Abstract
The Xifeng geothermal field is located in the Yangtze Craton, SW China, and is one of the most representative low-temperature geothermal fields in China. Widespread thermal anomalies, hot springs, and geothermal wells have been reported by previous studies. However, the nature and forming mechanisms of the field remain poorly understood. Element geochemical (ions, rare earth elements) and stable isotopic (D, O) composition of hot springs, geothermal fluids, rivers, and cold springs from different locations of the Xifeng geothermal field were analyzed in this study. The ions studies revealed that most samples featured the Ca-Mg-HCO3 type, except Xifeng hot springs, and which were characterized by the Ca-Mg-HCO3-SO4 type. Based on quartz geothermometers, the estimated reservoir temperature was 77°C. The results of stable isotopes (D, O) manifest that the Xifeng geothermal system was recharged by meteoric water at an elevation of 1,583 m from SW to NE. The research of rare earth elements (REE) revealed that their accumulation characteristics and obvious positive Eu anomaly were inherited from host feldspar-bearing reservoir dolomites through water-rock interactions. Combined with these observations, geological setting, and previous studies, it was concluded that the formation of the Xifeng geothermal field resulted from recharge, deep circulation, and secondary rising of the meteoric water along the faults. First, meteoric water infiltrated to depth through faults and crack zones. Second, the deep-infiltrated water was heated by radioactive heat, deep heat, and tectonic frictional heat. Finally, as the warmed-up waters underwent considerable deep circulation in the reservoir, it rose again along the main faults, and mixed with groundwater near the surface. Taken together, we suggest that the Xifeng geothermal system should be assigned as a faults-controlling, and deeply circulating meteoric water of low-temperature category.
Introduction
Geothermal resources are well developed in China and contribute significantly to the global supply of total resources (7.9%; Wang G. L. et al., 2017), while they are mainly produced as widespread medium-low temperature types (Wang G. L. et al., 2017; ). The occurrence of high-temperature types is limited and mainly formed in South China, e.g., southern Tibet, western Sichuan and Yunnan, as well as the south-east coastal area (; ; Zhang et al., 2016; , ; Tian et al., 2018; ; Zheng et al., 2021). These distribution characteristics mean that research on geothermal resources in South China mainly focuses on the high-temperature type, whereas studies on the medium-low type are limited.
South China has a significant geothermal potential and hosts many world-famous geothermal fields, including high-temperature Yangbajing, Tengchong, and Kangding, as well as low-temperature Xifeng in Guizhou Province (; ; ; Wang et al., 2018; Yang et al., 2018; Wang et al., 2019b; ). There are lots of hot springs, hydrothermal manifestations, and geothermal wells located in the Xifeng geothermal field, indicating great potential for exploration, and utilized prospects (Yang et al., 2018; Figure 1B). Although systematic exploration and utilization of Xifeng began in the 1950s, the scientific research on the overall field is poor, and attributed to the single application mode of geothermal resources. In recent years, with the increased need for renewable energy, a new round of exploration work and scientific study has been conducted to evaluate the potential of hydrothermal resources. Previous studies have focused on single hot springs or geothermal wells mainly based on hydrogeochemistry and geology (; Song et al., 2014; ). However, comprehensive comparative research on respective hot springs, geothermal wells, and related rivers from the whole geothermal field have not been conducted, meaning that the signature, evolution, and forming mechanisms of the Xifeng geothermal field remain obscure.
FIGURE 1
In this study, representative hot springs, geothermal fluids, cold springs, and related river waters were sampled for detailed element geochemistry (ions, rare earth elements) and stable isotopes (D, O) studies. This new comprehensive dataset allows us to confirm the feature, evolution, and genesis of the geothermal fluids, which will provide a favorable understanding of the forming mechanisms for the Xifeng geothermal field, and similar geothermal fields in South China and worldwide.
Geological Tectonic and Hydrogeological Settings
Geological Setting
The Xifeng geothermal field is situated in the central Guizhou Province, southwestern China (Figure 1A). The geological location is in the Guiyang Complex Tectonic Deformation Zone related to the central Guizhou uplift within the Yangtze Craton in South China (Figure 1A;
The stratigraphic succession of the Xifeng geothermal field consists of, from bottom to top, the Sinian Qingshuijiang, Nantuo, Doushantuo, and Dengying formations, lower Cambrian Niutitang, Mingxinsi, Jindingshan, Qingxudong, Gaotai, and Shilengshui formations and Loushanguan Group, Permian Liangshan Qixia, Maokou, Wujiaping, and Changxing formations, and Triassic Yelang and Maocaopu formations (Figure 1C;
The central Guizhou region experienced a series of tectonic events from Sinian to late Cambrian, such as the Yunan Movement (forming the central Guizhou uplift;
Tectonic Setting
Faults are well developed in the study area due to multi-stage tectonic activities, such as the Emeishan mantle-plume eruption, Yanshanian orogeny, and Himalayan crust uplift movement (Figure 1B). These faults are mainly thin-skinned with high hydraulic conductivities and resulted in greater exploitation potential relative to other geothermal fields in China. One of the most important faults is the compresso-shear strike-slip Baimadong fault, which is the main conduit and connects the deep heat source (
Hydrogeological Setting
The Xifeng geothermal field covers an area of 102.7 km2 (
FIGURE 2

Geological cross-section along section line A-A′ on the map in Figure 1B of the Xifeng geothermal field (modified from Wang H. S. et al., 2017;
Sampling and Study Methods
Water Sample and Analyses
Fieldwork was carried out in the Xifeng area for collecting samples and obtaining relevant field data in April 2021. A total of 16 water samples (six hot spring samples, two geothermal well samples, six river samples, and two cold spring samples) at Xifeng were collected for major ions, REE, and D-O isotope analyses. Sample locations are shown in Figure 1B.
Time sensitive parameters were tested on site using a portable water quality analyzer. Samples were stored in new 500 ml polyethylene bottles that were rinsed with deionized water twice before sampling. All mentioned hydrochemical analyses of the water samples were performed in the Laboratory of Beijing Research Institute of Uranium Geology. Samples used for analysis of cations were acidified after collection through adding Suprapur HNO3 to bring the pH to below 2. Analysis of major anions and cations was conducted by using Dionex ICS 1100 ion chromatography through Dionex ionpac AS-19HC and CS12A (4 mm × 250 mm) columns, respectively. The analysis of rare earth elements in water samples was documented using a Thermo Scientific ELEMENT XR inductively coupled plasma mass spectrometer (ICP-MS). The instrument was externally calibrated using a multielement standard solution before ICP-MS analysis. The analytical precision was better than 10% for duplicate analysis of the samples. The composition of deuterium (D) and oxygen (18O) isotopes of collected water samples was analyzed by a MAT 253 mass spectrometer in a continuous flow mode using a Gas-bench II preparation and introduction system. Isotopic data are expressed in the delta (δ) notation as the per mil (‰) deviation relative to the Standard Mean Ocean Water (SMOW); the analytic precisions (1σ) are ±1.0 and ±0.1‰ for δD and δ18O, respectively.
Geothermometry
Chemical geothermometers are helpful to estimate the reservoir equilibrium temperature of the geothermal system by using the distribution and relative contents of various chemical indicators (i.e., dissolved silica, cation, gas, and isotopes;
Various geothermometers can obtain different estimated reservoir temperatures as each geothermometer documents the last equilibrium of a specific chemical element and is directly affected by processes of boiling, dilution, and precipitation. Cation geothermometers (Na-K, K-Mg, and Na-K-Ca) and silica geothermometers (quartz no steam loss, quartz maximum steam loss, chalcedony no steam loss, chalcedony maximum steam loss, α-cristobalite, and β-cristobalite) applied in this study are shown in Table 1.
TABLE 1
| Geothermometer | Reference | Equations |
|---|---|---|
| Na-K | T = 1,217/[log(Na/K)+1.483]−273.15 | |
| Na-K | Truesdell, (1976) | T = 856/[log(Na/K)+0.857]−273.15 |
| Na-K | T = 1,390/[log(Na/K)+1.75]−273.15 | |
| Na-K | Tonani, (1980) | T = 883/[log(Na/K)+0.78]−273.15 |
| Na-K | T = 1,178/[log(Na/K)+1.47]−273.15 | |
| Na-K | T = 933/[log(Na/K)+0.993]−273.15 | |
| Na-K | T = 1,319/[log(Na/K)+1.699]−273.15 | |
| Na-K | T = 908/[log(Na/K)+0.7]−273.15 | |
| K-Mg | T = 4,410/[14−log(K2/Mg)]−273.15 | |
| Na-K-Ca | T = 1,647/{log(Na/K)+b[log(Ca1/2/Na)+2.06]+2.47}−273.15, where b = 4/3, if T < 100°C; b = 1/3, if T > 100°C | |
| Quartz, no steam loss (conductive) | T = [1,309/(5.19−logSiO2)]−273.15 | |
| Quartz, maximum steam loss at 100°C (adiabatic) | T = [1,522/(5.75−logSiO2)]−273.15 | |
| Chalcedony (no loss of steam) | T = [1,032/(4.69−logSiO2)]−273.15 | |
| Chalcedony (maximum steam loss) | T = [1,264/(5.31−logSiO2]−273.15 | |
| α-Cristobalite | T = [1,000/(4.78−logSiO2)]−273.15 | |
| β-Cristobalite | T = [781/(451−logSiO2)]−273.15 |
Geothermometry equations (in°C) for the cation and silica geothermometers used in this study.
Results
Ions Characteristics
The physico-chemical compositions of samples in this study are shown in Table 2. All samples showed alkaline pH values. In almost all the samples, the anions were dominated by HCO3− and the order of abundance was: HCO3- > SO42- > Cl−. Among the cations, the main ion was Ca2+, and the following order of abundance was Ca2+ > Mg2+ > Na+ > K+. As shown in the
TABLE 2
| Sample NO. | BY-1 | BY-2 | BD-1 | BD-2 | MR-1 | MR-2 | ML-1 | ML-2 | XQ-1 | XQ-2 | XF-1 | XF-2 | XF-3 | XF-4 | NS-1 | NS-2 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| PH | 8.05 | 7.98 | 8.06 | 8.12 | 8.01 | 7.92 | 7.83 | 7.96 | 8.19 | 8.15 | 8.05 | 8 | 8.08 | 8.05 | 8.06 | 8.19 |
| δ18OV-SMOW(‰) | −7.5 | −8.1 | −8.2 | −8.1 | −7.8 | −8.3 | −7.4 | −7 | −6.5 | −7 | −8 | −8.5 | −8.3 | −7.9 | −9.2 | −8.7 |
| δDV-SMOW(‰) | −51.1 | −53.7 | −54.1 | −55.6 | −56.2 | −57.4 | −48.3 | −47.9 | −45.9 | −47.7 | −56.3 | −59.1 | −58.8 | −58 | −65.6 | −65.6 |
| T(°C) | 12 | 12 | 13 | 13 | 43 | 43 | 14 | 14 | 14 | 14 | 56 | 56 | 56 | 56 | 48 | 48 |
| K+ | 1.2 | 1.13 | 2.23 | 2.17 | 1.04 | 1.08 | 7.96 | 7.64 | 2.2 | 2.16 | 3.51 | 3.41 | 3.56 | 3.7 | 3.08 | 2.98 |
| Na+ | 1.86 | 1.81 | 4.66 | 4.71 | 4.27 | 4.33 | 16 | 15.9 | 1.67 | 1.68 | 11.7 | 11.8 | 11.8 | 12.3 | 2.29 | 2.12 |
| Ca2+ | 34.7 | 35.1 | 47.2 | 49 | 45.1 | 44.6 | 62.1 | 61.2 | 57.2 | 57.3 | 52.7 | 52.5 | 52.8 | 54.3 | 36.9 | 36.9 |
| Mg2+ | 14.3 | 14.3 | 20.2 | 20.7 | 26.2 | 26 | 25 | 24.9 | 19.1 | 19.3 | 21.1 | 20.9 | 21.1 | 21.6 | 22.1 | 22.1 |
| HCO3- | 140 | 141 | 184 | 184 | 245 | 245 | 235 | 235 | 232 | 234 | 169 | 172 | 171 | 170 | 208 | 209 |
| SO42- | 20.5 | 20.8 | 39.6 | 40.4 | 17.6 | 16.6 | 41.5 | 40.1 | 16.5 | 16.6 | 88.4 | 91.5 | 88.3 | 91.4 | 10.7 | 10.4 |
| Cl- | 1.35 | 1.33 | 7.02 | 7.08 | 0.67 | 0.654 | 18.4 | 18 | 3.16 | 3.23 | 3.07 | 3.03 | 3.04 | 3.11 | 0.725 | 0.725 |
| SiO2 | 4.68 | 4.61 | 6.54 | 6.58 | 20.43 | 20.46 | 5.89 | 5.93 | 6.34 | 6.23 | 39.71 | 39.92 | 39.85 | 38.82 | 15.39 | 15.79 |
| La | 0.01 | 0.005 | 0.008 | 0.005 | 0.006 | 0.006 | 0.013 | 0.01 | 0.022 | 0.018 | 0.082 | 0.006 | <0.002 | <0.002 | 0.002 | 0.003 |
| Ce | 0.012 | 0.011 | 0.013 | 0.013 | 0.002 | <0.002 | 0.022 | 0.024 | 0.043 | 0.048 | 0.097 | 0.006 | 0.002 | 0.005 | 0.003 | 0.004 |
| Pr | 0.002 | 0.003 | <0.002 | 0.002 | <0.002 | <0.002 | 0.002 | 0.002 | 0.006 | 0.005 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.002 |
| Nd | 0.008 | 0.003 | 0.158 | 0.006 | 0.011 | 0.003 | 0.016 | 0.008 | 0.024 | 0.049 | 0.002 | 0.005 | 0.002 | 0.004 | 0.002 | 0.006 |
| Sm | <0.002 | 0.003 | 0.002 | 0.002 | 0.004 | 0.007 | 0.002 | 0.004 | 0.008 | 0.004 | 0.002 | 0.002 | <0.002 | <0.002 | <0.002 | 0.002 |
| Eu | 0.007 | 0.004 | 0.004 | 0.012 | 0.027 | 0.03 | 0.016 | 0.006 | 0.005 | 0.002 | <0.002 | 0.01 | 0.005 | 0.016 | 0.012 | 0.015 |
| Gd | 0.003 | 0.006 | <0.002 | 0.004 | 0.002 | 0.005 | 0.011 | 0.013 | 0.005 | 0.005 | 0.003 | 0.005 | <0.002 | 0.002 | 0.006 | 0.003 |
| Tb | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.007 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 |
| Dy | 0.003 | <0.002 | <0.002 | 0.003 | <0.002 | <0.002 | 0.004 | 0.002 | 0.007 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.004 |
| Y | 0.022 | 0.015 | 0.006 | 0.011 | 0.006 | 0.006 | 0.018 | 0.012 | 0.024 | 0.031 | 0.01 | 0.012 | 0.008 | 0.008 | 0.005 | 0.006 |
| Ho | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.002 |
| Er | 0.002 | 0.005 | <0.002 | 0.002 | <0.002 | 0.002 | 0.005 | <0.002 | 0.003 | <0.002 | <0.002 | 0.002 | <0.002 | <0.002 | <0.002 | 0.002 |
| Tm | 0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 |
| Yb | 0.004 | <0.002 | 0.007 | 0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.002 | 0.002 | <0.002 | <0.002 | <0.002 | <0.002 | 0.002 | 0.002 |
| Lu | 0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 | <0.002 |
| Total REE | <0.083 | <0.067 | <0.214 | <0.07 | <0.074 | <0.08 | <0.119 | <0.093 | <0.157 | <0.176 | <0.214 | <0.062 | <0.039 | <0.055 | <0.048 | <0.057 |
| δEu | >13.457 | 4.440 | >9.418 | 19.978 | 44.950 | 23.878 | 16.063 | 3.918 | 3.723 | 2.106 | <3.845 | 14.891 | >11.772 | >37.671 | >16.312 | 28.836 |
| δCe | 0.619 | 0.655 | >0.750 | 0.949 | >0.133 | 0.133 | 0.995 | 1.238 | 0.864 | 1.167 | >1.748 | >0.400 | 0.231 | 0.577 | >0.346 | 0.377 |
| Sample type | River | River | River | River | Hot spring | Hot spring | River | River | Cold spring | Cold spring | Hot spring | Hot spring | Hot spring | Hot spring | Well | Well |
| Water type | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3 | Ca-Mg-HCO3-SO4 | Ca-Mg-HCO3-SO4 | Ca-Mg-HCO3-SO4 | Ca-Mg-HCO3-SO4 | Ca-Mg-HCO3 | Ca-Mg-HCO3 |
Measured parameters, major ion chemistry (mg/L), SiO2 (mg/L), Rare Earth Element (μg/L), and δD-δ18O composition of water samples from the Xifeng geothermal field.
Notes: δEu = EuN/sqrt(SmN*GdN); δCe = CeN/sqrt(LaN*PrN); N=Post-Archean Shale normalized; LREE = La + Ce + Pr + Nd + Sm + Eu; HREE = Gd + Tb + Dy + Ho + Er + Tm + Yb + Lu.
FIGURE 3

Piper diagram for all water sampled from the Xifeng geothermal field.
FIGURE 4

Semi-logarithmic Schoeller diagram of all water from the Xifeng geothermal field.
FIGURE 5

Ternary plot of Cl-SO4-HCO3 for samples of the Xifeng geothermal field (after
FIGURE 6

A 10 Mg/(10 Mg + Ca) vs 10 K/(10 K + Na) plot of thermal and cold springs of the Xifeng geothermal field, using a Na/K-Mg-Ca diagram (after
FIGURE 7

The distribution of ionic ratios in water samples of the Xifeng geothermal field, (A) HCO3- vs Ca2+ + Mg2+; (B) Cl− vs Na+; (C) HCO3- + SO42- vs Ca2+ + Mg2+; and (D) SO42- vs Ca2+. BD represents samples labeled as BD-1 and BD-2; BY represents samples labeled as BY-1 to BY-4, ML represents samples labeled as ML-1 and ML-2; MR represents samples labeled as MR-1 and MR-2; NS represents samples labeled as NS-1 and NS-2; XF represents samples labeled as XF-1 to XF-4; and XQ represents samples labeled as XQ-1 and XQ-2.
Rare Earth Elements
The REE signatures of geothermal fluids can be used to assess the influences of water-rock interaction. REE composition of sampled waters were analyzed in this study, and the results are shown in Table 2. Four types of water appeared to have similar PAAS-normalized REE patterns, which were featured by heavy rare earth elements (HREE) enrichment compared to light rare earth elements (LREE), and positive Eu anomalies (Figure 8). The total rare earth elements (REE) contents in the geothermal well fluids (∼0.048 to ∼ 0.057 μg/L), hot spring waters (∼0.039–∼0.214 μg/L), river waters (∼0.067 to ∼0.214 μg/L), and cold spring waters (∼0.157 to 0.176 μg/L) were relatively low. The δCe values were 0.346–0.377, 0.133–0.577, 0.619–0.238, and 0.864–1.167, and δEu values were 16.312–28.836, 3.845–44.950, 3.918–19.978, and 2.106–3.723 for waters of the geothermal well, hot spring, river, and cold spring, respectively.
FIGURE 8

Post-Archean Australian Average Shale (PAAS) REE diagrams for water samples from the Xifeng geothermal field. For the values shown as ranges (<0.002), the maximum values (0.002) are used for plotting.
Hydrogen and Oxygen Isotope Compositions
Hydrogen and oxygen isotopic compositions of sampled waters in this study are shown in Table 2. The measured δDv-SMOW values ranged from −65.6 to −65.6‰ (avg. = −65.6‰, n = 2), −59.1 to −56.2‰ (avg. = −57.6‰, n = 6), −55.6 to −47.9‰ (avg. = −51.8‰, n = 6), and −47.7 to −45.9‰ (avg. = −46.8‰, n = 2) for the geothermal well, hot springs, river, and cold spring waters, respectively. The measured δ 18Ov-SMOW values were −9.2 to −8.7 (avg. = −8.95‰, n = 2), −8.5 to −7.8‰ (avg. = −8.13‰, n = 6), −8.2 to −7‰ (avg. = −7.71‰, n = 6), and −7 to −6.5‰ (avg. = −6.75‰, n = 2) for the geothermal well, hot spring, river, and cold spring waters, respectively.
Discussion
Source of Major Ions in the Geothermal Waters
Since most sampled waters were assigned to the Ca-Mg-HCO3 type (Figure 3), this bicarbonate and Ca-Mg dominated feature can be attributed to the interaction with reservoir rocks, which are mainly Sinian dolomites. Ca2+, Mg2+, and HCO3− were sourced from the dissolution of dolomites following the equation of
As illustrated in Figure 6, the water-rock interaction is a dominant process in thermal and cold springs of the Xifeng geothermal field, although water is not equalized with the host reservoir rocks. Water-rock reactions can be further evidenced by the δ18O results of geothermal waters, which deviate 2‰ of units from LMWL (Figure 11; Taylor, 1977). Additionally, most REE concentrations of sampled waters were above the detection limits (Table 2), indicating that REE in the samples were not derived from meteoric waters (
The characteristics of major ions and their intercorrelation can be used to deduce the geochemical processes caused by the water-rock reaction that the groundwater encounters along its flow path (
Geothermal Reservoir Temperature
The Giggenbach Na-K-Mg ternary diagram is used for categorizing waters as full equilibrium, partial equilibrium, or immaturity compared with reservoir rocks (
FIGURE 9

Ternary Na-K-Mg (mg/L) diagram for water samples from the Xifeng geothermal field.
TABLE 3
| Sample NO. | T(Na-K)① | T(Na-K)② | T(Na-K)③ | T(Na-K)④ | T(Na-K)⑤ | T(Na-K)⑥ | T(Na-K)⑦ | T(Na-K)⑧ | T(K-Mg)⑨ | T(Na-K-Ca)⑩ | Quartz, no steam loss (conductive)⑪ | Quartz, maximum steam loss at 100 °C (adiabatic)⑫ | Chalcedony (no loss of steam)⑬ | Chalcedony (maximum steam loss)⑭ | α-Cristobalite⑮ | β-Cristobalite⑯ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| MR-1 | 307.37 | 309.16 | 314.99 | 360.55 | 292.27 | 307.65 | 297.25 | 418.19 | 13.51 | −2.81 | 64.24 | 69.66 | 32.19 | 42.86 | 15.05 | −29.08 |
| MR-2 | 310.25 | 313.28 | 317.57 | 365.29 | 295.09 | 311.41 | 299.81 | 423.67 | 14.18 | −1.84 | 64.30 | 69.72 | 32.26 | 42.92 | 15.11 | −29.02 |
| XF-1 | 333.57 | 347.34 | 338.41 | 404.58 | 317.95 | 342.33 | 320.49 | 469.36 | 36.68 | 28.32 | 91.36 | 93.50 | 60.71 | 67.45 | 41.21 | −4.87 |
| XF-2 | 328.69 | 340.12 | 334.07 | 396.23 | 313.17 | 335.81 | 316.18 | 459.62 | 36.22 | 27.76 | 91.59 | 93.70 | 60.95 | 67.66 | 41.43 | −4.66 |
| XF-3 | 334.31 | 348.45 | 339.07 | 405.86 | 318.68 | 343.33 | 321.15 | 470.85 | 36.95 | 28.70 | 91.51 | 93.63 | 60.87 | 67.59 | 41.35 | -4.73 |
| XF-4 | 333.92 | 347.87 | 338.73 | 405.19 | 318.30 | 342.81 | 320.81 | 470.07 | 37.46 | 29.51 | 90.36 | 92.63 | 59.65 | 66.55 | 40.23 | −5.77 |
| NS-1 | 625.48 | 902.36 | 584.19 | 1082.63 | 605.11 | 806.36 | 566.83 | 1316.25 | 33.80 | 18.21 | 53.88 | 60.43 | 21.48 | 33.45 | 5.20 | −38.10 |
| NS-2 | 638.38 | 934.13 | 594.45 | 1123.74 | 617.84 | 830.84 | 577.20 | 1371.42 | 33.19 | 16.90 | 54.78 | 61.23 | 22.40 | 34.26 | 6.04 | −37.32 |
Cation and silica geothermometry of hot waters from the Xifeng geothermal field.
Notes: T(Na-K)① (
FIGURE 10

SiO2 concentration vs temperature plot for the samples of the Xifeng geothermal field. The amorphous SiO2 solubility curve is from
Source and Recharge of the Geothermal Fluid
Oxygen-18 (18O) and deuterium (D) contents in sampled waters from the Xifeng geothermal field were analyzed to confirm the source and circulation mechanism of geothermal fluids. On the δ18O-δD diagram (Figure 11), most samples were plotted close to the local meteoric water line (LMWL: δD = 8.83 δ18O+ 22.15, Zhang et al., 2005) and global meteoric water line (GMWL: δD = 8 δ18O+ 10,
FIGURE 11

Plot of δD vs δ18O values of water samples collected from the Xifeng geothermal field.
In Eq. 2, H (m) = recharge elevation; δ18Ogw = oxygen isotope value of groundwater; δ18Olw = oxygen isotope value of local meteoric water; grad18O (‰/km) = isotope elevation gradient of meteoric water, and h (m) = elevation of the local meteoric sampling point. The most depleted δ18O value (−9.2‰) in the geothermal samples was regarded as the δ18Ogw to minimize the positive isotopic shift effect in this study. The average oxygen isotope value (−7.7‰) of surface meteoric water obtained in this study was used as δ18Olw. Hence, the recharge elevation was calculated to be 1,583 m as the δ18O vertical gradient in Guizhou was assumed to be −3.1‰/km (Yu et al., 1984), and with the elevation of local meteoric sampling point at 1,100 m. Combined with the geological setting, this result is reasonable as the sampling elevation is around 1,250 m for the samples collected from southwest and 750 m for those from northeast and southeast of the geothermal field.
Forming Mechanisms for the Xifeng Geothermal Field
The formation of the Xifeng geothermal field resulted from recharge, deep circulation, and secondary rising meteoric water along the faults. Based on the topographic features and geological conditions (Figures 1, 2), we propose the basic conceptual model for the genesis of the Xifeng geothermal system, as illustrated in Figure 12 and discussed.
FIGURE 12

Genetic model of the Xifeng geothermal field.
Results of stable isotopes and geology revealed that the local meteoric water from the surrounding mountains seemed to infiltrate to depth through faults and crack zones and were the dominant recharge source for the geothermal system. Sedimentary rocks of Lower Cambrian Jindingshan, Mingxinsi, and Niutitang formations overlie the Upper Sinian Dengying reservoir units and act as cap rock (Figure 1C). Moreover, the black shale of the lower Cambrian Niutitang Formation in South China is well known to be enriched in radioactive heat-producing uranium elements, which are 10 and 6–20 times the content compared with that of crustal sedimentary rocks and the crust, respectively (
Once the meteoric water was warmed up, it would interact with the host rocks. The interaction between water and Sinian dolomites is the dominant process for the formation of Ca-Mg-HCO3 type waters in the Xifeng geothermal field. Moreover, the silicate weathering and ion exchange are also responsible for the formation of geothermal fluids in the Xifeng area. As to the Ca-Mg-HCO3-SO4 type in the Xifeng hot spring, it may be due to the dissolution of other sulphate minerals during the deeper, and long-duration circulation from high-elevation SW (i.e., 1,250 m, Baimadong area) towards low-elevation NE (i.e., 750 m, Xifeng area) in the study area (Figure 12; Song et al., 2014). This is consistent with the results of recharge elevation and geological setting.
Then finally, as the deep-infiltrated waters experienced considerable deep circulation, the geothermal fluids rose again along the main ENE-SE, NE-SE, and NW-NE faults. Moreover, the ascending geothermal fluids were mixed with cold groundwater in the subsidiary fractures near the surface (Figure 5;
Conclusion
The geothermal fluids in the Xifeng geothermal field are hosted in dolomite from the Sinian Dengying Formation, and are capped by sedimentary rocks of the lower Cambrian Jindingshan, Mingxinsi, and Niutitang formations. Radiogenic heat, deep heat, and tectonic frictional heat serve as heat sources for the formation of the large geothermal system. The reservoir temperature is estimated to be 77°C. D-O isotopic studies indicate that the Xifeng geothermal system is recharged by meteoric water from higher elevations at 1,583 m from SW to NE. It is the water-dolomite interactions that lead to the formation of the alkaline Ca-Mg-HCO3 type geothermal fluids. This is consistent with the research results of the REE, whose accumulation characteristics and positive Eu anomaly are inherited from host feldspar-bearing dolomites through the water-rock interaction. The high SO4 in the Xifeng hot spring are attributed to the deeper and long-duration circulation of waters from SW towards NE. Ternary relationships among major anions indicate that a mix of cold groundwater to the ascending geothermal fluids occurred when they migrated along the main faults near the surface. Taken together, the Xifeng geothermal system should be assigned as a faults-controlling and deeply circulating meteoric water of low-temperature category.
Statements
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Author contributions
YL wrote the manuscript with the support of the listed authors. All authors have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Funding
This study was financially supported by the National Natural Science Foundation of China (No. 42002299) and the Project of Chinese Academy of Geological Sciences (No. JKY202018).
Acknowledgments
We appreciate the kind help of Professor Hansheng Long from the Guizhou Institute of Technology on the field trip. The constructive comments made by the editor and anonymous reviewers are greatly thanked.
Conflict of interest
The handling editor declared a shared affiliation with the authors JD and CZ at the time of review
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
geology, element geochemistry, D-O isotopes, xifeng, SW China
Citation
Li Y, Dor J, Zhang C, Wang G, Zhang B, Zhang F and Xing Y (2021) Genesis of the Xifeng Low-Temperature Geothermal Field, Guizhou, SW China: Constrains From Geology, Element Geochemistry, and D-O Isotopes. Front. Earth Sci. 9:782943. doi: 10.3389/feart.2021.782943
Received
25 September 2021
Accepted
19 November 2021
Published
24 December 2021
Volume
9 - 2021
Edited by
Yinhui Zuo, Chengdu University of Technology, China
Reviewed by
Wei Xu, Xi’an Jiaotong University, China
Xiaoyin Tang, Chinese Academy of Geologi-cal Sciences, China
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© 2021 Li, Dor, Zhang, Wang, Zhang, Zhang and Xing.
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*Correspondence: Yanyan Li, liyanyan@cags.ac.cn
This article was submitted to Economic Geology, a section of the journal Frontiers in Earth Science
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