Geology topics

Stephen B. Brandt

Publications and source records attributed to Stephen B. Brandt.

9 recordsLinked to original sources

USGS2014

Assessing and addressing the re-eutrophication of Lake Erie: central basin hypoxia

Relieving phosphorus loading is a key management tool for controlling Lake Erie eutrophication. During the 1960s and 1970s, increased phosphorus inputs degraded water quality and reduced central basin hypolimnetic oxygen levels which, in turn, eliminated thermal habitat vital to cold-water organisms and contributed to the extirpation of important benthic macroinvertebrate prey species for fishes. In response to load reductions initiated in 1972, Lake Erie responded quickly with reduced water-column phosphorus concentrations, phytoplankton biomass, and bottom-water hypoxia (dissolved oxygen < 2 mg/l). Since the mid-1990s, cyanobacteria blooms increased and extensive hypoxia and benthic algae returned. We synthesize recent research leading to guidance for addressing this re-eutrophication, with particular emphasis on central basin hypoxia. We document recent trends in key eutrophication-related properties, assess their likely ecological impacts, and develop load response curves to guide revised hypoxia-based loading targets called for in the 2012 Great Lakes Water Quality Agreement. Reducing central basin hypoxic area to levels observed in the early 1990s (ca. 2000 km 2 ) requires cutting total phosphorus loads by 46% from the 2003–2011 average or reducing dissolved reactive phosphorus loads by 78% from the 2005–2011 average. Reductions to these levels are also protective of fish habitat. We provide potential approaches for achieving those new loading targets, and suggest that recent load reduction recommendations focused on western basin cyanobacteria blooms may not be sufficient to reduce central basin hypoxia to 2000 km 2 .

Great Lakes;Lake Erie↗

USGS2012

Macondo-1 well oil-derived polycyclic aromatic hydrocarbons in mesozooplankton from the northern Gulf of Mexico

Mesozooplankton (>200 μ m) collected in August and September of 2010 from the northern Gulf of Mexico show evidence of exposure to polycyclic aromatic hydrocarbons (PAHs). Multivariate statistical analysis revealed that distributions of PAHs extracted from mesozooplankton were related to the oil released from the ruptured British Petroleum Macondo-1 (M-1) well associated with the R/V Deepwater Horizon blowout. Mesozooplankton contained 0.03–97.9 ng g −1 of total PAHs and ratios of fluoranthene to fluoranthene + pyrene less than 0.44, indicating a liquid fossil fuel source. The distribution of PAHs isolated from mesozooplankton extracted in this study shows that the 2010 Deepwater Horizon spill may have contributed to contamination in the northern Gulf of Mexico ecosystem.

Gulf of Mexico↗

USGS2011

Effects of hypoxia on consumption, growth, and RNA:DNA ratios of young Yellow Perch

As in various freshwater and coastal marine ecosystems worldwide, seasonal bottom water hypoxia is a recurring phenomenon in Lake Erie’s central basin. While bottom hypoxia can strongly affect sessile benthic animals, its effects on mobile organisms such as fish are less understood. We evaluated the potential for bottom hypoxia to affect the growth rates of yellow perch Perca flavescens, a species of ecological and economic importance in the lake. To this end, we (1) conducted laboratory experiments to quantify the effects of reduced dissolved oxygen on consumption, somatic growth, and RNA:DNA ratios (an index of short-term growth) of young yellow perch and (2) explored the effects of bottom hypoxia on young yellow perch growth in Lake Erie’s central basin by collecting individuals in hypoxic and normoxic regions of the lake and quantifying their RNA:DNA ratios. Yellow perch consumption and growth in our experiments declined under hypoxic conditions (≤2 mg O2/L). While yellow perch RNA:DNA ratios responded strongly to experimental temperature, nucleic acid ratios were not significantly affected by dissolved oxygen or feeding ration. We did, however, observe a positive correlation between yellow perch growth and RNA:DNA ratios at low temperatures (11◦C). The nucleic acid ratios of yellow perch collected in Lake Erie varied spatiotemporally, but their patterns were not consistent with hypoxia. In short, while yellow perch consumption and growth rates respond directly and negatively to low oxygen conditions, these responses are not necessarily reflected in RNA:DNA ratios. Moreover, in central Lake Erie, where yellow perch can behaviorally avoid hypoxic areas, the RNA:DNA ratios of yellow perch do not respond strongly to bottom hypoxia. Thus, this study suggests that there is no strong negative effect of bottom hypoxia on the growth of young yellow perch in Lake Erie.

Transactions of the American Fisheries Society↗

USGS2006

Evaluation of a lake whitefish bioenergetics model

We evaluated the Wisconsin bioenergetics model for lake whitefish Coregonus clupeaformis in the laboratory and in the field. For the laboratory evaluation, lake whitefish were fed rainbow smelt Osmerus mordax in four laboratory tanks during a 133-d experiment. Based on a comparison of bioenergetics model predictions of lake whitefish food consumption and growth with observed consumption and growth, we concluded that the bioenergetics model furnished significantly biased estimates of both food consumption and growth. On average, the model overestimated consumption by 61% and underestimated growth by 16%. The source of the bias was probably an overestimation of the respiration rate. We therefore adjusted the respiration component of the bioenergetics model to obtain a good fit of the model to the observed consumption and growth in our laboratory tanks. Based on the adjusted model, predictions of food consumption over the 133-d period fell within 5% of observed consumption in three of the four tanks and within 9% of observed consumption in the remaining tank. We used polychlorinated biphenyls (PCBs) as a tracer to evaluate model performance in the field. Based on our laboratory experiment, the efficiency with which lake whitefish retained PCBs from their food (I?) was estimated at 0.45. We applied the bioenergetics model to Lake Michigan lake whitefish and then used PCB determinations of both lake whitefish and their prey from Lake Michigan to estimate p in the field. Application of the original model to Lake Michigan lake whitefish yielded a field estimate of 0.28, implying that the original formulation of the model overestimated consumption in Lake Michigan by 61%. Application of the bioenergetics model with the adjusted respiration component resulted in a field I? estimate of 0.56, implying that this revised model underestimated consumption by 20%.

Transactions of the American Fisheries Society↗

USGS2005

Preliminary evaluation of a lake whitefish ( Coregonus clupeaformis ) bioenergetics model

We conducted a preliminary evaluation of a lake whitefish ( Coregonus clupeaformis ) bioenergetics model by applying the model to size-at-age data for lake whitefish from northern Lake Michigan. We then compared estimates of gross growth efficiency (GGE) from our bioenergetis model with previously published estimates of GGE for bloater ( C. hoyi ) in Lake Michigan and for lake whitefish in Quebec. According to our model, the GGE of Lake Michigan lake whitefish decreased from 0.075 to 0.02 as age increased from 2 to 5 years. In contrast, the GGE of lake whitefish in Quebec inland waters decreased from 0.12 to 0.05 for the same ages. When our swimming-speed submodel was replaced with a submodel that had been used for lake trout ( Salvelinus namaycush ) in Lake Michigan and an observed predator energy density for Lake Michigan lake whitefish was employed, our model predicted that the GGE of Lake Michigan lake whitefish decreased from 0.12 to 0.04 as age increased from 2 to 5 years.

Conference Paper↗

USGS1997

The inverse problem of argon diffusion from minerals: Determination of kinetic parameters from stepwise-heating experiments

Results of two routine 40 Ar/ 39 Ar stepwise heating experiments on a biotite and a basanite are interpreted in terms of Fick's and Arrhenius' laws. Both patterns represent a saddle-shaped 39 Ar release. Argon isotope spectra are suggested to be controlled by the activation energy of diffusion E and the frequency factor D o . The activation energy of 39 Ar is lower than the one of 40 Ar. This results in a preferable release of 40 Ar relatively to 39 Ar at high-temperature steps and an increasing high-temperature wing in the saddle-shaped age spectrum. At low temperatures, considerable losses and irregularities in release of mainly 39 Ar are observed, which cause the decreasing low-temperature wing in the “saddle”. The suggestion of argon losses (mainly of 39 Ar) from a loose, “unstable” zone of the mineral structures becomes justified. The n -irradiation of the samples and the shift of E of 39 Ar towards lower values seems to explain the saddle-shaped age-spectra often encountered in 40 Ar/ 39 Ar-geochronometry.

Isotopes in Environmental and Health Studies↗

USGS1995

Effect of lake-wide planktivory by the pelagic prey fish community in Lakes Michigan and Ontario

We compared predatory demand by pelagic planktivorous prey fish with invertebrate production in Lake Michigan during 1987 and in Lake Ontario during 1990. Predation by the planktivores in Lake Ontario was nearly fourfold higher than in Lake Michigan (approx. 87&ensp;g wet weight∙m −2 ∙year −1 ). Predation rates on Mysis were comparable in Lakes Michigan and Ontario (approx. 21&ensp;g∙m −2 ∙year −1 ), while predation on Diporeia was markedly higher in Lake Michigan than in Lake Ontario (21.3&ensp;vs. 8.5&ensp;g wet weight∙m −2 ∙year −1 ). In Lake Ontario, predatory demand on zooplankton exceeded our best estimate of production by a factor of 1.7. Similarly, predation estimates on Mysis in Lake Ontario were 1.2–2.0 times the estimated rate of production, depending on the production model used. Lake Michigan planktivores consumed approximately 55% of available zooplankton production in 1987, indicating that competition for prey resources, if operating, was not as intense as that in Lake Ontario in 1990. It is unclear how to resolve the paradox that predation could markedly exceed available prey production in some cases. There could be sources of error in the estimates of both the supply and demand sides of these trophic relationships.

Canadian Journal of Fisheries and Aquatic Sciences↗

USGS1993

Applications of bioenergetics models to fish ecology and management: where do we go from here?

Papers and panel discussions given during a 1992 symposium on bioenergetics models are summarized. Bioenergetics models have been applied to a variety of research and management questions related to fish stocks, populations, food webs, and ecosystems. Applications include estimates of the intensity and dynamics of predator-prey interactions, nutrient cycling within aquatic food webs of varying trophic structure, and food requirements of single animals, whole populations, and communities of fishes. As tools in food web and ecosystem applications, bioenergetics models have been used to compare forage consumption by salmonid predators across the Laurentian Great Lakes for single populations and whole communities, and to estimate the growth potential of pelagic predators in Chesapeake Bay and Lake Ontario. Some critics say that bioenergetics models lack sufficient detail to produce reliable results in such field applications, whereas others say that the models are too complex to be useful tools for fishery managers. Nevertheless, bioenergetics models have achieved notable predictive successes. Improved estimates are needed for model parameters such as metabolic costs of activity, and more complete studies are needed of the bioenergetics of larval and juvenile fishes. Future research on bioenergetics should include laboratory and field measurements of key model parameters such as weight-dependent maximum consumption, respiration and activity, and thermal habitats actually occupied by fish. Future applications of bioenergetics models to fish populations also depend on accurate estimates of population sizes and survival rates.

Transactions of the American Fisheries Society↗

USGS1991

Acoustic measures of the abundance and size of pelagic planktivores in Lake Michigan

Based on acoustic data taken at night and vertically stratified by bottom depth (3–110 m only), the total number (± 95% Cl) of pelagic fishes in Lake Michigan was 43.4 ± 10.1 x 10 9 or 226.0 ± 55.2 kt in spring (mean density 0.7–3.8 fish·m -2 or 1.6–12.8 ga·m -2 ) and 115.8 ± 18.3 x 109 or 313.2 ± 74.3 kt in late summer, 1987 (mean density 1.1–7.0 fish·m -2 or 3.0–13.2 g·m -2 ); approximately 30% of this increase in numbers (35% of biomass) occurred within Green Bay. Abundance estimates from horizontally stratified (by water column depth) data were within 9-11% of vertically stratified estimates during spring but over 20% higher during summer. By extrapolation to all water depths, we estimated total pelagic biomass as 274.6 kt for spring and 410.8 kt for summer. During both seasons, smaller fishes were nearer to the surface and nearer shore than larger individuals, and acoustic measures of size approximated the sizes of fishes caught in trawls. Bioenergetic model simulations suggest that 60% of the available production of alewife (Alosa pseudoharengus) was either consumed by stocked salmonines (52.9%) or commercially harvested (7.1%) in 1987. Underwater acoustics proved a valuable tool for lakewide assessments of fish abundances in the Great Lakes.

Michigan↗