Littoral cladoceran community reassembly following the cessation of disturbance

The process of recovery from environmental impact provides insights into factors that drive community assembly. This study investigated community reassembly following perturbation, using littoral cladoceran microfossils. Whole-lake experimental manipulations of acids and nutrients in Lake 302N (L302N; 1972–1997) and acids in Lake 223 (L223; 1976–1994) at the Experimental Lakes Area (ELA; Ontario, Canada), provided an opportunity to use the sediment record to reconstruct the trajectory of recovery. Comparison was made to unmanipulated Lake 377 (L377) to estimate changes in regional baseline conditions. Recovery was evaluated at both the species and community level, using univariate and multivariate metrics. Up to 14 years after cessation of acid and nutrient additions, and following chemical recovery to pH > 6.5, both L302N and L223 littoral cladoceran communities failed to recover to their pre-manipulation states. Multivariate metrics demonstrated hysteresis along the recovery trajectory, and the movement to alternative states in littoral cladoceran communities in both lakes. The most recent littoral cladoceran community structure, reconstructed from the paleorecord, is driven by the persistence of species from the acidification period, suggesting biological resistance. Recovery states differed between L302N and L223, although their initial, pre-manipulation littoral cladoceran community structures were similar, reflecting multiple, independent recovery trajectories. Independent recovery trajectories are at odds with previous findings, which suggest that dispersal from an egg bank should support deterministic recovery trajectories. We conclude that littoral cladoceran microfossils can be used effectively to determine the community state with recovery and compare it to the pre-manipulation condition, particularly with the use of multivariate metrics.     

A Synthetic Haematite Reference Material for LA‐ICP‐MS U‐Pb Geochronology and Application to Iron Oxide‐Cu‐Au Systems

In both nature and synthetic experiments, the common iron oxide haematite (α‐Fe₂O₃) can incorporate significant amounts of U into its crystal structure and retain radiogenic Pb over geological time. Haematite is a ubiquitous component of many ore deposit types and, therefore, represents a valuable hydrothermal mineral geochronometer, allowing direct constraints to be placed on the timing of ore formation and upgrading. However, to date, no suitable natural haematite reference material has been identified. Here, a synthetic haematite U‐Pb reference material (MR‐HFO) is characterised using LA‐ICP‐MS and ID‐TIMS. Centimetre‐scale ‘chips’ of synthesised α‐Fe₂O₃ were randomly microsampled via laser ablation‐extraction and analysed using ID‐TIMS. Reproducible U/Pb and Pb/Pb measurements were obtained across four separate chips (n = 13). Subsequently, an evaluation of the suitability MR‐HFO in constraining U‐Pb data via LA‐ICP‐MS is presented using a selection of natural samples ranging from Cenozoic to Proterozoic in age. The MR‐HFO normalised U‐Pb ratios are more concordant and ages more accurate versus the same LA‐ICP‐MS spot analyses normalised to zircon reference material, when compared with independently acquired ID‐TIMS data from the same natural haematite grains. Results establish MR‐HFO as a suitable reference material for LA‐ICP‐MS haematite U‐Pb geochronology.     

Rare earth element geochemistry of feldspars: examples from Fe-oxide Cu-Au systems in the Olympic Cu-Au Province,South Australia

Mineralogy and Petrology - Rare earth element (REE) fractionation trends in feldspars are reported from Olympic Dam (including Wirrda Well and Phillip’s Ridge) and Cape Donington (Port...     

A modified light transmission visualization method for DNAPL saturation measurements in 2-D models

In this research, a light transmission visualization (LTV) method was used to quantify dense non-aqueous phase liquids (DNAPL) saturation in two-dimensional (2-D), two fluid phase systems. The method is an expansion of earlier LTV methods and takes into account both absorption and refraction light theories. Based on this method, DNAPL and water saturations can rapidly be obtained point wise across sand-packed 2-D flow chambers without the need to develop a calibration curve. A single point calibration step is, however, needed when dyed DNAPL is used to account for the change in the transmission factor at the dyed DNAPL–water interface. The method was applied to measure, for the first time, undyed DNAPL saturation in small 2-D chambers. Known amounts of DNAPL, modeled by tetrachloroethylene (PCE), were added to the chamber and these amounts were compared to results obtained by this LTV method. Strong correlation existed between results obtained based on this method and the known PCE amounts with an R² value of 0.993. Similar experiments conducted using dyed PCE showed a stronger correlation between results obtained by this LTV method and the known amounts of dyed PCE added to the chamber with an R² value of 0.999. The method was also used to measure dyed PCE saturation in a large 2-D model following sparging experiments. Results obtained from image analyses following each sparging event were compared to results obtained by two independent techniques, namely gas chromatography–mass spectrometry (GC/MS) analyses and carbon column extraction. There was a good agreement between the results obtained by this LTV method and those obtained by the two independent techniques when experiments were carried out under stable light source conditions and errors in mass balance were minor. The method presented here can be expanded to measure fluid contents in three fluid phase systems and provide a non-destructive, non-intrusive tool to investigate changes in DNAPL architecture and flow characteristics in laboratory experiments.     

Geoarchaeological analysis of an acheulean site at Kalambo Falls,Zambia

Acheulean sites are commonly recovered from sandy channel contexts, particularly in Africa. These sites frequently contain impressive concentrations of artifacts dominated by typical Acheulean large bifacial artifacts (‘handaxes,’ etc.). Possible influences of fluvial sedimentary processes in Acheulean site formation are explored through consideration of sedimentary context and detailed analysis of relevant artifact assemblage characteristics in part of a major Acheulean ‘Floor’ at Kalambo Falls, Zambia. The Kalambo Falls patterns are analyzed here with regard to influences of behavioral and natural processes in their formation, and are compared to those observed in Acheulean horizons at Montagu Cave, South Africa. Spatial concentration of bifaces and paucity of debitage at many Acheulean sites may be due largely to fluvial disturbance and winnowing, although a hominid preoccupation with large bifacial tools may be a bona fide behavior pattern at some sites. Better control over sedimentary context is necessary to elucidate the range of behaviorally-produced patterns at Acheulean sites.     

Climate change, ambient ozone, and health in 50 US cities

We investigated how climate change could affect ambient ozone concentrations and the subsequent human health impacts. Hourly concentrations were estimated for 50 eastern US cities for five representative summers each in the 1990s and 2050s, reflecting current and projected future climates, respectively. Estimates of future concentrations were based on the IPCC A2 scenario using global climate, regional climate, and regional air quality models. This work does not explore the effects of future changes in anthropogenic emissions, but isolates the impact of altered climate on ozone and health. The cities’ ozone levels are estimated to increase under predicted future climatic conditions, with the largest increases in cities with present-day high pollution. On average across the 50 cities, the summertime daily 1-h maximum increased 4.8 ppb, with the largest increase at 9.6 ppb. The average number of days/summer exceeding the 8-h regulatory standard increased 68%. Elevated ozone levels correspond to approximately a 0.11% to 0.27% increase in daily total mortality. While actual future ozone concentrations depend on climate and other influences such as changes in emissions of anthropogenic precursors, the results presented here indicate that with other factors constant, climate change could detrimentally affect air quality and thereby harm human health.     

The seasonal footprinting mechanism in CFSv2: simulation and impact on ENSO prediction

The seasonal footprinting mechanism (SFM) is thought to be a pre-cursor to the El Nino Southern Oscillation (ENSO). Fluctuations in the North Pacific Oscillation (NPO) impact the ocean via surface heat fluxes during winter, leaving a sea-surface temperature (SST) “footprint” in the subtropics. This footprint persists through the spring, impacting the tropical Pacific atmosphere–ocean circulation throughout the following year. The simulation of the SFM in the National Centers for Environmental Prediction (NCEP)/Climate Forecast System, version 2 (CFSv2) is likely to have an impact on operational predictions of ENSO and potentially seasonal predictions in the United States associated with ENSO teleconnection patterns. The ability of the CFSv2 to simulate the SFM and the relationship between the SFM and ENSO prediction skill in the NCEP/CFSv2 are investigated. Results indicate that the CFSv2 is able to simulate the basic characteristics of the SFM and its relationship with ENSO, including extratropical sea level pressure anomalies associated with the NPO in the winter, corresponding wind and SST anomalies that impact the tropics, and the development of ENSO-related SST anomalies the following winter. Although the model is able to predict the correct sign of ENSO associated with the SFM in a composite sense, probabilistic predictions of ENSO following a positive or negative NPO event are generally less reliable than when the NPO is not active.     

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in harbor sediments from Sea Lots, Port-of-Spain, Trinidad and Tobago

Concentrations of polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were determined in nearshore marine surficial sediments from three locations in Trinidad. Sediments were sampled at Sea Lots on the west coast, in south Port-of-Spain Harbor, south of Sea Lots at Caroni Lagoon National Park, and on Trinidad’s east coast at Manzanilla. Total PCB concentrations in Sea Lots sediments ranged from 62 to 601 ng/g (dry weight {dw}), which was higher than at Caroni and Manzanilla, 13 and 8 ng/g dw, respectively. Total OCP concentrations at Sea Lots were ranged from 44.5 to 145 ng/g dw, compared with 13.1 and 23.8 n/g (dw), for Caroni and Manzanilla respectively. The concentrations of PCBs and of some OCPs in sediments from Sea Lots were above the Canadian interim sediment quality guidelines. To date, this data is the first report on the levels of PCBs and other organochlorine compounds from Trinidad and Tobago.     

Intermobility of barium,strontium, and lead in chloride and sulfate leach solutions

Iron(III)-precipitates formed by the oxidation of dissolved Fe(II) are important sorbents for major and trace elements in aquatic and terrestrial systems. Their reductive dissolution in turn may result in the release of associated elements. We examined the reductive dissolution kinetics of an environmentally relevant set of Fe(II)-derived arsenate-containing Fe(III)-precipitates whose structure as function of phosphate (P) and silicate (Si) content varied between poorly-crystalline lepidocrocite, amorphous Fe(III)-phosphate, and Si-containing ferrihydrite. The experiments were performed with 0.2–0.5 mM precipitate-Fe(III) using 10 mM Na-ascorbate as reductant, 5 mM bipyridine as Fe(II)-complexing ligand, and 10 mM MOPS/5 mM NaOH as pH 7.0 buffer. Times required for the dissolution of half of the precipitate (t_50%) ranged from 1.5 to 39 h; spanning a factor 25 range. At loadings up to ~ 0.2 P/Fe (molar ratio), phosphate decreased the t_50% of Si-free precipitates, probably by reducing the crystallinity of lepidocrocite. The reductive dissolution of Fe(III)-phosphates formed at higher P/Fe ratios was again slower, possibly due to P-inhibited ascorbate binding to precipitate-Fe(III). The slowest reductive dissolution was observed for P-free Si-ferrihydrite with ~ 0.1 Si/Fe, suggesting that silicate binding and polymerization may reduce surface accessibility. The inhibiting effect of Si was reduced by phosphate. Dried-resuspended precipitates dissolved 1.0 to 1.8-times more slowly than precipitates that were kept wet after synthesis, most probably because drying enhanced nanoparticle aggregation. Variations in the reductive dissolution kinetics of Fe(II) oxidation products as reported from this study should be taken into account when addressing the impact of such precipitates on the environmental cycling of co-transformed nutrients and contaminants.