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The research presented here is an effort to characterize changes in marine oxygen availability across a portion of the later Cambrian noted for unique evolutionary dynamics and which includes a significant global oceanographic event known as the SPICE event (Steptoean Positive Carbon Isotope Excursion). Previous studies have revealed the SPICE caused large changes to the global cycles of carbon, sulfur, uranium, molybdenum and the overall trace metal content of seawater. Furthermore, the initiation of these changes appears to have been temporally coupled with marine extinctions across several paleocontinents raising the possibility of a common causal linkage between all these features. In particular, expanding marine anoxia has been invoked as the most parsimonious explanation for these co-occurring features. The research presented here tests this hypothesis directly across a range of spatial scales using the iron speciation paleoredox proxy to characterize redox conditions within individual basins and to facilitate comparison of conditions between basins. In addition to these analyses, we apply a new proxy, thallium stable isotopes to this interval to assess potential global changes in deoxygenation across the event. These iron speciation analyses showed shallow environments deoxygenated coincident with the initiation of the SPICE and extinction horizons, and these conditions were dominantly ferruginous. Importantly, this work also shows deeper-water environments were deoxygenated prior to and remained so across the event and these environments were also largely. Last we looked at changes in thallium isotopes during this same interval to see if this deoxygenation would be recorded as a positive shift across the interval if expanded anoxia were to impact the areal extent of manganese-oxide sedimentation and burial. We found it did record these changes, but with a different expression than during other more recent events explored using the isotope system. We attribute these differences to the unique chemical structure of the oceans during the Cambrian, which as documented herein were widely oxygen-deficient in their deeper depths. Given this recognition we suggest that thallium isotope studies in deep time should account for this redox structure of ancient oceans likely common under the less-oxygenated atmospheres of the ancient Earth. / Doctor of Philosophy / The research presented here is a story about oxygen in the oceans during an ancient portion of Earth history within the Cambrian Period (around 500 million years ago), soon after animal life first appears in the geologic record. The emerging biosphere of this time seems to have been particularly prone to extinctions, leading to the idea that environmental conditions, such as oxygen availability at the seafloor created difficult circumstances for animals in these ancient seas. This work seeks to quantify the levels of marine oxygenation at this time, however this remains a fundamental challenge because they cannot be directly measured from the rocks we study. Therefore, we rely on how the presence or absence of oxygen changed the chemistry of these rocks at the time they were sediments deposited on the seafloor. Here we use the behavior of two different elements, iron (Fe) and thallium (Tl), to understand changes in oxygen in the oceans around a large, globally-recorded extinction event called the SPICE event. Studying how much iron is concentrated in certain minerals in the rocks formed during this event allowed us to track how changes in oxygen may relate to these notable extinctions. We found that shallow coastal areas changed from oxygenated to deoxygenated at the same time of the extinctions, suggesting a direct role for this environmental shift in the biological crisis. Furthermore, we compared other locations from around the world using more new iron measurements in conjunction with previously published ones compiled by a collaborative geochemistry database project. This work revealed the deeper oceans were deoxygenated prior to and across the SPICE event and that the decline in oxygen in shallower environments was where most environmental change occurred during this time. Last we looked at changes in thallium isotopes during this same interval to see if this deoxygenation changed its global cycle. We found it did record global changes, but they were expressed differently than during other more recent events that have been studied. We attribute these differences to the unique chemical structure of the oceans during the Cambrian, which were widely oxygen-deficient in their deeper depths.

Yes / Sampling of dentine for stable carbon (δ13 C) and nitrogen (δ15 N) isotope ratios in the direction of tooth growth allows the study of temporal changes to the diet and physiological stress of an individual during tooth formation. Current methods of sampling permanent teeth using 1mm increments provide temporal resolution of six - nine months at best depending on the tooth chosen. While this gives sufficient sample sizes for reliable analysis by mass spectrometry, sectioning the dentine across the incremental structures results in a rolling average of the isotope ratios. A novel method of incremental dentine collagen sampling has been developed to decrease the collagen increment size to 0.35mm along the incremental structures thus reducing averaging and improving the temporal resolution of short-term changes within the δ13 C and δ15 N values. This study presents data for a MicroMill-assisted sampling method that allows for sampling at 0.35mm width x 1mm depth increments following the incremental growth pattern of dentine. A NewWave MicroMill was used to sample the demineralised dentine section of modern donated human third molars from Sudan and compared to data from the same teeth using the 1mm incremental sectioning method 2 from Beaumont et al. (2013). The δ13 C and δ15 N isotopic data showed an increased temporal resolution, with each increment providing data for two-four months of dentine formation. The data show the potential of this method for studying dietary reconstruction, nutritional stress, and physiological change with greater temporal resolution potentially to seasonal level and with less attenuation of the δ13 C and δ15 N values than was previously possible from human dentine.

The potential of Arctica islandica, a long lived marine bivalve with a lifespan of over 300 years, to reconstruct a high resolution (sub-annual) climate record is explored in this thesis. Fluctuations in trace element and isotopic data from live-collected specimens from Irvine Bay, NW Scotland are compared to instrumental (particularly temperature) data. X-ray absorption spectroscopy data demonstrate the coordination state of Sr and Mg within the shell. These are consistent with models in which Sr substitutes ideally for Ca in aragonite, and Mg is bound predominantly to organic molecules. Sr/Ca incorporation may be influenced by changes in the crystal nucleation, propagation and growth rate as well as vital effects. However any effect of seawater temperature on Sr/Ca incorporation was obscured by these other factors. Mg concentration is not a linear function of a single environmental variable or organic content within the shell, indicating that Mg uptake is biologically mediated. Ba variation shows sporadic increases (of >500% above baseline) in both shells, the timing of which is similar between the prismatic layer and umbo region. The maxima are, however, not synchronous between the two shells analysed. The controls on Ba uptake require further research, but low Ba/Ca may reflect Ba/Ca concentrations within the seawater. Aliquots taken from cod otoliths show that micromilling has negligible effect on δ¹⁸O. The range of reconstructed temperature from δ¹⁸O profiles Arctica islandica shows good agreement with the sea surface temperature data from the nearby Millport marine station to within 2.1 °C. However, both the interannual and intra-annual variation appears to be sensitive to changes in temporal resolution resulting from changes in growth rates. Modelling of δ¹⁸O highlights dependence on changes in temporal resolution of the sampling, in addition to temperature and salinity. Results from the radiocarbon pilot study show that Arctica islandica is a suitable archive for changes in radiocarbon associated with anthropogenic ¹⁴C fluxes.

"A Terminal Report Submitted 31 October, 1981 on the National Science Foundation grant EAR 78-04436 with the assistance of the Department of Energy contract no. EE-78-A-28-3274"

"A Final Technical Report Submitted 31 May 1985 on the National Science Foundation grant EAR-8018687 for the period 1 April 1981 to 31 October 1984 with the assistance of the Department of Energy contract no. DE-AC02-81EV10680 covering the period 1 May 1981 to 31 October 1982" / Since Edmund Schulman’s initial interest in 1953, the Laboratory of Tree-Ring Research has conducted dendrochronological studies of bristlecone pine (Pinus longaeva D. K. Bailey, sp. Nov.) in the White Mountains of east-central California where living trees reach ages in excess of 4,000 years. The focus of this report relates to the support by the Geology and Anthropology sections in the National Science Foundation under grant EAR-8018687 for the period 1 April 1981 to 31 October 1984 with the assistance of the Department of Energy contract no. DE-AC02-81EV10680 covering the period 1 May 1981 to 31 October 1982. A summary of this research was recently published in Radiocarbon (Ferguson and Graybill 1983). In most cases various facets of the work were related to projects sponsored by all agencies. Therefore the full range of activities during that period is described herein. The primary project goals were: To extend the bristlecone pine chronology from the White Mountains of California beyond 6700 B.C. and strengthen it by incorporating additional specimens. To develop bristlecone pine chronologies in new areas for applications in archaeology, isotopic studies, and other earth sciences. To furnish dendrochronologically dated wood to researchers engaged in the study of past variations in carbon isotopes and climate.

Aerosols change the Earth's energy balance. Black carbon (BC) aerosols are a product of incomplete combustion of fossil fuels and biomass burning and cause a net warming through aerosol radiation interactions (ari) and aerosol cloud interactions (aci). BC aerosols have potentially strong implications on the Arctic climate, yet the net global climate effect of BC is very uncertain. Best estimates assume a net warming effect, roughly half to that of CO2. However, the time scales during which CO2 emissions affect the global climate are on the order of hundreds of years, while BC is a short-lived climate pollutant (SLCP) with atmospheric life times of days to weeks. Climate models or atmospheric transport models struggle to emulate the seasonality and amplitude of BC concentrations in the Arctic, which are low in summer and high in winter/spring during the so called Arctic haze season. The high uncertainties regarding BC's climate impact are not only related to ari and aci, but also due to model parameterizations of BC lifetime and transport, and the highly uncertain estimates of global and regional BC emissions. Given the high uncertainties in technology-based emission inventories (EI), there is a need for an observation-based assessment of sources of BC in the atmosphere. We study short-term and long-term observations of elemental carbon (EC), the mass-based analog of optically-defined BC. EC aerosol concentrations and carbon-isotope-based (δ13C and ∆14C) sources were constrained (top-down) for three Arctic receptor sites in Abisko (northern Sweden), Tiksi (East Siberian Russia), and Zeppelin (on Svalbard, Norway). The radiocarbon (∆14C) signature allows to draw conclusion on the EC sources (fossil fuels vs. biomass burning) with high accuracy (&lt;5% variation). Stable carbon isotopic fingerprints (δ13C) give qualitative information of the consumed fuel type, i.e. coal, C3-plants (wood), liquid fossil fuels (diesel) or gas flaring (methane and non-methane hydrocarbons). These fingerprints can be used in conjunction with Bayesian statistics, to estimate quantitative source contributions of the sources. Finally, our observations were compared to predictions from a state of the art atmospheric transport model (coupled to BC emissions), conducted by our collaborators at NILU (Norwegian Institute for Air Research). Observed BC concentrations showed a high seasonality throughout the year, with elevated concentrations in the winter, at all sites. The highest concentrations were measured on Svalbard during a short campaign (Jan-Mar 2009) focusing on BC pollution events. Long-term observations showed that Svalbard (2013) had overall the lowest annual BC concentrations, followed by Abisko (2012) and Tiksi (2013). Isotope constraints on BC combustion sources exhibited a high seasonality and big amplitude all across the Eurasian Arctic. Uniform seasonal trends were observed in all three year-round studies, showing fractions of biomass burning of 60-70% in summer and 10-40% in winter. Europe was the major source region (&gt;80%) for BC emissions arriving at Abisko and the main sources were liquid fossil fuels and biomass burning (wood). The model agreed very well with the Abisko observations, showing good model skill and relatively well constrained sources in the European regions of the EI. However, for the Svalbard and East Siberian Arctic observatories the model-observation agreement was not as good. Here, Russia, Europe and China were the major contributors to the mostly liquid fossil and biomass burning BC emissions. This showed that the EI still needs to be improved, especially in regions where emissions are high but observations are scarce (low ratio of observations to emitted pollutant quantity). Strategies for BC mitigation in the (Eurasian) Arctic are probably most efficient, if fossil fuel (diesel) emissions are tackled during winter and spring periods, all across Eurasia. / <p>At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 2: Manuscript. Paper 3: Manuscript.</p>

Tree-ring studies have demonstrated that conifer latewood measurements contain information on long-term North American monsoon (NAM) variability, a hydroclimatic feature of great importance to plants, animals, and human society in the US Southwest. This paper explores data-treatment options for developing latewood chronologies aimed at NAM reconstruction. Archived wood samples for five Douglas-fir (Pseudotsuga menziesii, Mirb. Franco) sites in southeastern Arizona are augmented with new collections. The combined dataset is analyzed along with time series of regionally averaged observed precipitation to quantify the strength of regional precipitation signal in latewood time series and to identify ways of increasing the signal strength. Analysis addresses the signal strength influences of including or excluding ‘‘false’’ latewood bands in the nominal ‘‘latewood’’ portion of the ring, the necessary adjustment of latewood width for statistical dependence on antecedent earlywood width, and tree age. Results suggest that adjusted latewood width chronologies from individual sites can explain around 30% of the variance of regional summer (July–August) precipitation—increasing to more than 50% with use of multiple chronologies. This assessment is fairly insensitive to the treatment of false latewood bands (in intra-annual width and 𝛿¹³C variables), and to whether latewood-width is adjusted for dependence on earlywood-width at the core or site level. Considerations for operational chronology development in future studies are (1) large tree-to-tree differences in moisture signal, (2) occasional nonlinearity in EW-LW dependence, and (3) extremely narrow and invariant latewood width in outer portions of some cores. A protocol for chronology development addressing these considerations is suggested.

Current mining operators in the Athabasca oil sands deposit of Alberta, Canada have made commitments to zero discharge of oil sands process-affected waste materials (OSPM) from the mine site and rehabilitation of mined lands to a pre-mining state. As part of aquatic reclamation efforts, experimental test sites that contain a range of OSPM (solid and liquid components) were constructed to monitor the evolution and viability of aquatic habitats used as disposal sinks for OSPM produced by mining activities. In the present study, stable isotopes of carbon, nitrogen and sulphur were used to gauge some of the potential effects of OSPM site construction methods on aquatic food webs. Carbon and nitrogen isotopic signatures of sediment, dissolved inorganic carbon, dissolved organic carbon, particulate organic matter, periphytic material, plants, plankton, aquatic invertebrates and fish were used to assess differences related to the naphthenic acid (NA) concentration in OSPM and reference sites. For statistical analyses, sites were grouped into low (0 to 4 mg/L), medium (4 to 15 mg/L) and high (> 15 mg/L) NA concentrations. There were no significant differences in food web area or food web length among the low, medium and high NA concentration sites. In most cases, sample carbon isotope analyses of low, medium and high NA concentration sites were not significantly different, suggesting food web carbon sources did not include significant contributions from OSPM materials at OSPM sites. Significant differences, however, were found in the sample nitrogen isotope signatures between low, medium and high NA concentration sites. Ammonia from OSPM is suggested to be the main contributor to &delta;¹⁵N enrichment. <br /><br /> To determine the potential effects of site construction and OSPM within experimental test sites, carbon and sulphur stable isotopes of water, plankton, aquatic invertebrates and fish were analyzed. With the exception of <em>Chaoborus</em> and <em>Haliplus</em>, all carbon isotope signatures were not significantly different in constructed and reference sites. Also with the exception of <em>Haliplus</em>, sulphur isotope values for aquatic organisms from constructed and reference sites were significantly different. Aquatic organisms and water samples from constructed sites built in, or close, to the boundary of Kcw clays typically had &delta;³⁴S < 0 ?. Coinciding with depleted &delta;³⁴S signatures found in these aquatic systems were elevated sulphate concentrations. The waters at experimental test sites are in direct contact with the soil materials that facilitate the accumulation of sulphates as a result of the oxidation of substrate sulphide minerals. In general the results of the study suggest that aquatic food web structure and function do not change with the introduction of OSPM. Shifts in isotopic signatures suggestive of changes in food web structure, however, do occur when site construction exposes Kcw clays in the substrate.

Current mining operators in the Athabasca oil sands deposit of Alberta, Canada have made commitments to zero discharge of oil sands process-affected waste materials (OSPM) from the mine site and rehabilitation of mined lands to a pre-mining state. As part of aquatic reclamation efforts, experimental test sites that contain a range of OSPM (solid and liquid components) were constructed to monitor the evolution and viability of aquatic habitats used as disposal sinks for OSPM produced by mining activities. In the present study, stable isotopes of carbon, nitrogen and sulphur were used to gauge some of the potential effects of OSPM site construction methods on aquatic food webs. Carbon and nitrogen isotopic signatures of sediment, dissolved inorganic carbon, dissolved organic carbon, particulate organic matter, periphytic material, plants, plankton, aquatic invertebrates and fish were used to assess differences related to the naphthenic acid (NA) concentration in OSPM and reference sites. For statistical analyses, sites were grouped into low (0 to 4 mg/L), medium (4 to 15 mg/L) and high (> 15 mg/L) NA concentrations. There were no significant differences in food web area or food web length among the low, medium and high NA concentration sites. In most cases, sample carbon isotope analyses of low, medium and high NA concentration sites were not significantly different, suggesting food web carbon sources did not include significant contributions from OSPM materials at OSPM sites. Significant differences, however, were found in the sample nitrogen isotope signatures between low, medium and high NA concentration sites. Ammonia from OSPM is suggested to be the main contributor to &delta;¹⁵N enrichment. <br /><br /> To determine the potential effects of site construction and OSPM within experimental test sites, carbon and sulphur stable isotopes of water, plankton, aquatic invertebrates and fish were analyzed. With the exception of <em>Chaoborus</em> and <em>Haliplus</em>, all carbon isotope signatures were not significantly different in constructed and reference sites. Also with the exception of <em>Haliplus</em>, sulphur isotope values for aquatic organisms from constructed and reference sites were significantly different. Aquatic organisms and water samples from constructed sites built in, or close, to the boundary of Kcw clays typically had &delta;³⁴S < 0 ?. Coinciding with depleted &delta;³⁴S signatures found in these aquatic systems were elevated sulphate concentrations. The waters at experimental test sites are in direct contact with the soil materials that facilitate the accumulation of sulphates as a result of the oxidation of substrate sulphide minerals. In general the results of the study suggest that aquatic food web structure and function do not change with the introduction of OSPM. Shifts in isotopic signatures suggestive of changes in food web structure, however, do occur when site construction exposes Kcw clays in the substrate.