Loading and fate of particulate organic carbon from the Himalaya to the Ganga-Brahmaputra delta

We use the evolution of river sediment characteristics and sedimentary C_org from the Himalayan range to the delta to study the transport of C_org in the Ganga-Brahmaputra system and especially its fate during floodplain transit.A detailed characterisation of both mineral and organic particles for a sampling set of river sediments allows taking into account the sediment heterogeneity characteristic of such large rivers. We study the relationships between sediment characteristics (mineralogy, grain size, specific area) and C_org content in order to evaluate the controls on C_org loading. Contributions of C3 and C4 plants are estimated from C_org stable isotopic composition (δ¹³C_org). We use the evolution of δ¹³C_org values from the Himalayan range to the delta in order to study the fate of C_org during floodplain transit.Ganga and Brahmaputra sediments define two distinct linear relations with specific area. In spite of 4-5 times higher specific area, Ganga sediments have similar C_org content, grain size and mineralogy as Brahmaputra sediments, indicating that specific area does not exert a primary control on C_org loading. The general correlation between the total C_org content and Al/Si ratio indicates that C_org loading is mainly related to: (1) segregation of organic particles under hydrodynamic forces in the river, and (2) the ability of mineral particles to form organo-mineral aggregates.Bed and suspended sediments have distinct δ¹³C_org values. In bed sediments, δ¹³C_org values are compatible with a dominant proportion of fossil C_org derived from Himalayan rocks erosion. Suspended sediments from Himalayan tributaries at the outflow of the range have low δ¹³C_org values (−24.8‰ average) indicating a dominant proportion of C3 plant inputs. In the Brahmaputra basin, δ¹³C_org values of suspended sediments are constant along the river course in the plain. On the contrary, suspended sediments of the Ganga in Bangladesh have higher δ¹³C_org values (−22.4‰ to −20.0‰), consistent with a significant contribution of C4 plant derived from the floodplain. Our data indicate that, during the plain transit, more than 50% of the recent biogenic C_org coming from the Himalaya is oxidised and replaced by floodplain C_org. This renewal process likely occurs during successive deposition-erosion cycles and river course avulsions in the plain.     

A Reflection on Mg, Cd, Ca, Li and Si Isotopic Measurements and Related Reference Materials

This contribution aims to report the reflections we had with the scientific community during two international workshops on reference materials for stable isotopes in Davos (2002) and Nice (2003). After evaluating the isotopic homogeneity of some existing reference materials, based on either certificates, literature data or specific inter-laboratory rounds, we confirm these as primary reference materials or propose new ones relative to which stable isotope compositions should be reported. We propose DSM-3 for Mg, NIST SRM 915a for Ca, L-SVEC for Li and NBS28 for Si. Cadmium does not yet have a well identified delta zero material, although three commercial mono-elemental Cd solutions have yielded the same isotopic composition relative to one another. In order to scale the linearity of any mass spectrometer, some secondary reference materials are also proposed: Cambridge-1 solution for Mg, the "Münster-Cd" and JEPPIM Cd solutions for Cd and the "Big Batch" silicate for Si. The team from Nancy propose to prepare a mixed spike solution for Li isotopes. Well-characterised natural samples such as ocean or continental waters, diatoms, sponges, rocks and minerals are needed to validate the entire analytical procedure, particularly to take into account the effect of sample mineralisation and of chemical manipulations for elemental separation prior to analysis.     

Interpreting the Ca isotope record of marine biogenic carbonates

An 18 million year record of the Ca isotopic composition (δ^44/42Ca) of planktonic foraminiferans from ODP site 925, in the Atlantic, on the Ceara Rise, provides the opportunity for critical analysis of Ca isotope-based reconstructions of the Ca cycle. δ^44/42Ca in this record averages +0.37 ± 0.05 (1σ SD) and ranges from +0.21‰ to +0.52‰. The record is a good match to previously published Neogene Ca isotope records based on foraminiferans, but is not similar to the record based on bulk carbonates, which has values that are as much as 0.25‰ lower. Bulk carbonate and planktonic foraminiferans from core tops differ slightly in their δ^44/42Ca (i.e., by 0.06 ± 0.06‰ (n = 5)), while the difference between bulk carbonate and foraminiferan values further back in time is markedly larger, leaving open the question of the cause of the difference. Modeling the global Ca cycle from downcore variations in δ^44/42Ca by assuming fixed values for the isotopic composition of weathering inputs (δ^44/42Ca_w) and for isotope fractionation associated with the production of carbonate sediments (Δ_sed) results in unrealistically large variations in the total mass of Ca²⁺ in the oceans over the Neogene. Alternatively, variations of ±0.05‰ in the Ca isotope composition of weathering inputs or in the extent of fractionation of Ca isotopes during calcareous sediment formation could entirely account for variations in the Ca isotopic composition of marine carbonates. Ca isotope fractionation during continental weathering, such as has been recently observed, could easily result in variations in δ^44/42Ca_w of a few tenths of permil. Likewise a difference in the fractionation factors associated with aragonite versus calcite formation could drive shifts in Δ_sed of tenths of permil with shifts in the relative output of calcite and aragonite from the ocean. Until better constraints on variations in δ^44/42Ca_w and Δ_sed have been established, modeling the Ca²⁺ content of seawater from Ca isotope curves should be approached cautiously.     

Determination of Total Organic Carbon Content and δ13C in Carbonate-Rich Detrital Sediments

The determination of total organic carbon content and composition in detrital sediments requires careful removal of their carbonate minerals. In detrital sediments containing large amounts of carbonates, including dolomite, this can only be achieved by liquid acid leaching that may solubilise a significant proportion of the organic carbon. For a set of detrital sediments from the Himalayan system and the Amazon River as well as five geological reference materials, we determined the proportion of organic carbon (C_org) solubilised during acid leaching. This proportion is significant for all analysed sediments and generally tends to increase with the organic carbon content. Compared to other types of sediments analysed, clay fractions extracted from river sediments and bed sediments with very low organic carbon content have high and low proportions of acid soluble C_org respectively. In Himalayan and Amazon river sediments, the proportion of C_org solubilised during acid leaching was relatively constant with average values of 14 and 19 % respectively. Thus, it is possible to correct the C_org content for the dissolved organic carbon content measured after decarbonation. Data presented here show that C_org dissolved during liquid acid leaching must be taken into account. After careful calibration, the method presented here should, therefore, be applied to any carbonate-rich detrital sediment.     

Calcium and magnesium isotope systematics in rivers draining the Himalaya-Tibetan-Plateau region: Lithological or fractionation control?

In rivers draining the Himalaya-Tibetan-Plateau region, the ²⁶Mg/²⁴Mg ratio has a range of 2‰ and the ⁴⁴Ca/⁴²Ca ratio has a range of 0.6‰. The average δ²⁶Mg values of tributaries from each of the main lithotectonic units (Tethyan Sedimentary Series (TSS), High Himalayan Crystalline Series (HHCS) and Lesser Himalayan Series (LHS)) are within 2 standard deviation analytical uncertainty (0.14‰). The consistency of average riverine δ²⁶Mg values is in contrast to the main rock types (limestone, dolostone and silicate) which range in their average δ²⁶Mg values by more than 2‰. Tributaries draining the dolostones of the LHS differ in their values compared to tributaries from the TSS and HHCS. The chemistry of these river waters is strongly influenced by dolostone (solute Mg/Ca close to unity) and both δ²⁶Mg (−1.31‰) and (0.64‰) values are within analytical uncertainty of the LHS dolostone. These are the most elevated values in rivers and rock reported so far demonstrating that both riverine and bedrock values may show greater variability than previously thought.Although rivers draining TSS limestone have the lowest values at −1.41 and 0.42‰, respectively, both are offset to higher values compared to bedrock TSS limestone. The average δ²⁶Mg value of rivers draining mainly silicate rock of the HHCS is −1.25‰, lower by 0.63‰ than the average silicate rock. These differences are consistent with a fractionation of δ²⁶Mg values during silicate weathering. Given that the proportion of Mg exported from the Himalaya as solute Mg is small, the difference in ²⁶Mg/²⁴Mg ratios between silicate rock and solute Mg reflects the ²⁶Mg/²⁴Mg isotopic fractionation factor () between silicate and dissolved Mg during incongruent silicate weathering. The value of of 0.99937 implies that in the TSS, solute Mg is primarily derived from silicate weathering, whereas the source of Ca is overwhelmingly derived from carbonate weathering. The average value in HHCS rivers is within uncertainty of silicate rock at 0.39‰. The widespread hot springs of the High Himalaya have an average δ²⁶Mg value of −0.46‰ and an average value of 0.5‰, distinct from riverine values for δ²⁶Mg but similar to riverine values. Although rivers draining each major rock type have and δ²⁶Mg values in part inherited from bedrock, there is no correlation with proxies for carbonate or silicate lithology such as Na/Ca ratios, suggesting that Ca and Mg are in part recycled. However, in spite of the vast contrast in vegetation density between the arid Tibetan Plateau and the tropical Lesser Himalaya, the isotopic fractionation factor for Ca and Mg between solute and rocks are not systematically different suggesting that vegetation may only recycle a small amount of Ca and Mg in these catchments.The discrepancy between solute and solid Ca and Mg isotope ratios in these rivers from diverse weathering environments highlight our lack of understanding concerning the origin and subsequent path of Ca and Mg, bound as minerals in rock, and released as cations in rivers. The fractionation of Ca and Mg isotope ratios may prove useful for tracing mechanisms of chemical alteration. Ca isotope ratios of solute riverine Ca show a greater variability than previously acknowledged. The variability of Ca isotope ratios in modern rivers will need to be better quantified and accounted for in future models of global Ca cycling, if past variations in oceanic Ca isotope ratios are to be of use in constraining the past carbon cycle.     

Using Synthetic Aperture Radar Imagery for Flood Modelling

Airborne radar technology has traditionally been largely devoted to military applications. In recent years, applications in telecommunications, oil exploration and agriculture have proved that radar technology can also be used commercially. This paper focuses on an application of airborne radar technology in the insurance industry and describes the development of a large-scale flood risk assessment model for the River Thames. The model is based upon airborne Synthetic Aperture Radar (SAR) data and was built with commonly used Geographic Information Systems (GIS) and image processing tools. From the Orthorectified Images (ORIs) a land cover map was produced, from which a surface roughness map could be derived. A Digital Elevation Model (DEM) was processed to remove trees and other soft barriers and obtain the effective ground level. This was achieved by using standard GIS processes. The methodology may be applicable to any organisation exposed to flood risk.     

Petrological and mineralogical characteristics of younger granites and pegmatites in the Wadi Haleifiya area,southeastern Sinai,Egypt

This study is concerned with the radioactivity and mineralogy of the younger granites and pegmatites in the Wadi Haleifiya area, southeastern Sinai Peninsula, Egypt. The area is occupied by metasediments, migmatites, older and younger granites. Most of these rocks, especially granites, are dissected by mafic and felsic dykes as well as pegmatites. The younger granites are represented by three main varieties: monzogranites, syenogranites and alkali feldspar granites. The monzogranite consists essentially of quartz, plagioclase, potash feldspar and biotite with minor musco-vite. Iron oxide, titanite, zircon and allanite are the main accessory minerals. Syenogranite is massive, medium- to coarse-grained and commonly exhibits equigranular and hypidiomorphic textures. It is made up essentially of potash feldspar, quartz, plagioclase and biotite. Iron oxides, allanite, epidote, titanite, and zircon are accessory minerals. The alkali feldspar granite consists mainly of perthite, quartz, alkali amphibole (arfvedsonite and riebekite), biotite, sub-ordinate plagioclase and aegirine. Iron oxide, zircon and apatite are accessory minerals, whereas chlorite and sas-surite are secondary minerals. The altered monzogranite and pegmatite recorded high radioelement contents. The eU reaches up to 120 (av.=82×10-6) in the altered monzogranite and up to 55 (av.=27×10-6) in the pegmatites. The high radioactivity in the altered monzogranite is due to the presence of thorite, uranothorite and metamict zircon. In the pegmatites, it is re-lated to the presence of uranophane, uranothorite, thorite, zircon, samarskite, monazite, xenotime, magnetite, ilmen-ite, hematite and rutile.     

Significance of the clay mineral distribution in fluvial sediments of the Neogene to Recent Himalayan Foreland Basin (west‐central Nepal)

Clay mineral assemblages of the Neogene Himalayan foreland basin are studied to decipher their significance with respect to tectonic and climate processes. Fluvial deposits of the Siwalik Group (west‐central Nepal), and sediment of the Ganga River drainage system were analysed for clay mineralogy. The observed clay mineral assemblages are mainly composed of illite (dominant), chlorite, smectite and kaolinite. Illite and chlorite are chiefly of detrital origin, derived from Himalayan sources. Kaolinite and smectite are authigenic, and mainly developed within pore space and as coating of detrital particles. With increasing burial, diagenetic processes affected the original clay mineral signature. Illitisation of smectite and kaolinite occurred below 2500 and 3500 m depth, respectively. Therefore, illite in the lower parts of the Siwalik Group consists of a mixture of inherited illite and illitised smectite and kaolinite, as suggested by illite crystallinity. Detrital grains that make up the framework of the Siwalik Group sandstones mainly consist of quartz, feldspar and lithic fragments, which are principally of sedimentary and metamorphic origin. Lithoclast content increases over time at the expense of quartz and K‐feldspar in response to uplift and erosion of the Lesser Himalaya Series since about 11–10 Ma. Despite mainly felsic source rocks, dominantly physical erosion processes in the Himalayan belt, and high‐energy fluvial depositional systems, smectite is abundant in the <7 Ma Siwalik Group deposits. Analyses of the Siwalik deposits and comparison with the clay mineralogy of the modern drainage system suggest that smectite preferentially formed in floodplains and intermontane valleys during early diagenesis because of downward percolating fluids rich in cations from weathering and soil development. In general, increasing seasonality and aridity linked to variability of the Asian monsoon from about 8 Ma enhanced clay mineral formation and development of authigenic smectite in paleo‐plains on the southern side of the Himalaya.     

Erosion-driven drawdown of atmospheric carbon dioxide: The organic pathway

Rapidly eroding, coastal mountain belts, where steep rivers and submarine channels connect upland sources to nearby marine sinks are hotspots of organic carbon transfer from life biomass, soil and exhumed bedrock into geological storage. Using observations from the Southern Alps of New Zealand, and Taiwan, we have mapped this organic pathway to geological carbon sequestration, and can evaluate the magnitude and efficiency of transfers between sources and sinks. We demonstrate that POC is harvested by landsliding, but importantly also by common and widespread surface runoff on steep hillslopes. Although terrestrially sourced POC is found in many sedimentary environments associated with mountain belts and frontier basins, it appears to be most abundantly trapped and preserved in marine turbidites. The loss of all forms of POC in onward transport through short, steep routing systems to this repository is limited. This is in marked contrast to larger routing systems, in which only the most resilient forms of POC survive into long-term deposition.     

Mg isotope heterogeneity in the Allende meteorite measured by UV laser ablation-MC-ICPMS and comparisons with O isotopes

First results from a new UV laser ablation MC-ICPMS method for measuring Mg isotope ratios in situ in meteoritical materials show that there are mass-dependent variations in δ²⁵Mg and δ²⁶Mg up to 1.5 ‰ per amu in chondrules and 0.3‰ per amu in a CAI from the Allende meteorite. In both cases the mass-dependent fractionation is associated with alteration. Comparisons with laser ablation O isotope data indicate that incorporation of pre-existing grains of forsterite with distinct Mg and O isotopic compositions and post-formation alteration both contributed to the variability in Mg isotope ratios in the chondrules, resulting in a correlation between high δ²⁵Mg and low Δ¹⁷O. The laser ablation analyses of the CAI show that high-precision determinations of both δ²⁵Mg and δ²⁶Mg can be used to discriminate features of the ²⁶Al-²⁶Mg isotope system that are relevant to chronology from those that result from element mobility.