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40 results for “Rhizophora”
Figure 2 in Sex change and reproductive output of the protandric shrimp Merguia rhizophorae (Rathbun, 1900) (Decapoda, Merguiidae)
Figure 2. Anatomical and morphological characteristics of the male phase (a–c) and female phase (d– f) individuals of Merguia rhizophorae (Rathbun 1900). (a) Close-up of the endopod of the first pleopod (arrow points to the cincinnuli); (b) Endopod of the second pleopod (upper and lower arrows point to the appendix interna and the appendix masculina, respectively); (c) Gonopore on the coxae of the fifth pereiopod (arrow points to the gonopore); (d) Close-up of the endopod of the first pleopod (arrow points to the area where cincinnuli would be located in a male phase); (e) Endopod of the second pleopod, lacking an appendix masculina (arrow points to the appendix interna); (f) Coxae of the fifth pereiopod, lacking a gonopore (arrow points to the area where gonopore would be located in a male phase). Scale bar: A–D, 0.2 mm; B–E, 1.0 mm; C–F, 0.5 mm. Legend: CI, cincinnuli; AI, appendix interna; AM, appendix masculina; GO, gonopore; P, pereiopod.
Figure 1 in Sex change and reproductive output of the protandric shrimp Merguia rhizophorae (Rathbun, 1900) (Decapoda, Merguiidae)
Figure 1. (a) Occurrence of Merguia rhizophorae along the western Atlantic. The red circle shows Vaza- Barris estuarine region of Sergipe State, northeastern coast of Brazil and blue circle shows the previous records of the species (obtained from literature and Global Biodiversity Information Facility – GBIF; http://www.gbif.org); (b–c) Sampling site in a fringe mangrove forest; (d) Excavation of the burrows using a spatula; (e) Burrows (white arrows) inhabited by mud shrimps (yellow arrow) distributed on the sediment of the intertidal zone; (f) lateral view of Merguia rhizophorae (Rathbun 1900). Photo credits: Douglas F.R. Alves.
Figure 3 in Sex change and reproductive output of the protandric shrimp Merguia rhizophorae (Rathbun, 1900) (Decapoda, Merguiidae)
Figure 3. Sex change in Merguia rhizophorae (Rathbun 1900). (a) Size frequency distribution of body size (CL, mm); (b) Adjustment of the logistic function, indicating the carapace length (CL, mm) where 50% of the female phase shrimps are morphologically mature. Legend: MP, male phase; FPNO, female phase non-ovigerous; FPO, female phase ovigerous.
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. Selected species from the flora of Quiçama National Park. A. Adansonia digitata. B. Euphorbia candelabrum. C. Acacia welwitschii. D. Hyphaene guineensis. E. Rhizophora racemosa. F. Guibourtia carrissoana var. gossweileri. G. Tessmannia camoneana. H. Sterculia setigera. I. Carissa spinarum. J. Boscia urens. K. Maerua angolensis. L. Grewia villosa. M. Sesuvium crithmoides. N. Aloe zebrina. O. Barleria elegans. P. Setaria welwitschii. (Photographs by the authors). in An annotated checklist of the vascular flora of Quiçama National Park, Angola
FIGURE. Selected species from the flora of Quiçama National Park. A. Adansonia digitata. B. Euphorbia candelabrum. C. Acacia welwitschii. D. Hyphaene guineensis. E. Rhizophora racemosa. F. Guibourtia carrissoana var. gossweileri. G. Tessmannia camoneana. H. Sterculia setigera. I. Carissa spinarum. J. Boscia urens. K. Maerua angolensis. L. Grewia villosa. M. Sesuvium crithmoides. N. Aloe zebrina. O. Barleria elegans. P. Setaria welwitschii. (Photographs by the authors).
FIGURE 1. RAxML tree resulting from analyzed partial ACT dataset. The scale bar indicates 0.05 in Sexual morph of Phaeoacremonium aureum from Rhizophora mucronata collected in southern Thailand
FIGURE 1. RAxML tree resulting from analyzed partial ACT dataset. The scale bar indicates 0.05 changes. ML, MP bootstrap support values> 65 % from 1,000 replicates and PP> 0.95 from 1 million generations in Markov chains are shown at the nodes. Newly generated sequences are in bold text. The tree was rooted to Pleurostoma richardsiae (CBS 270.33) (Pleurostomataceae).
FIGURE 2 in Sexual morph of Phaeoacremonium aureum from Rhizophora mucronata collected in southern Thailand
FIGURE 2. Sexual morph of Phaeoacremonium aureum (MFLU 17-1581). a–c. Appearance of ascomata on host surface. d. Vertical section through ascoma. e, f. Peridium. g, k, l. Asci. h. Asci stained with Congo red. i, n. Ascospores. j. Paraphyses. m. Apical thickening. Scale bars c, d = 100 μm, e, f = 20 μm, g = 20 μm, h = 50 μm, i–l = 10 μm, m, n = 5 μm.
Rhizophora complete chloroplast genome sequences
<p>Historical processes of long-distance migration and ocean-wide expansion feature the global biogeographic pattern of <i>Rhizophora</i> species. Throughout the Indian Ocean, <i>R. stylosa</i> and <i>R. mucronata</i> appear as a young phylogenetic group with expansion of <i>R. mucronata</i> towards the Western Indian Ocean (WIO) driven by the South Equatorial Current. Nuclear microsatellites revealed genetic patterns and breaks, however, estimating propagule dispersal routes requires maternally inherited cytoplasmic markers. Here, we examine the phylogeography of 21 <i>R. mucronata</i> provenances across a >4,200 km coastal stretch in the WIO using <i>R. stylosa</i> as outgroup. Full length chloroplast genome (164,474 bp) and nuclear ribosomal RNA cistron (8,033 bp) sequences were assembled. Boundaries, junction point, sequence orientation and stretch between LSC/IRb/SSC/IRa/LSC showed no differences with the <i>R. stylosa</i> chloroplast genome. A total of 58 mutations in <i>R. mucronata</i> encompassing transitions/transversions, insertion-deletions and mononucleotide repeats revealed three major haplogroups. Haplonetwork, Bayesian ML and Approximate Bayesian Computation (ABC) analyses supported discrete historical migration events. An ancient haplogroup A in the Seychelles and eastern Madagascar was as divergent from other <i>R. mucronata</i> haplogroups as it was from <i>R. stylosa</i>. A star-like haplonetwork referred to recent range expansion of haplogroup B from northern Madagascar towards the African mainland coastline, including a single variant spanning >1,800 km across the Mozambique Channel Area. Populations south of Delagoa Bight contained haplogroup C and originate from a unique bottleneck dispersal event. Divergence estimates of pre- and post-Last Glacial Maximum illustrated a recent emergence of WIO <i>Rhizophora </i>mangroves compared to other oceans. Connectivity patterns could be aligned with directionality of major ocean currents. Madagascar and the Seychelles each harbored haplogroups A and B, albeit among spatially separated populations, explained from a different migration era. Likewise, the Aldabra Atoll harbored spatially distinct haplotypes. Nuclear ribosomal cistron (8,033bp) variants corresponded to haplogroups and confirmed admixtures in the Seychelles and Aldabra. These findings shed new light on the origins and dispersal routes of <i>R. mucronata</i> lineages that have shaped their contemporary populations in large regions of the WIO, which may be important information for defining marine conservation units, both at ocean scale and at level of small islands.</p>
Data from: Short-distance barriers affect genetic variability of Rhizophora mangle L. in the Yucatan Peninsula
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Data from: Genetic differentiation and phylogeography of partially sympatric species complex Rhizophora mucronata Lam. and R. stylosa Griff. using SSR markers
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Data from: Effects of maternal genotypic identity and genetic diversity of the red mangrove Rhizophora mangle on associated soil bacterial communities: a field-based experiment
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Data from: Postglacial expansion pathways of red mangrove, Rhizophora mangle, in the Caribbean Basin and Florida
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Data from: Molecular identification of natural mangrove hybrids of Rhizophora in Peninsular Malaysia
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Rhizophora complete chloroplast genome sequences
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FIGURE 1. Ilyograpsus rhizophorae Barnard, 1955 in Brachyuran crabs of the family Macrophthalmidae Dana, 1851 (Decapoda: Brachyura: Macrophthalmidae) of the Persian Gulf
FIGURE 1. Ilyograpsus rhizophorae Barnard, 1955: female (SMF 36859), dorsal view.
Figure 1 from: Ragavan P, Mohan PM, Jayaraj RSC, Ravichandran K, Saravanan S (2015) Rhizophora mucronata var. alokii – a new variety of mangrove species from the Andaman and Nicobar Islands, India (Rhizophoraceae). PhytoKeys 52: 95-103. https://doi.org/10.3897/phytokeys.52.5037
Figure 1 - Cluster dendrogram (group average) showing similarity among the Rhizophora species of the ANI.
Figure 2 from: Ragavan P, Mohan PM, Jayaraj RSC, Ravichandran K, Saravanan S (2015) Rhizophora mucronata var. alokii – a new variety of mangrove species from the Andaman and Nicobar Islands, India (Rhizophoraceae). PhytoKeys 52: 95-103. https://doi.org/10.3897/phytokeys.52.5037
Figure 2 - Rhizophora mucronata var. alokii (A) habit (B) stem base with stilt roots (C) bark (D) branches (E) leafy branch end with flowers (F)leaf apex with mucro (G) inflorescence (H) minute bract at dichotomous inflorescence branch (I) mature bud with minute bracteole below calyx (J) cross section of bud (K) mature propagules (L) thick leathery petal (M) stamens (N) flower (O) pistil showing four-sided ovary (P) flower with one petal removed (Q) pear-shaped fruit (R) stamens with pollen.
Data from: Treated Rhizophora mucronata tannin as a corrosion inhibitor in chloride solution
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Rhizophora mucronata Lam. de novo transcriptome - Gene expression estimation
GEO Series GSE112162. Rhizophora mucronata. 1 samples. Type: Expression profiling by high throughput sequencing.
Figure 4 in Sex change and reproductive output of the protandric shrimp Merguia rhizophorae (Rathbun, 1900) (Decapoda, Merguiidae)
Figure 4. Reproductive output in Merguia rhizophorae (Rathbun 1900). (a) Mean (± SD) (vertical bars) of fecundity in shrimps carrying embryos in Stages I, II, and III of development; (b) Relationship between the number of embryos and carapace length (CL, mm) of female phase shrimps; (c) Mean (± SD) (vertical bars) of embryo volume in shrimps carrying embryos in Stages I, II, and III of development; (d) Relationship between the embryo volume (mm3) and carapace length (CL, mm) of female phase shrimps. In (a) and (c), different letters indicate significant differences between embryo development stages. In (b) and (d), linear regression equations obtained after log–log transformation of the data are shown. In (b), Stages I and II of the development represent a single straight line since the mean of fecundity among these stages did not show significant difference.
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