Simulating transport pathways of pelagic Sargassum from the Equatorial Atlantic into the Caribbean Sea

Since 2011, beach inundation of massive amounts of pelagic Sargassum algae has occurred around the Caribbean nations and islands. Previous studies have applied satellite ocean color to determine the origins of this phenomenon. These techniques, combined with complementary approaches, suggest that, rather than blooms originating in the Caribbean, they arrive from the Equatorial Atlantic. However, oceanographic context for these occurrences remains limited. Here, we present results from synthetic particle tracking experiments that characterize the interannual and seasonal dynamics of ocean currents and winds likely to influence the transport of Sargassum from the Equatorial Atlantic into the Caribbean Sea. Our findings suggest that Sargassum present in the western Equatorial Atlantic (west of longitude 50°W) has a high probability of entering the Caribbean Sea within a year’s time. Transport routes include the Guiana Current, North Brazil Current Rings, and the North Equatorial Current north of the North Brazil Current Retroflection. The amount of Sargassum following each route varies seasonally. This has important implications for the amount of time it takes Sargassum to reach the Caribbean Sea. By weighting particle transport predictions with Sargassum concentrations at release sites in the western Equatorial Atlantic, our simulations explain close to 90% of the annual variation in observed Sargassum abundance entering the Caribbean Sea. Additionally, results from our numerical experiments are in good agreement with observations of variability in the timing of Sargassum movement from the Equatorial Atlantic to the Caribbean, and observations of the spatial extent of Sargassum occurrence throughout the Caribbean. However, this work also highlights some areas of uncertainty that should be examined, in particular the effect of “windage” and other surface transport processes on the movement of Sargassum. Our results provide a useful launching point to predict Sargassum beaching events along the Caribbean islands well in advance of their occurrence and, more generally, to understand the movement ecology of a floating ecosystem that is essential habitat to numerous marine speciesNFP, GJG, LJG, EJ and JT acknowledge support from the NOAA Atlantic Oceanographic and Meteorological Laboratory. JT was also supported by NOAA/OceanWatch. CH and MW acknowledge support from NASA (NNX14AL98G, NNX16AR74G, and NNX17AE57G) and the William and Elsie Knight Endowed Fellowship. Funding for the development of HYCOM has been provided by the National Ocean Partnership Program and the Office of Naval ResearchS

Exploring functional candidate genes for genetic association in German patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma

purpose. Pseudoexfoliation (PEX) syndrome is a generalized elastic microfibrillopathy characterized by fibrillar deposits in intra- and extraocular tissues. Genetic and nongenetic factors are known to be involved in its etiopathogenesis. This study was focused on six functional candidate genes involved in PEX material deposition and the analysis of their potential association with PEX syndrome and PEX glaucoma (PEXG). methods. Fifty single-nucleotide polymorphisms (SNPs) capturing >95% of overall genetic variance observed in Europeans at loci for FBN1, LTBP2, MFAP2, TGM2, TGF-b1, and CLU were genotyped in 333 unrelated PEX-affected and 342 healthy individuals of German origin, and a genetic association study was performed. To replicate the findings, two SNPs of the CLU gene were genotyped in a further 328 unrelated German patients with PEX as well as in 209 Italian patients with PEX and 190 Italian control subjects. results. Association with PEX was observed only for the SNP rs2279590 in intron 8 of the CLU gene coding for clusterin (corrected P = 0.0347, OR = 1.34) in our first German cohort. Likewise, a frequent haplotype encompassing the associated risk allele showed nominally significant association. None of remaining SNPs or SNP haplotypes were associated with PEX. The association found was confirmed in a second German cohort (P = 0.0244) but not in the Italian cohort (P = 0.7173). In addition, the association with CLU SNP rs2279590 was more significant in German patients with PEX syndrome than in those with PEXG. conclusions. Genetic variants in the gene encoding clusterin may represent a risk factor for PEX in German patients but not in Italian patients. Variants in FBN1, LTBP2, MFAP2, TGF-b1, and TGM2 do not play a major role in the etiology of PEX syndrome, at least in German patients