Abstract: Cacao from South America is especially used to produce premium quality chocolate. Although the European Food Safety Authority has not established a limit for cadmium (Cd) in chocolate raw material, recent studies demonstrate that Cd concentrations in cacao beans can reach levels higher than the legal limits for dark chocolate (0.8 mg kg−1, effective January 1st, 2019). Despite the fact that the presence of Cd in agricultural soils is related to contamination by fertilizers, other potential sources must be considered in Ecuador. This field study was conducted to investigate Cd content in soils and cacao cultivated on Ecuadorian farms in areas impacted by oil activities. Soils, cacao leaves, and pod husks were collected from 31 farms in the northern Amazon and Pacific coastal regions exposed to oil production and refining and compared to two control areas. Human gastric bioaccessibility was determined in raw cacao beans and cacao liquor samples in order to assess potential health risks involved. Our results show that topsoils (0–20 cm) have higher Cd concentrations than deeper layers, exceeding the Ecuadorian legislation limit in 39% of the sampling sites. Cacao leaves accumulate more Cd than pod husks or beans but, nevertheless, 50% of the sampled beans have Cd contents above 0.8 mg kg−1. Root-to-cacao transfer seems to be the main pathway of Cd uptake, which is not only regulated by physico-chemical soil properties but also agricultural practices. Additionally, natural Cd enrichment by volcanic inputs must not be neglected. Finally, Cd in cacao trees cannot be considered as a tracer of oil activities. Assuming that total Cd content and its bioaccessible fraction (up to 90%) in cacao beans and liquor is directly linked to those in chocolate, the health risk associated with Cd exposure varies from low to moderate.

Abstract: Ethanol extract of Bagassa guianensis was tested as corrosion inhibitor for zinc in ASTM medium using polarization and electrochemical impedance spectroscopy (EIS). The results obtained show that this plant extract could serve as an effective inhibitor for the corrosion of zinc in sodium chloride media. The extract obtained give inhibition around 85%. Polarization curves show that Bagassa guianensis extract affects the anodic and cathodic reactions and the corrosion potential values were shifted to the positive potentials in the presence of the crude extract in the ASTM medium. The experimental data obtained from EIS method show a frequency distribution and therefore a modelling element with frequency dispersion behavior, a constant phase element (CPE alpha,Q ) has been used. Graphical methods are illustrated by synthetic data to determine the parameter of CPE (alpha, Q). Studies on the phytochemical constituents of thetotal extract were also established. Electrochemical studies, on the chemical families present in the crude extract, were also carried out to find the main constituents responsible for corrosion inhibition properties of the plant extract.

Abstract: In neotropical landscapes, a substantial fraction of the still waters available is found within tank bromeliads, plants which hold a few milliliters to several litres of rainwater within their leaf axils. The bromeliad ecosystem is integrated into the functioning of rainforest environments, but no study has ever estimated the secondary production, nor the biomass turnover rates of bromeliad macroinvertebrates in relation to other functional traits. We estimated secondary production at invertebrate population to metacommunity level in bromeliads of French Guiana. Coleoptera, Diptera and Crustacea with traits that confer resistance to drought had lower biomass turnover, longer generation times, and slower individual growth than species without particular resistance traits, suggesting convergent life history strategies in phylogenetically distant species. Detritivores and predators accounted for 87% and 13% of the overall annual production, respectively, but had similar production to biomass ratios. An average bromeliad sustained a production of 23.93 g dry mass m−2 year−1, a value which exceeds the medians of 5.0–14.8 g DM m−2 year−1 for lakes and rivers worldwide. Extrapolations to the total water volumes held by bromeliads at our field site yielded secondary production estimates of 226.8 ± 32.5 g DM ha−1 year−1. We conclude that the ecological role of tank bromeliads in neotropical rainforests may be as important as that of other freshwater ecosystems. © 2018, Springer International Publishing AG, part of Springer Nature.

Abstract: A thorough understanding of how tropical forests respond to climate is important to improve ecosystem process models and to reduce uncertainties in current and future global carbon balance calculations. The Amazon rainforest, a major contributor to the global carbon cycle, is subject to strong intra- and interannual variations in climate conditions. Understanding their effect on carbon fluxes between the ecosystem and the atmosphere and on the resulting carbon balance is still incomplete. We examined the long-term (over a 12-year period; 2004–2015) variations in gross primary productivity (GPP), ecosystem respiration (RE) and net ecosystem exchange (NEE) in a tropical rainforest in French Guiana and identified key climatic drivers influencing the changes. The study period was characterized by strong differences in climatic conditions among years, particularly differences in the intensity of the dry and wet seasons, as well as differences in annual carbon fluxes and balance. Annual average GPP varied from 3384.9?g?C?m-2?yr?1 (95% CI [3320.7, 3445.9]) to 4061.2?g?C?m-2?yr?1 (95% CI [3980.1, 4145.0]). RE varied even more than GPP, with a difference of 933.1?C?m-2?yr?1 between the minimum (3020.6?g?C?m-2?yr?1; 95% CI [2889.4, 3051.3]) and maximum (3953.7?g?C?m-2?yr?1; 95% CI [3887.6, 4019.6]) values. Although NEE showed large interannual variability (nine-fold), from ?65.6?g?C?m-2?yr?1 (95% CI [?4.4, ?126.0]) to ?590.5?g?C?m-2 yr?1 (95% CI [?532.3, ?651.6]), the forest remained a carbon sink over the 12-year period. A combination of global radiation (Rg), relative extractable water (REW) and soil temperature (Ts) explained 51% of the daily variations for GPP, 30% for RE and 39% for NEE. Global radiation was always the best predictor of these variations, but soil water content and temperature did also influence carbon fluxes and balance. Seasonally, Rg was the major controlling factor for GPP, RE and NEE during the wet season. During the dry season, variations in carbon fluxes and balance were poorly explained by climate factors. Yet, REW was the key driver of variations in NEE during the dry season. This study highlights that, over the long-term, carbon fluxes and balance in such tropical rainforest ecosystems are largely controlled by both radiation and water limitation. Even though variations in Rg have a greater impact on these fluxes, water limitation during seasonal droughts is enough to reduce ecosystem productivity, respiration and carbon uptake. The reduced precipitation expected in tropical rainforest areas under future climatic conditions will therefore strongly influence carbon fluxes and carbon uptake. This study also highlights the importance for land surface or dynamic global vegetation models to consider the main drivers of carbon fluxes and balance separately for dry and wet seasons.

Abstract: In Neotropical rainforest canopies, phytotelmata (“plant-held waters”) shelter diverse aquatic macroinvertebrate communities, including vectors of animal diseases. Studying these communities is difficult because phytotelmata are widely dispersed, hard to find from the ground and often inaccessible. We propose here a method for placing in tree crowns “artificial phytotelmata” whose size and shape can be tailored to different research targets. The efficacy of this method was shown while comparing the patterns of community diversity of three forest formations. We noted a difference between a riparian forest and a rainforest, whereas trees alongside a dirt road cutting through that rainforest corresponded to a subset of the latter. Because rarefied species richness was significantly lower when the phytotelmata were left for three weeks rather than for six or nine weeks, we recommend leaving the phytotelmata for twelve weeks to permit predators and phoretic species to fully establish themselves.