Holocene lake-level fluctuations and beach-ridge development along the northern shore of Lake Michigan, USA

Geomorphology of a beach-ridge complex and adjacent lake basins along the northern shore of Lake Michigan records fluctuations in the level of Lake Michigan for the last 8000 to 10 000 ¹⁴C yr B.P. (radiocarbon years Before Present). A storm berm at 204.7–206 m (671.6–675.9 ft) exposed in a sandpit provides evidence of a pre-Chippewa Low lake level that is correlated with dropping water levels of Glacial Lake Algonquin (c. 10 300–10 100 ¹⁴C yr B.P.). Radiocarbon dates from organic material exposed in a river cutbank and basal sediments from Elbow Lake, Mackinac Co., Michigan, indicate a maximum age of a highstand of Lake Michigan at 6900 ¹⁴C yr B.P., which reached as high as 196.7 m (645 ft), during the early-Nipissing transgression of Lake Michigan. Basal radiocarbon dates from beach swales and a second lake site (Beaverhouse Lake, Mackinac Co.) provide geomorphic evidence for a subsequent highstand which reached 192.6 m (632 ft) at 5390±70 ¹⁴C yr B.P.Basal radiocarbon dates from a transect of sediment cores, along with tree-ring data, and General Land Office Surveyor notes of a shipwreck, c. A.D. 1846, reveal a late-Holocene rate for isostatic rebound of 22.6 cm/100 radiocarbon years (0.74 ft/100 radiocarbon years) for the northern shore of Lake Michigan, relative to the Lake Michigan-Lake Huron outlet at Port Huron, Michigan. Changes in sediment stratigraphy, inter-ridge distance, and sediment accumulation rates document a mid- to late-Holocene retreat of the shoreline due to isostatic rebound. This regression sequence was punctuated by brief, periodic highstands, resulting in progressive development over the past 5400 ¹⁴C yr of 75 pairs of dune ridges and swales each formed over an interval of approximately 72 years. Times of lake-level fluctuation were identified at 3900, 3200, and 1000 ¹⁴C yr B.P. based on changes in inter-ridge spacing, shifts in the course of Millecoquins River, and reorientation of beach-ridge lineation. Soil type, dune development, and selected pollen data provide supporting evidence for this chronology. Late-Holocene beach-ridge development and lake-level fluctuations are related to a retreat of the dominant Pacific airmass and the convergence of the Arctic and Tropical airmasses resulting in predominantly meridional rather than zonal air flow across the Great Lakes region.This is the 13th in a series of papers published in this special AMQUA issue. These papers were presented at the 1994 meeting of the American Quaternary Association held 19–22 June, 1994, at the University of Minnesota, Minneapolis, Minnesota, USA. Dr Linda C. K. Shane served as guest editor for these papers.     

Effects of stormwater nutrient discharges on eutrophication processes in nearshore waters of the Florida keys

Rainfall events cause episodic discharges of groundwaters contaminated with septic tank effluent into nearshore waters of the Florida keys, enhancing eutrophication in sensitive coral reef communities. Our study characterized the effects of stormwater discharges by continuously (30-min intervals) measuring salinity, temperature, tidal stage, and dissolved oxygen (DO) along an offshore eutrophication gradient prior to and following heavy rainfall at the beginning of the 1992 rainy season. The gradient included stations at a developed canal system (PP) on Big Pine Key, a seagrass meadow in a tidal channel (PC), a nearshore patch reef (PR), a bank reef at Looe Key National Marine Sanctuary (LK), and a blue water station (BW) approximately 9 km off of Big PIne Key. Water samples were collected at weekly intervals during this period to determine concentrations of total nitrogen (TN), ammonium (NH₄ ⁺), nitrate plus nitrite NO₃ ^? plus NO₂ ^?), total phosphorus (TP), total dissolved phosphorus (TDP), soluble reactive phosphorus (SRP), and chlorophyll a (chl a). Decreased salinity immediately followed the first major rainfall at Big Pine Key, which was followed by anoxia (DO <0.1 mg I^?1), high concentrations of NH₄ ⁺ (≈24 μM), TDP (≈1.5 μM), and chl a (≈20 μg I^?1). Maximum concentration of TDP (≈0.30 μM) also followed the initial rainfall at the PC, PR, and LK stations. In contrast, NH₄ ⁺ (≈4.0 μM) and chl a (0.45 μg I^?1) lagged the rain event by 1–3 wk, depending on distance from shore. The highest and most variable concentrations of NH₄ ⁺, TDP, and chl a occurred at PP, and all nutrient parameters correlated positively with rainfall. DO at all stations was positively correlated with tide and salinity and the lowest values occurred during low tide and low salinity (high rainfall) periods. Hypoxia (DO <2.5 mg I^?1) was observed at all stations follwing the stormwater discharges, including the offshore bank reef station LK. Our study demonstrated that high frequency (daily) sampling is necessary to track the effects of episodic rainfall events on water quality and that such effects can be detected at considerable distances (12 km) from shore. The low levels of DO and high levels of nutrients and chl a in coastal waters of the Florida Keys demand that special precautions be exercised in the treatment and discharge of wastewaters and land-based runoff in order to preserve sensitive coral reef communities.     

The impact of doubled CO2 on the energetics and hydrologic processes of mid-latitude transient eddies

The Northern Hemisphere winter (DJF) stationary eddy response of a general circulation model (GCM) to a doubling of atmospheric CO₂ is simulated with a linear steady state model as a response to anomalies in diabatic heating (latent, sensible and radiative), mountain and transient eddy effects. For this analysis the doubled CO₂ experiment performed by Wilson and Mitchell (1987) is used. The linear simulations of the control and perturbation climate capture most of the important features of the GCMs stationary eddies. The simulation of the anomalous stationary eddy pattern in the Northern Hemisphere captures only some of the important features of the GCMs anomalies. The climate anomalies in the Southern Hemisphere are poorly simulated. In the Northern Hemisphere the climate anomalies are dominated by the effect of transient eddies and mountains. In low latitudes also the contribution of latent heating is important. The contributions of sensible and radiative heating are small.     

Helium isotope geochemistry of mid-ocean ridge basalts from the South Atlantic

We report new helium isotope results for 49 basalt glass samples from the Mid-Atlantic Ridge between 1°N and 47°S.³He/⁴He in South Atlantic mid-ocean ridge basalts (MORB) varies between 6.5 and 9.0 R_A (R_A is the atmospheric ratio of1.39 × 10⁻⁶), encompassing the range of previously reported values for MORB erupted away from high³He/⁴He hotspots such as Iceland. He, Sr and Pb isotopes show systematic relationships along the ridge axis. The ridge axis is segmented with respect to geochemical variations, and local spike-like anomalies in³He/⁴He, Pb and Sr isotopes, and trace element ratios such as(La/Sm)_N are prevalent at the latitudes of the islands of St. Helena, Tristan da Cunha and Gough to the east of the ridge. The isotope systematics are consistent with injection beneath the ridge of mantle “blobs” enriched in radiogenic He, Pb and Sr, derived from off-axis hotspot sources. The variability in³He/⁴He along the ridge can be used to refine the hotspot source-migrating-ridge sink model.

MORB from the 2–7°S segment are systematically the least radiogenic samples found along the mid-ocean ridge system to date. Here the depleted mantle source is characterized by⁸⁷Sr/⁸⁶Sr of 0.7022, Pb isotopes close to the geochron and with²⁰⁶Pb/²⁰⁴Pb of 17.7, and³He/⁴He of 8.6–8.9 R_A. The “background contamination” of the subridge mantle, by radiogenic helium derived from off-ridge hotspots, displays a maximum between 20 and 24°S. The HePb and HeSr isotope relations along the ridge indicate that the³He/⁴He ratios are lower for the hotspot sources of St. Helena, Tristan da Cunha and Gough than for the MORB source, consistent with direct measurements of³He/⁴He ratios in the island lavas. Details of the HeSrPb isotope systematics between 12 and 22°S are consistent with early, widespread dispersion of the St. Helena plume into the asthenosphere, probably during flattening of the plume head beneath the thick lithosphere prior to continental breakup. The geographical variation in theHe/Pbratio deduced from the isotope systematics suggests only minor degassing of the plume during this stage. Subsequently, it appears that the plume component reaching the mid-Atlantic ridge was partially outgassed of He during off-ridge hotspot volcanism and related melting activity.

Overall, the similar behavior of He and Pb isotopes along the ridge indicates that the respective mantle sources have evolved under conditions which produced related He and Pb isotope variations.     

Calcification, photosynthesis and growth of the bloom-forming coccolithophore, Emiliania huxleyi

Measurements were made of photosynthesis and calcification in a bloom of coccolithophores in the Gulf of Maine as well as in laboratory batch cultures of the Emiliania huxleyi strain 88E. The¹⁴C technique for measuring calcification was evaluated with calcifying and noncalcifying coccolithophore strains. Shipboard bloom observations showed physiological evidence of stratification between surface and deep populations within the surface mixed layer. Photosynthesis and calcification rates were enhanced within hours of addition of KNO₃ or nitrate-rich deep water (to the same final concentration). Such rates were strongly temperature dependent in laboratory cultures, decreasing over a factor of two from 15 to 20°C. Calcification was considerably less light-dependent than photosynthesis and consistently had a measurable dark rate. In culture, maximum calcification rates and degree of cell plating were limited to logarithmic growth phase. This was followed by rapid increase in the coccolith shedding rate 1 day prior to the onset of stationary phase which continued several days after cell division stopped. The regional significance of these features to total organic and inorganic carbon production as well as calcite burial is discussed.     

Glycol Ethers As Groundwater Contaminants

Ether derivatives of dihydroxy alcohols, which are formed from ethylene or propylene, comprise an important group of groundwater contaminants known as glycol ethers. Compounds in this group are used as solvents, cleaning agents, and emulsifiers in many chemical products and manufacturing operations. Glycol ethers have been associated with a variety of toxic effects, and some compounds in the group are relatively potent teratogens. The limited information available suggests that glycol ethers are contaminants in groundwater, especially in anaerobic plumes emanating from disposal of mixed industrial and household waste. Most methods used to analyze groundwater samples cannot adequately detect 7g/’ (ppb) concentrations of glycol ethers, and the existing methods perform worst for the most widely used and toxic species. A new method capable of analyzing 7g/’ concentrations of glycol ethers was recently developed, and its use is recommended for groundwater samples where glycol ethers are likely to be present. Résumé. Les éthers glycol, polluants des eaux souterraines. Les dérivés d'éther de dihydroxy-alcool, formés à partir de l'éthylène ou du propylène, constituent un important groupe de polluants des eaux souterraines connus sous le nom d'éthers glycol. Les composés de ce groupe sont utilisés comme solvants, comme agents de nettoyage et comme émulsifiants dans de nombreux produits chimiques et dans de nombreux processus de fabrication. Des effets toxiques variés ont été attribués aux éthers glycol et certains des composés sont des agents tératogènes relativement puissants. Les données disponibles, qui sont limitées, indiquent que les éthers glycol sont des polluants communs dans les eaux souterraines, particulièrement dans les panaches anaéorobies émis par les décharges mixtes de déchets industriels et domestiques. La plupart des méthodes d'analyse d'échantillons d'eau souterraine ne sont pas capables de détecter convenablement des concentrations en éthers glycol de l'ordre du 7g/l (ppb); les méthodes actuelles sont médiocres pour doser les espèces toxiques les plus courantes. Une nouvelle méthode permettant de doser des concentrations en éthers glycol de l'ordre du 7 g/l a été récemment mise au point; son utilisation est préconisée pour les échantillons d'eau souterraine contenant des éthers glycol.     

Experimentally determined mineral-melt partition coefficients for Sc,Y and REE for olivine,orthopyroxene, pigeonite,magnetite and ilmenite

Our current lack of understanding of the partitioning behavior of Sc, Y and the REE (rare-earth elements) can be attributed directly to the lack of a sufficiently large or chemically diverse experimental data set. To address this problem, we conducted a series of experiments using several different natural composition lavas, doped with the elements of interest, as starting compositions. Microprobe analyses of orthopyroxene, pigeonite, olivine, magnetite, ilmenite and co-existing glasses in the experimental charges were used to calculate expressions that describe REE partitioning as a function of a variety of system parameters. Using expressions that represent mineral-melt reactions (versus element ratio distribution coefficients) it is possible to calculate terms that express low-Ca pyroxene-melt partitioning behavior and are independent of both pyroxene and melt composition. Compositional variations suggest that Sc substitution in olivine involves either a paired substitution with Al or, more commonly, with vacancies. The partitioning of Sc is dependent both on melt composition and temperature. Our experimentally determined olivine-melt REE Ds (partition coefficients) are similar to, but slightly higher than those reported by McKay (1986) and support their conclusions that olivines are strongly LREE depleted. Y and REE mineral/melt partition coefficients for magnetite range from 0.003 for La to 0.02 for Lu. Ilmenite partition coefficients range from 0.007 for La to 0.029 for Lu. These experimental values are two orders of magnitude lower than many of the published values determined by phenocryst/matrix separation techniques.