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Figs 10–14 in Halyomorpha halys fixed as the type species of the genus Halyomorpha (Hemiptera: Heteroptera: Pentatomidae)
Figs 10–14. Halyomorpha picus (Fabricius, 1794), male genitalia of the specimen from Mayr collection (NHMW). 10–13 – genital capsule (10 – posterior view, magnification 42×; 11 – lateral view, 42×; 12 – ventral view, 30×; 13 – dorsal view, 32×); 14 – paramere in posterior mediolateral view (100×). Abbreviations: pa – parameres, plp – posterolateral lobes of genital capsule. Scale bars: 0.5 mm. Orig. P. Kment.
Correlation of urban avian species diversity present in heterogenous habitat types of the Silk city, Odisha, Eastern India
<p>This is the complete metadata and the R code required to do the analysis of the paper regarding birds of Berhampur city.</p>
Figures 7–12. Phyllophaga type specimens. 7 in A new species of Phyllophaga Harris (Coleoptera: Scarabaeidae: Melolonthinae) from Puerto Rico
Figures 7–12. Phyllophaga type specimens. 7) Genitalia of P. bobevelynorum, female allotype, ventral view. 8) Genitalia of P. bobevelynorum, female allotype, lateral view. 9) Sclerotized median lobe of genitalia of P. bobevelynorum, male holotype, caudal view. 10) Sclerotized median lobe of genitalia of P. adjuntas, male holotype, caudal view. 11) Posterior tarsal claw of P. bobevelynorum, male holotype. 12) P. adjuntas, holotype specimen labels.
Fig. 24 in Redescription Of The Type Species Of The Genus Argistes (Aranei, Liocranidae)
Fig. 24. Distribution records of Argistes velox. Filled circles refer to literature data and open circles refer to present data.
Figs 16–23 in Redescription Of The Type Species Of The Genus Argistes (Aranei, Liocranidae)
Figs 16–23. Somatic characters and copulatory organs of Argistes velox: 16 — innerets of male; 17–18 bulb, ventral and anterior, embolus is broken; 19 — epigyne, dorsal; 20 — right part of epigyne, antero-dorsal; 21 — tibia and cymbium of male palp, retrolateral; 22 — epiandrous region; 23 — male abdomen, ventral. Scale = 0.1 mm if not otherwise indicated. Abbreviations: Ar — accessorial receptacle, Bc — bursa copulatrix, Cd — copulatory duct, Cf — cymbial fold, Cl — colulus, Co — conductor, Ea — epiandrus, Em — embolus, Re — receptacle, Rg — gland of receptacle, Rs — round swelling, Ta — tegular apophysis.
Figs 1‒7 in Redescription Of The Type Species Of The Genus Argistes (Aranei, Liocranidae)
Figs 1‒7. Habitus and male palp of Argistes velox: 1–2 — female habitus, lateral and dorsal; 3 — male habitus, lateral; 4‒5 — male palp, retro- and prolateral; 6‒7 — prosoma frontal in female and male. Scale = 0.2 mm if not otherwise indicated.
Figs 8‒15 in Redescription Of The Type Species Of The Genus Argistes (Aranei, Liocranidae)
Figs 8‒15. Copulatory organs and abdomen of Argistes velox: 8–10 — male palp, ventral, ventro-prolateral and dorsal; 11–12 — ventral side of abdomen in female and male; 13 — intact epigyne, ventral; 14–15 — macerated epigyne, ventral and dorsal. Scale = 0.2 mm. Abbreviations: Ar — accessorial receptacle, Bc — bursa copulatrix, Cd — copulatory duct, Co conductor, Ea — epiandrus, Em — embolus, Mp — median pocket, Re — receptacle, Rg — gland of receptacle, Ta — tegular apophysis.
Data from: eDNA metabarcoding of log hollow sediments and soils highlights the importance of substrate type, frequency of sampling and animal size, for vertebrate species detection
<p>Fauna monitoring often relies on visual monitoring techniques such as camera trappings, which have biases leading to underestimates of vertebrate species diversity. Environmental DNA (eDNA) has emerged as a new source of biodiversity data that may improve biomonitoring; however, eDNA based assessments of species richness remain relatively untested in terrestrial environments. We investigated the suitability of fallen log hollow sediment as a source of vertebrate eDNA, across two sites in south-western Australia - one with a Mediterranean climate and the other semi-arid. We compared two different approaches (camera trapping and eDNA metabarcoding) for monitoring of vertebrate species, and investigated the effect of other factors (frequency of species, timing of visits, frequency of sampling, body size) on vertebrate species detectability. Metabarcoding of hollow sediments resulted in the detection of higher species richness in comparison Hollow sediment detected higher species richness (29 taxa: six birds, three reptiles and 20 mammals) to metabarcoding of soil at the entrance of the hollow (13 taxa: three birds, two reptiles and eight mammals). We detected 31 taxa in total with eDNA metabarcoding and 47 with camera traps, with 14 taxa detected by both (12 mammals and two birds). By comparing camera trap data with eDNA read abundance, we were able to detect vertebrates through eDNA metabarcoding that had visited the area up to two months prior to sample collection. Larger animals were more likely to be detected, and so were vertebrates that were identified multiple times in the camera traps. These findings demonstrate the importance of substrate selection, frequency of sampling, and animal size, on eDNA based monitoring. Future eDNA experimental design should consider all these factors as they affect detection of target taxa. </p>
Text-fig. 3. Tendency of changes in IPM and PE width indicators in different types of enamel of the Equidae species of the "tarpan" group. I–III – types of enamel. a: IPM; b: PE. in The Ultrastructure Of The Tooth Enamel Of Small Equus Of The "Tarpan" Group And Their Possible Phylogenetic Connections
Text-fig. 3. Tendency of changes in IPM and PE width indicators in different types of enamel of the Equidae species of the "tarpan" group. I–III – types of enamel. a: IPM; b: PE.
FIGURE 1. Odontonema aliciae. A. Habit showing distal leaves with subauriculate bases and inflorescence. B. Habit and habitat. C. Capsule. D. Seed. A, B from the type A in Odontonema aliciae, a New Heterostylous Species of Acanthaceae from Panama
FIGURE 1. Odontonema aliciae. A. Habit showing distal leaves with subauriculate bases and inflorescence. B. Habit and habitat. C. Capsule. D. Seed. A, B from the type A. Ibáñez et al. 6928, photos by A. Ibáñez, used with permission; C, D from Nee & Andres 46341.
Рис. 4. Распределение станций отбора проб по глубине и типу грунта (круЖком обведены станции, на которых макробентос не обнаруЖен; БО – биогенные остатки, ГМ – галька мелкаЯ, Гр – гравий, И – ил, П – песок). Fig. 4. Distribution of sampling stations by depth and type of bottom sediments (circles are around the stations where no macrobenthos was detected; БО – biogenic residues, ГМ – pebbles, Гр – gravel, И – silt, П – sand). in Species composition and distribution of bivalve mollusks in plankton and benthos in Nevelsky Strait in summer
Рис. 4. Распределение станций отбора проб по глубине и типу грунта (круЖком обведены станции, на которых макробентос не обнаруЖен; БО – биогенные остатки, ГМ – галька мелкаЯ, Гр – гравий, И – ил, П – песок). Fig. 4. Distribution of sampling stations by depth and type of bottom sediments (circles are around the stations where no macrobenthos was detected; БО – biogenic residues, ГМ – pebbles, Гр – gravel, И – silt, П – sand).
А – типовые местонахоЖдениЯ: Зал. ЛаврентиЯ (красный маркер), б. ПровидениЯ (Зеленый маркер); B, B' – иЗобраЖениЯ раковины (B) и Зуба радулы (B') Bela violacea var. nodulosa. Вр=14.5 мм, ДЗ=0.25 мм, иЗ: Krause [1885, pl. 18, figs. 4, 12]; C, C' – синтип Bela violacea var. nodulosa (C) и увеличенный участок предпоследнего оборота (C'), ZMB 37860, Вр=12 мм (фотографиЯ – с раЗрешениЯ ZMB); D–I – иЗменчивость Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN беЗ номера, ЗФИ, о-в Аполлонова, Американский Залив, 3–4 м. Вр=8.2 мм; E – Defrancia becki. ZIN беЗ номера, ЗФИ, о-в Кука, 3–4 м. Вр=9.1 мм; F – Bela violacea var. laevior. Вр=12 мм, иЗ: Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Баренцево море, Югорский Шар, 13 м. Вр=8.7 мм; H – Pleurotoma bicarinata. ZIN 41203/156, ЗФИ, о-в ГрЭм-БЭм, 12–15 м. Вр=8.4 мм; I, I' – Зубы радулы типичной (I) и беЗкилевой (I') форм. ДЗ=0.12 мм и 0.21 мм, соответственно, иЗ: [Sars, 1878, pl. 9, figs. 7, 8]; J – иЗобраЖение раковины Lora inequita. Вр=11 мм, иЗ: Dall [1919, pl. 16, fig. 9]; K – голотип Lora inequita, USNM 222238. Вр=11 мм (фотографиЯ – с раЗрешениЯ USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: раковины (L) и Зуб радулы (L'). Вр=12 мм и 11.6 мм, соответственно, ДЗ=0.15 мм, иЗ: Богданов [1990, рис. 175, 176, 422 (7)]. A – type localities: Lawrence Bay (red circle), Providence Bay (green circle); B, B' – images of the shell (B) and tooth of the radula (B') of Bela violacea var. nodulosa. H=14.5 mm, L=0.25 mm, after Krause [1885, pl. 18, figs. 4, 12]; C, C' – a syntype of Bela violacea var. nodulosa (C) and the enlarged section of the penultimate whorl (C'), ZMB 37860, H=12 mm (photo – courtesy of ZMB); D–I – variability of Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN uncatalogued, Franz Josef Land, Apollonova Isl., American Gulf, 3–4 m. H=8.2 mm; E – Defrancia becki. ZIN uncatalogued, Franz Josef Land, Cook Isl., 3–4 m. H=9.1 mm; F – Bela violacea var. laevior. H=12 mm, after Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Barents Sea, Ugra Shar, 13 m. H=8.7 mm; H – Pleurotoma bicarinata. ZIN 41203/156, Franz Josef Land, Graham-Bam Isl., 12–15 m. H= 8.4 mm; I, I' – teeth of typical (I) and keelless (I') forms. L=0.12 mm and 0.21 mm, respectively; after Sars [1878, pl. 9, figs. 7,8]; J – image of Lora inequita. H=11 mm, after Dall [1919, pl.16, fig. 9]; K – the holotype of Lora inequita, USNM 222238. H=11 mm (photo – courtesy of USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: shells (L) and tooth (L'). H=12 mm and 11.6 mm, respectively, L=0.15 mm, after Bogdanov [1990, figs. 175, 176, 422 (7)]. in Curtitoma nodulosa (Krause, 1885) comb. nov. (Gastropoda: Mangeliidae), a rare species twice described from the northern part of Bering Sea
А – типовые местонахоЖдениЯ: Зал. ЛаврентиЯ (красный маркер), б. ПровидениЯ (Зеленый маркер); B, B' – иЗобраЖениЯ раковины (B) и Зуба радулы (B') Bela violacea var. nodulosa. Вр=14.5 мм, ДЗ=0.25 мм, иЗ: Krause [1885, pl. 18, figs. 4, 12]; C, C' – синтип Bela violacea var. nodulosa (C) и увеличенный участок предпоследнего оборота (C'), ZMB 37860, Вр=12 мм (фотографиЯ – с раЗрешениЯ ZMB); D–I – иЗменчивость Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN беЗ номера, ЗФИ, о-в Аполлонова, Американский Залив, 3–4 м. Вр=8.2 мм; E – Defrancia becki. ZIN беЗ номера, ЗФИ, о-в Кука, 3–4 м. Вр=9.1 мм; F – Bela violacea var. laevior. Вр=12 мм, иЗ: Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Баренцево море, Югорский Шар, 13 м. Вр=8.7 мм; H – Pleurotoma bicarinata. ZIN 41203/156, ЗФИ, о-в ГрЭм-БЭм, 12–15 м. Вр=8.4 мм; I, I' – Зубы радулы типичной (I) и беЗкилевой (I') форм. ДЗ=0.12 мм и 0.21 мм, соответственно, иЗ: [Sars, 1878, pl. 9, figs. 7, 8]; J – иЗобраЖение раковины Lora inequita. Вр=11 мм, иЗ: Dall [1919, pl. 16, fig. 9]; K – голотип Lora inequita, USNM 222238. Вр=11 мм (фотографиЯ – с раЗрешениЯ USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: раковины (L) и Зуб радулы (L'). Вр=12 мм и 11.6 мм, соответственно, ДЗ=0.15 мм, иЗ: Богданов [1990, рис. 175, 176, 422 (7)]. A – type localities: Lawrence Bay (red circle), Providence Bay (green circle); B, B' – images of the shell (B) and tooth of the radula (B') of Bela violacea var. nodulosa. H=14.5 mm, L=0.25 mm, after Krause [1885, pl. 18, figs. 4, 12]; C, C' – a syntype of Bela violacea var. nodulosa (C) and the enlarged section of the penultimate whorl (C'), ZMB 37860, H=12 mm (photo – courtesy of ZMB); D–I – variability of Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN uncatalogued, Franz Josef Land, Apollonova Isl., American Gulf, 3–4 m. H=8.2 mm; E – Defrancia becki. ZIN uncatalogued, Franz Josef Land, Cook Isl., 3–4 m. H=9.1 mm; F – Bela violacea var. laevior. H=12 mm, after Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Barents Sea, Ugra Shar, 13 m. H=8.7 mm; H – Pleurotoma bicarinata. ZIN 41203/156, Franz Josef Land, Graham-Bam Isl., 12–15 m. H= 8.4 mm; I, I' – teeth of typical (I) and keelless (I') forms. L=0.12 mm and 0.21 mm, respectively; after Sars [1878, pl. 9, figs. 7,8]; J – image of Lora inequita. H=11 mm, after Dall [1919, pl.16, fig. 9]; K – the holotype of Lora inequita, USNM 222238. H=11 mm (photo – courtesy of USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: shells (L) and tooth (L'). H=12 mm and 11.6 mm, respectively, L=0.15 mm, after Bogdanov [1990, figs. 175, 176, 422 (7)].
Morphospace disparity and species diversity in Sri Lankan phytophagous scarab beetles – a comparison by forest types, altitude, and sites
<p>The files contain the supporting information and raw data of the masnucript, Morphospace disparity and species diversity in Sri Lankan phytophagous scarab beetles – a comparison by forest types, altitude, and sites.</p> <p>It includes the following:</p> <p><strong>Raw Data:</strong></p> <p><strong><span>Suppl. Table 1: </span></strong><span>Details of sampling sites (Sri Lanka); L number, coordinates, elevation, elevation zone and forest types. </span><span>Elevation zones; EZ1: 0-500m, EZ2: 501-1000m, EZ3: 1001-1500m, EZ4: 1501-2000m, EZ5; 2001-2500m. </span><span>Forest types; WL: evergreen wet lowland forests, DL: evergreen dry lowland forests, SM: sub-montane forests, MO: montane forests.</span></p> <p><strong>Suppl. Table 2. </strong>Morphometric measurements and metadata of all studied specimens. Metadata include species identification, voucher number, occurrence data regarding sampling location in Sri Lanka, elevation zone (EZ), and forest type (F). Units of measurements are mm. WL: evergreen wet lowland forests, LD: evergreen dry lowland forests, SM: sub-montane forests, MO: montane forests; EZ1: 0-500m, EZ2: 501-1000m, EZ3: 1001-1500m, EZ4: 1501-2000m, EZ5; 2001-2500m; L1: Aranayake; L2: Riverston; L3: NIFS Arboretum; L4: Deenston; L5: Nuwara Eliya; L6: Horton Plains; L8: Hiyare; L9: Kottawa; L10: Kanneliya; L11: Piduruthalagala; L12: Uda Peradeniya; L13: Gannoruwa; L14: Udawattakele. Morphological measurements abbreviations are explained in Sup. Fig.1.</p> <p><strong>Results:</strong></p> <p><strong><span>Suppl. Table 3: </span></strong><span>Proportion of</span><strong><span> </span></strong><span>variance explained by PC axes in principal component analysis for the data subsets of lineages </span><span>(derived from shape and size data). Values of axes reflecting the 95% of explained cumulative variation are highlighted in bold.</span></p> <p><strong><span>Suppl. Table 4</span></strong><strong><span>: </span></strong><span>Euclidean distances between species (mean/median/maximum) for shape and size partitioned by </span><span>forest types </span><span>and lineages (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). </span><span>WL: Wet lowland; DL: Dry lowland; SM: Sub-montane; MO: Montane.</span></p> <p><strong><span>Suppl. Table 5: </span></strong><span>Euclidean distances between species mean/median/maximum) for shape and size partitioned by elevational zones and lineages (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). </span><span>EZ1: 0-500m. EZ2: 501-1000m. EZ3: 1001-1500m. EZ4: 1501-2000m. EZ5: 2001-2500m.</span></p> <p><strong><span>Suppl. Table 6: </span></strong><span>Euclidean distances between species (mean/median/maximum) for shape and size partitioned by localities (L1-14), and lineages (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). </span></p> <p><strong><span>Suppl. Table 7</span></strong><strong><span>: </span></strong><span>Pairwise p-values from non-parametric MANOVA on PCA scores partitioned for shape and size <u>forest types</u> and lineages (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). Significant correlations (p value <0.05) are shown in bold italics. WL: Wet lowland; DL: Dry lowland; SM: Sub-montane; MO: Montane.</span></p> <p><strong><span>Suppl. Table 8</span></strong><strong><span>: </span></strong><span>Pairwise p-values from non-parametric MANOVA on PCA scores for shape and size partitioned for <u>elevational zones</u> and lineages (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). Significant correlations (p value <0.05) are shown in bold italics. EZ1: 0-500m. EZ2: 501-1000m. EZ3: 1001-1500m. EZ4: 1501-2000m. EZ5: 2001-2500m.</span></p> <p><strong><span>Suppl. Table 9: </span></strong><span>Pairwise p-values from non-parametric MANOVA on PCA scores partitioned for <u>localities</u> and lineages for shape (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). Significant correlations (p value <0.05) are shown in bold italics.</span></p> <p><strong><span>Suppl. Table 10: </span></strong><span>Pairwise p-values from non-parametric MANOVA on PCA scores partitioned for <u>localities</u> and lineages for size (all Pleurosticts, Sericini only, and Pleurosticts excluding Sericini (*)). Significant correlations (p value <0.05) are shown in bold italics.</span></p> <p> </p> <p><strong>Figure S1.</strong> Illustration of the measured morphological traits (after Eberle et al., 2014). Schematic drawings of a Sericini beetle, in (A) dorsal, (B) ventral, and (C) lateral aspect. Body: BH - maximal body height, EH - maximal elytra height, EL - maximal elytra length, Eld - maximal diagonal elytra length, Elmb - length from maximal body width to elytral apex, EW - maximal elytra width, Ewb - elytral width at middle of scutellum, PL - maximal pronotum length, PW - maximal pronotum width; Head: ED - maximal eye diameter, HW - maximal head with including eyes, IOD - minimal interocular distance (dorsal view); Legs: MCL - maximal length of metacoxa, MFL - maximal length of metafemur, MFW - maximal width of metafemur, MTL - maximal length of metatibia, MTW - maximal width of metatibia, PFL - maximal length of profemur, PFW - maximal width of profemur, PTL - maximal length of protibia.</p> <p><strong>Figure S2.</strong> Biplots of PC1 and 2 from principal components analysis, illustrating trait contribution to the principal patterns of morphospace (raw measurements). Trait abbreviations are explained in Figure S1.</p> <p><strong>Figure S3. </strong>Patterns of morphospace disparity of all Pleurosticts derived from raw measurements in individual localities. Symbols represent genus or other family-group level, color of symbols single species.<br> <br><strong>Figure S4. </strong>Patterns of morphospace disparity of Sericini derived from raw measurements in individual localities. Colored dots represent single species. Locality L12 had no Sericini recorded.<br> <br><strong>Figure S5. </strong>Patterns of morphospace disparity (PCA plots of PC1 and PC2) derived from raw measurements of Sericini chafers partitioned for forest types (A), elevation zones (B), localities (C)(enlarged visualization from Fig. 2). Colored dots represent single species, outlines grouping entities grouped by forest types, elevation zone, or locality.</p>
Рис. 1. ВоЗмоЖный синтип Mactra sulcataria Deshayes in Reeve, 1854 иЗ коллекции МуЗеЯ естественной истории, Лондон (коллекциЯ Х. Каминга), регистрационный номер № NHMUK 20130005. Рисунок Этого ЭкЗемплЯра опубликован Л. Ривом [Reeve, 1854, pl. 2, fig. 5]; воспроиЗведен в настоЯЩей статье (рис. 2А). in Notes on type material of Mactra sulcataria Deshayes in Reeve, 1854 (Bivalvia: Mactridae) and taxonomic history of the species
Рис. 1. ВоЗмоЖный синтип Mactra sulcataria Deshayes in Reeve, 1854 иЗ коллекции МуЗеЯ естественной истории, Лондон (коллекциЯ Х. Каминга), регистрационный номер № NHMUK 20130005. Рисунок Этого ЭкЗемплЯра опубликован Л. Ривом [Reeve, 1854, pl. 2, fig. 5]; воспроиЗведен в настоЯЩей статье (рис. 2А).
Fig. 2 in Notes on type material of Mactra sulcataria Deshayes in Reeve, 1854 (Bivalvia: Mactridae) and taxonomic history of the species
Fig. 2. Illustrations of Mactra sulcataria Deshayes in Reeve, 1854 in monographs of the 19th century: A – Reeve [1854, pl. 2, fig. 5]; B – Weinkauff [1881, Taf. 18, Fig. 3]; in references as: Küster, Weinkauff [1841–1884].
Рис. 3. ОписаниЯ Mactra sulcataria Deshayes in Reeve, 1854 в статье Ж.П. ДехЭ [Deshayes, 1854, p. 15] (вверху) и монографии Л. Рива [Reeve, 1854, species 5] (вниЗу). in Notes on type material of Mactra sulcataria Deshayes in Reeve, 1854 (Bivalvia: Mactridae) and taxonomic history of the species
Рис. 3. ОписаниЯ Mactra sulcataria Deshayes in Reeve, 1854 в статье Ж.П. ДехЭ [Deshayes, 1854, p. 15] (вверху) и монографии Л. Рива [Reeve, 1854, species 5] (вниЗу).
Fig. 13. Lamprobityle magnifica Heller, 1923 in Type specimens of the genera Doliops Waterhouse, 1841 and Lamprobityle Heller, 1923 (stat. nov.) (Coleoptera: Cerambycidae) and description of two new species deposited in Senckenberg Natural History collections Dresden, Germany
Fig. 13. Lamprobityle magnifica Heller, 1923 (=Doliops magnifica (Heller, 1923)) (A – dorsal view, B – lateral view, C – labels)
Рис. 2. ИЗобраЖениЯ Mactra sulcataria Deshayes in Reeve, 1854 в работах 19 в.: A – Reeve [1854, pl. 2, fig. 5]; B – Weinkauff [1881, Taf. 18, Fig. 3]; в списке литературы как: Küster, Weinkauff [1841–1884]. in Notes on type material of Mactra sulcataria Deshayes in Reeve, 1854 (Bivalvia: Mactridae) and taxonomic history of the species
Рис. 2. ИЗобраЖениЯ Mactra sulcataria Deshayes in Reeve, 1854 в работах 19 в.: A – Reeve [1854, pl. 2, fig. 5]; B – Weinkauff [1881, Taf. 18, Fig. 3]; в списке литературы как: Küster, Weinkauff [1841–1884].
Figure 3 in Original specimens and type localities of early described polychaete species (Annelida) from Norway, with particular attention to species described by O.F. Müller and M. Sars
Figure 3. Example of text page from Zoologia Danica prodromus for polychaetes with armed mouth ('ore forcipato') and with eversible pharynx ('ore proboscideo'). From Müller (1776).
Figure 2 in Original specimens and type localities of early described polychaete species (Annelida) from Norway, with particular attention to species described by O.F. Müller and M. Sars
Figure 2. Text page and plate for descriptions of Scoletoma fragilis (= Lumbricus fragilis) and Scoloplos armiger (= Lumbricus armiger) from Zoologia Danica Vol. I (Müller, 1777–84).
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Allen Brain Atlas
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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
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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.