Geochemical characteristics of stream sediments,sediment fractions,soils, and basement rocks from the Mahaweli River and its catchment,Sri Lanka

Geochemical variations in stream sediments (n = 54) from the Mahaweli River of Sri Lanka have been evaluated from the viewpoints of lithological control, sorting, heavy mineral concentration, influence of climatic zonation (wet, intermediate, and dry zones), weathering, and downstream transport. Compositions of soils (n = 22) and basement rocks (n = 38) of the catchment and those of <180 μm and 180–2000 μm fractions of the stream sediments were also examined. The sediments, fractions, soils and basement rocks were analyzed by X-ray fluorescence to determine their As, Pb, Zn, Cu, Ni, Cr, V, Sr, Y, Nb, Zr, Th, Sc, Fe₂O₃, TiO₂, MnO, CaO, P₂O₅ and total sulfur contents. Abundances of high field strength and ferromagnesian elements in the sediments indicate concentration of durable heavy minerals including zircon, tourmaline, rutile, monazite, garnet, pyriboles, and titanite, especially in <180 μm fractions. The sediments show strong correlation between Ti and Fe, further suggesting presence of heavy mineral phases containing both elements, such as ilmenite and magnetite. The basement rocks range from mafic through to felsic compositions, as do the soils. The river sediments lack ultrabasic components, and overall have intermediate to felsic compositions. Elemental spikes in the confluences of tributary rivers and high values in the <180 μm fractions indicate sporadic inputs of mafic detritus and/or heavy minerals to the main channel. Al₂O₃/(K₂O + Na₂O) and K₂O/Na₂O ratios of the sediments and LOI values of the soils correlate well with the climatic zones, suggesting intense weathering in the wet zone, lesser weathering in the intermediate zone, and least weathering in the dry zone. Low Sr and CaO contents and Cr/V ratios in stream sediments in the wet zone also suggest climatic influence. Fe-normalized enrichment factors (EFs) for As, Pb, Zn, Cu, Ni and Cr in stream sediments in the main channel are nearly all <1.5, indicating there is no significant environmental contamination. The chemistry of the sediments, rocks and the soils in the Mahaweli River are thus mainly controlled by source lithotype, weathering, sorting, and heavy mineral accumulation.     

Transportation and evolution of trace element bearing phases in stream sediments in a mining – Influenced basin (Upper Isle River,France)

Arsenic-bearing stream sediments enter the Upper Isle River, an Au mining-influenced basin (France), by the discharge of mining sites, tailings runoff and weathering of mineralized veins in granites and gneiss. Some fresh ochreous As-rich deposits on the river banks and in floodplains are identified as additional As-rich point sources (As between 0.07 and 6.5 wt.%). The <63 μm fraction of stream sediments contains elevated As bulk concentrations, ranging from 160 to 890 mg/kg, compared to the geochemical background (70 mg/kg on average). It is also enriched in Cd, Hg and W. Spatial variations of these trace elements show 3 significant increases corresponding to the 3 drained mining districts. They decrease down river but are still enriched 30 km downstream of the mining districts due to downstream transportation. Three types of trace element-bearing phases have been identified as: (i) detrital primary sulfides, with high in situ As percentages (up to 43.7 wt.%). They also carry significant amounts of W according to the differences in chemical compositions of the total and light <63 μm fractions. These sulfide particles do not show any sign of alteration in the oxygenated stream sediments; (ii) Secondary Fe–Mn oxyhydroxides,some with very high in situ As₂O₅ concentrations (up to 59.8 wt.%) and with about 40% of the total Cd composition. They occur as fresh precipitates in the river banks and floodplains and as discrete particles in stream sediments and (iii) Al–Si fine-grained phases. Their major element composition is highly variable with in situ As₂O₅ concentrations ranging between 430 and 5020 mg/kg. This type of solid phase is also the major carrier of Hg.     

Provenance, tectonics and source weathering of modern fluvial sediments of the Brahmaputra–Jamuna River, Bangladesh: Inference from geochemistry

This present study describes the elemental geochemistry of fluvial sediments in the Kurigram (upstream) to Sirajganj–Tangail (downstream) section of the Brahmaputra–Jamuna River, Bangladesh, with the aim of evaluating their provenance, weathering and tectonic setting. Petrographically, the sediments are rich in quartz (68%), followed by feldspars (8.5%) and lithic grains (7%). The bulk sediment chemistry is influenced by grain size. Concentrations of TiO₂, Fe₂O₃, MgO, K₂O, P₂O₅, Rb, Nb, Cr, V, Y, and, Ce, Th and Ga slightly decrease with increasing SiO₂/Al₂O₃ and grain size, suggesting clay matrix control. In contrast, concentrations of CaO, Na₂O, Sr and Pb increase with increasing SiO₂/Al₂O₃ and grain size, suggesting residence of these substances in feldspar. Decrease in Zr as grain size increases is likely controlled both by clay matrix and heavy minerals. In addition, heavy minerals' sorting also influences Ce, Th, Y and Cr abundances in some samples. The sediments are predominantly quartzose in composition with abundant low-grade metamorphic and sedimentary lithics, low feldspars and trace volcanic detritus, indicating a quartzose recycled orogen province as a source of the sediments. Discriminant diagrams together with immobile element ratio plots show that, the Brahmaputra–Jamuna River sediments are mostly derived from rocks formed in an active continental margin. Moreover, the rare earth element ratios as well as chondrite-normalized REE patterns with flat HREE, LREE enrichment, and negative Eu anomalies indicate derivation of the sediments of Brahmaputra–Jamuna River from felsic rock sources of upper continental crust (UCC). The chemical indices of alteration suggest that Brahmaputra–Jamuna River sediments are chemically immature and experienced low chemical weathering effects. In the A–CN–K ternary diagram, most of the samples close to the plagioclase–K-feldspar join line and to the UCC plot, and in the field of various lithologies of Higher Himalayan Crystalline Series, suggesting that rocks in these series are likely source rocks. Therefore, the elemental geochemistry of the Brahmaputra–Jamuna River sediments is controlled mostly by mechanical breakdown of lithic fragments and subsequent preferential attrition of muscovite > albite > quartz.     

Geochemical characteristics of modern river sediments in Myanmar and Thailand: Implications for provenance and weathering

The elemental composition of organic matter and the major and trace element compositions of stream sediments from Myanmar (Ayeyarwady and Sittaung rivers) and Thailand (Mekong and Chao Phraya rivers, and their tributaries) were determined to examine their distributions, provenance, and chemical weathering processes. Higher total organic carbon (TOC) and total nitrogen (TN) contents in the finer grained sediments indicate hydrodynamic energy may control their distributions. TOC/TN ratios indicate inputs of both aquatic macrophyte and higher vascular plant material to the river sediments. The major element abundances of the sediments are characterized by predominance of SiO₂ in coarser fractions and a marked negative correlation with Al₂O₃, representing primary grain size primarily control on SiO₂ content. Marked depletion of most labile elements (Na₂O, CaO, K₂O, Ba and Sr) relative to UCC (upper continental crust), indicate destruction of feldspar during chemical weathering in the source area or during transport. However, enrichment of some high field strength elements (Zr, Th, Ce and Y) relative to UCC and higher Zr/Sc ratios indicate moderate concentration of resistant heavy minerals in finer-grained samples. Discriminant diagrams and immobile trace element characteristics indicate that the Mekong, and Chao Phraya river sediments were largely derived from felsic sources with compositions close to typical rhyolite, dacite/granodiorite, UCC, I- and S-type granites. Relative enrichment of ferromagnesian elements (e.g. MgO, Cr, Ni) and high Cr/V and low Y/Ni ratios in Ayeyarwady and Sittaung sediments indicate the presence of a mafic or ultramafic component in their sources. The ICV (Index of Compositional Variability), CIA (Chemical Index of Alteration), PIA (Plagioclase Index of Alteration), α^Al, Rb/Sr and K₂O/Rb ratios indicate that the Ayeyarwady and Sittaung sediments record low to moderate degrees of chemical weathering in their source, compared to moderate to intense chemical weathering in the Mekong and Chao Phraya river basins. These results are compatible with existing major ion data for river waters collected at the same locations.     

Floodplain deposits: A geochemical archive of flood history – A case study on the River Rhine,Germany

Based on the correlation between discharge and carbonate content of the suspended load of the River Rhine, Germany, a systematic geochemical, mineralogical and granulometric study was carried out to verify whether this geochemical signal is transferred to floodplain deposits and in what way these sediments and their chemostratigraphic characterization can be used as a tool for the reconstruction of the river flood history. The analysis of the time resolved changes in the composition of particulate matter during a flood event revealed that the increase of carbonate content (represented by CaO, Sr) with discharge was coupled to a simultaneous decrease in the relative amount of siliciclastics (K₂O, Rb). The association of these two groups of diametrical parameters with specific grain size fractions (carbonates with 40–200 μm; siliciclastics with >200 μm) were found to be slightly shifted relative to each other and showed different gradients during the surging and fading flood wave. This, together with the covariance of elements pertaining to minerals with different density (e.g., carbonate and heavy minerals) suggests a chemical response to the changes in discharge, which is controlled primarily by hydraulic equivalence rather than grain size. There is also a time lag between the amount of suspended load and discharge, with a maximum in suspended load shortly after the peak discharge, when the flood has already started to abate. The flood plain sediments have similar composition to the suspended load, suggesting the direct transfer of the geochemical flood signal to the floodplain sediments.     

Effects of grain size distribution on mineralogical and chemical compositions: a case study from size‐fractional sediments of the Huanghe (Yellow River) and Changjiang (Yangtze River)

The influence of hydrodynamics on the chemical composition of sediments is based on the uneven distribution of element abundances in different size fractions. In this study, 72 size‐fractional sediments from the Huanghe (Yellow River) and Changjiang (Yangtze River) riverbeds were measured with XRD, SEM, ICP‐AES and ICP‐MS. The analysis results show that the mineral and chemical characteristics change with grain size in the Huanghe and Changjiang sediments. According to the principal components analysis, three independent geochemical factors were found. The first factor elements, Zr, Hf, Th, U, Y, La and TiO₂ are influenced by the existence of heavy minerals. The second factor elements, Al₂O₃, alkalis, alkaline earth (excluding Ca and Sr) and most of the transitional metals are dominated by clay minerals. The third factor group includes Ca and Sr, which were controlled by calcium‐bearing mineral contents and chemical weathering intensities. The various grain size distributions greatly affect the mineralogical and chemical compositions of bulk sediments. Compared to other size fractions, the 5–6PHI size fractions of the Huanghe and Changjiang sediments have special mineralogical and chemical compositions, and intermediate volume percentages. Weight or volume percentage of each size fraction may be more suitable than mean grain‐size of the bulk sediment to elucidate the grain size effects. Chemical Index of Alteration (CIA) values increase steeply with decreasing grain size, while Weathering Index of Parker (WIP) values are relatively stable. Because of the big influence of the abundance of clay minerals on CIA values, it is questionable to use CIA as a proxy of weathering intensity. Considering the clay mineral effects, stability in values and heterogeneous material properties, WIP has the potential to indicate the chemical weathering intensity of sediments. Copyright © 2014 John Wiley & Sons, Ltd.     

Sources of stream sediments in the granulite terrain of the Walawe Ganga Basin,Sri Lanka,indicated by rare earth element geochemistry

Thirty-eight samples of stream sediments draining high-grade metamorphic rocks in the Walawe Ganga (river) Basin, Sri Lanka, were analysed for their REE contents, together with samples of metamorphic suites from the source region. The metamorphic rocks are enriched in light REE (LREE) compared to heavy REE (HREE) and are characterised by high La/Lu ratios and negative Eu anomalies. The chondrite-normalised patterns for these granulite-grade rocks are similar to that of the average post-Archaean upper crust, but they are slightly enriched with La and Ce. The REE contents of the <63-μm fraction of the stream sediments are similar to the probable source rocks, but the other grain size fractions show more enriched patterns. The <63-μm stream sediments fraction contains lower total REE, more pronouncd negative Eu anomalies, higher Eu_N/Sm_N and lower La _N/Lu_N ratios relative to other fractions. The lower La _N/Lu_N ratio is related to the depletion of heavy minerals in the <63-μm fraction. The 63–125-μm and 125–177-μm grain size fractions of sediments are particularly enriched in LREE (average ΣLREE=2990 μg/g and 3410 μg/g, respectively). The total HREE contents are surprisingly uniform in all size fractions. However, the REE contents in the Walawe Ganga sediments are not comparable with those of the granulite-grade rocks from the source region of the sediments. The enrichment of REE is accounted for by the presence of REE containing accessory mineral phases such as zircon, monazite, apatite and garnet. These minerals are derived from an unknown source, presumably from scattered bodies of granitic pegmatites.     

Alteration of As-bearing phases in a small watershed located on a high grade arsenic-geochemical anomaly (French Massif Central)

At a watershed scale, sediments and soil weathering exerts a control on solid and dissolved transport of trace elements in surface waters and it can be considered as a source of pollution. The studied subwatershed (1.5 km²) was located on an As-geochemical anomaly. The studied soil profile showed a significant decrease of As content from 1500 mg kg⁻¹ in the 135–165 cm deepest soil layer to 385 mg kg⁻¹ in the upper 0–5 cm soil layer. Directly in the stream, suspended matter and the <63 μm fraction of bed sediments had As concentrations greater than 400 mg kg⁻¹. In all these solid fractions, the main representative As-bearing phases were determined at two different observation scales: bulk analyses using X-ray absorption structure spectroscopy (XAS) and microanalyses using scanning electron microscope (SEM) and associated electron probe microanalyses (EPMA), as well as micro-Raman spectroscopy and synchrotron-based micro-scanning X-ray diffraction (μSXRD) characterization. Three main As-bearing phases were identified: (i) arsenates (mostly pharmacosiderite), the most concentrated phases As in both the coherent weathered bedrock and the 135–165 cm soil layer but not observed in the river solid fraction, (ii) Fe-oxyhydroxides with in situ As content up to 15.4 wt.% in the deepest soil layer, and (iii) aluminosilicates, the least concentrated As carriers. The mineralogical evolution of As-bearing phases in the soil profile, coupled with the decrease of bulk As content, may be related to pedogenesis processes, suggesting an evolution of arsenates into As-rich Fe-oxyhydroxides. Therefore, weathering and mineralogical evolution of these As-rich phases may release As to surface waters.     

Geochemistry,provenance and tectonic setting of the Late Cambrian–Early Ordovician Seydişehir Formation in the Çaltepe and Fele areas,SE Turkey

The major, trace and rare earth element (REE) contents of metapelite (MPL), metapsammite (MPS) and metamarl (MM) samples from the Cambro-Ordovician Seydi?ehir Formation were analyzed to investigate their provenance and tectonic setting. The MPS, MPL, and MM samples have variable SiO₂ concentrations, with average values of 72.36, 55.54, and 20.95 wt%, moderate SiO₂/Al₂O₃ ratios (means of 6.88, 3.23, and 3.80), moderate to high Fe₂O₃ + MgO contents (means of 5.14, 9.55, 3.56 wt%), and high K₂O/Na₂O ratios (means of 3.26, 3.64, 2.90), respectively. On average, the chemical index of alteration (CIA) values of the MPS and the MPL are 65.87 and 71.96, respectively, while the chemical index of weathering (CIW) values are 74.54 and 85.09, respectively. These data record an intermediate to high degree of alteration (weathering) of plagioclase to illite/kaolinite in the samples’ provenance. The chondrite-normalized REE patterns of all the sample groups are similar and are characterized by subparallel light rare earth elements (LREE)-enriched, relatively flat heavy rare earth elements (HREE) patterns with pronounced Eu anomalies (mean of 0.69) and moderate fractionation [average (La/Yb)_N = 8.7]. Plots of sediments in ternary diagrams of La, Th, Sc and elemental ratios (La/Sc, Th/Sc, Cr/Th, Eu/Eu*, La/Lu, Co/Th, La/Sc and Sc/Th), which are critical for determining provenance, and REE patterns indicate that the metaclastic units of the Seydi?ehir Formation were derived dominantly from felsic to intermediate magmatic rocks and not from a mafic source. The La–Sc–Th and Th–Sc–Zr/10 ternary diagrams of the Seydi?ehir Formation are typical of continental island arc/active continental margin tectonic settings. The geologic location and geochemistry of the Seydi?ehir Formation suggest that it was deposited in an Andean-type retroarc foreland basin during the Late Cambrian–Early Ordovician period. The Neoproterozoic intermediate to felsic magmatic rocks and metaclastic sediments with felsic origins of the Sand?kl?–Afyon Basement Complex (SBC) and their equivalent units, which are thought to be overlain by the younger units in the study area, may be the dominant source rocks for the Seydi?ehir Formation.     

Detection of manure-derived organic compounds in rivers draining agricultural areas of intensive manure spreading

It is essential to have suitable tools able to trace the fate of manure organic matter in the environment to assess whether manure disposal on the soils of catchments could affect the organic quality of rivers. Sterol compounds – mainly expressed as C_29 + 28/C₂₇ and 5β/C₂₇ ratios – have been shown to be specific molecular tracers of pig, dairy and poultry manures in soils. The objective of this study was to measure C_29 + 28/C₂₇ and 5β/C₂₇ ratios in five Brittany rivers (Elorn, Yar, Léguer, Min Ran and Couesnon) draining agricultural catchments receiving massive annual inputs of pig, poultry and dairy manures and compare these ratios with ratios published for enriched soils and manure samples. The particulate organic fractions from the studied rivers yielded steroid signatures typical of animal manures. More specifically, a stanol compound diagnostic of pig slurry – the 5β-stanol known as coprostanol – was found to be very widespread, with particularly high concentrations in one of the rivers (Elorn). The C_29 + 28/C₂₇ and 5β/C₂₇ ratios of the particulate fractions of the rivers were compared with ratios measured directly in pig, dairy and poultry manure samples, as well as with the breeding activities on river catchments. These comparisons show that the steroid profiles of the five investigated rivers correlate closely with the types of manure (i.e. pig, poultry or dairy) spread on soils in their catchments. For instance, the C_29 + 28/C₂₇ and 5β/C₂₇ ratios in the Elorn river are similar to the values typical of pig slurry (e.g. 5β/C₂₇ > 4); compared with other catchments, the soils in this area receive by far the largest amount of pig slurry. By contrast, the Yar river drains a catchment receiving only poultry and dairy manures, and its soils exhibit C_29 + 28/C₂₇ and 5β/C₂₇ ratios similar to those of dairy and poultry manures (e.g. 5β/C₂₇ ∼ 1). Thus, this study indicates that the organic quality of rivers is modified in catchments where there is intense manure spreading on soils. It also provides evidence that rivers draining areas receiving different manure types may exhibit differences in the long-term evolution of their OM content. Indeed, two of the investigated river catchments receive dominantly dairy and poultry manure, and exhibit clear long-term upward trends in OM. On the other hand, one catchment receiving high proportions of pig slurry clearly shows a long-term downward trend in OM contents. A survey of the literature shows that the relative amount of OM and N received by soils in agricultural catchments could be the key parameter in determining the direction of the long-term OM trend of the river, rather than the absolute amount and/or type of manure that is applied to the soil. In any case, the present study suggests that sterol/stanol compounds may be of diagnostic value in determining whether a stream or a river is undergoing contamination by manure-derived organic matter.     

How important is it to integrate riverine suspended sediment chemical composition with depth? Clues from Amazon River depth-profiles

The vertical variability in mineralogical, chemical and isotopic compositions observed in large river suspended sediments calls for a depth-integration of this variability to accurately determine riverine geochemical fluxes. In this paper, we present a method to determine depth-integrated chemical particulate fluxes of large rivers, based on river sampling along depth-profiles, and applied to the Amazon Basin lowland tributaries. The suspended particulate matter (SPM) concentration data from depth-profiles is modeled for a number of individual grain size fractions using the Rouse model, which allows to predict the grain size distribution of suspended sediment throughout the whole river cross-section. Then, using (1) the relationship between grain size distribution and the Al/Si ratio (2) relationships between the Al/Si ratio and the chemical concentrations, the chemical composition of river sediment is predicted throughout the river cross-section, and integrated to yield the depth-integrated chemical particulate flux for a number of chemical elements (e.g. Si, Al, Fe, Na, REEs, …). For elements such as Al, Fe, REEs, Th, the depth-integrated flux is around twice as high as the one calculated from river surface sample characteristics. For Na and Si, the depth-integrated flux is three times higher than the “surface” estimate, due to the enrichment of albite and quartz at the bottom of the river. Depth-integrated ⁸⁷Sr/⁸⁶Sr composition of suspended sediment, also predictable using this method, differs by more than 10⁻³ from the surface sample composition.Finally, potential implications of depth-integrated estimates of Amazon sediment chemistry are explored. Depth-integration of particulate ⁸⁷Sr/⁸⁶Sr isotopic ratios is necessary for a reliable use of Sr isotopes as a provenance tracer. The concept of steady-state weathering of a large river basin is revisited using depth-integrated sediment composition. This analysis shows that, in the Amazon Basin river, the previously observed discrepancy between (1) weathering intensities of channel surface sediment and (2) silicate-derived dissolved fluxes is only slightly accounted for by the vertical variability of suspended sediment weathering intensities. This observation confirms that most large rivers basins are not eroding at steady-state.     

Pleistocene chemical weathering history of Asian arid and semi-arid regions recorded in loess deposits of China and Tajikistan

Quaternary loess-soil sequences in China and Tajikistan are valuable archives of the chemical weathering history for arid and semi-arid regions of Asia. The development of new proxies independent of grain size are vital to reconstruct the long-term chemical weathering history of eolian deposits. In this study, we analyze major elemental and Rb, Sr, and Ba concentrations of decarbonated residue from representative loess and soil units along a north-south transect on the Chinese Loess Plateau and compare these concentrations among different grain-size fractions. Results show that most of the elemental abundances and ratios vary considerably among different grain-size fractions for both loess and paleosols, indicating transport-driven compositional differentiation of minerals during subaerial transport. However, (CaO + Na₂O + MgO)/TiO₂ ratios show little variation among different size fractions for the loess-soil transect. Loess-soil sequences at Lingtai (northern China) and Chashmanigar (southern Tajikistan) for the past 1.50-1.77 Ma show lower (CaO + Na₂O + MgO)/TiO₂ ratios in soil units than in adjacent loess horizons, in good agreement with greater weathering intensity in soils than in loess units. The (CaO + Na₂O + MgO)/TiO₂ ratio of the decarbonated residue is therefore a reliable proxy for chemical weathering of loess deposits that is independent of grain size. The (CaO + Na₂O+MgO)/TiO₂ ratios of the Lingtai and Chashmanigar sections display a relatively regular oscillation within a narrow range in the early Pleistocene, and a rapid increase in average values and in variance from 0.85-0.6 Ma to the present, indicating lowered chemical weathering intensity in both the dust source regions and the depositional areas. This event may be causally related to the expansion of northern hemisphere ice and/or the regional tectonic uplift of high mountains in Asia since the mid-Pleistocene.     

Geochemistry of late quaternary sediments from Tecocomulco lake, central Mexico: Implication to chemical weathering and provenance

This paper presents the first detailed multi-element geochemical data from the late Quaternary sediments of the Tecocomulco lake basin (central Mexico) and rocks exposed in the basin catchments to understand the extents of chemical weathering and provenance of the siliciclastic fractions. Ternary diagrams of A-CN-K, A-C-N and A-CNK-FM and elemental ratios suggest that most of the lacustrine sediments were derived from mafic volcanic deposits comprising the Chichicuatla and the Apan-Peñon andesites and the Apan-Tezontepec basaltic-andesites. The felsic tephra layers have chemical compositions comparable to the Acoculco volcanic sequences. The calculated indices of chemical weathering such as chemical index of alteration (CIA), plagioclase index of alteration (PIA) and chemical index of weathering (CIW) indicate low to extreme chemical weathering for the lacustrine sediments and low chemical weathering for tephra layers. The varying degree of chemical weathering in lacustrine sediments is related to the fluctuating average annual precipitation during the late Quaternary. However, the low weathering of tephra layers are due to their higher rate of deposition. The dacite-rhyolitic tephra layers of ca. 31,000 ¹⁴C yr BP are relatively more weathered compared to the unweathered rhyolitic tephra of ca. 50,000 ¹⁴C yr BP. This could be due to the rapid deposition of ca. 200 cm of tephra layers during the ca. 50,000 ¹⁴C yr BP volcanic eruption that might have prevented the interaction between tephra layers and weathering agents.     

Geochemistry and provenance of bed sediments of the large rivers in the Tibetan Plateau and Himalayan region

We investigated the geochemical characteristics of major, trace and rare earth elements and Sr–Nd isotope patterns of bed sediments from the headwaters and upper reaches of the six large rivers draining the Tibetan Plateau (the Jinsha River—Yangtze, Lancang River—Mekong, Nujiang River—Salween, Huang He—Yellow, Indus, and Yarlung Tsangpo—Brahmaputra). By using Ca/Al versus Mg/Al, La/Sc versus Co/Th, and ⁸⁷Sr/⁸⁶Sr versus ε_Nd (0) binary differentiation diagrams of provenance, some typical contributors to the different catchment sediments can be identified. In the Three-River (the Jinsha, Lancang, and Nujiang Rivers) tectonomagmatic belt, acidic–intermediate-acidic volcanic rocks are very important provenance of sediments. Carbonate rocks and Permian Emeishan basalts are dominant in the Jinsha River. The Yellow River sediments have similar geochemical characteristics with loess in catchments. The Indus and Yarlung Tsangpo Rivers sediments are mainly from ultra-K volcanic rocks and Cenozoic granitoids widely distributed in the Indus–Yarlung suture. The intensity of chemical weathering in these river catchments is evaluated by calculating the chemical indices of alteration (CIA) of sediments and comparing them with bedrocks. The CIA values of the six river sediments are from 46.5 to 69.6, closing to those of bedrocks in the corresponding catchment, which indicates relatively weak chemical weathering intensity. Lithology, climate, and topography affect the chemical weathering intensity in these river catchments.     

The CO2 system in rivers of the Australian Victorian Alps: CO2 evasion in relation to system metabolism and rock weathering on multi-annual time scales

The patterns of dissolved inorganic C (DIC) and aqueous CO₂ in rivers and estuaries sampled during summer and winter in the Australian Victorian Alps were examined. Together with historical (1978–1990) geochemical data, this study provides, for the first time, a multi-annual coverage of the linkage between CO₂ release via wetland evasion and CO₂ consumption via combined carbonate and aluminosilicate weathering. δ¹³C values imply that carbonate weathering contributes ∼36% of the DIC in the rivers although carbonates comprise less than 5% of the study area. Baseflow/interflow flushing of respired C3 plant detritus accounts for ∼50% and atmospheric precipitation accounts for ∼14% of the DIC. The influence of in river respiration and photosynthesis on the DIC concentrations is negligible. River waters are supersaturated with CO₂ and evade ∼27.7 × 10⁶ mol/km²/a to ∼70.9 × 10⁶ mol/km²/a CO₂ to the atmosphere with the highest values in the low runoff rivers. This is slightly higher than the global average reflecting higher gas transfer velocities due to high wind speeds. Evaded CO₂ is not balanced by CO₂ consumption via combined carbonate and aluminosilicate weathering which implies that chemical weathering does not significantly neutralize respiration derived H₂CO₃. The results of this study have implications for global assessments of chemical weathering yields in river systems draining passive margin terrains as high respiration derived DIC concentrations are not directly connected to high carbonate and aluminosilicate weathering rates.     

白水黄土-红粘土化学风化强度的剖面特征与粒度效应

白水剖面黄土-红粘土全样化学分析表明,以CIA指数为代表的化学风化强度从剖面下部往上逐步变弱,波动增大,总体趋势与深海氧同位素代表的全球冰量变化可以很好对比。分粒级组分化学分析则显示,黄土-红粘土主要元素迁移及化学风化强度与粒度强烈相关,CIA指数表征的化学风化强度变化在相当程度上受到粒度变化的控制。总体上,黄土-红粘土各粒级颗粒的风化程度都不高,而且沉积之后的成土风化作用对其主要元素含量的影响有限,黄土-红粘土化学成分的长期变化趋势主要受到物源的新加入和混合过程的影响。从剖面变化看,粗粒级部分(5～20μm和20～63μm)的风化指数的变化特征与细粒级部分(<5μm)不完全相同,表明不同粒级组分接受化学风化以及在物源区停留的历史不尽相同。1Ma以来,各粒级CIA指数都整体降低,显示物源区新鲜、弱风化碎屑影响到各粒级颗粒的混合过程。进一步对细粒级部分(<5μm)化学成分演化进行的分析显示,其元素含量呈现不同组分递次变化的"序列模式",从红粘土下部(约4.5Ma)到黄土上部(约0.6Ma),K₂O/Al₂O₃,Na₂O/Al₂O₃,CaO/Al₂O₃和MgO/Al₂O₃比率的变化依次出现转折,这很可能与晚新生代黄土-红粘土物源区构造抬升、冰川剥蚀能力不断加大,使得新鲜基岩不断被剥蚀、去顶,由此造成主要造岩矿物顺序剥蚀、接受风化,成为粉尘新物源有关。     

Particulate-associated potentially harmful elements in urban road dusts in Xi’an,China

Sixty five urban road dust samples were collected from different land use areas of ∼240 km² in Xi’an, China. The concentrations of Ag, As, Cr, Cu, Hg, Pb, Sb and Zn were determined to investigate potentially harmful element (PHE) contamination, distribution and possible sources. In addition, the concentrations in different size fractions were measured to assess their potential impact on human health. The highest concentrations were found in the fraction with particle diameters between 80 μm and 101 μm, the finest particles (<63 μm) were not the most important carriers for Ag, As, Cd, Cr, Cu, Hg, Pb and Zn. The percentages of these elements in particles with diameters less than 63 μm (PM₆₃) and less than 101 μm (PM₁₀₁) were in the range of 7–15%, and 30–55%, respectively. Three main factors influencing element distributions have been identified: (a) industrial activities; (b) prior agricultural land use; and (c) other activities commonly found in urban areas, such as traffic, coal combustion, waste dumping, and building construction/renovation. The highest concentrations were found in industrial areas for As (20 mg kg⁻¹), Cr (853 mg kg⁻¹), Cu (1071 mg kg⁻¹), Pb (3060 mg kg⁻¹) and Zn (2112 mg kg⁻¹), and in previous agricultural areas for Ag and Hg, indicating significant contributions from industrial activities and prior agricultural activities.     

Time scale and conditions of weathering under tropical climate: Study of the Amazon basin with U-series

The Rio Solimões/Amazonas (Amazon River) and its major tributaries have been analyzed for U-series nuclides. ²³⁸U-²³⁴U-²³⁰Th-²²⁶Ra disequilibria have been measured in the dissolved (<0.2 μm) and suspended loads (>0.2 μm) as well as bed sands. U-series disequilibria are closely related to major and trace element compositions and therefore reflect elemental fractionation during chemical weathering. Moreover, while the dissolved load records present-day weathering, suspended particles integrate the erosion history over much longer time scales (>100 ka). Lowland rivers are characterized by long time scales of chemical erosion (?100 ka) resulting in a high weathering intensity. Moreover, exchange between suspended particles and the dissolved load may explain the U-series signature for these rivers. By combining U-series and Pb isotopes in suspended particles, we show that erosion in the Rio Madeira basin occurred as a multi-step process, whereby the pristine continental crust was eroded several hundreds of Ma ago to produce sediments that have then been integrated in the Cordillera by crustal shortening and are currently eroded. In contrast, recent erosion of a pristine crust is more likely for the Rio Solimões/Amazonas (<10 ka). The suspended particles of the rivers draining the Andes (Solimões/Amazonas, Madeira) suggest time scales of weathering ranging between 4 and 20 ka. This indicates that suspended particles transported by those rivers are not stored for long periods in the Andean foreland basin and the tropical plain. The sediments delivered to the ocean have resided only a few ka in the Amazon basin (6.3 ± 1 ka for the Rio Amazonas at Óbidos). Nevertheless, a large fraction of the sediments coming out from the Andes are trapped in the foreland basin and may never reach the ocean. Erosion in the Andes is not operating in steady state. U-series systematics shows unambiguously that rivers are exporting a lot more sediments than predicted by steady-state erosion and that is a consequence of soil destruction greater than production. By relating this observation to the short time scales of weathering inferred for the Andes (a few ka), it appears that the erosion regime has been recently perturbed, resulting in high denudation rates. A possible explanation would be the increase in precipitation less than 5 ka proposed by recent paleoclimatic studies. Our results indicate that erosion responds rapidly to high-frequency climatic fluctuations.     

Metal speciation in rivers affected by enhanced soil erosion and acidity

Dissolved (<1 kDa), colloidal (1 kDa–0.45 μm) and particulate (>0.45 μm) size fractions of 30 elements were determined for four rivers (Sirppujoki, Laajoki, Mynäjoki and Paimionjoki), including 12 low-order inflow streams, largely affected by soil erosion and acidity in SW Finland. In addition, geochemical modelling was used to predict the formation of free ions and complexes in these rivers. Total metal concentrations were relatively high but most of the elements occurred mainly in a colloidal or particulate form and even elements expected to be very soluble occurred to a large extent in colloidal form. According to geochemical modelling these patterns could be explained by in-stream metal complexation/adsorption only to a limited extent. Instead there were strong indications that the high metal concentrations and dominant solid fractions were largely caused by erosion of metal bearing phyllosilicates. A strong influence of acid sulphate (AS) soils, known to exist in the catchment, could be clearly distinguished in Sirppujoki river as it had very high concentrations of dissolved metals, while in the two nearby rivers (Laajoki and Mynäjoki) the influence of AS soils was largely masked by eroded phyllosilicates. In Paimionjoki river the colloidal and particulate fractions dominated very strongly, indicating that total metal concentrations are almost solely controlled by erosion of phyllosilicates. Consequently, rivers draining clay plains sensitive to erosion, like those in SW Finland, have generally high “background” metal concentrations due to erosion of relatively non-toxic colloidal/particulate phyllosilicates. Thus, relying on only semi-dissolved (<0.45 μm) concentrations obtained in routine monitoring and/or speciation modelling can lead to a great overestimation of the water toxicity in this environment.     

Lower Palar River Sediments,Southern Peninsular,India: Geochemistry,Source-Area Weathering,Provenance and Tectonic Setting

This present study describes the geochemistry of fluvial sediments of the Palar river (lower reaches), Southern Peninsular India, with an aim to evaluate their provenance, weathering and tectonic setting. The bulk sediment chemistry is influenced by grain size. The river sediments are enriched with SiO₂ and depleted in Al₂O₃, K₂O, CaO, Na₂O, MgO, P₂O₅, MnO, Fe₂O₃ as compared with UCC values. Geochemical classification indicate that the sediments are mainly arkose, wacke and shale in composition. Discriminant diagrams together with immobile element ratio plots reveal that, the Palar river sediments are mostly derived from rocks formed in an active continental margin. Additionally, the rare earth element ratios as well as chondrite-normalized REE patterns with flat HREE, LREE enrichment, and negative Eu anomalies indicate felsic rock sources. The chemical indices of alteration suggest that Palar river sediments are chemically immature and have experienced low chemical weathering effects. This is further supported by the Th/U Rb/Sr ratio and A-CN-K ternary diagram, with most of the sample data points falling close to the plagioclase-smectite line. The bivariate plot of Th/Sc versus Zr/Sc suggest a moderate recycled origin of the sediments.