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1,650 results for “Acariformes”

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Fig. 5 in Redescription of the Snail Mite Riccardoella reaumuri (Acariformes: Prostigmata: Ereynetidae)

Fig. 5. Riccardoella (Proriccardoella) reaumuri: holotype, female. A–D: Leg I–IV without coxae. Scale bar 50 µm.

opencc-by-4.0May 2019View details →
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Fig. 6 in Redescription of the Snail Mite Riccardoella reaumuri (Acariformes: Prostigmata: Ereynetidae)

Fig. 6. Riccardoella (Proriccardoella) reaumuri: holotype, female. Tarsi I–IV in lateral view (A–D). Scale bar 20 µm.

opencc-by-4.0May 2019View details →
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Fig. 2 in Redescription of the Snail Mite Riccardoella reaumuri (Acariformes: Prostigmata: Ereynetidae)

Fig. 2. Riccardoella (Proriccardoella) reaumuri: holotype, female. A. Body in ventral view. B. Dorsal view of idiosoma. Scale bar 100 µm. Arrow: base lacking setae 1a.

opencc-by-4.0May 2019View details →
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Fig. 3 in Redescription of the Snail Mite Riccardoella reaumuri (Acariformes: Prostigmata: Ereynetidae)

Fig. 3. Riccardoella (Proriccardoella) reaumuri: holotype, female. Aggenital region. Scale bar 50 µm. Arrows: bases lacking setae. Open arrow: right g4 adjacent to right g5.

opencc-by-4.0May 2019View details →
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Fig. 1 in Redescription of the Snail Mite Riccardoella reaumuri (Acariformes: Prostigmata: Ereynetidae)

Fig. 1. Holotype of Riccardoella (Proriccardoella) reaumuri: A. Slide with mounted holotype. B. Body in dorsal view. Scale bar 100 µm.

opencc-by-4.0May 2019View details →
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Fig. 4 in Redescription of the Snail Mite Riccardoella reaumuri (Acariformes: Prostigmata: Ereynetidae)

Fig. 4. Riccardoella (Proriccardoella) reaumuri: holotype, female. Gnathosoma in ventral view. Scale bar 50 µm.

opencc-by-4.0May 2019View details →
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Figure 3 Nycteridocaulus sulcatussp. n in Two new feather mites of the subfamily Proctophyllodinae (Acariformes: Proctophyllodidae) from the Yellow-bellied Flycatcher Empidonax flaviventris (Passeriformes: Tyrannidae) in Canada

Figure 3 Nycteridocaulus sulcatussp. n., details: A–C – legs I–III of male, respectively, D – tibia and tarsus IV of male, E – tibia and tarsus IV of female, F – spermatheca and spermaducts, G – opisthosoma of male, ventral view. Abbreviations: ad– adanal shield, ga– genital arch, hs– head of spermatheca, pd– primary spermaduct, pg – pregenital apodemes, sd – secondary spermaducts, tl– terminal lamella.

opencc-by-4.0Nov 2020View details →
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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

opencc-by-4.0May 2021View details →
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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

opencc-by-4.0May 2021View details →
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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

opencc-by-4.0May 2021View details →
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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

opencc-by-4.0May 2021View details →
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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

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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

opencc-by-4.0May 2021View details →
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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

opencc-by-4.0May 2021View details →
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Figure 2 in The eriophyid mite Aculops ailanthi Lin, Jin, & Kuang, 1997 (Acariformes: Prostigmata: Eriophyidae) from tree-of-heaven in the United States - new state records and morphological observations

Figure 2 Stereomicrographs (2a–b) and SEMs (2c–f) ofAculops ailanthi: General aspect of colonies on leaves and morphological traits:** 2a–b – prodorsal shield; 3c – mite infestation of a leaf; 2d – mite feeding on a trichome; 2e – nymph next to an egg, note the lack of reticulate cells on the prodorsal shield; 2f – dorsum.

opencc-by-4.0Feb 2021View details →
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Figure 1 in The eriophyid mite Aculops ailanthi Lin, Jin, & Kuang, 1997 (Acariformes: Prostigmata: Eriophyidae) from tree-of-heaven in the United States - new state records and morphological observations

Figure 1 Tree­of­heaven damaged byAculops ailanthi Lin, Jin, & Kuang feeding: 1a – healthy leaf without mite infestation; 1b – leaf showing severe stippling; 1c – leaf showing yellowing, stippling, and necrosis; 1d – leaf necrosis; 1e – mites on leaf surface after an application of a 2% solution of M­Pede insecticidal soap.

opencc-by-4.0Feb 2021View details →
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Fig. 1 in Functional And Ecological Adaptations Of Several Acaridid Mite Species (Acariformes, Astigmata) For Feeding On Stored Produce

Fig. 1. Cluster analysis of similarity of acaridid complexes in studied substrates (Ward's method, correlation coefficient 0.5844).

opencc-by-4.0Jul 2018View details →
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Figure 3 in On the perception of leaf morphology and visible light byTetranychus urticae Koch (Acariformes, Tetranychidae)

Figure 3 Distribution of Tetranychus urticae females (A) and daily oviposition rate (B) on bean leaves: A1, B1 (BNI); A2, B2 (BNS); A3, B3

opencc-by-4.0Apr 2022View details →
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Figure 2 in On the perception of leaf morphology and visible light byTetranychus urticae Koch (Acariformes, Tetranychidae)

Figure 2 Survival (squares) and oviposition rate (circles) of Tetranychus urticae females fed on adaxial (AdSU-open squares and circles) or abaxial (AbSU-closed squares and circles) surface of bean (A) and lemon (B) leaves. Different letters denote significant differences (P<0.05)

opencc-by-4.0Apr 2022View details →
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Figure 1 Minteracarus mombasa n in A new genus and species of bat chiggers (Acariformes: Trombiculidae) from Kenya

Figure 1 Minteracarus mombasa n. sp., holotype: A – arrangement of dorsal idiosomal setae; B – arrangement of ventral idiosomal setae; C

opencc-by-4.0Apr 2022View details →

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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.

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neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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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.

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electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record