Oxygen and hydrogen isotope studies of contact metamorphism in the Santa Rosa Range,Nevada and other areas

The O¹⁸/O¹⁶ and D/H ratios have been determined for rocks and coexisting minerals from several granitic plutons and their contact metamorphic aureoles in the Santa Rosa Range, Nevada, and the Eldora area, Colorado, with emphasis on pelitic rocks. A consistent order of O¹⁸/O¹⁶ and D/H enrichment in coexisting minerals, and a correlation between isotopic fractionations among coexisting mineral pairs are commonly observed, suggesting that mineral assemblages tend to approach isotopic equilibrium during contact metamorphism. In certain cases, a systematic decrease is observed in the oxygen isotopic fractionations of mineral pairs as one approaches the intrusive contacts. Isotopic temperatures generally show good agreement with heat flow considerations. Based on the experimentally determined quartz-muscovite O¹⁸/O¹⁶ fractionation calibration curve, temperatures are estimated to be 525 to 625° C at the contacts of the granitic stocks studied.Small-scale oxygen isotope exchange effects between intrusive and country rock are observed over distances of 0.5 to 3 feet on both sides of the contacts; the isotopic gradients are typically 2 to 3 per mil per foot. The degree of oxygen isotopic exchange is essentially identical for different coexisting minerals. This presumably occurred through a diffusion-controlled recrystallization process. The size of the oxygen isotope equilibrium system in the small-scale exchanged zones varies from about 1.5 to 30 cm. A xenolith and a re-entrant of country rock projecting into an intrusive have both undergone much more extensive isotopic exchange (to hundreds of feet); they also show higher isotopic temperatures than the rocks in the aureole. The marginal portions of most plutons have unusually high O¹⁸/O¹⁶ ratios compared to normal igneous rocks, presumably due to large-scale isotopic exchange with metasedimentary country rocks when the igneous rocks were essentially in a molten state. The isotopic data suggest that outward horizontal movement of H₂O into the contact metamorphic aureoles is very minor, but upward movement of H₂O is important. Also, direct influx and absorption of H₂O from the country rock appears to have occurred in certain intrusive stocks. The D/H ratios of biotites in the contact metamorphic rocks and their associated intrusions show a geographic correlation that is similar to that shown by the D/H ratios of meteoric surface waters, perhaps indicating that meteoric waters were present in the rocks during crystallization of the biotites.Except in the exchanged zones, the O¹⁸/O¹⁶ ratios of pelitic rocks do not change appreciably during contact metamorphism, even in the cordierite and sillimanite grades; this is in contrast to regional metamorphic rocks which commonly decrease in O¹⁸ with increasing grade. Thus, contact metamorphic rocks generally do not exchange with large quantities of igneous H₂O, but regional metamorphic rocks appear to have done so.Publications of the Division of Geological Sciences, California Institute of Technology, Contribution No. 1565.     

On the causes of 18O-depletion and 18O/16O homogenization during regional metamorphism; the East Humboldt Range core complex,Nevada

 Previous stable isotope studies at Lizzies Basin revealed that metasedimentary rocks are ¹⁸O-depleted relative to protolith values, particularly in the lower parts of the section (Lower Zone) where the rocks are also isotopically homogeneous on a scale of hundreds of meters (quartz δ¹⁸O=+9.0 to +9.6 per mil). In contrast, metasedimentary rocks at higher levels at Lizzies Basin (Upper Zone) are less ¹⁸O-depleted and more heterogeneous in δ¹⁸O. In order to understand more fully the isotopic evolution of this terrane, a series of detailed, meter-scale traverses across various metamorphic and igneous lithologies were completed at Lizzies Basin, and at the structurally higher Angel Lake locality. Traverses in the Lizzies Basin Lower Zone and in the lower parts of Angel Lake (Angel Lake Lower Sequence) across various silicate lithologies, including abundant granitoids, reveal similar degrees of homogeneity, although the average δ¹⁸O values are higher at Angel Lake. In contrast, traverses which include substantial thicknesses of marble and calc-silicate gneiss and very little granitoid have more heterogeneous quartz δ¹⁸O values (+11.9 to +13.4 per mil), and also have a higher average δ¹⁸O (+12.9 per mil), than observed elsewhere. The scale of ¹⁸O/¹⁶O homogeneity in quartz observed at Lizzies Basin and Angel Lake (meters to hundreds of meters) requires fluid-mediated isotope exchange, which accompanied Tertiary metamorphism. There is a correlation between the degree of ¹⁸O-depletion in metasedimentary rocks, ¹⁸O/¹⁶O homogenization between lithologies, and the proportion of granitoids (leucogranites in particular) within any part of the section, and a corresponding anticorrelation with the proportion of marble. This points to a causal relationship, whereby the leucogranites (as well as the Tertiary hornblende diorite and biotite monzogranite) acted as both a relatively low-¹⁸O reservoir and a source of fluids to enhance exchange, while the marbles hindered isotope depletion and homogenization by acting as relatively high-¹⁸O reservoirs and impermeable layers. Material balance calculations help delineate the plausible mechanisms of exchange between granitoids and metasediments. Single-pass infiltration of magmatic fluids from the granitoids is not capable of reproducing all of the observations. Fluid-mediated exchange by convective recirculation of magmatic fluids on a scale of meters is the mechanism which explains all of the observations. The generalized model for the isotopic evolution of the East Humboldt Range core complex provides an excellent opportunity to establish the main causes and controlling factors of ¹⁸O-depletion and ¹⁸O/¹⁶O homogenization during regional metamorphism. Received: 27 July 1993 / Accepted: 1 July 1994     

Oxygen and carbon isotope profiles in metasediments from Lizzies Basin,East Humboldt Range,Nevada: constraints on mid-crustal metamorphic and magmatic volatile fluxes

¹⁸O/¹⁶O ratios vary systematically in the 1,000 m section of interlayered metasediments and granitoids at Lizzies Basin, the deepest structural level exposed in the East Humboldt Range metamorphic core complex. In the lower 300 m of the section (the Lower Zone) ¹⁸O is homogeneous and low (+6.6 to +8.8 in silicate rocks, +8.7 to +12.1 in marbles). A detailed oxygen isotope profile across an individual marble layer within the Lower Zone has a similar range in ¹⁸O (+9.5 to +11.9) with the highest values preserved in the middle of the layer. In the upper 700 m of the section (the Upper Zone) metasediments have been less strongly ¹⁸O depleted. The ¹⁸O values are higher and more heterogeneous and in a profile across a marble layer of similar thickness, rise steeply from marginal values of +12 to core values of +23. Quartz from silicate metasediments throughout the Upper Zone ranges from +11 to +13 and is thus fairly homogeneous, particularly where detailed profiles have been measured adjacent to the ¹⁸O-rich marble layers. Covariation of ¹⁸O/¹⁶O and ¹³C/¹²C ratios in marbles suggests that the isotopic composition of these elements has been altered by exchange with infiltrating, water-rich, CO₂–H₂O fluids with mantle-like isotopic composition. In most cases, marble cores preserve protolith ¹³C values and these vary systematically throughout the section according to structural level, including some exceptionally ¹³C-rich values up to +12. This range may reflect stratigraphic variation in ¹³C of the Proterozoic sedimentary protoliths of these rocks. The Upper/Lower Zone boundary, and the contrast in isotope systematics to either side, has been previously explained either as an impermeable barrier to fluid flow, or as an infiltration front (Wickham and Peters 1990). The second alternative has been tested using a numerical model in which low-¹⁸O aqueous fluid flows vertically upward through an alternating sequence of monomineralic quartz (¹⁸O=+12) and calcite (¹⁸O=+22) layers in a regime in which the oxygen isotopic composition is controlled by advection, diffusion (in the fluid), and fluid/solid exchange. Solutions to the relevant transport equations indicate that the abrupt change in the average ¹⁸O value of the layers at the Upper/Lower Zone boundary can be reproduced by the model with a uniform porosity throughout the system, but the observed contrast in the shapes of the marble layer profiles in the Upper and Lower Zones cannot be reproduced under these conditions. However, if the calcite layers have two orders of magnitude lower porosity in comparison with the quartz layers and exchange within them is diffusion-dominated (as opposed to advection-dominated in the quartz) the contrasting shapes of the marble profiles in the two zones are reproduced, as well as the Upper/Lower Zone discontinuity. The range of conditions that generates both an infiltration front (at the appropriate scale) and contrasting marble profiles (at the appropriate scale) is quite narrow but requires a volatile flux that could be generated by plausible volumes of mantle-derived magma crystallizing at depth beneath the area, providing support for this mechanism as a viable agent of ¹⁸O depletion in the deep-level rocks of this terrane.     

Strontium and oxygen isotope profiles across marble-silicate contacts,Lizzies Basin,East Humboldt Range,Nevada: constraints on metamorphic permeability contrasts and fluid flow

 Sr isotope profiles across marble-silicate rock contacts are used in conjunction with previously published oxygen isotope profiles to constrain fluid movement, porosity and permeability contrasts in migmatitic rocks from Lizzies Basin in the East Humboldt Range, Nevada. The ¹⁸O/¹⁶O systematics in the high-grade sequence have been interpreted to reflect infiltration of ∼2×10² m³/m² of a relatively low ¹⁸O hydrous fluid through the sequence, but with preservation of δ¹⁸O anomalies in thin marble bands due to a 30-fold lower porosity in the marble compared with silicate rocks (Wickham and Peters 1992). The Sr isotope profiles confirm that tracer exchange between marble and silicate rock was primarily by diffusion, and in one case, indicate that porosities differed by less than a factor of four in the ∼10 cm boundary layer which exhibits diffusive modification of ⁸⁷Sr/⁸⁶Sr ratios. This contrasts with modelling of the oxygen isotope profiles which imply porosity contrasts >10 for one marble band and >50 for a second marble band. Either strontium and oxygen isotope diffusion reflect different events (possible if fluid Sr contents varied with time) or porosity varied substantially with the silicate rocks. Oxygen isotope profiles in the deeper part of the metamorphic section in which δ¹⁸O values of silicate rocks have been homogenised and lowered, indicate similar diffusion distances (and thus porosity-time evolution) to oxygen isotopic profiles higher in the section. Comparison of strontium and oxygen isotope diffusion distances constrains fluid Sr contents to between ∼50 and ∼500 ppm deep in the section, but less than ∼10 ppm higher in the section. The difference is related to release of relatively saline, Sr-rich fluids, by the abundant leucogranites and associated skarns deep in the section (cf. Peters and Wickham 1995). Received: 9 December 1994/Accepted: 13 April 1995     

Oxygen and hydrogen isotope relations in water and acid residues of carbonaceous chondrites

Oxygen isotope compositions of the carbon-rich, acid-resistant fraction of four carbonaceous chondrites (Orgueil, Renazzo, Murchison and Murray) are reported, along with results of experiments wherein bulk samples of Orgueil and Renazzo were selectively outgassed.Variations of the whole rock isotopic compositions of Orgueil and Renazzo with the temperature of vacuum outgassing show that the water released, presumably from hydroxyl radicals bound to the phyllosilicates, has an O-isotope composition distinct from that of the rest of the silicates. A model of formation of carbonaceous chondrite phyllosilicates requiring a single water reservoir with this composition is proposed.The acid residues are only slightly different from the whole rocks and from terrestrial compositions in their ¹⁶O-content. A hydrogen-oxygen isotope relation is found, which can be interpreted in terms of low temperature reactions in the primitive solar nebula.     

The oxygen isotope composition of granitoid and sedimentary rocks of the southern Snake Range,Nevada

Six diverse intrusive igneous types are exposed as discrete outcrops within an area of 900 km² in the southern Snake Range, White Pine County, Nevada. The previously recognized variety among these igneous types is reflected in the wide range of ¹⁸O values (–1.1 to 13.4 permil) found in these rocks. This range of ¹⁸O values probably results from differences in source material and post-crystallization history of the different intrusive types.The Jurassic intrusive of the Snake Creek-Williams Canyon area represents the chemical equivalent of a large part of a differentiation sequence, with the entire range of composition (63–76 percent SiO₂) exposed over a horizontal distance of about five km. The rather regular increase of ¹⁸O values from the most mafic to the most felsic parts of this pluton, together with ¹⁸O values determined for constituent minerals recovered from five of the samples, supports a fractional crystallization model. The high ¹⁸O values found (10.2–12.2 permil) indicate that the magma likely was derived from or assimilated sedimentary materials.Nine samples of the Cretaceous two-mica granite of the Pole Canyon-Can Young Canyon area have ¹⁸O values in the range 10.6–12.1 permil. These high ¹⁸O values, an initial⁸⁷Sr/⁸⁶Sr ratio of 0.7165, and the presence of muscovite along with an accessory mineral suite limited to monazite, apatite, zircon, and an allanite-like mineral, characterize this intrusive mass as an S-type granite. It probably formed through anatexis of late Precambrian pelitic rocks.The granitoid rock exposed in the Young Canyon-Kious Basin area is Tertiary (32 m.y.). Most of this intrusive has been cataclastically deformed as a result of late (18 m.y.) movement on the overlying Snake Range decollement. The undeformed portion of this intrusive has ¹⁸O values of 8.7–10.0 permil. However, the deformed portion of this intrusive has ¹⁸O values as low as –1.1 permil, apparently resulting from isotopic exchange between this rock and ground water at the time of cataclasis.Although the igneous types exposed in the southern Snake Range differ petrologically and range in age from Jurassic to Tertiary, most have relatively high ¹⁸O values compared with other granitoid rocks of the Basin-Range Province.     

Behavior of carbonate-associated sulfate during meteoric diagenesis and implications for the sulfur isotope paleoproxy

Although carbonate-associated sulfate (CAS) is used widely as a proxy for the sulfur isotope composition of ancient seawater, little is known about the effects of diagenesis on retention of primary δ³⁴S signals. Our case study of the Key Largo Limestone, Pleistocene, Florida, is the first systematic assessment of the impact of meteoric diagenesis on CAS properties. Geochemical and petrographic data show that meteoric diagenesis has affected the exposed coralline facies to varying degrees, yielding differences now expressed as sharp reaction fronts between primary and secondary carbonate minerals within individual coral heads. Specifically, analyses across high-resolution transects in the Key Largo Limestone show that concentrations of strontium and sodium decrease across the recrystallization front from original aragonite to meteoric low-magnesium calcite by factors of roughly 5 and 10, respectively. Predictably, δ¹⁸O values decrease across these same fronts. The δ¹³C relationships are more complex, with the most depleted values observed in the latest-formed calcite. Such trends likely reflect carbon isotope buffering capacity that decreased as reaction progressed, as well as protracted development of soil profiles and the associated terrestrial biomass and thus depleted δ¹³C during sea-level lowstand. Conversely, δ³⁴S values of CAS vary within a narrow ‘buffered’ range from 20.6 to 22.6‰ (compared to 20.8-22.0‰ of coeval Pleistocene seawater) across the same mineralogical transition, despite sulfate concentrations that drop in the diagenetic calcite by an average factor of 12. Collectively, these data point to robust preservation of primary δ³⁴S for carbonates that have experienced intense meteoric diagenesis, which is encouraging news for those using the isotopic composition of CAS as a paleoceanographic proxy. At the same time, the vulnerability of CAS concentrations to diagenetic resetting is clear.     

云蒙山变质核杂岩抬升过程中伸展拆离和岩浆底辟联合作用的证据

北京地区云蒙山变质核杂岩在白垩纪阶段抬升的早期,伴随着沿四合堂剪切带由北向南的拆离滑脱和大型花岗闪长岩的垂向侵位,晚期变形发生在花岗闪长岩岩基周边及其邻近围岩中,形成云蒙山剪切带,并伴随大量同构造的花岗岩和伟晶岩岩脉灌入。剪切带中所有的岩脉都随时间发生了不同程度的变形,较老的岩脉形成紧闭的圆柱状褶皱,枢纽与剪切带的线理和面理接近平行。岩脉与剪切带中L-S组构的平行化作用主要是由于这种转动的结果。岩脉的成分和长英指数随它们的变形程度发生变化,说明持续的岩浆分异作用与韧性剪切变形是同时发生的。云蒙山剪切带由岩浆底辟引起的上盘岩石重力所驱动,并不断得到同构造侵位岩脉的补充,起到存储和不断改造侵位岩脉的作用。早期伸展体制下形成的四合堂剪切带局部遭受云蒙山剪切带的改造或复合。该地区的岩石、构造和同构造岩脉的变形几何学和运动学证据表明,太古宙结晶基底的抬升是下部岩浆底辟与上部地壳伸展拆离共同作用的结果。     

云蒙山变质核杂岩抬升过程中伸展拆离和岩浆底辟联合作用的证据

北京地区云蒙山变质核杂岩在白垩纪阶段抬升的早期,伴随着沿四合堂剪切带由北向南的拆离滑脱和大型花岗闪长岩的垂向侵位,晚期变形发生在花岗闪长岩岩基周边及其邻近围岩中,形成云蒙山剪切带,并伴随大量同构造的花岗岩和伟晶岩岩脉灌入。剪切带中所有的岩脉都随时间发生了不同程度的变形,较老的岩脉形成紧闭的圆柱状褶皱,枢纽与剪切带的线理和面理接近平行。岩脉与剪切带中L-S组构的平行化作用主要是由于这种转动的结果。岩脉的成分和长英指数随它们的变形程度发生变化,说明持续的岩浆分异作用与韧性剪切变形是同时发生的。云蒙山剪切带由岩浆底辟引起的上盘岩石重力所驱动,并不断得到同构造侵位岩脉的补充,起到存储和不断改造侵位岩脉的作用。早期伸展体制下形成的四合堂剪切带局部遭受云蒙山剪切带的改造或复合。该地区的岩石、构造和同构造岩脉的变形几何学和运动学证据表明,太古宙结晶基底的抬升是下部岩浆底辟与上部地壳伸展拆离共同作用的结果。     

Geochemical and C, O, Sr, and U-series isotopic evidence for the meteoric origin of calcrete at Solitario Wash, Crater Flat, Nevada, USA

Calcite-rich soils (calcrete) in alluvium and colluvium at Solitario Wash, Crater Flat, Nevada, USA, contain pedogenic calcite and opaline silica similar to soils present elsewhere in the semi-arid southwestern United States. Nevertheless, a ground-water discharge origin for the Solitario Wash soil deposits was proposed in a series of publications proposing elevation-dependent variations of carbon and oxygen isotopes in calcrete samples. Discharge of ground water in the past would raise the possibility of future flooding in the unsaturated zone at Yucca Mountain, Nevada, site of a proposed high-level nuclear waste repository. New geochemical and carbon, oxygen, strontium, and uranium-series isotopic data disprove the presence of systematic elevation-isotopic composition relations, which are the main justification given for a proposed ground-water discharge origin of the calcrete deposits at Solitario Wash. Values of δ¹³C (−4.1 to −7.8 per mil [‰]), δ¹⁸O (23.8–17.2‰), ⁸⁷Sr/⁸⁶Sr (0.71270–0.71146), and initial ²³⁴U/²³⁸U activity ratios of about 1.6 in the new calcrete samples are within ranges previously observed in pedogenic carbonate deposits at Yucca Mountain and are incompatible with a ground-water origin for the calcrete. Variations in carbon and oxygen isotopes in Solitario Wash calcrete likely are caused by pedogenic deposition from meteoric water under varying Quaternary climatic conditions over hundreds of thousands of years.     

Stable isotopic evidence for fluid infiltration during contact metamorphism in a multiply-metamorphosed terrane: the Reynolds Range, Arunta Block, central Australia

The Lander Rock Beds form the local basement of the Reynolds Range in the Arunta Inlier of central Australia. These dominantly quartzose and pelitic lithologies underwent low-grade ( c.   400  °C) regional metamorphism prior to contact metamorphism ( c.   2.5  kbar) around S-type megacrystic granitoids at 1820–1800  Ma. The Lander Rock Beds are overlain by metasediments of the Reynolds Range Group, which were subsequently intruded by granitoids at c. 1780  Ma. Regional metamorphism at 1590–1580  Ma produced grades varying from greenschist (400  °C at 4–5  kbar) to granulite (750–800  °C at 4–5  kbar) from north-west to south-east along the length of the Reynolds Range. Oxygen isotope ratios of the Lander Rock Beds were reset from 13.4±0.8 to as low as 6.7 adjacent to the contacts of the larger plutons, and to 10.3±1.1 around the smaller plutons. Biotite in all the major rock types found in the aureoles has δD values between −52 and −69, probably reflecting resetting by a cooling igneous+metamorphic fluid near the plutons. Sapphirine-bearing and other Mg- and Al-rich rock types have low δ¹⁸O values (4.0±0.7). The precursors to these rocks were probably low-temperature ( c. 200  °C) diagenetic–hydrothermal deposits of Mg-rich chlorite, analogous to those in Proterozoic stratiform precious metal and uranium deposits that form by the infiltration of basin brines or seawater. As in the overlying Reynolds Range Group, regional metamorphism involved little fluid–rock interaction and isotopic resetting.     

Petrology of Upper Amphibolite Facies Marbles from the East Humboldt Range, Nevada, USA; Evidence for High-Temperature, Retrograde, Hydrous Volatile Fluxes at Mid-Crustal Levels

Petrographic and petrologic investigations of upper amphibolitefacies metacarbonates from the East Humboldt Range core complex,Nevada, provide important constraints on P-T-X_CO2 conditionsand fluid flow during metamorphism. Three marble assemblagesare observed [(1)dol+cc+bt+cpx+q+ruscapkspamph; (2) cc+bt+cpx+plag+q+sphscapksp;(3) cc+cpx+plag+q+sphscapksp], all of which equilibrated withrelatively CO₂-rich fluid compositions, at P-T conditions of6 kbar and 600–750C. The most recent equilibration eventis recorded in some calcsilicate gneisses where retrograde amphiboleand epidotegarnet replace clinopyroxene and plagioclase, respectively.This is attributed to infiltration of H₂O-rich fluids at and/orafter peak metamorphic temperatures, which continued as therocks were cooled and rapidly uplifted after a Tertiary extension-relatedheating event. Likely sources for the retrograde fluids are the abundant pegmatiticleucogranites in the area. Volumetric fluid-rock ratios of 0.02–0.4are required to generate the retrograde assemblage, and observedleucogranite proportions are more than adequate to provide therequired volume of fluid. Estimates of retrograde fluid fluxesrange from 0.25 to 510² cm³/cm² for a transient temperaturegradient of 5C/m, to 310³ to 710⁴ cm³/cm² for a temperaturegradient of 35C/km. These gradients are characteristic of askarn-type contact metamorphic environment and a regional crustalgeotherm, respectively. They imply different time-scales andlength-scales for the retrograde fluid flow system, with theformer more akin to a contact metamorphic setting with local,meter-scale retrograde fluid flow, and the latter to a regionalmetamorphic setting with regionally high mid- and lower-crustaltemperatures and fluid flow throughout a significant thicknessof the middle crust. Higher gradients are considered more likelygiven the proximity of leucogranites to retrogressed calc-silicategneisses, and the resultant relatively small fluxes are consistentwith a magmatic source. The length-scale of reaction within the retrograde fluid flowsystem was of the order of meters to hundreds of meters andinvolved both pervasive and (later) fracture-controlled down-temperatureflow. Retrograde fluid flow in this terrance, as well as othersdominated by magmatic volatiles, is in the form of multiplediscrete bursts of fluid released in a discontinuous mannerpotentially over long periods of time (1–10 Ma) with locallyvariable thermal gradients along the flow path.     

Oxygen,hydrogen and carbon isotope studies of the franciscan formation,Coast Ranges,California

Analyses of 230 Franciscan rock and mineral samples, including the San Luis Obispo ophiolite, show that metamorphism produces no change in the δ¹⁸O of the graywackes (+11 to +14), but that igneous rocks become enriched in ¹⁸O by 2–6% and the cherts depleted by 5–10%. The shales are of two types, a high-¹⁸O type (+16 to +20) associated with chert and a low-¹⁸O type isotopically and mineralogically similar to the graywackes. The vein quartz (δ = + 15 to + 20) is invariably richer in ¹⁸O than the host rock quartz and in most of the rocks the δ¹⁸O of the clastic quartz is similar to the δ¹⁸O of the whole rock. Mineral assemblages are typically not in isotopic equilibrium. Although the δ¹⁸O values are very uniform (+13 to +16). the δ¹³C of vein aragonite and calcite is widely variable (0 to ? 14), implying that a major source of the carbon is oxidized organic material. The δD values of 83 igneous and sedimentary rocks are -45 to -80, exceptions are the Fe-rich minerals howieite and deerite, which have δD = ?100. All of these samples could have equilibrated with H₂O having δD ≈ +10 to ?20 and δ¹⁸O ≈ ?3 to +8. assuming temperatures of 100–300°C. However, the serpentines (δD ≈ ?85 to ?110) and the vein minerals (δD = ?23 to ?55) are exceptions. The vein minerals are 10–20%, richer in deuterium than the adjacent wall rocks; they formed from a relatively D-rich metamorphic water, typically at lower temperatures than did their host rocks. The isotopic compositions of the other Franciscan rocks were affected by three distinct events: (1) hydrothermal alteration of the ophiolite complexes and volcanic rocks as a result of submarine igneous activity at a spreading center or in an island-arc environment; (2) low-temperature, high-pressure regional metamorphism and diagenesis; and (3) a late-stage, very low temperature (<100°C) alteration of the ultramafic bodies by meteoric ground waters, producing lizardite-chrysotile serpentine. In the first two cases, the pore fluid involved in the alteration of the Franciscan rocks was sea water. However, this water became somewhat depleted in D and enriched in ¹⁸O during blueschist metamorphism, evolving to values of δD ≈ ? 20 and δ¹⁸O ≈ + 6 to + 8 at the highest grades. Except for one graywacke sample, the meteoric waters that affected the serpentinites did not significantly change the $\text{D}\text{H}$ ratios of the OH-bearing minerals in any other Franciscan rock.The δ¹⁸O values of orogenic andesites are too low for such magmas to have formed by direct partial melting of Franciscan-type materials in a subduction zone. Andesites either form in some other fashion, or the melts must undergo thorough isotopic exchange with the upper mantle. The great Cordilleran granodiorite-tonalite batholiths, however, are much richer in ¹⁸O and may well have formed by large-scale melting or assimilation of Franciscan-type rocks. The range of δD values of Franciscantype rocks is identical to the ?50 to ?80 range shown by most igneous rocks. This suggests that ‘primary magmatic H₂O’ throughout the world may be derived mainly by partial melting of Franciscantype materials, or by dehydration of such rocks in the deeper parts of a Benioff zone.     

Occurrence and origin of marialitic scapolite in the Humboldt lopolith,N.W. Nevada

The occurrence and origin of marialitic scapolite in the Humboldt lopolith was investigated in the field and in the laboratory using petrographic and experimental techniques. Scapolite occurs in three modes: as a pervasive replacement of plagioclase and other minerals in gabbro, diorite and extrusive rocks; as a poikiloblastic mineral in scapolitite dikes; and as a fracture-filling mineral with analcime, albite and sphene in scapolite veins. Additional secondary minerals associated with scapolite include epidote, prehnite, hornblende and diopside-salite clinopyroxene. Relations with these minerals suggest that most marialitic scapolite grew at temperatures around 400° C. Scapolite composition varies from EqAn₁₂ to EqAn₃₇, containing from 72 to 96 atomic% Cl in the R position. Experiments on systems of similar compositions indicate that NaCl-H₂O fluid having more than 40 mol% NaCl is needed to stabilize the scapolite.Variation in scapolite compositions is due to thermal and fluid compositional gradients normal to conduits of hydrothermal fluids, and occurs on a scale up to 100 m. The likely source of Na and Cl is pre-existing evaporites or evaporitic brine derived from the wallrocks. Salinity could have been increased to a level sufficient to stabilize scapolite by hydration of an originally dry magma, possibly aided by hydrothermal boiling. Results may be applied to hydrothermal alteration in areas of rifting or back-arc spreading, and in mid-ocean ridge hydrothermal systems.     

Anomalous gold, antimony, arsenic, and tungsten in ground water and alluvium around disseminated gold deposits along the Getchell Trend, Humboldt County, Nevada

Ground-water, alluvium, and bedrock samples were collected from drill holes near the Chimney Creek, Preble, Summer Camp, and Rabbit Creek disseminated gold deposits in northern Nevada to determine if Au and ore-related metals, such as As, Sb, and W, are being hydromorphically mobilized from buried mineralized rock, and, if they are, to determine whether the metal-enriched ground water is reacting with the alluvial material to produce a geochemical anomaly within the overburden.Results of chemical analyses of drill-hole water samples show the presence of hydromorphic dispersion anomalies of Au, As, Sb, and W in the local ground-water systems associated with these deposits. Background concentrations for Au in the ground water up-gradient from the buried deposits was less than 1 nanogram per liter (ng/L), near the deposits the Au values ranged from 1 to 140 ng/ L, and in drill holes penetrating mineralized rock, concentrations of Au in the ground water were as high as 4700 ng/L. Highest concentrations of Au were found in ground-water samples where the measured E_h and the distribution of arsenic species, arsenite [As(III)] and arsenate [As(V)], indicated oxidizing redox potentials. Similarly, As, Sb, and W concentrations in the ground water near the deposits were significantly enriched relative to concentrations in the ground water up-gradient from the deposits. In general, however, the highest concentrations of As, Sb, and W occurred in ground-water samples where the measured E_h and the distribution of arsenic species indicated reducing conditions. Arsenic concentrations ranged from 9 to 710 micrograms per liter (μg/L); Sb, from less than 0.1 to 250 μg/L; and W, from 1 to 260 μg/L.In addition, analysis of sequential dissolution and extraction solutions of drill cuttings of alluvium and bedrock indicate geochemical anomalies of gold and ore-related metals in the overburden at depths corresponding to the location of the present-day water table. This relationship suggests that water-rock reactions around these buried deposits are active and that this information could be very useful in exploration programs for concealed disseminated gold deposits.     

沧县隆起献县变质核杂岩的发育特征及成因模式

渤海湾盆地周缘发育的多个变质核杂岩,很好地记录了华北克拉通东部晚中生代以来的地壳伸展过程。文中以渤海湾盆地西部献县凸起和饶阳凹陷为研究区,试图揭示盆地内部变质核杂岩的发育特征。根据井、震结合的方法,通过精细的构造解释,厘定了献县断层及其上盘的构造变形特征;利用凹陷内的钻井资料对献县凸起上发育地层的时代和岩性进行限定;结合区域上变质核杂岩的发育特征和形成背景,讨论了献县变质核杂岩的发育时间和成因演化模式。结果表明:在研究区内呈弧形展布的献县断层具有主拆离断层的特征,断层上盘的饶阳凹陷南部残留有中元古界和下古生界,且凹陷内发育有数量众多、不同倾向的次级断层;献县凸起上发育的地层为太古宇-古元古界,岩性包括角闪片麻岩、黑云二长片麻岩,局部发育有花岗片麻岩。研究认为,献县变质核杂岩具有典型变质核杂岩的基本特征,其形成时间为晚中生代(K1?),发育于华北克拉通东部岩石圈大规模减薄的背景下,并以滚动枢纽模式发展演化。     

White mica trace element and boron isotope evidence for distinctive infiltration events during exhumation of deeply subducted continental crust

ABSTRACT

Previous study of subducted continental crust within the Luliang Shan terrane in Northwest China has documented metasomatic formation of thick, hydrated phengite + garnet-rich selvages at the interface between mafic eclogite blocks and quartzofeldspathic host gneiss. Whole rock concentrations of Cs and Ba within the selvage are enriched by two orders of magnitude relative to the eclogite blocks and host gneiss. We performed in situ ion microprobe analyses of Li, Be, B, Rb, Sr, Cs and Ba and δ¹¹B of phengite within the Luliang Shane terrane to better constrain the source(s) of the infiltrating fluid. The phengite within the selvage are enriched in Li, Cs and Ba and yield δ¹¹B values between ?30‰ and ?9‰, values that are lower than mantle values. High Ba/Rb, Cs/Rb coupled with low B/Be, B/Li and highly negative δ¹¹B values indicate that the high-pressure fluid that formed the selvage was derived from highly devolatilized rocks within the subduction channel. In contrast, muscovite, which crystallized in the adjacent host gneiss during a subsequent lower pressure phase of fluid infiltration at approximately 0.9 GPa depths, has much lower Li, Cs and Ba relative to the high-pressure phengite. These retrograde muscovite have very high concentrations of B (up to 5500 ppm) and Be (up to 50 ppm) and high (?2 to +8‰) δ¹¹B values that are consistent with crystallization from a fluid derived from shallower and less devolatilized regions of the subduction zone. Additional host gneiss samples, regionally distributed and kilometres away from the studied area lack the B-rich signature and indicate that the late stage fluids were likely localized to the region near the studied traverse.     

Extreme oxygen isotope signature of meteoric water in magmatic zircon from metagranite in the Sulu orogen, China: Implications for Neoproterozoic rift magmatism

Unusual ¹⁸O depletion, with δ¹⁸O values as negative as −10‰ to −4‰ relative to VSMOW, was reported in zircons from ultrahigh-pressure eclogite-facies metamorphic rocks in the Dabie-Sulu orogenic belt, China. But it is critical for the negative δ¹⁸O zircons to be distinguished between magmatic and metamorphic origins, because the ¹⁸O depletion can be acquired by high-T eclogite-facies metamorphism of meteoric-hydrothermally altered low δ¹⁸O rocks. While zircon O diffusion kinetics has placed a reasonable constraint on this, zircon trace element compositions can provide a straightforward distinction between the magmatic and metamorphic origins. This paper reports our finding of unusual ¹⁸O depletion in zircon from granitic gneiss in the northeastern end of the Sulu orogen. Zircon δ¹⁸O values vary from −7.8‰ to −3.1‰ along a profile of 50 m length at Zaobuzhen. They are close to extremely low δ¹⁸O values of −9.0‰ to −5.9‰ for metagranite at Qinglongshan and adjacent areas in the southwestern end of the Sulu orogen. CL imaging suggests that the low δ¹⁸O zircons at Zaobuzhen are primarily of magmatic origin, but underwent different degrees of metamorphic modification. Zircon U-Pb dating yields middle Neoproterozoic ages of 751 ± 27 to 779 ± 25 Ma for protolith crystallization and Triassic ages of 214 ± 10 to 241 ± 33 Ma for metamorphic resetting. However, no metamorphic modification occurs in zircon REE patterns that only indicate magmatic recrystallization and hydrothermal alteration, respectively. Thus, the negative δ¹⁸O zircons are interpreted as crystallizing from negative δ¹⁸O magmas due to melting of meteoric-hydrothermally altered negative δ¹⁸O rocks in an active rift setting at about 780 Ma. The variation in zircon δ¹⁸O values indicates considerable O isotope heterogeneity in its granitic protolith. Zircon Lu-Hf isotope analyses give positive ε_Hf(t) values of 1.6-4.1 and Hf model ages of 1.18-1.30 Ga. This suggests that the granitic protolith was derived from the mid-Neoproterozoic reworking of late Mesoproterozoic juvenile crust. The metagranites at Zaobuzhen and Qinglongshan, about 450 km apart, are two known occurrences of the unusually low δ¹⁸O zircons below −6‰ so far reported in the Sulu orogen. They are similar to each other in both protolith and metamorphic ages, so that they share the same nature of both Neoproterozoic protolith and Triassic metamorphism. Therefore, the locally negative δ¹⁸O zircons may register centers of low δ¹⁸O magmatism during the supercontinental rifting.