female from slide GOS F9222, lectotype from locality marked as "S.A.Mus. I" (194) and from Soetendalsvlei wetland, Western Cape Province, Republic of South Africa, coll. 25.08.2000 by G. Jones (195–203). 195–196. Adult anf juvenile. 197–198. Dorsal head pores. 199. Labrum. 200. A fragment of valve. 201–203. Armature of ventral, postero-ventral and posterior margin of valve. Scale bar denotes 100 µm.
FIGURE 8. Bosminopsis zernowi, parthenogenetic female from a in On the taxonomic status of Oriental populations of the genus Bosminopsis Richard 1895 (Crustacea: Cladocera)
FIGURE 8. Bosminopsis zernowi, parthenogenetic female from a tributary of Dnieper River near Kremenchug, Poltava Area, Ukraine. A, valve of large parthenogenetic female. B. its antero-ventral portion. C, valve of smaller parthenogenetic female. D–G, Its postero-ventral valve portion. H–K, postabdomen. Scale bar denotes 0.1 mm.
Figure 6 in Ant crickets and their secrets: Myrmecophilus acerŋorum is not always parthenogenetic (Insecta: Orthoptera: Myrmecophilidae)
Figure 6. Haplotype distribution map based on COI sequences, parthenogenetic populations are depicted in red, magenta and orange. Size of the pie chart is proportional to the sample size. Location numbers correspond to the notation in the Supporting Information, Table S1.
Figure 5 in Ant crickets and their secrets: Myrmecophilus acerŋorum is not always parthenogenetic (Insecta: Orthoptera: Myrmecophilidae)
Figure 5. Haplotype networks of Myrmecophilus acerƲorum A, based on 41 sequences of COI gene. B, based on 30 concatenated sequences of COI and 16S. Circle size reflects haplotype frequency; missing haplotypes are represented by nodes and small perpendicular lines represent mutational steps. Haplotypes in magenta, red and orange represent parthenogenetic western populations.
Figure 2 in Ant crickets and their secrets: Myrmecophilus acerŋorum is not always parthenogenetic (Insecta: Orthoptera: Myrmecophilidae)
Figure 2. SEM images of male and female Myrmecophilus acerƲorum: A, hairs on male antenna; B, details of body hairs on male abdomen; C, male supragenital plate; D, male subgenital plate; E, epiphallus; F, female ovipositor valves. Scale 100 µm.
Figure 1 in Ant crickets and their secrets: Myrmecophilus acerŋorum is not always parthenogenetic (Insecta: Orthoptera: Myrmecophilidae)
Figure 1. Habitus of adults of Myrmecophilus acerƲorum: A, male from CoȘereni, Ialomiţa county, Romania, 11.V.2013; B, female from Letea, Tulcea county, 2.V.2019.
Figure 4 in Ant crickets and their secrets: Myrmecophilus acerŋorum is not always parthenogenetic (Insecta: Orthoptera: Myrmecophilidae)
Figure 4. Maximum likelihood tree of Myrmecophilus acerƲorum based on concatenated sequences of COI and 16S mtDNA, with GTR nucleotide substitution model and M. nonƲeilleri, M. fuscus, M. gallicus and M. balcanicus as outgroups. Numbers at nodes indicate bootstrap values (values <50 are not shown). The clade marked with blue represents the haplotypes from parthenogenetic populations. Coloured bars represent the different delimitation schemes obtained with> 3% of genetic differentiation on both COI alone, as well as on concatenated COI and 16S sequences, with ABGD (calculated with JC69, K2P and p genetic distances), PTP, TCS and GMYC sequence-based delineation tests, and white bars are due to missing sequences.
Figure 3 in Ant crickets and their secrets: Myrmecophilus acerŋorum is not always parthenogenetic (Insecta: Orthoptera: Myrmecophilidae)
Figure 3. Tip of the abdomen of Myrmecophilus acerƲorum: A, male supragenital plate and cerci, dorsal view; B, male subgenital plate, ventral view; C, female ovipositor and subgenital plate, ventral view. Scale 0.5 mm.
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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.