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J.V. Klump

Publications and source records attributed to J.V. Klump.

3 recordsLinked to original sources

Sedimentary phosphorus cycling and a phosphorus mass balance for the Green Bay (Lake Michigan) ecosystem

The tributaries of Green Bay have long been recognized as major sources of phosphorus in the Lake Michigan basin. The status of Green Bay as a sink or source of phosphorus for Lake Michigan proper has been less well defined. The bay receives nearly 70% of its annual load of phosphorus ( 700 metric tons (t) &middot; year-1) from a single source: the Fox River. Most of this phosphorus is deposited in sediments accumulating at rates that reach 160 mg &middot; cm-2 &middot; year-1 with an average of 20 mg &middot; cm-2 &middot; year-1. The phosphorus content of these sediments varies from <5 to >70 &micro;mol &middot; g-1. Deposition is highly focused, with ~70% of the total sediment accumulation and at least 80% of the phosphorus burial occurring within 20% of the surface area of the bay. Diagenetic and stoichiometric models of phosphorus cycling imply that >80% of the phosphorus deposited is permanently buried. External phosphorus loading to the bay is combined with sediment fluxes of phophorus to arrive at a simple phosphorus budget. Green Bay acts as an efficient nutrient trap, with the sediments retaining an estimated 70-90% of the external phosphorus inputs before flowing into Lake Michigan.

Wisconsin

Benthic biogeochemical cycling, nutrient stoichiometry, and carbon and nitrogen mass balances in a eutrophic freshwater bay

Green Bay, while representing only ~7% of the surface area and ~1.4% of the volume of Lake Michigan, contains one‐third of the watershed of the lake, and receives approximately one‐third of the total nutrient loading to the Lake Michigan basin, largely from the Fox River at the southern end of the bay. With a history of eutrophic conditions dating back nearly a century, the southern portion of the bay behaves as an efficient nutrient and sediment trap, sequestering much of the annual carbon and nitrogen input within sediments accumulating at up to 1 cm per year. Depositional fluxes of organic matter varied from ~0.1 mol C m22 yr21 to >10 mol C m −2 yr −1 and were both fairly uniform in stoichiometric composition and relatively labile. Estimates of benthic recycling derived from pore‐water concentration gradients, whole‐sediment incubation experiments, and deposition‐burial models of early diagenesis yielded an estimated 40% of the carbon and 50% of the nitrogen recycled back into the overlying water. Remineralization was relatively rapid with ~50% of the carbon remineralized within ~15 yr of deposition, and a mean residence time for metabolizable carbon and nitrogen in the sediments of 20 yr. On average, organic carbon regeneration occurred as 75% CO 2 , 15% CH 4 , and 10% dissolved organic carbon (DOC). Carbon and nitrogen budgets for the southern bay were based upon direct measurements of inputs and burial and upon estimates of export and production derived stoichiometrically from a coupled phosphorus budget. Loadings of organic carbon from rivers were ~3.7 mol m −2 yr −1 , 80% in the form of DOC and 20% as particulate organic carbon. These inputs were lost through export to northern Green Bay and Lake Michigan (39%), through sediment burial (26%), and net CO 2 release to the atmosphere (35%). Total carbon input, including new production, was 4.54 mol m −2 yr −1 , equivalent to ~10% of the gross annual primary production. Nitrogen budget terms were less well quantified, with nitrogen export ~54% of total inputs and burial ~24%, leaving an unquantified residual loss term in the nitrogen budget of ~22%.

Green Bay

Beryllium-7 as a tracer of short-term sediment deposition and resuspension in the Fox River Wisconsin

Short-term (∼monthly) sediment deposition and resuspension rates of surficial bed sediments in two PCB-laden impoundments on the Fox River, WI, were determined in the summer and fall of 1998 using 7 Be, a naturally occurring radioisotope produced in the atmosphere. Decay-corrected activities and inventories of 7 Be were measured in bed sediment and in suspended particles. Beryllium-7 activities generally decreased with depth in the top 5−10 cm of sediments and ranged from undetectable to ∼0.9 pCi cm - 3 . Inventories of 7 Be, calculated from the sum of activities from all depths, ranged from 0.87 to 3.74 pCi cm - 2 , and the values covaried between sites likely reflecting a common atmospheric input signal. Activities of 7 Be did not correlate directly with rainfall. Partitioning the 7 Be flux into “new” and “residual” components indicated that net deposition was occurring most of the time during the summer. Net erosion, however, was observed at the upstream site from the final collection in the fall. This erosion event was estimated to have removed 0.10 g (cm of sediment) - 2 , corresponding to ∼0.5 cm of sediment depth, and ∼6−10 kg of polychlorinated biphenyls (PCBs) over the whole deposit. Short-term accumulation rates were up to ∼130 times higher than the long-term rates calculated from 137 Cs profiles, suggesting an extremely dynamic sediment transport environment, even within an impounded river system.

Environmental Science & Technology