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Fig. 4 in Diurnal activity, temperature responses and endothermy in three South American cicadas (Homoptera: Cicadidae: Dorisiana bonaerensis, Quesada gigas and Fidicina mannifera)
Fig. 4. Distribution of Tb of as a function of Ta when Dorisiana bonaerensis were not exposed to solar radiation. The slope of the linear regression for " active " animals (closed circles) is significantly different from one, suggesting thermoregulation is occurring with endogenous heat. The slope of the linear regression for " inactive " animals (open circles) is not significantly different from one, suggesting no thermoregulation is occurring when the animals do not generate heat for activity.
Fig. 1 in Diurnal activity, temperature responses and endothermy in three South American cicadas (Homoptera: Cicadidae: Dorisiana bonaerensis, Quesada gigas and Fidicina mannifera)
Fig. 1. Diurnal distribution of Tb of Dorisiana bonaerensis and Quesada gigas on the 13th December 1986. A rainstorm from 07.00 to 08.00 h followed by a misting rain until 09.45 h delayed the start of activity approx. 2 h. Body temperatures are below ambient temperature before activity begins. Body temperatures are elevated at the start of activity (10.00 h) and regulated throughout the day. Body temperatures of quiescent animals decrease with ambient temperature after sunset (20.10 h). Animals participating in the evening chorus have body temperatures in or near the body temperature range measured during the day. Closed circles, Tb of singing D. bonaerensis; open circles, Tb of D. bonaerensis engaged in other activities (including no activity); closed triangles, Tb of singing Q. gigas; open triangles, Tb of Q. gigas performing other activities; solid line, ambient air temperature.
Figure 7 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 7. Reconstruction of the postpharyngeal genital organs of Dreuxiola philippi sp. nov., seen from the right. Refer to the Appendix for a list of abbreviations.
Figure 4 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 4. Hard parts of the copulatory organ of Meidiama uruguayensis sp. nov. (A; inset, terminal opening in the holotype), Meidiama lutheri (B), and Meidiama schockaerti (C).
Figure 15 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 15. The needles and the muscular supports of the copulatory organ in the species of Serrula. A, Serrula byronensis sp. nov.; B, Serrula maxillaria sp. nov.; C, Serrula concharum sp. nov.; D, Serrula acuta sp. nov. Refer to the Appendix for a list of abbreviations.
Figure 3 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 3. Reconstruction of the copulatory organ in Meidiama lutheri and Meidiama uruguayensis sp. nov., seen from the left, based on sections of M. uruguayensis sp. nov. and the whole mounts of both species. Refer to the Appendix for a list of abbreviations.
Figure 14 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 14. Posteriormost body part in live animals. A, Serrula byronensis sp. nov.; B, Serrula maxillaria sp. nov.; C, Serrula concharum sp. nov. Refer to the Appendix for a list of abbreviations.
Figure 2 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 2. Sagittal reconstruction of the female system, seen from the left, of the species of Meidiama, mainly based on sections of Meidiama uruguayensis sp. nov. The lower figure is the continuation of the upper part. Refer to the Appendix for a list of abbreviations.
Figure 5. A in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 5. A living animal of Dreuxiola philippi sp. nov. Refer to the Appendix for a list of abbreviations.
Figure 11 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 11. Sagittal reconstruction of the postpharyngeal genital organs of Yorknia aprostatica sp. nov., seen from the left. Refer to the Appendix for a list of abbreviations.
Figure 12 in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 12. Copulatory organ of Yorknia aprostatica sp. nov., as seen in the whole mounts. A, in the holotype; B, in the paratype. Refer to the Appendix for a list of abbreviations.
Figure 10. Drawings from a in A new family of lithophoran Proseriata (Platyhelminthes), with the description of seven new species from the Indo-Pacific and South America, and the proposal of three new genera
Figure 10. Drawings from a living animal of Yorknia aprostatica sp. nov. A, the whole animal; B, the postpharyngeal genital organs. Refer to the Appendix for a list of abbreviations.
Figure 10 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 10. Maximum-likelihood tree of Weddell Sea gromiids (shaded boxes), Arabian Sea gromiids (Aranda da Silva et al., 2006), and Gromia oviformis from shallow-water localities (Burki et al., 2002), based on partial small subunit ribosomal DNA (SSU rDNA) sequences. The numbers at the nodes represent the percentage of bootstrap support,> 50%. Weddell Sea gromiids are grouped into three distinct clades (A, B, and C).
Figure 3 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 3. Gromia marmorea sp. nov. A, B, scanning electron microscope (SEM) photographs of wall consisting of multiple layers. C, transmission electron microscope (TEM) photograph of 'honeycomb membrane' layer. D, detail of (C).
Figure 4 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 4. Gromia marmorea sp. nov. scanning electron microscope (SEM) photographs. A, oral capsule (the arrow indicates the direction of the photograph sequence shown in panels Ci–Civ). B, perforations of the test surface. Ci–Civ, sequence of photographs over a distance of 250 Mm showing test pores (each pore is highlighted by a white circle), with the number of pores increasing with increasing distance from the aperture (from left to right); 4000¥ magnification. D, E, interior of broken specimen showing stercomata and other structures.
Figure 1 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 1. Stations sampled in the Weddell Sea during the RV Polarstern cruise, leg ANT-XXII/3, from 22nd January to 6th April, 2006. Filled circles indicate sample stations for Gromia marmorea sp. nov. (133#2) at 1584-m depth, Gromia winnetoui sp. nov. (121#7) at ~2600-m depth, and Gromia melinus sp. nov. (81#8 and 80#9) at 3101- and 4392-m depth, respectively.
Figure 2 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 2. Gromia marmorea sp. nov. A–D, reflected-light photographs of preserved specimens, from station 133#2, 1584-m depth. Photographed in water. A, holotype, reg. no. SMF XXVII 7398, spherical morphotype. B, paratype, reg. no. SMF XXVII 7399, droplet-shaped morphotype. C, paratype, reg. no. SMF XXVII 7399, oval morphotype. D, detail of oral capsule. E, scanning electron microscope (SEM) photograph of oral capsule. F, unfixed specimens.
Figure 6 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 6. Gromia melinus sp. nov. A, reflected light photograph, station 80#9, at 3103-m depth. B, transmission electron microscope (TEM) photograph of 'honeycomb membrane' layer at a 5000¥ magnification. C, TEM photograph at a 50 000¥ magnification. D, TEM photograph at a 100 000¥ magnification.
Figure 7 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 7. Gromia winnetoui sp. nov. A–D, reflected-light photographs, station 121#7, ~2600-m depth. A, holotype, reg. no. SMF XXVII 7402, agglutinated specimen. B, paratype, reg. no. SMF XXVII 7403, elongate oval specimen (the circle indicates the oral capsule). C, D, irregularly shaped specimen (the circles indicate the oral capsules).
Figure 9 in Three new species of deep-sea Gromia (Protista, Rhizaria) from the bathyal and abyssal Weddell Sea, Antarctica
Figure 9. Gromia winnetoui sp. nov. A–D, transmission electron microscope (TEM) photographs of the test wall, including the 'honeycomb membrane' layer (hm), station 121#7, ~2600-m depth.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.