Vulnerability of headwater catchment resources to incidences of <Superscript>210</Superscript>Pb excess and <Superscript>137</Superscript>Cs radionuclide fallout

Recent identification of elevated excess ²¹⁰Pb (≤302.6 mBq L⁻¹) and ¹³⁷Cs (≤111.3 mBq L⁻¹) activity in drinking water wells up to 20 m depth indicates some transport of airborne radionuclide fallout beyond soils in the Shaker Village catchment, Maine. Estimated airborne mass loading ²¹⁰Pb_ex fluxes of about 0.9 mBq m⁻³, canvass this headwater catchment and may be sufficient to pose risks to unprotected shallow wells. Inventories of ²¹⁰Pb_ex and ¹³⁷Cs in pond sediments indicate maximum median activities of 943 mBq g⁻¹ and 40.0 mBq g⁻¹, respectively. Calculated ²¹⁰Pb_ex fluxes in the catchment soils range from 0.62–0.78 Bq cm⁻² year⁻¹ and yield a mean residence time of near 140 years. Measured ¹³⁷Cs activity up to 51.1 mBq g⁻¹ occurs in sediments at least to 5 m depth. Assumed particle transport in groundwater with apparent ⁸⁵Kr ages less than 5 years BP (2005) may explain the correlation between these particle-reactive radionuclides and elevated activity in some drinking water wells.     

Tracing sources of carbon in urban groundwater using δ<Superscript>13</Superscript>C<Subscript>TDIC</Subscript> ratios

Total dissolved inorganic carbon (TDIC) and its stable isotope ratio δ¹³C_TDIC are used to trace the evolution of the carbon system of groundwater in three UK Permo-Triassic sandstone aquifers. Samples were collected from multilevel piezometers, open boreholes and sewer sampling points in the British Midlands (Nottingham, Birmingham and Doncaster) to evaluate both local and regional variations in δ¹³C_TDIC. δ¹³C samples of matrix and pore water have also been analysed in each aquifer to further constrain the interpretations. Combining δ¹³C_TDIC ratios with measurements of TDIC and pH clearly distinguishes the principal processes underlying the geochemical evolution of groundwater in Triassic sandstone aquifers, where processes can be both natural (e.g. carbonate dissolution) and anthropogenic (sewer-derived recharge). The paper shows that δ¹³C_TDIC resolves ambiguities that arise from the interpretation of TDIC and pH measurements in isolation. Field measurements demonstrate that, under natural conditions, the carbonate system evolves similarly in each aquifer. An open-system evolution during recharge largely saturates the groundwater with carbonate depending upon its availability in the sandstone matrix. The contribution of sewer exfiltration to urban recharge is readily distinguished by lower pH and higher TDIC values without significant changes in δ¹³C_TDIC.     

Groundwater age dating and recharge mechanism of Arusha aquifer,northern Tanzania: application of radioisotope and stable isotope techniques

The continuous abstraction of groundwater from Arusha aquifers in northern Tanzania has resulted in a decline in water levels and subsequent yield reduction in most production wells. The situation is threatening sustainability of the aquifers and concise knowledge on the existing groundwater challenge is of utmost importance. To gain such knowledge, stable isotopes of hydrogen and oxygen, and radiocarbon dating on dissolved inorganic carbon (DIC), were employed to establish groundwater mean residence time and recharge mechanism.¹⁴C activity of DIC was measured in groundwater samples and corrected using a δ¹³C mixing method prior to groundwater age dating. The results indicated that groundwater ranging from 1,400 years BP to modern is being abstracted from deeper aquifers that are under intensive development. This implies that the groundwater system is continuously depleted due to over-pumping, as most of the sampled wells and springs revealed recently recharged groundwater. High ¹⁴C activities observed in spring water (98.1?±?7.9 pMC) correspond with modern groundwater in the study area. The presence of modern groundwater suggests that shallow aquifers are actively recharged and respond positively to seasonal variations.     

Radiocarbon dating and the <Superscript>36</Superscript>Cl/Cl evolution of three Great Artesian Basin wells at Dalhousie,South Australia

The use of ¹⁴C (half-life?=?5,730 years) in modeling the evolution of the ³⁶Cl/Cl ratios in groundwater is reported for the first time. The complexity of the Cl–³⁶Cl system due to the occurrence of different Cl and ³⁶Cl sources and the difficulty of the determination of the initial groundwater ³⁶Cl/Cl ratios have raised concerns about the reliability of using ³⁶Cl (half-life?=?301 thousand years, a) as a groundwater-dating tool. This work uses groundwater ¹⁴C age as a calibrating parameter of the Cl–³⁶Cl/Cl decay-mixing models of three wells from the southwestern Great Artesian Basin (GAB), Australia. It aims to allow for the different sources of Cl and ³⁶Cl in the southwestern GAB aquifer. The results show that the initial Cl concentrations range from 245 to 320 mg/l and stable Cl is added to groundwater along flowpaths at rates ranging from 1.4 to 3.5 mg/l/ka. The ³⁶Cl content of the groundwater is assumed to be completely of atmospheric origin. The samples have different Cl–³⁶Cl/Cl mixing-decay models reflecting recharge under different conditions as well as the heterogeneity of the aquifer.     

Changes of δ<Superscript>18</Superscript>O and δD along the Dousitu River,Inner Mongolia,China, and their evidence of river water evaporation

On the basis of the hydrogeology of the Dousitu River drainage basin, the changes of water flow rate, δ¹⁸O and δD along the Dousitu River are discussed according to measured and analytical results. Changes of flow rate along the Dousitu River agree well with groundwater level contours and the recharge and discharge of groundwater to the river. When compared with other types of water in the area, it is obvious that the ¹⁸O and D of river waters have experienced evaporation. The changes of δ¹⁸O and δD along the Dousitu River are mainly caused by combined effects of groundwater recharge and river water evaporation. The recharge of groundwater makes δ¹⁸O and δD of the river water decrease. Evaporation makes δ¹⁸O and δD of the river water increase. The evaporation fractions of the river water are calculated using the kinetic fractionation theory. Results showed as much as 10–30% of water was evaporated in different segments of Dousitu River.     

Effects of rainwater-harvesting-induced artificial recharge on the groundwater of wells in Rajasthan, India

In light of the increasing deterioration of groundwater supplies in Rajasthan, India, rainwater harvesting practices in southern Rajasthan were studied to determine the effects of artificially recharged groundwater on the supply and quality of local groundwater. A physical and geochemical investigation utilizing environmental tracers (δ¹⁸O and Cl^–), groundwater level and groundwater quality measurements, and geological surveys was conducted with two objectives: (1) to quantify the proportion of artificially recharged groundwater in wells located near rainwater harvesting structures and (2) to examine potential effects of artificial recharge on the quality of groundwater in these wells. A geochemical mixing model revealed that the proportion of artificial recharge in these wells ranged from 0 to 75%. Groundwater tracer, water table, and geological data provided evidence of complex groundwater flow and were used to explain the spatial distribution of artificial recharge. Furthermore, wells receiving artificial recharge had improved groundwater quality. Statistical analysis revealed a significant difference between the water quality in these wells and wells determined not to receive artificial recharge, for electrical conductivity and SO ₄ ^– . The findings from this study provide quantitative evidence that rainwater harvesting structures in southern Rajasthan influence the groundwater supply and quality of nearby wells by artificially recharging local groundwater.     

Investigation of young water inflow in karst aquifers using SF6–CFC–3H/He–85Kr–39Ar and stable isotope components

Karst aquifers are known for their wide distribution of water transfer velocities. From this observation, a multiple geochemical tracer approach seems to be particularly well suited to provide a significant assessment of groundwater flows, but the choice of adapted tracers is essential. In this study, several common tracers in karst aquifers such as physicochemical parameters, major ions, stable isotopes, and δ¹³C to more specific tracers such as dating tracers – ¹⁴C, ³H, ³H–³He, CFC-12, SF₆ and ⁸⁵Kr, and ³⁹Ar – were used, in a fractured karstic carbonated aquifer located in Burgundy (France). The information carried by each tracer and the best sampling strategy are compared on the basis of geochemical monitoring done during several recharge events and over longer time periods (months to years).This study’s results demonstrate that at the seasonal and recharge event time scale, the variability of concentrations is low for most tracers due to the broad spectrum of groundwater mixings. The tracers used traditionally for the study of karst aquifers, i.e., physicochemical parameters and major ions, efficiently describe hydrological processes such as the direct and differed recharge, but require being monitored at short time steps during recharge events to be maximized. From stable isotopes, tritium, and Cl⁻ contents, the proportion of the fast direct recharge by the largest porosity was estimated using a binary mixing model. The use of tracers such as CFC-12, SF₆, and ⁸⁵Kr in karst aquifers provides additional information, notably an estimation of apparent age, but they require good preliminary knowledge of the karst system to interpret the results suitably. The CFC-12 and SF₆ methods efficiently determine the apparent age of baseflow, but it is preferable to sample the groundwater during the recharge event. Furthermore, these methods are based on different assumptions such as regional enrichment in atmospheric SF₆, excess air, and flow models among others. ⁸⁵Kr and ³⁹Ar concentrations can potentially provide a more direct estimation of groundwater residence time. Conversely, the ³H–³He method is inefficient in the karst aquifer for dating due to ³He degassing.     

An infrared and <Superscript>1</Superscript>H MAS NMR investigation of strong hydrogen bonding in ussingite,Na<Subscript>2</Subscript>AlSi<Subscript>3</Subscript>O<Subscript>8</Subscript>(OH)

The mineral ussingite, Na₂AlSi₃O₈(OH), an interrupted tectosilicate, has strong hydrogen bonding between OH and the other nonbridging oxygen atom in the structure. Infrared spectra contain a strongly polarized, very broad OH-stretching band with an ill-defined maximum between 1500 and 1800 cm^–1, and a possible OH librational bending mode at 1295 cm^–1. The IR spectra confirm the orientation of the OH vector within the triclinic unit cell as determined from X-ray refinement (Rossi et al. 1974). There are three distinct bands in the ¹H NMR spectrum of ussingite: a predominant band at 13.5 ppm (TMS) representing 90% of the structural hydrogen, a second band at 15.9 ppm corresponding to 8% of the protons, and a third band at 11.0 ppm accounting for the remaining 2% of structural hydrogen. From the correlation between hydrogen bond length and ¹H NMR chemical shift (Sternberg and Brunner 1994), the predominant hydrogen bond length (H...O) was calculated to be 1.49 Å, in comparison to the hydrogen bond length determined from X-ray refinement (1.54 Å). The population of protons at 15.9 ppm is consistent with 5–8% Al–Si disorder. Although the ussingite crystal structure and composition are similar to those of low albite, the bonding environment of OH in low albite and other feldspars, as characterized through IR and ¹H NMR, is fundamentally different from the strong hydrogen bonding found in ussingite.     

Identifying groundwater recharge connections in the Moscow (USA) sub-basin using isotopic tracers and a soil moisture routing model

Globally, aquifers are suffering from large abstractions resulting in groundwater level declines. These declines can be caused by excessive abstraction for drinking water, irrigation purposes or industrial use. Basaltic aquifers also face these conflicts. A large flood basalt area (1.1?×?10⁵ km²) can be found in the Northwest of the USA. This Columbia River Basalt Group (CRBG) consists of a thick series of basalt flows of Miocene age. The two major hydrogeological units (Wanapum and Grand Ronde formations) are widely used for water abstraction. The mean decline over recent decades has been 0.6 m year^?1. At present day, abstraction wells are drying up, and base flow of rivers is reduced. At the eastern part of CRBG, the Moscow sub-basin on the Idaho/Washington State border can be found. Although a thick poorly permeable clay layer exists on top of the basalt aquifer, groundwater level dynamics suggest that groundwater recharge occurs at certain locations. A set of wells and springs has been monitored bi-weekly for 9 months for δ¹⁸O and δ²H. Large isotopic fluctuations and d-excess values close to the meteoric water line in some wells are indicating that recharge occurs at the granite/basalt interface through lateral flow paths in and below the clay. A soil moisture routing (SMR) model showed that most recharge occurs on the granitic mountains. The basaltic aquifer receives recharge from these sedimentary zones around the granite/basalt interface. The identification of these types of areas is of major importance for future managed-aquifer recharge solutions to solve problems of groundwater depletion.     

Recharge and discharge controls on groundwater travel times and flow paths to production wells for the Ammer catchment in southwestern Germany

Travel times and flow paths of groundwater from its recharge area to drinking-water production wells will govern how the quality of pumped groundwater responds to contaminations. Here, we studied the 180 km² Ammer catchment in southwestern Germany, which is extensively used for groundwater production from a carbonate aquifer. Using a 3-D steady-state groundwater model, four alternative representations of discharge and recharge were systematically explored to understand their impact on groundwater travel times and flow paths. More specifically, two recharge maps obtained from different German hydrologic atlases and two plausible alternative discharge scenarios were tested: (1) groundwater flow across the entire streambed of the Ammer River and its main tributaries and (2) groundwater discharge via a few major springs feeding the Ammer River. For each of these scenarios, the groundwater model was first calibrated against water levels, and subsequently travel times and flow paths were calculated for production wells using particle tracking methods. These computed travel times and flow paths were indirectly evaluated using additional data from the wells including measured concentrations of major ions and environmental tracers indicating groundwater age. Different recharge scenarios resulted in a comparable fit to observed water levels, and similar estimates of hydraulic conductivities, flow paths and travel times of groundwater to production wells. Travel times calculated for all scenarios had a plausible order of magnitude which were comparable to apparent groundwater ages modelled using environmental tracers. Scenario with groundwater discharge across the entire streambed of the Ammer River and its tributaries resulted in a better fit to water levels than scenario with discharge at a few springs only. In spite of the poorer fit to water levels, flow paths of groundwater from the latter scenario were more plausible, and these were supported by the observed major ion chemistry at the production wells. We concluded that data commonly used in groundwater modelling such as water levels and apparent groundwater ages may be insufficient to reliably delineate capture zones of wells. Hydrogeochemical information relating only indirectly to groundwater flow such as the major ion chemistry of water sampled at the wells can substantially improve our understanding of the source areas of recharge for production wells.     

Coupling isotopic and piezometric data to infer groundwater recharge mechanisms in arid areas: example of Samail Catchment,Oman

Hydrochemistry and well hydrographs are coupled to assess groundwater recharge in the regional catchment of Samail, Oman. The complex geology comprises three aquifers: limestones of the Hajar Supergroup (HSG) at the highlands of North Oman Mountains (NOM); fractured/weathered ophiolites; and Quaternary alluvium. Groundwater flows south–north from the NOM to the coast. Samples from groundwater wells and springs (38) were analyzed for isotopes and major ions. Corrected ¹⁴C dating reveals modern groundwater across the entire catchment, while ⁸⁷Sr/⁸⁶Sr (0.70810–0.70895) shows greater homogeneity. Groundwater in the upper catchment is depleted in ²H and ¹⁸O, indicating a high-altitude recharge source (NOM), and becomes enriched downstream, with a slope indicating an evaporation effect. The hydrographs of nested piezometers located in the upper, middle and lower catchment show different recharge responses between deep and shallower depths. Head difference in response to recharge is observed upstream, suggesting a lateral recharge mechanism, contrary to vertical recharge downstream reflected in identical recharge responses. The homogeneous ⁸⁷Sr/⁸⁶Sr ratio, head changes, downstream enrichment of ²H and ¹⁸O, and the presence of modern groundwater throughout the catchment suggest that groundwater recharge takes place across the entire catchment and that the three aquifers are hydraulically connected. The recharge estimated using the chloride mass balance method is in the range of 0–43% of the mean annual rainfall.     

Hydrochemical framework of groundwater in the Ankobra Basin,Ghana

Hydrochemical and stable isotope (¹⁸O and ²H) analyses of groundwater samples were used to establish the hydrochemistry of groundwater in the Ankobra Basin. The groundwater was generally mildly acidic, low in conductivity and undersaturated with respect to carbonate phases. Major ions except bicarbonate were low and dissolved silica was moderately high. Silicate minerals weathering is probably the main process through which major ions enter the groundwater. Groundwater samples clustered tightly along the Global Meteoric Water Line suggesting integrative, smooth and rapid recharge from meteoric origin. The majority of the boreholes and a few hand dug wells cluster towards the Ca–Mg–HCO₃ dominant section of the phase diagram, in conformity with the active recharge and short residence time shown by the isotope data. Aluminium, arsenic, manganese, iron and mercury were the only trace metals analysed with concentrations significantly above their respective detection limits. Approximately 20%, 5%, 40% and 25% respectively of boreholes had aluminium, arsenic, iron and manganese concentrations exceeding the respective WHO maximum acceptable limits for drinking water. The relatively large percentage of boreholes with high concentration of aluminium reflects the acidic nature of the groundwater.     

A multi-tracer approach to delineate groundwater dynamics in the Rio Actopan Basin,Veracruz State,Mexico

Geochemistry and environmental tracers were used to understand groundwater resources, recharge processes, and potential sources of contamination in the Rio Actopan Basin, Veracruz State, Mexico. Total dissolved solids are lower in wells and springs located in the basin uplands compared with those closer to the coast, likely associated with rock/water interaction. Geochemical results also indicate some saltwater intrusion near the coast and increased nitrate near urban centers. Stable isotopes show that precipitation is the source of recharge to the groundwater system. Interestingly, some high-elevation springs are more isotopically enriched than average annual precipitation at higher elevations, indicating preferential recharge during the drier but cooler winter months when evapotranspiration is reduced. In contrast, groundwater below 1,200 m elevation is more isotopically depleted than average precipitation, indicating recharge occurring at much higher elevation than the sampling site. Relatively cool recharge temperatures, derived from noble gas measurements at four sites (11–20 °C), also suggest higher elevation recharge. Environmental tracers indicate that groundwater residence time in the basin ranges from 12,000 years to modern. While this large range shows varying groundwater flowpaths and travel times, ages using different tracer methods (¹⁴C, ³H/³He, CFCs) were generally consistent. Comparing multiple tracers such as CFC-12 with CFC-113 indicates piston-flow to some discharge points, yet binary mixing of young and older groundwater at other points. In summary, groundwater within the Rio Actopan Basin watershed is relatively young (Holocene) and the majority of recharge occurs in the basin uplands and moves towards the coast.     

Factors of <Superscript>18</Superscript>O/<Superscript>16</Superscript>O fractionation in corundum estimated from the calculation of isotopic shifts on vibration frequencies

The β-factors of corundum were estimated on the basis of DFT calculations of vibrational frequency changes due to ¹⁶O–¹⁸O isotope substitution in a harmonic approximation using an all-electron Gaussian-type basis set and the B3LYP hybrid functional (the CRYSTAL program). Calculations were performed accounting for eight phonon wave vectors within the first Brillouin zone. The results are approximated by the relation 1000ln β _crn = 9.19874x–0.12326x ² + 0.00213x ³ (x = 10⁶/T(K)², 400 < T(K) < 1300), which can be used in isotope geochemical studies in combination with the known temperature effects on the β-factors of other phases.     

Stable water isotope climate archives in springs from the Olympic Mountains,Washington

The ¹⁸O and ²H (HDO) compositions are summarized for sampled springs (n = 81) within the Elwha watershed (≈692 km²) on the northern Olympic Peninsula. Samples, collected during 2001–2009, of springs (n = 158), precipitation (n = 520), streams (n = 176), and firn (n = 3) assisted the determinations for meteoric composition of recharge waters. The local mean water line (LMWL) is defined as δ²H = 8.2δ¹⁸O − 9.3 for the watershed. Recharge history is surmised from groundwater ages ranging from 5 ± 3 years (apparent ⁸⁵Kr) to 9,490 ± 420 ¹⁴C cal years BP. About 56% of the springs were recharged over the last 1,000 years while 13% of springs were recharged over 5,000 years ago. Spring HDO values fluctuate between −11.8 to −15.6‰ δ¹⁸O and −90.9 to −119.4‰ δ²H. Deuterium excess values predominate around 4–6‰. The HDO proxy records from springs suggest a pronounced paleoclimate shift in air masses near 5,000 year BP on the Peninsula.     

Probing the relationship between surface waters and aquifers by <Superscript>18</Superscript>O measurements on the top of the Araripe Plateau/NE Brazil

The Araripe Plateau in northeastern Brazil has an area of about 8,000 km², confined by 39°05E and 40°55E, and 7°10S and 7°50S. Due to high permeability of soils, a surface drainage system is practically inexistent. Water is stored in excavations with clayey soil, the barreiros. Monthly samples were taken for ¹⁸O measurements, from September 1999 to August 2000, from four barreiros, three dug wells and five drilled wells. Results show that (1) groundwaters in the eastern part of the plateau are derived from present-day rainfall (¹⁸O–3.2), whereas groundwaters in the western portion are isotopically different (¹⁸O–5.0); (2) barreiros are strongly marked seasonally by elevated ¹⁸O during the dry period due to elevated evaporation; (3) a dug well at a distance of 30 m from a barreiro exhibits ¹⁸O similar to that of the reservoir, indicating a strong interaction between groundwater and surface water; and (4) a tubular well of 242-m depth, located in a fault, exhibits strong seasonal changes in ¹⁸O and electrical conductivity, revealing downward leakage between aquifers.     

Hydrogeological and hydrogeochemical characterization of a karstic mountain region

Karstic limestone formations in the Mediterranean basin are potential water resources that can meet a significant portion of groundwater demand. Therefore, it is necessary to thoroughly study the hydrogeology and hydrogeochemistry of karstic mountain regions. This paper presents a detailed hydrogeological and hydrogeochemical characterization of the Nif Mountain karstic aquifer system in western Turkey, an important recharge source for the densely populated surrounding area. Based on the geological and hydrogeological studies, four major aquifers were identified in the study area including the allochthonous limestone in Bornova flysch, conglomerate-sandstone and clayey-limestone in Neogene series, and the Quaternary alluvium. Physicochemical characteristics of groundwater were measured in situ, and samples were collected at 59 locations comprised of springs and wells. Samples were analyzed for major ions, isotopic composition, arsenic, boron and heavy metals among other trace elements. It was found that the hydrogeological structure is complex with many springs having a wide range of discharge rates. High-discharge springs originate from allochthonous limestone units, whereas low-discharge springs are formed at the contacts with claystone and limestone units. Using stable isotope analysis data, a δ¹⁸O-deuterium relationship was obtained that lies between the Mediterranean meteoric and mean global lines. Tritium analyses showed that low-discharge springs originating from contact zones had longer circulation times compared to the high-discharge karstic springs. Furthermore, hydrogeochemical data revealed that groundwater quality significantly deteriorated as water moved from the mountain to the plains. Heavy metal, arsenic and boron concentrations were generally within drinking-water quality standards with a few exceptions occurring in residential and industrial areas located at the foothills of the mountain. Elevated arsenic concentrations were related to local geologic formations, which are likely to contain oxidized sulfite minerals in claystones. It is concluded that Nif Mountain overall has a significant potential to provide high-quality water with a safe yield of at least 50 million m³/year, which corresponds to about 28% of the mean annual inflow to the Tahtali reservoir, a major water resource for the city of Izmir. An erratum to this article can be found at     

Quantification of groundwater–surface water interactions using environmental isotopes: A case study of Bringi Watershed,Kashmir Himalayas,India

Environmental isotopes including \({\updelta }^{18}\)O, \({\updelta }^{2}\)H and \(^{3}\)H of precipitation, streams and springs were determined in the mountainous Bringi catchment of Kashmir Himalaya, dominated by carbonate lithology. The isotopic signature of winter precipitation is reflected in stream and spring water in late spring and is, therefore, representative of snow melting. The spring waters in September bear the enriched isotopic signatures of summer rainfall. The strong correlation (\(r^{2} = 0.97\)) between the isotopic composition of streams and springs indicates the streams and springs either share similar catchments or the springs are recharged by the streams. Chloride mass balance and isotopic mass balance studies suggest that the surface recharge component averages 337.35 m\(^{3}\)/s, which is about 75% of total stream discharge during the high flow period. Similarly, the contribution of surface water to groundwater recharge during the low flow period averages 7.5 m\(^{3}\)/s, which is about 18.6% of total stream flow. Furthermore, the mean residence time of the springs calculated from the tritium decay equation is very short (<1 year). The residence time is longer for Kongamnag and short for Achabalnag, which is further supported by dye testing.     

Cosmogenic radionuclide <Superscript>7</Superscript>Be concentration in seven species of lichens and its correlation with <Superscript>40</Superscript>K, <Superscript>137</Superscript>Cs and <Superscript>226</Superscript>Ra

In this work, accumulation of cosmogenic radionuclide ⁷Be in seven species of lichens was determined using HPGe detectors in autumn season. Ramsar city which is located in the north of Iran as one of the high-level natural radiation areas in the world was considered. Lichen species represented good potential in accumulation of ⁷Be radionuclide. The foliose species of Xanthoria parietina with the highest activity concentration value of 112.8 ± 1.8 Bq kg^?1 was introduced as bioindicator for accumulation of ⁷Be radionuclide. Cladonia rangiformis species has got minimum concentration of 64.5 ± 0.8 Bq kg^?1. Also from thallus morphology viewpoint, results showed that ⁷Be accumulation in foliose species is higher than in fruticose and crustose lichens species. Also there was relatively large positive correlation between ⁷Be and ²²⁶Ra activity concentrations in lichens species.     

Zinclipscombite,ZnFe<Stack><Subscript>2</Subscript><Superscript>3+</Superscript></Stack>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript>(OH)<Subscript>2</Subscript>, a new mineral species

Zinclipscombite, a new mineral species, has been found together with apophyllite, quartz, barite, jarosite, plumbojarosite, turquoise, and calcite at the Silver Coin mine, Edna Mountains, Valmy, Humboldt County, Nevada, United States. The new mineral forms spheroidal, fibrous segregations; the thickness of the fibers, which extend along the c axis, reaches 20 μm, and the diameter of spherulites is up to 2.5 mm. The color is dark green to brown with a light green to beige streak and a vitreous luster. The mineral is translucent. The Mohs hardness is 5. Zinclipscombite is brittle; cleavage is not observed; fracture is uneven. The density is 3.65(4) g/cm³ measured by hydrostatic weighing and 3.727 g/cm³ calculated from X-ray powder data. The frequencies of absorption bands in the infrared spectrum of zinclipscombite are (cm^?1; the frequencies of the strongest bands are underlined; sh, shoulder; w, weak band) 3535, 3330sh, 3260, 1625w, 1530w, 1068, 1047, 1022, 970sh, 768w, 684w, 609, 502, and 460. The Mössbauer spectrum of zinclipscombite contains only a doublet corresponding to Fe³⁺ with sixfold coordination and a quadrupole splitting of 0.562 mm/s; Fe²⁺ is absent. The mineral is optically uniaxial and positive, ω = 1.755(5), ? = 1.795(5). Zinclipscombite is pleochroic, from bright green to blue-green on X and light greenish brown on Z (X > Z). Chemical composition (electron microprobe, average of five point analyses, wt %): CaO 0.30, ZnO 15.90, Al₂O₃ 4.77, Fe₂O₃ 35.14, P₂O₅ 33.86, As₂O₅ 4.05, H₂O (determined by the Penfield method) 4.94, total 98.96. The empirical formula calculated on the basis of (PO₄,AsO₄)₂ is (Zn_0.76Ca_0.02)_Σ0.78(Fe _1.72 ³⁺ Al_0.36)_Σ2.08[(PO₄)_1.86(AsO₄)_0.14]_Σ2.00(OH)_{1. 80} · 0.17H₂O. The simplified formula is ZnFe ₂ ³⁺ (PO₄)₂(OH)₂. Zinclipscombite is tetragonal, space group P4₃2₁2 or P4₁2₁2; a = 7.242(2) Å, c = 13.125(5) Å, V = 688.4(5) ų, Z = 4. The strongest reflections in the X-ray powder diffraction pattern (d, (I, %) ((hkl)) are 4.79(80)(111), 3.32(100)(113), 3.21(60)(210), 2.602(45)(213), 2.299(40)(214), 2.049(40)(106), 1.663(45)(226), 1.605(50)(421, 108). Zinclipscombite is an analogue of lipscombite, Fe²⁺Fe ₂ ³⁺ (PO₄)₂(OH)₂ (tetragonal), with Zn instead of Fe²⁺. The mineral is named for its chemical composition, the Zn-dominant analogue of lipscombite. The type material of zinclipscombite is deposited in the Mineralogical Collection of the Technische Universität Bergakademie Freiberg, Germany.