Spatial and temporal hydrochemistry variations of karst water in Gunung Sewu,Java, Indonesia

A hydrogeochemical study was conducted in the Gunung Sewu Karst, Java Island, Indonesia. The main objective of this study is to describe the spatial and temporal variations of hydrochemistry that occur in the central and western parts of Gunung Sewu. Discharge measurements for a one-year period are taken in some karst springs or underground rivers to define their discharge hydrograph. Furthermore, baseflow separation analysis was conducted to determine the base flow percentage throughout the year. Water sampling for hydrogeochemical analysis was taken every month to represent the dry and rainy season conditions. To describe the hydrogeochemical processes, a scatter plot analysis with a small sample size was conducted. The results showed that the hydrochemistry of karst water in the study area has different characteristics spatially and temporally. Within the dry season, the dominant hydrogeochemical process is water–rock interaction (precipitation of calcite mineral), indicated by achieving the maximum level of Ca²⁺, HCO₃ ^?, electrical conductivity, base flow percentage, and SI calcite, with the lowest level of log \(P_{{{\text{CO}}_{2} }}\) in the water. In addition, the dry season hydrochemistry is characterized by a strong relationship between electrical conductivity–calcium/bicarbonate, base flow percentage-discharge, base flow percentage-SI calcite, and SI calcite-log \(P_{{{\text{CO}}_{2} }}\). Spatially, the different level of correlations between these parameters depended on the sampling location, flow recharge, and the conduit development. Conversely, in the rainy season, the hydrogeochemical process shifted from water–rock interaction to dilution of rainwater as a result of rain water supply through a conduit system channel, which is characterized by declining Ca²⁺, HCO₃ ^?, electrical conductivity, base flow percentage, and SI calcite, with the highest level of log \(P_{{{\text{CO}}_{2} }}\) in the water. The dilution of rainwater process also caused a decline in the correlation of some hydrogeochemical parameters.     

A comparative study of aquifer systems occurring at the Paraná sedimentary basin, Brazil: major hydrochemical trends

This investigation was carried out within the Paraná sedimentary basin, Brazil, and involved the sampling of 80 pumped tubular wells for evaluating the hydrochemistry in three aquifer systems (Bauru, Serra Geral and Guarani) occurring in 21 localities of S?o Paulo and Mato do Grosso Sul states. The Guarani aquifer of Triassic?CJurassic age has continental dimensions and extends over some 1.2 million km² within the Paraná basin. A thick (up to 1,500?m) basaltic package of the Serra Geral Formation overlies this aquifer that is covered by Cretaceous sediments of the Bauru Group. Major hydrochemical data were obtained and compared in each aquifer system, allowing the establishment of the principal trends among the parameters analyzed. The redox potential Eh decreased according to the pH increase in the three aquifers. A consistent database has been assured from expected relationships found for typical parameters commonly evaluated in hydrogeochemical surveys. Thus, direct relationships of conductivity with ionic strength (IS) were determined and, despite bicarbonate, assumed an important role in justifying such trends; other direct significant correlations involving IS were also identified with Na⁺, Cl^?, F^? and SO₄ ^2?. Precipitation of carbonates was evidenced by opposite relations among CO₃ ^2?, Ca²⁺ and Mg²⁺ that are strongly linked to the temperature effects on Ca²⁺ and Mg²⁺ dissolution as often reported from theoretical constraints.     

Factors which determine the hydrogeochemical behaviour of karstic springs. A case study from the Betic Cordilleras,Spain

The Cabra-Alcaide karstic massif situated in the south of Spain constitutes an important part of the so-called Natural Park of the Subbetic Sierras. This aquifer system is drained by various springs which supply a population of some 100,000 inhabitants. The feed areas of these springs show very different characteristics with respect to their geological structure, size of the drainage area, thickness of the vadose zone, elevation and degree of karstification. In addition, the carbonate rocks lie over a clayey substratum which contains large masses of intercalated evaporites. Due to these conditions, the hydrochemical composition of the springs is relatively variable. In this study a hydrogeochemical characterization of the aquifer in both space and time is undertaken and the factors that determine it are discussed. To achieve this, 19 monthly samples were taken from the 6 most significant springs of the hydrogeological system. The commencement of sampling coincided with the transition from a period of several years of severe drought and a very wet two-year period, which amplified considerably the hydrochemical and hydrodynamic response of the springs to the recharge. Identification of hydrogeochemical processes was performed by studying hydrographs, the temporal evolution of physico-chemical parameters, ionic ratios (mainly Mg/Ca) and by means of simple and multivariate statistical analyses. The saturation status was established using the WATEQF program and the mass transfer was quantified using PHREEQC. With the exception of the epikarstic subsystem (i.e. the Zarza spring), the majority of the results indicate that the aquifer exhibits a diffuse flow model, in which piston flow phenomena are seen, closely linked to the most intense precipitation. Along the direction of flow hydrochemical trends are seen as the water type changes from Ca–HCO₃ to Ca–Mg–HCO₃; at the same time enrichment in some ions, derived from the dissolution of evaporitic minerals of the impermeable substratum, and dedolomitization processes occur. In this way, almost 90% of the water samples were oversaturated in calcite, the majority of cases being a consequence of the dissolution of the gypsum of the substratum. Only in the epikarstic springs can it be considered that the oversaturation in calcite is due to loss of CO₂ from the emerging groundwater. It is concluded that hydrodynamic aspects together with hydrogeochemical characteristics need to be taken into account to correctly explain the hydrochemical evolution of the karstic springs. Moreover, the use of both approaches permits a more accurate establishment of the degree of aquifer karstification, which in turn needs to be known in order to assess its vulnerability to contamination and to protect recharge zones.     

Investigating the hydrogeological properties of springs in a karstic aquifer in Dorfak region (Guilan Province,Iran)

Karstic aquifers are considered as the main sources of groundwater in the northeast of Rudbar, Iran. The present study was conducted to evaluate the hydrogeological properties of karstic springs in this region. For this purpose, saturation indices (SI values) were calculated using the geochemical PHREEQC model for a number of minerals in the groundwater in the karstic aquifer. Moreover, AqQA-RockWare software packages were used to prepare hydrogeochemical plots for the aquifer, using which the sources of the ions in the water were identified. The origin of bicarbonate, calcium, and magnesium ions in water was determined using chloro-alkaline indices. Moreover, through plotting a Piper diagram for spring water samples, it was discovered that water type of all springs is the Ca-HCO₃ type, confirming the karstic characteristic of springs in the area. A Durov diagram also suggests that the water composition of the springs is of the bicarbonate type with the dominant Ca cation, suggesting the calcareous effects of the region on the quality of groundwater and exhibiting a single source for the springs. The calculated saturation indices show that most of the water samples are undersaturated with respect to calcite, dolomite, and CO₂. The stable isotopes (δ¹⁸O and δ²H) and deuterium excess values were used to get information about transport pathways in groundwater, atmospheric moisture, and the degree of interaction between these reservoirs. The degree of karstification of the recharge area of the karst aquifer was determined to be 5.5 from an analysis of the hydrograph Sefidab Spring.     

Hydrogeochemistry and isotope techniques to determine water interactions in groundwater-dependent shallow lakes,Wet Pampa Plain,Argentina

This paper gives an account of the implementation of hydrochemical and isotopic techniques to identify and explain the processes that govern solute exchange in two groundwater-dependent shallow lakes in the Southeastern Pampa Plain of Argentina. Water samples (lakes, streams, spring water and groundwater) for hydrochemical and stable isotopic determination were collected and the main physical–chemical parameters were measured. The combination of stable isotope data with hydrogeochemical techniques was used for the identification of sources and preferential recharge areas to these aquatic ecosystems which allowed the explanation of the lake water origin. The hydrochemical processes which explain Los Padres Lake water chemistry are evaporation from groundwater, CO₂ input, calcite dissolution, Na⁺ release by Ca²⁺ and Mg²⁺ exchange, and sulfate reduction. The model that best aligns with La Brava Lake hydrochemical constraints includes: mixing, CO₂ and calcite dissolution, cationic exchange with Na⁺ release and Mg²⁺ adsorption, and to a lesser extent, Ca/Na exchange. This model suggests that the fractured aquifer contribution to this water body is greater than 50 %. An isotopic-specific fingerprint for each lake was identified, finding a higher evaporation rate for La Brava Lake compared to Los Padres Lake. Isotopic data demonstrate the importance of these shallow lakes as recharge areas to the regional aquifer, becoming areas of high groundwater vulnerability. The Tandilia Range System, considered in many hydrogeological studies as the impermeable bedrock of the Pampean aquifer, acts as a fissured aquifer in this area, contributing to low salinity waters and with a fingerprint similar to groundwater isotopic composition.     

Using non-conservative tracers to characterise karstification processes in the Merinos-Colorado-Carrasco carbonate aquifer system (southern Spain)

The systematic sampling of the chemical composition of the groundwater from five karst springs (including an overflow spring) and one outflowing borehole have permitted to determine distinctive chemical changes in the waters that reflect the geochemical processes occurring in a carbonate aquifer system from southern Spain. The analysis of the dissolution parameters revealed that geochemical evolution of the karst waters basically depends on the availability of the minerals forming aquifer rocks and the residence time within the aquifers. In the three proposed scenarios in the aquifers, which include the preferential flow routines, the more important geochemical processes taking place during the groundwater flow from the recharge to the discharge zones are: CO₂ dissolution and exsolution (outgassing), calcite net dissolution, calcite and dolomite sequential dissolution, gypsum/anhydrite and halite dissolution, de-dolomitization and calcite precipitation. A detailed analysis of the hydrochemical data set, saturation indices of the minerals and partial pressure of CO₂ in the waters joined to the application of geochemical modelling methods allowed the elaboration of a hydrogeochemical model of the studied aquifers. The developed approach contributes to a better understanding of the karstification processes and the hydrogeological functioning of carbonate aquifers, the latter being a crucial aspect for the suitable management of the water resources.     

Groundwater hydrochemistry and origin in the south-eastern part of Wadi El Natrun,Egypt

The demand for water is rapidly increasing in Egypt, because of high population and agriculture production growth rate, which makes research of water resources necessary. The regional multi-aquifer system of the Miocene–Pleistocene age is discharged in Wadi El Natrun area. Intensive aquifer overexploitation and agricultural development in the area are related to groundwater quality deterioration. Hydrochemical and hydrogeological data was evaluated to determine the groundwater origin and quality in the south-eastern part of wadi, which appears to be more significant for water supply owing to lower groundwater salinity. The dominance of the high mineralised Cl groundwater type was found; however, also less mineralised SO₄ and HCO₃ types were identified there. Based on the ion relations, halite and gypsum dissolution and ion exchange are the most important hydrochemical processes forming the groundwater chemical composition. The Cl dominated groundwater matches the discharge part of the regional hydrogeological system. Contrary, the presence of HCO₃ and SO₄ hydrochemical types corresponds to the infiltration and transferring parts of the hydrogeological system indicating the presence of zones conducting low mineralised groundwater. The discharge area of the over-pumped aquifer in Wadi El-Natrun lies 23 m beneath the sea level with the shoreline being at the distance of 100 km, thus there is a real risk of seawater intrusion. Using the hydrochemical facies evolution diagram, four samples in the centre of the discharge area indicate advanced seawater intrusion. The zones of the highest demand for groundwater quality protection were indicated based on a spatial pattern of hydrogeochemical composition.     

Assessing hydrochemical evolution of groundwater in limestone terrain via principal component analysis

This paper describes the use of multivariate statistical analysis to trace hydrochemical evolution in a limestone terrain at Zagros region, Iran. The study area includes a deep confined aquifer, overlaid by an unconfined aquifer. The method involves the use of principal component analysis (PCA) to assess and evaluate the hydrochemical evolution based on chemical and isotope variables of 12 piezometers drilled in both the unconfined and confined aquifers. First PCA on all variables shows that water–rock interaction under different conditions with respect to the atmospheric CO₂ is the main process responsible for chemical constituents. As a result, combinations of several ratios such as Ca/TDS, SO₄/TDS and Mg/TDS with physico-chemical and isotope variables reveal different hydrochemical evolution trend in the aquifers. Second PCA on the selective samples and variables reveals that displacement of the unconfined samples from dry to wet season follows a refreshing trend towards river samples that is characterized by reducing electrical conductivity and increasing sulphate and tritium contents. However, the refreshing trend cannot be traced in the confined aquifer samples suggesting no recharge from river to the confined aquifer. Third PCA reveals that, chemical composition of water samples in the unconfined aquifer tends to have considerable difference from each other in the end of recharge period. In contrast, the confined aquifer samples have a tendency to show similar chemical composition during recharge period in comparison to end of dry period. This difference is caused by different mechanism of recharge in the unconfined aquifer (through the whole aquifer surface) and the confined aquifer (through the limited recharge area).     

Hydrochemical variations of epikarst springs in vertical climate zones: a case study in Jinfo Mountain National Nature Reserve of China

High temporal resolution (15 min) measurements of stage, pH, electric conductivity, temperature, and other hydrochemical parameters of groundwater at two sites in the Jinfo Mountain Nature Reserve of China were collected using automatic data loggers. Bitan Spring (BS 700 m a.s.l.) sits in subtropical climate zone, while Shuifang Spring (SS 2,060 m a.s.l.) is located in plateau temperate climate. The data show that hydrochemistry of epikarst springs at different altitudes is very sensitive to the changes of their physical environment, especially two factors: air temperature and soil CO₂ concentration. Springs at lower altitude are associated with higher air temperature and soil CO₂ concentration, thus more likely leading to more active karst processes than those at higher elevation. Water temperature and pH of BS showed a noticeable diurnal circle with high values in daytime and low values at night. The data also indicate that at least there are two effects that could impact the variations of groundwater hydrochemistry during flood pulse: dilution effect and CO₂ effect.     

采动条件下沉积变质型铁矿床水化学特征及控制因素:以司家营铁矿南区为例

为了解沉积变质型铁矿床开采后矿区地下水化学特征的变化趋势,在充分掌握矿区含水系统划分和流动系统发育规律的基础上,通过对四含上、四含下、基岩含水层148个水样常规离子的相关性、水化学类型及公因子的分析,得出水化学类型分区和公因子得分等值线,将二者叠加,分析各含水层潜在的形成作用及其控制因素.研究结果表明,四含上以碳酸盐溶滤、污染、氧化作用为主;四含下以污染、溶滤、局部脱硫酸作用为主;基岩含水层以离子交换吸附、第四系水的混合、硅酸盐矿物的不全等溶解作用为主.除了背景因素外,矿山开采后的三维流场控制了基岩含水层的形成作用和原生水化学类型,影响了第四系含水层的局部形成作用,水化学类型分区界线明显移动.      

Integrated hydrochemical assessment of the Quaternary alluvial aquifer of the Guadalquivir River, southern Spain

The alluvial aquifer of the Guadalquivir River comprises shallow Quaternary deposits located in the central-eastern part of the Province of Jaén in southern Spain, where groundwater resources are used mainly for crop irrigation in an important agricultural area. In order to establish the baseline hydrochemical conditions and processes determining the groundwater quality, groundwater and river water samples were collected as part of an integrated investigation that coupled multivariate statistical analysis with hydrochemical methods to identify and interpret the groundwater chemistry of the aquifer system. Three main hydrochemical types (Mg–Ca–HCO₃, Ca–Mg–SO₄–HCO₃–Cl and Na–Ca–Mg–Cl–SO₄) were identified. Further interpretation, using R-mode principal components analysis (PCA) conducted with 13 hydrochemical variables, identified two principal components which explain ⅔ of the variance in the original data. In combination with the hydrochemical interpretation, mineralogical analyses of the aquifer sediment together with inverse geochemical modelling using NETPATH showed that dedolomitization (calcite precipitation and dolomite dissolution driven by gypsum dissolution) is the principal hydrochemical process controlling the regional groundwater chemistry. Other processes such as silicate weathering, ion exchange, mixing between river water and groundwater, and agricultural practices also affect the groundwater chemistry.     

玛曲高原区潜水水化学和氢氧同位素特征

玛曲高原区地下水是黄河的重要补给水源,然而其水化学特征及形成机理认识还十分有限。通过采集玛曲潜水、河水和黄河河道沉积物,系统研究了玛曲高原区地下水水化学、同位素特征以及水文地球化学过程。结果表明:河水和潜水的溶解性总固体含量低,分别为72~195 mg/L和207~459 mg/L,水化学成分以Ca2+和HCO3-为主,水样中砷浓度为0.46~17.7μg/L。氢氧同位素结果表明,地下水和河水补给来源为当地大气降水,河水相对潜水富集δ18O和δD。河水水化学组成主要受蒸发浓缩作用的影响,而潜水主要受碳酸盐岩溶解作用的影响。潜水水样SI白云石小于0的占68%,表明潜水中白云石处于不饱和状态。某些潜水砷含量超标的原因可能是沉积物铁锰氧化物矿物的还原性溶解,而砷的来源可能是玛曲河道和浅层松散沉积物中吸附态砷。研究成果有助于揭示黄河上游玛曲段地下水的来源及地下水化学成分的形成机理。     

伊犁河支流大西沟河水与地下水转化关系研究

开展河流和地下水转换关系研究对于区域水资源合理开发利用具有重要意义。文章以大西沟河水与地下水转换关系为目标,在分析地下水动力场的基础上,通过水化学类型、溶解性总固体(TDS)、氯离子（Cl-）等水化学以及环境同位素18O、D、T等指标作为示踪剂,分析大西沟河和地下水的转换关系和转化强度。结果表明:研究区河流和地下水化学类型主要为HCO3—Ca,水化学类型空间分布特征相似;TDS和Cl-浓度表现为先增加后下降,但地下水的变化幅度大于河水。通过对大西沟河水和地下水中的水化学和环境同位素指标对比分析,发现研究区河流与地下水之间补给排泄关系具有明显的分段性;从河流出山口到下游地区,河水和地下水之间发生了三次转化关系:在山前倾斜砾质平原区以河水入渗补给地下水为主,补给量占该段潜水径流量的56%;到了细土平原区出现地下水补给河水地段,补给源为承压水越流补给潜水后的混合水体,潜水和承压水补给比例占该段河水径流量的20.4%与58.4%;风成沙漠区河水沿途渗漏补给地下水直至河流断流。本次研究结果为建立研究区水循环演化模式和水资源合理开发利用提供了理论和技术支持。     

Carbon river fluxes and weathering CO2 consumption in the Congo and Amazon river basins

Data on carbon river fluxes recently obtained by the authors for the Congo basin within the framework of the PIRAT Program (INSU-CNRS/ORSTOM) are compared with results previously obtained for the Amazon basin. A special interest is devoted to the bicarbonate river fluxes and to their relationships with river discharges. The flux of atmospheric and soil CO₂ consumed by rock weathering is estimated to be 3.1 × 10⁵ and 0.5 × 10⁵ moles/a/km² respectively for the Amazon and the Congo basin. These CO₂ fluxes represent, respectively, 67.4% and 74.7% of the total bicarbonate river fluxes. A comparison to other large river basins shows that this contribution is directly related to the proportion of carbonate rock areas. A transfer function between the weathering CO₂ flux and the river discharge is calculated for each basin and allows the reconstitution of the variations of this flux using the river discharge fluctuations during the last century. These interannual CO₂ fluctuations present average increasing trends of 10% for Amazon basin and only 0.7% for the Congo basin during the last century.     

Hydrochemical and PCO2 variations of a cave stream in a subtropical karst area,Chongqing, SW China: piston effects,dilution effects,soil CO2 and buffer effects

The role of CO₂ in karst has been of interest for decades, and emphasized by IGCP 379, International Geoscience Programme, UNESCO started in 1995. There are still open questions about the dynamics of carbon in karst systems, particularly the flux of carbon between the surface and subsurface and between different components in the karst subsurface. This research report focuses on the variations of hydrochemistry and PCO₂ (partial pressures of carbon dioxide) in subtropical karst groundwater, using high-resolution auto-monitoring hydrochemical data (15-min intervals). The aim of this study was to understand how hydrochemistry and PCO₂ in karst systems respond to recharge over different time scales and what the controlling factors are. An auto-monitoring hydrochemistry station was installed about 300 m upstream from the exit in the active stream channel of Xueyu Cave, a typical subtropical karst cave. Four years of high-resolution continuous pH, specific conductivity (Spc), temperature and water-level data were collected. A thermodynamic model was used to link the continuous data to monthly water quality data, allowing the calculation of CO₂ partial pressures and calcite saturation (SIc) levels on a continuous basis. Seasonal, diurnal and storm-scale variations were captured in the hydrochemistry and calculated PCO₂ records, indicating that the cave stream is a dynamic and variable system. Seasonal features (higher specific conductivity and lower pH in summer; lower specific conductivity and higher pH in winter) tend to covary with temperature which influences the production of CO₂ in soils, thus being the driving force for the variations (the soil CO₂ effect). Due to the buffer effect of a thick vadose zone and large void cave space, diurnal variations are not obvious compared with epikarst springs in SW China. Storm-scale fluctuations due to storm events occur during the summer rainy season. Piston flow effects, dilution and soil CO₂ effects determine the variations in different storm events. At the beginning of the rains, the piston effect drives the variations, characterized by increase in Spc, SIc and pH in the cave stream and decrease in PCO₂. With heavy rainfall, decrease in Spc shows control by the dilution effect, while decrease in SIc and pH and increase in PCO₂ indicates the greater influence of soil CO₂. These results imply that the soil and cave voids are important factors influencing the hydrochemical evolution of karst groundwater. Future works need to use such high-resolution technology widely for tracing the PCO₂ and hydrochemical variations in different karst aquifers.     

鄂尔多斯沙漠高原白垩系地下水水化学演化的多元统计分析

结合稳定同位素( D、18O、13C) ,应用聚类分析和因子分析两种多元统计分析方法,对鄂尔多斯沙漠高原白垩系含水层地下水水化学演化特征进行研究。结果表明: 研究区环河组和洛河组地下水均可分为3 大类,且大致在地下水补给区、径流区和排泄区分别聚类,每一类的水化学特征和同位素特征均存在一定的差异; 研究区地下水均起源于大气降水,发生了岩盐溶滤、碳酸盐矿物溶解、硫酸盐矿物溶解、硅酸盐矿物溶解和阳离子交换等水文地球化学作用。相对洛河组地下水,环河组地下水水化学演化特征还受到了大气降水稀释作用和酸碱演化的影响。     

利用水化学特征识别桑树坪煤矿突水水源

及时准确地找到突水水源,是解决矿井突水问题的关键。通过对桑树坪煤矿主要含水层水样进行常规水质分析,并通过Piper三线图揭示了矿区不同地下水含水层的水化学特征,并通过出水点与背景值的水文地球化学特征对比,正确地判断出了该矿区突水水源为奥灰岩溶水。研究认为,水化学特征分析是一种快速判别突水水源的有效方法。      

石期河流域岩溶水系统及其水资源构成分析

在深入研究石期河流域岩溶水系统含水介质结构特征、水资源形成的基础上,通过对流域岩溶水总排泄口流量动态长观资料系列的分析,选择2005年丰水期内最后一次洪峰(年内最大洪峰)后的流量衰减过程,根据该过程的数据资料建立本流域岩溶水总排泄口的流量衰减方程,并利用该流量衰减方程对流域岩溶水资源的构成进行定量分析研究。结果表明,石期河流域岩溶水系统在2005年最大洪峰状态下,可自然排泄的岩溶水资源总量为69 469.95×104 m3, 其中:流域坡面产流占3.64%,赋存于大型溶洞或管道中的溶洞-管道水占4.53%,赋存于小型管道或强岩溶化裂隙中的管道-裂隙水占74.10%,赋存于细小溶蚀裂隙中的溶隙水占17.73%。从衰减期的初始时刻起,它们各自可供消耗(可作为有效利用岩溶水资源)的时效分别为2日、8日、35日和126日以上。      

Long-term hydrochemical earthquake precursor studies at the Koyna-Warna reservoir site in western India

Koyna-Warna region of western India is an active seismic zone due to the Reservoir Triggered Seismicity (RTS). Earthquake precursor studies are carried out monitoring hydrochemical and stable isotope signatures in the groundwater from 15 bore wells since January 2005, for more than 12 years (January 2005 to February 2017). Depth of these boreholes ranges from 100 to 250 m. Cyclic or temporal variation in hydrochemistry is observed in few sensitive wells in Koyna region. The Govare well in Koyna is found to be most sensitive and the observed hydrochemical cycle is closely associated with local earthquakes of M > 5. The earthquakes M <5 occurring either in Warna cluster or close to the observation wells, did not generate hydrochemical precursory changes. The increase in hydrochemistry is hypothesized as mixing of two aquifer waters with different hydrochemistry. It is noted that a precursory hydrochemical cycle is observed during first quarter of 2015, but no earthquake M > 5.0 occurred till date. The cyclic changes in hydrochemistry, however, indicate on-going earthquake processes and an impending earthquake of M > 5 in the region.