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112 results for “mangrove forest”
Data from: Mangrove above-ground biomass and production are related to forest age at Low Isles, Great Barrier Reef
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Figure 1. Sarcofahrtiopsis terezinhae n in A new species of Sarcofahrtiopsis (Insecta, Diptera, Sarcophagidae) from mangrove forests in the Brazilian Amazon, with a key to species identification
Figure 1. Sarcofahrtiopsis terezinhae n. sp., male paratype. A. Epandrium, surstylus and cercus, left lateral view; B. Sternite 5, ventral view; C. Right gonite, lateral view; D. Phallus, lateral view. Scale bars = 0.1 mm, except in Fig. 1A where it represents 0.2 mm. Abbreviations: pa = postgonal apodeme, prg = pregonite; ptg = postgonite; tp = toe-like projections; v = vesica; ve = vesical extension.
Figure 2. Sarcofahrtiopsis terezinhae n in A new species of Sarcofahrtiopsis (Insecta, Diptera, Sarcophagidae) from mangrove forests in the Brazilian Amazon, with a key to species identification
Figure 2. Sarcofahrtiopsis terezinhae n. sp., habitus of male holotype, lateral view. Scale bar = 1.0 cm. This figure is in color in the electronic version.
Data from: Habitat-dependent occupancy and movement in a migrant songbird highlights the importance of mangroves and forested lagoons in Panama and Colombia
Climate change is predicted to impact tropical mangrove forests due to decreased rainfall, sea-level rise, and increased seasonality of flooding. Such changes are likely to influence habitat quality for migratory songbirds occupying mangrove wetlands during the tropical dry season. Overwintering habitat quality is known to be associated with fitness in migratory songbirds, yet studies have focused primarily on territorial species. Little is known about the ecology of non-territorial species that may display more complex movement patterns within and among habitats of differing quality. In this study, we assess within season survival and movement at two spatio-temporal scales of a non-territorial overwintering bird, the prothonotary warbler (Protonotaria citrea), that depends on mangroves and tropical lowland forests. Specifically, we (1) estimated within-patch survival and persistence over a six-week period using radio-tagged birds in central Panama and (2) modelled abundance and occupancy dynamics at survey points throughout eastern Panama and northern Colombia as the dry season progressed. We found that site persistence was highest in mangroves; however, the probability of survival did not differ among habitats. The probability of warbler occupancy increased with canopy cover, and wet habitats were least likely to experience local extinction as the dry season progressed. We also found that warbler abundance is highest in forests with the tallest canopies. This study is one of the first to demonstrate habitat-dependent occupancy and movement in a non-territorial overwintering migrant songbird, and our findings highlight the need to conserve intact, mature mangrove and lowland forests.
FIGURE 3 in A new species of Nephochaetopteryx Townsend (Diptera: Sarcophagidae) from the Brazilian Amazon mangrove forest
FIGURE 3. Nephochaetopteryx aryi sp. nov., holotype male (MPEG), terminalia. A. Epandrium, surstylus and cercus, left lateral view. B. Cerci, posterior view (setation omitted on left side). C. Sternite 5, ventral view (setation omitted on left side). D. Gonites, left lateral view. E. Phallus, left lateral view. Abbreviations: bp = basiphallus; ce = cercus; dp = distiphallus; ep = epandrium; ip = inner process of vesica; jx = juxta; ls = lateral stylus; ms = median stylus; pce = projections of cercus; pg = pregonite; pt = postgonite; su = surstylus; ve = vesica. Scale bars: A–C = 0.5 mm; D–E = 0.25 mm.
FIGURE 1. Study area. A in A new species of Nephochaetopteryx Townsend (Diptera: Sarcophagidae) from the Brazilian Amazon mangrove forest
FIGURE 1. Study area. A. Detail of satellite image of South America, with state of Pará highlighted by red box. B. State of Pará. C. Satellite image of the area highlighted by red box in Fig. 1B. D. Satellite image of area highlighted by red box in Fig. 1C. The white star points to the Village of Calafate and the white circle to the mangrove forest where the collections were carried out.
FIGURE 2 in A new species of Nephochaetopteryx Townsend (Diptera: Sarcophagidae) from the Brazilian Amazon mangrove forest
FIGURE 2. Nephochaetopteryx aryi sp. nov., male. A. Habitus of paratype (MPEG, collected 16–18.I.2021), lateral view. B. Terminalia of paratype (MPEG, collected 16–18.XII.2015), posterior view. C. Same, left lateral view. Abbreviations: ce = cercus; ep = epandrium; jx = juxta; pce = projections of cercus; pg = pregonite; pt = postgonite; ve = vesica. Scale bars: A = 0.7 mm; B–C = 0.5 mm.
Predicting changes in molluscan spatial distributions in mangrove forests in response to sea-level rise
<p class="MsoNormal"><span>Molluscs are an important component of the mangrove ecosystem, and the vertical distributions of molluscan species in this ecosystem are primarily dictated by tidal inundation. Thus, sea-level rise (SLR) may have profound effects on mangrove mollusc communities. Here, we used dynamic empirical models, based on measurements of surface elevation change, sediment accretion, and molluscan zonation patterns, to predict changes in molluscan spatial distributions in response to different sea-level rise rates in the mangrove forests of Zhenzhu Bay (Guangxi, China). The change in surface elevation was 4.76–9.61 mm yr</span><sup><span>−</span></sup><sup><span>1</span></sup><span> during the study period (2016–2020), and the magnitude of surface-elevation change decreased exponentially as original surface elevation increased. Based on our model results, we predicted that mangrove molluscs might successfully adapt to a low rate of SLR (2.00–4.57 mm yr</span><sup><span>−</span></sup><sup><span>1</span></sup><span>) by 2100, with molluscs moving seaward and those in the lower intertidal zones expanding into newly available zones. However, as SLR rate increased (4.57–8.14 mm yr</span><sup><span>−</span></sup><sup><span>1</span></sup><span>), our models predicted that surface elevations would decrease beginning in the high intertidal zones and gradually spread to the low intertidal zones. Finally, at high rates of SLR (8.14–16.00 mm yr</span><sup><span>−</span></sup><sup><span>1</span></sup><span>), surface elevations were predicted to decrease across the elevation gradient, with molluscs moving landward and species in higher intertidal zones blocked by landward barriers. Tidal inundation and the consequent increases in interspecific competition and predation pressure were predicted to threaten the survival of many molluscan groups in higher intertidal zones, especially arboreal and infaunal molluscs at the landward edge of the mangroves, resulting in a substantial reduction in the abundance of original species on the landward edge. Thus, future efforts to conserve mangrove floral and faunal diversity should prioritize species restricted to landward mangrove areas and protect potential species habitats.</span></p>
FIGURE. Landscapes and vegetation types at Quiçama National Park. A. Wooded savannah with Adansonia digitata. B. Mosaic of wooded savannah and thicket. C. Grassy savannah. D. Slope with thicket. E. Grassy savanna with Setaria welwitschi. F. Wooded savannah. G. Cuanza River shores with herbaceous vegetation. H. Herbaceous vegetation on the banks of the Cuanza River and slope with open forest. I. Coastal sands. J. Mangrove at the Cuanza River estuary, with Rhizophora racemosa. (Photographs by the authors). in An annotated checklist of the vascular flora of Quiçama National Park, Angola
FIGURE. Landscapes and vegetation types at Quiçama National Park. A. Wooded savannah with Adansonia digitata. B. Mosaic of wooded savannah and thicket. C. Grassy savannah. D. Slope with thicket. E. Grassy savanna with Setaria welwitschi. F. Wooded savannah. G. Cuanza River shores with herbaceous vegetation. H. Herbaceous vegetation on the banks of the Cuanza River and slope with open forest. I. Coastal sands. J. Mangrove at the Cuanza River estuary, with Rhizophora racemosa. (Photographs by the authors).
FIGURE 3 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 3. Thalassina cangioensis sp. nov., paratype ♀, ZMMU Ma-6231 (a, h, i) and holotype ♂, ZMMU Ma-6230 (b–f, g): a, b—carapace, lateral view; c—anterior part of carapace, lateral view; d—rostrum, dorsal view; e—posterodorsal median process and pleomere I, dorsal view; f, h—pleon, dorsal view; g, i—pleomeres, lateral view; k—pleomere III, ventral view.
FIGURE 6 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 6. Thalassina cangioensis sp. nov., holotype ♂, ZMMU Ma-6230 (a, g, h), paratype ♀, ZMMU Ma-6231, (b, c–f), and Thalassina squamifera De Man, 1915, ♂, ZMMU Ma-3226 (i, j): a—anterior part of carapace, lateral view; b—antennula; c—antenna; d—chela of pereopod II; e—dactylus of pereopod III; f—sternites III; ventral view; g, i—pleopod I; h, j—distal part of pleopod I.
FIGURE 2 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 2. Thalassina cangioensis sp. nov., general view of holotype ♂, ZMMU Ma-6230: a—lateral view; b—dorsal views; c—carapace, dorsal view. Scale bar—5 cm.
FIGURE 1 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 1. The map of the distribution of the species of Thalassina Latreille, 1806 in the Indo-West Pacific region.
FIGURE 5 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 5. Thalassina cangioensis sp. nov., holotype ♂, ZMMU Ma-6230: a—pereopod II; b—pereopod III; c—merus of pereopod III; d—pereopod IV. Scale bar 2 cm.
FIGURE 4 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 4. Thalassina cangioensis sp. nov., holotype ♂, ZMMU Ma-6230: a, b—larger pereopod I (cheliped); c, d—fingers (dactylus and pollex) of larger pereopod I (cheliped); e—larger pereopod I, dorsal view; f—smaller pereopod I (cheliped); g—fingers (dactylus and pollex) of smaller pereopod I; h—smaller pereopod I, dorsal view. Scale bar—1 cm.
FIGURE 9 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 9. Phylogenetic relationships of Thalassina cangioensis sp. nov. and other species of the genus Thalassina. Bootstrap support indicated at nodes.
FIGURE 7 in A new mud lobster of the genus Thalassina Latreille, 1806 (Crustacea: Decapoda: Gebiidea: Thalassinidae) from the mangrove forest of the Cần Giờ Mangrove Reserve, South Vietnam
FIGURE 7. Thalassina cangioensis sp. nov., paratype ♀, ZMMU Ma-6231: a—anterior part of carapace, lateral view; b—rostrum, dorsal view; c—posterodorsal median process and pleomere I, dorsal view; d, e—larger pereopod I (cheliped); f—fingers (dactylus and polex) of larger pereopod I (cheliped); g—larger pereopod I, dorsal view; h, i—smaller pereopod I (cheliped); j—fingers (dactylus and polex) of larger pereopod I (cheliped); k—larger pereopod I, dorsal view; l—pleomere III, ventral view. Scale bar—1 cm.
FIGURE 3 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 3. Parastomonema papillosum sp. nov. Male (A, E, F, holotype ZIHU 3137; H, additional specimen) and female (B–C, ZIHU 3138; D, ZIHU 3139; G, ZIHU 3142): A) Anterior region. B) Transverse section at level anterior to cephalic setae, cephalic papillary nerves (arrowed). C) Transverse section at level of amphids. D) Two amphids located in tandem. E) Anterior and posterior testes near the arrowed point in Fig. 2A. F) Cloacal region. G) Posterior region. H) Head sensilla, sequentially arranged from the surface (a) to the deeper focal plane (d). A, E, F, H, left side view; D, G, right side view; B, C, en face view, top is dorsal side. Bar scales: A, E–H = 10 µm; B–D = 5 µm. Abbreviations: amp = amphid, cgl = caudal gland, cp = cephalic papilla/papillary nerve, cs = cephalic seta, gub = gubernaculum, gut = rudimentary gut, m = microorganisms, nr = nerve ring, spic = spicule, T1 and T2 = anterior and posterior testis, vs = vacuolated structure.
FIGURE 1 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 1. Location of the sampling site in the mangrove forest of Ban Khlong Khon, Samut Songkhram, Thailand. Asterisk, sampling site (13°19'7 N, 99°58'19 E); dotted area, mangrove forest.
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.
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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.