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1.
Rocks of the Miocene Macquarie Island ophiolite, south of New Zealand, have oxygen and carbon isotopic compositions comparable to those of seafloor rocks. Basalt glass and weathered basalts have δ18O values at 5.8–6.0‰ and 7.9–9.5‰, respectively, similar to drilled seafloor rocks including samples from the Leg 29 DSDP holes near Macquarie Island. Compared to the basalt glass, the greenschist to amphibolite facies metaintrusives are depleted in18O (δ18O=3.2–5.9‰) similar to dredged seafloor samples, whereas the metabasalts are enriched (δ18O=7.1–9.7‰). Although the gabbros are only slightly altered in thin-section they have exchanged oxygen with a hydrothermal fluid to a depth of at least 4.5 km. There is an approximate balance between18O depletion and enrichment in the exposed ophiolite section. The carbon isotopic composition of calcite in the weathered basalts (δ13C=1.0–2.0‰) is similar to those of drilled basalts, but the metamorphosed rocks have low δ13C values (?14.6 to 0.9‰).These data are compatible with two seawater circulation regimes. In the upper regime, basalts were weathered by cold seawater in a circulation system with high water/rock ratios (?1.0). Based on calcite compositions weathering temperatures were less than 20°C and the carbon was derived from a predominantly inorganic marine source. As previously suggested for the Samail ophiolite, it is postulated that the lower hydrothermal regime consisted of two coupled parts. At the deeper levels, seawater circulating at low water/rock ratios (0.2–0.3) and high temperatures (300–600°C) gave rise to18O-depleted gabbro and sheeted dikes via open system exchange reactions. During reaction the seawater underwent a shift in oxygen isotopic composition (δ18O=1.0–5.0‰) and subsequently caused18O enrichment of the overlying metabasalts. In the shallower part of the hydrothermal regime the metabasalts were altered at relatively high water/rock ratios (1.0–10.0) and temperatures in the range 200–300°C. The relatively low water/rock ratios in the hydrothermal regime are supported by the low δ13C values of calcite, interpreted as evidence of juvenile carbon in contrast to the inorganic marine carbon found in the weathered basalts.  相似文献   

2.
El Chichón crater lake appeared immediately after the 1982 catastrophic eruption in a newly formed, 1-km wide, explosive crater. During the first 2 years after the eruption the lake transformed from hot and ultra-acidic caused by dissolution of magmatic gases, to a warm and less acidic lake due to a rapid “magmatic-to-hydrothermal transition” — input of hydrothermal fluids and oxidation of H2S to sulfate. Chemical composition of the lake water and other thermal fluids discharging in the crater, stable isotope composition (δD and δ18O) of lake water, gas condensates and thermal waters collected in 1995–2006 were used for the mass-balance calculations (Cl, SO4 and isotopic composition) of the thermal flux from the crater floor. The calculated fluxes of thermal fluid by different mass-balance approaches become of the same order of magnitude as those derived from the energy-budget model if values of 1.9 and 2 mmol/mol are taken for the catchment coefficient and the average H2S concentration in the hydrothermal vapors, respectively. The total heat power from the crater is estimated to be between 35 and 60 MW and the CO2 flux is not higher than 150 t/day or ~ 200 gm− 2 day− 1.  相似文献   

3.
High-frequency metre-scale cycles are present within the Lower-Middle Ordovician carbonate successions in northern Tarim Basin, NW China. These metre-scale cycles were variably dolomitised from top to bottom. Three types of replacive dolomites were recognised, including dololaminite(very finely to finely crystalline, planar-s to nonplanar-a dolomite;type-1), patterned dolomite(finely crystalline, planar-s dolomite; type-2), and mottled dolomite(finely to medium crystalline,nonplanar-a(s) dolomite; type-3). Petrographic evidence indicate these dolomites were primarily deposited in supratidal to restricted subtidal environments, and formed in near-surface to shallow burial realms. Geochemically, all types of dolomites have similar δ13C and 87Sr/86 Sr ratios comparable to calcite precipitated in equilibrium with the Early-Middle Ordovician seawater. These geochemical attributes indicate that these dolomites were genetically associated and likely formed from connate seawater-derived brines. Of these, type-1 dolomite has δ18O values(.4.97‰ to.4.04‰ VPDB) slightly higher than those of normal seawater dolomite of the Early-Middle Ordovician age. Considering the absence of associated evaporites within type-1 dolomite, its parental fluids were likely represented by slightly evaporated(i.e., mesosaline to penesaline) seawater with salinity below that of gypsum precipitation. More depleted δ18O values(.7.74‰ to.5.20‰ VPDB) of type-2 dolomite and its stratigraphic position below type-1 dolomite indicate the generation of this dolomite from mesosaline to penesaline brines at higher temperatures in near-surface to shallow burial domains. Type-3 dolomite yields the most depleted δ18O values(–9.30‰to –7.28‰ VPDB), pointing to that it was most likely formed from coeval seawater-derived brines at highest temperatures in a shallow burial setting. There is a downward decreasing trend in δ18O values from type-1 through type-2 to type-3 dolomites, and in abundance of dolomites, indicating that the dolomitising fluids probably migrated downward from above and persisted into shallow burial conditions.  相似文献   

4.
Stable isotope ratios of S, O and Sr have been measured for active vent materials which were first found and sampled in April 1987 from the Mariana backarc spreading axis at 18°N. Chimneys consisted mostly of barite with a lesser proportion of sulfide minerals such as sphalerite, galena, chalcopyrite and pyrite. Theδ34S values of sphalerite and galena taken from several chimneys and various parts of a chimney showed a narrow range from 2.1 to 3.1‰, suggesting uniform conditions of fluid chemistry during chimney growth. The sulfur isotopic results imply a contribution of hydrogen sulfide reduced from seawater sulfate in the deep hydrothermal reaction zone, considering that fresh glasses of the Mariana Trough basalts haveδ34S= −0.6 ± 0.3‰. Sulfur isotopic compositions of hydrogen sulfide in the high temperature vent fluids (δ34S= 3.6–4.8‰) which are higher than those of the sulfide minerals suggest the secondary addition of hydrogen sulfide partially reduced from entrained seawater SO42− at a basal part of the chimneys. This interpretation is consistent with theδ34S values of barite (21–22‰) that are higher than those of seawater sulfate. The residence time of the entrained SO42− was an order of an hour on a basis of oxygen isotopic disequilibrium of barite. Strontium isotopic variations of barite and vent waters indicated that Sr in barite was mostly derived from the Mariana Trough basalts with a slight contribution from Sr in circulating sea-water, and that 10–20% mixing of seawater with ascending hydrothermal fluids induced precipitation of barite at the sea-floor.  相似文献   

5.
Low18O/16O values have been found in rocks from the Captains Bay pluton and surrounding country rocks on Unalaska Island in the Aleutian Islands. The pluton is surrounded by a metamorphic aureole in which the country rocks have been domed, faulted and chaotically fractured. Samples with lower18O/16O values (δ18O = ?4.1 to +2.7‰, SMOW) commonly have interstitial micrographic intergrowths of quartz and turbid potassium feldspar. These facts suggest extensive interaction of circulating meteoric waters with the pluton. Unalaska Island must have been subaerially exposed at or shortly after the time of intrusion of the pluton. The pervasive low-grade metamorphism of the “early series” volcanic rocks of all of the Aleutian Islands might be a result of the interaction of intrusive bodies with meteoric waters rather than the consequence of ridge subduction.  相似文献   

6.
We provide two new determinations of the oxygen isotopic composition of seawater during the last glacial maximum (LGM). High-resolution oxygen isotopic measurements were made on interstitial waters from Ocean Drilling Program (ODP) Sites 1168 and 1170 in the southeast Indian Ocean sector of the Southern Ocean. We use a diffusion-advection numerical model to calculate the glacial-interglacial change in bottom-water δ18Osw from the pore water δ18O profiles; the first such determinations from this part of the oceans. Statistical analyses of the model runs indicate that Circumpolar Deep Water (CDW) δ18Osw changed by 1.0-1.1±0.15‰ since the last glacial maximum (LGM). Our results are consistent with a previous calculation from a South Atlantic Southern Ocean location (ODP Site 1093) also situated within CDW. The new values determined in this study, together with previous estimates, are converging on a global average Δδ18Osw of 1.0-1.1‰.Using the calculated bottom-water δ18Osw, we have extracted the temperature component from the benthic foraminiferal δ18O record at Sites 1168 and 1170. Since the LGM, bottom waters at these two sites warmed by 2.6 and 1.9°C, respectively. The absolute temperature estimates for the LGM (−0.5°C [Θ=−0.6°C] at Site 1168 and −0.2°C [Θ=−0.4°C] at Site 1170) are slightly warmer than those reported from previous studies using the same technique, but are consistent with more homogenous deep-ocean temperatures during the LGM relative to the modern.  相似文献   

7.
Oxygen and hydrogen isotope ratios were measured on coexisting minerals from quartz diorites and quartz monzonites from a section across the Coast Range batholith in the Skagway area, Alaska, including a variety of outlying plutons west of the batholith in the Yakutat Bay-Mt. St. Elias region (latitudes 59–60°N). The extremely low and variable δ18Oand δD results indicate widespread meteoric-hydrothermal alternaiton of the Coast Range batholith, and to a lesser extent, of the Yakutat Bay plutons as well. In the Yakutat Bay area, the plutons with K—Ar ages younger than 50 m.y. have widely varying δD values of ?72 to ?148, compared to δD = ?69to?90 for all but one sample in the 50–225 m.y. age grouping (one biotite has δD = ?109). This suggests that the major meteoric-hydrothermal episodes in this area occurred during the Eocene and Miocene. This involved relatively small meteoric water/rock ratios(<0.1), as none of the δ18O values show any clear-cut evidence of alteration (δ18Oquartz= 7.4 ?11.8; δ18Ofeldspar= 5.7?10.0). However, in the section across the Coast Range batholith, 85% of the plutonic rocks have very low δD values of ?100 to ?167, and the δ18O values are extremely variable δ18Ofeldspar= + 10.3to?4.0 and Δ18Oquartz-feldspar= 0.4?10.5. These data indicate that a major portion of the batholith, particularly the quartz monzonite-rich eastern part, but also including many of the quartz diorite plutons as well, interacted with meteoric-hydrothermal convective systems that involved water/rock ratios of about 0.3–1.4. The quart diorite plutons are most depleted in18O near their northeast contacts against the younger quartz monzonite intrusions. The primary igneous δ18O values of the quartz diorites were apparently higher than those of the quartz monzonites; they are also unusually high in18O compared to most other analyzed quartz diorites, suggesting derivation from, exchange with, or assimilation of high-18O metasediments or altered volcanic rocks. These data and conclusions are very similar to those reached previously on a similar isotopic study of the Coast Range batholith in British Columbia, 700 km to the southeast at latitudes 54–55°N, except that in the Skagway area an even greater proportion of the batholith was apparently depleted in deuterium. This implies that deep (?5km?) circulation of meteoric groundwaters is probably a characteristic of the later stages of emplacement of the Cordilleran batholiths of western North America, suggesting that the eastern sections of these batholiths in particular were emplaced at relatively shallow depths.  相似文献   

8.
Multiple sulfur and oxygen isotope compositions in Beijing aerosol   总被引：1，自引：0，他引：1  
Multiple sulfur isotopes(32S, 33 S, 34 S, 36S) and oxygen isotopes(16O, 18O) in Beijing aerosols were measured with MAT-253 isotope mass spectrometer. The δ34S values of Beijing aerosol samples range from 1.68‰ to 12.57‰ with an average value of 5.86‰, indicating that the major sulfur source is from direct emission during coal combustion. The δ18O values vary from 5.29‰ to 9.02‰ with an average value of 5.17‰, revealing that the sulfate in Beijing aerosols is mainly composed of the secondary sulfate. The main heterogeneous oxidation of SO2 in atmosphere is related to H2O2 in July and August, whereas H2O2 oxidation and Fe3+ catalytic oxidation with SO2 exist simultaneously in September and October. Remarkable sulfur isotope mass-independent fractionation effect is found in Beijing aerosols, which is commonly attributed to the photochemical oxidation of SO2 in the stratosphere. In addition, thermochemical reactions of sulfur-bearing compounds might be also a source of sulfur isotope anomalies based on the correlation between ?33S and CAPE.  相似文献   

9.
Shallow submarine gas vents in Levante Bay, Vulcano Island (Italy), emit around 3.6t CO2 per day providing a natural laboratory for the study of biogeochemical processes related to seabed CO2 leaks and ocean acidification. The main physico-chemical parameters (T, pH and Eh) were measured at more than 70 stations with 40 seawater samples were collected for chemical analyses. The main gas vent area had high concentrations of dissolved hydrothermal gases, low pH and negative redox values all of which returned to normal seawater values at distances of about 400 m from the main vents. Much of the bay around the vents is corrosive to calcium carbonate; the north shore has a gradient in seawater carbonate chemistry that is well suited to studies of the effects of long-term increases in CO2 levels. This shoreline lacks toxic compounds (such as H2S) and has a gradient in carbonate saturation states.  相似文献   

10.
Phosphorites from sedimentary sequences ranging in age from Archaean to Recent were analysed for δ18O in both the PO4 (δ18Op) and CO3 (δ18Oc) in the apatite lattice. The oxygen isotope record is considerably better preserved in phosphates than in either carbonates or cherts. The use of the Longinelli and Nuti [8] temperature equation yields temperatures for Recent phosphorites that are in good agreement with those measured in the field. The δ18Op values of ancient phosphorites decrease with increasing age. These changes with time are not likely to be due to post-depositional exchange. Changes in δ18O values of seawater and variations of temperature with time can account for the δ18Op time trend, but the latter explanation is preferred. In Ancient phosphorites δ18Oc in structurally bound carbonate in apatite is not a reliable geochemical indicator.  相似文献   

11.
 Two geochemical surveys carried out in March 1991 and September 1992 revealed the existence of a hydrothermal system in the southern portion of Montserrat Island, below Soufrière Hills Volcano. This conclusion is supported by the presence of: (a) the thermal springs of Plymouth which are fed by deep Na–Cl waters (Cl concentration ∼25 000 mg/kg, temperature ca. 250  °C) mixed with shallow steam-heated waters; (b) the four fumarolic fields of Galway's Soufrière, Gages Upper Soufrière, Gages Lower Soufrière, and Tar River Soufrière, where acid to neutral, steam-heated waters are present together with several fumarolic vents, discharging vapors formed through boiling of hydrothermal aqueous solutions. Involvement of magmatic fluids in the recharge of the hydrothermal aquifers is suggested by: (a) the high 3He/4He ratios of fumarolic fluids, i.e., 8.2 RA at Galway's Soufrière and 5.9 RA at Gages Lower Soufrière; (b) the δD and δ18O values of Na–Cl thermal springs and steam condensates, indicating the involvement of arc-type magmatic water in the formation of deep geothermal liquids; and (c) the CH4/CO2 ratios of fumarolic fluids, which are lower than expected for equilibrium with the FeO–FeO1.5 hydrothermal rock buffer, but being shifted towards the SO2–H2S magmatic gas buffer. Received: 26 March 1996 / Accepted: 19 July 1996  相似文献   

12.
This paper reports a detailed geochemical study of thermal occurrences as observed in the edifice and on the flanks of Mendeleev Volcano, Kunashir Island in August and September 2015. We showed that three main types of thermal water are discharged there (neutral chloride sodium, acid chloride sulfate, and acid sulfate types); these waters exhibit a zonality that is typical of volcano-hydrothermal island arc systems. Spontaneous and solfataric gases have relatively low 3He/4He ratios, ranging between 5.4Ra and 5.6Ra, and δ13C-CO2 between –4.8‰ and –3.1‰, and contain a light isotope of carbon in methane (δ13C ≈ –40‰). Gas and isotope geothermometers yield relatively low temperatures around 200°C. The isotope compositions in all types of water are similar to that of local meteoric water. The distribution of microcomponents varies among different types. The isotope composition of dissolved Sr varies considerably, from 0.7034 as observed in Kunashir rocks on an average to 0.7052 in coastal springs, which may have resulted from admixtures of seawater. The total hydrothermal transport rates of magmatic Cl and SO4, as observed for Mendeleev Volcano, are 7.8 t/d and 11.6 t/d, respectively. The natural outward transport of heat by the volcano’s hydrothermal system is estimated as 21 MW.  相似文献   

13.
To be used as proxies of seawater surface temperature(SST), the δ 18Oc values and Sr/Ca and Mg/Ca ratios of scleractinian coral skeletons must be verified by coral culture experiments in the laboratory. This paper describes a coral culture experiment that was conducted at several seawater temperatures T(21–28°C) using a tandem aquarium system and the new method for depositing coral skeletons grown under controlled conditions. The δ 18Oc values and the Sr/Ca and Mg/Ca ratios of the cultured coral were measured. We concluded that the δ 18Oc values and Sr/Ca and Mg/Ca ratios of the cultured coral are clearly correlated with T. The linear regression curve is δ18Oc(‰)=δ0.1427δT(°C)δ0.1495(n=18, r=0.955, p0.0001), and the slope of δ0.1427‰/°C is at the low end of the range of published values(δ0.13–δ0.29‰/°C). The Sr/Ca ratio decreases with increasing T, whereas the Mg/Ca ratio increases with increasing T, indicating a negative correlation between Sr/Ca and Mg/Ca. Their linear regression curves are Sr/Ca(mmol/mol)=δ0.04156δT+10.59(n=15, r=0.789, p0.005) and Mg/Ca(mmol/mol)= 0.04974δT+2.339(n=17, r=0.457, p0.05), respectively, which demonstrate that when Mg/Ca and Sr/Ca are increased by one unit, T increases by 5.19°C and decreases by 15.62°C, respectively. These variations are significantly lower than published values.  相似文献   

14.
《Marine pollution bulletin》2014,87(1-2):238-243
We analyzed δ13C, δ15N and δ18O in the muscle and liver from killer whales stranded on the coast of Japan. The δ15N values in the muscle samples from calves were apparently higher than those in their lactating mothers, suggesting that nursing may result in the higher δ15N values in the muscle samples of calves. The δ15N value in the muscle samples of male and female whales, except for the calves, were positively correlated with the δ13C values and body length, suggesting that the increases in δ15N were due to the growth of the whales and increase in their trophic level. In contrast, the δ18O values in the muscle samples of female whales except for the calves were negatively correlated with the δ13C and δ15N values. The δ18O may be lower in whales occupying higher trophic positions (δ15N), although it might also be affected by geographic and climatic conditions.  相似文献   

15.
An area of massive barite precipitations was studied at a tectonic horst in 1500 m water depth in the Derugin Basin, Sea of Okhotsk. Seafloor observations and dredge samples showed irregular, block- to column-shaped barite build-ups up to 10 m high which were scattered over the seafloor along an observation track 3.5 km long. High methane concentrations in the water column show that methane expulsion and probably carbonate precipitation is a recently active process. Small fields of chemoautotrophic clams (Calyptogena sp., Acharax sp.) at the seafloor provide additional evidence for active fluid venting. The white to yellow barites show a very porous and often layered internal fabric, and are typically covered by dark-brown Mn-rich sediment; electron microprobe spectroscopy measurements of barite sub-samples show a Ba substitution of up to 10.5 mol% of Sr. Rare idiomorphic pyrite crystals (∼1%) in the barite fabric imply the presence of H2S. This was confirmed by clusters of living chemoautotrophic tube worms (1 mm in diameter) found in pores and channels within the barite. Microscopic examination showed that micritic aragonite and Mg-calcite aggregates or crusts are common authigenic precipitations within the barite fabric. Equivalent micritic carbonates and barite carbonate cemented worm tubes were recovered from sediment cores taken in the vicinity of the barite build-up area. Negative δ13C values of these carbonates (>−43.5‰ PDB) indicate methane as major carbon source; δ18O values between 4.04 and 5.88‰ PDB correspond to formation temperatures, which are certainly below 5°C. One core also contained shells of Calyptogena sp. at different core depths with 14C-ages ranging from 20?680 to >49?080 yr. Pore water analyses revealed that fluids also contain high amounts of Ba; they also show decreasing SO42- concentrations and a parallel increase of H2S with depth. Additionally, S and O isotope data of barite sulfate (δ34S: 21.0-38.6‰ CDT; δ18O: 9.0-17.6‰ SMOW) strongly point to biological sulfate reduction processes. The isotope ranges of both S and O can be exclusively explained as the result of a mixture of residual sulfate after a biological sulfate reduction and isotopic fractionation with ‘normal’ seawater sulfate. While massive barite deposits are commonly assumed to be of hydrothermal origin, the assemblage of cheomautotrophic clams, methane-derived carbonates, and non-thermally equilibrated barite sulfate strongly implies that these barites have formed at ambient bottom water temperatures and form the features of a Giant Cold Seep setting that has been active for at least 49?000 yr.  相似文献   

16.
The Ca isotope compositions of 37 late Mesozoic skeletal carbonates, belemnites and brachiopods, from the Tethyan realm were analyzed by thermal (TIMS) and plasma (MC-ICP-MS) ionization mass spectrometry. A poor correlation between δ44/40Ca and δ18O values of belemnites suggests only a weak temperature dependency for the Ca isotope composition of belemnites, likely less than 0.02‰/°C. The δ44/40Ca record of belemnites was therefore used to reconstruct the Ca isotope composition of paleo-seawater (δ44/40CaSW), based on an experimentally determined fractionation factor between seawater Ca and belemnite calcite (αCC–SW) of ∼ 0.9986. The inferred δ44/40CaSW record, with an average stratigraphic resolution of 1 Ma, shows systematic temporal variation of ∼ 0.5‰ with the Middle/Late Jurassic (∼ 154 Ma) minimum of ∼ 1.4‰ and a subsequent general increase to the Early Cretaceous (∼ 124 Ma) maximum of ∼ 1.9‰. The global nature of the δ44/40CaSW record is supported by identical Ca isotope compositions of coeval (Kimmeridgian) belemnites collected from two distinct paleogeographic regions, the southern (New Zealand) and northern (Germany) margin of the Tethys Ocean. The observed late Mesozoic δ44/40CaSW record was simulated using a simple Ca isotope mass balance model, and the results indicate that the variation in δ44/40CaSW record can be explained by changes in oceanic input fluxes of Ca that were independent of the carbonate ion fluxes, such as the hydrothermal Ca flux or the release of Ca to the oceans via dolomitization of marine carbonates.  相似文献   

17.
Isotopic analyses have been made on five species of planktonic foraminifera collected in two deployments of PARFLUX Mark II time-series sediment traps in the Panama Basin. The automated sampling system on the traps provided 4 one-month samples from 29 July to 16 November 1979 and 6 two-month samples from December 1979 to November 1980.The δ18O values of Globigerinoides ruber and Globigerinoides sacculifer in this region are primarily affected by a low-salinity surface layer that forms during the early winter. These species each show a 1‰ total range in δ18O. The δ18O values of the colder-water species Globorotalia menardii, Neogloboquadrina dutertrei, and Globorotalia theyeri show smaller seasonal changes in δ18O. The δ13C values of G. ruber and G. sacculifer exhibit small seasonal changes (0.35 and 0.4‰ respectively) despite large seasonal changes in surface water productivity. The colder-water species exhibit only slightly larger changes in δ13C (up to 0.55‰) throughout the year. All colder-water species exhibit minimum or near minimum δ13C values during February and March, which is the period of maximum upwelling and primary productivity. Seasonal variations in the flux of foraminifera in the water column at this location will have only a small effect on the isotopic composition of the sediment assemblage; extreme values of δ18O and δ13C do not occur during the periods which are associated with the high flux of foraminiferal tests.  相似文献   

18.
Coral-reef terraces on tectonically elevated coasts provide important data on variations of sea level. In this paper a systematic approach is presented for the construction of synthetic reef terraces. Idealized reef terraces are generated assuming a constant rate of tectonic uplift ν and a harmonic variation of sea level with amplitudehwo and period τ. It is further assumed that coral terraces grow only during periods of relative sea-level rise. The behavior is governed by the parameter u = τυ/2π hwo. If u > 1 no reef terraces form. If 0.217 < u < 1 a discontinuous series of terraces form on the uplifting basement. If 0 < u < 0.217 the basement is covered with coral and a series of coral terraces forms on this coral. Uplifted coral-reef terraces on the Huon Peninsula, Papua New Guinea, compare reasonably well with terraces generated by our model with τ = 20,000 years andhwo = 21.4 m. We also compare the observed terraces with model terraces using the paleo sea level inferred from18O/16O data. The observed terraces are qualitatively similar to those predicted using the oxygen isotope data, however, the model terraces require larger relative sea-level variations with a near 20,000 year period than those inferred directly from the18O/16O data.  相似文献   

19.
We explore the potential of tree-ring cellulose δ18O and δ13C records for reconstructing climate variability in the southeast Tibetan Plateau. Our sampling strategy was designed to investigate intra and inter-tree variability, and the effects of the age of tree on δ18O variation. We show that intra-tree δ13C and δ18O variability is negligible, and inter-tree coherence is sufficient to build robust tree-ring δ18O or δ13C chronologies based on only four trees. There is no evidence of an age effect regarding δ18O, in contrast with tree-ring width. In our warm and moist sampling site, young tree δ13C is not clearly correlated with monthly mean meteorological data. Tree-ring δ18O appears significantly anti-correlated with summer precipitation amount, regional cloud cover, and relative humidity. Simulations conducted with the ORCHIDEE land surface model confirm the observed contribution of relative humidity to tree cellulose δ18O, and explain the weak correlation of δ13C with climate by the non-linear integration linked with photosynthesis. Altogether, the tree-ring cellulose δ18O is shown to be a promising proxy to reconstruct regional summer moisture variability prior to the instrumental period.  相似文献   

20.
At three sample sites where there are good exposures of the upper 15 m of the 1912 ash-flow sheet in the Valley of Ten Thousand Smokes (VTTS), Alaska, 18O/16O studies indicate that fumarolic activity produced a very wide range of δ18O values (?0.1 to +12.6; n=32) in the groundmass adjacent to fossil fissure fumaroles. This contrasts sharply with the uniformity of δ18O in the groundmass away from fumarolic conduits (δ18O=+5.9 to +7.1; n=7) and in all of the feldspar phenocrysts (δ18O=+6.11 to +7.5 1 for 11 samples from this study and Hildreth 1987), independent of whether these were collected from fossil fumaroles or from unaltered tuff. Only one sample contained feldspars that were even slightly 18O-enriched relative to the others (cloudy plagioclase δ18O=+8.45). and this sample also contained the most 180-enriched groundmass of any of those analyzed (δ18O=+12.6). This preservation of primary magmatic δ18O values in the VTTS feldspar phenocrysts is clearly a consequence of the extremely short time span (i.e., 1912 to ≈1923) of vigorous, high-temperature, fumarolic activity in the 1912 ash-flow sheet. These 18O/l6O systematica are strikingly similar to those discovered in the 2.8-Ma intracaldera Chegem Tuff (Gazis et al. 1996) and in the fossil fumaroles in the outflow sheet of the 0.76 Ma Bishop Tuff (Holt and Taylor 1998), thus confirming that a similar type of fumarolic meteoric-hydro-thermal activity occurred above the zone of intense welding in all three of these ash-flow tuffs. This is particularly important, because it provides a direct linkage between the older tuffs and the actual observations at the VTTS of steam chemistry, water/rock interaction, circulation geometry, flow velocities, and fumarolic temperatures (up to 645°C). The 18O/l6O effects in the VTTS can all be explained in terms of a two-stage history: (a) an early, 10- to 15-year-long, high-temperature (τ;450°C), fumarolic 18O-depletion event (groundmass δ18O=?0.1 to +4.8); and (b) a subsequent, much longer-lived, low-temperature (<150°C), 18O-enrichment episode (groundmass as high as δ18O=+12.6). Steam in these low-temperature fumaroles probably passed through various parts of the same hydrothermal system associated with the earlier, higher-temperature, fumarolic activity, and a weakened form of this low-temperature hydrothermal circulation continues to the present day (Keith et al. 1992; Lowell and Keith 1991). This low-temperature 18O/16O exchange probably occurred in combination with mineralogical alteration of both the groundmass and the calcium-rich portions of feldspar phenocrysts during the waning (<150°C) stages of fumarolic activity (Spilde et al. 1993). The slight 18O enrichment of apparently pristine, transparent feldspar phenocrysts (δ18O=+7.51) in one of the 18O-depleted, meteoric-hydrothermally altered fumarolic samples (whole-rock δ18O=+4.8) probably indicates that this sample was incipiently altered at low temperatures as fumarolic activity waned, and thus may have had a whole-rock δ18O value much lower than +4.87‰ prior to 1923.  相似文献   

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