Trace metals and radionuclides reveal sediment sources and accumulation rates in Jordan Cove, Connecticut

Many small estuaries are influenced by flow restrictions resulting from transportation rights-of-way and other causes. The biogeochemical functioning and history of such systems can be evaluated through study of their sediments. Ten long and six short cores were collected from the length of Jordan Cove, Connecticut, a Long Island Sound subestuary, and analyzed for stratigraphy, radionuclides (¹⁴C, ²¹⁰Pb, ²²⁶Ra, ¹³⁷Cs, and ⁶⁰Co), and metals (Ag, Cd, Cu, Pb, Zn, Fe, and Al). For at least 3,800 yr, rising sea level has gradually inundated Jordan Cove, filling it with mud similar to that currently being deposited there. Long-term sediment accumulation in the cove averaged close to 0.1 cm yr⁻¹ over the last three millennia. Recent sediment accumulation rates decrease inland from 0.84 cm yr⁻¹ to 0.40 cm yr⁻¹, and are slightly faster than relative sea-level rise at this site (0.3 cm yr⁻¹). Similarity of depth distributions of trace metals was used to confirm relative sediment accumulation rates. ⁶⁰Co and Ag are derived from sources outside the cove and its watershed, presumably the Millstone nuclear power plant and regional contaminated sediments, respectively. The combined data suggest that Long Island Sound is an important source of sediment to the cove; a minor part of total sediment is supplied from the local watershed. Trace metal levels are strongly correlated with Fe but not with either organic matter or Al. Sediment quality has declined in the cove over the past 60 yr, but only slightly. Cu, Pb, and Zn data correlate strongly with Fe but not with either organic matter or aluminum. Ratios of Ag to Fe and to trace metals suggest that Ag in the cove is derived almost entirely from Long Island Sound. This result supports the notion that Fenormalized Ag can serve as a better tracer of some kinds of contamination than more common and abundant metals, like Cu, Pb, and Zn. *** DIRECT SUPPORT *** A01BY085 00008     

Unprecedented last-glacial mass accumulation rates determined by luminescence dating of loess from western Nebraska

A high-resolution chronology for Peoria (last glacial period) Loess from three sites in Nebraska, midcontinental North America, is determined by applying optically stimulated luminescence (OSL) dating to 35–50 μm quartz. At Bignell Hill, Nebraska, an OSL age of 25,000 yr near the contact of Peoria Loess with the underlying Gilman Canyon Formation shows that dust accumulation occurred early during the last glacial maximum (LGM), whereas at Devil’s Den and Eustis, Nebraska, basal OSL ages are significantly younger (18,000 and 21,000 yr, respectively). At all three localities, dust accumulation ended at some time after 14,000 yr ago. Mass accumulation rates (MARs) for western Nebraska, calculated using the OSL ages, are extremely high from 18,000 to 14,000 yr—much higher than those calculated for any other pre-Holocene location worldwide. These unprecedented MARs coincide with the timing of a mismatch between paleoenvironmental evidence from central North America, and the paleoclimate simulations from atmospheric global circulation models (AGCMs). We infer that the high atmospheric dust loading implied by these MARs may have played an important role, through radiative forcing, in maintaining a colder-than-present climate over central North America for several thousand years after summer insolation exceeded present-day values.     

Recharge characteristics of a phreatic aquifer as determined by storage accumulation

The cumulative storage accumulation curve (CSAC) is a tool for saturated-volume fluctuation (SVF) analysis of transient recharge to shallow phreatic aquifers discharging only to springs. The method assumes that little underflow or phreatic evapotranspiration occurs. The CSAC is a modified water-table hydrograph that distinguishes storage increase caused by recharge from loss due to springflow-induced recession. Required for the analysis are water-table fluctuations at a single representative location within the catchment of a single spring and either direct measurements or robust interpolations of springflows at different aquifer stages. The method employs empirical manipulation of head observations, varying spring catchment area to minimize CSAC water-level changes in late portions of long recessions. Results include volumetric estimates of recharge integrated over individual events and instantaneous rates of recharge to the water table, at the temporal resolution of the water-level sampling interval. The analysis may also yield physically realistic information on spring catchment and recharge focusing. In a test case in West Virginia, USA, recharge estimates by this technique were consistent with integrated springflow time series but greater than estimates based on potential evapotranspiration. Results give insight into dynamic recharge behavior over time as well as an indication of recharge catchment size. Electronic Publication     

Sediment accumulation rates and geochronologies measured in the Saguenay Fjord using the Pb-210 dating method

Sediment accumulation rates were estimated from-the vertical distribution of excess Pb-210 measured in sediment cores collected at seven stations in the Saguenay Fjord, Quebec. These rates decrease with increasing water depth and distance from the mouth of the Saguenay River, ranging from 4.0 g cm^?2 yr^?1 (～- 7 cm yr^?1) near the head of the fjord to 0.07 g cm^?2 yr^?1 (～- 0.1 cm yr^?1) in the deep inner basin of the fjord. In one core from the head of the fjord, layered sediment structures, having different physical characteristics and composition, appear related to recent, pulsed inputs of older raised marine deposits displaced by a landslide in 1971. Synchronous depositional anomalies in several cores provide evidence of other large scale sediment redistribution processes in the fjord. Pb-210 geochronologies are generally in good agreement with time-stratigraphic horizons inferred both from Cs-137 activity profiles and from the analysis of pollen assemblages in one core.     

Assessing the natural recovery of a lake contaminated with Hg using estimated recovery rates determined by sediment chronologies

Deer Lake is an impoundment located near Ishpeming, Michigan, USA. Iron mining assay laboratories located in Ishpeming disposed of Hg salts to the city sewer whose outfall was located along an inlet to Deer Lake. An effort to remediate the system in the mid 1980s which consisted of drawing down water in the impoundment in order to volatize Hg from the sediments did not result in recovery of the system. Since the mid 1990s, the remediation strategy has been to allow the continual burial of the contaminated sediments, i.e., natural recovery. The goal of this study was to assess the effectiveness of this strategy. This was accomplished by investigating the state of the system in terms of its recovery and estimating the time frame for recovery. Sediment cores were collected in 2000 to determine historical trends in accumulation rates and concentrations of Hg and other metals. Sedimentation rates and sediment ages were estimated using ²¹⁰Pb. Event-based dating (e.g., peak of ¹³⁷Cs in 1963) was used to supplement ²¹⁰Pb data due to non-monotonic features in the ²¹⁰Pb profile and activities that were not at supported levels at the base of the core. Selected results are that: (1) drawdown significantly influenced sedimentation patterns causing slopes for ²¹⁰Pb profiles that reflected the influx of older sediment, (2) periods of Fe production correlate to Hg loading indicating the point source for contamination, a relationship not previously identified, (3) Hg:Al ratios indicate a recent change to a watershed pathway for Hg loading and (4) Hg concentrations had decreased from their peak, remain elevated, and were increasing after 1997. The cause of the recent Hg concentrations may be related to influx of contaminated watershed soils or sediments. Estimating the time frame for recovery is challenging in this system because the process of natural recovery seems to have been arrested and deeper, uncontaminated sediments, were not recovered as a basis for reference. However, a recovery to background conditions is likely not achievable since rates of Hg loading to nearby lakes and the current rate of atmospheric deposition are greater than an estimate of background conditions for Deer Lake. Assuming recovery continued after 2000, estimates of the time required for recovery varied based on the system state used to define it (e.g., recent rates of wet Hg deposition or Hg surface concentrations/fluxes from similar systems), but were less than 12 a. However, the recent increasing values of recovery indicators (e.g., Hg concentrations) suggests that these estimates are conservative and will be longer if recovery remains arrested, which may in part be due to the legacy of Hg contamination on the landscape. This study shows that estimates of recovery of highly disturbed lake systems can be made in the absence of within lake reference conditions by using comparisons to reference systems and challenges of estimating ages from atypical ²¹⁰Pb activity profiles can be overcome in part using event-based dating techniques.     

Correlations of natural radionuclides in sediment from Danube

The correlation between specific activities of some natural radionuclides (²³⁸U, ²²⁶Ra, ²³²Th, ⁴⁰K) measured in sediment taken from river bottom was studied. The sediment was taken from the Serbian part of the Danube River. Good correlation between some of the isotopes is observed, so that their specific activity ratios are spread over a lower range than specific activities themselves. This suggests that evaluation of specific activity ratios of some natural radionuclides could be a more sensitive method for the determination of increased levels of some of them than the straightforward analysis of specific activities.     

Sediment accumulation in lake chicot,Arkansas

Lake Chicot is an oxbow lake located along the western side of the Mississippi River in southeastern Arkansas. A major flood in 1927, levee construction, land use changes from bottomland hardwood to agriculture, a large increase in drainage area, and stream channelization have altered the appearance of contributing watersheds and the lake. The lake often has high suspended sediment concentrations making it undesirable for recreation and aquatic production. As part of a coordinated study to determine changes in the lake, sediment accumulation patterns and rates were determined in Lake Chicot using the¹³⁷Cs technique. Major sediment accumulation is occurring near the major inlet and along the thalweg of the oxbow. Average sediment accumulation of 1.8 cm/yr since 1963 was measured for twelve samples. Calculations show sediment accumulation is decreasing. This study has shown that the¹³⁷Cs technique can provide useful planning information for the environmental geologist or reservoir manager. Results of the current study will be used to develop better sediment and water management strategies for Lake Chicot. Contribution of the U.S. Department of Agriculture, Agricultural Research Service, in cooperation with the Vicksburg District of the U.S. Army Corps of Engineers.     

Sediment and heavy metal accumulation in the Cauvery basin

Eleven cores were collected from the Cauvery basin. Radiometric dates were used to determine modern sediment accumulation rates. Sediment accumulation rates ranged from 0.4 to 4 mm yr^–. Heavy metal concentration decreases with the increase of depth. The heavy metal concentrations at certain depths are attributed to the irregular input of metals and their remobilization. Heavy metal accumulations have been computed using sediment accumulation rates, and accumulation rates show an additional anthropogenic input of metals and sediments in the recent past. Factor analysis and correlation analysis show the diverse source and accumulation mechanism influencing the metal distribution in the basin.     

Halite karst geohazards (natural and man-made) in the United Kingdom

In the United Kingdom, Permian and Triassic halite (rock salt) deposits have been affected by natural and artificial dissolution producing karstic landforms and subsidence. Brine springs from the Triassic salt have been exploited since Roman times or possibly earlier, indicating prolonged natural dissolution. Medieval salt extraction in England is indicated by the names of places ending in "wich", indicating brine spring exploitation at Northwich, Middlewich, Nantwich and Droitwich. Later, Victorian brine extraction in these areas accentuated salt karst development, causing severe subsidence problems which remain a legacy. The salt was also mined, but the mines flooded and consequent brine extraction caused the workings to collapse, resulting in catastrophic surface subsidence. Legislation was enacted to pay for the damage and a levy is still charged for salt extraction. Some salt mines are still collapsing, and the re-establishment of the post-brine extraction hydrogeological regimes means that salt springs may again flow, causing further dissolution and potential collapse.     

Spatial and isotopic analysis of watershed soil loss and reservoir sediment accumulation rates in Lake Anna, Virginia, USA

Soil erosion and associated sedimentation are a threat to the sustainable use of surface water resources through the loss of volume storage capacity and conveyance of pollutants to receiving water bodies. The RUSLE2 empirical model and isotopic sediment core analyses were used to evaluate watershed erosion and reservoir sediment accumulation rates for Lake Anna, in Central Virginia. A sediment flux rate of 66,000 Mg/year was estimated from the upper basin and land use was determined to be the primary factor contributing to soil erosion. Barren lands and agricultural activities were estimated to contribute the most sediment (>20 Mg/ha/year), whereas forested and herbaceous landscapes were less likely to erode (<0.3 Mg/ha/year). Eleven separate ²¹⁰Pb-based estimates of sediment accumulation were used to construct reservoir-scale sedimentation rates. Sedimentation rates in the upper reaches of the reservoir were variable, ranging from 2.3 to 100 Mg/ha/year, with a median rate of 8.4 Mg/ha/year. Historical sedimentation showed an increase in annual accumulation from 1972 to present. Based on these data the reservoir has experienced a 2% loss of volume storage capacity since impoundment in 1972. Results from this study indicate that Lake Anna is not currently experiencing excessive sedimentation and erosion problems. However, the predominance of highly erosive soils (soil erodibility factor >0.30) within the watershed makes this system highly vulnerable to future anthropogenic stressors.     

Sediment storage and severity of contamination in a shallow reservoir affected by historical lead and zinc mining

A combination of sediment-thickness measurement and bottom-sediment coring was used to investigate sediment storage and severity of contamination in Empire Lake (Kansas), a shallow reservoir affected by historical Pb and Zn mining. Cd, Pb, and Zn concentrations in the contaminated bottom sediment typically exceeded baseline concentrations by at least an order of magnitude. Moreover, the concentrations of Cd, Pb, and Zn typically far exceeded probable-effects guidelines, which represent the concentrations above which toxic biological effects usually or frequently occur. Despite a pre-1954 decrease in sediment concentrations likely related to the end of major mining activity upstream by about 1920, concentrations have remained relatively stable and persistently greater than the probable-effects guidelines for at least the last 50 years. Cesium-137 evidence from sediment cores indicated that most of the bottom sediment in the reservoir was deposited prior to 1954. Thus, the ability of the reservoir to store the contaminated sediment has declined over time. Because of the limited storage capacity, Empire Lake likely is a net source of contaminated sediment during high-inflow periods. The contaminated sediment that passes through, or originates from, Empire Lake will be deposited in downstream environments likely as far as Grand Lake O’ the Cherokees (Oklahoma).     

Sediment permeability change on natural gas hydrate dissociation induced by depressurization

The permeability of a natural gas hydrate reservoir is a critical parameter associated with gas hydrate production. Upon producing gas from a hydrate reservoir via depressurization, the permeability of sediments changes in two ways with hydrate dissociation, increasing with more pore space released from hydrate and decreasing due to pore compression by stronger effective stress related to depressurization. In order to study the evolution of sediment permeability during the production process with the depressurization method, an improved pore network model (PNM) method is developed to establish the permeability change model. In this model, permeability change induced by hydrate dissociation is investigated under hydrate occurrence morphology of pore filling and grain coating. The results obtained show that hydrate occurrence in sediment pore is with significant influence on permeability change. Within a reasonable degree of pore compression in field trial, the effect of pore space release on the reservoir permeability is greater than that of pore compression. The permeability of hydrate containing sediments keeps increasing in the course of gas production, no matter with what hydrate occurrence in sediment pore.     

伏龙泉断陷白垩系油气成藏规律及优势储层特征

伏龙泉断陷是松辽盆地东南隆起区的次级构造单元,处在反转构造较为强烈的背斜带上。在研究区基本成藏条件研究的基础上,总结了伏龙泉断陷油气成藏规律及优势储层特征。伏龙泉断陷油气主要来自沙河子组和营城组的烃源岩;成藏期分为三期:泉头组—嫩江组沉积时期、嫩江组沉积末期构造运动时期、嫩江组沉积末期构造运动之后至现今。构造是控制伏龙泉断陷成藏的重要因素,断陷深部油气藏具有先成藏后致密、近源早成藏的特征,早期成藏的储层具有好的物性条件;浅部油气藏均为次生油气藏,成藏受嫩江组末期构造运动控制。     

The oxidation state of sulfur in synthetic and natural glasses determined by X-ray absorption spectroscopy

Sulfur K-edge X-ray absorption near edge structure (XANES) spectra were recorded for experimental glasses of various compositions prepared at different oxygen fugacities (fO₂) in one-atmosphere gas-mixing experiments at 1400 °C. This sample preparation method only results in measurable S concentrations under either relatively reduced (log fO₂ < −9) or oxidised (log fO₂ > −2) conditions. The XANES spectra of the reduced samples are characterised by an absorption edge crest at 2476.4 eV, typical of S²⁻. In addition, spectra of Fe-bearing compositions exhibit a pronounced absorption edge shoulder. Spectra for all the Fe-free samples are essentially identical, as are the spectra for the Fe-bearing compositions, despite significant compositional variability within each group. The presence of a sulfide phase, such as might exsolve on cooling, can be inferred from a pre-edge feature at 2470.5 eV.The XANES spectra of the oxidised samples are characterised by an intense transition at 2482.1 eV, typical of the sulfate anion SO₄²⁻. Sulfite (SO₃²⁻) has negligible solubility in silicate melts at low pressures. The previous identification of sulfite species in natural glass samples is attributed to an artefact of the analysis (photoreduction of S⁶⁺). S⁴⁺ does, however, occur unambiguously with S⁶⁺ in Fe-free and Fe-poor compositions prepared in equilibrium with CaSO₄ at 4-16 kbar, and when buffered with Re/ReO₂ at 10 kbar. Solubility of S⁴⁺ thus requires partial pressures of SO₂ considerably in excess of 1 bar. A number of experiments were undertaken in an attempt to access intermediate fO₂s more applicable to terrestrial volcanism. Although these were largely unsuccessful, S²⁻ and S⁶⁺ were found to coexist in some samples that were not in equilibrium with the imposed fO₂.The XANES spectra of natural olivine-hosted melt inclusions and submarine glasses representative of basalts at, or close to, sulfide saturation show mainly dissolved S²⁻, but with minor sulfate, and additionally a peak at 2469.5 eV, which, although presumably due to immiscible sulfide, is 1 eV lower than that typical of FeS. These sulfate and sulfide-related peaks disappear with homogenisation of the inclusions by heating to 1200 °C followed by rapid quenching, suggesting that both these features are a result of cooling under natural conditions. The presence of small amounts of sulfate in otherwise reduced basaltic magmas may be explained by the electron exchange reaction: S²⁻ + 8Fe³⁺ = S⁶⁺ + 8Fe²⁺, which is expected to proceed strongly to the right with decreasing temperature. This reaction would explain why S²⁻ and S⁶⁺ are frequently found together despite the very limited fO₂ range over which they are thermodynamically predicted to coexist. The S XANES spectra of water-rich, highly oxidised, basaltic inclusions hosted in olivine from Etna and Stromboli confirm that nearly all S is dissolved as sulfate, explaining their relatively high S contents.     

Metal accumulation rates in northwest Atlantic pelagic sediments

Measurements of ²³⁰Th, ${}^{87}\text{Sr}{}^{86}\text{Sr}$ and twenty-four metals were made on cores from the Nares Abyssal Plain. The sediment is characterized by slowly-accumulating (0.3–0.7 g/cm² 10³ yr) pelagic red clays and rapidly deposited grey clays transported by turbidity currents. Despite their colour differences and the enrichment of Mn, Fe, Cu, Co, Ni, Zn, V and, to a lesser degree, the rare earths in the red clays, Sr isotope evidence demonstrates that the clays have the same terrigenous origin. The excesses of metals in the red clays have been attributed to metal removal from the water column and a comparison with the grey clays has enabled the authigenic fluxes of metals to be estimated. The fluxes obtained are in the ranges 20–50 μmol/cm² 10³ yr for Mn and Fe, 0.1–0.4 μmol/cm² 10³ yr for Cu, Co, Ni, Zn, V, Sr and Ce, 10–20 nmol/cm² 10³ yr for La and Nd, and 0.5-3 nmol/cm² 10³ yr for Sm, Eu, Gd, Dy, Er and Yb. Authigenic fluxes of Y, Nb, Cr, Zr, Rb, U and Th were not resolvable. Fluxes appear to be near constant on the Plain but comparison with other areas shows that they are quite variable both between and within ocean basins. The chief factor controlling authigenic fluxes is the geochemical abundances of the elements but fractionation within both the transition element and rare earth series can be recognized from inter-element comparisons and from differences in fluxes between Atlantic and Pacific red clays corresponding to the oceanic reactivities of the elements.     

Accretion rates and sediment accumulation in Rhode Island salt marshes

In order to test the assumption that accretion rates of intertidal salt marshes are approximately equal to rates of sea-level rise along the Rhode Island coast,²¹⁰Pb analyses were carried out and accretion rates calculated using constant flux and constant activity models applied to sediment cores collected from lowSpartina alterniflora marshes at four sites from the head to the mouth of Narragansett Bay. A core was also collected from a highSpartina patens marsh at one site. Additional low marsh cores from a tidal river entering the bay and a coastal lagoon on Block Island Sound were also analyzed. Accretion rates for all cores were also calculated from copper concentration data assuming that anthropogenic copper increases began at all sites between 1865 and 1885. Bulk density and weight-loss-on-ignition of the sediments were measured in order to assess the relative importance of inorganic and organic accumulation. During the past 60 yr, accretion rates at the eight low marsh sites averaged 0.43±0.13 cm yr^?1 (0.25 to 0.60 cm yr^?1) based on the constant flux model, 0.40±0.15 cm yr^?1 (0.15 to 0.58 cm yr^?1) based on the constant activity model, and 0.44±0.11 cm yr^?1 (0.30 to 0.59 cm yr^?1) based on copper concentration data, with no apparent trend down-bay. High marsh rates were 0.24±0.02 (constant flux), 0.25±0.01 (constant activity), and 0.47±0.04 (copper concentration data). The cores showing closest agreement between the three methods are those for which the excess²¹⁰Pb inventories are consistent with atmospheric inputs. These rates compare to a tide gauge record from the mouth of the bay that shows an average sea-level rise of 0.26±0.02 cm yr^?1 from 1931 to 1986. Low marshes in this area appear to accrete at rates 1.5–1.7 times greater than local relative sea-level rise, while the high marsh accretion rate is equal to the rise in sea level. The variability among the low marsh sites suggests that marshes may not be poised at mean water level to within better than ±several cm on time scales of decades. Inorganic and organic dry solids each contributed about 9% by volume to low marsh accretion, while organic dry solids contributed 11% and inorganic 4% to high marsh accretion. Water/pore space accounted for the majority of accretion in both low and high marshes. If water associated with the organic component is considered, organic matter accounts for an average of 91% of low marsh and 96% of high marsh accretion. A dramatic increase in the organic content at a depth of 60 to 90 cm in the cores from Narragansett Bay appears to mark the start of marsh development on prograding sand flats.     

Weathering and weathering rates of natural stone

Physical and chemical weathering were studied as separate processes in the past. Recent research, however, shows that most processes are physicochemical in nature. The rates at which calcite and silica weather by dissolution are dependent on the regional and local climatic environment. The weathering of silicate rocks leaves discolored margins and rinds, a function of the rocks' permeability and of the climatic parameters. Salt action, the greatest disruptive factor, is complex and not yet fully understood in all its phases, but some of the causes of disruption are crystallization pressure, hydration pressure, and hygroscopic attraction of excess moisture. The decay of marble is complex, an interaction between disolution, crack-corrosion, and expansion-contraction cycies triggered by the release of residual stresses. Thin spalls of granites commonly found near the street level of buildings are generally caused by a combination of stress relief and salt action. To study and determine weathering rates of a variety of commercial stones, the National Bureau of Standards erected a Stone Exposure Test Wall in 1948. Of the many types of stone represented, only a few fossiliferous limestones permit a valid measurement of surface reduction in a polluted urban environment.     

柴达木盆地昆北油田切16区路乐河组沉积特征与储层预测

柴达木盆地西南部昆北构造带发现以古近系路乐河组陆源碎屑岩为储层的油田.根据昆北油田切16区探井岩心观察、测录井资料分析,结合岩石铸体薄片观测、电子扫描显微镜镜下分析等结果,初步确定了昆北油田切16区路乐河组主要发育两期辫状三角洲体系;路乐河组储层岩石类型分布相对稳定,成分成熟度较低,主要为岩屑长石砂岩,岩屑成份以花岗岩为主,骨架偏刚性,储层中杂基含量相对较高、胶结物含量较低;储集层孔隙较发育且分布相对较均匀,孔隙连通性较好,孔隙类型主要以残余原生粒间孔为主;储层物性受沉积相带分布,成岩作用以及杂基含量共同控制,压实作用是储层物性的主控因素.通过结合主力油层段测井响应特征及层控地震振幅属性分析,认为昆北油田切16区、切15井与切169井的东部以及切20井的西南部的构造相对较高部位为今后有利勘探目标.     

Iron isotopes in natural carbonate minerals determined by MC-ICP-MS with a Fe-Fe double spike

We have developed a method for iron isotope analysis by multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) using a ⁵⁸Fe-⁵⁴Fe double spike. A 20 min analysis produces mass-bias-corrected iron isotope data with an external reproducibility of ±0.05 (2 SD) on δ⁵⁶Fe, which represents a decrease in analysis time compared to sample-standard bracketing techniques. The estimation of external reproducibility is based on replicate analysis of the ETH hematite in-house standard. The double spike method has two advantages. First, matrix effects during MC-ICP-MS analysis are decreased with tests showing that accurate iron isotope data can, in some cases, be obtained even when matrix levels exceed iron concentration (Na/Fe, Mg/Fe, and Ca/Fe up to 5, 2, and 0.1, respectively). Because chemical separation reduces matrix/Fe to levels more than three orders of magnitude lower than this, measured Fe isotope compositions are unlikely to be compromised by matrix effects. Second, it is possible to spike samples before chemical purification, which enables any isotopic fractionation effect because of incomplete recovery of iron from a sample to be accounted for. This may be important where obtaining quantitative iron yields from samples is difficult, such as the extraction of dissolved iron from water samples. Fe isotope data on a set of standard reference materials (igneous rocks, ferromanganese nodules, sedimentary rocks, and ores) are presented, which are in agreement with previously published data considering analytical uncertainties. Mantle-derived standard rock samples that are the source of iron for surficial, (bio)geochemical cycling yield a mean δ⁵⁶Fe of 0.041 ± 0.11‰ (n = 8; 2 SD) with reference to IRMM-14. Hydrothermal and metamorphic calcium carbonate rocks with a relatively low iron content (100-4000 ppm) have δ⁵⁶Fe = −1.25 to −0.07‰. Structural Fe(II) in hydrothermal calcites has δ⁵⁶Fe = −1.25 to −0.27‰. The light iron in this range of carbonate minerals may reflect the iron isotope composition of the hydrothermal fluids from which the carbonate precipitated, or the presence of Fe(III) and/or organic material in the hydrothermal fluids during calcite precipitation.