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Figure 4 in Influence of CO -induced seawater acidification on the development and lifetime reproduction of Tigriopus japonicus Mori, 1938
Figure 4. Effect of carbon dioxide (CO2)-driven seawater acidification on total number of nauplii (N = 3) produced by Tigriopus japonicus females over the duration of the experiment (median indicated with a bar; quartiles, minimum and maximum shown).
Figure 3 in Influence of CO -induced seawater acidification on the development and lifetime reproduction of Tigriopus japonicus Mori, 1938
Figure 3. Proportion of egg sacs that successfully produced nauplii (N = 3) at four pH levels (median indicated with a bar; quartiles, minimum and maximum also shown).
Figure 6 in Influence of CO -induced seawater acidification on the development and lifetime reproduction of Tigriopus japonicus Mori, 1938
Figure 6. Variation in number of nauplii [mean ± standard deviation (SD), N = 3] produced by Tigriopus japonicus females over successive broods at four pH levels.
Figure 2 in Influence of CO -induced seawater acidification on the development and lifetime reproduction of Tigriopus japonicus Mori, 1938
Figure 2. Effect of carbon dioxide (CO2)-induced seawater acidification on the number of broods (N = 3) produced by females of Tigriopus japonicus over the duration of the experiment (median indicated with a bar; quartiles, minimum and maximum also shown).
Figure 1 in A new subterranean Maraenobiotus (Crustacea: Copepoda) from Slovenia challenges the concept of polymorphic and widely distributed harpacticoids
Figure 1. Maraenobiotus slovenicus sp. nov., SEM micrographs, paratype female 1: (A) habitus, dorsal; (B) cephalothorax, dorsal; (C) anterior part of cephalothorax, dorsal; (D) right antennule, dorsal; (E) free pedigerous somites, dorsal; (F) first three urosomites, dorsal; (G) last three urosomites and caudal rami, dorsal; (H) right caudal ramus, dorsal.
Figure 8 in On a small collection of Tetragonicipitidae Lang, 1944 (Copepoda: Harpacticoida) from Mexico: new records and new species
Figure 8. Phyllopodopsyllus parastigmosus sp. nov. Female. (A) Urosome, dorsal, P5 bearingsomite omitted; (B) urosome, dorsal, P5 bearing somite omitted. Scale bars: A, B, 100 µm.
Figure 26 in On a small collection of Tetragonicipitidae Lang, 1944 (Copepoda: Harpacticoida) from Mexico: new records and new species
Figure 26. Adoginiceps camaxeni gen. nov. et sp. nov. Male. (A) P5, anterior; (B) P6, anterior. Scale bars: A, B, 50 µm.
Figure 5 in On a small collection of Tetragonicipitidae Lang, 1944 (Copepoda: Harpacticoida) from Mexico: new records and new species
Figure 5. Phyllopodopsyllus tenuis Wells and Rao, 1987. Male. (A) Habitus, dorsal; (B) habitus, lateral; (C) anal somite and left caudal ramus, dorsal. Scale bars: A, B, 100 µm; C, 286 µm.
Figure 15 in On a small collection of Tetragonicipitidae Lang, 1944 (Copepoda: Harpacticoida) from Mexico: new records and new species
Figure 15. Phyllopodopsyllus parastigmosus sp. nov. Male. (A) P2, anterior; (B) P4, anterior; (C) P5 anterior; (D) P3 ENP. Scale bars: A–D, 100 µm.
Figure 4 in On a small collection of Tetragonicipitidae Lang, 1944 (Copepoda: Harpacticoida) from Mexico: new records and new species
Figure 4. Phyllopodopsyllus tenuis Wells and Rao, 1987. Female. (A) P4 ENP, anterior; (B) P3 EXP2, anterior; (C) P3 EXP3, anterior; (D) P3 EXP1, anterior; (E) P3 ENP, anterior; (F) P5, anterior. Scale bars: A–E, 50 µm; F, 100 µm.
Figure 6 in Spatiotemporal distribution of planktonic copepod communities in Tokyo Bay where Oithona davisae Ferrari and Orsi dominated in mid-1980s
Figure 6. Horizontal distributions of the identified community groups in Tokyo Bay (the letters in parentheses in legends show the indicator species).
Figure 6 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 6. Characteristics of P5 in oncaeid species. Different types of length to width ratio of P5 exopod segment (blue), number of exopodal setae (green) and length of outer basal seta (red). (A) Oncaea serrata (notopus-group) [from Böttger-Schnack 2011]; (B) Triconia similis [from Böttger-Schnack 1999]; (C) Spinoncaea humesi [from Böttger-Schnack 2003].
Figure 5 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 5. Characteristics of P1- or P2-bearing somite in oncaeid species. (A) P1-bearing somite with dorsal protrusion ([original] undescribed morphospecies Oncaea sp. 4.2, cf. Böttger-Schnack and Schnack 2013, table 3); (B) and (C) P2-bearing somite with dorsal projection or swelling: (B) Triconia conifera [from Böttger-Schnack 1999]; (C) T. rufa [from Böttger-Schnack 1999].
Figure 3 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 3. Seasonal changes in sea ice concentration, surface chl. a (from satellite) and total mass flux (a), and daylight hours (b) at St. NAPt from October 2010 to September 2012.
Figure 8 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 8. Seasonal changes in sea ice concentration, daylight hours, chl. a, and total mass flux from January to December (upper panel). The ecological characteristics of the five dominant copepods (lower panel). The open and solid bars indicate the high abundance and reproductive periods for each species, respectively.
Figure 4 in Inter-oceanic comparison of planktonic copepod ecology (vertical distribution, abundance, community structure, population structure and body size) between the Okhotsk Sea and Oyashio region in autumn
Figure 4. Copepod species composition (centre) and copepodid stage structures of the dominant species (left: Oyashio region, right: Okhotsk Sea). All data are integrated means of a 0– 500 m water column based on the IONESS samples in the Oyashio region (St. 19) and Okhotsk Sea (St. OK24) from October to November 1996. Error bars for the copepodid stage indicate standard deviations of each daily duplicate.
Figure 3 in Inter-oceanic comparison of planktonic copepod ecology (vertical distribution, abundance, community structure, population structure and body size) between the Okhotsk Sea and Oyashio region in autumn
Figure 3. Vertical distribution of zooplankton biovolume in the Oyashio region (upper panels) and Okhotsk Sea (lower panels) from September to December in 1996–1998. Note that the biovolume axes are not the same between panels. Tc: thermocline.
Figure 4 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 4. Characteristics of cephalosome shape in oncaeid species. (A) Lateral view of species (Oncaea longipes [from Kršinić and Malt 1985]) and front sections of cephalosome ([original] undescribed morphospecies of longipes-group, cf. Böttger-Schnack 1994, table 2) showing distal spinous process; (B) and (C) dorsal view of species showing bilateral protrusion of cephalosome (arrowed) at posterior margin (O. minima [from Kršinić and Malt 1985]) or at midregion (O. vodjanitskii [G.A. Boxshall, pers. comm.]).
Figure 50. Pegomya solennis, mandibles removed from a in Diverse mechanisms of feeding and movement in Cyclorrhaphan larvae (Diptera)
Figure 50. Pegomya solennis, mandibles removed from a puparium, ventral view, maximum length 0.1 mm.
Figure 53 in Diverse mechanisms of feeding and movement in Cyclorrhaphan larvae (Diptera)
Figure 53. Stegana coleoptrata, thorax and head cleared in KOH, lateral view, head to the right, as = anterior spiracle; ms = mesothorax; mt = metathorax; os = oral sclerite; pro = prothorax; ps = pseudocephalon.
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.