Modeling biodiversity loss by global warming on Pantepui, northern South America: projected upward migration and potential habitat loss

This work aims to estimate the potential effects of the global warming projected for the twenty-first century on the biodiversity of a remote and pristine region of the Neotropics called Pantepui. Habitat loss and fragmentation by upward migration of bioclimatic conditions is analyzed using Species-Area Relationships (SAR) and Altitudinal Range Displacement (ARD) analysis. The ARD is a tool that uses the present-day lapse rate to estimate the upward migration of the species based on the global warming predicted by the IPCC. The results show that around 80% of the vascular flora, ca. 1,700 species of which up to 400 would be Pantepui endemics, are threatened of extinction. These estimates should be considered preliminary, but the danger is real. Therefore, suitable conservation or mitigation strategies are needed.     

Residence time of S-type anatectic magmas beneath the Neogene Volcanic Province of SE Spain: a zircon and monazite SHRIMP study

Zircon and monazite from three restitic enclaves and one host dacite have been dated by ion microprobe (SHRIMP), with the aim of characterising their Miocene history and defining the timing relationships between crustal melting and eruption in the high-K calc-alkaline volcanics of the Neogene Volcanic Province of SE Spain. The studied samples are from the volcanic edifices of El Joyazo (Cerro del Hoyazo) and Mazarrón. Zircons in the enclaves are characterized by a thin euhedral rim overgrowing a detrital core. The core-rim boundary is marked by tiny glass inclusions of S-type granitic composition, which attest to the growth of zircon rims during a crustal melting event. At El Joyazo, where lavas erupted at 6.3 Ma (Zeck and Williams 2002), U-Pb ages of zircon overgrowths define an age of anatexis of 9.63±0.26 Ma (95% c.l.), in agreement with monazite ages of 9.74±0.21 Ma (95% c.l.). At Mazarrón, the age of anatexis provided by monazite at 9.13±0.18 Ma (95% c.l.) overlaps with that of melt-precipitated zircon in the host dacite, dated at 9.06±0.53 Ma (95% c.l.). These results indicate that after partial melting, the enclaves and the syngenetic S-type melts resided at depth for >3 m.y. at El Joyazo. Compared with the results from Mazarrón, the long residence time obtained at El Joyazo is probably due to the greater depth of melting (c. 25 km vs. c. 15 km). At such depth, corresponding to the Miocene palaeo-Moho, the more ductile regime of the crust is likely to have favoured magma ponding. The thermal anomaly beneath the Neogene Volcanic Province, which generated the S-type crustal melts, is today visible from geophysical data and can be traced back to the Lower Miocene. As a consequence, residence times longer than determined in this work may be expected.Editorial responsibility: J. Hoefs     

Fate of polycyclic aromatic hydrocarbon (PAH) contamination in a mangrove swamp in Hong Kong following an oil spill

The fate of polycyclic aromatic hydrocarbon (PAH) contamination in a mangrove swamp (Yi O) in Hong Kong after an oil spill accident was investigated. The concentrations and profiles of PAHs in surface sediments collected from five quadrats (each of 10 m×10 m) covering different degrees of oil contamination and the most contaminated mangrove leaves were examined in December 2000 (30 days after the accident) and March 2001 (126 days later). The concentrations of total PAHs in surface sediments ranged from 138 to 2135 ng g⁻¹, and PAHs concentrations decreased with time. In the most contaminated sediments, total PAHs dropped from 2135 (30 days) to 1196 ng g⁻¹ (120 days), and the decrease was smaller in less contaminated sediments. The percentage reduction in sediment PAHs over three months (44%) was less significant than that in contaminated leaves (85%), indicating PAH in or on leaves disappeared more rapidly. The PAH profiles were very similar in sediments collected from quadrats Q1 and Q2 with benzo[a]anthracene and pyrene being the most abundant PAH compounds, but were different in the other three quadrats. The proportion of the light molecular weight PAHs to total PAHs increased after three months, especially phenanthrene. Results suggest that physical and photo-chemical weathering (tidal washing and photo-oxidation) of crude oil in surface sediments and on plant leaves were important processes in the first few months after the oil spill. The PAH contamination in Yi O swamp came from both petrogenic and pyrolytic sources. The petrogenic characteristic in the most contaminated sediment was confirmed with high values of phenanthrene to anthracene ratio (>10) and low values of fluoranthene to pyrene ratio (0.3–0.4).     

Effects of industrial by-product amendments on As,Cd and Tl retention/release in an element-spiked acidic soil

To asses the efficiency of two by-products (phosphogypsum (PG) and sugar foam (SF), rich in gypsum and calcium carbonate, respectively) in the immobilization of three toxic elements (As, Cd and Tl) in an acidic soil, batch-scale sorption and desorption experiments were conducted after 18 months of in situ amendment application. The Langmuir isotherms applied for sorption studies showed that the estimated maximum sorption capacity of the elements was highest in the SF-treated samples. The amount of element retained and the percentage of extraction after TCLP tests indicated that those samples amended with sugar foam (SF and PG + SF) had the potential to immobilize As, Cd and Tl in an acidic soil with low sorptive capacity. In addition to sorption and desorption experiments, scanning electron microscopy in back-scattered electron mode (SEM-BSE) showed the formation of Al-hydroxy polymers which provides the soil with additional sorption capacity. The three target elements were associated with the Al-hydroxy polymers, probably through direct coordination or the formation of ternary complexes. By means of statistical analysis it has been found that sorption processes of As, Cd and Tl in this soil mainly depend on the treatment, whereas desorption is an element-dependent process.