Intra- and inter-specific variability in total and methylmercury bioaccumulation by eight marine fish species from the Azores

We relate fish biological and ecological characteristics to total and organic mercury concentrations to determine whether accumulation is influenced by trophic level, Hg concentration in the diet, and vertical distribution. Levels of total mercury and methylmercury were determined in the muscle tissue of eight species of fish: Pagellus acarne, Trachurus picturatus, Phycis phycis, P. blennoides, Polyprion americanus, Conger conger, Lepidopus caudatus and Mora moro, caught in the Azores. All such fishes are commercially valuable and were selected to include species from a wide range of vertical distributions from epipelagic (<200 m) to mesopelagic (>300 m) environments. Methylmercury was the major form accumulated in all species, comprising an average of 88.1% of total mercury. Concentrations of mercury (total and methylmercury) increased with age, length and weight. Based on data from other studies, mercury concentrations in fish diet were estimated. Mercury levels in food ranged from 0.08 to 0.32 ppm, dry weight. Hg concentrations in the food and in muscle tissue from different species were positively correlated. Total Hg levels in the muscles were approximately nine times those estimated in food. Total mercury concentrations in muscle were positively correlated with both trophic level and median depth. Such enhanced mercury bioaccumulation in relation to depth appears to be determined primarily by concentrations in food and ultimately by water chemistry, which controls mercury speciation and uptake at the base of the food chain.     

Organic carbon accumulation in oligotrophic coastal lakes in southern Brazil during the last century

Journal of Paleolimnology - We report organic carbon (OC) accumulation rates in three freshwater ecosystems in southern Brazil, along the largest shallow coastal lagoon ecosystem in the world, the...     

Pattern and pathways for mercury lifespan bioaccumulation in Carcinus maenas

Carcinus maenas is an important and exploited natural resource in temperate estuaries, being consumed by local populations and also used as fish bait. Through bioaccumulation and bioamplification processes occurring in polluted estuarine ecosystems, this species may directly or indirectly represent a major pathway for Human contamination. No information is available on the overall lifespan bioaccumulation pattern of mercury for this species, which would be an invaluable tool for assessing the risks associated with C. maenas harvest in contaminated areas. Taking that in mind, the main objectives of this work were to clarify the lifespan bioaccumulation pattern of mercury for this species. A consistent lifespan accumulation pattern was found for this species, both for total and organic mercury, and coherent differences were found between genders, suggesting different physiological responses to contamination. From our results two scenarios emerge: (a) for low mercury contamination areas where the diet is the major pathway for metal uptake, with higher levels in muscle and hepatopancreas (twice as high as in gills) and higher organic mercury fractions (as high as 80-90% in muscle), crabs bioaccumulate with age and (b) on high contaminated areas, environmental exposure is predominant, with higher levels found in gills (reaching 0.8 mg kg(-1)), lower organic fractions and no mercury increment with age. Detoxification strategies, dietary differences and species mobility may account for these two accumulation patterns.     

Predicting monthly precipitation along coastal Ecuador: ENSO and transfer function models

Theoretical and Applied Climatology - It is well known that El Niño-Southern Oscillation (ENSO) modifies precipitation patterns in several parts of the world. One of the most impacted areas is...     

Reply to ‘Comment on: Rainfall,fog and throughfall dynamics in a subtropical ridge top cloud forest,National Park of Garajonay (La Gomera,Canary Islands,Spain)’ by A. Ritter and C.M. Regalado

This Reply aims to clarify and address many of the errors introduced to the discussion of our original paper (García‐Santos and Bruijnzeel, 2011; referred to henceforth as GSB2011) in the comment by Ritter and Regalado (2012) (henceforth referred to as RRR2012) as explained more fully under replies nos. 1–6, 8–12 and 14–18 below. Two (largely inconsequential) shortcomings in our original paper as detected by RRR2012 are acknowledged (see replies nos. 7 and 13 below). It is concluded that the majority of the comments offered by RRR2012 are unfounded as well as unnecessary. In summary, the two errors in GSB2011 spotted by RRR2012 (see points 7 and 13 below) could easily have been addressed in an erratum. Copyright © 2013 John Wiley & Sons, Ltd.