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Figure 3 in Contribution to knowledge of the oribatid mite genus Idiozetes (Acari, Oribatida, Idiozetidae), with description of a new sexually dimorphic species from Vietnam
Figure 3 Idiozetes schusteri sp. n., adult, male (A) and female (B–J): A, B — posterior view; C — subcapitulum (dissected), ventral view; D — left lip with adoral seta, ventral view; E — palp, right, antiaxial view; F — chelicera, left, paraxial view; G — tibia and tarsus of leg I, right, antiaxial view; H — trochanter and femur of leg I, left, paraxial view; I — tibia and tarsus of leg II, left, paraxial view; J — leg IV, right, paraxial view. Scale bars 50 μm (A, B), 25 μm (G–J), 20 μm (C, D, F), 10 μm (E).
Figs. 6-14 in The Aplocnemus Stephens, 1830, of Greece (Coleoptera, Cleroidea, Dasytidae). A contribution to their knowledge
Figs. 6-14 - Right antennae, ♂♂. 6) A. nigricornis (Fabricius, 1792) (from Aragnouet, Hautes Pyrenées, F). 7) A. pertusus Kiesenwetter, 1859 (from Girne, CY). 8) A. rufipes Miller, 1862 (from Stavrodromi, Ahaia, GR). 9) A. basalis (Küster, 1849) (from Budva, MNE). 10) A. jejunus Kiesenwetter, 1863 (from Castelfranco di Sopra, Arezzo, I). 11) A. caelatus (Brullé, 1832) (from Agios Nicolaos, Lakonia, GR). 12) A. cribrarius (Brullé, 1832) (from Kalanistra, Ahaia, GR). 13) A. reitteri Schilsky, 1894 (from Yenice, Çanakkale, TR). 14) A. henrici n. sp. (paratypus from Pissoderi, Florina, GR). Scale: 1 mm.
Fig. 1 in The Aplocnemus Stephens, 1830, of Greece (Coleoptera, Cleroidea, Dasytidae). A contribution to their knowledge
Fig. 1 - The greek provinces [taken, with modifications, from the "Euro Atlas" of Greece, scale 1: 3000,000 (see under "Notes to discussion of the species")].
Figs. 32-52 - 32, 34, 36, 39, 42, 43, 47 in The Aplocnemus Stephens, 1830, of Greece (Coleoptera, Cleroidea, Dasytidae). A contribution to their knowledge
Figs. 32-52 - 32, 34, 36, 39, 42, 43, 47) Median lobes in lateral view. 33) Median lobe apex in sternal view. 35, 37, 40, 44, 48) Median lobes in sternal view. 46, 50) Tegmens. 45, 49) Spicular forks. 38, 41, 51) Last sternites. 52) Last tergite. 32-33) A. basalis (Küster, 1849); 32) Papigko on Timfi Mts., Ioannina, GR; 33) Vinisce near Trogir, HR). 34-35) A. cribriarius (Brullé, 1832) (both Kalanistra, Ahaia, GR). 36-38) A. caelatus (Brullé, 1832); 36) Stavrodromio, Arkadia, GR; 37-38) Agios Nikolaos, Lakonia, GR). 39-41) A. henrici n. sp. 39) Lake Batak near Velingrad, BG; 40) Bosnek-Chupetlovo near Mt. Vitoscia, BG; 41) Pissoderi, Florina, GR; all paratypes). 42-46) A. reitteri Schilsky, 1894. 42) Abant Gölü near Bolu, TR; 43-46) Dikili, Izmir, TR. 47-52) A. (Diplambe) abietum Kiesenwetter, 1859. 47, 49-52) Arahova, Ahaïa, GR; 48) Oros Parnitha, Atiki, GR, topotype. Scale 0.5 mm.
Figs. 15-31 - 15-16 in The Aplocnemus Stephens, 1830, of Greece (Coleoptera, Cleroidea, Dasytidae). A contribution to their knowledge
Figs. 15-31 - 15-16) Aedeagus, spicular fork and last ventrite (tergite and sternite) in sternal view, as they appear on dissection: all sternites and tergites – but the last ones – have been removed. 17) Aedeagus (median lobe with dorsal lever and tegmen), lateral view. 18) Aedeagus (median lobe with dorsal lever and tegmen), dorsal view. 20) aedeagus (median lobe with dorsal lever and tegmen), laeral view. 19, 23-24, 28) Median lobes, lateral view. 21, 25-26, 29) Median lobe apices, sternal view. 22, 27, 30) Basal half of tegmen. 31) Last sternite. 15) A. (Ischnopalpus) subcostatus Schilsky, 1894 from Tizi n'Test, 2000 m, Haut Atlas, Maroc. 16) A. rufipes Miller, 1862 from Anogia, Crete, GR. 17-18) A. (Ischnopalpus) subcostatus Schilsky, 1894 from Tizi n'Test, 2000 m, Haut Atlas, Maroc. 19-22) A. serratus (Brullé, 1832); 19) Karteri; 20-21) Vavouri near Tsamantas; 22) Agia Kiriaki all in Thesprotia, GR. 23-27) A. rufipes Miller, 1862; 23, 25) Lagavouni near Kalavrita, Ahaia GR; 24, 26) Anogia, Crete; 27) Hortiatis near Thessaloniki, GR. 28-31) A. pertusus Kiesenwetter, 1859; 28-30) Paliouri on Kassandra, Halkidiki, GR; 31) Silifke, Mersin, TR. Scales: 0.5 mm. Scale a: Figs. 15, 16. Scale b: all others.
Eye morphology contributes to the ecology and evolution of the avian tree of life
<p>The avian eye is the single most important external anatomical trait for interpreting light environments by birds and varies widely in size and shape across the avian tree of life. The attached dataset provides measurements on eye size taken from preserved museum specimens for roughly one third of the avian tree of life (N = 3,475 species). The original dataset was collected by Stanley Ritland and Alice Hutchinson and archived as appendices in Stanley Ritland's Dissertation from the University of Chicago (1982): "The Allometry of the Vertebrate Eye".</p>
Fig. 3 in Fish kill in Ismarida lake, Greece: identification of drivers contributing to the event Abstract
Fig. 3: a) Upper panel: Water level variability in Ismarida Lake, as recorded by the auto-recording hydrographic station (blue line) and water level reconstruction model, based on harmonic analysis results (red line); b) Lower panel: Residual (non-tidal) fluctuation of sea level variability in Ismarida Lake. Rectangle represents the period of the fish mortality event.
Fig. 1 in Fish kill in Ismarida lake, Greece: identification of drivers contributing to the event Abstract
Fig. 1: Map of the study area. The fish fauna sampling stations are marked as triangles (see table 1 for a short description of each site), where the dot labeled as "WEIR" is its position, the one labeled "PFD" represents the position of the Permanent Fishing Devices, and the dot labeled "HS" shows the position of the hydrographic station.
Fig. 4 in Fish kill in Ismarida lake, Greece: identification of drivers contributing to the event Abstract
Fig. 4: a) Upper panel: Water conductivity in Ismarida Lake, as recorded by the auto-recording hydrographic station (blue line) and water conductivity reconstruction model, based on harmonic analysis results (red line); b) Lower panel: Residual (no-tidal) fluctuation of water conductivity variability in Ismarida Lake. Rectangle represents the period of the fish mortality event.
Figs 5–8 in Contribution To The Knowledge Of The Hungarian Oribatida Fauna (Acari) I.
Figs 5–8. Cyranozetes nasalis gen. et sp. n. – 5–6 = lateral part of podosoma; 7 = femur of leg II; 8 = tibia and tarsus of leg I
Figs 1–4 in Contribution To The Knowledge Of The Hungarian Oribatida Fauna (Acari) I.
Figs 1–4. Cyranozetes nasalis gen. et sp. n. – 1 = body in dorsal view; 2 = body in ventral view; 3 = rostrum; 4 = pigidial part of the body
Data for: Spatial variability in the contribution of termites to the decay of plant detritus
<p>Drylands are characterized by high spatial variability in resource availability due to sporadic rainfall, topography of the landscape and important effects of animals. Resource availability gradients may trigger patterns in decomposer population abundances and activity which could affect ecosystem functions such as decomposition. Here, we examined the influence of resource availability gradients on the importance of termites in the decomposition of wood and grass litter. We placed wood blocks and grass litter baits in bags accessible and inaccessible to termites across wood and grass resource gradients as determined by the presence or absence of a top mammalian predator and across topographic gradients during a 9-month period in arid Australia. We hypothesized that grass-eating termite activity would track grass abundance and wood-eating termite activity would track wood abundance. Termites were the predominant decomposition agent at these sites. Termites contributed to 99.5% of wood decomposition and 83.9% of grass decomposition during our study period. For wood, the termite effect was spatially variable and increased with habitat wood availability which was greatest on dunes and where top predators were absent. However, the contribution of termites to grass litter decomposition did not track grass availability or termite abundance. The highest effects of termites on grass decomposition rates were found in habitats where the absence of top predators led to low grass availability. Our findings highlight how spatial variability in resources in addition to other factors that we do not document but are known to be influenced by the presence of top predators, such as insectivore predation rates, across the landscape could affect ecosystem functions such as decomposition. </p>
Figure 7 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 7. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag =(Erciyas-dagi), 2100 m a. s. l., Asia Minor: A= pereopod 5; B= pereopod 6; C= pereopod 7; D= uropod 3 (slide); E= telson (slide) [A, B, C= female 7.8 mm ovig., paratype; D, E= female, unknown size, paratype, slide).
Figure 8 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 8. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor, female 7.8 mm ovig., paratype: A-B= gnathopod 1; C-D= gnathopod 2.
Figure 1 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 1. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor: A= head; B-C= left antenna 1; D= accessory flagellum of right antenna 1; E= antenna 2; F= uropod 3 (numerous setae are broken); G= telson; H= telson [A, B, C, D, E, F, G= male 8.0 mm, paratype; H= male, holotype].
Figure 5 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 5. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor: A= peduncle of antenna 1 (slide); B= antenna 2 (slide); C= uropod 3, slide; D= urosome; E= epimeral plates 1 - 3; F= telson [A, B, C= male, holotype; D, E, F= female ovig. 7.8 mm, paratype].
Figure 4 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 4. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor: A-B= pereopod 5; C= pereopod 6; D= pereopod 7; E= urosome; F= basipodit of pereopod 7 [A, B, C, D, E= male 8.0 mm, paratype; F= male, holotype].
Figure 6 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 6. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor, female ovig. 7.8 mm, paratype: A= antenna 2; B= pereopod 3; C= pereopod 4; D= uropod 3.
Figure 3 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 3. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor, male 8.0 mm, paratype: A= right mandible and lacinia mobilis; B= left mandible and lacinia mobilis; C= mandibular palpus [A, B, D and E setae]; D= epimeral plates 1-3; E= pereopod 3; F= pereopod 4.
Figure 2 in New data of poorly known species Gammarus orientalis (S. Karaman, 1934) (family Gammaridae) from Asia Minor (Contribution to the Knowledge of the Amphipoda 292)
Figure 2. Gammarus orientalis (S. Karaman 1934), Derbend, Erdschias-dag (=Erciyas-dagi), 2100 m a. s. l., Asia Minor: A-B= gnathopod 1; C-D= gnathopod 2; E= distal part of gnathopod 1; F= distal part of gnathopod 2 [A, B, C, D= male 8.0 mm, paratype; E, F= male, holotype].
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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.