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Figures 5–8 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 5–8. Eurygeophilus multistiliger (Verhoeff, 1899), female, 32 mm long, Coimbra (Iberian Peninsula), holotype, mounted on a slide. (5) Forcipular segment, ventral. (6) Calyx inside the left forcipule, ventral. (7) Sternum of leg-bearing segment XII. (8) Last leg-bearing segment and terminal segments, ventral. Images from light microscopy. Scale bars: 200 Mm (5); 100 Mm (6, 8); 50 Mm (7).
Figures 9–13 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 9–13. Eurygeophilus multistiliger (Verhoeff, 1899), female, 24 mm long, Campu Omo (Sardinia). (9) Head, dorsal (right antenna and setae not drawn). (10) Head, ventral (antennae not drawn). (11) Forcipular segment, ventral. (12) Sternum of leg-bearing segment V, ventral. (13) Last leg-bearing segment and terminal segments, ventral (right telopodite and setae on the relevant coxopleuron not drawn).
Figures 1–4 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 1–4. (1–3) Eurygeophilus pinguis (Brölemann, 1898), female, 33 mm long, M. La Marzola (near Trento, Alps). (1) Distal articles of the left antenna, ventral. (2) Left claw of the second maxillae, ventral. (3) Right part of the forcipular coxosternum, ventral. (4) Geophilus linearis C. L. Koch, 1835, male, 34 mm long, Cologna Veneta (near Verona, Italy): right part of the forcipular coxosternum, ventral. Arrows indicate the putative position of the forcipular chitin-lines. Micrographs from ESEM Philips XL30. Scale bars: 20 Mm (1, 2); 50 Mm (3, 4).
Fig. 1 in Dependence of the sperm number on the adult age of the male black field cricket Teleogryllus commodus W ALKER (Insecta: Orthoptera)
Fig. 1: Shape and morphology of the spermatophore (total length: ca. 5 mm) separated from males of the black field cricket Teleogryllus commodus.
Fig. 2 in Dependence of the sperm number on the adult age of the male black field cricket Teleogryllus commodus W ALKER (Insecta: Orthoptera)
Fig. 2: Results of sperm quantification of male crickets belonging to different age categories: (a) Age-dependence of the percentage of filled/unfilled spermatophores (N = 80); (b) Age-dependence of the number of sperm per spermatophore (N = 80). The asterisk indicates a significant difference (p <0.05) between adjacent mean values.
Figure 2 in Four submarginal cells on a forewing of Melitoma taurea (Say) (Hymenoptera: Apidae), and a summary of known records of atypical and variable numbers of submarginal cells
Figure 2. Melitoma taurea. Female; USGS_DRO205857; left forewing with atypical 4 SM. (The distorted appearance is due to the wing being partially folded over.) Photographed by Brooke Alexander, BIML.
Figure 1 in Four submarginal cells on a forewing of Melitoma taurea (Say) (Hymenoptera: Apidae), and a summary of known records of atypical and variable numbers of submarginal cells
Figure 1. Melitoma taurea. Female; USGS_DRO205857; right forewing with typical 3 SM. Photographed by Brooke Alexander, BIML.
Text-fig. 3. Phylogenetic relationship of Peignecyon felinoides n. gen. et n. sp., within some selected Amphicyonidae, and some extinct caniform carnivorans. Paramiacis exilis is the outgroup. Searches were performed by means of the Branch and Bound and a Bootstrap analysis through 1,000 replicates. One tree is obtained (length 73 steps, consistency index (CI) = 0.6301, retention index (RI) = 0.7000). The numbers below nodes are Bremer indices, and the numbers above nodes are Bootstrap support percentages (only shown ≥ 50). in A New Thaumastocyoninae (Amphicyonidae, Carnivora) From The Early Miocene Of Tuchořice, The Czech Republic
Text-fig. 3. Phylogenetic relationship of Peignecyon felinoides n. gen. et n. sp., within some selected Amphicyonidae, and some extinct caniform carnivorans. Paramiacis exilis is the outgroup. Searches were performed by means of the Branch and Bound and a Bootstrap analysis through 1,000 replicates. One tree is obtained (length 73 steps, consistency index (CI) = 0.6301, retention index (RI) = 0.7000). The numbers below nodes are Bremer indices, and the numbers above nodes are Bootstrap support percentages (only shown ≥ 50).
Text-fig. 2. The relation between number of genera and localities in MN 5 of central Europe (CE) and the Iberian Peninsula (IB). a. Localities ordered from highest to lowest number of taxa; the distribution is more equitable in the Iberian Peninsula. b. Genera ordered from most common to rarest; the distribution of genera is more equitable in central Europe. The low number of common genera is an artefact of incomplete faunal lists (see text). in Generically Speaking, A Survey On Neogene Rodent Diversity At The Genus Level In The Now Database
Text-fig. 2. The relation between number of genera and localities in MN 5 of central Europe (CE) and the Iberian Peninsula (IB). a. Localities ordered from highest to lowest number of taxa; the distribution is more equitable in the Iberian Peninsula. b. Genera ordered from most common to rarest; the distribution of genera is more equitable in central Europe. The low number of common genera is an artefact of incomplete faunal lists (see text).
Text-fig. 8. The limited differentiation the schmelzmuster in Allosorex (Allosoricinae) indicates its phylogenetic position in Soricomorpha. The numbers to the right refer to the different types of schmelzmuster found in Soricidae: 1 – Soricella-schmelzmuster, 2 – Anourosorex- schmelzmuster, 3 – Crocidura-schmelzmuster, 4 – Notiosorex-schmelzmuster, 5 – Sorex-schmelzmuster, and 6 – Blarina-schmelzmuster (ex Koenigswald and Reumer 2020). in Allosorex Stenodus Fejfar, 1966 (Eulipotyphla, Soricidae): Re-Description Of Type Material And Re-Interpretation Of Its Fossil Record
Text-fig. 8. The limited differentiation the schmelzmuster in Allosorex (Allosoricinae) indicates its phylogenetic position in Soricomorpha. The numbers to the right refer to the different types of schmelzmuster found in Soricidae: 1 – Soricella-schmelzmuster, 2 – Anourosorex- schmelzmuster, 3 – Crocidura-schmelzmuster, 4 – Notiosorex-schmelzmuster, 5 – Sorex-schmelzmuster, and 6 – Blarina-schmelzmuster (ex Koenigswald and Reumer 2020).
Text-fig. 2. Map of the Mikhailovka quarry. 1 – wall of the quarry, 2 – roads, 3 – position and number of sections. in Late Pleistocene (Eemian) Mollusk And Small Mammal Fauna From Mikhailovka-5 (Kursk Oblast, Central Russia)
Text-fig. 2. Map of the Mikhailovka quarry. 1 – wall of the quarry, 2 – roads, 3 – position and number of sections.
Fig. 53 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Fig. 53. Eggs of some cleptoparasitic bees from some of my recent publications, all reproduced in the same scale to illustrate the often complex shape of those that are hidden in open cells (above horizontal line) and the simple elongate shapes of those that are introduced into closed cells (below horizontal line). The size difference between the oocytes in these two categories is noteworthy, but is best analyzed in terms of oocyte length compared with body size of the female, i.e., the egg index; see Analyses and Results, subsection Size of Mature Oocytes.
Figs. 43, 44 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 43, 44. SEM micrographs of mature oocyte of Ericrocis lata. 43. Anterior end with micropylar area barely visible just below follicular debris; note smooth, platelike, polygonal patterning on outcurved (upper) surface and nodular patterning on incurved surface. 44. Midbody, showing platelike surface on outcurved surface changing to nodular patterning on incurved surface, lateral view.
Figs. 30, 31 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 30, 31. SEM micrographs of mature oocyte of Rhathymus bicolor. 30. Micropylar area. 31. Polygonal pattern just below micropyle on incurved side.
Fig. 29 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Fig. 29. Diagrams of mature oocytes of (from top to bottom) Rhathymus bicolor, Rhathymus species A, and Epiclopus gayi, lateral views, anterior ends to the left. Scale line (= 1.0 mm) refers to all figures.
Figs. 16–19 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 16–19. SEM micrographs of operculum of mature oocyte of Leiopodus abnormis. 16. Late stage, anterodorsal view. 17. Closeup of micropyle; note opercular rim causing micropyle to be recessed. 18. Early stage mature oocyte, with tubercles starting to be deposited, rim thin, and micropyle exposed (except for follicular debris appearing to divide it) anterodorsal view. 19. Intermediatestage mature oocyte, with tubercles partly developed and micropyle becoming recessed by rim, posterodorsal view.
Figs. 13–15 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 13–15. SEM micrographs of mature oocyte of Melectoides triseriatus, anterior end toward left. 13. Entire oocyte, dorsal view. 14. Closeup of micropylar area as outlined by rectangle in fig. 13. 15. Entire oocyte, lateral view.
Figs. 58–61 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 58–61. SEM micrographs of mature oocyte of Coelioxys novomexicana. 58. Entire oocyte, ventral view; anterior end toward the left. 59. Anterior end, frontal view. 60. Closeup of micropylar area; absence of strongly raised polygonal boundaries below unexplained but possibly due to dissection damage. 61. Closeup of micropyle.
Fig. 10 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Fig. 10. Diagrams of mature oocytes of Isepeolus luctuosus (above) and Melectoides triseriatus (below), anterior ends toward left. Scale line refers to both.
Figs. 11, 12 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 11, 12. SEM micrographs of anterior end of mature oocyte of Isepeolus luctuosus. 11. Dorsal view; note polygonal pattern of eclosion line anterior to micropyle. 12. Closeup of micropyle.
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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.