Interpreting temporal variations in river response functions: an example from the Arkansas River,Kansas, USA

Groundwater/surface-water interactions can play an important role in management of water quality and quantity, but the temporal and spatial variability of these interactions makes them difficult to incorporate into conceptual models. There are simple methods for identifying the presence of groundwater/surface-water interactions; however, identifying flow mechanisms and pathways can be challenging. More complex methods are available to better identify these mechanisms and pathways but are often too time consuming or costly. In this work, a simple method for interpreting and identifying flow mechanisms and sources using temporal variations of river response functions is presented. This approach is demonstrated using observations from two sites along the Arkansas River in Kansas, USA. A change in flow mechanisms between the rising and falling limbs of river hydrographs was identified, along with a second surface-water source to the aquifer, a finding that was validated with stable isotope analyses.     

Application of the titanium-in-quartz thermometer to pelitic migmatites from the Adirondack Highlands, New York

The 'TitaniQ' (Ti-in-quartz) solubility thermometer was applied to migmatitic metapelites from the southern and western Adirondack Highlands, New York, to examine the effect of granulite facies metamorphism on the distribution of Ti in quartz. Both cathodoluminescence imaging and quantitative traverses revealed that individual grains of Adirondack quartz are highly zoned with respect to Ti, and that core-to-rim decreases of Ti are common. Large ranges in calculated temperature were observed within each sample. One sample, not considered to be saturated with respect to TiO₂, gave maximum temperatures more than 100 °C lower than previously estimated peak temperatures. Rutile-saturated southern and western Adirondack samples yielded peak estimates of ≥803 ± 11 °C and ∼860–870 °C, respectively, which are similar to previous estimates from major phase thermometry. Minimum Ti-in-quartz matrix temperatures from rutile-saturated samples are 630 °C, which is interpreted as the closure temperature for Ti diffusion in quartz in these samples. This study demonstrates that Ti-in-quartz thermometry can yield details of rock evolution if the textural setting and reaction history of the quartz is clear, and can yield near-peak metamorphic temperatures in some cases, if care is taken to test for post-peak diffusional resetting.     

Hornblende geothermometry of amphibolite layers of the Popple Hill gneiss, north-west Adirondack Lowlands, New York, USA

The exchange reaction tschermakite+2 diopside+2 quartz=tremolite+2 anorthite (HPCQ), in combination with the thermodynamic database TWQ (version 1.02, Berman, 1991), has been evaluated for its usefulness as a geothermometer. This reaction, which is both water conserving (independent of water fugacity) and which does not require the presence of garnet, is well suited for studying pyroxene‐bearing amphibolites. As an application of this geothermometer, we have re‐examined the amphibolites occurring in the Popple Hill gneiss of the Adirondack Lowlands of New York, USA, to better understand the magnitude of temperature variation preserved in the amphibolites themselves in this classic locality. At an assumed constant pressure of 7 kbar, the temperatures range from 619 to 682 °C from Edwards to Pierrepont and are uncorrelated with either distance along the strike of the region or with modal mineralogical variations. Hornblende exhibits a narrow compositional range suggesting that there has been little or no thermal gradient along the strike of the Lowlands. Temperatures recorded just north of Colton are, however, distinctly higher (694–758 °C). Although it is likely that the Popple Hill gneiss amphibolites experienced some effects of progressive metamorphism, particularly in the vicinity of Colton, the variations in modal mineralogy are most likely the result of such factors as local variations in the bulk chemistry of the protolith and in the fugacity of H₂O due to infiltration of diluting species (e.g. CO₂, CH₄), rather than a regional temperature variation. Temperatures recorded by the HPCQ geothermometer reported here are similar in magnitude and geographic trend to those reported for graphite–calcite carbon‐isotope thermometry by Kitchen & Valley (1995), suggesting that peak metamorphism in the Adirondack Lowlands involved laterally extensive and fairly uniform isotherms.     

The origin of olivine-plagioclase coronas in metagabbros from the Adirondack Mountains, New York

Olivine-plagioclase coronas in metagabbros from the Adirondack Mountains, New York (USA) are spatially well-organized reaction textures consisting most commonly of sequential layers of orthopyroxene, clinopyroxene, plagioclase, and garnet; the textures are characteristic of diffusion-controlled reaction kinetics. Although similar coronas have been interpreted by previous workers in terms of an isochemical steady-state diffusion model, petrographical relations and material-balance calculations establish that coronas in the Adirondack metagabbros cannot be treated as isochemical and do not form in a single-stage steady-state process; instead they evolve through time in a complex open-system reaction. In this study, the isochemical diffusion model is modified to account for elemental fluxes across the outer boundaries of the coronal reaction band, thereby approximating the open-system behaviour of the coronas. The sequence and relative proportions of product minerals calculated by the open-system steady-state model correspond closely to those observed in coronas of the Adirondacks, over a wide range of values for the relative diffusivities of chemical components involved in the reaction, regardless of the particular method used to determine material balance in the reaction texture. Despite this correspondence, petrographical evidence for successive replacement of coronal product layers reveals that the Adirondack coronas evolved through one or more transient states, rather than forming in a single-stage steady-state process. There is no evidence that the successive replacement of coronal product layers resulted from changes in pressure or temperature, but there is petrographical evidence that these changes resulted from modification of the composition of reactant plagioclase as the corona-forming reaction proceeded. This is confirmed by the fact that the evolution of the coronas over time can be replicated with the open-system diffusion model by simulating the effect of the gradual exhaustion of plagioclase as a source of the Ca and Si components required for reaction. These simulations suggest that successive stages in the evolution of the coronas are characterized by these product sequences: (i) orthopyroxene-clinopyroxene-plagioclase-garnet; (ii) orthopyroxene-clinopyroxene-garnet; and (iii) orthopyroxene-garnet. All of these stages, and the transitions between them, are observed petrographically. Coronas in Adirondack metagabbros appear, therefore, to have originated in a complex, open-system, diffusion-controlled reaction in which the product assemblages changed as the reaction progressed.     

Origin of biotite-hornblende-garnet coronas between oxides and plagioclase in olivine metagabbros,Adirondack region,New York

Complex multivariant reactions involving Fe-Ti oxide minerals, plagioclase and olivine have produced coronas of biotite, hornblende and garnet between ilmenite and plagioclase in Adirondack olivine metagabbros. Both the biotite (6–10% TiO₂) and the hornblende (3–6% TiO₂) are exceptionally Titanium-rich. The garnet is nearly identical in composition to the garnet in coronas around olivine in the same rocks. The coronas form in two stages:

1. Plagioclase+Fe-Ti Oxides+Olivine+water =Hornblende+Spinel+Orthopyroxene±Biotite +more-sodic Plagioclase
2. Hornblende+Orthopyroxene±Spinel+Plagioclase =Garnet+Clinopyroxene+more-sodic Plagioclase

The Orthopyroxene and part of the clinopyroxene form adjacent to olivine. Both reactions are linked by exchange of Mg²⁺ and Fe²⁺ with the reactions forming pyroxene and garnet coronas around olivine in the same rocks. The reactions occur under granulite fades metamorphic conditions, either during isobaric cooling or with increasing pressure at high temperature.     

Genesis of metapelitic migmatites in the Adirondack Mountains, New York

Oxygen isotope ratios and rare earth element (REE) concentrations provide independent tests of competing models of injection v. anatexis for the origin of migmatites from amphibolite and granulite facies metasedimentary rocks of the Adirondack Mountains, New York. Values of δ¹⁸O and REE profiles were measured by ion microprobe in garnet–zircon pairs from 10 sample localities. Prior U–Pb SIMS dating of zircon grains indicates that inherited cores (1.7–1.2 Ga) are surrounded by overgrowths crystallized during the Grenville orogenic cycle (～1.2–1.0 Ga). Cathodoluminescence imaging records three populations of zircon: (i) featureless rounded ‘whole grains’ (interpreted as metamorphic or anatectic), and rhythmically zoned (igneous) cores truncated by rims that are either (ii) discordant rhythmically zoned (igneous) or (iii) unzoned (metamorphic or anatectic). These textural interpretations are supported by geochronology and oxygen isotope analysis. In both the amphibolite facies NW Adirondacks and the granulite facies SE Adirondacks, δ¹⁸O_(Zrc) values in overgrowths and whole zircon are highly variable for metamorphic zircon (6.1–13.4‰; n = 95, 10 μm spot). In contrast, garnet is typically unzoned and δ¹⁸O_(Grt) values are constant at each locality, differing only between leucosomes and corresponding melanosomes. None of the analysed metamorphic zircon–garnet pairs attained oxygen isotope equilibrium, indicating that zircon rims and garnet are not coeval. Furthermore, REE profiles from zircon rims indicate zircon growth in all regions was prior to significant garnet growth. Thus, petrological estimates from garnet equilibria (e.g. P–T) cannot be associated uncritically with ages determined from zircon. The unusually high δ¹⁸O values (>10‰) in zircon overgrowths from leucocratic layers are distinctly different from associated metaigneous rocks (δ¹⁸O_(Zrc) < 10‰) indicating that these leucosomes are not injected magmas derived from known igneous rocks. Surrounding melanosomes have similarly high δ¹⁸O_(Zrc) values, suggesting that leucosomes are related to surrounding melanosomes, and that these migmatites formed by anatexis of high δ¹⁸O metasedimentary rocks.     

Carbon isotope thermometry in marbles of the Adirondack Mountains, New York

Abstract Carbon isotope thermometry has been applied to coexisting calcite and graphite in marbles from throughout the Adirondack Mountains, New York. Eighty-nine calcite-graphite pairs from the amphibolite grade NW Adirondacks change systematically in temperature north-westwards from 680 to 640 to 670° C over a 30-km distance, reflecting transitions from amphibolite facies towards granulite facies to the north-west and to the south-east. Temperature contours based on calcite-graphite thermometry in the NW Adirondacks parallel mineral isograds, with the orthopyroxene isograd falling above 675° C, and indicate that regional metamorphic temperatures were up to 75° C higher than temperatures inferred from isotherms based on cation and solvus thermometry (Bohlen et al. 1985). Fifty-five calcite-graphite pairs from granulite grade marbles of the Central Adirondacks give regional metamorphic temperatures of 670–780° C, in general agreement with cation and solvus thermometry. Data for amphibolite and granulite grade marbles show a 12%oo range in δ¹³C_cal and δ¹³C_gr. A strong correlation between carbon isotopic composition and the abundance of graphite (C_gr/C_rock) indicates that the large spread in isotopic compositions results largely from exchange between calcite and graphite during closed system metamorphism. The trends seen in δ¹³C _vs. C_gr/C_rock and δ¹³C_cal vs. δ¹³C_gr could not have been preserved if significant amounts of CO₂-rich fluid had pervasively infiltrated the Adirondacks at any time. The close fit between natural data and calculated trends of δ¹³C vs. C_gr/C_rock indicates a biogenic origin for Adirondack graphites, even though low δ¹³C values are not preserved in marble. Delamination of 17 graphite flakes perpendicular to the c-axis reveals isotopic zonation, with higher δ¹³C cores. These isotopic gradients are consistent with new graphite growth or recrystallization during a period of decreasing temperature, and could not have been produced by exchange with calcite on cooling due to the sluggish rate of diffusion in graphite. Samples located >2km from anorthosite show a decrease of 0.5-0.8%oo in the outer 100 μ of the grains, while samples at distances over 8 km show smaller core-to-rim decreases of c.0.2%oo. Correlation between the degree of zonation and distance to anorthosite suggests that the isotopic profiles reflect partial overprinting of higher temperature contact metamorphism by later granulite facies metamorphism. Core graphite compositions indicate contact metamorphic temperatures were 860–890° C within 1 km of the Marcy anorthosite massif. If samples with a significant contact metamorphic effect (Δ(_cal-gr) <3.2%oo) are not included, then the remaining 38 granulite facies samples define the relation Δ¹³C(_cal-gr) = 3.56 ± 10⁶T^-2 (K).     

Debris slide hazards in the Adirondack Province of New York state

More than 400 debris slide scars have been identified in the Adirondack Province through aerial photographic interpretation. Debris slides are concentrated in the high relief, east-central portion of the province, although some isolated scars occur in the north and southwest. Intense rainfall, relief, slope angle, slope form, and slope exposure are recognized as factors in Adirondack slide formation and distribution. Vegetational, pedological, and geological characteristics also influence slope stability conditions, but complexities in after-the-fact analyses obscure their exact function in slide activity. On the basis of slope angle and slope form, more than 600 major valley systems which exhibit slide potential were identified in the Adirondacks. Approximately 25 percent of these sites of potential slides are on private land. The prospect for higher land-use in these areas warrants serious consideration of the hazards of debris slides. Debris slides cannot be prevented, or even accurately predicted, but certain measures may possibly be taken to avert extensive economic damage or loss of life.     

Complex baseflow in urban streams: an example from central Ohio, USA

Baseflow in urban streams remains an under-researched topic, given the critical roles it plays and the extensive and ever-increasing pace of urbanization and its impacts on stream ecosystems. This study is designed to characterize the complexity of baseflow in Dry Run, an urban stream in Columbus, Ohio. A hierarchical modeling approach combined with observations of streamflow discharge (Q) and specific conductance (SC) of the stream water was applied. The streamflow measurements showed that baseflow in Dry Run is small (below 1 m³ s^?1) and being impacted by anthropogenic activities that directly discharge water into the stream. Model analyses using IHACRES and SWMM showed that baseflow is mainly composed of two different components—groundwater inflow and slowly released flows from storm-water detention ponds. The complex origins of baseflow are exemplified by hysteresis, which can be described with a plot of SC versus discharge. Overall, the study shows the value of geochemical measurements that constrain conceptual models of source-water inflows to the stream.     

Periglacial disruption and subsequent glacitectonic deformation of bedrock: an example from Anglesey,North Wales,UK

The deformed metasedimentary bedrock and overlying diamictons in western Anglesey, NW Wales, record evidence of glacier-permafrost interactions during the Late Devensian (Weichselian). The locally highly brecciated New Harbour Group bedrock is directly overlain by a bedrock-rich diamicton which preserves evidence of having undergone both periglacial (brecciation, hydrofracturing) and glacitectonic deformation (thrusting, folding), and is therefore interpreted as periglacial head deposit. The diamicton locally posses a well-developed clast macrofabric which preserves the orientation of the pre-existing tectonic structures within underlying metasedimentary rocks. Both the diamicton and New Harbour Group were variably reworked during the deposition of the later Irish Sea diamicton, resulting in the detachment of bedrock rafts and formation of a pervasively deformed glacitectonite. These structural and stratigraphic relationships are used to demonstrate that a potentially extensive layer of permafrost developed across the island before it was overridden by the Irish Sea Ice Stream. These findings have important implications for the glacial history of Anglesey, indicating that the island remained relatively ice-free prior to its inundation by ice flowing southwards down the Irish Sea Basin. Palynological data obtained from the diamictons across Anglesey clearly demonstrates that they have an Irish Sea provenance. Importantly no Lower Palaeozoic palynomorphs were identified, indicating that it is unlikely that Anglesey was overridden by ice emanating from the Snowdon ice cap developed on the adjacent Welsh mainland. Permafrost was once again re-established across Anglesey after the Irish Sea Ice Stream had retreated, resulting in the formation of involutions which deform both the lower bedrock-rich and overlying Irish Sea diamictons.     

Pressure, temperature and cooling rates of granulite facies migmatitic pelites from the southern Adirondack Highlands, New York

Detailed petrographic analysis was performed on samples from five localities within the southern Adirondacks. Textures and zoning patterns in garnet from all samples provide evidence for dehydration melting of biotite. Zoning of grossular in garnet – providing a record of prograde growth – shows both increasing and decreasing trends in garnet from the same sample. However, Ca concentrations at the garnet rims of most samples are identical (grossular = 3.4%). These observations have been interpreted as evidence for the differential timing of garnet nucleation and growth. All Fe/(Fe + Mg) and some spessartine distributions are consistent between samples, displaying diffusive profiles established largely upon cooling. Only one sample, in which retrogression was minimal, contains garnet with flat Fe/(Fe + Mg) profiles. A general pelitic pseudosection constructed in the system MnNCKFMASH reveals a maximum for Ca in garnet where the plagioclase‐out isopleth intersects the solidus (muscovite = 0). The pseudosection predicts bell‐shaped core‐to‐rim profiles of grossular during anatexis, similar to those observed in the rocks. Garnet–biotite thermometry and GASP barometry indicate peak temperatures of at least 790 °C at about 7–9 kbar, similar to conditions determined for the central Adirondacks. Cooling rates determined from finite difference modelling of spessartine and Fe/(Fe + Mg) diffusional profiles indicate a multi‐stage cooling history in which some period of rapid cooling (>200 °C Myr^?1) is required.     

Experimental examination of two-pyroxene graphical thermometers using natural pyroxenes with application to metaigneous pyroxenes from the Adirondack Mountains,New York

Clinopyroxene with exsolved orthopyroxene and coexisting orthopyroxene with exsolved clinopyroxene (inverted pigeonite) in metaigneous rocks from the Adirondacks, New York, were experimentally homogenized at temperatures near those inferred for their original crystallization. The purposes were several: (1) to test the graphical two-pyroxene geothermometer of Lindsley (1983); (2) to test the hypothesis of Bohlen and Essene (1978) that these were originally igneous pyroxenes; and (3) to test whether modal recombination of complexly exsolved pyroxenes yields realistic compositions. Experiments on Fe-rich compositions at 930° and 870° C (1 GPa) are compatible with the graphical thermometer of Lindsley (1983); however, this graphical thermometer yields apparent temperatures approximately 50° C too high for experiments at 1050° C and 1100° C (0 MPa). This suggests that at intermediate Mg/Fe the augite isotherms for these temperatures lie at lower wollastonite compositions than shown by Lindsley. The results are, however, in good agreement with isotherms derived from the solution model of Davidson (1985). When these isotherms are applied to a variety of terrestrial and lunar igneous rocks and the metaigneous rocks from the Adirondacks, temperatures given by augite and pigeonite compositions from coexisting pairs are similar. Comparison of the experimentally homogenized compositions with modally recombined compositions of Bohlen and Essene (1978) show that discrepancies between augite and pigeonite temperatures may nevertheless arise if pyroxene grains formed by granular exsolution are not correctly reintegrated.     

Composition and petrogenesis of oxide-, apatite-rich gabbronorites associated with Proterozoic anorthosite massifs: examples from the Adirondack Mountains,New York

Mafic dikes and sheets rich in Fe, Ti-oxides and apatite are commonly associated with Proterozoic massif anorthosites and are referred to as oxide-apatite gabbronorites (OAGN). Within the Adirondacks, field evidence indicates that during middle to late stages of anorthositic evolution, these bodies were emplaced as magmas with unspecified liquid-crystal ratios. Sixty whole rock analyses of Adirondack OAGN and related rocks define continuous oxide trends on Harker variation diagrams (SiO₂=37–54%). Similar trends exist for Sr, Y, Nb, Zr, and REE and together suggest a common origin via fractional crystallization. A representative parental magma (plagioclase-rich crystal mush) has been chosen from this suite, and successive daughter magmas have been produced by removal of minerals with compositions corresponding to those determined in actual rocks. Least squares, mass balance calculations of major element trends indicate that removal of intermediate plagioclase (An_40–50) plus lesser amounts of pyroxene account for the compositional variation of this suite and produce very low sums of the squares of the residuals (R² _s>0.25). The extracted mineral phases correspond volumetrically and compositionally to those of the anorthositic suite, and the model succeeds in accounting for the observed OAGN trends. The major element model is utilized to calculate trace elejent concentrations for successive magmas, and these agree closely with observation. We conclude that, beginning with a plagioclase-rich crystal mush, the extraction of intermediate plagioclase (An_40–50) drives residual magmas to increasingly Fe-, Ti-, and P-rich and SiO₂-poor conditions characteristic of Fenner-type fractionation. The crystallization sequence is plagioclaseplagioclase+orthopyroxeneplagioclase+orthopyroxene (pigeonite)+augite. Fe, Ti-oxides begin to crystallize near the end of the sequence and are followed by apatite and fayalitic olivine which appears in place of pigeonite. Augitic pyroxene becomes the dominant ferromagnesian phase in late stages of fractionation. Resultant OAGN magmas are injected into congealed anorthosite by filter pressing of liquid-rich interstitial fractions. Varying compositions of the dikes reflect filter pressing at different stages during fractionation and thereby provide information on the fractionation history of Proterozoic massif anorthosites.     

The Petrology and Geochemistry of Mafic Igneous Rocks in the Anorthosite-Bearing Adirondack Highlands, New York

Igneous rocks of broadly basaltic composition are widely distributedin the anorthosite-bearing Adirondack Highlands of New York.They constitute a mafic series of rocks that occurs on the marginsof the anorthosite series and up to 50 km away from the anorthosite.On an Sr reference diagram, the mafic series has an apparentinitial ⁸⁷Sr/⁸⁶Sr value of 0.7036, which is consistent with1100 Ma subcontinental mantle. The series was probably emplacedin the interval 1150–1100 Ma, during which time anorthositeand granitic magmas were also emplaced. The rocks were metamorphosedshortly thereafter ({small tilde} 1088 Ma) under upper-amphiboliteand granulite facies conditions. Individual bodies of maficrocks range in thickness from small enclaves and layers >>1 m thick to large lensoid masses several tens of meters thick.Despite deformation and metamorphic recrystallization, manyof the rocks retain chiHed margins, cross-cutting relationships,and relict igneous textures. Selected samples of the mafic series have been analyzed fortheir major and trace element compositions. Metamorphism didnot significantly alter the igneous geochemical relationships,and the rocks retain mantle-like values for Zr/Nb, K/Zr, K/Rb,Rb/Sr, and ⁸⁷Sr/⁸⁶Sr. The most primitive rocks of the seriesare silica-undersaturated gabbroic troctolites, and the moreevolved rocks are basaltic in composition. The mafic seriesas a whole has high abundances of A1₂O₃, FeO, the light rareearth elements (LREE), and other incompatible trace elements.Even the most geochemically primitive compositions have highFeO contents. The Fe enrichment and Si depletion that are shownby chemically evolved compositions are consistent with a Fennertrend of fractionation. Low levels of normative di indicatethat high Fe is not a result of the extensive fractionationof cpx. The geochemical trends that are defined by the traceelements, including the REE, suggest the basaltic rocks maybe differentiates of a parental magma of gabbroic troctolitecomposition. The main compositional trend of the mafic seriescan be simulated by 61% crystallization of olivine and plagioclaseof a gabbroic troctolite, followed by 13% crystallization ofolivine, plagioclase, clinopyroxene, and titanomagnetite atthe final stages. The modelled ratio of olivine to plagioclasecrystallization changes from 1–8: 1 to 0–64: 1.These non-cotectic ratios may reflect a delay in the crystallizationof plagioclase relative to olivine, possibly as a result oflow nucleation rates. At later stages of differentiation, plagioclasewas more important in the crystallization of the series. Delayedcrystallization of plagioclase may also have resulted in thehigh A1₂O₃ contents and enhancement of Eu and Sr relative toother trace elements at early stages of differentiation. The mafic series and the silica-saturated anorthosite seriestogether form an anorthosite-norite-troctolite (ANT) suite.More than one mantle composition may have been involved in generatingthe Adirondack mafic magmas. The rocks retain geochemical evidenceof a source that was depleted in basaltic components (cpx) butenriched in Fe, Ti, K, and the LREE. Previously documented evidenceof anticlockwise cooling paths (Bohlen, 1987) and of a regionalgravity high centered beneath the Adirondack region (Simmons,1964) suggests that of the continental crust by basaltic magmasmay have underplating of the continental crust by basaltic magmasmay have been an important feature of the tectonic evolutionofthe region. A model of mantle upwelling beneath thinning continentalcrust explains the geochemically hybrid nature of the maficseries magmas. It is also consistent with a tectonic settingof incipient or failed continental rifting, to which the generationof the anorthosites is commonly attributed.     

Distribution of asbestos in the bedrock of the northern New Jersey area

Asbestos has been identified at fifty-five locations in the bedrock of the northern New Jersey area. Most occurrences are confined to (1) The Precambrian rocks of the New Jersey Highlands, particularly the marbles; (2) the Paleozoic serpentinites of Staten Island, New York, and Hoboken, New Jersey; and (3) the Mesozoic basaltic rocks of the Newark Basin. Chrysotile and tremolite asbestos are present in local concentrations in the marbles. In the most extensive exposure of the marble, the Franklin band, traces of tremolite-actinolite asbestos are commonly present. Crocidolite asbestos occurs in localized areas associated with fracture systems in Precambrian pegmatites and associated rocks. The Paleozoic serpentinites contain chrysotile asbestos as a major component in deformed zones. Megascopic chrysotile and anthophyllite asbestos veins occur locally in the serpentinites. Actinolite asbestos occurs in the Mesozoic basaltic rocks of the Newark Basin. Potential environmental problems associated with asbestosbearing bedrock include production and use of rock products containing asbestos, introduction of asbestos into environments surrounding excavations, and asbestos contamination of soils and water supplies.     

Chemistry and transport of soluble humic substances in forested watersheds of the Adirondack Park,New York

Studies were conducted in conjunction with the Integrated Lake-Watershed Acidification Study (ILWAS) to examine the chemistry and leaching patterns of soluble humic substances in forested watersheds of the Adirondack region. During the summer growing season, mean dissolved organic carbon (DOC) concentrations in the ILWAS watersheds ranged from 21–32 mg C l^?1 in O/A horizon leachates, from 5–7 mg C l^?1 in B horizon leachates, from 2–4 mg C l^?1 in groundwater solutions, from 6–8 mg C l^?1 in first order streams, from 3–8 mg C l^?1 in lake inlets, and from 2–7 mg C l^?1 in lake outlets. During the winter, mean DOC concentrations dropped significantly in the upper soil profile. Soil solutions from mixed and coniferous stands contained as much as twice the DOC concentration of lysimeter samples from hardwood stands. Results of DOC fractionation analysis showed that hydrophobia and hydrophilic acids dominate the organic solute composition of natural waters in these watersheds. Charge balance and titration results indicated that the general acid-base characteristics of the dissolved humic mixture in these natural waters can be accounted for by a model organic acid having an average_pK_a of 3.85, an average charge density of 4–5 μeq mg^?1 C at ambient pH, and a total of 6–7 meq COOH per gram carbon.     

Evidence for Differential Unroofing in the Adirondack Mountains, New York State, Determined by Apatite Fission-Track Thermochronology

Apatite fission-track ages of 168-83 Ma for 39 samples of Proterozoic crystalline rocks, three samples of Cambrian Potsdam sandstone, and one Cretaceous lamprophyre dike from the Adirondack Mountains in New York State indicate that unroofing in this region occurred from Late Jurassic through Early Cretaceous. Samples from the High Peaks section of the Adirondack massif yielded the oldest apatite fission-track ages (168-135 Ma), indicating that it was exhumed first. Unroofing along the northern, northwestern, and southwestern margins of the Adirondacks began slightly later, as shown by younger apatite fission-track ages (146-114 Ma) determined for these rocks. This delay in exhumation may have resulted from burial of the peripheral regions by sediment shed from the High Peaks. Apatite fission-track ages for samples from the southeastern Adirondacks are distinctly younger (112-83 Ma) than those determined for the rest of the Adirondack region. These younger apatite fission-track ages are from a section of the Adirondacks dissected by shear zones and post-Ordovician north-northeast-trending normal faults. Differential unroofing may have been accommodated by reactivation of the faults in a reverse sense of motion with maximum compressive stress, sigma1, oriented west-northwest. A change in the orientation of the post-Early Cretaceous paleostress field is supported by a change in the trend of Cretaceous lamprophyre dikes from east-west to west-northwest.     

Quartz–garnet isotope thermometry in the southern Adirondack Highlands (Grenville Province, New York)

Quartz–garnet oxygen isotope thermometry of quartz‐rich metasedimentary rocks from the southern Adirondack Highlands (Grenville Province, New York) yields metamorphic temperatures of 700–800 °C, consistent with granulite facies mineral assemblages. Samples from the Irving Pond quartzite record Δ¹⁸O(Qtz–Grt) = 2.68 ± 0.21‰ (1 s.d. , n = 15), corresponding to peak metamorphic conditions of 734 ± 38 °C. This agrees well with the estimates from garnet–biotite exchange thermometry. Similar temperature estimates are obtained from Swede Pond (682 ± 47 °C, n = 3) and King's Station (c. 700 °C). The Whitehall area records higher temperatures (798 ± 25 °C, n = 3). All of these temperatures are higher than previous regional temperature estimates. The c. 800 °C temperatures near Whitehall are consistent with preservation of pre‐granulite contact temperatures adjacent to anorthosite. The preservation of peak metamorphic temperatures in garnet of all sizes is consistent with slow oxygen diffusion in garnet, and closure temperatures of at least 730 °C. Peak metamorphic fractionations are preserved in rocks with varying quartz:feldspar ratios, indicating that the modal percentage of feldspar does not affect retrograde oxygen exchange in these rocks. The lack of this correlation suggests slow rates of oxygen diffusion in quartz and feldspar, consistent with the results of anhydrous oxygen diffusion experiments.