Inventário de algas bentônicas de praias e matacões rochosos da costa nordeste do Pará, Amazônia brasileira / Checklist of benthic algae from beaches and rocky outcrops on the northeast coast of Pará state, Brazilian Amazonia

Apresentamos um inventário com 23 táxons da flora ficológica bentônica em praias da costa nordeste do estado do Pará, na Amazônia brasileira, uma região raramente amostrada para algas. As coletas foram realizadas em substratos como matacões no município de Salinópolis, e em troncos, galhos e pneumatóforos de Laguncularia racemosa e substratos artificiais no município de Marapanim. Apesar das limitações da amostragem, nós registramos dez novas citações de algas marinhas e estuarinas bentônicas para a costa do estado do Pará: seis Chlorophyta (Bryopsis pennata, Cladophora coelothrix, C. conferta,Gayralia brasiliensis, Pseudorhizoclonium africanum e Ulva chaetomorphoides), duas Rhodophyta (Caloglossa confusa e Centroceras gasparrinii), uma Ochrophyta (Bachelotia antillarum) e uma Cyanophyta (Coleofasciculus chthonoplastes).(AU)

Isolation and characterization of high quality DNA from marine benthic macroalgae.

The isolation of high quality DNA is essential for many molecular biology applications including polymerase chain reaction (PCR) and endonuclease restriction digestion based techniques. An easy and inexpensive protocol has been developed for extracting genomic DNA from seven species of algae viz. Lola capillaries, Enteromorpha intestinalis, Ulva lactuca and Rhizoclonium sp belonging to Chlorophyceae, Catenella nipae, Polysiphonia mollis belonging to Rhodophyceae and Dictyota ceylanica belonging to Phaeophyceae group were collected from the coastal regions of Sunderban delta in West Bengal, India dominantly growing on mud flats, bark of different mangrove trees, pneumatophores, stilt roots, concrete surfaces, wooden and bamboo poles, sides of the boats and other water vehicles inundated during high tides. The DNA was found suitable for restriction endonuclease digestion and PCR amplification with randomely amplified polymorphic DNA (RAPD) primers. The A260/A280 ratio of 1.15 0.14 to 1.94 indicated little contamination from proteins and polysaccharides. The PCR amplification with RAPD primers showed its suitability in PCR based techniques and the restriction digestion with Eco RV confirmed its suitability for hybridization based techniques. The protocol is equally good for isolating DNA from both fresh as well as preserved materials.

Taxonomic reappraisal of Antithamnion sparsum Tokida (Ceramiaceae, Rhodophyta).

The taxonomic criterion of Antithamnion sparsum was reappraised in comparison with A. densum and A. defectum based on crossing experiments, morphological observation, chromosome study and Random Amplified Polymorphic DNA (RAPD) analysis. These species had a very similar morphology but were sexually isolated. The chromosome number was n = ca. 24 for A. densum, n = ca. 21 for A. defectum, and n = ca. 44 for A. sparsum. All isolates of A. sparsum and A. densum showed polysiphonia-type life history Asexual reproduction was induced by favorable environmental conditions. In A. sparsum, 1-2% of male plants developed mitotic tetrasporangia together with spermatangia. In A. densum, 5-10% of tetraspores developed into asexual tetrasporophytes. Phylogenetic relationships between these species were examined using RAPD analysis, and A. glanduliferum was used as an outgroup. A total of 167 polymorphic RAPD markers amplified from 15 different primers were analyzed. Results suggested that these species were closely related, with A. defectum placed in the middle of A. sparsum and A. densum. Chromosome study and RAPD analysis implied that A. sparsum first separated from A. defectum through polyploidization and later A. densum evolved. These species may present another example of the narrow species concept in the genus Antithamnion.