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Fig. 4 in Rediscovery of two species of Croton (Euphorbiaceae) from littoral habitats of eastern Madagascar
Fig. 4. – Croton chapelieri Baill. (A-F) and C. vatomandrensis Leandri (G-L). A-C. Staminate flower: side view (A), top view (B) and top view with stamens removed to show the five nectaries (C). D-F. Pistillate flower: side view (D), top view (E), and top view with ovary removed to show the five nectaries (F). G-I. Staminate flower: side view (G), top view (H), and top view with stamens removed to show the five nectaries (I). J-L. Pistillate flower: side view (J), top view (K), and top view with ovary removed to show the five nectaries (L). [A-F: van Ee et al. 1181; G-L: van Ee et al. 1194]
Fig. 2. – Croton chapelieri Baill. A in Rediscovery of two species of Croton (Euphorbiaceae) from littoral habitats of eastern Madagascar
Fig. 2. – Croton chapelieri Baill. A. Typical littoral habit at Mahabo, Atsimo-Atsinanana Region, Fianarantsoa Province; B. Shrubs growing
Рис. 2. Размерная структура G. lacustris в ΛитораΛьной зоне озера АрахΛей: 1 — июнь; 2 — август; 3 — октябрь Fig. 2. G. lacustris population size structure in the Lake Arakhley littoral zone: 1 — June, 2 — August, 3 — October in The life cycle of Gmelinoides fasciatus (Stebbing, 1899) and Gammarus lacustris (Sars, 1863) amphipods in the lake Arakhley littoral during the extreme low-water phase of the hydrological cycle
Рис. 2. Размерная структура G. lacustris в ΛитораΛьной зоне озера АрахΛей: 1 — июнь; 2 — август; 3 — октябрь Fig. 2. G. lacustris population size structure in the Lake Arakhley littoral zone: 1 — June, 2 — August, 3 — October
Рис. 1. Размерная структура Gm. fasciatus в ΛитораΛьной зоне озера АрахΛей: 1 — в июне; 2 — в августе; 3 — в октябре; 4 — в Αекабре 2017 г. и июне 2018 г. Fig. 1. Gm. fasciatus population size structure in the Lake Arakhley littoral zone: 1 — June; 2 — August; 3 — October; 4 — December, 2017 and June, 2018 in The life cycle of Gmelinoides fasciatus (Stebbing, 1899) and Gammarus lacustris (Sars, 1863) amphipods in the lake Arakhley littoral during the extreme low-water phase of the hydrological cycle
Рис. 1. Размерная структура Gm. fasciatus в ΛитораΛьной зоне озера АрахΛей: 1 — в июне; 2 — в августе; 3 — в октябре; 4 — в Αекабре 2017 г. и июне 2018 г. Fig. 1. Gm. fasciatus population size structure in the Lake Arakhley littoral zone: 1 — June; 2 — August; 3 — October; 4 — December, 2017 and June, 2018
US reservoir surface and littoral area
<p>These datasets include estimates for littoral area and surface areas (based on water occurrence and recurrence) for reservoirs in the US that are documented in HydroLakes.</p>
Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm
Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm
Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm
Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm
Рис. 1. Карта-схема района иссΛеΑования и места сбора материаΛа: 1 — район косы НюкΛя; 2 — бухта Гертнера; 3 — бухта Батарейная; 4 — бухта Нагаева; 5 — Амахтонский заΛив, вбΛизи устья р. Армань in Species diversity and dominant species of the littoral area fishes of Tauysk bay, the Sea of Okhotsk
Рис. 1. Карта-схема района иссΛеΑования и места сбора материаΛа: 1 — район косы НюкΛя; 2 — бухта Гертнера; 3 — бухта Батарейная; 4 — бухта Нагаева; 5 — Амахтонский заΛив, вбΛизи устья р. Армань
Рис. 2.Соотношение виΑов рыб на ΛитораΛи Тауйской губы: А — по их зоогеографической принаΑΛежности; Б — по принаΑΛежности к ихтиоцену. Обозначения см. в табΛице 1 Fig. 2. Ratio of fish species in the littoral zone of Tauysk Bay: А — according to their zoogeographic affiliation; Б — by belonging to the ichthyocene. Designations are similar to those in Table 1. in Species diversity and dominant species of the littoral area fishes of Tauysk bay, the Sea of Okhotsk
Рис. 2.Соотношение виΑов рыб на ΛитораΛи Тауйской губы: А — по их зоогеографической принаΑΛежности; Б — по принаΑΛежности к ихтиоцену. Обозначения см. в табΛице 1 Fig. 2. Ratio of fish species in the littoral zone of Tauysk Bay: А — according to their zoogeographic affiliation; Б — by belonging to the ichthyocene. Designations are similar to those in Table 1.
Figure 2 in Description of three new species of Quadriacanthus (Monogenea: Ancyrocephalidae) gill parasites of Clarias submarginatus (Siluriformes: Clariidae) from Lake Ossa (Littoral region, Cameroon)
Figure 2. Morphometrics of Quadriacanthus spp. used in this study are based on GUSSEV (1962) and modified by N'DOUBA et al. (1999). (An) Anchor: (a) length, (ba) base width, (e) point length; (Cc) copulatory complex: (Ap) accessory piece length, (Pe) penis length; (Cn) cuneus: (j) length, (i) width; (Db) dorsal bar: (ct) centre length, (h) median process length, (w) width, (x) length, (H) hooklet length; (Vb) ventral bar: (w) width, (x) length, (Vg) vagina.
Fig. 1 in The invasive white ginger lily (Hedichium coronarium) simplifies the trait composition of an insect assemblage in the littoral zone of a Savanna reservoir
Fig. 1. Location and characterization of plant composition banks of Fazzari reservoir in the Brazilian Savanna (Cerrado Biome, Brazil).
Fig. 3 in The invasive white ginger lily (Hedichium coronarium) simplifies the trait composition of an insect assemblage in the littoral zone of a Savanna reservoir
Fig. 3. The average values of CWM-trait values of aquatic insect assemblages in invaded and non-invaded banks by white ginger lily of a reservoir in Brazilian Savanna (Cerrado Biome). A – CWM-FFG, B – CWM-feed, C – CWM-habit, D – CWM body length. CWM, Community level Weight-Mean.
Fig. 1 in Conservation status, range extension, and call analysis of the Littoral Glassfrog, Cochranella litoralis (Ruiz-Carranza and Lynch 1996)
Fig. 1. Distribution map of Cochranella litoralis. White circles indicate verifiable localities reported in the literature; the white star denotes the type locality; the blue X marks the iNaturalist observation from the Río Palenque Research Center, Los Ríos; and yellow plus symbols indicate new records reported herein.
Fig. 2 in Conservation status, range extension, and call analysis of the Littoral Glassfrog, Cochranella litoralis (Ruiz-Carranza and Lynch 1996)
Fig. 2. Dorsal and ventral aspects of Cochranella litoralis in life. (A) Adult male, CJ12588, from Los Laureles, Cotopaxi, Ecuador. (B–E) Adult male, CJ12587a–d, from Cristobal Colón Quininde, Esmeraldas, Ecuador. Photos by: Jaime Culebras (A); Ross J. Maynard (B–E).
Fig. 3 in Conservation status, range extension, and call analysis of the Littoral Glassfrog, Cochranella litoralis (Ruiz-Carranza and Lynch 1996)
Fig. 3. Audio spectrogram (top), oscillogram (middle), and power spectrum (bottom) of an adult male Cochranella litoralis from Los Laureles, Cotopaxi, Ecuador (A), and an adult male C. granulosa from Jardín de los Sueños, Cotopaxi, Ecuador (B).
Fig. 4 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition
Fig. 4. Comparison among Bray-Curtis dissimilarity indices of aquatic insect assemblages associated with white ginger lily banks and native vegetation profile in the littoral zone of a tropical reservoir in the Brazilian Savanna (Group 1, white ginger lily; Group 2, invaded forest; Group 3, native macrophyte; Group 4, riparian vegetation).
Fig. 2 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition
Fig. 2. Comparison between ecological variables of aquatic insect assemblages associated with invasive white ginger lily bank and other native vegetation banks in the littoral zone of a tropical reservoir in the Brazilian Savanna (A, abundance; B, richness; C, Simpson diversity; IM, invasive macrophyte; IF, invaded forest; NM, native macrophyte; RV, riparian vegetation).
Fig. 1 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition
Fig. 1. Location and characterization of vegetation profile banks of the Fazzari reservoir in the Brazilian Savanna (Cerrado Biome, Brazil).
ScienceDex guides
Understand access before you commit
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.