identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
03CB87D7743E3A4FEB8FFAEA69110644.text	03CB87D7743E3A4FEB8FFAEA69110644.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Chroodactylon ornatum (C. Agardh) Basson 1979	<div><p>Chroodactylon ornatum (Figs 1 A–B)</p> <p>Conferva ornata Agardh (1824: 104).</p> <p>Thallus erect, filamentous, uniseriate, having pseudodichotomous ramifications, greenish colored, up to 1.7 mm in height, fixed by a lobed basal cell. Filament diameter (25–)30(–35) µm in the basal region, (15–)21(–25) µm in the median region, and 15 µm in the apical region. Vegetative cells square to sub-square, (10–)13(–15) µm in diameter, each with a star-shaped chloroplast with a conspicuous central pyrenoid; wrapped in a mucilaginous sheath 2.5–5.0 µm thick. Apical cell cylindrical with rounded apex, longer than width, (15.0–)18.5(–25.0) µm long and 10.0– 12.5 µm in diameter.</p> <p>Representative specimens examined:— BRAZIL. Bahia: Ilha de Itaparica, Vera Cruz, Praia da Penha, 25/ XI/2007, Santos (HUEFS 130889).</p> <p>Geographic distribution along the west coast of Atlantic Ocean:—North Carolina, Florida, Isla Mujeres, Yucatán Peninsula, Aruba, Bonaire, Bahamas, Bermuda, Cuba, Grenada, Hispaniola, Virgin Islands, Venezuela (Howe 1920, Taylor 1960, Vroman &amp; Stegenga 1988, Ganesan 1989, Schneider &amp; Searles 1991, Suárez 2005, Mendoza-González et al. 2007, Dawes &amp; Mathieson 2008) and Brazil (this study).</p> <p>Comments:— Chroodactylon Hansgirg (1885: 14) is a widely distributed genus in tropical marine and temperate environments, estuaries, as well as fresh-water areas (Brodie &amp; Nielsen 2005). Both the genus and the species C. ornatum are reported here for the first time as occurring in the American South Atlantic. The species had previously been recorded from the coast of Connecticut (USA) to Venezuela, including the Caribbean Islands (Wynne 2011, Guiry &amp; Guiry 2011).</p> <p>Chroodactylon ornatum has characteristics very similar to Stylonema alsidii (Zanardini) Drew (1956: 72), including a filamentous thallus, uniseriate, ramified, and a star-shaped chloroplast with central pyrenoid; it differs, however, in terms of the dimensions and shapes of its cells and the thickness of the mucilaginous sheath. Chroodactylon ornatum has generally square cells, large (ca. 15 µm in diameter), with a thinner sheath (2.5–5.0 µm) (Fig. 1B), while S. alsidii has spherical or elliptical cells, rarely square, smaller (7.5 µm diameter) and with thick sheaths (up to 25 µm) (Santos 2010). Some authors consider the color of the thallus to be a useful character for distinguishing between the two species, for the thallus of C. ornatum is greenish and that of S. alsidii is pink to vinaceous (Taylor 1960, Schneider &amp; Searles 1991); this characteristic is easily lost, however, in fixed material (Børgesen 1915). According to Abbott (1999), the characteristic greenish coloring of C. ornatum is due to the predominance of phycocyanin in the plastids.</p> <p>The specimens analyzed here had dimensions very close to those described by Howe (1920) for the Bahamas, and by Basson (1979) for Saudi Arabia. Taylor (1960), Schneider &amp; Searles (1991) and Dawes &amp; Mathieson (2008) described the thalli of C. ornatum as being up to 10 mm high.</p> <p>Descriptions in the literature (Børgesen 1915, Howe 1920, Basson 1979, Schneider &amp; Searles 1991, Abbott 1999, Dawes &amp; Mathieson 2008) indicated that the branching patterns and the cell shapes of C. ornatum are variable. The thalli are described as ranging from simple filaments to densely ramified, unilateral, dichotomous, pseudo-dichotomous or irregular; the cells are described as having diverse shapes (oval, elliptical, elongated, globose, square, or sub-square), although they all are essentially the same size. The material analyzed here had pseudo-dichotomous ramifications (Fig. 1A) and filaments with squared cells, except the apical cells that were cylindrical with rounded apices.</p> <p>No reproductive structures were observed in the specimens analyzed; however, according to Howe (1920), Børgesen (1927), Taylor (1960), Schneider &amp; Searles (1991) and Dawes &amp; Mathieson (2008), C. ornatum reproduces by way of monospores or by subglobose or ellipsoidal akinetes with thick cell walls that arise from vegetative cells in the filaments that are liberated laterally by the rupturing of the mucilaginous sheath.</p> <p>Chroodactylon ornatum was considered uncommon in the present study area as it was only found once on the beach at Penha. According to Dawes &amp; Mathieson (2008), this species is common in Florida and grows on marine phanerograms. This alga has been found as an epiphyte on many different macroalgae, including Ceramium sp., Corallina sp. and Ganonema farinosum (J.V. Lamouroux) Fan &amp; Wang (1974: 492) (Børgesen 1915, Howe 1920, Børgesen 1927, Basson 1979, Vroman &amp; Stegenga 1988, Schneider &amp; Searles 1991, Abbott 1999).</p> </div>	http://treatment.plazi.org/id/03CB87D7743E3A4FEB8FFAEA69110644	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Santos, Alana Araujo Dos;Moura, Carlos Wallace Do Nascimento	Santos, Alana Araujo Dos, Moura, Carlos Wallace Do Nascimento (2011): Additions to the epiphytic macroalgae flora of Bahia and Brazil. Phytotaxa 28: 53-64, DOI: 10.11646/phytotaxa.28.1.7, URL: http://biotaxa.org/Phytotaxa/article/view/phytotaxa.28.1.7
03CB87D7743C3A48EB8FFB656C480167.text	03CB87D7743C3A48EB8FFB656C480167.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Chondria collinsiana Howe 1920	<div><p>Chondria collinsiana (Figs 1 C–J)</p> <p>Thallus erect, cylindrical, delicate, of soft consistency, 2.5–4.0 cm high, brownish, fixed to the substrate by a discoid holdfast and rhizoids along the basal region of the thallus, presence of anastomoses in the basal region of the thallus. Ramification radial, dense, with 3–4 orders of branches. Branches of the last order with constricted bases, apices truncated and with a slight apical depression. The basal region of the principal axis is (580–)610(–640) µm in diameter; the median region (500–)540(–600) µm in diameter; and the apical region (300–)360(–430) µm in diameter. First order branches 500–530 µm in diameter; second order branches 300– 460 µm in diameter; and third order branches 120–330 µm in diameter. Trichoblasts present on the apices of truncated branches. Trichoblast scars frequent at the distal region of the thallus. Thallus with polysiphonic organization; transversal cuts show 5 periaxial cells (75.0–)78.0(–112.5) µm long and 62.5–80.0 µm in diameter, with lenticular thickening and wrapped by 3 layers of medullar cells, colorless, (30–)48(–62) µm in diameter; cortical region with 1 layer of pigmented cells, (10–)13(–20) µm in diameter. In surface view, cortical cells elongated, (70.0–)100.0(–112.5) µm long and 17–22 µm in diameter, with pit connections between the cells. Cistocarps spherical to ovoid, not adnate, 0.5–1.0 mm long and 0.5 mm in diameter, growing on the last branchlets, with protuberance at base. Spermatangial bodies laminar, discoid, (210–)250(– 330) µm in diameter, with rounded spermacia, wrapped in 1 layer of sterile and rectangular cells, 3–5 on the apices branches and branchlets. Tetrasporangia formed from the pericentral cells on the branchlets; in transversal section, 3–5 tetrahedral tetrasporangia, 60–80 µm in diameter.</p> <p>Representative specimens examined:— BRAZIL. Bahia: Ilha de Itaparica, Vera Cruz, Praia da Penha, 18/ III/2007, Moura (HUEFS 130885); 14/VII/2007, Alves &amp; Peixoto (HUEFS 130887). Praia da Barra Grande, 19/III/2007, Santos (HUEFS 147560); 18/V/2007, Santos (HUEFS 147561); 14/VII/2007, Santos (HUEFS 147562); 27/IX/2007, Oliveira &amp; Oliveira (HUEFS 130890).</p> <p>Geographic distribution along the west coast of Atlantic Ocean:—Florida, Bahamas, Belize, Cuba, Venezuela, Brazil (Taylor 1960, Ganesan 1989, Littler et al. 1995, Littler &amp; Littler 2000, Bacci 2005, Suárez 2005, Ribeiro 2008).</p> <p>Comments:— Chondria collinsiana is restricted to the Caribbean Sea, the South Atlantic, and the Indian Ocean (Jaasund 1976, Littler et al. 1995, Bacci 2005, Ribeiro 2008). Along the Brazilian coast this species was previously known only from the states of Espírito Santo (Bacci 2005) and Rio de Janeiro (Ribeiro 2008). The present study expanded the distribution of this species to the northeastern coast of Brazil.</p> <p>The specimens analyzed are in agreement with the characteristics described and illustrated by Littler et al. (1995) and Bacci (2005). According to Bacci (2005), this species differs from the others along the coast of the states of Espírito Santo and São Paulo by having an erect thallus, delicate, densely radially branched, slight depressions at the apices of the branches and branchlets, and by the presence of lenticular thickenings on the medullar cell walls.</p> <p>In addition to these morphological characteristics, the shapes of the sterile cells of the spermatangial bodies and the characteristics of the cistocarp are useful in identifying species of C hondria C.Agardh (Bacci 2005). This is the first report of masculine gametophytes of this species from the Brazilian coast. They were described earlier by Littler et al. (1995) for the flora of Belize. The spermatangial bodies of Chondria collinsiana are laminar, discoidal, with rounded spermacia, surrounded by a layer of rectangular sterile cells, as can be seen in Fig. 1I. Thalli were observed growing isolated on the thallus of A. crenulata, sometimes forming dense tufts when attachments are present in the basal region of the thallus.</p> </div>	http://treatment.plazi.org/id/03CB87D7743C3A48EB8FFB656C480167	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Santos, Alana Araujo Dos;Moura, Carlos Wallace Do Nascimento	Santos, Alana Araujo Dos, Moura, Carlos Wallace Do Nascimento (2011): Additions to the epiphytic macroalgae flora of Bahia and Brazil. Phytotaxa 28: 53-64, DOI: 10.11646/phytotaxa.28.1.7, URL: http://biotaxa.org/Phytotaxa/article/view/phytotaxa.28.1.7
03CB87D7743B3A4AEB8FFC446CE2061E.text	03CB87D7743B3A4AEB8FFC446CE2061E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Phaeophila dendroides (P. Crouan & H. Crouan) Batters 1902	<div><p>Phaeophila dendroides (Figs 2 A–H)</p> <p>Oclochaete dendroides Crouan &amp; Crouan (1852: 128).</p> <p>Thalli growing in tufts, light to dark green, composed of uniseriate filaments, densely aggregated, intertwined, with sparse unilateral ramifications. Filaments with cylindrical to irregular cells, longer than wide, (30.0–)41.5(–55.0) µ m long and (8.5–)15.0(–18.5) µ m in diameter, sometimes with slight intumescense. Cells with dense contents, chloroplast parietal, sometimes with lobate margins, 9–14 pyrenoids. Hairs erect, colorless, straight, sinuous, sometimes with dilated base, (100.0–)172.5(–280.0) µm long. When cultivated, tufts growing free or aggregated on the flask, filaments uniseriate with cylindrical cells, elongated, surrounded by spherical cells, (12.5–)17.0(–20.0) µm in diameter. Ellipsoid reproductive structures were observed in cultivated specimens, 10 µm long and 2.5 µm in diameter, with an eye spot and two flagella (gametes or spores), although it was not possible to identify the cell type that gave rise to them.</p> <p>Representative specimens examined:— BRAZIL. Bahia: Ilha de Itaparica, Vera Cruz, Praia da Penha, 19/ V/2007, Santos (HUEFS 130886); 25/XI/2007, Santos &amp; Alves (HUEFS 130889); 08/III/2008, Santos (HUEFS 147559). Praia da Barra Grande, 18/V/2007, Santos (HUEFS 147561); 14/VII/2007, Santos (HUEFS 147562); 27/IX/2007, Oliveira &amp; Oliveira (HUEFS 130890); 25/XI/2007, Alves &amp; Ramos (HUEFS 147563).</p> <p>Geographic distribution along the west coast of Atlantic Ocean:—Newfoundland to North Carolina, Florida, Gulf of Mexico, Bermuda, Venezuela, Brazil (Oliveira &amp; Ugadim 1976, Ganesan 1989, Schneider &amp; Searles 1991, Reis &amp; Yoneshigue-Valentin 1996, Dawes &amp; Mathieson 2008).</p> <p>Comments:—According to O’Kelly &amp; Yarish (1980), Phaeophila dendroides is characterized in terms of the structure and development of its zoosporangia and by the architecture of the flagella apparatus of the zoospore. These characteristics led Chappel et al. (1990) to consider P. dendroides as having a well-delimited evolutionary lineage within the Ulvophyceae, and they suggested creating a new family (Phaeophilaceae) and order (Phaeopilales). This proposal was recently supported by O’Kelly et al. (2004) based on molecular studies which revealed that morphologically indistinguishable specimens of P. dendroides from distinct localities were genetically distinct.</p> <p>Phaeophila dendroides was described as being endophytic, epiphytic on the peduncle of Acetabularia Lamouroux (1812: 185) (as P. divaricata Huber (1893: 332)) (Thyvi 1943) and endolithic, growing on stones and shells (O’Kelly et al. 2004). In the present study, this species was found growing on the thallus of A. crenulata, as well as isolated in culture.</p> <p>A number of studies have reported that the morphology of the filament cells of Phaeophila dendroides varies according to the host type. Thyvi (1943) observed that specimens of P. dendroides (as Phaeophila engleri Reinke (1889: 86)) growing on mollusk shells had cells with extremely irregular outlines, forming lateral and vertical papilla and having thickened cell walls. The specimens studied by Nielsen (1987), however, had filaments whose cells had numerous intumescences, few hairs and cylindrical, cruciform or spherical shapes (Nielsen 1987, Fig. 10). In the present study, the cultivated specimens grew tufts of filaments having elongated cylindrical cells as well as spherical cells (Fig. 2C).</p> <p>The filaments of the specimens analyzed had 1–2 long and sinuous hairs per cell that were continuous with the cell lumen, sometimes with a thickened base (Fig. 2E). Thyvi (1943) described specimens of P. dendroides (as P. engleri) with few hairs, sometimes absent, sinuous or straight, continuous with the lumen of the support-cell, or septate when continuous with the dilated base. Although the presence of hairs is characteristic of the genus, Wilkinson (1975) noted that these hairs were not useful characteristics for distinguishing the species for when members of Chaetophorales are exposed to different degrees of salinity these hairs can be lost. The hairs apparently have absorption functions, as deduced from experimental cultivation of species of Phaeophyceae and Chaetophorales in media deficient in certain nutrients (Thyvi 1942).</p> <p>Reproductive structures (gametes or spores, Fig. 2H) were observed in the cultivated specimens, although it was not possible to identify the cells from which they arose. According to O’Kelly &amp; Yarish (1980), reproduction in Phaeophila Hauck (1876: 56) occurs by way of quadriflagellated zoospores derived simultaneously from multinucleated sporangia; the sporangia develop from vegetative cells with the same morphology and an elongated necks.</p> <p>Among the valid 11 species of the genus Phaeophila, four were cited for the American Atlantic Ocean; of those, only the type-species (P. dendroides) was known from the Brazilian coast, specifically from Rio de Janeiro (Reis &amp; Yoneshigue-Valentin 1996) and Atol das Rocas (Oliveira &amp; Ugadim 1976).</p> </div>	http://treatment.plazi.org/id/03CB87D7743B3A4AEB8FFC446CE2061E	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Santos, Alana Araujo Dos;Moura, Carlos Wallace Do Nascimento	Santos, Alana Araujo Dos, Moura, Carlos Wallace Do Nascimento (2011): Additions to the epiphytic macroalgae flora of Bahia and Brazil. Phytotaxa 28: 53-64, DOI: 10.11646/phytotaxa.28.1.7, URL: http://biotaxa.org/Phytotaxa/article/view/phytotaxa.28.1.7
03CB87D774393A44EB8FFB9C6D0A051F.text	03CB87D774393A44EB8FFB9C6D0A051F.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Ulva clathrata (Roth) Agardh 1811	<div><p>Ulva clathrata (Figs 3 A–E)</p> <p>Conferva clathrata Roth (1806: 175–178).</p> <p>Thallus erect, cylindrical, flaccid to rigid, densely branched, olive-green, up to 4 cm long, fixed by extensions of rhizoid cells originating from the basal portion of the thallus, forming a small holdfast. Principal axis (100.0–)108.5(–115.0) µm width, with long branches from the basal region to the apex, (55–)71(–100) µm width; short, spiny multiseriate proliferations along the thallus. Cells square to polygonal, without any apparent organizing pattern, (20.0–)28.5(–40.0) µm long and (20–)33(–40) µm in diameter along the principal axis, and branches (15.0–)18.5(–27.5) µm in diameter. Chloroplast parietal, margin lobed, 6 to 9 pyrenoids.</p> <p>Representative specimens examined:— BRAZIL. Bahia: Ilha de Itaparica, Vera Cruz, Praia da Penha, 25/ XI/2007, Santos &amp; Alves (HUEFS 130889). Praia da Barra Grande, 19/III/2007, Santos (HUEFS 147560); 18/ V/2007, Santos (HUEFS 147561); 14/VII/2007, Santos (HUEFS 147562).</p> <p>Geographic distribution along the west coast of Atlantic Ocean:— Canada to Georgia, Bermuda, Cuba, Puerto Rico, Venezuela, Brazil (Taylor 1960, Kanagawa 1983, Santos 1983, Ganesan 1989, Schneider &amp; Searles 1991, Littler &amp; Littler 2000, Suárez 2005, Dawes &amp; Mathieson 2008).</p> <p>Comments:—The general aspects of the thalli (which are densely ramified, with multiseriate proliferations, spiny along their entire length) (Figs 3A–C) as well as the great numbers of pyrenoids are important characteristics for delimiting this species (Fig. 3E). Some authors have reported variations in the numbers of pyrenoids per cell within the different regions of the thallus of U. clathrata. Brodie et al. (2007) reported 5–15 pyrenoids in cells in the basal region of the thallus, and (1–)2–3 pyrenoids in cells in the apical region. Kraft (2007) reported 5–9 pyrenoids in cells in the basal region and 2–4 pyrenoids in cells in the apical region of the thallus. In the specimens analyzed here, the numbers of pyrenoids were not observed to vary between the basal and apical regions of the thallus, with 6–9 pyrenoids per cell being uniformly found. This data was similar to that published by Burrows (1991; 5–10 pyrenoids per cell) for the British Islands and Kanagawa (1983; 2–8 pyrenoids per cell) for São Paulo.</p> <p>The general aspect of the thallus of specimens of U. clathrata from Australia, as described and illustrated by Kraft (2007), with branches with bulbous apices, differed from the other references consulted that described the species as having densely ramified thalli with spiny proliferations (Kanagawa 1983, Burrows 1991, Brodie et al. 2007).</p> <p>This is the first citation of U. clathrata for the coast of Bahia State, although the species is widely distributed along the Brazilian coast with records from the states of Maranhão (Ferreira-Correia &amp; Brandão 1974), Ceará (Pinheiro-Joventino et al. 1998), Alagoas (Muniz 1983), Espírito Santo (Barata 2004), Rio de Janeiro (Reis &amp; Yoneshigue-Valentin 1996), São Paulo (Kanagawa 1983), Paraná (Shirata et al. 1991), Santa Catarina (Santos 1983), and Rio Grande do Sul (Horta 2000).</p> <p>Ulva flexuosa subsp. paradoxa (Figs 3 F–K)</p> <p>Conferva paradoxa Dillwyn (1809: xxii).</p> <p>Thallus erect, cylindrical, flaccid, delicate, light green, (0.6–)3.0(–10.0) mm long, fixed by prolongations of rhizoidal cells at the base, forming a small holdfast. Principal axis (60–)115(–150) µm width, with dense ramifications, opposite to irregular, with pluriseriate branches and short uniseriate branchlets (up to 900 µm long) along the thallus. Cells square or rectangular, organized longitudinally, (15.0–)26.5(–37.5) µm long and (10–)24(–45) µm width; branches uniseriate with isodiametric cells (5.0–)9.5(–15) µm width. Chloroplast parietal, laminar, lobed, with (4–)6–7 pyrenoids.</p> <p>Representative specimens examined:— BRAZIL. Bahia: Vera Cruz, Ilha de Itaparica, Praia da Penha, 18/ III/2007, Moura (HUEFS 130885); 19/V/2007, Santos (HUEFS 130886); 14/VII/2007, Alves &amp; Peixoto (HUEFS 130887); 27/IX/2007, Santos &amp; Peixoto (HUEFS 130888); 23/I/2008, Santos (HUEFS 147558); 08/ III/2008, Santos (HUEFS 147559); Praia da Barra Grande, 19/III/2007, Santos (HUEFS 147560); 18/V/2007, Santos (HUEFS 147561); 14/VII/2007, Santos (HUEFS 147562); 27/IX/2007, Oliveira &amp; Oliveira (HUEFS 130890).</p> <p>Geographic distribution along the west coast of Atlantic Ocean:— Canada to South Carolina, Florida, Gulf of Mexico, Cuba, Venezuela, Brazil, Uruguay (Taylor 1960, Kanagawa 1984, Ganesan 1989, Schneider &amp; Searles 1991, Littler &amp; Littler 2000, Suárez 2005, Dawes &amp; Mathieson 2008).</p> <p>Comments:— Ulva flexuosa subsp. paradoxa was cited for Paraíba State along the Brazilian coast by Kanagawa (1984, as Enteromorpha paradoxa (Dilwin) Kützing (1845: 247), for Espírito Santo State by Barata (2004, as E. paradoxa), for São Paulo State by Coto (2007, as Ulva paradoxa Agardh (1817: xxii)), and for Rio de Janeiro by Reis &amp; Yoneshigue-Valentin (1996, as E. paradoxa). This is the first reference of this taxon for the coast of Bahia State.</p> <p>Of all of the descriptions and illustrations presented by Brazilian authors, apparently only Kanagawa (1984) was referring to Ulva flexuosa subsp. paradoxa. The specimens described by Barata (2004) and Coto (2007) are morphologically similar to the specimens of U. flexuosa subsp. flexuosa, although the numbers of pyrenoids are similar to those reported by Kanagawa (1984) and in the present study (Fig. 3K). Additionally, these authors did not mention the characteristic uniseriate branches of this taxon (Figs 3G–H); both described the presence of spiny branches along the thallus, although these are not evident in their illustrations. In light of these discrepancies, it will be necessary to review the citations of this taxon for the Brazilian coast.</p> <p>Bliding (1963), Wynne (2011) and Kraft (2007) referred to this taxon as a subspecies of Ulva flexuosa, a designation that was adopted in the present study; all of the citations of this subspecies for Brazil are referred to as Enteromorpha paradoxa or U. paradoxa as these authors considered the morphological differences between U. flexuosa subsp. flexuosa (as U. flexuosa) and U. flexuosa subsp. paradoxa (as E. paradoxa or U. paradoxa) consistent, delimiting it as a distinct species (Kanagawa 1984, Barata 2004, Coto 2007).</p> </div>	http://treatment.plazi.org/id/03CB87D774393A44EB8FFB9C6D0A051F	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Santos, Alana Araujo Dos;Moura, Carlos Wallace Do Nascimento	Santos, Alana Araujo Dos, Moura, Carlos Wallace Do Nascimento (2011): Additions to the epiphytic macroalgae flora of Bahia and Brazil. Phytotaxa 28: 53-64, DOI: 10.11646/phytotaxa.28.1.7, URL: http://biotaxa.org/Phytotaxa/article/view/phytotaxa.28.1.7
