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Fig. 2 in Pine Forest Earthworms From Canary Islands (Tenerife And Gran Canaria)
Fig. 2. The projection of the species and edaphic variables: CA = calcium, OM = organic matter, K = potassium, PH = pH in water. Ac = A. chlorotica, Ar = A. rosea bimastoides, At = A. trapezoi-
Figure 1 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 1: Line drawings of female Delatylus andersoni n. gen., n. sp: (A) head and pharynx, (B) lip region and stylet, (C) deirids, (D) vulva and the anus viewed ventrally, (E) vulva and the tail viewed laterally, (F) oviduct and quadricolumella, (G) oocytes.
Figure 1. A in Structural and diversity changes in coastal dunes from the Mexican Caribbean: the case of the invasive Australian pine (Casuarina equisetifolia)
Figure 1. A) Location of Cozumel Island within the Yucatán Peninsula. B) Study area on the north side of Cozumel Island. C) The distribution of Casuarina equisetifolia, shown as dark gray polygons and the sampling plots (numbered circles). Plots 1, 6–9 are the invaded, while plots 2–5, 10 are non-invaded.
Figure 3 in Structural and diversity changes in coastal dunes from the Mexican Caribbean: the case of the invasive Australian pine (Casuarina equisetifolia)
Figure 3. Grouping of invaded (triangles) and non-invaded (squares) sampling plots according to their species composition similarity (PERMANOVA). The numbers close to the symbols are the assigned sampling plot number. The dotted lines represent the scores' standard deviation of each group. The solid black lines represent the distance (similarity) between sampling plots.
Fig. 7 in Differences Of The Bog And Dry Site Scots Pine Population Seedlings Germination And Early Growth
Fig. 7. Comparison of development stage when the terminal bud is formed between seedlings from bog site and dry site (mean development stage and standard error).
Fig. 5 in Differences Of The Bog And Dry Site Scots Pine Population Seedlings Germination And Early Growth
Fig. 5. Dry site seedlings early growth stages change during the first season till terminal bud formation.
Fig. 6 in Differences Of The Bog And Dry Site Scots Pine Population Seedlings Germination And Early Growth
Fig. 6. Bog site seedlings early growth stages change during the first season till terminal bud formation.
Fig. 3 in Variation In Cone And Seed Morphology Traits Among The Mitochondrial Dna Haplotypes Of Scots Pine (Pinus Sylvestris L.)
Fig. 3. Dependence of seed number per cone on cone length for the type A and type B mitotypes of Scots pine. Individual cone values are shown.
Рис. 4. Нора поΑземной поΛевки (компΛекс KS-11, октябрь 1984 г., «Αес на ВорскΛе»). А — горизонтаΛьная проекция; Б — боковая реконструкция Fig. 4. A common pine vole burrow (complex No. KS-11, October, 1984; "Forest on the Vorskla"). A — horizontal projection; Б — lateral projection in Spatial Organization Of Common Pine Vole (Microtus Subterraneus Selys-Longchamps, 1836) Colonies
Рис. 4. Нора поΑземной поΛевки (компΛекс KS-11, октябрь 1984 г., «Αес на ВорскΛе»). А — горизонтаΛьная проекция; Б — боковая реконструкция Fig. 4. A common pine vole burrow (complex No. KS-11, October, 1984; "Forest on the Vorskla"). A — horizontal projection; Б — lateral projection
Рис. 1. Пространственное распреΑеΛение скопΛений земΛяных выбросов поΑземной поΛевки в преΑеΛах пΛощаΑи поΛигона 1 га (октябрь 1985 г., «Αес на ВорскΛе») in Spatial Organization Of Common Pine Vole (Microtus Subterraneus Selys-Longchamps, 1836) Colonies
Рис. 1. Пространственное распреΑеΛение скопΛений земΛяных выбросов поΑземной поΛевки в преΑеΛах пΛощаΑи поΛигона 1 га (октябрь 1985 г., «Αес на ВорскΛе»)
Fig. 10. Males possess a in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 10. Males possess a well-developed file on the lef elytron a), with a relatively underdeveloped file on the right elytron b). The development of a file in female D. approximatus was highly variable and ofen almost non-existent. Lef elytron of female with a well-developed file, relative to most other observed female files c), and of female with poorly-developed file d).
Fig. 7. Waveform a in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 7. Waveform a) and spectrogram b) of simple chirps produced by a male (first and third chirps) and female (second and fourth chirps) when paired together in gallery. The spectral profile c) was taken at the center time of the first chirp, highlighted in a and b. Center time is the point during a sample about which energy is divided equally.
Fig. 8. Waveform a in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 8. Waveform a) and spectrogram b) of overlapping chirps produced by female and male D. approximatus. The first chirp in the sequence was produced by the female and is repeated approximately every 0.5 s. The female chirp overlaps with male chirps between 2 and 5 s in the recording. Sound occurring just past 4 s was not produced by either beetle, but rather was accidental noise produced by the recorder.
Fig. 9 in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 9. Abdominal segments of male a) and female b) D. approximatus. The male plectrum is shown circled in a).
Fig. 6. Waveform a in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 6. Waveform a), and spectrogram b) of a male interrupted chirp showing individual syllables within each chirp.
Fig. 5. Waveform a in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 5. Waveform a), and spectrogram b) of female simple chirp in a disturbance context. The waveform shows the relative amplitude in generic units and the spectrogram shows frequency over time with darker shades indicating higher relative energy.
Fig. 4. Waveform a in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 4. Waveform a), spectrogram b), and spectral profile c) of male simple chirp in a disturbance context. The waveform shows the relative amplitude in generic units and the spectrogram shows frequency over time with darker shades indicating higher relative energy. The spectral profile was taken at the midpoint of the first chirp, highlighted in a and b.
Fig. 2 in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 2. File length was measured posteriorly from the most posterior ridge (see lower arrow) up anteriorly to the last well-developed ridge (top arrow). Ridges at the anterior edge become poorly developed (circle) and these were not measured. See Methods for further description.
Fig. 3 in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 3. Temporal and spectral characteristics assessed for simple chirps made in a disturbance context. Train of individual pulses a), waveform b), and spectrogram c) from sample chirp produced by male in a disturbance context. The peak frequency (3.468 kHz) is noted for the first recorded chirp (occurring at 0.3 s).
Fig. 1 in Characterization of stridulatory structures and sounds of the larger Mexican pine beetle, Dendroctonus approximatus (Coleoptera: Curculionidae: Scolytinae)
Fig. 1. Phloem slide positioned under dissecting scope. The ultrasonic electronic insertion microphone is shown positioned in the center of the slide (see circle), inserted into the tunnel entrance. A small piezo transducer, shown at the far end of the phloem slide, was not used in recordings for this study.
ScienceDex guides
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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.