Systematics and distribution of freshwater Audouinella (Arochaetiaceae, Rhodophyta) in Brazil

Forty-five Brazilian populations of freshwater Audouinella were analysed using multivariate morphometrics. These populations were statistically related to seven type specimens. Five species are recognised on the basis of qualitative (plant colour and size, basal system type and branch angle) and quantitative (length and diameter of vegetative cells and monosporangia) characters. A. hermannii (syn. A. violacea) is characterised by a reddish colour, an irregular prostrate basal system, open branch angles (greater than or equal to 25 degrees) and small monosporangia (less than or equal to 15 mu m in diameter). A. macrospora (syn. A. chalybea var. brasiliensis) is distinguished from the other Brazilian species by having a bluish colour, a basal system composed of well-developed rhizoids, narrow branch angles (< 25 degrees) and large monosporangia (greater than or equal to 15 mu m in diameter). A. meiospora is microscopic and has a reddish colour, a basal system composed of creeping filaments, narrow branch angles and small monosporangia. A. pysmaea (syn. A. leibleinii) is characterised by being bluish, having an irregular prostrate basal system, narrow branch angles and small monosporangia. A, tenella is distinct from the other species by having a reddish colour, an irregular prostrate basal system, open branch angles, small monosporangia and small vegetative cells (less than or equal to 6 mu m in diameter). An identification key and revised descriptions and synonyms are presented for the five species. A. meiospora and A. tenella are reported for the first time for Brazil. A. macrospora and A. pygmaea were the most widespread species and occurred in tropical and subtropical regions. A. meiospora was found at two sites in a tropical rainforest region, whereas A. hermannii and A. tenella were found at only one site. Selected physical and chemical environmental data (temperature, specific conductance, current velocity, turbidity, pH and dissolved oxygen) are presented for most species.

Changes in cells's secretory organelles and extracellular matrix during endochondral ossification in the mandibular condyle of the growing rat

The mandibular condyle from 20-day-old rats was examined in the electron microscope with particular attention to intracellular secretory granules and extracellular matrix. Moreover, type II collagen was localized by an immunoperoxidase method. The condyle has been divided into five layers: (1) the most superficial, articular layer, (2) polymorphic cell layer, (3) flattened cell layer, (4) upper hypertrophic, and (5) lower hypertrophic cell layers. In the articular layer, the cells seldom divide, but in the polymorphic layer and upper part of the flattened cell layer, mitosis gives rise to new cells. In these layers, cells produce two types of secretory granules, usually in distinct stacks of the Golgi apparatus; type a, cylindrical granules, in which 300-nm-long threads are packed in bundles which appear lucent after formaldehyde fixation; and type b, spherical granules loaded with short, dotted filaments. The matrix is composed of thick banded lucent fibrils in a loose feltwork of short, dotted filaments. The cells arising from mitosis undergo endochondral differentiation, which begins in the lower part of the flattened cell layer and is completed in the upper hypertrophic cell layer; it is followed by gradual cell degeneration in the lower hypertrophic cell layer. The cells produce two main types of secretory granules: type b as above; and type c, ovoid granules containing 300-nm-long threads associated with short, dotted filaments. A possibly different secretory granule, type d, dense and cigar-shaped, is also produced. The matrix is composed of thin banded fibrils in a dense feltwork. In the matrix of the superficial layers, the lucency of the fibrils indicated that they were composed of collagen I, whereas the lucency of the cylindrical secretory granules suggested that they transported collagen I precursors to the matrix. Moreover, the use of ruthenium red indicated that the feltwork was composed of proteoglycan; the dotted filaments packed in spherical granules were similar to, and presumably the source of, the matrix feltwork. The superficial layers did not contain collagen II and were collectively referred to as perichondrium. In the deep layers, the ovoid secretory granules displayed collagen II antigenicity and were likely to transport precursors of this collagen to the matrix, where it appeared in the thin banded fibrils. That these granules also carried proteoglycan to the matrix was suggested by their content of short dotted filaments. Thus the deep layers contained collagen II and proteoglycan as in cartilage; they were collectively referred to as the hyaline cartilage region.

Ecological distribution of stream macroalgal communities from a drainage basin in the Serra da Canastra National Park, Minas Gerais, Southeastern Brazil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Structural and functional insights into the conductive pili of Geobacter sulfurreducens revealed in molecular dynamics simulations

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Ecological distribution of stream macroalgal communities from a drainage basin in the Serra da Canastra National Park, Minas Gerais, Southeastern Brazil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fechamento de defeitos em padrão de figura geométrica associado ao emprego de anestesia por tumescência com lidocaína em coelhos (oryctolagus cuniculus)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Citotoxicidade do ácido peracético: avaliação metabólica, estrutural e de morte em fibroblastos L929

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)