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Figure 6 in Two species of Acaricis (Acari: Tenuipalpidae) from New Zealand, moved from the genus Tenuipalpus, with a key to the known species
Figure 6 Differential interference contrast (DIC) image ofAcaricis alpinus (Collyer) (Female): dorsum.
Figure 4 in Two species of Acaricis (Acari: Tenuipalpidae) from New Zealand, moved from the genus Tenuipalpus, with a key to the known species
Figure 4 Acaricis montanus (Collyer) female, dorsal aspect, right side, of: A – leg I; B – leg II; C – leg III; D – leg IV.
FIG. 8. — Paragiopagurus schnauzer n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 8. — Paragiopagurus schnauzer n. sp., ♂ holotype 3.3 mm, BIOGEOCAL, stn CP 214, New Caledonia (MNHN-Pg 7615): A, propodus and dactyl of left fourth pereopod, lateral; B, propodus and dactyl of left fifth pereopod, lateral; C, thoracic region, ventral; D, anterior and posterior lobes of thoracic sternite XII (third pereopods), ventral; E, uropods and telson, dorsal; F, left first pleopod, mesial; G, left second pleopod, anterior. Scale bars: A-D, F, G, 1 mm; E, 0.5 mm.
FIG. 3. — Oncopagurus conicus n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 3. — Oncopagurus conicus n. sp., ♂ holotype 2.0 mm, HALIPRO 1, stn C 858, New Caledonia (MNHN-Pg 7612): A, left second pereopod, lateral; B, dactyl of same, mesial; C, left third pereopod, lateral; D, dactyl of same, mesial; E, propodus and dactyl of left fourth pereopod, lateral; F, propodus and dactyl of left fifth pereopod, lateral. Scale bars: A-D, 1 mm; E, F, 0.20 mm.
FIG. 4. — Oncopagurus conicus n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 4. — Oncopagurus conicus n. sp., ♂ holotype 2.0 mm, HALIPRO 1, stn C 858, New Caledonia (MNHN-Pg 7612); A, thoracic region, ventral;B, anterior and posterior lobes of thoracic sternite XII (third pereopods), ventral; C, uropods and telson, dorsal; D, left first pleopod, mesial; E, left second pleopod, anterior. Scale bars: A, 0.50 mm; B, D, E, 0.20 mm; C, 0.25 mm.
FIG. 9 in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 9. — Right ocular peduncle and cornea (stippling indicates weakly calcified portion): A-C, Typhlopagurus foresti de Saint Laurent, 1972, ♂ 3.7 mm, SALOMON 1, stn CP 1781 (USNM 1084207, ex MNHN-Pg 6706); D, Sympagurus acinops Lemaitre, 1989, ♂ paratype 3.2 mm, Tongue of the Ocean, Bahamas, 1438 m (USNM 231834); E, Parapagurus saintlaurentae Lemaitre, 1999, ♂ paratype 12.8 mm, N of Madagascar, 4810 m (USNM 276123); A, D, E, lateral; B, mesial; C, ventral. Scale bars: A-D, 0.25 mm; E, 1 mm.
FIG. 7. — Paragiopagurus schnauzer n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 7. — Paragiopagurus schnauzer n. sp., ♂ holotype 3.3 mm, BIOGEOCAL, stn CP 214, New Caledonia (MNHN-Pg 7615): A, right second pereopod, lateral; B, dactyl of same, mesial; C, right third pereopod, lateral; D, dactyl of same, mesial. Scale bar: 1 mm.
FIG. 1. — Oncopagurus conicus n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 1. — Oncopagurus conicus n. sp., New Caledonia: A, ♀ paratype 2.0 mm, HALIPRO 1, stn C 858 (MNHN-Pg 7613); B-D, F-J, ♂ holotype 2.0 mm, HALIPRO 1, stn C 858 (MNHN-Pg 7612); E, ovig. ♀ paratype 2.1 mm, BIOGEOCAL, stn CP 214 (MNHN-Pg 7614); A, gill lamella; B, shield and cephalic appendages, dorsal (stippling indicates weakly calcified portion); C, right ocular peduncle and cornea, lateral; D, epistome, dorsolateral (es, epistomial spine; ls, labral spine); E, anterior portion of shield and cephalic appendages, dorsal; F, right antennal peduncle, lateral; G, right cheliped, dorsal; H, chela of same, lateral; I, same, mesial; J, left cheliped, dorsal. Scale bars: A, 0.10 mm; B, 0.50 mm; C-F, 0.25 mm; G-J, 1 mm.
FIG. 6. — Paragiopagurus schnauzer n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 6. — Paragiopagurus schnauzer n. sp., ♂ paratype 3.2 mm, HALIPRO 2, stn BT 105, Loyalty Islands (MNHN-Pg 6705), left mouthparts, internal: A, mandible; B, maxillule; C, maxilla; D, first maxilliped; E, second maxilliped; F, third maxilliped. Scale bars: 0.25 mm.
FIG. 5. — Paragiopagurus schnauzer n in Two new species of Parapaguridae (Crustacea, Decapoda, Anomura, Paguroidea) with subconical corneas, and new data on biology of some rare species
FIG. 5. — Paragiopagurus schnauzer n. sp., ♂ holotype 3.3 mm, BIOGEOCAL, stn CP 214, New Caledonia (MNHN-Pg 7615): A, gill lamella; B, shield and cephalic appendages, dorsal (stippling indicates weakly calcified portion); C, right ocular peduncle and cornea, lateral; D, epistome, dorsolateral (es, epistomial spine; ls, labral spine); E, right antennal peduncle, lateral; F, right cheliped, dorsal; G, chela of same, lateral; H, same, mesial; I, left cheliped, dorsal. Scale bars: A, C, D, 0.25 mm; B, F-I, 1 mm; E, 0.50 mm.
Figure 7 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 7 Stylostomes of Neotrombicula talmiensis(Schluger, 1955) larvae in the skin of the Asian chipmunkTamias sibiricus(Laxmann, 1769). Histological sections of aural cavity. Azure II-Eosin. A – Young stylostome composed of one eosinophil cone with the already developed feeding cavity situated within the upper epidermal layers. Note the grayish substance underneath the eosinophil cone arrow(). Scale bar – 50 μm; B – Young stylostome at the initial stage of development with the nearly empty feeding cavity underneath it. Note that the pale-grey substance
Figure 6 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 6 Skin injury of the Asian chipmunkTamias sibiricus(Laxmann, 1769) during feeding ofNeotrombicula talmiensis(Schluger, 1955) larvae. Histological sections of aural cavity. Azure II-Eosin. A - General view of aural cavity damaged by numerous feeding larvae. Note the differently developed stylostomes evolving within scabs. Scale bar – 500 μm; B – Two young closely disposed stylostomes evolving within epidermis. Note the numerous larvae at different feeding stages occupying the aural cavity. The feeding cavity is barely expressed. Scale bar 200 μm; C – Two young stylostomes of the recently attached larvae at different developmental stages evolving within the epidermis showing the large feeding cavity filled with numerous inflammatory cells. — car – aural cartilage, der – dermis, ec – eosinophil cone, ep – epidermis fc – feeding cavity, lar – larvae, sb – scab, st – stylostome, stc – stratum corneum
Figure 5 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 5 Skin injury of voles Myodes rufocanusSundevall, 1846 and stylostomes ofNeotrombicula talmiensis(Schluger, 1955) larvae. Histological sections. Azure II-Eosin. A – Several stylostomes evolving in both hypertrophic epidermis and penetrating into the strongly expressed feeding cavities filled with numerous infiltrating cells and cell debris. Note the grayish substance at the periphery of stylostomesarrows(). Scale bar – 100 μm; B – Two closely disposed stylostomes evolving within the cell association of the broken inflammatory and epidermal cells (arrows). Scale bar – 50 μm; C – Three differently arranged stylostomes evolving within the pronounced feeding cavity tightly packed with the broken inflammatory and epidermal cells fused to form a scab. Note the grayish substance at the periphery of stylostomesarrows(). Scale
Figure 4 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 4 Stylostomes of Neotrombicula talmiensis(Schluger, 1955) larvae in the skin of volesMyodes rufocanusSundevall, 1846. Histological sections. Azure II-Eosin. A – Young stylostome evolved in the hypertrophic stratum corneum. Note the active stratum lucidum surrounding growing stylostome and feeding cavity filled with a flocculent material without inflammatory cells. Stylostome canal is also empty. Scale bar
Figure 3 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 3 Skin injury of voles Myodes rufocanusSundevall, 1846 during feeding ofNeotrombicula talmiensis(Schluger, 1955) larvae. Histological sections of aural cavity. Azure II-Eosin. A – General view of aural cavity damaged by feeding larvae. Scale bar – 200 μm; B
Figure 2 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 2 Cheliceral blades and sites of attachment ofNeotrombicula talmiensis(Schluger, 1955) larvae. SEM. A – Cheliceral blades, dorsal view. Arrows show two small barbs on the tip of the cheliceral blades, the third barb is not visible.Arrowheadpoints to a groove on the medial surface of the cheliceral blade. Scale bar – 10 μm; B – Cheliceral blades, lateral view.Arrows indicate hardly noticeable barbs on the tip of the cheliceral blades (tricuspid cap). Scale bar – 10 μm; C – Sites of the larval attachment on the vole skin (arrows). Scale bar – 40 μm; D
Figure 1 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 1 Organization ofNeotrombicula talmiensis(Schluger, 1955) larvae. SEM. A – Scutum (one of sensilla broken). Scale bar – 40 μm; B – Paired eye and posterolateral seta of scutum.Arrow points to a pore on the scutal surface. Scale bar – 10 μm; C – Gnathosoma, dorsal view (palpal claws not visible). Arrows show branched setae on palpal femur, genu, and tibia (ventral seta of tibia and palpal tarsus not shown
FIG. 3. — Opisthacanthus milloti n in Scorpions of the Réserve spéciale d'Ankarana, Madagascar, with particular reference to cave-dwelling animals and the description of two new species (Arachnida, Scorpiones)
FIG. 3. — Opisthacanthus milloti n. sp., ventral aspect, showing coxapophysis, sternum,genital operculum, pectines and sternite III: A, ♂ holotype; B, ♀ paratype. Scale bar: 2 mm.
FIG. 7. — Opisthacanthus pauliani n in Scorpions of the Réserve spéciale d'Ankarana, Madagascar, with particular reference to cave-dwelling animals and the description of two new species (Arachnida, Scorpiones)
FIG. 7. — Opisthacanthus pauliani n. sp., ♂ holotype, trichobothrial pattern: A-C, chela dorso-external, external and ventral aspects; D, femur, dorsal aspect; E, fixed finger, internal aspect; F-H, patella, dorsal, external and ventral aspects; I, cutting edge of movable finger with rows of granules. Scale bars: 2 mm.
FIG. 2. — Opisthacanthus milloti n in Scorpions of the Réserve spéciale d'Ankarana, Madagascar, with particular reference to cave-dwelling animals and the description of two new species (Arachnida, Scorpiones)
FIG. 2. — Opisthacanthus milloti n. sp., ♂ holotype and ♀ paratype: A, carapace; B, chelicera; C, hemispermatophore external aspect (♂); D, E, metasomal segment V and telson, lateral aspect (♂ and ♀). Scale bars: 2 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.