Pore water trace metal chemistry in polluted sediments of a tropical estuary of SE Brazil

The Sepetiba Bay is a shallow water body semi enclosed located on the west side of Rio de Janeiro City. Almost 80% of flesh water discharge, from the St Francisco canal, coming from the northern side of the bay develops an estuarine environment. Fishing and tourism are some of the most important economic activities in the area. During 35 years a zinc/cadmium smelter has polluted the bay. The objective of this investigation is to demonstrate the diagenetic processes and cadmium remobilization into pore water from the contaminated sediments. Two sites were selected to compare diagenetic processes. Site P1 is located next to domestic effluents discharge into the bay and approximately 20km away from the smelter. Site P2 is located near the same smelter and next to the Mazomba estuary, which is not influenced directly by domestic effluents. Peeper samplers of 25 cells with a resolution of 2.5 cm were deployed at both the sites. After a 3-weeks period of equilibrium, the pore waters were separated from the cells and analyzed immediately （within 24 h） for alkalinity, NH3 and reactive soluble phosphorus on a spectrophotometer. An ICP-AESΣH2S spectrometer was used to analyze Na, Mg, Li, Ba, Sr, Si, Fe and Mn. Total and labile dissolved Cd in pore waters were determined by differential-pulse stripping voltametry. The dissolved constituents in the pore waters have shown that the intensities of diagenetic reactions are different between sites. The reactions are stronger at site P1 site than at site P2, especially between 7.5 cm and 22.5 cm, which is evident by the organic rich sediment.     

Major ion chemistry,weathering processes and water quality assessment in upper catchment of Damodar River basin,India

The chemical characteristics of surface, groundwater and mine water of the upper catchment of the Damodar River basin were studied to evaluate the major ion chemistry, geochemical processes controlling water composition and suitability of water for domestic, industrial and irrigation uses. Water samples from ponds, lakes, rivers, reservoirs and groundwater were collected and analysed for pH, EC, TDS, F, Cl, HCO₃, SO₄, NO_3, Ca, Mg, Na and K. In general, Ca, Na, Mg, HCO₃ and Cl dominate, except in samples from mining areas which have higher concentration of SO₄. Water chemistry of the area reflects continental weathering, aided by mining and other anthropogenic impacts. Limiting groundwater use for domestic purposes are contents of TDS, F, Cl, SO₄, NO₃ and TH that exceed the desirable limits in water collected from mining and urban areas. The calculated values of SAR, RSC and %Na indicate good to permissible use of water for irrigation. High salinity, %Na, Mg-hazard and RSC values at some sites limit use for agricultural purposes.     

Deeper groundwater chemistry and geochemical modeling of the arsenic affected western Bengal basin,West Bengal,India

A regional scale hydrogeochemical study of a ∼21,000-km² area in the western Bengal basin shows the presence of hydrochemically distinct water bodies in the main semiconfined aquifer and deeper isolated aquifers. Spatial trends of solutes and geochemical modeling indicate that carbonate dissolution, silicate weathering, and cation exchange control the major-ion chemistry of groundwater and river water. The main aquifer water has also evolved by mixing with seawater from the Bay of Bengal and connate water. The isolated aquifers contain diagenetically altered water of probable marine origin. The postoxic main aquifer water exhibits overlapping redox zones (metal-reducing, sulfidic and methanogenic), indicative of partial redox equilibrium, with the possibility of oxidation in micro-scale environments. The redox processes are depth-dependent and hydrostratigraphically variable. Elevated dissolved As in the groundwater is possibly related to Fe(III) reduction, but is strongly influenced by coupled Fe–S–C redox cycles. Arsenic does not show good correlations with most solutes, suggesting involvement of multiple processes in As mobilization. The main river in the area, the Bhagirathi–Hoogly, is chemically distinctive from other streams in the vicinity and probably has little or no influence on deep groundwater chemistry. Arsenic in water of smaller streams (Jalangi and Ichamati) is probably introduced by groundwater discharge during the dry season.     

Seasonal and spatial variations in water chemistry and nitrate sources in six major Korean rivers

Seasonal and spatial variations in water chemistry and contaminant sources were investigated in six major rivers in South Korea that vary widely in drainage area and length. The dissolved-load content of the rivers varied seasonally, and some dissolved ions such as Cl^? and NO₃ ^? showed large spatial differences in all of the rivers. The water type changed from Ca–HCO₃ in the upper reaches to Na–Cl–NO₃ in the lower reaches, indicating anthropogenic contamination in the lower reaches. Compared with two relatively pristine rivers (the Sumjin and Mankyung rivers), the other four rivers, which flow through agricultural and urban areas, registered much higher Cl^? and NO₃ ^? concentrations. Statistical analysis showed that seasonal and spatial variations in water chemistry occurred in all the rivers. The nitrogen and oxygen isotopes of dissolved nitrate indicated that the rivers flowing through urban and agricultural areas were significantly affected by manure, sewage, or both.     

Hydrochemistry of reservoirs of Damodar River basin, India: weathering processes and water quality assessment

Water samples collected from the six reservoirs of Damodar River basin in pre- and post-monsoon, have been analysed, to study the major ion chemistry and the weathering and geochemical processes controlling the water composition. Ca, Na and HCO₃ dominate the chemical composition of the reservoir water. The seasonal data shows a minimum concentration of most of the ions in post-monsoon and a maximum concentration in pre-monsoon seasons, reflecting the concentrating effects due to elevated temperature and increased evaporation during the low water level period of the pre-monsoon season. Water chemistry of the reservoirs strongly reflects the dominance of continental weathering aided by atmospheric and anthropogenic activities in the catchment area. Higher concentration of SO₄ and TDS in Panchet, Durgapur and Tenughat reservoirs indicate mining and anthropogenic impact on water quality. The high contribution of (Ca+Mg) to the total cations, high concentration of dissolved silica, relatively high (Na+K)/TZ⁺ ratio (0.3) and low equivalent ratio of (Ca+Mg)/(Na+K) suggests combined influence of carbonate and silicate weathering. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the chemistry of reservoir water favours kaolinite formation. The calculated values of SAR, RSC and sodium percentage indicate the ‘excellent to good quality’ of water for irrigation uses.     

恒河流域地下水As中毒的特征及其对中国区域生态地球化学评价的启示

恒河流域地下水舡中毒事件始于20世纪80年代。通过对恒河流域地下水舡中毒例案的时空演变、生态效应和成因的分析，指出中国正在开展的区域生态地球化学评价应从恒河流域舡中毒事件中吸取教训，尤其应关注中国长江流域发现的Cd异常带。沿江各省应有全局观念，把长江流域作为一个整体，开展Cd异常的区域生态地球化学评价。     

The chemistry of Offatts Bayou,Texas: A seasonally highly sulfidic basin

Offatts Bayou basin was created by use of this are as a borrow pit for landfill by the city of Galveston, Texas, in the first half of this century. Restricted exchange of water with the adjacent West Bay results in this basin changing, on a seasonal time scale, between oxic winter and highly sulfidic summer (greater than 500 μM ΣH₂S) bottom water conditions. It is, therefore, a “natural laboratory” for the investigation of the behavior of toxic metals in an estuarine environment where redox conditions undergo major variations. Here we report the first study of the chemistry of Offatts Bayou’s waters and sediment-associated trace metals. The high concentrations of dissolved sulfide in bottom water during summer cause a loss of macrofauna from most of the water deeper than about 4 m and the bottom of the basin. The potential exists for major mortality of organisms living in the oxic surface waters if rapid mixing of waters were to occur during the summer. Reactions of toxic metals with sulfides are probably the dominant influence on their potential bioavailability in this type of environment, as evidenced by large seasonal changes in concentrations of sedimentary sulfide minerals and associated trace metals. The trace metals As, Cu, and Hg are dominantly found in the pyrite phase (greater than 75% pyritization), Ag and Mn are moderately pyritized (40% to 60%), and Zn is not strongly associated with pyrite (less than 20% pyritization).     

A geochemical assessment of coastal groundwater quality in the Varahi river basin, Udupi District, Karnataka State, India

The Varahi Irrigation project site is located at 13°39′15″N (latitude) and 74°57′E (longitude) in Hole Shankaranarayana village, approximately 6 km from Siddapura, Kundapura taluk, Udupi district. A total of 59 groundwater samples were collected from dug and tube wells in November 2008 to evaluate hydrochemistry and suitability for drinking and irrigation purposes. The physico-chemical parameters estimated include pH, electrical conductivity (EC), total dissolved solids (TDS), redox potential (Eh), total hardness (TH), total alkalinity (TA), temperature, major cations and anions, besides irrigation quality parameters like boron, sodium absorption ratio (SAR), % Na, residual sodium carbonate (RSC), residual sodium bicarbonate (RSBC), chlorinity index, soluble sodium percentage (SSP), exchangeable sodium ratio (ESR), non-carbonate hardness, potential salinity (PS), permeability index (PI), Kelly index (KI), magnesium hazard (MH), magnesium ratio (MR), index of base exchange. Chloride, sulphate and bicarbonate concentrations classified the groundwater samples into normal chloride, normal sulphate and normal bicarbonate water types, respectively. The Salinity (Class I; 98.3%), Chlorinity (Class I; 100%) and Sodicity (Class 0; 96.6%) indices suggest the suitability of groundwater for irrigation. The Wilcox diagram illustrates that 96.6% of the samples belongs to excellent to good category, while the US Salinity Laboratory (USSL) diagram indicates the low salinity/low sodium content in 86.44% of samples (C1S1). Positive index of base exchange in majority of the samples (91.52%) indicates direct base exchange reaction or chloro-alkaline equilibrium in the study area. The positive value of RSC in majority of samples signifying higher concentrations of HCO₃ over alkaline earths indicates that groundwater are base exchange-softened water as there is an exchange of alkaline earths for Na⁺ ions. Majority of water samples fall in the precipitation dominance field based on Gibbs’ ratio.     

Seasonal variations in water quality of Al-Wehda Dam north of Jordan and water suitability for irrigation in summer

Al-Wehda dam is an impoundment on the Yarmouk River basin north of Jordan, which came recently into operation. The reservoir is designated to provide water for agricultural, domestic, and industrial uses. Evaluation of seasonal trends in water quality of Al-Wehda dam over the year 2010 showed strong influences by weathering and leaching of geologic units along with discharge of effluents from the adjacent agricultural lands. Seasonal trends in TDS level showed slight variations, though its concentrations have been affected by events of rainfall and evaporation. The presence of total nitrogen (TN) and total phosphorus (TP) promoted the development of photosynthetic algae. Temporal fluctuations in TN, TP, chlorophyll a, COD, and BOD have been observed with peaks occurred in spring season. TN to TP ratios varied seasonally with a minimum ratio observed in spring concurrent with algal bloom. Eutrophication tends to occur throughout the year, though its intensity increased in springtime. A variety of water quality parameters has been used to evaluate water for irrigation use during summer time when the water demand for irrigation increased. Of all parameters evaluated, Na% and TH indicated that the reservoir water is not suitable for irrigation purposes.     

A methodological approach to water quality assessment in an ungauged basin,Buenos Aires,Argentina

The Reconquista River is one of the most polluted rivers in Latin America. This paper aims at identifying the dynamics of water quality in an area with low or “background” concentrations of pollutants within the Reconquista River system in order to better define levels of pollution in the main system. In order to describe the dynamics of water quality in the background area, we propose a methodology based on flow estimation with the instantaneous unit hydrograph model and on measurements of physical and chemical water variables under different hydrological conditions. Because of high dissolved oxygen and low ammonium and o-phosphate concentrations, the Arroyo Durazno, a tributary stream of the Reconquista River, is defined as a background area. When a storm event begins, the concentration of nitrates and the electrical conductivity diminish. An increase in dissolved organic carbon suggests an important input of carbon from hillslope runoff. The proportion of fulvic and humic acids also increases. On the receding limb of the hydrograph, nitrate concentration was lower than during maximum flow and organic carbon concentration remained high. This behavior, known as the “flushing effect”, suggests that the soluble material accumulated in the drainage area during dry periods is transported to the stream by leaching or “lixiviation” and surface runoff, thus raising solute concentrations during the first few hours of the storm. Water quality changes rapidly, even in background areas, due to its dependence on the flow. The methodology followed in this paper can also be applied to other basins with similar characteristics. Due to the difficulty in defining baseline areas for surface waters, a knowledge of background water quality and its dynamics is essential for understanding pollution trends and anthropogenic impacts on rivers.     

Origin of rare earth element anomalies in mangrove sediments,Sepetiba Bay,SE Brazil: used as geochemical tracers of sediment sources

Elemental contents were determined in two mangrove habitats along Sepetiba Bay, SE Brazil, an area impacted by local industrial activities, as well as hinterland water diversion networks. This study demonstrates how specific REEs (La, Ce, Nd, Sm, Eu, Tb, Yb and Lu) may be used as a sediment source tracer to mangrove-dominated coastlines. From the two stations studied, a pair of cores was collected, one in the mangrove forest and the other in the tidal flat. Station 1 results show a general enrichment in most of the fractioned patterns of the REEs normalised by Post-Archean Australian Shale. The relatively light rare earth elements are similarly enriched in the generally more polluted Station 1. Despite the probable difference in background sediment characteristics, a common sharp increase in mud contents patterns in the upper part of the mangrove sediment core was related to a lower REE content as well as Eu anomalies. With existing knowledge of clockwise water circulation in the bay, these patterns can be explained by man-made water diversion from the São Francisco and Guandu rivers, initiated more than 30 years ago, whereby suspended matter with relatively large contents of REEs and material originating from industrial sources accumulate in the eastern sector of the bay. This is the first comprehensive assessment of REEs as sedimentary tracers in a mangrove ecosystem in Brazil.     

Ground water chemistry and geochemical modeling of water-rock interactions at the Osamu Utsumi mine and the Morro do Ferro analogue study sites, Poços de Caldas, Minas Gerais, Brazil

Surface and ground waters, collected over a period of three years from the Osamu Utsumi uranium mine and the Morro do Ferro thorium/rare-earth element (Th/REE) deposits, were analyzed and interpreted to identify the major hydrogeochemical processes. These results provided information on the current geochemical evolution of ground waters for two study sites within the Poços de Caldas Natural Analogue Project.The ground waters are a K---Fe---SO₄---F type, a highly unusual composition related to intense weathering of a hydrothermally altered and mineralized complex of phonolites. Tritium and stable isotope data indicate that ground waters are of meteoric origin and are not affected significantly by evaporation or water-rock interactions. Recharging ground waters at both study sites demonstrate water of less than about 35 years in age, whereas deeper, more evolved ground waters are below 1 TU but still contain in most cases detectable tritium. These deeper ground waters may be interpreted as being of 35 to 60 or more years in age, resulting mainly from an admixture of younger with older ground waters and/or indicating the influence of subsurface produced tritium.Geochemical processes involving water-rock-gas interactions have been modeled using ground water compositions, mineralogic data, ion plots and computations of speciation, non-thermodynamic mass balance and thermodynamic mass transfer. The geochemical reaction models can reproduce the water chemistry and mineral occurrences and they were validated by comparing the results of thermodynamic mass transfer calculations (using the PHREEQE program, Parkhurst et al., 1980). The results from the geochemical reaction models reveal that the dominant processes are production of CO₂ in the soil zone through aerobic decay of organic matter, dissolution of fluorite, calcite, K-feldspar, albite, chlorite and manganese oxides, oxidation of pyrite and sphalerite, and precipitation of ferric oxides, silica and kaolinite. Gibbsite precipitation can be modeled for the shallow (recharge) water chemistry at Morro do Ferro, consistent with known mineralogy. Recharge waters are undersaturated with respect to barite and discharging waters and deeper ground waters are saturated to supersaturated with respect to barite demonstrating a strong solubility control. Strontium isotope data demonstrate that sources other than calcium-bearing minerals are required to account for the dissolved strontium in the ground waters. These may include K-feldspar, smectite-chlorite mixed-layer clays and goyazite [SrAl₃(PO₄)₂(OH)₅·H₂O].     

Environmental geochemistry and quality assessment of surface and subsurface water of Mahi River basin, western India

The hydrogeochemical study of surface and subsurface water of Mahi River basin was undertaken to assess the major ion chemistry, solute acquisition processes and water quality in relation to domestic and irrigation uses. The analytical results show the mildly acidic to alkaline nature of water and dominance of Na⁺ and Ca²⁺ in cationic and HCO₃ ⁻ and Cl⁻ in anionic composition. In general, alkaline-earth elements (Ca²⁺ + Mg²⁺) exceed alkalis (Na⁺ + K⁺) and weak acids (HCO₃ ⁻) dominate over strong acids (SO₄ ²⁺ + Cl⁻) in majority of the surface and groundwater samples. Ca²⁺–Mg²⁺–HCO₃ ⁻ is the dominant hydrochemical facies both in surface and groundwater of the area. The weathering of rock-forming minerals mainly controlled the solute acquisition process with secondary contribution from marine and anthropogenic sources. The higher concentration of sodium and dissolved silica, high equivalent ratios of (Na⁺ + K⁺/TZ⁺), (Na⁺ + K⁺/Cl⁻) and low ratio of (Ca²⁺ + Mg²⁺)/(Na⁺ + K⁺) suggest that the chemical composition of the water is largely controlled by silicate weathering with limited contribution from carbonate weathering and marine and anthropogenic sources. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the chemistry of river water favors kaolinite formation. Assessment of water samples for drinking purposes suggests that the majority of the water samples are suitable for drinking. At some sites concentrations of TDS, TH, F⁻, NO₃ ⁻ and Fe are exceeding the desirable limit of drinking. However, these parameters are well within the maximum permissible limit except for some cases. To assess the suitability for irrigation, parameters like SAR, RSC and %Na were calculated. In general, both surface and groundwater is of good to suitable category for irrigation uses except at some sites where high values of salinity, %Na and RSC restrict its uses.     

Distribution and evolution of water chemistry in Heihe River basin

Surface- vs. ground-water chemistry in the Heihe River basin, assessed through field sampling of precipitation, surface water and groundwater, allowed geographical zones and chemical types to be differentiated. The geographical zones included: alpine ice-snow (>3,900 m), alpine meadow (3,400–3,900 m), mountain forest and shrub (2,600–3,400 m), mountain grassland (1,900–2,600 m) and desert grassland (1,500–1,900 m). Groundwater chemical types included: (1) mountain fissure and piedmont gravel, bicarbonate, (2) piedmont diluvial, alluvial and lacustrine plain, sulphate, and (3) desert salt-accumulating depression, chloride. Since the 1960s, large volumes of river water diverted for irrigation have been found to re-emerge as spring water at the edge of alluvial fans and then reintegrate the Heihe River. After a number of reuses and re-emergences in the middle reaches, the rivers level of mineralization has doubled. Hydrological changes have resulted in the marked degradation of aquatic habitats, and caused substantial, and expanding, land salinization and desertification. Solving these largely anthropogenic problems requires concerted, massive and long-term efforts.     

Impact of AMD on water quality in critical watershed in the Hudson River drainage basin: Phillips Mine,Hudson Highlands,New York

A sulfur and trace element enriched U–Th-laced tailings pile at the abandoned Phillips Mine in Garrison, New York, releases acid mine drainage (AMD, generally pH < 3, minimum pH 1.78) into the first-order Copper Mine Brook (CMB) that drains into the Hudson River. The pyrrhotite-rich Phillips Mine is located in the Highlands region, a critical water source for the New York metro area. A conceptual model for derivation/dissolution, sequestration, transport and dilution of contaminants is proposed. The acidic water interacts with the tailings, leaching and dissolving the trace metals. AMD evaporation during dry periods concentrates solid phase trace metals and sulfate, forming melanterite (FeSO₄·7H₂O) on sulfide-rich tailings surfaces. Wet periods dissolve these concentrates/precipitates, releasing stored acidity and trace metals into the CMB. Sediments along CMB are enriched in iron hydroxides which act as sinks for metals, indicating progressive sequestration that correlates with dilution and sharp rise in pH when mine water mixes with tributaries. Seasonal variations in metal concentrations were partly attributable to dissolution of the efflorescent salts with their sorbed metals and additional metals from surging acidic seepage induced by precipitation.     

福建省寿宁县1:25万土地质量地球化学评估

基于多目标区域地球化学调查所获得大量高精度表层土壤重金属元素和养分元素数据,参照土壤环境质量标准(GB15618—1995)和相关行业标准,采用单因子指数法和综合因子评价法对福建省寿宁县土壤环境质量和土壤养分质量进行评价,并在此基础上,将两者叠加分析,对研究区进行土地质量地球化学分等。结果表明:福建寿宁县土地总体质量较好,以三等、四等土地为主,土壤较清洁,两者面积之和占全区的80.80%,且三等、四等土地覆盖区内有占全区10.46%的富硒土壤分布,适宜于发展一般性农业和富硒特色农业;一等、二等土地次之,土壤清洁,是发展绿色、无公害农产品的最佳区域,应加强保护并合理利用;五等、六等土地分布很少,仅占全区的6.07%。     

Recharge,geochemical processes and water quality in karst aquifers: Central West Bank,Palestine

The Central West Bank aquifer (CWB) is one of the most important resources of fresh groundwater of Palestine. The geology of the area consists mainly of karstic and permeable limestones and dolomites interbedded with argillaceous beds of late Albian–Turonian age. Exploitation of the CWB aquifer, combined with lack of information required to understand the groundwater pattern, represents a challenge for reservoir management. The present work reports hydrogeochemistry, microbiology and environmental isotope data from spring water samples, which were utilized to understand recharge mechanisms, geochemical evolution and renewability of groundwater in CWB aquifer. Besides the major chemical compositions, ionic ratios were used to delineate mineral-solution reactions and weathering processes. Interpretation of chemical data suggests that the chemical evolution of groundwater is primarily controlled by (1) water–rock interactions, involving dissolution of carbonate minerals (calcite and dolomite), and (2) cation exchange processes. The measured equation of the local meteoric water line is δD?=?5.8 δ¹⁸O?+?9.9. Stable isotopes show that precipitation is the source of recharge to the groundwater system. The evaporation line has a linear increasing trend from south to north direction in the study area. All analyzed spring waters are suitable for irrigation, but not for drinking purposes. The results from this study can serve as a basis for decision-makers and stakeholders, with the intention to increase the understanding of sustainable management of the CWBs.     

Classification of rivers based on water quality assessment using factor analysis in Taizi River basin, northeast China

A method for river classification based on water quality assessment (WQA) was introduced using factor analysis (FA) in this paper. Sixty-nine sampling sites and 20 water quality parameters in Taizi River basin were selected for monitoring and analysis. Five factors were determined in FA, denoted as general, hardness, trophic, nitrogen pollution, and physical factors. The total factor scores (TFSs) of the WQA results from all sampling sites were calculated by the eigenvalue and factor score of each factor. The TFSs of 69 sites were interpolated with the measure of inverse distance weighted in the river buffer zone generated by ArcGIS 9.2 software to form a continuous spatial distribution along river channels. All streams were divided into five classes marked “excellent”, “good”, “fair”, “poor”, and “seriously polluted”. The classification result showed that the water quality of Taizi River basin deteriorated gradually from the mountain area to the plain area. Sewage and intensive human activities contributed to the deterioration of water quality since towns and farmland were dotted densely along the river basin.     

The Hunghae Formation, SE Korea: Miocene debris aprons in a back-arc intraslope basin

ABSTRACT During early to middle Miocene times a sudden opening of the Ulleung (Tsushima) back-arc basin in the East Sea (Sea of Japan) led to the development of intraslope basins along the rifted southwestern margin (southeast Korea). Abrupt subsidence resulted in the deposition of the 200 m thick Hunghae Formation (middle Miocene), a sand/mudstone sequence that can be divided into five facies. Facies I (sand and mudstone couplet) and II (coarse sand) are turbiditic in origin, as evidenced by massive, graded, crudely-layered and parallel-laminated sand beds. Facies III (homogeneous mudstone) is characterized by various lignite and plant fragments, clastic and biogenic grains that are randomly oriented, suggestive of hemipelagic deposition. Facies IV (chaotic deposit) is characterized by the disruption of beds, the presence of isolated siltstone blocks (or balls) and large clasts in the muddy matrix, indicative of retrogressive rockfall and slide/slump. Facies V (conglomerate) is of debris flow origin, as evidenced by clast- and matrix-supported features, floating large clasts and absence of traction structures. Individual facies are organized into two types of facies association: (1) homogeneous mudstone (facies III) associated randomly with the rest (facies I, II, IV and V), indicative of hemipelagic and episodic sediment-gravity flow processes, respectively; (2) conglomerate (facies V), coarse sand (facies II) and sand/mudstone couplet (facies I), representing the flow transformation from debris flow to high- and low-concentration turbidity currents. These facies associations are similar in many respects to modern and ancient debris (or slope) aprons found elsewhere. Numerous isolated slide/slump blocks, wedged conglomerates with armoured mudstone balls, discontinuous lignite-containing sand/mudstone beds, chaotic structure and growth faults suggest that the deposition occurred on a steep slope (intraslope basin) off coalescing fan-deltas, mainly by unchannellized sediment-gravity flows. Ancient deposits with irregular facies sequences can be viewed as debris-apron systems, which provide alternatives to submarine-fan models in many clastic basins with a line rather than point source.