Mountain glaciers under a changing climate

Mountain glaciers are found around the world in ranges such as the Himalaya, the Andes and the European Alps. The majority of mountain glaciers world‐wide are shrinking. However, the rugged alpine topography through which these glaciers flow governs their dynamics and impacts on the regional climate systems that modify glacier mass balance. As a result, the response of mountain glaciers to climate change is difficult to predict, and highly spatially variable even across one mountain range, particularly where orography controls precipitation distributions. To understand how mountain glaciers behave and change, geologists combine many different techniques based on direct observations and dating of glacial geology, measurements of present‐day glaciers, and predictive numerical (computer) models. Recent advances in these techniques and their applications to glacial environments have demonstrated that the glacial geological record is a rich archive of information about how climate has changed in the past, and gives greater confidence in predictions of glacier change in the future, which is required if populations living in glacerised catchments are able to adapt to the rapid response of glaciers to a changing climate.     

Late Pleistocene baldcypress (Taxodium distichum) forest deposit on the continental shelf of the northern Gulf of Mexico

Approximately 13 km south of Gulf Shores, Alabama (United States), divers found in situ baldcypress (Taxodium distichum) stumps 18 m below the ocean surface. These trees could have only lived when sea level fell during the Pleistocene subaerially exposing the tectonically stable continental shelf. Here we investigate the geophysical properties along with microfossil and stratigraphical analyses of sediment cores to understand the factors that lead to this wood’s preservation. The stumps are exposed in an elongated depression (~100 m long, ~1 m deep) nested in a trough of the northwest–southeast trending Holocene sand ridges and troughs with 2–5 m vertical relief and ~0.5 km wavelength. Radiocarbon ages of the wood were infinite thus optically stimulated luminescence (OSL) dating was used to constrain the site’s age. Below the Holocene sands (~0.1–4 m thick), separated by a regional erosional unconformity, are Late Pleistocene mud-peat (72±8 ka OSL), mud-sand (63±5, 73±6 ka OSL), and palaeosol (56±5 ka OSL) facies that grade laterally from west to east, respectively. Foraminiferal analysis reveals the location of the terrestrial-marine transitional layer above the Pleistocene facies in an interbedded sand and mud facies (3940±30 (1σ) ¹⁴C a BP), which is part of a lower shoreface or marine-dominated estuarine environment. The occurrence of palaeosol and swamp facies of broadly similar ages and elevation suggests the glacial landscape possessed topographic relief that allowed wood, mud and peats to be preserved for ~50 ka of subaerial exposure before transitioning to the modern marine environment. We hypothesize that rapid sea-level rise occurring ~60 or ~40 ka ago provided opportunities for local flood-plain aggradation to bury the swamp thus preserving the stumps and that other sites may exist in the northern Gulf of Mexico shelf.     

Stable isotope constraints on the fluid source of hydrothermal breccia pipes in the Tankwa Karoo depocentre,South Africa: Breakdown of authigenic minerals during sill intrusion

The Karoo Basin covers much of South Africa and is an area of prospective shale gas exploration, with the Whitehill Formation the target shale unit. However, the sedimentary succession, including the Whitehill, has been intruded by a series of sills and dykes associated with the Karoo Large Igneous Province (~183 Ma), which are expected to have modified the thermal history of the basin dramatically. Here, we investigate a secondary effect of these intrusions: a series of hydrothermal vent complexes, or breccia pipes, focusing on using O, H, and C isotopes to constrain the origin and evolution of fluids produced during the intrusion of basaltic sills. A cluster of breccia pipes have been eroded down to the level of the Ecca Group at Luiperdskop on the western edge of the Karoo basin; a small isolated pipe of similar appearance crops out 13 km to the east. The Luiperdskop pipes are underlain by a Karoo dolerite sill that is assumed to provide the heat driving fluidization. The pipes consist of fine‐grained matrix and about 8% clasts, on average, of mostly sedimentary material; occasional large rafts of quartzite and dolerite are also present. The presence of clasts apparently from the Dwyka Group is consistent with the depth of formation of the pipes being at, or near, the base of the Karoo Supergroup, between 400 and 850 m below present surface. The presence of chlorite as the dominant hydrous mineral is consistent with an emplacement temperature between 300 and 350°C. The major and trace element, and O‐ and H‐isotope composition of the Tankwa breccias is homogenous, consistent with them being derived from the same source. The δ¹⁸O values (vsVSMOW) of the breccias are relatively uniform (7.1‰–8.7‰), and are similar to that of the country rock shale, and both are lower than expected for shale. The water content of the breccia is between 2.7 and 3.1 wt.% and the δD values range from ?109‰ to ?144‰. Calcite in vesicles has δ¹³C and δ¹⁸O (VSMOW) values of ?4.2‰ and 24.0‰, respectively. The low δD value of the breccia rocks does not appear to be due to the presence of methane in the fluid. Instead, it is proposed that low δD and δ¹⁸O values are the result of the fluid being derived from the breakdown of clay minerals that formed and were deposited at a time of cold climate at ~290 Ma.     

Tidal river sediments in the Washington,D.C. area. III. Biological effects associated with sediment contamination

Sediment toxicity and benthic macroinvertebrate community structure were measured as one component of a study cohceived to determine the distribution and effect of sediment contamination in tidal freshwater portions of the Potomac and Anacostia rivers in the Washington, D.C., area. Samples were collected at 15 sites. Analyses included a partial life cycle (28 d) whole sediment test using the amphipod Hyalella azteca (Talitridae) and an assessment of benthic community structure. Survival and growth (as estimated by amphipod length) were experimental endopoints for the toxicity test. Significant mortality was observed in 5 of 10 sites in the lower Anacostia River basin and at the main channel Potomac River site. Sublethal toxicity, as measured by inhibition of amphipod growth, was not observed. Toxicity test results were in general agreement with synoptically measured sediment contaminant concentrations. Porewater total ammonia (NH₃+NH₄ ⁺) appears to be responsible for the toxicity of sediments from the Potomac River, while correlation analysis and simultaneously extracted metals: acid volatile sulfide (SEM∶AVS) results suggest that the toxicity associated with Anacostia River sediments was due to organic compounds. Twenty-eight macroinvertebrate taxa were identified among all sites, with richness varying from 5 to 17 taxa per site. Groups of benthic assemblages identified by group-average cluster analysis exhibited variable agreement with sediment chemical and sediment toxicity results. Integration of toxicological, chemical, and ecological components suggests that adverse environmental effects manifest in the lower Anacostia River benthos result from chemical contamination of sediment.     

Implications of model uncertainty for the mapping of hillslope‐scale soil erosion predictions

An integrated modelling approach (MIRSED) which utilizes the process‐based soil erosion model WEPP (Water Erosion Prediction Project) is presented for the assessment of hillslope‐scale soil erosion at five sites throughout England and Wales. The methodology draws upon previous uncertainty analysis of the WEPP hillslope soil erosion model by the authors to qualify model results within an uncertainty framework. A method for incorporating model uncertainty from a range of sources is discussed as a first step towards using and learning from results produced through the GLUE (Generalized Likelihood Uncertainty Estimation) technique. Results are presented and compared to available observed data, which illustrate that levels of uncertainty are significant and must be taken into account if a meaningful understanding of output from models such as WEPP is to be achieved. Furthermore, the collection of quality, observed data is underlined for two reasons: as an essential tool in the development of soil erosion modelling and also to allow further constraint of model uncertainty. Copyright © 2001 John Wiley & Sons, Ltd.     

A comparison of sediment microbial communities associated with<Emphasis Type="Italic">Phragmites australis</Emphasis> and<Emphasis Type="Italic">Spartina alterniflora</Emphasis> in two brackish wetlands of New Jersey

The extensive spread ofPhragmites australis throughout brackish marshes on the East Coast of the United States is a major factor governing management and restoration decisions because it is assumed that biogeochemical functions are altered by the invasion. Microbial activity is important in providing wetland biogeochemical functions such as carbon and nitrogen cycling, but there is little known about sediment microbial communities inPhragmites marshes. Microbial populations associated with invasivePhragmites vegetation and with native salt marsh cordgrass,Spartina alterniflora, may differ in the relative abundance of microbial taxa (community structure) and in the ability of this biota to decompose organic substrates (community biogeochemical function). This study compares sediment microbial communities associated withPhragmites andSpartina vegetation in an undisturbed brackish marsh near Tuckerton, New Jersey (MUL), and in a brackish marsh in the anthropogenically affected Hackensack meadowlands (SMC). We use phospholipid fatty acid (PLFA) analysis and enzymataic activity to profile sediment microbial communities associated with both plants in each site. Sediment analyses include bulk density, total organic matter, and root biomass. PLFA profiles indicate that the microbial communities differ between sites with the undisturbed site exhibiting greater fatty acid richness (62 PLFA recovered from MUL versus 38 from SMC). Activity of the 5 enzymes analyzed (β-glucosidase, acid phosphatase, chitobiase, and 2 oxidases) was higher in the undisturbed site. Differences between vegetation species as measured by Principal Components Analysis were significantly greater at the undisturbed MUL site than at SMC, and patterns of enzyme activity and PLFAs did not correspond to patterns of root biomass. We suggest that in natural wetland sediments, macrophyte rhizosphere effects influence the community composition of sediment microbial populations. Physical and chemical site disturbances may impose limits on these rhizosphere effects, decreasing sediment microbial diversity and potentially, microbial biogeochemical functions.     

Situated knowledges and the spaces of consent

Informed consent has often been presented as a kind of ethical panacea, the best way of guarding against medical and scientific abuses of human rights. However recent empirical research has led bioethicists to question both the feasibility and the value of informed consent procedures. This paper also seeks to critique informed consent, but focuses less on its empirical shortcomings. Instead, this paper questions the assumption that ethics involves engaging in the kind of rational, distanced, objective reflection traditionally considered the basis of both scientific observation and ethical decision making. Drawing on recent insights from ethical geography and geographers studying the biotechnology industry, I wish to argue that ethical reflection is a relational and situated process, less about being distanced and objective, and more about recognizing how our ethical decisions are shaped by our social and material environment.     

Geology and tectonics of Neoproterozoic salt diapirs and salt sheets in the eastern Willouran Ranges,South Australia

Allochthonous salt structures and associated primary and secondary minibasins are exposed in Neoproterozoic strata of the eastern Willouran Ranges, South Australia. Detailed geologic mapping using high‐quality airborne hyperspectral remote‐sensing data and satellite imagery, combined with a qualitative structural restoration, are used to elucidate the evolution of this complex, long‐lived (>250 Myr) salt system. Field observations and interpretations at a resolution unobtainable from seismic or well data provide a means to test published models of allochthonous salt emplacement and associated salt‐sediment interaction derived from subsurface data in the northern Gulf of Mexico. Salt diapirs and sheets are represented by megabreccias of nonevaporite lithologies that were originally interbedded with evaporites that have been dissolved and/or altered. Passive diapirism began shortly after deposition of the Callanna Group layered evaporite sequence. A primary basin containing an expulsion‐rollover structure and megaflap is flanked by two vertical diapirs. Salt flowed laterally from the diapirs to form a complex, multi‐level canopy, now partly welded, containing an encapsulated minibasin and capped by suprasalt basins. Salt and minibasin geometries were modified during the Late Cambrian–Ordovician Delamerian Orogeny (ca. 500 Ma). Small‐scale structures such as subsalt shear zones, fractured or mixed ‘rubble zones’ and thrust imbricates are absent beneath allochthonous salt and welds in the eastern Willouran Ranges. Instead, either undeformed strata or halokinetic drape folds that include preserved diapir roof strata are found directly below the transition from steep diapirs to salt sheets. Allochthonous salt first broke through the diapir roofs and then flowed laterally, resulting in variable preservation of the subsalt drape folds. Lateral salt emplacement was presumably on roof‐edge thrusts or, because of the shallow depositional environment, via open‐toed advance or extrusive advance, but without associated subsalt deformation.