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Fig. 60 in Cochlostoma Jan, 1830 revised: an overview of the subgenus Turritus Westerlund, 1883 and its species (Caenogastropoda, Cochlostomatidae)
Fig. 60. Topotypical Cochlostoma (T.) montanum (Issel, 1866), 1- top of Pania della Croce, I (WP-99-.
Operating diagram of IF incubator, two identical incubators were used for eggs that were already sorted. They are made up of an isothermal enclosure and contain three tiers (100 × 60 × 17 cm). The water circulating in each tier comes from the same filtration, cooling and sterilisation device. As a result, the eggs placed in the different tiers are subject to the same temperature regime. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of IF incubator, two identical incubators were used for eggs that were already sorted. They are made up of an isothermal enclosure and contain three tiers (100 × 60 × 17 cm). The water circulating in each tier comes from the same filtration, cooling and sterilisation device. As a result, the eggs placed in the different tiers are subject to the same temperature regime.
Operating diagram of the incubator, two tiered modules contain six independent incubators. Three shallow hatching are (220 × 60 × 17 cm) stacked on top of each other to create a compact assembly in which each tier functions independently. Eighteen trays covered with eggs can be placed in each tier, allowing the simultaneous incubation of seven to nine lays. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of the incubator, two tiered modules contain six independent incubators. Three shallow hatching are (220 × 60 × 17 cm) stacked on top of each other to create a compact assembly in which each tier functions independently. Eighteen trays covered with eggs can be placed in each tier, allowing the simultaneous incubation of seven to nine lays.
Figure 60. Borboropactus nanda Lin & Li in Taxonomic notes on some spider species (Arachnida: Araneae) from China and Vietnam
Figure 60. Borboropactus nanda Lin & Li, sp. nov., alive. A. Holotype male; B. Paratype female. Photoed by Fan Gao.
Figure 60 in Thirty-eight spider species (Arachnida: Araneae) from China, Indonesia, Japan and Vietnam
Figure 60. Tekellina spp., dorsal view, holotype males (A, C) and paratype females (B, D), habitus. A–B. T. haosiwen Lin & Li, sp. nov.; C–D. T. huihangi Lin & Li, sp. nov. Scale bars = 0.2 mm.
Figs 57–60. Abdomen morphology. 57 in ON SPLITTING OF THE GENUS NOTOCUPES (COLEOPTERA: ARCHOSTEMATA): NEW DATA ON MORPHOLOGY AND TAXONOMY
Figs 57–60. Abdomen morphology. 57 – Rhabdocupes rostratus; 58 – Conexicoxa longicollis; 59 – Brachilatus caducus; 60 – Notocupes lapidarius. Scale bar = 1 mm.
Figures 59–60 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)
Figures 59–60. Olivierus przewalskii (Birula, 1897), tergites of male from Ghulja (Yining) County (59) and female from Yarkant (Shache) County (60) under UV light.
Figures 60–61 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 60–61. Parabuthus evae sp. n., male holotype, in dorsal (60) and ventral (61) views. Scale bar: 10 mm.
Figures 53–60. Nephrotoma nigrostylata Alexander, 1935. 53. Hypopygium, lateral view. 54. Tergite ninth, dorsal view. 55. Hypopygium, ventral view. 56 in Description of a new species in the genus Nephrotoma (Diptera: Tipuloidea: Tipulidae) from China, with redescriptions of hypopygiums of six species
Figures 53–60. Nephrotoma nigrostylata Alexander, 1935. 53. Hypopygium, lateral view. 54. Tergite ninth, dorsal view. 55. Hypopygium, ventral view. 56. Outer gonostylus and inner gonostylus, lateral view. 57. Inner gonostylus, inner view. 58. Ejaculatory apodeme, dorsal view. 59. Semen pump, lateral view. 60. Semen pump, dorsal view. Scale bars = 0.2 mm.
Plate VII (Figures 55–64). Streblocera (Eutanycerus) sharifi Shamim, sp. nov. Figure 55. Head dorsal view. Figure 60. Metasoma showing ovipositor and ovipositor sheath. Figure 56. Head ventral view. Figure 61. Forewing. Figure 57. Pronotal side. Figure 62. Hind leg. Figure 58. Mesosoma in dorsal view. Figure 63. Part of hindwing. Figure 59. First metasomal tergite. Figure 64. Antenna. in The genus Streblocera Westwood (Hymenoptera: Braconidae: Euphorinae) from India, with descriptions of 9 new species
Plate VII (Figures 55–64). Streblocera (Eutanycerus) sharifi Shamim, sp. nov. Figure 55. Head dorsal view. Figure 60. Metasoma showing ovipositor and ovipositor sheath. Figure 56. Head ventral view. Figure 61. Forewing. Figure 57. Pronotal side. Figure 62. Hind leg. Figure 58. Mesosoma in dorsal view. Figure 63. Part of hindwing. Figure 59. First metasomal tergite. Figure 64. Antenna.
Figs 60–63. Ommatius normus Curran,1928 in A new species of Cerozodus and new records of Asilinae and Ommatiinae (Diptera: Asilidae) from Tocantins, Brazil
Figs 60–63. Ommatius normus Curran,1928, male, habitus: 60, lateral view; 61, dorsal view; head: 62, frontal view; 63, lateral view.
Figures 60–78 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 60–78: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (60, 61) Cocconeis antigua. (62) Diploneis smithii. (63) Diploneis weissflogii. (64) Diploneis sp. (65) Caloneis sp. (66, 67) Navicula cancellate. (68) Navicula directa. (69, 70) Navicula perminuta. (71) Navicula sp. (72, 73) Pseudogomphonema kamtchaticum. (74) Trachyneis aspera. (75, 76) Biremis ambigua. (77) Parlibellus crucicula. (78) Pinnularia quadratarea.
FIGURE 60 in Taxonomic Revision of the Spider Genus Actinopus Perty, 1833 (Araneae, Mygalomorphae, Actinopodidae)
FIGURE 60. Actinopus cornelli sp. nov., male: A–F MCN 23400: A. Abdomen, dorsal; B. Carapace, dorsal; C. Sternum, ventral; D. Cheliceral teeth, ventral; E. Rastellum, dorsal; F. Rastellum, ventral.
Fig. 60 in The Changhsingian (Late Permian) ammonoids from Baghuk Mountain (Central Iran)
Fig. 60. Abichites infirmis Korn & Hairapetian sp. nov. A. Lateral and dorsal view, holotype MB.C.30086, section G, -0.40 m. B. Suture line, holotype MB.C.30086, at 21.5 mm dm, 9.1 mm wh. Abbreviations: see Material and methods. Scale bar units = 1 mm.
Fig. 60 in Hydromedusae observed during night dives in the Gulf Stream
Fig. 60. Rhopalonema velatum. (A-B) Specimen of 04-MAR-2019, diameter ca. 11 mm. (A) Oblique view from aboral side. (B) Tentacle tips. (C-E) BFLA4292, 7 mm diameter. (C) Oblique view from aboral side, yellow arrow points to short, interradial tentacle, red arrow points to long, perradial tentacle. (D) Oblique view from oral side. (E) Near lateral view, note the slight apical process.
Data from: Monitoring microarthropods assemblages along a pH gradient in a forest soil over a 60 years' time period
<p>The goal of this study was to assess the development, over 60 years, of microarthropod communities over a pH gradient in forest soil.</p> <p>Site Description</p> <p>Hackfort is an oak coppice grove in the East-Southeast of the city of Zutphen in the province of Gelderland, the Netherlands, 52°06′09.7″ N, 6°15′56.0″ E (see Figure 1). The experimental area is about 1.5 ha and is divided in a 10 m × 10 m grid. Vegetation is dominated by common oak (<em>Quercus robur</em>), mixed with birch (<em>Betula pendula</em>), and had in 1959, an understory of wood sage plugs (<em>Teucrium scorodonia</em>), wood anemone (<em>Anemone nemorosa</em>), bracken (<em>Pteridium aquilinum</em>), and wavy-hair grass (<em>Deschampsia flexuosa</em>). In later years, the understory became more dominated by bramble species (<em>Rubus fruticosus </em>and<em> R. idaeus</em>) and common nettles (<em>Urtica dioica</em>) at the edges of the forest, due to increased N deposition from adjacent farmland. The forest is situated at the transition from western riverine deposits and eastern periglacial cover sands. The soil is a riverine deposit with a few elevation differences, making a number of gradients in clay and loam content, which results in many short-distance gradients in soil types, varying from typic haplaquolls with the largest loam contents, via psammaquentic haplorthods to humaqueptic spodic psammaquents, slightly elevated and low in loam contents.</p> <p>Microarthropod Sampling and pH Measurement</p> <p>In 1959, samples were taken at three subsequent dates: 11 September, 9 October, and 30 October. Samples in 1987 were taken on one date, 9 October, just as on 30 October 2019. Samples were taken following a standard procedure, developed at the Institute for Applied Biological Research in Nature, Wageningen, the Netherlands (later merged into the Research Institute for Nature management, Institute for Forestry and Nature Research and Alterra resp., now known as Wageningen Environmental Research); this procedure has been published by Siepel and van de Bund in 1988 (Siepel and van de Bund, 1988). Each mineral soil sample has 100 cc: a volume of 5 cm diameter and 5 cm depth plus litter on top. In 1959, two samples per date were taken on each plot, making a total of 6 samples (only pooled data are available); in 1987 and in 2019, 4 and 5 samples for each plot were taken on, respectively (data per sample available).</p> <p>Soil cores were put on a Tullgren funnel for 1 week, during which temperature was increased from 35 to 45 °C, and then, microarthropods were collected in 70% alcohol and later put into 20% lactic acid for clarification and identification (Siepel, 1990; Siepel and van de Bund, 1988). The Tullgren funnel used for extraction (Siepel, 1990) has been used ever since 1936 and efficiency has not changed as the tool and protocol was the same all over the years.</p> <p>Identification was done to the species level as much as possible using at present the keys for Oribatida(Weigmann and G., 2006), for Gamasina (Lehtinen, 1994), for Uropodina (Karg, 1989), and for Collembola (Hopkin, 2007). Material from the extractions of 1959 and 1987 was re-examined as far as possible to check the correct species identification. In the 1959 and 1987 samples, only oribatid mites were identified to the species level, whereas in 1959, all species of <em>Quadroppiidae, Oppiidae</em>, and <em>Suctobelbidae</em> were pooled. In 2019, all microarthropods were identified to the species level.</p> <p>Sorting and identification of the 1959 microarthropods was carried out by an experienced acarologist (J.G. de Gunst), in 1987, this was done by a student (C. Arnold) and completed and checked by the second author. For the 2019 samples, we decided to demonstrate the potential difference in picking out the microarthropods from the extraction fluid into the slides for identification as part of the experiment: the first author made a first series of slides including all distinguished animals (dataset 2019 a), while the second author made an extra set of slides with the animals missed by the first (dataset 2019 b). The first author did know since the beginning that the second author would check all samples after her sorting session. In this way, we intended to demonstrate the potential difference in this crucial part of the procedure by a starting and an experienced professional. In the analysis, we compare dataset (2019 a) with (2019 a + b), in order to highlight the difference between a starting and an experienced acarologist. Nomenclature adopted was updated according to current standards, following, e.g., the checklists for Oribatida (Siepel et al., 2009), for Astigmatina (Siepel et al., 2016), and for Mesostigmata (Siepel, 2018). Values of pH-KCl were measured in the core material after the extraction of the microarthropods, both in 1959, 1987, and 2019.</p> <p> </p> <p>We have four data files:</p> <p>1959 hackfort microarthropods data.csv</p> <p>1989 hackfort microarthropods data.csv</p> <p>2019 hackfort microarthropods data.csv</p> <p>pH data Hackfort 1959-2019.csv.</p> <p> </p> <p>Explanation of the variables in the datasets:</p> <p>higher taxon: Oribatida, Astigmata, Mesostigmata, Prostigmata, Collembola or Protura</p> <p>Name in De Gunst 1959: taxonomic identification by De Gunst in 1959</p> <p>Valid name: Henk Siepel re-checked these species names in 2019</p> <p>Plot: plot 1, plot 2, plot 3, plot 4, plot 5</p> <p>a: identified by Yuxi Guo</p> <p>b: re-checked by Henk Siepel from remaining soil microarthropods in slide</p> <p>pH(KCL) and pH(H2O): pH values based on indicated methods</p> <p> </p>
Figs 57–65. 57–60 in Braconidae (Hymenoptera) From Korea Xxii. Subfamily Alysiinae
Figs 57–65. 57–60. Aspilota deserta PAPP: 57 = head in dorsal view, 58 = mandible, 59 = distal part of right fore wing, 60 = propodeum. – 61–65. A. inflatitempus FISCHER: 61 = mandible, 62 = head in dorsal view, 63 = distal part of right fore wing, 64–65 = propodeum
Figures 49–60 in Somalibuthus sabae sp. n., a new buthid scorpion from Kenya (Scorpiones: Buthidae)
Figures 49–60: Somalibuthus sabae sp. n., paratype male, right pedipalp under UV fluorescence. Figures 49–52. Chela in dorsal (49), external (50), ventral (51) and internal (52) views. Figures 53–56. Patella in dorsal (53), external (54), ventral (55) and internal (56) views. Figures 57–60. Femur and trochanter in dorsal (57), external (58), ventral (59) and internal (60) views. Scale bar: 2 mm.
Figures 60–67 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXVI. Records of Hottentotta polystictus (Pocock, 1896), with descriptions of H. haudensis sp. n. and H. nigrimontanus sp. n. (Buthidae) from Somaliland
Figures 60–67: Hottentotta haudensis sp. n. Figures 60, 62–64. Male holotype, telson lateral (60), and metasoma and telson lateral (62), ventral (63), and dorsal (64). Figures 61, 65–67. Female paratype, telson lateral (61), and metasoma and telson lateral (65), ventral (66), and dorsal (67). Scale bar: 10 mm (62–67).
Figures 60–65 in Further review of Orthochirus Karsch, 1892 (Scorpiones: Buthidae) from Asia: taxonomic position of O. melanurus, O. persa, O. scrobiculosus, and description of six new species
Figures 60–65: Orthochirus formozovi sp. n., metasoma and telson under UV light. Figures 60–62. lateral (60), ventral (61), and dorsal (62) views. Figures 63–65. Holotype male, lateral (63), ventral (64), and dorsal (65) views.
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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.