Light-dependence of the metabolic balance of a highly productive Philippine seagrass community

Seagrass meadows are important primary producers in SE-Asia coastal areas that are increasingly threatened by human activities resulting in a deterioration of the underwater light environment. The resilience of seagrass meadows to decreasing light availability should be approached in an integrative manner, because they shelter complex communities of primary and secondary producers. The aim of this study was to measure the in situ metabolism of a seagrass community under different levels of light availability following changes in the water column dissolved oxygen (DO) and dissolved inorganic carbon (DIC), the sediment redox potential and seagrass production. Net community production (NCP) and respiration were measured along two diel cycles to produce a balance of NCP under different light treatments. On a daily basis, at full irradiance, the community metabolism presented a net production which was close to zero, with values of −7.75 to 16.6 mmol O₂ m⁻² day⁻¹ for DO, and −56.8 to 22.7 mmol C m⁻² day⁻¹ for DIC in the first and second incubation runs, respectively. Compensation irradiance for the NCP was thus found to be close to 80% of the present light availability. Shading resulted in a general decrease in the sediment redox potential, while the initial redox potential had not recovered 6 days after exposure to full sunlight. This community appears to be in a fragile equilibrium with the environment, and any minor decrease in the water transparency would lead to a shift from an autotrophic to a heterotrophic system.     

MiR-101 and miR-144 Regulate the Expression of the CFTR Chloride Channel in the Lung

The Cystic Fibrosis Transmembrane conductance Regulator (CFTR) is a chloride channel that plays a critical role in the lung by maintaining fluid homeostasis. Absence or malfunction of CFTR leads to Cystic Fibrosis, a disease characterized by chronic infection and inflammation. We recently reported that air pollutants such as cigarette smoke and cadmium negatively regulate the expression of CFTR by affecting several steps in the biogenesis of CFTR protein. MicroRNAs (miRNAs) have recently received a great deal of attention as both biomarkers and therapeutics due to their ability to regulate multiple genes. Here, we show that cigarette smoke and cadmium up-regulate the expression of two miRNAs (miR-101 and miR-144) that are predicted to target CFTR in human bronchial epithelial cells. When premature miR-101 and miR-144 were transfected in human airway epithelial cells, they directly targeted the CFTR 3′UTR and suppressed the expression of the CFTR protein. Since miR-101 was highly up-regulated by cigarette smoke in vitro, we investigated whether such increase also occurred in vivo. Mice exposed to cigarette smoke for 4 weeks demonstrated an up-regulation of miR-101 and suppression of CFTR protein in their lungs. Finally, we show that miR-101 is highly expressed in lung samples from patients with severe chronic obstructive pulmonary disease (COPD) when compared to control patients. Taken together, these results suggest that chronic cigarette smoking up-regulates miR-101 and that this miRNA could contribute to suppression of CFTR in the lungs of COPD patients.     

Reversal of digestive interactions between Pacific reef corals: Mediation by sweeper tentacles

Summary Aggressive interactions among reef corals involving direct interference through extracoelenteric digestion has previously been considered as a potential mechanism for the maintenance of high species diversity. In this report I show that induced development of sweeper tentacles can reverse initial digestive interactions. In the eastern Pacific these reversals contribute to resource monopolization by fast growing pocilloporid corals. This suggests that other mechanisms must account for the maintenance of local species diversity.     

A MONTE CARLO SIMULATION OF CLONE GROWTH

A Monte Carlo simulation of clone growth is discussed from the point of view of clonal volume. It is shown that clone volume is a good representation of the number of cells per clone for a wide range of single cell growth equations. However, the rate at which the coefficient of variation in clonal volume approaches that of cell number per clone is strongly dependent upon the particular growth equation.