Botryocladia franciscana J. A. S. Santiago, P. B. M. Carneiro, A. P. Santiago, R. G. Feijó & R. Maggioni, 2016

Santiago, Janaína De Araújo Sousa, Carneiro, Pedro Bastos De Macedo, Santiago, André Prata, Feijó, Rubens Galdino & Maggioni, Rodrigo, 2016, A New Species of Rhodymeniaceae (Rhodophyta, Rhodymeniales) from the Northern Brazilian Coast: Botryocladia franciscana sp. nov., Phytotaxa 243 (2), pp. 137-146 : 140-141

publication ID

https://doi.org/ 10.11646/phytotaxa.243.2.3

DOI

https://doi.org/10.5281/zenodo.14222200

persistent identifier

https://treatment.plazi.org/id/03DC0136-AB70-FF9C-FF5E-736B569FFEBE

treatment provided by

Felipe

scientific name

Botryocladia franciscana J. A. S. Santiago, P. B. M. Carneiro, A. P. Santiago, R. G. Feijó & R. Maggioni
status

sp. nov.

Botryocladia franciscana J. A. S. Santiago, P. B. M. Carneiro, A. P. Santiago, R. G. Feijó & R. Maggioni , sp. nov. ( Figs. 1 View FIGURE 1 , 2 View FIGURE 2 )

Type:— BRAZIL, Piauí: Luis Correia, Praia do Coqueiro, Parnaíba River Delta ; 2 o 53’52.20”S, 41 o 34’20.82”W, 26 April 2013, J.A.S. Santiago and A.P. Santiago. (holotype: HMAR 2594 !, female gametophyte). Molecular vouchers: rbc L (GenBank no. KR866021 ), cox 1 (GenBank no. KR011965 ) and UPA (GenBank no. KR872421 ) GoogleMaps .

Paratype:— BRAZIL, Piauí: Luis Correia, Praia do Coqueiro, Parnaíba River Delta ; 2 o 53’31.82”S, 41 o 33’28.63”W, 26 April 2013, J.A.S. Santiago and A.P. Santiago. ( HMAR 2452 !, HMAR 2453 ! infertile) GoogleMaps .

Etymology:—This species is named in honour of Prof. Francisca Pinheiro Joventino, professor and researcher at the Institute of Marine Sciences (LABOMAR), for her contribution as one of the founders of the institute and for her pioneering research on taxonomy of marine macroalgae in the state of Ceará.

Description:—Plants erect, brownish red in colour, 60–74 mm tall; stipes solid, terete and subterete, branched, 1000–1400 μm in diameter ( Fig. 1A View FIGURE 1 ); attached by small discoid holdfasts, giving rise to stipes bearing many vesicles; vesicles spherical, obovoid and often elongating ( Fig. 1B View FIGURE 1 ), 2.5–5 mm wide and 8–12 mm long, with complete cortication of vesicle wall ( Fig. 1D View FIGURE 1 ); in transverse section, the vesicle walls consist of three (to four) cell layers ( Fig. 2B View FIGURE 2 ); innermost cells of the medulla in surface view with large and small polygonal cells intermingled ( Fig. 2C View FIGURE 2 ); gland cells obovoid to pyriform, 10–19 μm wide and 14–30 μm long, produced from inner medullary cells, which project into the vesicle cavity ( Fig. 2B View FIGURE 2 ); 1–7 gland cells per supporting cell ( Fig. 2A View FIGURE 2 ); cystocarps forming in upper portions of the vesicles wall, 700–1000 μm wide ( Fig. 2D View FIGURE 2 ). The morphological and anatomical features of the paratype match the descriptions above, except for the cystocarp. Morphological characteristics of B. franciscana and similar species are summarized in Table 2 View TABLE 2 .

DNA sequences:—Partial sequences of the target genes were obtained only from the holotype. A sequence of 775 bp was obtained for rbc L (GenBank no. KR866021), a sequence of 650 bp for cox 1 (GenBank no. KR011965) and a sequence of 369 for UPA (GenBank no. KR872421). All sequences showed high homology to the corresponding sequences of other Botryocladia species, as revealed by searches with BLAST ( Altschul et al. 1990). The mean sequence divergence observed between B. franciscana and B. occidentalis and B. pyriformis , was 9.19% and 9.93%, respectively, for rbc L. B. occidentalis and B. pyriformis are two of the three Botryocladia species reported for the Brazilian coast.

Phylogenetic results:—Phylogenetic analyses of rbc L sequences included the species found on the Brazilian coast and 14 Botryocladia species found worldwide. The B. franciscana rbc L sequence was consistently resolved in a separate clade with high support, both in BI and ML analyses ( Fig. 3 View FIGURE 3 ). One highly supported clade grouped Brazilian and Caribbean species: B. bermudana Schneider & Lane (2008: 615) , B. caraibica Gavio & Fredericq (2003: 95) and B. franciscana . However, B. occidentalis , which is found in Brazil as well, was placed in a different clade. The NJ analysis of rbc L sequences showed considerable interspecific divergence between B. franciscana and other Botryocladia species ( Fig. 3 View FIGURE 3 ). In some instances, the pairwise distance is far higher than those found between accepted species. As observed in BI and ML trees, the NJ rbc L tree clustered B. franciscana with morphologically similar B. caraibica and B. bermudana . The sequences presented here for cox 1 and UPA could be compared only to a small number of recorded Botryocladia species. For cox 1, the sequence divergence observed between B. franciscana and B. pseudodichotoma (Farlow) Kylin (1931: 18) and B. skottsbergii (Børgesen) Levring (1941: 645) was 10.7% and 11.6%, respectively. For UPA, divergence values of 4.4% and 4.1% were found between B. franciscana and sequences from two B. skottsbergii .

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