Construction of detrital mineral populations: insights from mixing of U–Pb zircon ages in Himalayan rivers

Fission‐track, U–Pb and Pb–Pb analyses of detrital heavy mineral populations in depositional basins and modern river sediments are widely used to infer the exhumational history of mountain belts. However, relatively few studies address the underlying assumption that detrital mineral populations provide an accurate representation of their entire source region. Implicit in this assumption is the idea that all units have equal potential to contribute heavy minerals in proportion to their exposure area in the source region. In reality, the detrital mineral population may be biased by variable concentrations of minerals in bedrock and differential erosion rates within the source region. This study evaluates the relative importance of these two variables by using mixing of U–Pb zircon ages to trace zircon populations from source units, through the fluvial system, and into the foreland. The first part of the study focuses on the Marsyandi drainage in central Nepal, using tributaries that drain single formations to define the U–Pb age distributions of individual units and using trunk river samples to evaluate the relative contributions from each lithology. Observed mixing proportions are compared with proportions predicted by a simple model incorporating lithologic exposure area and zircon concentration. The relative erosion rates that account for the discrepancy between the observed and predicted mixing proportions are then modelled and compared with independent erosional proxies. The study also compares U–Pb age distributions from four adjacent drainages spanning ～250 km along the Himalayan front using the Kolmogorov–Smirnov statistic and statistical estimates of the proportion of zircon derived from each upstream lithology. Results show that, along this broad swath of rugged mountains, the U–Pb age distributions are remarkably similar, thereby allowing data from more localized sources to be extrapolated along strike.     

Continental rift systems and anorogenic magmatism

Precambrian Laurentia and Mesozoic Gondwana both rifted along geometric patterns that closely approximate truncated-icosahedral tessellations of the lithosphere. These large-scale, quasi-hexagonal rift patterns manifest a least-work configuration. For both Laurentia and Gondwana, continental rifting coincided with drift stagnation, and may have been driven by lithospheric extension above an insulated and thermally expanded mantle. Anorogenic magmatism, including flood basalts, dike swarms, anorthosite massifs and granite-rhyolite provinces, originated along the Laurentian and Gondwanan rift tessellations. Long-lived volcanic regions of the Atlantic and Indian Oceans, sometimes called hotspots, originated near triple junctions of the Gondwanan tessellation as the supercontinent broke apart. We suggest that some anorogenic magmatism results from decompression melting of asthenosphere beneath opening fractures, rather than from random impingement of hypothetical deep-mantle plumes.     

Foreword

Destructive earthquakes have caused great damage in China and the United States and collapsing buildings havecaused many deaths and injuries. The field of earthquake engineering studies earthquake hazards, the occurrence ofearthquakes of various magnitudes, the nature of the ground shaking during an earthquake, the vibration of structuresduring earthquakes, the strengthening of existing structures and the design of new structures to be earthquake resistant,and finally, how to cope with earthquake damage and restore a city to normal functioning. Such efforts are in progressin both countries, but unfortunately, the language barrier interferes with the free flow of information between China andthe Untied States. It would be mutually beneficial if some means could be developed to promote the exchangeof information across the Pacific Ocean. This new journal has been established for this purpose and its success willbe an important step in promoting earthquake engineering in China and the United States.     

Preliminary investigation of the surficial sediments in the Cap-Breton Canyon (southwest France) and the surrounding continental shelf

A total of 120 grab samples of the surficial sediments in the Cap-Breton submarine canyon and surrounding continental shelf were collected and analyzed by grain-size sieving. A Q-mode Factor Analysis was made on the grain-size data in order to define the most meaningful facies types. Four distinct lithological facies were found to exist: silt and clay, very fine sand, fine sand, and coarse sand. Comparison with previous work and a ¹⁴C date on the silt and clay facies showed that the facies are not contemporaneous. The sands and coarse sands on the shelf were emplaced during the pre-Würm and Würm regressions, and later probably reworked during the Holocene (Flandrian) transgression. The silty clays found in the canyon and on the shelf to the south are younger and represent sediments brought in as suspended load by the Adour and other nearby rivers during the Holocene (Flandrian) transgression.     

pp′-DDT adsorption to suspended particulate matter in sea water

A procedure was devised to study pp′-DDT [2,2-bis($\text{p-}\text{chlorophenyl}$)-1,1,1-trichloroethane] adsorption and desorption to suspended particulates in aqueous solutions. DDT adsorption to a marine sediment, sediment fractions, clay and humic acid suspended in sea water was investigated and the humic fraction was found to have a greater adsorbing capacity than the clay or sediment. Removal of the humic fraction from sediment reduced the adsorption capacity to less than 60 per cent of the original sediment sample. It was concluded that suspended humic particulates may be important agents for transporting chlorinated hydrocarbons through the water column and for concentrating them in sediments and in detritus-feeding organisms.     

Nature of polymerization and properties of silicate melts and glasses at high pressure

The structures of sodium silicate and aluminosilicate glasses quenched from melts at high pressure (6-10 GPa) with varying degrees of polymerization (fractions of nonbridging oxygen) were explored using solid-state NMR [¹⁷O and ²⁷Al triple-quantum magic-angle spinning (3QMAS) NMR]. The bond connectivity in melts among four and highly coordinated network polyhedra, such as ^[4]Al, ^[5,6]Al, ^[4]Si, and ^[5,6]Si, at high pressure is shown to be significantly different from that at ambient pressure. In particular, in the silicate and aluminosilicate melts, the proportion of nonbridging oxygen (NBO) generally decreases with increasing pressure, leading to the formation of new oxygen clusters that include 5- and 6-coordinated Si and Al in addition to 4-coordinated Al and Si, such as ^[4]Si-O-^[5,6]Si, ^[4]Si-O-^[5,6]Al and Na-O-^[5,6]Si. While the fractions of ^[5,6]Al increase with pressure, the magnitude of this increase diminishes with increasing degrees of ambient-pressure polymerization under isobaric conditions. Incorporating the above structural information into models of melt properties reproduces the anomalous pressure-dependence of O²⁻ diffusivity and viscosity often observed in silicate melts.     

Iron and Sulfur Chemistry in a Stratified Lake: Evidence for Iron-Rich Sulfide Complexes

A four month study of a man-made lake used for hydroelectric power generation in northeastern Pennsylvania USA was conducted to investigate seasonal anoxia and the effects of sulfide species being transported downstream of the power generation equipment. Water column analyses show that the system is iron-rich compared to sulfide. Total Fe(II) concentrations in the hypolimnion are typically at least twice the total sulfide levels. In situ voltammetric analyses show that free Fe(II) as [Fe(H₂O)₆]²⁺ or free H₂S as H₂S/HS^- are either not present or at trace levels and that iron-rich sulfide complexes are present. From the in situ data and total Fe(II) and H₂S measurements, we infer that these iron-rich sulfide complexes may have stoichiometries such as Fe₂SH³⁺ (or polymeric forms of this and other stoichiometries). These iron-rich sulfide complexes appear related to dissolution of the iron-rich FeS mineral, mackinawite, because IAP calculations on data from discrete bottle samples obtained from bottom waters are similar to the pK_sp of mackinawite. Soluble iron-sulfide species are stable in the absence of O₂ (both in lake waters and the pipeline) and transported several miles during power generation. However, iron-sulfide complexes can react with O₂ to oxidize sulfide and can also dissociate releasing volatile H₂S when the waters containing them are exposed to the atmosphere downstream of the powerplant. Sediment analyses show that the lake is rich in oxidized iron solids (both crystalline and amorphous). Fe concentrations in FeS solids are low (<5 μmole/gr_{dry wt}) and the pyrite concentration ranges from about equal to the solid FeS to 30 times the solid FeS concentration. The degree of pyritization is below 0.12 indicating that pyrite formation is limited by free sulfide, which can react with the iron-rich sulfide complexes.     

A long‐term study of stable isotopes as tracers of processes governing water flow and quality in a lowland river basin: the upper Thames,UK

A long‐term study of O, H and C stable isotopes has been undertaken on river waters across the 7000‐km² upper Thames lowland river basin in the southern UK. During the period, flow conditions ranged from drought to flood. A 10‐year monthly record (2003–2012) of the main River Thames showed a maximum variation of 3‰ (δ¹⁸O) and 20‰ (δ²H), although interannual average values varied little around a mean of –6.5‰ (δ¹⁸O) and –44‰ (δ²H). A δ²H/δ¹⁸O slope of 5.3 suggested a degree of evaporative enrichment, consistent with derivation from local rainfall with a weighted mean of –7.2‰ (δ¹⁸O) and –48‰ (δ²H) for the period. A tendency towards isotopic depletion of the river with increasing flow rate was noted, but at very high flows (>100 m³/s), a reversion to the mean was interpreted as the displacement of bank storage by rising groundwater levels (corroborated by measurements of specific electrical conductivity). A shorter quarterly study (October 2011–April 2013) of isotope variations in 15 tributaries with varying geology revealed different responses to evaporation, with a well‐correlated inverse relationship between Δ¹⁸O and baseflow index for most of the rivers. A comparison with aquifer waters in the basin showed that even at low flow, rivers rarely consist solely of isotopically unmodified groundwater. Long‐term monitoring (2003–2007) of carbon stable isotopes in dissolved inorganic carbon (DIC) in the Thames revealed a complex interplay between respiration, photosynthesis and evasion, but with a mean interannual δ¹³C‐DIC value of –14.8 ± 0.5‰, exchange with atmospheric carbon could be ruled out. Quarterly monitoring of the tributaries (October 2011–April 2013) indicated that in addition to the aforementioned factors, river flow variations and catchment characteristics were likely to affect δ¹³C‐DIC. Comparison with basin groundwaters of different alkalinity and δ¹³C‐DIC values showed that the origin of river baseflow is usually obscured. The findings show that long‐term monitoring of environmental tracers can help to improve the understanding of how lowland river catchments function. Copyright © NERC 2015. Hydrological Processes © 2015 John Wiley & Sons, Ltd.