Crystal chemistry of suspended matter in a tropical hydrosystem, Nyong basin (Cameroon, Africa)

Suspended matter (SM) from the Nyong basin (Cameroon, Africa), a tropical watershed, was collected by tangential flow ultrafiltration to separate particulate (>0.45 μm) and colloidal (<0.45 μm; >20 kDa) fractions. In this basin, two distinctive systems in a selected small catchment (Nsimi–Zoétélé) of the Nyong river basin have been considered: (i) colourless water (groundwater and spring) with a low suspended load (<3 mg/l) and a low total organic carbon content (TOC<1 mg/l) and (ii) coloured water (Mengong brook and Nyong river), which is organic rich (TOC>10 mg/l) and contains higher amounts of SM (10–20 mg/l) than the colourless water. Freeze-dried samples of SM have been analysed by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), electron paramagnetic resonance spectroscopy (EPR), and visible diffuse reflectance spectroscopy (DRS).

Colourless water mainly contains mineral phases, such as poorly ordered kaolinite, plus quartz and goethite in the particulate fraction, and euhedral kaolinite plus amorphous iron oxyhydroxides in the colloidal fraction. In contrast, the SM in coloured water is mainly organic in nature. The mineral phases in the particulate fraction are similar to those from clear water, but with additional phytoliths and diatom frustules composed of biogenic opal. In the colloidal fraction, complexation of Fe³⁺ and Mn²⁺ with organic matter is evidenced by EPR, together with significant occurrence of Fe oxyhydroxides associated with organic matter.

The sites of Al, Si, Fe, Mn in colloidal fractions derived from spectroscopic analyses are discussed with reference to chemical analyses performed by inductively coupled plasma mass spectrometry. Most of the observed solid phases or species correspond to those expected from published thermodynamic calculations for the same hydrosystem, except the colloidal iron oxyhydroxides in the coloured water. The presence of such iron phases is emphasised since they are expected to have large sorption capacities for numerous trace elements.

The crystal chemistry of SM is used to discuss the origin of the mineral particles transported from the soil to the main rivers in terms of mechanical and chemical erosion processes.     

青藏高原东部金沙江流域盆地陆地风化特征

青藏高原东部金沙江流域是研究高原隆升与陆地风化的理想地区。本文通过对金沙江河流系统的取样,从河流溶质载荷主要离子和悬浮载荷粘土矿物等方面揭示青藏高原东部金沙江流域盆地陆地风化特征。研究表明,金沙江流域盆地陆地岩石风化主要是碳酸盐岩、蒸发盐岩和硅酸盐岩。利用S i、S i/TZ+*、S i/Na*+K和S i/K以及(Na*+K)/TZ+等5个指标结合流域区域岩石分布和土壤特征揭示出流域硅酸盐岩为浅表性初级风化,风化产物主要是富含阳离子的次生粘土矿物。     

Hydrogeochemical controls and usability of groundwater in the semi-arid Mayo Tsanaga River Basin: far north province,Cameroon

Deuterium, δ ¹⁸O, major ions and dissolved silica in groundwater from semi-arid Mayo-Tsanaga river basin in the Far North Province, Cameroon were used to trace hydrogeochemical processes that control their concentrations and to explore for usability of the water. Electrical conductivity ranges from 57–2,581 μs/cm with alternating low and high values along the hydraulic gradient. Waters from piedmont alluvium show low concentrations in major cations, which peak in Mg within basalt, Na within plain alluvium, and Ca within basalt and the sandy Limani-Yagoua ridge. The initial dominant groundwater composition is CaHCO₃, which did not evolve within the basalt and piedmont alluvium, but evolved to NaHCO₃ in the granite and plain alluvium. The main processes controlling the major ions composition include the following: (1) dissolution of silicates and fluorite; (2) precipitation of fluorite and carbonate; (3) cation exchange of Ca in water for Na in clay; (4) and anthropogenic activities. The δD and δ ¹⁸O ratios vary from −35 to 0.7 and −5.3 to 1.1‰, respectively. The lowest and highest isotope ratios are observed in groundwater within the downstream sandy Limani-Yagoua ridge and the upstream graintes respectively. Variation in isotope ratios depends on altitude effect of −0.48‰ per 100 m between 600 and 850 m asl, and on evaporation, which had insignificant effect on the water salinity. Seventy percent of the groundwater shows poor drinking quality and 90% is suitable for irrigation. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

砒砂岩区小流域沟冻融风化侵蚀模型研究

文章通过砒砂岩区西召沟小流域冻融风化侵蚀实测资料,分析了冻融风化侵蚀与沟道各变量之间的关系。确定了该流域相同种类支沟上、中、下游的冻融风化坡面侵蚀模数、单位沟沿线沟角线长度和侵蚀量值,不同种类支沟冻融风化坡面蚀模数及单位长度沟沿线沟角线长度和的侵蚀量的比例关系,及上、中、下游冻融风化侵蚀侵蚀量的比例关系。据此建立了小流域单位长度沟沿线沟角线冻融风化侵蚀量比例模型和冻融风化侵蚀模数比例模型。根据西召沟小流域上游20条沟谷的资料,利用两种模型对该流域的冻融风化侵蚀量进行了模拟计算,两种模型的模拟计算结果分别为23757．9t和29165．1t,相差18．5％。     

Soil and plant composition in the Noun river catchment basin,Western Cameroon: a contribution to the development of a biogeochemical baseline

Soils and selected edible plants of the Noun river catchment basin of western Cameroon were sampled to investigate the distribution of trace elements, based on the preliminary idea of unusual anomalies. Analytical techniques for trace elements included ICP-AES, GF-AAS, and ICP-MS. Further soil analyses comprised the mineralogy and contents of the biogenic elements carbon, nitrogen and sulphur (CNS). The trace element concentrations in the soils reflect those of the lithogeochemical background of the pluto-volcanic rocks of the region. This is consistent with the results from the mineralogical analyses and physicochemical parameters such as pH, taken in the field, which also do not suggest any geochemical anomaly. Most trace elements analyzed in the plants showed concentrations that reflect those of the soils (Al, Fe, Ti, and Rb). However, some trace elements were enriched in the plants as compared to the soils, such as Zn, Cu, Cd, Mo (excluding yam), Ni (peanut), Ba (peanut), Sr (peanut, bean), and B. Trace elements such as As, Cr, V, and Se were not bioavailable for all the analyzed plants. Besides, trace elements such as Cu, Zn, Mo, Fe, Al, Ni, B, Ti, Rb, Cs, and Ba were in the range of phytotoxicity and reached or exceeded human food tolerance level (Cu). The plants with seeds showed a higher absorption of trace elements compared to plants with tubercles.     

Areal versus linear evaluation of relationship between drainage basin lithology and geochemistry of stream and overbank sediments in low-order mountainous drainage basins

The comparison of two multiple regression models is based on the assumption that geochemical composition of the drainage basin alluvial sediments is derived primarily from the underlying bedrock lithology. The parent material is integrated with both stream sediment and overbank sediment geochemistry via the two essentially different approaches as regards the drainage basin geomorphological data: (1) as the relative area of influence representing a portion of the catchment basin occupied by a specific rock type and (2) as the relative “line” of influence representing a narrow zone of the underlying bedrock traversed by the perennial streams which form the active stream network. The model comparison is established on the goodness-of-fit test for both experimental designs and for the same set of data. Both experiments converge on the linear approach as the more appropriate model in evaluating the lithologic influence on the analysed sample media in small mountainous watersheds.     

Relationships between major and trace elements during weathering processes in a sedimentary context: Implications for the nature of source rocks in Douala,Littoral Cameroon

In Douala (Littoral Cameroon), the Cretaceous to Quaternary formation composed of marine to continental sediments are covered by ferrallitic soils. These sediments and soils have high contents of SiO₂ (≥70.0 wt%), intermediate contents of Al₂O₃ (11.6–28.4 wt%), Fe₂O₃ (0.00–20.5 wt%) and TiO₂ (0.04–4.08 wt%), while K₂O (≤0.18 wt%), Na₂O (≤0.04 wt%), MgO (≤0.14 wt%) and CaO (≤0.02 wt%) are very low to extremely low. Apart from silica, major oxides and trace elements (REE included) are more concentrated in the fine fraction (<62.5 μm) whose proportions of phyllosilicates and heavy minerals are significant. The close co-associations between Zr, Hf, Th and ∑REE in this fraction suggest that REE distribution is controlled by monazite and zircon. CIA values indicate intense weathering. Weathering products are characterized by the association Al₂O₃ and Ga in kaolinite; the strong correlation between Fe₂O₃ and V in hematite and goethite; the affinity of TiO₂ with HFSE (Hf, Nb, Th, Y and Zr) in heavy minerals. The ICV values suggest mature sediments. The PCI indicates a well-drained environment whereas U/Th and V/Cr ratios imply oxic conditions. La/Sc, La/Co, Th/Cr, Th/Sc and Eu/Eu* elemental ratios suggest a source with felsic components. Discrimination diagrams are consistent with the felsic source. The REE patterns of some High-K granite and granodiorite of the Congo Craton resemble those of the samples, indicating that they derive from similar source rocks.     

黔中小流域水体C、S同位素特征及主要风化过程

选取贵州省红枫湖流域四条支流为研究对象,通过对水体中C、S元素浓度及稳定同位素特征的分析,探讨了典型碳酸盐小流域的主要风化过程对流域C、S循环的贡献。红枫湖流域河水中的C同位素组成在-7．47‰--11．68‰之间,硫酸根浓度为295．5～1315．6μmol／L,除受当地煤矿影响较大的区域外,其余部分水体中离子的δ^34S值在-3‰--7‰之内,反映了这些河段中硫化物矿物的氧化的影响。通过质量守恒的方法,得到硫化物的氧化、蒸发岩溶解以及大气输入对河水硫酸根离子的贡献率分别为63．8％、30．8％和5．4％。来自硫酸对碳酸盐岩、碳酸对碳酸盐岩以及碳酸对硅酸盐岩风化的DIC比例为1：3．58：1．37,三种不同的风化过程对区域二氧化碳的净吸收量为7．97×10^9mol／a。     

Natural and anthropogenic budgets of a small watershed in the massif central (France): Chemical and strontium isotopic characterization of water and sediments

A small watershed (160 km²) located in the Massif Central (France) has been chemically, isotopically and hydrologically studied through its dissolved load, bed sediments and soils. This watershed is underlain by basaltic bedrock and associated soils in which the vegetation is dominated mainly by meadows.Dissolved concentrations of major ions (Cl, SO₄, NO₃, HCO₃, Ca, Na, Mg, K, Al and Si), trace elements (Rb and Sr) and strontium isotopes have been determined for two different hydrologic periods on the main stream of the Allanche river and its tributaries.The major objectives of this study were to characterize the chemical and isotopic signatures of each reservoir occurring in the watershed. Changes in chemical and isotopic signatures are interpreted in terms of fluctuations of the different components inputs: rainwater, weathering products, anthropogenic addition.Water quality may be influenced by natural inputs (rainwater, weathering processes) and anthropogenic additions (fertilizers, road salts, etc.). Precipitation serves as a major vehicle for dissolved chemical species in addition to the hydrosystem and, in order to constrain rain inputs, a systematic study of rainwaters is carried out over a one year period using an automatic collector. Corrections of rainwater addition using chloride as an atmospheric input reference were computed for selected elements and the Sr/Sr ratio. After such corrections, the geochemical budget of the watershed was determined and the role of anthropogenic additions evaluated through the relationship between strontium isotopes and major and trace element ratios. Thus, 10% of Ca and Na originate in rainwater input, 40 to 80% in fertilizer additions and 15 to 50% in rock weatheringThe cationic denudation rates for this watershed are around 0.3 g s^–1 km² during low water discharge and 0.6 g s^–1 km² in high water stage. This led to a chemical denudation rate of 5.3 mm/1000 years.For solid matter, the normalization of chemical species relative to parent rocks shows the depletion or enrichment in soils and sediments. The use of K and Ca as mobile reference illustrates the weathering state of soils and sediments relative to parent rocks. This weathering state for bed sediments range from 15 to 45% for the K normalization and from 2 to 50% for the Ca normalization. For the soils, the weathering state ranges from 15 to 57% for the K normalization and from 17 to 90% for the Ca normalization.     

Silicate and carbonate weathering in the drainage basins of the Ganga-Ghaghara-Indus head waters: Contributions to major ion and Sr isotope geochemistry

The role of silicate and carbonate weathering in contributing to the major cation and Sr isotope geochemistry of the headwaters of the Ganga-Ghaghara-Indus system is investigated from the available data. The contributions from silicate weathering are determined from the composition of granites/ gneisses, soil profiles developed from them and from the chemistry of rivers flowing predominantly through silicate terrains. The chemistry of Precambrian carbonate outcrops of the Lesser Himalaya provided the data base to assess the supply from carbonate weathering. Mass balance calculations indicate that on an average ∼ 77% (Na + K) and ∼ 17% (Ca + Mg) in these rivers is of silicate origin. The silicate Sr component in these waters average ∼40% and in most cases it exceeds the carbonate Sr. The observations that (i) the⁸⁷Sr/⁸⁶Sr and Sr/Ca in the granites/gneisses bracket the values measured in the head waters; (ii) there is a strong positive correlation between⁸⁷Sr/⁸⁶Sr of the rivers and the silicate derived cations in them, suggest that silicate weathering is a major source for the highly radiogenic Sr isotope composition of these source waters. The generally low⁸⁷Sr/⁸⁶Sr (< 0.720) and Sr/Ca (∼ 0.2 nM/ μM) in the Precambrian carbonate outcrops rules them out as a major source of Sr and⁸⁷Sr/⁸⁶Sr in the headwaters on a basin-wide scale, however, the high⁸⁷Sr/⁸⁶Sr (∼ 0.85) in a few of these carbonates suggests that they can be important for particular streams. The analysis of⁸⁷Sr/⁸⁶Sr and Ca/Sr data of the source waters show that they diverge from a low⁸⁷Sr/⁸⁶Sr and low Ca/Sr end member. The high Ca/Sr of the Precambrian carbonates precludes them from being this end member, other possible candidates being Tethyan carbonates and Sr rich evaporite phases such as gypsum and celestite. The results of this study should find application in estimating the present-day silicate and carbonate weathering rates in the Himalaya and associated CO₂ consumption rates and their global significance.     

Chemical and physical weathering in a hot‐arid,tectonically active alluvial system of Anza Borrego Desert,California

Investigation of chemical and physical weathering of bedrock and alluvial sediment in the Anza Borrego Desert, California, sheds light on weathering processes in hot‐arid systems and clarifies interpretations of climate from alluvial sediment. All of the alluvial sediment in the study area emanates from Cretaceous tonalite of the Peninsular Range, enabling exploration of the effects of external variables – climate, transport distance and tectonics – on the physical and chemical properties of the sediment. Chemical weathering in this area is dominated by plagioclase alteration observed in both bedrock outcrops and sediment, evinced most clearly by changes in the Eu anomaly. Biotite chemical weathering, manifested by interlayer K⁺ loss, is not evident in bedrock, but clearly observed in the sediment. Despite the weak intensity of chemical weathering (Chemical Index of Alteration = 56 to 62), fine‐grained (<63 μm) sediment displays a clear weathering trend in A–CN–K space and contains up to 25% clay minerals. Physical abrasion and grain‐size reduction in biotite during transport predominates in the sediment, whereas physical (insolation) weathering affecting bedrock is inferred from estimates of differential thermal expansion of mineral phases in response to extreme temperature changes in the study area. Chemical alteration and Brunauer–Emmett–Teller surface area both increase within the active Elsinore fault zone at the distal end of the depositional transect, reflecting tectonic‐induced fracturing and associated accelerated weathering. Extensive fracturing, together with a more humid Pleistocene climate, probably facilitated in situ bedrock weathering, preceding arid alluvial deposition in the Holocene. This study demonstrates that both climate and tectonic processes can affect chemical and physical weathering, resulting in alteration of plagioclase, leaching of K⁺ from biotite in the sediment and formation of clay minerals, even in hot, arid systems.     

The effects of source rocks and chemical weathering on the petrogenesis of siliciclastic sand from the Neto River (Calabria, Italy): implications for provenance studies

Plutonic and gneissic rocks of the Sila Massif in the uppermost portion of the Neto drainage basin (Calabria, Southern Italy) weather and erode under a humid Mediterranean climate. During the development of weathering profiles, a combination of chemical weathering and granular disintegration processes occurred. Chemical weathering involves a loss of both plagioclase (mainly during grus generation) and K-feldspar (mainly during soil formation). This loss is attributed to transformation of plagioclase to clay minerals and to leaching and dissolution of K-feldspar. Sand composition is quartzofeldspathic and nearly homogeneous along the main channel of the Neto River, even where the river cuts across a blanket of sedimentary cover. Thus, fluvial transport does not alter sand composition within the Neto drainage basin. Petrographic indices are effective in (1) discriminating between contributions from similar (granite and gneiss) source rocks (Qm/F); (2) relating the provenance of plutoniclastic and gneissiclastic sand found in the headwaters to grus horizons (Qm/F; Q/Rg); and (3) distinguishing between upstream first-cycle and downstream multicycle sand (Q/Rg). This last distinction is further emphasized by considering both aphanitic and phaneritic varieties of rock fragments (RgRmRs diagram). Chemical weathering is the main sand producer within the regolithic environment in northern Calabria. In addition, rapid erosion resulting from steep slopes removes weathered products, and rapid and short transport leads to minimal sediment maturation. In general, the F/Q index is climate and relief dependent; thus, it should be used in conjunction with palaeoclimatic and palaeophysiographic evidence for provenance interpretations of ancient quartzofeldspathic sandstones.     

The Sis palaeovalley: a record of proximal fluvial sedimentation and drainage basin development in response to Pyrenean mountain building

The Sis conglomerate body represents the Middle Eocene to Oligocene transfer‐zone trunk palaeovalley fill of the Sis fluvial system, a drainage system established within the Pyrenees during Late Palaeocene times. The spatial stability of the fluvial transfer zone (active for at least 38 My), and hence the longevity of its aggradational palaeovalley component (>19·5 My), was controlled by its location between long‐lived pre‐existing structures. Coarse‐grained fluvial facies dominate the palaeovalley fill, with alluvial fan facies shed from its defining marginal structures. The detailed sedimentology of very proximal fluvial facies deposited within the dominantly erosional realm of an active mountain belt has rarely been documented before because of their poor preservation potential. The Sis conglomerate body contains a robust internal stratigraphy with stratigraphic units defined by distinct bounding surfaces, across which there are pronounced changes in facies and provenance. These mark the reorganization of the headward portions of the Sis fluvial system during the evolution of the Pyrenean Axial Zone antiformal stack. Major changes in discharge resulted, demonstrating the highly variable nature of even mountain belt‐scale fluvial systems when viewed on timescales of several to tens of millions of years. Provenance details indicate that initial unroofing of Hercynian granitoids, situated within the Pyrenean Axial Zone, occurred around 54·5 Ma (early Ypresian) immediately before the first significant exhumation event within the drainage basin of the Sis fluvial system. This is earlier than previously constrained by apatite fission track studies. Rock uplift accelerated in the Lutetian and Bartonian with the initial aggradation of the palaeovalley fill (the Cajigar and Cornudella Formations and Sis One and Two Members). This became marked in the Priabonian (Sis Three and Four Members), with significant activity on local structures including the Morreres backthrust. An increase in basement‐derived clasts and a headwater decapitation event also indicate pronounced Axial Zone antiformal stack development at this time. Axial Zone development intensified further in the Oligocene with the deposition of the Collegats Formation and the switch in the main depositional loci of the system from the Tremp‐Graus thrust‐sheet‐top basin to the Ebro Basin to the south.     

Geochemistry of peridotite and granite xenoliths during the early stage of weathering in the Nyos volcanic region (NW Cameroon): Implications for PGE exploration

Peridotite and granite xenoliths, in the early stage of weathering, occur in the Nyos volcanic region (NW Cameroon). Geochemical data shows that peridotites are marked by high concentrations of MgO (42.30 wt.%, with SiO₂/MgO ∼ 1), chromium (2100 ppm), nickel (2100 ppm) and cobalt (104 ppm), as well as by low lanthanide contents (ΣREE: 7.41 ppm). Granites display SiO₂ contents (70–73 wt.%), and are mostly peraluminous (1.40 > A/CNK < 1.6). They are also characterized by low contents in chromium (<24 ppm), nickel (ranging from 6 to 15 ppm) and cobalt (ranging from 3 to 6 ppm). Granites possess high lanthanide contents (ΣREE varying between 248.00 and 463.00 ppm), particularly in light lanthanides (LREE/HREE ratios ranging from 21 to 32). The chondrite-normalized patterns of the studied xenoliths are characterized by: (i) LREE enrichments in both rock types; (ii) negative Eu anomalies ([Eu/Eu*] ranging from 0.45 to 0.64) and weak positive Ce anomalies ([Ce/Ce*] ranging from 1.06 to 1.46) in granites. The weathering process provokes a remobilization of several trace elements notably light lanthanides.The geochemical survey of Platinum-Group Elements (PGE) done in these rocks in the early stage of weathering shows that PGE contents are less than 7 ppb in the peridotites. The highly concentrated elements are ruthenium (6.26 ppb) and platinum (5.53 ppb). The total PGE content is 14.57 ppb. These concentrations normalized with respect to chondrites display a flat spectrum from iridium to platinum. PGE contents in the granites are below detection limit except for two samples (LNY01 and LNY02) whose platinum content is close to 0.23 ppb.     

Chemical weathering in the Hong (Red) River basin: Rates of silicate weathering and their controlling factors

The Hong (Red) River drains the prominent Red River Fault Zone that has experienced various tectonic activities—intrusion of magma, exhumation of basement rocks, and influx of thermal waters—associated with the Cenozoic collision of India and Eurasia. We report dissolved major element and Sr isotope compositions of 43 samples from its three tributary systems (Da, Thao/Hong main channel, and Lo) encompassing summer and winter seasons. Carbonic acid ultimately derived from the atmosphere is the main weathering agent, and sulfuric acid from pyrite oxidation plays a minor role. Seasonality is manifested in higher calcite saturation index and Mg/TZ⁺ and lower Ca/Mg in summer, suggesting calcite precipitation, and in higher Si/(Na^∗ + K) ratios in summer suggesting more intensive silicate weathering. We quantified the input from rain, evaporite, carbonate, and silicate reservoirs using forward and inverse models and examined the robustness of the results. Carbonate dissolution accounts for a significant fraction of total dissolved cations (55-97%), and weathering of silicates makes a minor contribution (1-40%). Our best estimate of the spatially averaged silicate weathering rate in the Hong basin is 170 × 10³ mol/km²/yr in summer and 51 × 10³ mol/km²/yr in winter. We tested for correlations between the rate of CO₂ consumption by silicate weathering and various climatic (air temperature, precipitation, runoff, and potential evapotranspiration) and geologic (relief, elevation, slope, and lithology) parameters calculated using GIS. Clear correlations do not emerge (except for ?CO₂ and runoff in winter) which we attribute to the complex geologic setting of the area, the seasonal regime change from physical-dominant in summer to chemical-dominant in winter, and the incoherent timescales involved for the different parameters tested.     

Typology of Natural Hazards and Assessment of Associated Risks in the Mount Bambouto Caldera (Cameroon Line,West Cameroon)

Abstract: Mount Bambouto is a polygenic stratovolcano of the Cameroon Volcanic Line, built between 21?Ma and 4.5?Ma. It is situated approximately 200?km NE of Mount Cameroon, between 09°55′ and 10°15′ longitude east and, 05°25′ and 05°50′ latitude north. The volcano covers an area of 500?km2 and culminates at 2740?m at Mélétan dome and bears a collapsed caldera at the summit (13?×?8?km). Mount Bambouto is characterized by several natural hazards of different origins: meteorological, such as landslides and rock falls; anthropogenic, such as bushfires, tribal wars and deforestation; and volcanological, such as volcanic eruption. The thematic map shows that 55–60% of the caldera has high probability of occurrence of mass movement. The caldera has a high population density (3000 inhabitants), which increases the level of risk, evaluated at approximately $US3.8 million for patrimony, 3000 civilian deaths and destruction of biodiversity.     

Mineralogical and geochemical features of alluvial sediments from the Lobo watershed (Southern Cameroon): Implications for rutile exploration

This paper is focused on the morphological, mineralogical, and geochemical features of alluvial sediments from the Neoproterozoic Pan-African belt to explore rutile. The fine-grained sediments, which contain a large proportion of rutile, are made up of quartz, rutile, zircon, brookite, tourmaline, andalusite, and kyanite. The high SiO₂ and TiO₂ contents highlight the predominance of silica minerals in the alluvia from the humid tropical zone. La/Sc, La/Co, Th/Sc and Zr/Cr ratios reflect the contribution of felsic and mafic sources. The highest Ti contents, which occur at the outlet of the Lobo watershed, indicate the resistance of rutile. The REE distribution could be linked to the heavy mineral sorting. The low (La/Yb)_N ratios and high Zr contents are attributed to the high proportion of zircon. Chondrite-normalized REE patterns indicate high felsic sources, which are the regional rocks. Ultimately, the Yaoundé Group constitutes a favorable potential target for further rutile exploration.     

Geologic correlation between the Neoproterozoic Sergipano belt (NE Brazil) and the Yaoundé belt (Cameroon, Africa)

The Yaoundé belt (Cameroon) and the Sergipano belt (NE Brazil) belonged to a major and continuous Neoproterozoic orogen at the northern margin of the ancient Congo-São Francisco craton. The Yaoundé belt comprises schists, quartzites, gneisses and migmatitic gneisses grouped into three domains; the low-grade Mbalmayo Group in south and the medium- to high-grade Yaoundé and Bafia Group in north. The Sergipano belt is divided into six domains, the three southernmost of which are mostly made up of clastic and chemical metasedimentary rocks whereas the others are more diverse with a migmatite–gneiss complex, and two metavolcanicplutonic complexes. In general, the two belts show structural vergence and decrease of metamorphic grade towards the craton; three main deformation phases are recognized in the Sergipano belt in contrast with two described in the Yaoundé belt. The minimum age of Pan-African-Brasiliano collision in the Sergipano belt is constrained at 628 ± 12 Ma on syn-collision granites, whereas in the Yaoundé belt collision took place between 620 and 610 Ma, i.e. the age of granulite facies metamorphism. Sm–Nd isotope geochemistry and U–Pb age dating indicate that most clastic metasedimentary rocks in both belts were derived from sources to the north and, to a lesser degree, from the cratons to the south.     

Monsoon variability and chemical weathering during the late Pleistocene in the Goriganga basin, higher central Himalaya, India

Stable isotope analysis along with radiocarbon and luminescence dating of late Pleistocene lacustrine deposits at Burfu in the higher central Himalaya are used to interpret hydrologic changes in the lake basin. From 15.5 ka to ~ 14.5 ka the Burfu lake was largely fed by melting glaciers. A warming event at 14.5 ka suggests an enhanced monsoon and increased carbonate weathering. From ~ 13.5 ka to ~ 12.5 ka the isotopic data suggest large-amplitude climate variability. Following this, the isotope data suggest a short-lived, abrupt cooling event, comprising a ~ 300-yr intense cool period followed by a ~ 500-yr interval of moderate climate. A shift in isotope values at ~ 11.3 ka may signify a strengthening monsoon in this region. The inferred climatic excursions appear to be correlative, at least qualitatively, with global climatic events, and perhaps the Burfu lake sequence provides regional evidence of globally recorded excursions. This study also suggests a potential use of radiocarbon ages in specific environments as a paleoenvironmental proxy.