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Dive into the research topics where Brian J. Eadie is active.

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Featured researches published by Brian J. Eadie.


Journal of Great Lakes Research | 1984

Sediment Trap Studies in Lake Michigan: Resuspension and Chemical Fluxes in the Southern Basin

Brian J. Eadie; Richard L. Chambers; Wayne S. Gardner; Gerald L. Bell

The results of 4 years (1977–80) of sediment trap sample collection in the southeastern region of Lake Michigan are summarized and compared with water column and sediment characteristics. Mass flux data indicate strong seasonal patterns, with maximum fluxes recorded during the unstratified period. The large amount of winter resuspension is a mechanism which provides an intimate coupling of recent sediments and the water column. Also these trap study results indicate that there is a near-bottom (10-m-thick) benthic nepheloid layer whose chemical composition approaches that of deep water (fine grain) sediments. The amount of resuspended NaOH extractable phosphorus injected into the euphotic zone is estimated as approximately equal to the load of new phosphorus entering southern Lake Michigan. The role of resuspension in the cycling of organic carbon and contaminants associated with it appears to be important.


Organic Geochemistry | 1993

Sources, degradation and recycling of organic matter associated with sinking particles in Lake Michigan

Brian J. Eadie

Sediment trap material collected at five depths from two locations in Lake Michigan has been studied to determine the sources of particulate organic matter and the early diagenetic changes which occur during sinking of particles. Aquatic material dominates in shallower depths whereas land-derived material is more important in near-bottom depths. Organic carbon concentrations decrease with depth as a result of remineralization of organic matter by microbial activity and dilution by resuspended bottom sediments. Preferential remineralization of algal organic matter and downslope transport of particulate matter from coastal areas create differences in the lipid biomarker characteristics of settling particles found at different depths in the water column. Calculations of apparent decomposition rate constants from lipid distri- butions at different depths show that shorter chainlength n-alkanoic acids are degraded faster than longer components. Carbon and nitrogen isotopic compositions of total organic matter are nearly unaffected by large-scale amounts of remineralization during sinking.


Estuaries | 1994

Records of nutrient-enhanced coastal ocean productivity in sediments from the Louisiana continental shelf

Brian J. Eadie; Brent A. McKee; Margaret B. Lansing; John A. Robbins; Simonne Metz; John H. Trefry

Shelf sediments from near the mouth of the Mississippi River were collected and analyzed to examine whether records of the consequences of anthropogenic nutrient loading are preserved. Cores representing approximately 100 yr of accumulation have increasing concentrations of organic matter over this period, indicating increased accumulation of organic carbon, rapid early diagenesis, or a combination of these processes. Stable carbon isotopes and organic tracers show that virtually all of this increase is of marine origin. Evidence from two cores near the river mouth, one within the region of chronic seasonal hypoxia and one nearby but outside the hypoxic region, indicate that changes consistent with increased productivity began by approximately the mid-1950s when the inorganic carbon in benthic forams rapidly became isotopically lighter at both stations. Beginning in the mid-1960s, the accumulation of organic matter, organic δ13C, and δ15N all show large changes in a direction consistent with increased productivity. This last period coincides with a doubling of the load of nutrients from the Mississippi River, which levelled off in the mid-1980s. These data support the hypothesis that anthropogenic nutrient loading has had a significant impact on the Louisiana shelf.


Organic Geochemistry | 1998

Perylene: an indicator of alteration processes or precursor materials?

James E. Silliman; Brian J. Eadie

Abstract Perylene is a polycyclic aromatic hydrocarbon (PAH) that is found pervasively in both marine and freshwater sediments, yet its origin remains obscure. We have explored relationships between perylene and possible precursor materials in two 210 Pb-dated sediment cores from Lake Ontario in which contributions of aquatic and land-plant organic matter and concentrations of anthropogenic PAHs have been measured. No significant correlations were identified between perylene occurrence and indicators of terrigenous or aquatic sources of organic matter. Distinct differences between perylene and anthropogenic PAH sedimentary profiles rule out an industrial source for perylene at these locations. The general pattern of low-to-absent perylene concentrations in upper, oxic sediments and increasing concentrations with depth indicates that in situ diagenesis under anoxic conditions produces perylene and that its formation is kinetically controlled. The results of our study suggest that perylene is formed from non-specific precursor materials by biotic or abiotic transformation processes. If this scenario accurately describes its formation, then perylene is an indicator of depositional conditions rather than the source of organic matter.


Ecological Modelling | 2002

A model study of the coupled biological and physical dynamics in Lake Michigan

Changsheng Chen; Rubao Ji; David J. Schwab; Dmitry Beletsky; Gary L. Fahnenstiel; Mingshun Jiang; Thomas H. Johengen; Henry A. Vanderploeg; Brian J. Eadie; Judith Wells Budd; Marie H. Bundy; Wayne S. Gardner; James B. Cotner; Peter J. Lavrentyev

A coupled physical and biological model was developed for Lake Michigan. The physical model was the Princeton ocean model (POM) driven directly by observed winds and net surface heat flux. The biological model was an eight-component, phosphorus-limited, lower trophic level food web model, which included phosphate and silicate for nutrients, diatoms and non-diatoms for dominant phytoplankton species, copepods and protozoa for dominant zooplankton species, bacteria and detritus. Driven by observed meteorological forcings, a 1-D modeling experiment showed a controlling of physical processes on the seasonal variation of biological variables in Lake Michigan: diatoms grew significantly in the subsurface region in early summer as stratification developed and then decayed rapidly in the surface mixed layer when silicate supplied from the deep stratified region was reduced as a result of the formation of the thermocline. The non-diatoms subsequently grew in mid and late summer under a limited-phosphate environment and then declined in the fall and winter as a result of the nutrient consumption in the upper eutrophic layer, limitation of nutrients supplied from the deep region and meteorological cooling and wind mixing. The flux estimates suggested that the microbial loop had a significant contribution in the growth of microzooplankton and hence, to the lower-trophic level food web system. The model results agreed with observations, suggesting that the


Estuaries | 1994

Transport of particulate organic carbon by the Mississippi River and its fate in the Gulf of Mexico

John H. Trefry; Simone Metz; Terry A. Nelsen; Robert P. Trocine; Brian J. Eadie

This study was designed to determine the amount of particulate organic carbon (POC) introduced to the Gulf of Mexico by the Mississippi River and assess the influence of POC inputs on the development of hypoxia and burial of organic carbon on the Louisiana continental shelf. Samples of suspended sediment and supporting hydrographic data were collected from the river and >50 sites on the adjacent shelf. Suspended particles collected in the river averaged 1.8±0.3% organic carbon. Because of this uniformity, POC values (in μmol l−1) correlated well with concentrations of total suspended matter. Net transport of total organic carbon by the Mississippi-Atchafalaya River system averaged 0.48×1012 moles y−1 with 66% of the total organic carbon carried as POC. Concentrations of POC decreased from as high as 600 μmol l−1 in the river to <0.8 μmol l−1 in offshore waters. In contrast, the organic carbon fraction of the suspended matter increased from <2% of the total mass in the river to >35% along the shelf at ≥10 km from the river mouth. River flow was a dominant factor in controlling particle and POC distributions; however, time-series data showed that tides and weather fronts can influence particle movement and POC concentrations. Values for apparent oxygen utilization (AOU) increased from ∼60 μmol l−1 to >200 μmol l−1 along the shelf on approach to the region of chronic hypoxia. Short-term increases in AOU were related to transport of more particle-rich waters. Sediments buried on the shelf contained less organic carbon than incoming river particles. Orgamic carbon and δ13C values for shelf sediments indicated 3 that large amounts of both terrigenous and marine organic carbon are being decomposed in shelf waters and sediments to fuel observed hypoxia.


Chemosphere | 1990

Three-phase partitioning of hydrophobic organic compounds in Great Lakes waters

Brian J. Eadie; Nancy R. Morehead; Peter F. Landrum

Abstract Great Lakes waters were freshly collected, innoculated with radiolabelled hydrophobic organic compounds and, after equilibration, separated into particle bound, dissolved organic matter bound and freely dissolved phases. In these ambient suspended matter (0.2–5 ppm) and dissolved organic carbon (1–6 ppm) media, the freely dissolved phase generally dominates and the amounts associated with dissolved organic matter rarely exceeds 5% for most compounds. Solubility controls the constituent distribution between particle bound and freely dissolved but plays a much smaller role in mediating the binding to dissolved organic matter. Differences observed in the binding to dissolved and particulate organic matter support the need to consider the distribution of constituents among three phases. Although the concentration and composition of the substrate changes significantly, there is no apparent seasonal effect on the distribution of compounds among the three phases in the Great Lakes.


Chemical Geology | 2001

A hypothesis for the origin of perylene based on its low abundance in sediments of Green Bay, Wisconsin

James E. Silliman; Brian J. Eadie; J. Val Klump

Abstract Perylene, a polycyclic aromatic hydrocarbon (PAH) that is common in sediments, is believed to originate principally from anaerobic diagenesis of organic matter, but its precursor material remains enigmatic. We have investigated the formation of perylene in a dated sediment core from Green Bay, WI. Comparisons of sedimentary profiles of perylene, anthropogenic PAHs, land-plant-derived hydrocarbons, and aquatic contributions of organic matter rule out a specific industrial, terrigenous, or aquatic precursor for perylene. Instead, perylene seems to be formed from any kind of organic matter as a consequence of a specific type of microbial activity in sub-bottom sediments. Despite an abundance of organic matter, the amount of perylene is low in Green Bay and in other organic-carbon-rich lake sediments. The abundant availability of organic matter that stimulates microbial activity in Green Bay sediments would seem to favor perylene formation in such sediments. We therefore hypothesize that the microorganisms responsible for perylene formation do not compete successfully with those that flourish in sediments rich in organic matter. Perylene formation consequently does not become significant until deeper in sediments after the more-reactive types of organic matter have been consumed.


Geochimica et Cosmochimica Acta | 1986

The partitioning of 7beryllium in fresh water

Nathan Hawley; John A. Robbins; Brian J. Eadie

Abstract Field observations and experimental measurements of the partitioning coefficient ( K d ) of 7 Be in fresh water show that it varies inversely with the solids concentration at typical environmental values (up to 30 mg/1). This behavior is similar to that of many other metals and organic pollutants, which means that 7 Be may be useful as a tracer of the movement of these substances in the water column. However, the wide range in the percentage of 7 Be adsorbed by solids over this range of concentrations (over 50%) means that in order to use 7 Be either to measure total sedimentation rates or to trace lateral sediment movement it will be necessary to monitor changes in sediment concentration over the area and time period of interest. The wide scatter in our data at both high and low solids concentrations suggests that other factors also affect K d . Until these factors are identified, application of our results to other systems will be risky. At high (greater than 100 mg/1) solids concentrations over 90% of 7 Be is associated with the solid phase, so it may be a useful tracer of reworking rates in bottom sediments. 7 Be has a slightly greater affinity for the solid phase in fresh water than in seawater.


Eos, Transactions American Geophysical Union | 1996

Development of recurrent coastal plume in Lake Michigan observed for first time

Brian J. Eadie; David J. Schwab; Raymond A. Assel; Nathan Hawley; Margaret B. Lansing; Gerald S. Miller; Nancy R. Morehead; John A. Robbins; P. L. Van Hoof; George Leshkevich; Thomas H. Johengen; Peter J. Lavrentyev; Ruth E. Holland

NOAA CoastWatch satellite imagery from early 1996 captured the initiation, development, and decay of a recurrent coastal plume in southern Lake Michigan (Figure 1). For the past 4 years intermittent satellite coverage has revealed a late winter-early spring plume in the lake, a feature also observed by Mortimer [1988]. In 1996, clear weather conditions allowed researchers to observe the plumes development for the first time and they also collected water samples from helicopter and a small boat.

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John A. Robbins

Great Lakes Environmental Research Laboratory

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Margaret B. Lansing

Great Lakes Environmental Research Laboratory

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Peter F. Landrum

Southern Illinois University Carbondale

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Wayne S. Gardner

University of Texas at Austin

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David J. Schwab

National Oceanic and Atmospheric Administration

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Nathan Hawley

Great Lakes Environmental Research Laboratory

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Henry A. Vanderploeg

Great Lakes Environmental Research Laboratory

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