The viscosity effect on marine particle flux: A climate relevant feedback mechanism

Oceanic uptake and long-term storage of atmospheric carbon dioxide (CO2) are strongly driven by the marine “biological pump,” i.e., sinking of biotically fixed inorganic carbon and nutrients from the surface into the deep ocean (Sarmiento and Bender, 1994; Volk and Hoffert, 1985). Sinking velocity of marine particles depends on seawater viscosity, which is strongly controlled by temperature (Sharqawy et al., 2010). Consequently, marine particle flux is accelerated as ocean temperatures increase under global warming (Bach et al., 2012). Here we show that this previously overlooked “viscosity effect” could have profound impacts on marine biogeochemical cycling and carbon uptake over the next centuries to millennia. In our global warming simulation, the viscosity effect accelerates particle sinking by up to 25%, thereby effectively reducing the portion of organic matter that is respired in the surface ocean. Accordingly, the biological carbon pump's efficiency increases, enhancing the sequestration of atmospheric CO2 into the ocean. This effect becomes particularly important on longer time scales when warming reaches the ocean interior. At the end of our simulation (4000 A.D.), oceanic carbon uptake is 17% higher, atmospheric CO2 concentration is 180 ppm lower, and the increase in global average surface temperature is 8% weaker when considering the viscosity effect. Consequently, the viscosity effect could act as a long-term negative feedback mechanism in the global climate system

Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia.

We and others have reported mutations in LONP1, a gene coding for a mitochondrial chaperone and protease, as the cause of the human CODAS (cerebral, ocular, dental, auricular and skeletal) syndrome (MIM 600373). Here, we delineate a similar but distinct condition that shares the epiphyseal, vertebral and ocular changes of CODAS but also included severe microtia, nasal hypoplasia, and other malformations, and for which we propose the name of EVEN-PLUS syndrome for epiphyseal, vertebral, ear, nose, plus associated findings. In three individuals from two families, no mutation in LONP1 was found; instead, we found biallelic mutations in HSPA9, the gene that codes for mHSP70/mortalin, another highly conserved mitochondrial chaperone protein essential in mitochondrial protein import, folding, and degradation. The functional relationship between LONP1 and HSPA9 in mitochondrial protein chaperoning and the overlapping phenotypes of CODAS and EVEN-PLUS delineate a family of "mitochondrial chaperonopathies" and point to an unexplored role of mitochondrial chaperones in human embryonic morphogenesis