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1,071 results for “Mangroves”
Fig. 5 in A new genus and three new species of mangrove slugs from the Indo-West Pacific (Mollusca: Gastropoda: Euthyneura: Onchidiidae)
Fig. 5. Diagram that helps to visualize the data on pairwise genetic distances between COI sequences within and between mitochondrial units in Paromoionchis gen. nov. (see Table 3). Ranges of minimum to maximum distances are indicated (in percentages). For instance, within P. tumidus (Semper, 1880) unit #1, individual sequences are between 0 and 3.2% divergent; individual sequences between P. tumidus unit #1 and the other units are minimally 5% and maximally 8.4% divergent; overall, the distance gap between P. tumidus unit #1 and the eight other units is between 3.2 and 5%. The colors used for each unit are the same as those used in Figs 1–4 and 6.
Fig. 4. Maximum parsimony consensus tree within Paromoionchis gen. nov., performed with ITS2 DNA sequences from 80 in A new genus and three new species of mangrove slugs from the Indo-West Pacific (Mollusca: Gastropoda: Euthyneura: Onchidiidae)
Fig. 4. Maximum parsimony consensus tree within Paromoionchis gen. nov., performed with ITS2 DNA sequences from 80 individuals (including 7 outgroups). Numbers by the branches are the bootstrap values (only numbers>50% are indicated). Numbers for each individual correspond to unique identifiers for DNA extraction. All sequences for specimens of Paromoionchis gen. nov. are new. Information on specimens can be found in the lists of material examined and in Table 1. The letter A corresponds to a clade referred to in the text. The color used for each (mitochondrial) unit is the same as that used in Figs 1–3 and 5–6.
Fig. 2 in A new genus and three new species of mangrove slugs from the Indo-West Pacific (Mollusca: Gastropoda: Euthyneura: Onchidiidae)
Fig. 2. (continued) Phylogenetic relationships within Paromoionchis gen. nov. based on COI sequences of 166 individuals.
Fig. 1 in A new genus and three new species of mangrove slugs from the Indo-West Pacific (Mollusca: Gastropoda: Euthyneura: Onchidiidae)
Fig. 1. Phylogenetic relationships within Paromoionchis gen. nov. based on concatenated COI, 16S and 12S sequences for 53 individuals (including 7 outgroups). Numbers by the branches are the bootstrap values (maximum likelihood analysis, ML) and the posterior probabilities (Bayesian analysis). Only numbers>70% (ML) and>0.9 (Bayesian) are indicated. Numbers for each individual correspond to unique identifiers for DNA extraction. All sequences for specimens of Paromoionchis gen. nov. are new. Some outgroup sequences are from previous studies (Dayrat et al. 2011a, 2016; Dayrat & Goulding 2017). Information on specimens can be found in the lists of material examined and in Table 1. The letters A, B and C correspond to three clades which are referred to in the text. The color used for each (mitochondrial) unit is the same as that used in Figs 2–6.
Fig. 13 in Species turnover between the northern and southern part of the South China Sea in the Elaphropeza Macquart mangrove fly communities of Hong Kong and Singapore (Insecta: Diptera: Hybotidae)
Fig. 13. Elaphropeza riatanae Shamshev & Grootaert, 2007, male terminalia (19M1), RBINS (leg. C. Taylor and U. Chang). A. Tip of right epandrial lamella. B. Right epandrial lamella. C. Epandrium dorsal view. D. Left surstylus. Scale bar: 0.1 mm.
Fig. 10 in Species turnover between the northern and southern part of the South China Sea in the Elaphropeza Macquart mangrove fly communities of Hong Kong and Singapore (Insecta: Diptera: Hybotidae)
Fig. 10. Elaphropeza hongshulin sp. nov., holotype, ♂, habitus, RBINS (leg. C. Taylor and U. Chang; photo A. Samoh).
Fig. 12 in Species turnover between the northern and southern part of the South China Sea in the Elaphropeza Macquart mangrove fly communities of Hong Kong and Singapore (Insecta: Diptera: Hybotidae)
Fig. 12. Elaphropeza riatanae Shamshev & Grootaert, 2007, ♂, habitus, RBINS (leg. C. Taylor and U. Chang; photo A. Samoh).
Supplementary material 1 from: Robertson DR, Domínguez-Dominguez O, Aroyo YML, Mendoza RM, Simões N (2019) Reef-associated fishes from the offshore reefs of western Campeche Bank, Mexico, with a discussion of mangroves and seagrass beds as nursery habitats. ZooKeys 843: 71-115. https://doi.org/10.3897/zookeys.843.33873
: Data type: multimedia
Figure 3 in Diversity of Ctenophores in the Sundarban Mangroves, Northern Indian Ocean
Figure 3. Comparison between Mesozooplankton abundance and Ctenophore abundance in the selected study sites of Sundarbans.
Figure 1. The sampling sites for capturing C in Influence of environmental variability on the body condition of the mangrove horseshoe crab Carcinoscorpius rotundicauda from Banyuasin Estuarine, South Sumatra, Indonesia
Figure 1. The sampling sites for capturing C. rotundicauda in Banyuasin Estuary Waters. The sampling was conducted together with local fishermen using a trammel net.
Fig. 20 in Alpheid Shrimps From The Mangroves And Mudflats Of Singapore. Part I. Genera Salmoneus, Athanas And Potamalpheops, With The Description Of Two New Species (Crustacea: Decapoda: Caridea)
Fig. 20. Colour patterns of some Alpheidae from Sungei Buloh, Singapore: a, b, Potamalpheops tigger Yeo & Ng; c, d, Potamalpheops johnsoni, new species; e, f, Athanas polymorphus Kemp. All more or less to scale.
Fig. 2 in Xyleborus bidentatus (Motschulsky, 1863), a Newly Discovered Ambrosia Beetle in Mangrove Forests of Southern Iran (Coleoptera: Curculionidae: Scolytinae)
Fig. 2. Mangrove forest, Mardu Island, Iran.
Fig. 1 in Xyleborus bidentatus (Motschulsky, 1863), a Newly Discovered Ambrosia Beetle in Mangrove Forests of Southern Iran (Coleoptera: Curculionidae: Scolytinae)
Fig. 1. Xyleborus bidentatus, dorsal (left) and lateral (right) habitus.
Fig. 5 in Xyleborus bidentatus (Motschulsky, 1863), a Newly Discovered Ambrosia Beetle in Mangrove Forests of Southern Iran (Coleoptera: Curculionidae: Scolytinae)
Fig. 5. Distribution map of Xyleborus bidentatus in Iran.
Figs. 3–4 in Xyleborus bidentatus (Motschulsky, 1863), a Newly Discovered Ambrosia Beetle in Mangrove Forests of Southern Iran (Coleoptera: Curculionidae: Scolytinae)
Figs. 3–4. Traps in mangrove forest, Mardu Island, Iran. 3) Light trap; 4) Ethanol-baited trap.
FIGURE 1 in Cheсklist of gastropod molluscs in mangroves of Khanh Hoa province, Vietnam
FIGURE 1. Map of Vietnamese coast divided into four zones by Hong & San 1993.
FIGURE 2. A in Cheсklist of gastropod molluscs in mangroves of Khanh Hoa province, Vietnam
FIGURE 2. A. Notoacmea sp. (9 mm). B–C. Monodonta sp. (12 mm).
Data from: Dissolved iron elution from mangrove ecosystem associated with polyphenols and a herbivorous snail
Interest in the systems supplying dissolved forms of iron to the sea from upland-forests and wetlands has increased because iron is abundant on land but has low bioavailability in seawater. This can be a limiting factor for the growth of marine phytoplankton. Organic complex iron, a typical form of iron dissolved in seawater, is supplied to the ocean through rivers from forest and wetland soils. As a related study, we focus on mangrove ecosystems located at the boundary between the land and sea and on polyphenols present in leaves as ligands for the formation of iron complexes. When mangrove leaf litter falls on the wet forest floor, phenolic compounds leach out from the leaves and might solubilize insoluble iron in the sediments (i.e., iron complexation). However, the reaction mechanism is not simple in the field, and it might be made more complex by tidal currents and intervention by crabs and snails, which consume mangrove leaf litter. In the present study, we focused on a detritivorous snail, Terebralia palustris, as a facilitator of iron solubilization associated with phenolic compounds, and examined how the snail contribute to iron solubilization processes. Our results indicated that the amounts of phenolic compounds in mangrove sediments are strongly related to iron solubilization. Furthermore, the average dissolved iron and phenolic contents in sediments from areas inhabited by the snail were significantly higher than those of sediments where the snail was not present. We additionally report that the solubilization of iron was promoted when snail feces were added to mangrove sediments. In conclusion, we propose that iron solubilization in mangrove sediments is promoted by the interaction between i) iron in the sediment, ii) phenolic compounds derived from mangroves, and iii) the consumption of leaves and the deposition of feces by the snail.
Fig. 3 in On The Taxonomy And Ecology Of The Mangrove Crab Perisesarma Maipoense (Soh, 1978) (Crustacea: Decapoda: Brachyura: Sesarmidae) From Vietnam
Fig. 3. Perisesarma maiponense, male (31.7 × 25.9 mm) (ZRC), major chela: A, outer view; B, dorsal view of palm and dactylar finger; C, dorsal view of dactylar finger.
Figs. 22–25 in Paraclius (Diptera: Dolichopodidae: Dolichopodinae) Of Singapore, With New Species From Mangroves
Figs. 22–25. Paraclius polychaetus, new species: 22, wing; 23, antenna; 24, cercus; 25, male genitalia.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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OpenNeuro
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