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Geochemistry and geothermometry of Breitenbush Hot Springs, Oregon, USA

机译:美国俄勒冈州尔伊尼堡温泉的地球化学与地热测定

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The aqueous chemistry, isotopic composition (delta O-18 and delta H-2), and geothermometry of the Breitenbush Hot Springs area in the central Oregon Cascades were examined. Water samples were collected from springs (5), wells (8), and the Breitenbush River (2). Geothermometry was interpreted using the Reservoir Temperature Estimator (RTEst) software package and constrained by the reported mineralogy. Reservoir temperature was calculated assuming equilibration with chalcedony, celadonite, laumontite, heulandite, and epidote. Because of its relatively rapid reaction rate, calcite was presumed to remain equilibrated during cooling of the ascending reservoir waters. CO2(g) degassing from the springs was accounted for by adjusting the carbon content and temperature to be consistent with a cooling curve passing through the chemical composition of the deep well waters. The average estimated reservoir temperature of 137.1 +/- 2.0 degrees C is lower than the 174 to 180 degrees C reported in other multicomponent geothermometric studies. However, our new estimate is consistent with mineralogical, aqueous geochemical, and fluid inclusion data, and with geothermal borehole temperature measurements near the site.Stable oxygen and hydrogen isotope data indicate that the thermal waters at Breitenbush and Austin Hot Springs are a mixture of 4 to 8% "andesitic water" (Giggenbach, 1992) and local meteoric waters recharged at elevations of 1750 to 2200 m, along the crest of the Cascade Mountains. Br/Cl ratios, delta O-18, and delta D, and their correlation with Cl- concentrations from our study combined with data and analyses from other sources, suggests that Cl-, other halogens, and CO2 in the Breitenbush hot springs are primarily derived from degassing fluids rising from the serpentinized forearc mantle.The calculated reservoir temperature and average measured thermal water Cl- concentration were used with previously reported chloride-flux-based measurements by the USGS to estimate a hydrothermal discharge of 13.7 +/- 1.6 L/s and an advective heat discharge of 7.1 +/- 0.8 MW. This calculated hydrothermal heat loss is slightly less than Ingebritsen et al.'s (1992) previous estimate of 9 MW. However, it still represents a substantial transfer of heat from a relatively small, constant groundwater discharge.
机译:水化学,同位素组成(△-O-18和delta H-2),和Breitenbush温泉区在俄勒冈州瀑布中央的地热测量进行检测。水样品从弹簧(5),孔(8)收集,并且所述Breitenbush河(2)。地热测量用的是储层温度估计(RTEST)软件包解释和所报告矿物学限制。储层温度计算假设用玉髓,绿鳞石,浊沸石,片沸石,和绿帘平衡。由于其相对快速的反应速率,方解石推测升贮存水的冷却过程中保持平衡。 CO 2(g)从弹簧脱气通过调节碳含量和温度,以与穿过所述深阱水的化学组成的冷却曲线一致的解释。的137.1±2.0摄氏度的平均估计储层温度比174至180摄氏度报道在其他多组分geothermometric研究低。然而,我们的新的估计值与矿物,含水地球化学和流体夹杂物数据一致,并且具有接近site.Stable氧和氢同位素数据的地热埋管温度测量表明,在Breitenbush和奥斯汀温泉热水域是4:1的混合物至8%“安山岩水”(Giggenbach,1992),并在2200米1750海拔充电本地大气水,沿着梯级山脉的顶峰。 BR /氯比率,δ-O型18,和delta d,以及它们与氯离子浓度从我们的研究中结合数据和来自其他来源的分析的相关性,表明氯离子,其它卤素,和CO 2在Breitenbush温泉主要从脱气流体从蛇纹石弧前mantle.The计算储层温度和平均测得的热水氯离子浓度上升的衍生是由美国地质调查局与基于氯化物的焊剂先前报告的测量结果来估计的13.7 +/- 1.6升的水热放电/ S和7.1 +/- 0.8兆瓦对流热排放。此计算出的水热的热损失比Ingebritsen等略少是。(1992)的9 MW先前估计。然而,它仍然表示从相对小的,恒定地下水排放的热量的大量转移。

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