Distribution of quaternary siliceous sponge spicules in sediments of ODP Leg 180 sites

Siliceous sponge spicules were found in Quaternary sediments recovered during drilling of Leg 180. The assemblage consists mainly of monaxon forms. Relative abundances of the various types are tabulated.

(Table T2) Rock magnetic parameters of ODP Leg 180 sites

Rock magnetic measurements were performed on sediments above 20 meters below seafloor (mbsf) (general) and above 2.5 mbsf (detailed) at Sites 1109, 1110, and 1115 (Ocean Drilling Program Leg 180) in the western Woodlark Basin. Rock magnetic parameters imply the presence of magnetite as a principal magnetic mineral in the sediments. The hysteresis ratios lay in the pseudo-single domain field and generally showed the trend close to that for the mixture of single domain and multidomain magnetite The sediments in the oxidized zones at the top at Sites 1109 and 1115 provided a different trend in the logarithmic plot of the hysteresis ratios, and the oxidized samples were characterized by higher coercivity.

(Table T3) Distribution of radiolarian taxa in sediments of ODP Leg 180 sites

Cores from the 11 sites drilled during Leg 180 showed radiolarian assemblages that appear only in the Quaternary sediments. The most diverse and well-preserved assemblages were found in hemipelagic sediments from Holes 1108A, 1110A, and 1115B.

The Ruthenium Complex cis-(Dichloro)tetraammineruthenium(III) Chloride Presents Selective Cytotoxicity Against Murine B Cell Lymphoma (A-20), Murine Ascitic Sarcoma 180 (S-180), Human Breast Adenocarcinoma (SK-BR-3), and Human T Cell Leukemia (Jurkat) Tumor Cell Lines

The aim of present study was to verify the in vitro antitumor activity of a ruthenium complex, cis-(dichloro)tetraammineruthenium(III) chloride (cis-[RuCl(2)(NH(3))(4)]Cl) toward different tumor cell lines. The antitumor studies showed that ruthenium(III) complex presents a relevant cytotoxic activity against murine B cell lymphoma (A-20), murine ascitic sarcoma 180 (S-180), human breast adenocarcinoma (SK-BR-3), and human T cell leukemia (Jurkat) cell lines and a very low cytotoxicity toward human peripheral blood mononuclear cells. The ruthenium(III) complex decreased the fraction of tumor cells in G0/G1 and/or G2-M phases, indicating that this compound may act on resting/early entering G0/G1 cells and/or precycling G2-M cells. The cytotoxic activity of a high concentration (2 mg mL(-1)) of cis-[RuCl(2)(NH(3))(4)]Cl toward Jurkat cells correlated with an increased number of annexin V-positive cells and also the presence of DNA fragmentation, suggesting that this compound induces apoptosis in tumor cells. The development of new antineoplastic medications demands adequate knowledge in order to avoid inefficient or toxic treatments. Thus, a mechanistic understanding of how metal complexes achieve their activities is crucial to their clinical success and to the rational design of new compounds with improved potency.

The central pathway of primary olfactory axons is abnormal in mice lacking the N-CAM-180 isoform

Although N-CAM has previously been implicated in the growth and fasciculation of axons, the development of axon tracts in transgenic mice with a targeted deletion of the 180-kD isoform of the neural cell adhesion molecule (N-CAM-180) appears grossly normal in comparison to wild-type mice. We examined the organization of the olfactory nerve projection from the olfactory neuroepithelium to glomeruli in the olfactory bulb of postnatal N-CAM-180 null mutant mice. Immunostaining for olfactory marker protein revealed the normal presence of fully mature primary olfactory neurons within the olfactory neuroepithelium of mutant mice. The axons of these neurons form an olfactory nerve, enter the nerve fiber layer of the olfactory bulb, and terminate in olfactory glomeruli as in wild-type control animals. The olfactory bulb is smaller and the nerve fiber layer is relatively thicker in mutants than in wild-type mice. Previous studies have revealed that the plant lectin Dolichos biflorus agglutinin (DBA) clearly stains the perikarya and axons of a subpopulation of primary olfactory neurons. Thus, DBA staining enabled the morphology of the olfactory nerve pathway to be examined at higher resolution in both control and mutant animals. Despite a normal spatial pattern of DBA-stained neurons within the nasal cavity, there was a distorted axonal projection of these neurons onto the surface of the olfactory bulb in N-CAM-180 null mutants. In particular, DBA-stained axons formed fewer and smaller glomeruli in the olfactory bulbs of mutants in comparison to wild-type mice. Many primary olfactory axons failed to exit the nerve fiber layer and contribute to glomerular formation. These results indicate that N-CAM-180 plays an important role in the growth and fasciculation of primary olfactory axons and is essential for normal development of olfactory glomeruli. (C) 1997 John Wiley & Sons, Inc.

Portaria n?? 180, de 28 de novembro de 2014: trata do Gestor de Seguran??a da Informa????o e Comunica????es (GeSIC), e do Comit?? de Seguran??a da Informa????o e Comunica????es (CSIC)

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