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1,071 results for “Mangroves”
FIGURE 2 in New mouthless nematode of the genus Parastomonema Kito, 1989 (Nematoda: Siphonolaimidae) from a mangrove forest on the coast of Thailand, and erection of the new subfamily Astomonematinae within the Siphonolaimidae
FIGURE 2. Parastomonema papillosum sp. nov. Male (A–E, holotype ZIHU 3137): A) Entire body, posterior testis reflexed at arrowed point. B) Anterior region. C) Head. D) Posterior region. E) Spicule and gubernaculum. Female (F–I, K, ZIHU 3142; J, ZIHU 3140; L, ZIHU 3141): F) Entire body, vulva (arrowed). G) Head. H–J) Vulval region. K, L) Posterior region. A–E, L, left side view; F–I, K, right side view; J, ventral view.
Figs 15–23 in Three new species of the genus Argyrochlamys Lamb, 1922 (Diptera: Dolichopodidae) from mangroves of Iran and Oman
Figs 15–23. Argyrochlamys tomkovichi, sp.n., male (15–22), female (23): 15 — habitus; 16 — head; 17 — antenna; 18 — wing; 19 — hypopygium, lateral view; 20 — details of hypopygial appendages, lateral view; 21 — details of hypopygial appendages, ventral view; 22 — hypandrium, ventral view; 23 — antenna. Рис. 15–23. Argyrochlamys tomkovichi, sp.n., самец (15–22), самка (23): 15 —внеШний вид; 16 — голова; 17 — усик; 18 — крыло; 19 — гипопигий, вид сбоку; 20 — детали придатков гипопигиЯ, вид сбоку; 21 — детали придатков гипопигиЯ, вид сниЗу; 22 — гипандрий, вид сниЗу; 23 — усик.
Figs 25–28 in Three new species of the genus Argyrochlamys Lamb, 1922 (Diptera: Dolichopodidae) from mangroves of Iran and Oman
Figs 25–28. Habitats of the Argyrochlamys species in Iran: 25 — the Azini wharf of the Sirik mangrove forest (Argyrochlamys hajiesmaeiliani, sp.n. and A. nigrescens, sp.n.); 26 — Qeshm Island, DoKuhak (Argyrochlamys hajiesmaeiliani, sp.n.); 27 — the Gabrik protected area (Argyrochlamys hajiesmaeiliani, sp.n.); 28 — mangrove forest near the Nayband Gulf at the Asalouyeh firth (the Iranian Argyrochlamys species). Photoes by M. Mofidi. Рис. 25–28. МестообитаниЯ видов Argyrochlamys в Иране: 25 — причал АЗини в мангровом лесу Сирик (Argyrochlamys hajiesmaeiliani, sp.n. и A. nigrescens, sp.n.); 26 — остров КеШм, Докухак (Argyrochlamys hajiesmaeiliani, sp.n.); 27 —Заповедник Габрик (Argyrochlamys hajiesmaeiliani, sp.n.); 28 — мангровый лес у Залива Найбанд в устье реки Эселуйе (местообитание иранских видов Argyrochlamys). Фото М. Мофиди.
Fig. 24 in Three new species of the genus Argyrochlamys Lamb, 1922 (Diptera: Dolichopodidae) from mangroves of Iran and Oman
Fig. 24. Distribution of the Argyrochlamys species in Iran and Oman: A — Bushehr Prov., Asaluyeh, Nayband (A. hajiesmaeiliani, sp.n., A. nigrescens, sp.n., A. impudicus, Argyrochlamys sp. A); B — Hormozgan prov., Bandar-e Khamir, Marduo Island (Argyrochlamys sp. A); C — Hormozgan Prov., Qeshm Island, DoKuhak (A. hajiesmaeiliani, sp.n.); D — Hormozgan prov., Sirik, Azini wharf (A. hajiesmaeiliani, sp.n., A. nigrescens, sp.n.); E — Hormozgan prov., Gabrik protected area, Keyki (A. hajiesmaeiliani, sp.n.); F — Oman, Barr al-Hikman peninsula (A. hajiesmaeiliani, sp.n., A. tomkovichi, sp.n.). Рис. 24. Распространение видов Argyrochlamys species в Иране и Омане: А — остан БуШир, Эселуйе, Найбанд (A. hajiesmaeiliani, sp.n., A. nigrescens, sp.n., A. impudicus, Argyrochlamys sp. A); B — остан ХормоЗган, Бендер-Хемир, о-в Мардуо (Argyrochlamys sp. A); C — остан ХормоЗган, о-в КеШм, Докухак (A. hajiesmaeiliani, sp.n.); D — остан ХормоЗган, Сирик, пристань АЗини (A. hajiesmaeiliani, sp.n., A. nigrescens, sp.n.); E — остан ХормоЗган, Заповедник Габрик, Кейки (A. hajiesmaeiliani, sp.n.); F — Оман, п-ов Барр-Эль-Хикман (A. hajiesmaeiliani, sp.n., A. tomkovichi, sp.n.).
Figs 7–14 in Three new species of the genus Argyrochlamys Lamb, 1922 (Diptera: Dolichopodidae) from mangroves of Iran and Oman
Figs 7–14. Argyrochlamys nigrescens sp.n., male: 7 — habitus; 8 — head; 9 — antenna; 10 — wing; 11 — abdomen, dorsal view; 12 — hypopygium, lateral view; 13 — hypopygium, ventral view; 14 — details of hypopygial appendages. Рис. 7–14. Argyrochlamys nigrescens sp.n., самец: 7 — внеШний вид; 8 — голова; 9 — усик; 10 — крыло; 11 — брЮШко, вид сверху; 12 — гипопигий, вид сбоку; 13 — гипопигий, вид сниЗу; 14 — детали придатков гипопигиЯ.
Fig. 1 a–c Lignincola laevis. a Ascoma inside mangrove wood. b Ascus. c Ascospore. Bars a 50 in Genetic variation within the cosmopolitan aquatic fungus Lignincola laevis (Microascales, Ascomycota)
Fig. 1 a–c Lignincola laevis. a Ascoma inside mangrove wood. b Ascus. c Ascospore. Bars a 50 μm; b, c 10 μm
Fig. 6 in Salinity Variation in a Mangrove Ecosystem: A Physiological Investigation to Assess Potential Consequences of Salinity Disturbances on Mangrove Crabs
Fig. 6. NKA immunolabelling and activity for Neosarmatium meinerti (A, C, E) and Tubuca urvillei (B, D, F). NKA immunolabelling is shown for anterior (A, C) and posterior (B, D) gills (here, gill 8 for N. meinerti and gill 6 for T. urvillei). NKA activity (E, F) was measured from the last three gill pairs of crabs exposed to SW or dSW. Different letters show statistically significant differences based on a twoway ANOVA followed by Tukey's HSD test (p <0.05). GL: gill lamellae; arrow heads indicate NKA labelling. This labelling occurs along the basal side of the epithelial cells and appears reduced in the anterior gills but thicker in the posterior gills. Scale bar = 40 µm.
Fig. 2 in Salinity Variation in a Mangrove Ecosystem: A Physiological Investigation to Assess Potential Consequences of Salinity Disturbances on Mangrove Crabs
Fig. 2. Dorsal view of Neosarmatium meinerti (A) and Tubuca urvillei (B). (C) Schematic representation of the experimental setup. For those analyses considering gill tissues (morphology, NKA activity and labelling), anterior and posterior gills were considered separately. The macroscopic view of N. meinerti and T. urvillei gill cavities are shown in D and E, respectively. The branchiostegite covering the branchial cavity has been removed. Gills are numbered from the anterior side of the crabs. Both species present a similar gill organization but different total gill number: whilst there are 2 podobranchs and 4 arthrobranchs for T. urvillei, N. meinerti possess 3 podobranchs and 4 arthrobranchs. (F) Histological section of a phyllobranchiate gill (T. urvillei) with flat leaf-like lamellae connected to a central axis distributing and collecting the circulating hemolymph. Anterior and posterior gills of both species present a similar branchial organisation. CA: central axis; cSW: concentrated seawater; dSW: diluted seawater; FW: freshwater; GL: gill lamellae; GT: gill tip; iSW: isosmotic seawater; N: dissecting needle; SW: seawater. Scale bars: A = 3 cm, B = 2 cm; C = 2 cm; D = 7 mm; E = 500 µm. *values adjusted to the isosmotic point of each of the two species according to the results provided in figure 3A.
Fig. 3 in Salinity Variation in a Mangrove Ecosystem: A Physiological Investigation to Assess Potential Consequences of Salinity Disturbances on Mangrove Crabs
Fig. 3. Hemolymph osmolality (in mOsm·kg-1) at different salinities (A) and osmoregulatory capacity after salinity challenge (B, C) shown by Neosarmatium meinerti (B) and Tubuca urvillei (C). Grey bar: salinity range of water collected at low tide along the rivulet banks. Black bar: salinity range of water collected at low tide in burrows of N. meinerti.
Fig. 5 in Salinity Variation in a Mangrove Ecosystem: A Physiological Investigation to Assess Potential Consequences of Salinity Disturbances on Mangrove Crabs
Fig. 5. Histological sections (A to D) and epithelial thickness of gill lamellae (E, F) of Neosarmatium meinerti (A, C, E) and Tubuca urvillei (B, D, F) after dSW acclimation. Subpanels A and B correspond to anterior (mainly respiratory) gills (here pairs 1 and 3 for N. meinerti and T. urvillei, respectively). Subpanels C and D correspond to posterior (osmoregulatory) gills (here, pairs 8 and 6 for N. meinerti and T. urvillei, respectively). B: bacterial layer; C: cuticle; E: epithelium; H: hemocyte; HL: hemolymphatic lacuna; N: nucleus; S: septum. Scale bar = 20 µm. * p <0.001 (t-test).
Fig. 4 in Salinity Variation in a Mangrove Ecosystem: A Physiological Investigation to Assess Potential Consequences of Salinity Disturbances on Mangrove Crabs
Fig. 4. Whole animal rates of oxygen consumption (A, B) and ROS/RNS production in hemolymph (C, D) from Neosarmatium meinerti (A, C) and Tubuca urvillei (B, D). Different letters represent significantly different groups according to a one-way ANOVA test followed by a SNK multiple comparison test (p <0.05). iSW: isosmotic SW (750 mOsm·kg-1 for N. meinerti and 820 mOsm·kg-1 for T. urvillei). FWB: fresh body weight.
Fig. 1 in Salinity Variation in a Mangrove Ecosystem: A Physiological Investigation to Assess Potential Consequences of Salinity Disturbances on Mangrove Crabs
Fig. 1. Characteristics of the study site. (A) Location of the Comoros archipelago and Malamani mangrove (Mayotte Island). (B) Detailed view of the Malamani mangrove and Neosarmatium meinerti and Tubuca urvillei collection zones. Continuous line indicates the upper limit of the Ceriops tagal belt while the discontinuous line represents the approximate limit between the C. tagal and Rhizophora mucronata belts. The red dot corresponds to the position where pictures E and F were taken. Areas marked in red and blue represent the collection sites for N. meinerti and T. urvillei, respectively. (C) Schematic representation of the mangrove structure, representing the habitats of the two crab species. (D) General view of the mangrove (area marked in red in subpanel B) at high tide. E-F: General view of the rivulet at low tide during a dry day (E) and after rainfall (F).
An Excel spreadsheet including 7-year eddy covariance-based evapotranspiration and auxilary data at Yunxiao mangrove flux tower
<p>An Excel spreadsheet including 7-year eddy covariance-based evapotranspiration and auxilary data at Yunxiao mangrove flux tower required to reproduce key results in the main text of a manuscript (each figure corresponds to a single sheet). Contact Xudong Zhu at Xiamen University (xdzhu@xmu.edu.cn) if you have any question.</p>
FIGURE 3 in Achlya catenulata sp. nov., a new Saprolegniales (Oomycetes, Straminipila) from Brazilian mangrove swamp
FIGURE 3. Maximum likelihood tree inferred from LSU rDNA sequences of isolates of Achlya. Numbers next to branches indicate bootstrap support (%) and the bar shows the number of substitutions per site.
FIGURE 2 in Achlya catenulata sp. nov., a new Saprolegniales (Oomycetes, Straminipila) from Brazilian mangrove swamp
FIGURE 2. Maximum likelihood tree inferred from ITS rDNA sequences of isolates of Achlya. Numbers next to branches indicate bootstrap support (%) and the bar shows the number of substitutions per site.
FIGURE 1 A–E. Achlya catenulata. A in Achlya catenulata sp. nov., a new Saprolegniales (Oomycetes, Straminipila) from Brazilian mangrove swamp
FIGURE 1 A–E. Achlya catenulata. A. Achlyoid discharge of the zoosporangia. B. Sympodial renewal of the zoosporangia. C. Catenulate oogonia and diclinous antheridia. D–E. Oogonia, failed to mature and eccentric oospores and antheridia. Bars: 10 μm.
FIGURE 6 in Description of a new marine planktonic cyanobacterial species Synechococcus moorigangaii (Order Chroococcales) from Sundarbans mangrove ecosystem
FIGURE 6. (A) Growth of Synechococcus moorigangaii sp. nov. in presence of different nitrogen sources; (B) Chlorophyll a concentration of Synechococcus moorigangaii sp. nov. in presence of different nitrogen sources; (C) Growth of Synechococcus moorigangaii sp. nov. in presence of different concentrations of nitrate; (D) Chlorophyll a concentration of Synechococcus moorigangaii sp. nov. in presence of different concentrations of nitrate.
FIGURE 5 in Description of a new marine planktonic cyanobacterial species Synechococcus moorigangaii (Order Chroococcales) from Sundarbans mangrove ecosystem
FIGURE 5. (A) Growth rate of Synechococcus moorigangaii sp. nov. at salinity 15; (B) Chlorophyll concentration of Synechococcus moorigangaii sp. nov. at salinity 15; (C) Salinity tolerance of Synechococcus moorigangaii sp. nov. measured by optical density in presence of salinity 0–40; (D) Chlorophyll a concentration of Synechococcus moorigangaii sp. nov. in presence of salinity 0–40.
FIGURE 2 in Description of a new marine planktonic cyanobacterial species Synechococcus moorigangaii (Order Chroococcales) from Sundarbans mangrove ecosystem
FIGURE 2. FESEM micrographs of isolate CMS01; (A) Single dividing cell; (B and C) Short chain filament; (D) Clusters of short chains.
FIGURE 1 in Description of a new marine planktonic cyanobacterial species Synechococcus moorigangaii (Order Chroococcales) from Sundarbans mangrove ecosystem
FIGURE 1. (A and B) Light micrographs of CMS01; (C) Differential interference contrast micrograph of isolate CMS01; (D) Autofluorescence micrograph of CMS01.
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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.