Temporal and spatial variability of Chl-a and SST on the South Atlantic Bight: Revisiting with cloud-free reconstructions of MODIS satellite imagery     

Travis N. Miles  Ruoying He 《Continental Shelf Research》2010

Daily, cloud-free data interpolating empirical orthogonal function (DINEOF) reconstructions of sea-surface temperature (SST) and chlorophyll (Chl-a) satellite imagery are compiled into monthly mean images for a six-year period (2003–2008) and used to identify their spatial and temporal variability on the South Atlantic Bight. Monthly-mean SST has the highest variability on the inner-shelf, decreasing seaward approaching the more stable temperatures of the Gulf Stream (GS). Monthly-mean Chl-a concentrations are similarly highest on the inner shelf throughout the year and decrease cross-shelf toward the nutrient depleted open ocean. Empirical orthogonal function (EOF) analyses on SST and Chl-a show a clear seasonal cycle in their 1st mode of variability, with SST lagging behind Chl-a by approximately one month. The 1st EOF modes account for 95.8% and 46.4% variance of SST and Chl-a, respectively. Chl-a EOF mode 1 in particular shows a highly regionalized spatial pattern with values on the central SAB clearly out of phase with the southern and northern SAB. This regional difference is likely a result of shelf geometry and stratification, which modulate GS influence on the shelf. SST EOF mode 2 exhibits a seasonal cycle as well, which previous studies have shown to be a function of local wind. Chl-a EOF mode 2 is well correlated with the cumulative river transport onto the SAB, but accounts for a relatively small 10.8% of Chl-a variability.  相似文献   

Short-Term Response of a Downstream Marine System to the Partial Opening of a Tidal-River Causeway     

Travis G. Gerwing  Diana J. Hamilton  Myriam A. Barbeau  Katy Haralampides  Gordon Yamazaki 《Estuaries and Coasts》2017,40(3):717-725

The spillway gates of the Petitcodiac Causeway, a hydraulic structure ~35 km upstream of the mouth of the Petitcodiac River in New Brunswick, Canada, were permanently opened in April 2010. The short-term effect opening the spillway gates had on downstream intertidal mudflats of the upper Bay of Fundy was investigated. Specifically, a multivariate before-after-control-impact design was used to determine if opening the spillway gates affected the invertebrate community (crustaceans, polychaetes, and molluscs), abiotic sediment conditions (sediment water content, mean particle size, penetrability, and depth of the apparent redox potential discontinuity), or resource availability (sediment chlorophyll a concentration and organic matter content) of five intertidal mudflats (two impacted sites, three reference sites) spanning Chignecto Bay, the northern arm of the upper Bay of Fundy, up to 5 months post-opening. No biologically or statistically meaningful differences were detected between impacted and reference sites for any of the measured variables. This suggests that opening the causeway did not have a quantifiable impact on these intertidal mudflats, at least within half a year of the opening. This is likely a result of the macrotidal nature of the Bay of Fundy that overwhelmed any immediate changes to hydrodynamics that occurred after the opening of the causeway gates.  相似文献   

Melting of a Hydrous Mantle: I. Phase Relations of Natural Peridotite at High Pressures and Temperatures with Controlled Activities of Water, Carbon Dioxide, and Hydrogen   总被引：4，自引：4，他引：4  

MYSEN  BJ?RN O.; BOETTCHER  A. L. 《Journal of Petrology》1975,16(1):520-548

Four natural peridotite nodules ranging from chemically depletedto Fe-rich, alkaline and calcic (SiO₂=43?7–45?7 wt. percent, Al₂O3=1?6O–8?21 wt. per cent, CaO=0?70–8?12wt. per cent,alk=0?10–0?90 wt. per cent and Mg/(Mg+Fe²⁺)=0?94–0?85)have been investigated in the hypersolidus region from 800?to 1250?C with variable activities of H₂O, CO₂, and H₂. Thevapor-saturated peridotite solidi are 50–200?C below thosepreviously published. The temperature of the beginning of meltingof peridotite decreases markedly with decreasing Mg/(Mg+Fe)of the starting material at constant CaO/Al₂O₃. Conversely,lowering CaO/Al₂O₃ reduces the temperature at constant Mg/(Mg+Fe)of the starting material. Temperature differences between thesolidi up to 200?C are observed. All solidi display a temperatureminimum reflecting the appearance of garnet. This minimum shiftsto lower pressure with decreasing Mg/(Mg+Fe) of the startingmaterial. The temperature of the beginning of melting decreasesisobarically as approximately a linear function of the mol fractionof H₂O in the vapor (X_H2O). The data also show that some CO₂may dissolve in silicate melts formed by partial melting ofperidotite. Amphibole (pargasitic hornblende) is a hypersolidus mineralin all compositions, although its P/T stability field dependson bulk rock chemistry. The upper pressure stability of amphiboleis marked by the appearance of garnet. The vapor-saturated (H₂O) liquidus curve for one peridotiteis between 1250? and 1300?C between 10 and 30 kb. Olivine, spinel,and orthopyroxene are either liquidus phases or coexist immediatelybelow the temperature of the peridotite liquidus. The data suggest considerable mineralogical heterogeneity inthe oceanic upper mantle because the oceanic geotherm passesthrough the P/T band covering the appearance of garnet in variousperidotites. The variable depth to the low-velocity zone is explained byvariable a_H2O conditions in the upper mantle and possibly alsoby variations in the composition of the peridotite itself. It is suggested that komatiite in Precambrian terrane couldform by direct melting of hydrous peridotite. Such melting requiresabout 1250?C compared with 1600?C which is required for drymelting. The genesis of kimberlite can be related to partial meltingof peridotite under conditions of (). Such activities of H₂Oresult in melting at depths ranging between 125 and 175 km inthe mantle. This range is within the minimum depth generallyaccepted for the formation of kimberlite.  相似文献   

Melting of a Hydrous Mantle: II. Geochemistry of Crystals and Liquids Formed by Anatexis of Mantle Peridotite at High Pressures and High Temperatures as a Function of Controlled Activities of Water, Hydrogen, and Carbon Dioxide   总被引：3，自引：6，他引：3  

MYSEN  BJ?RN O.; BOETTCHER  A. L. 《Journal of Petrology》1975,16(1):549-593

The system peridotite-H₂O-CO₂ serves as a simplified model forthe phase relations of mantle peridotite involving more thanone volatile component. Run products obtained in a study ofphase relations of four mantle peridotites in the presence ofH₂O- and (H₂O+CO₂)-bearing vapors and with controlled hydrogenfugacity (f_H2) at high pressures and temperatures have beensubjected to a detailed chemical investigation, principallyby the electron microprobe. Mg/(Mg+Fe) of all phases generally increases with increasingtemperature and with increasing Mg/(Mg+Fe) of the starting material.This ratio appears to decrease with increasing pressure forolivine, and for amphibole coexisting with garnet. DecreasingfH₂from that of IW buffer to that of MH buffer decreases Mg/(Mg+Fe)of the partial melt from approximately 0?85 to approximately0?50, whereas the Fo content of coexisting olivine increasesslightly less than 3 per cent and the Mg/(Mg+Fe) of clinopyroxeneincreases about 4 per cent. However, the variations in Fo contentof olivines are within those observed in olivines from naturalmantle peridotite. The chemistry of other silicate mineralsdoes not significantly reflect variations of fH₂. Consequently,the peridotite mineralogy and/or chemistry is not a good indicatorfor the fH₂ conditions during crystallization. All crystalline phases, except amphibole, and to some extentgarnet, show increasing Cr content with increasing temperatureand increasing Cr content of the starting material, resultingin a positive correlation with Mg/(Mg+Fe). Partial melts aredepleted in Cr₂O₃ relative to the crystalline phases. High Mg/(Mg+Fe)and Cr₂O₃ are thus expected in crystal residues after partialmelting. The absolute values depend on degree of melting andthe composition of the parent peridotite.  相似文献   

Melting of a Hydrous Mantle: II. Geochemistry of Crystals and Liquids Formed by Anatexis of Mantle Peridotite at High Pressures and High Temperatures as a Function of Controlled Activities of Water, Hydrogen, and Carbon Dioxide   总被引：1，自引：0，他引：1  

MYSEN  BJ?RN O.; BOETTCHER  A. L. 《Journal of Petrology》1975,16(3):549-593

The system peridotite-H₂O–CO₂ serves as a simplified modelfor the phase relations of mantle peridotite involving morethan one volatile component. Run products obtained in a studyof phase relations of four mantle peridotites in the presenceof H₂O- and (H₂O+CO₂)- bearing vapors and with controlled hydrogenfugacity (f_H2) at high pressures and temperatures have beensubjected to a detailed chemical investigation, principallyby the electron microprobe. Mg/(Mg+Fe) of all phases generally increases with increasingtemperature and with increasing Mg/(Mg+Fe) of the starting material.This ratio appears to decrease with increasing pressure forolivine, and for amphibole coexisting with garnet. Decreasingf_H2 from that of IW buffer to that of MH buffer decreases Mg/(Mg+Fe)of the partial melt from approximately 0-85 to approximately0.50, whereas the Fo content of coexisting olivine increasesslightly less than 3 per cent and the Mg/(Mg+Fe) of clinopyroxeneincreases about 4 per cent. However, the variations in Fo contentof olivines are within those observed in olivines from naturalmantle peridotite. The chemistry of other silicate mineralsdoes not significantly reflect variations of f_H2. Consequently,the peridotite mineralogy and/or chemistry is not a good indicatorfor the f_H2 conditions during crystallization. All crystalline phases, except amphibole, and to some extentgarnet, show increasing Cr content with increasing temperatureand increasing Cr content of the starting material, resultingin a positive correlation with Mg/(Mg+Fe). Partial melts aredepleted in Cr₂O₃ relative to the crystalline phases. High Mg/Mg+Fe)and Cr₂O₃ are thus expected in crystal residues after partialmelting. The absolute values depend on degree of melting andthe composition of the parent peridotite. Liquids formed by anatexis of mantle peridotite are andesiticunder conditions of X_H2O^v > 0.6 to at least 25 kb total pressureand to more than 200?C above the peridotite solidus. This observationsupports numerous suggestions that andesite genesis in islandarcs may result from partial melting of underlying peridotitemantle. In contrast to basaltic rocks, the absence of amphibole(paragasitic hornblende) does not affect the silica-saturatednature of the liquids. Increasing K₂O content of the startingmaterial (up to 1 wt. per cent K₂O) results in increasing potassiumcontent of the amphibole (1 wt. per cent K₂O) as well as theappearance of phlogopite. The liquid under these conditionsis relatively K₂0-poor (less than 1 wt. per cent K₂O). Partial melts are olivine normative with X_H2O 0.5, and initialliquids contain normative ol and ne at X_H2O 0.4. The alkalinityof these liquids increases with decreasing X_H2O below valuesof 0.5. The (ol+opx)-normative liquids resemble oceanic basaltswhereas (ol+ne)-normative liquids resemble olivine nepheliniteand melilite basalt. Low aHlo and high a_Co2 conditions may bethose under which kimberlites and related rocks are formed inthe mantle.  相似文献   

Oxygen and Hydrogen Isotopic Signatures of Large Atmospheric Ice Conglomerations     

J. Martinez-FrÍAs  A. Delgado  M. MillÁN  E. Reyes  F. Rull  D. Travis  R. Garcia  F. LÓPez-Vera  J. A. RodrÍGuez-Losada  J. A. Martin-Rubi  J. Raya  E. Santoyo 《Journal of Atmospheric Chemistry》2005,52(2):185-202

Specific studies about the stable isotope composition (¹⁸O/¹⁶O and D/H) of atmospheric icy conglomerations are still scarce. The present work offers, for the first time, a very detailed analysis of oxygen and hydrogen isotopic signatures of unusually large ice conglomerations, or “megacryometeors”, that fell to the ground in Spain during January 2000. The hydrochemical analysis is based on the bulk isotopic composition and systematic selective sampling (deuterium isotopic mapping) of eleven selected specimens. δ¹⁸O and δD (V-SMOW) of all samples fall into the Meteoric Water Line matching well with typical tropospheric values. The distribution of the samples on Craig's line suggests either a variation in condensation temperature and/or different residual fractions of water vapour (Rayleigh processes). Three of the largest megacryometeors exhibited unequivocally distinctive negative values (δ¹⁸O = −17.2%₀ and δD = −127 %₀ V-SMOW), (δ¹⁸O = −15.6%₀ and δD = −112%₀ V-SMOW) and (δ¹⁸O = −14.4%₀ and δD = −100%₀ V-SMOW), suggesting an atmospheric origin typical of the upper troposphere. Theoretical calculations indicate that the vertical trajectory of growth was lower than 3.2 km. During the period in which the fall of megacryometeors occurred, anomalous atmospheric conditions were observed to exist: a substantial lowering of the tropopause with a deep layer of saturated air below, ozone depression and strong wind shear. Moreover, these large ice conglomerations occurred during non-thunderstorm conditions, suggesting an alternative process of ice growth was responsible for their formation.  相似文献   

Genetic effects of a large-scaleSpartina alterniflora (smooth cordgrass) dieback and recovery in the northern Gulf of Mexico     

Keith R. Edwards  Steven E. Travis  C. Edward Proffitt 《Estuaries and Coasts》2005,28(2):204-214

A large-scale dieback event struck marshes along the northwestern Gulf of Mexico coast during summer 2000, in apparent response to a prolonged and severe drought. Along the Louisiana coast, large areas of the dominant marsh species,Spartina alterniflora, turned brown, followed by death of at least the aboveground structures of entire plant mortality. Key ecological and genetic measures were studied in a dieback-affected marsh in southwest Louisiana (C83 marsh, Sabine National Wildlife Refuge), for which existed predieback ecologic and genetic datasets. Effects on genetic diversity only were studied in a second set of sites in southeastern Louisiana (near Bay Junop), where the dieback was more widespread. We hypothesized that stem density, live aboveground biomass, and genetic diversity would be significantly reduced compared to predieback conditions and to nearby unaffected marshes. Stem densities and biomass levels approached predieback conditions 14 months after first observance of the dieback in the Sabine marsh and were similar to or exceeded the same measures for a nearby unaffected marsh. DNA extracted from leaf samples in the Sabine and Bay Junop sites was used to construct genotype profiles using AFLPs and analyzed using the complement of Simpson’s Index (1-D), the richness measure G/N, average heterozygosity <H>, and the estimated proportion of polymorphic genes <P>. Genetic diversity was relatively unaffected by the dieback at either the Sabine or Bay Junop sites. Evidence from field observations and the results of the genetic analyses suggest that seedling recruitment is an important factor in the recovery of both the Bay Junop and C83 sites, although re-growth from surviving below-ground rhizomes appeared to dominate recovery at the latter site. Survival of below-ground structures, leading to the rapid recovery observed, indicates a high level of resilience of the Sabine marsh to drought-induced stress. Still, the genetic diversity ofS. alterniflora-dominated marshes may be promoted by occasional disturbance events, which produce open areas in which seedling recruitment can occur.  相似文献   

Turbulent 3-D thermal convection in an infinite Prandtl number, volumetrically heated fluid: implications for mantle dynamics     

E. M. Parmentier  C. Sotin  B. J. Travis 《Geophysical Journal International》1994,116(2):241-251

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Temporal and Spatial Variabilities of Chemical and Physical Parameters on the Heron Island Coral Reef Platform     

Kekuewa  Samuel A. H.  Courtney  Travis A.  Cyronak  Tyler  Kindeberg  Theodor  Eyre  Bradley D.  Stoltenberg  Laura  Andersson  Andreas J. 《Aquatic Geochemistry》2021,27(4):241-268

Globally, coral reefs are threatened by ocean warming and acidification. The degree to which acidification will impact reefs is dependent on the local hydrodynamics, benthic community composition, and biogeochemical processes, all of which vary on different temporal and spatial scales. Characterizing the natural spatiotemporal variability of seawater carbonate chemistry across different reefs is critical for elucidating future impacts on coral reefs. To date, most studies have focused on select habitats, whereas fewer studies have focused on reef scale variability. Here, we investigate the temporal and spatial seawater physicochemical variability across the entire Heron Island coral reef platform, Great Barrier Reef, Australia, for a limited duration of six days. Autonomous sensor measurements at three sites across the platform were complemented by reef-wide boat surveys and discrete sampling of seawater carbonate chemistry during the morning and evening. Variability in both temporal and spatial physicochemical properties were predominantly driven by solar irradiance (and its effect on biological activity) and the semidiurnal tidal cycles but were influenced by the local geomorphology resulting in isolation of the platform during low tide and rapid flooding during rising tides. As a result, seawater from previous tidal cycles was sometimes trapped in different parts of the reef leading to unexpected biogeochemical trends in space and time. This study illustrates the differences and limitations of data obtained from high-frequency measurements in a few locations compared to low-frequency measurements at high spatial resolution and coverage, showing the need for a combined approach to develop predictive capability of seawater physicochemical properties on coral reefs.

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Do carbonate liquids become denser than silicate liquids at pressure? Constraints from the fusion curve of K<Subscript>2</Subscript>CO<Subscript>3</Subscript> to 3.2 GPa     

Qiong Liu  Travis J. Tenner  Rebecca A. Lange 《Contributions to Mineralogy and Petrology》2007,153(1):55-66

Brackets on the melting temperature of K₂CO₃ were experimentally determined at 1.86 ± 0.02 GPa (1,163–1,167°C), 2.79 ± 0.03 GPa (1,187–1,195°C), and 3.16 ± 0.04 GPa (1,183–1,189°C) in a piston-cylinder apparatus. These new data, in combination with published experiments at low pressure (<0.5 GPa), establish the K₂CO₃ fusion curve to 3.2 GPa. On the basis of these experiments and published thermodynamic data for crystalline and liquid K₂CO₃, the high-pressure density and compressibility of K₂CO₃ liquid were derived from the fusion curve. The pressure dependence of the liquid compressibility (K′₀ = dK ₀/dP, where K ₀ = 1/β₀) is between 16.2 and 11.6, with a best estimate of 13.7, in a third-order Birch–Murnaghan equation of state (EOS). This liquid K′₀ leads to a density of 2,175 ± 36 kg/m³ at 4 GPa and 1,500°C, which is ∼30% lower than that reported in the literature on the basis of the falling-sphere method at the same conditions. The uncertainty in the liquid K′₀ leads to an error in melt density of ± 2% at 4 GPa; the error decreases with decreasing pressure. With a K′₀ of 13.7, the compressibility of K₂CO₃ at 1,500°C and 1 bar (K ₀ = 3.8 GPa) drops rapidly with increasing pressure ( ), which prevents a density crossover with silicate melts, such as CaAlSi₂O₈ and CaMgSi₂O₆, at upper mantle depths.  相似文献