Recharge into Southern High Plains aquifer—possible mechanisms,unresolved questions

The High Plains aquifer in the Southern High Plains (Texas and New Mexico), consisting of Tertiary, Cretaceous, and Triassic formations, has traditionally been considered to be recharged by its uppermost water-bearing unit, the Tertiary Ogallala aquifer. This article provides hydrologic, chemical, and isotopic evidence that in the Southern High Plains: (1) Cretaceous rocks actually contain independent recharge sources; (2) Triassic rocks cannot currently be recharged by the Ogallala aquifer in significant quantities; and (3) in places, both Cretaceous and Triassic aquifers recharge the overlying Ogallala aquifer. On the basis of chemical and isotopic data, playa lakes seem to act as the predominant recharge source of the Ogallala aquifer, suggesting recharge rates greater than 30 mm/yr, as opposed to the much lower rates reported by others. The Cretaceous aquifers are being recharged by cross-formational flow from the Ogallala aquifer but also from overlying Quaternary sands and the underlying Triassic aquifer in eastern New Mexico. Current recharge into the Triassic aquifer may be insignificant.     

Relative importance and chemical effects of diffuse and focused recharge in an eogenetic karst aquifer: an example from the unconfined upper Floridan aquifer, USA

Karst aquifer studies often focus on allogenic water inputs and large conduit flow. However, diffuse recharge can be significant, particularly in unconfined eogenetic karst aquifers that retain high matrix permeability. This study examines an unconfined region of the upper Floridan aquifer (USA) that hosts a sinking stream, its resurgence, and a large conduit system. Daily diffuse recharge was approximated using a water-budget method and ranged from 17% of precipitation during a low precipitation year to >53% during the highest precipitation year, illustrating the highly variable nature of diffuse recharge in this region. The total allogenic input via the sinking stream over the 5 years of the study was significantly larger than the volume of diffuse recharge. However, only about 2% of the allogenic recharge flows from the conduit into the surrounding aquifer. That flow is restricted to storm events when hydraulic heads in the conduits exceed those in the surrounding aquifer. The estimated volume of dissolution is similar for allogenic recharge and diffuse recharge to the unconfined region surrounding the conduits, but dissolution from the diffuse recharge is distributed over a larger area than dissolution from allogenic recharge. These results exemplify how recharge type impacts flow and water–rock interactions in eogenetic karst aquifers.     

Groundwater flow patterns in the San Luis Valley,Colorado, USA revisited: an evaluation of solute and isotopic data

Groundwater systems in the San Luis Valley, Colorado, USA have been re-evaluated by an analysis of solute and isotopic data. Existing stream, spring, and groundwater samples have been augmented with 154 solute and isotopic samples. Based on geochemical stratification, three groundwater regimes have been identified within 1,200 m of the surface: unconfined, upper active confined, and lower active confined with maximum TDS concentrations of 35,000, 3,500 and 600 mg/L, respectively. The elevated TDS of northern valley unconfined and upper active confined systems result from mineral dissolution, ion exchange and methanogenesis of organic and evaporate lake sediments deposited in an ancient lake, herein designated as Lake Sipapu. Chemical evolutions along flow paths were modeled with NETPATH. Groundwater ages, and δ¹³C, δ²H and δ¹⁸O compositions and distributions, suggest that mountain front recharge is the principle recharge mechanism for the upper and lower confined aquifers with travel times in the northern valley of more than 20,000 and 30,000 ¹⁴C years, respectively. Southern valley confined aquifer travel times are 5,000 ¹⁴C years or less. The unconfined aquifer contains appreciable modern recharge water and the contribution of confined aquifer water to the unconfined aquifer does not exceed 20%.     

Identifying the recharge sources and age of groundwater in the Songnen Plain (Northeast China) using environmental isotopes

The recharge sources and groundwater age in the Songnen Plain, Northeast China, were confirmed using environmental isotopes. The isotopic signatures of the unconfined aquifers in the southeast elevated plain and the north and west piedmont, cluster along local meteoric water lines (LMWLs) with a slope of about 5. The signature of source water was obtained by the intersection of these LMWLs with the regional meteoric water line (RMWL). This finding provides evidence that the recharge water for these areas originate from the Changbai Mountains and the Low and High Hingan Mountains, respectively. Groundwater in the unconfined aquifer in the low plain yields a LMWL with a slope of 4.4; its nitrate concentration indicates the admixture of irrigation return flow. The δ-values of the unconfined aquifer in the east elevated plain plot along the RMWL, reflecting recharge by local precipitation. The mean residence time of groundwater in these aquifers is less than 50?years. However, the ¹⁴C age of the groundwater in the confined Quaternary aquifer ranges from modern to 19,500?years, and in the Tertiary confined aquifer from 3,100 to 24,900?years. Modern groundwater is mainly recharged to the Quaternary confined aquifer on the piedmont by local precipitation and lateral subsurface flow.     

Modeling of water–rock interactions in an aquitard of sandy clay in the coastal area near Beihai,China

Unconsolidated sand, gravel and clay deposits near Beihai and in the Leizhou Peninsula in southern China form an unconfined aquifer, aquitard and a confined aquifer. Water and soil samples were collected from the two aquifers in the coastal Beihai area for the determination of chemical compositions, minerals and soluble ions. Hydrogeochemical modeling of three flow paths through the aquitard are carried out using PHREEQC to determine water–rock interactions along the flow paths. The results indicate that the dissolution of anorthite, fluorite, halite, rhodochrosite and CO₂, and precipitation of potash feldspar and kaolinite may be occurring when groundwater leaks through the aquitard from the unconfined aquifer to the confined aquifer. Cation exchanges between Na and Ca can also happen along the flow paths.     

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.     

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).     

Effects of human-induced alteration of groundwater flow on concentrations of naturally-occurring trace elements at water-supply wells

The effects of human-induced alteration of groundwater flow patterns on concentrations of naturally-occurring trace elements were examined in five hydrologically distinct aquifer systems in the USA. Although naturally occurring, these trace elements can exceed concentrations that are considered harmful to human health. The results show that pumping-induced hydraulic gradient changes and artificial connection of aquifers by well screens can mix chemically distinct groundwater. Chemical reactions between these mixed groundwaters and solid aquifer materials can result in the mobilization of trace elements such as U, As and Ra, with subsequent transport to water-supply wells. For example, in the High Plains aquifer near York, Nebraska, mixing of shallow, oxygenated, lower-pH water from an unconfined aquifer with deeper, confined, anoxic, higher-pH water is facilitated by wells screened across both aquifers. The resulting higher-O₂, lower-pH mixed groundwater facilitated the mobilization of U from solid aquifer materials, and dissolved U concentrations were observed to increase significantly in nearby supply wells. Similar instances of trace element mobilization due to human-induced mixing of groundwaters were documented in: (1) the Floridan aquifer system near Tampa, Florida (As and U), (2) Paleozoic sedimentary aquifers in eastern Wisconsin (As), (3) the basin-fill aquifer underlying the California Central Valley near Modesto (U), and (4) Coastal Plain aquifers of New Jersey (Ra). Adverse water-quality impacts attributed to human activities are commonly assumed to be related solely to the release of the various anthropogenic contaminants to the environment. The results show that human activities including various land uses, well drilling, and pumping rates and volumes can adversely impact the quality of water in supply wells, when associated with naturally-occurring trace elements in aquifer materials. This occurs by causing subtle but significant changes in geochemistry and associated trace element mobilization as well as enhancing advective transport processes.     

Controls on the regional-scale salinization of the Ogallala aquifer,Southern High Plains,Texas, USA

An extensive saline plume (>250 km²) within the regionally important unconfined aquifer in the Neogene Ogallala Formation overlies the Panhandle oil and gas field in the Southern High Plains, Texas, USA. Relative to upgradient Ogallala water, the plume waters have δ¹⁸O (−6.7 to −8.8‰) and δD (−42 to −88‰) values that tend to be depleted and have higher Cl (>150 mg/l) and SO₄ (>75 mg/l) concentrations. Various end-member-mixing models suggest that the plume composition reflects the presence of paleowaters recharged during Middle to Late Wisconsinan time rather than salinization associated with petroleum production. Paleowaters probably mixed with salt-dissolution zone waters from the underlying Upper Permian formations before discharging upward into the Ogallala Formation. Cross-formational discharge is controlled primarily by the geometry of the underlying units, as influenced by the Amarillo uplift, pinch-out of the laterally adjoining confined aquifer in the Triassic Dockum Group, variations in the saturated thickness of the Ogallala aquifer and the presence of potential pathways related to salt dissolution.     

Sources of groundwater pumpage in a layered aquifer system in the Upper Gulf Coastal Plain, USA

Understanding groundwater-pumpage sources is essential for assessing impacts on water resources and sustainability. The objective of this study was to quantify pumping impacts and sources in dipping, unconfined/confined aquifers in the Gulf Coast (USA) using the Texas Carrizo-Wilcox aquifer. Potentiometric-surface and streamflow data and groundwater modeling were used to evaluate sources and impacts of pumpage. Estimated groundwater storage is much greater in the confined aquifer (2,200?km³) than in the unconfined aquifer (170?km³); however, feasibility of abstraction depends on pumpage impacts on the flow system. Simulated pre-development recharge (0.96?km³/yr) discharged through evapotranspiration (ET, ～37%), baseflow to streams (～57%), and to the confined aquifer (～6%). Transient simulations (1980–1999) show that pumpage changed three out of ten streams from gaining to losing in the semiarid south and reversed regional vertical flow gradients in ～40% of the entire aquifer area. Simulations of predictive pumpage to 2050 indicate continued storage depletion (41% from storage, 32% from local discharge, and 25% from regional discharge capture). It takes ～100?yrs to recover 40% of storage after pumpage ceases in the south. This study underscores the importance of considering capture mechanism and long-term system response in developing water-management strategies.     

Review: Recharge rates and chemistry beneath playas of the High Plains aquifer, USA

Playas are ephemeral, closed-basin wetlands that are hypothesized as an important source of recharge to the High Plains aquifer in central USA. The ephemeral nature of playas, low regional recharge rates, and a strong reliance on groundwater from the High Plains aquifer has prompted many questions regarding the contribution and quality of recharge from playas to the High Plains aquifer. As a result, there has been considerable scientific debate about the potential for water to infiltrate the relatively impermeable playa floors, travel through the unsaturated zone sediments that are tens of meters thick, and subsequently recharge the High Plains aquifer. This critical review examines previously published studies on the processes that control recharge rates and chemistry beneath playas. Reported recharge rates beneath playas range from less than 1.0 to more than 500 mm/yr and are generally 1–2 orders of magnitude higher than recharge rates beneath interplaya settings. Most studies support the conceptual model that playas are important zones of recharge to the High Plains aquifer and are not strictly evaporative pans. The major findings of this review provide science-based implications for management of playas and groundwater resources of the High Plains aquifer and directions for future research.     

The geochemistry of boron and its isotopes in groundwaters from marine and non-marine sandstone aquifers

The geological evolution of B in two UK sandstone aquifers is followed from precipitation chemistry through to groundwaters in both the unconfined and confined zones. Measurements have been made of major element geochemistry, B concentrations and B isotopic ratios. The isotopic measurements were carried out using ICP/MS following a simple preconcentration step. Isotopic measurements of rainfall show a bimodal distribution and it is suggested that enriched signatures are characteristic of Atlantic air over Britain and depleted signatures representative of continental air. In the marine Lower Greensand aquifer dissolution of glauconite results in the mobilisation of B and a correlation with SO₄ suggests that this dissolution is related to the oxidation of pyrite which appears to be the SO₄-forming reaction in the aquifer. In the non-marine Hastings beds isotopic ratios and a correlation with HCO₃ suggest that B is associated with the dissolution of ferroan carbonates. In both aquifers the geochemical evolution of B is complex and more information is needed on the behaviour of B isotopes during evapotranspiration and groundwater recharge.     

An appraisal of groundwater quality in Seymour and Blaine aquifers in a major agro-ecological region in Texas,USA

Aquifer-based groundwater quality assessment offers critical insight into the major hydrochemical processes, and aids in making groundwater resources management decisions. The Texas Rolling Plains (TRP), spanning over 22 counties, is a major agro-ecological region in Texas from where highest groundwater nitrate (NO₃ ^?) levels in the state have been reported. In this study, we present a comparative assessment of major hydrochemical facies pertaining to NO₃ ^? contamination and a host of species such as sulfate (SO₄ ^2?), chloride (Cl^?), and total dissolved solids (TDS) in different water use classes in the Seymour and Blaine aquifers, underlying the TRP. Aquifer-stratified groundwater quality information from 1990 to 2010 was obtained from the Texas Water Development Board and aggregated over decadal scale. High groundwater salinization was found in the municipal water use class in the Blaine aquifer with about 100, 87 and 50 % of observations exceeding the secondary maximum contaminant level for TDS, SO₄ ^2?, and Cl^?, respectively in the 2000s (2000–2010). The NO₃-contamination was more alarming in the Seymour aquifer with 82 and 61 % of observations, respectively, exceeding the maximum contaminant level (MCL) in the irrigation and municipal water use classes in the 2000s. Salinization was more influenced by SO₄ ^2? and Cl^? in the Blaine aquifer and by NO₃ ^? in the Seymour aquifer. High NO₃ ^? (>MCL) observations in the Seymour aquifer occurred in the Ca–HCO₃ and Ca–Mg–HCO₃ facies, the domains of fresh water recharge and anthropogenic influences (e.g., agricultural activities, waste disposal). High SO₄ ^2?, Cl^? and TDS observations in the Blaine aquifer dominated the Ca–Cl, Na–Cl, and mixed Ca(Mg)–SO₄(Cl) facies indicating evaporite dissolution, mixing and solute exchange, and lack of fresh recharge.     

Effects of model layer simplification using composite hydraulic properties

The effects of simplifying hydraulic property layering within an unconfined aquifer and the underlying confining unit were assessed. The hydraulic properties of lithologic units within the unconfined aquifer and confining unit were computed by analyzing the aquifer-test data using radial, axisymmetric two-dimensional (2D) flow. Time-varying recharge to the unconfined aquifer and pumping from the confined Upper Floridan aquifer (USA) were simulated using 3D flow. Conceptual flow models were developed by gradually reducing the number of lithologic units in the unconfined aquifer and confining unit by calculating composite hydraulic properties for the simplified lithologic units. Composite hydraulic properties were calculated using either thickness-weighted averages or inverse modeling using regression-based parameter estimation. No significant residuals were simulated when all lithologic units comprising the unconfined aquifer were simulated as one layer. The largest residuals occurred when the unconfined aquifer and confining unit were aggregated into a single layer (quasi-3D), with residuals over 100% for the leakage rates to the confined aquifer and the heads in the confining unit. Residuals increased with contrasts in vertical hydraulic conductivity between the unconfined aquifer and confining unit. Residuals increased when the constant-head boundary at the bottom of the Upper Floridan aquifer was replaced with a no-flow boundary.     

Characterization of hydrogeologic properties of the Tabriz plain multilayer aquifer system,NW Iran

A detailed hydrogeological investigation was carried out in the Tabriz plain in Iran using conventional hydrogeological field investigations and hydrochemistry. The study was carried out because the aquifers are of particular importance as they are more or less the only source of water supply available to the rural population and for agricultural and industrial activities. Analytical and numerical methods were applied to the constant rate pumping test data from the Tabriz airport and the Tabriz Power Station well fields. Two types of aquifers of different water quality were identified in the study area: an unconfined aquifer that extends over the plain and confined aquifers that are found in the deeper layers of the multilayered sediment terraces of the Aji-Chay River course. Therefore, the central part of the Tabriz plain contains both unconfined and confined aquifers, while close to the highlands, there is only an unconfined aquifer. There was evidence of minor leakage in the confined aquifers when the numerical method was used for analysis. The groundwater in the area can be identified by three main geochemical facies: Na-Cl, Ca-HCO₃, and mixed Ca-Mg-Cl-SO₄. The processes responsible for the hydrochemical evolution in the area fall into five categories: dissolution of evaporate minerals, precipitation of carbonate minerals, evaporation, ion exchange, and anthropogenic activity.     

Arsenic enrichment in unconfined sections of the southern Gulf Coast aquifer system, Texas

Groundwater arsenic concentrations exceeding the federal drinking water standard are common in the southern Gulf Coast aquifer system in Texas, including in aerobic, unconfined groundwater which provides much of the municipal and domestic water supplies for the region. The objective of this study was to determine geochemical factors affecting the occurrence and distribution of groundwater As in unconfined portions of the southern Gulf Coast aquifer system through a comparative transect study of groundwater across three major hydrostratigraphic units (the Catahoula Formation, Jasper aquifer and Evangeline aquifer) and analysis of regional water quality data. Results show that As concentrations decrease with increasing distance from the Catahoula Formation, which is consistent with Miocene volcanic ash as the main source of As to groundwater in the region. Arsenic concentrations correlate with V, SiO₂ and K, all of which were released during weathering of volcanic sediments and their degradation products. In all three units, carbonate weathering and active recharge in the unconfined zones result in circum-neutral pH and oxidizing groundwater, which are typically amenable to As immobilization by adsorption of arsenate onto mineral oxides and clays. However, As concentrations exceed 10 μg/L in approximately 30% of wells. Silica that was co-released with As may compete for sorption sites and reduce the capacity for arsenate adsorption.     

The impact of the geologic setting on the Quaternary aquifer,El-Tur area,Southwest Sinai,Egypt

The groundwater extracted from the unconfined Quaternary aquifer is the main source of water supply in El-Tur area. The area is bounded from the east by the elevated basement complex of Southern Sinai and from the west by El-Qabaliyat Ridge. The wadis dissecting these highlands form effective watersheds of the Quaternary aquifer. These wadis form areas of focused recharge. Recharge also occurs directly via the Quaternary sediments covering El-Qaa Plain. Subsurface lateral groundwater flow from the fractured basement contributes significant recharge to the aquifer as well. The aquifer sediment facies affect the type and quality of groundwater. In the eastern part where the aquifer is composed mainly of gravel and coarse sand with fragments of weathered basement, the Na-Cl-SO₄ water dominates. In the west where the facies change is rapid and complex, many water types arise. The base exchange index (BEX) is positive in this part reflecting the role of clay minerals in changing the water types via cation exchange. In the east where clays are insignificant in the aquifer, the BEX is negative. In the western part next to El-Qabaliyat Ridge, the wells discharging from the calcareous sand zone have low groundwater salinities compared to the wells discharging from the alluvium. In general, the groundwater salinity increases in the direction of groundwater flow from the northeast to the southwest which reflects the dissolution of aquifer sediments. The concentration relationships between the major ions on one hand and chloride on the other reflect the dissolution of calcium carbonates, precipitation of K- and Mg-bearing minerals, and cation exchange of Ca for Na on clay minerals. The hydrochemical models support these reactions. In addition, they show that the effect of evaporation on the recharge water in the western catchment is about four times its effect on the eastern recharge water which reflects the rapid recharge through the wadis draining the fractured basement. Moreover, the contribution from the eastern catchment in sample No. 23 is more than four-folds the contribution from the western recharge area. The stable isotopes (²H and ¹⁸O) show that the Quaternary aquifer is recharging from recent rainfall. However, upward leakage of Paleogene groundwater (depleted in ¹⁸O) also occurs. The groundwater level map shows strong overpumping impact especially in the areas close to El-Tur city.     

Geochemical and isotopic composition of groundwater in the Complex Terminal aquifer in southwestern Tunisia,with emphasis on the mixing by vertical leakage

The Complex Terminal (CT) confined aquifer of the Djerid basin, southwestern Tunisia, was studied using major ion concentrations and stable isotope contents in order to (1) investigate the changes on its hydrodynamic functioning due to the long-term over-pumping and the large-scale flood irrigation practices, (2) determine the principal mineralization processes of its fossil groundwater, and (3) examine the mode of recharge of this aquifer and whether it contains part of modern hydrological regime. The observed geochemical patterns indicated that the main mineralization processes affecting the CT groundwater water/rock interactions and mixing. The native Na > Cl and Cl > SO₄ > Ca > Na waters, resulting from the dissolution of halite and gypsum and from pyrite oxidation, interacted with those of the underlying and the overlying aquifers without changing their chemical facies. Stable isotope data provided evidences about upward and downward leakage into the CT aquifer and their relationships with anthropogenic activities. They demonstrated that the long-term over-pumping of the CT aquifer, which contributed to the loss of its potentiometric pressure, favored the upward leakage of the artesian deep groundwater along parts of the major faults. Moreover, the large-scale flood irrigation practices in the oases domain, which ensured the recharge of the shallow water table by return flow, enhanced the downward leakage toward the CT aquifer.     

Using geochemical indicators to investigate groundwater mixing and residence time in the aquifer system of Djeffara of Medenine (southeastern Tunisia)

Stable isotopes (??²H, ??¹⁸O and ??¹³C) and radiocarbon (¹⁴C) have been used in conjunction with chemical data to evaluate recharge mechanisms and groundwater residence time, and to identify inter-aquifer mixing in the Djeffara multi-aquifer in semi-arid southeastern Tunisia. The southern part of this basin, the Djeffara of Medenine aquifer system, is comprised of two main aquifers of Triassic and Miocene sandstone. The Triassic aquifer presents two compartments; the first one (west of the Medenine fault system) is unconfined with a well-defined isotope fingerprint; the second compartment is deeper and confined. Multi-tracer results show groundwater of different origins, ages and salinities, and that tectonic features control groundwater flows. Fresh and brackish groundwater from the unconfined part of the Triassic aquifer was mostly recharged during the Holocene. The recharge rates of this aquifer, inferred by ¹⁴C ages, are variable and could reach 3.5?mm/year. Brackish water of the deep confined part of the Triassic aquifer has stable isotope composition and ¹⁴C content that indicates earlier recharge during late Pleistocene cold periods. Brackish to saline water of the Miocene aquifer presents variable isotope composition. Groundwater flowing through the Medenine fault system is mainly feeding the Miocene aquifer rather than the deep confined part of the Triassic aquifer.     

Geochemistry,radiocarbon ages,and paleorecharge conditions along a transect in the central High Plains aquifer,southwestern Kansas,USA

Water samples from short-screen monitoring wells installed along a 90-km transect in southwestern Kansas were analyzed for major ions, trace elements, isotopes (H, B, C, N, O, S, Sr), and dissolved gases (He, Ne, N₂, Ar, O₂, CH₄) to evaluate the geochemistry, radiocarbon ages, and paleorecharge conditions in the unconfined central High Plains aquifer. The primary reactions controlling water chemistry were dedolomitization, cation exchange, feldspar weathering, and O₂ reduction and denitrification. Radiocarbon ages adjusted for C mass transfers ranged from <2.6 ka (¹⁴C) B.P. near the water table to 12.8 ± 0.9 ka (¹⁴C) B.P. at the base of the aquifer, indicating the unconfined central High Plains aquifer contained a stratified sequence of ground water spanning Holocene time. A cross-sectional model of steady-state ground-water flow, calibrated using radiocarbon ages, is consistent with recharge rates ranging from 0.8 mm/a in areas overlain by loess to 8 mm/a in areas overlain by dune sand. Paleorecharge temperatures ranged from an average of 15.2 ± 0.7 °C for the most recently recharged waters to 11.6 ± 0.4 °C for the oldest waters. The temperature difference between Early and Late Holocene recharge was estimated to be 2.4 ± 0.7 °C, after taking into account variable recharge elevations. Nitrogen isotope data indicate NO₃ in paleorecharge (average concentration=193 μM) was derived from a relatively uniform source such as soil N, whereas NO₃ in recent recharge (average concentration=885 μM) contained N from varying proportions of fertilizer, manure, and soil N. Deep water samples contained components of N₂ derived from atmospheric, denitrification, and deep natural gas sources. Denitrification rates in the aquifer were slow (5 ± 2× 10⁻³ μmol N L⁻¹ a⁻¹), indicating this process would require >10 ka to reduce the average NO₃ concentration in recent recharge to the Holocene background concentration.