Jeffrey M. Heikoop

Extended megadroughts in the southwestern United States during Pleistocene interglacials

The potential for increased drought frequency and severity linked to anthropogenic climate change in the semi-arid regions of the southwestern United States (US) is a serious concern. Multi-year droughts during the instrumental period and decadal-length droughts of the past two millennia were shorter and climatically different from the future permanent, ‘dust-bowl-like’ megadrought conditions, lasting decades to a century, that are predicted as a consequence of warming. So far, it has been unclear whether or not such megadroughts occurred in the southwestern US, and, if so, with what regularity and intensity. Here we show that periods of aridity lasting centuries to millennia occurred in the southwestern US during mid-Pleistocene interglacials. Using molecular palaeotemperature proxies to reconstruct the mean annual temperature (MAT) in mid-Pleistocene lacustrine sediment from the Valles Caldera, New Mexico, we found that the driest conditions occurred during the warmest phases of interglacials, when the MAT was comparable to or higher than the modern MAT. A collapse of drought-tolerant C4 plant communities during these warm, dry intervals indicates a significant reduction in summer precipitation, possibly in response to a poleward migration of the subtropical dry zone. Three MAT cycles ∼2 °C in amplitude occurred within Marine Isotope Stage (MIS) 11 and seem to correspond to the muted precessional cycles within this interglacial. In comparison with MIS 11, MIS 13 experienced higher precessional-cycle amplitudes, larger variations in MAT (4–6 °C) and a longer period of extended warmth, suggesting that local insolation variations were important to interglacial climatic variability in the southwestern US. Comparison of the early MIS 11 climate record with the Holocene record shows many similarities and implies that, in the absence of anthropogenic forcing, the region should be entering a cooler and wetter phase.

Nitrogen-15 Signals of Anthropogenic Nutrient Loading in Reef Corals

The 15N content of tissue from the coral Porites lobata was enriched, relative to corals from reference sites, at 5 of 7 Indo-Pacific sewage-affected reefs. Enrichment was as high as 3.7‰. The δ13C of sewage-affected corals suggests they maintained a high degree of autotrophic nutrition. 15N-enriched wastewater dissolved inorganic nitrogen (DIN), derived from untreated sewage, is the most likely cause for enrichment in coral tissue 15N, though changes in coral nutrition, metabolism and zooxanthellae population dynamics are possible additional factors. Isotopic measurements of coral tissue can provide a simple means of detecting wastewater uptake by corals.

Bacterial communities inhabiting the healthy tissues of two Caribbean reef corals: interspecific and spatial variation

Bacterial communities inhabiting healthy tissues of the reef-building corals Diploria strigosa and Montastraea annularis were evaluated across a human-induced environmental gradient along the southern coast of Curaçao, Netherlands Antilles. Variations in bacterial communities inhabiting coral tissues were determined using terminal restriction fragment length polymorphisms (T-RFLP) of 16S rRNA genes, and the δ15N value of coral tissue was used to assess the relative amount of human contaminants at each reef locality. Bacterial communities of D. strigosa were more variable than M. annularis, but there were no systematic differences in the populations of healthy M. annularis and D. strigosa. The δ15N value of coral tissues showed as much as a 1.5‰ increase in the impacted versus the non-impacted localities. While M. annularis showed no significant variation in bacterial community structure due to local reef conditions, the bacterial communities of D. strigosa showed dramatic shifts in community structure. The most abundant bacterial taxa inhabiting D. strigosa display increased dominance at impacted localities. By linking variations in microbial communities with an understanding of variations in local environmental conditions, this study provides a means of assessing potential factors that may impact the microbial habitat of coral tissues as well as overall reef health.

Potential climate signals from the deep-sea gorgonian coral Primnoa resedaeformis

The deep-sea gorgonian coral Primnoa resedaeformis has an arborescent skeleton composed of both calcite and a horn-like structural protein called gorgonin. We have investigated potential climate records in corals from Alaska, the eastern seaboard of Canada and the United States, and a Southern Ocean (Pacific sector) seamount. Temperatures at these sites range from 4 to ∼10 °C. δ18O values of the calcite show strong evidence for isotopic disequilibrium. Extraction of δ18O paleotemperatures is therefore not straightforward. Sr/Ca data, analyzed by Secondary Ion Mass Spectrometry (SIMS), suggest that temperature might be a control on calcite Sr/Ca in Primnoa resedaeformis, but that growth-related kinetic effects could also be important. Based on previous 14C, δ13C and δ15N measurements, it has been suggested that particulate organic matter (POM) from the surface is an important carbon source to the polyps and the gorgonin fraction of the Primnoa skeleton. δ15N and δ13C of polyps and gorgonin show similar regional differences to δ15N and δ13C of surface POM. Polyps and contemporaneous gorgonin correlate strongly for both δ13C and δ15N. The influence of nutrient isotopic composition and climate and productivity variations on the isotopic composition of surface POM may therefore be recorded in gorgonin layers. These corals have very long lifespans (several centuries). The potential exists, therefore, to obtain extended records of surface productivity, deep ocean temperature and chemistry of value to climatologists and fisheries managers.

Skeletal Mg/Ca in Primnoa resedaeformis: relationship to temperature?

It has been suggested that the deep-sea gorgonian coral Primnoa resedaeformis may be an important paleoceanographic archive. Seventeen colonies collected from the upper slope of the NW Atlantic margin (229 – 447 m) were analyzed to see if skeletal Mg/Ca is related to temperature. Analyses were focused on the calcite cortex region of skeletal sections to avoid interference from organic Mg in the horny layers found closer to the center of sections. Comparison of bulk skeletal Mg/Ca with hydrographic temperature yielded the relationship Mg/Ca (mmol/mol)=5 (+/− 1.4) T (°C)+64 (+/− 10). This relationship was used to calibrate profiles of Mg/Ca measured across the annual rings of one large, well-dated colony, over the period 1950–2002. Mg/Ca profiles were broadly consistent among three sections spaced 10 cm apart along the main trunk of the colony. These profiles were in general agreement with the local instrumental record of temperature at 375 – 450 m. Some discrepancies between the coral and instrumental records of temperature may be a result of chronological error, poor sampling density, or additional factors influencing Mg partitioning in the coral. Overall, these preliminary results support the hypothesis that temperature drives Mg/Ca in the skeletal calcite of this species. It appears that environmentally meaningful records from Primnoa resedaeformis will be found at decadal scales or longer.

Microtopographic and depth controls on active layer chemistry in Arctic polygonal ground

Polygonal ground is a signature characteristic of Arctic lowlands, and carbon release from permafrost thaw can alter feedbacks to Arctic ecosystems and climate. This study describes the first comprehensive spatial examination of active layer biogeochemistry that extends across high- and low-centered, ice wedge polygons, their features, and with depth. Water chemistry measurements of 54 analytes were made on surface and active layer pore waters collected near Barrow, Alaska, USA. Significant differences were observed between high- and low-centered polygons suggesting that polygon types may be useful for landscape-scale geochemical classification. However, differences were found for polygon features (centers and troughs) for analytes that were not significant for polygon type, suggesting that finer-scale features affect biogeochemistry differently from polygon types. Depth variations were also significant, demonstrating important multidimensional aspects of polygonal ground biogeochemistry. These results have major implications for understanding how polygonal ground ecosystems function, and how they may respond to future change.

Pretreatment technique for siderite removal for organic carbon isotope and C:N ratio analysis in geological samples

A method for the removal of siderite from geological samples to determine organic carbon isotope compositions using elemental analysis isotope ratio mass spectrometry is presented which includes calculations for % organic carbon in samples that contain diagenetic carbonate. The proposed method employs in situ acidification of geological samples with 6 N HCl and silver capsule sample holders and was tested on modern peach leaf samples (NIST 1547) and ancient lacustrine samples from Valles Caldera, New Mexico. The in situ acidification technique eliminates potential errors associated with the removal of soluble organic material using standard acid decanting techniques and allows for removal of the less soluble siderite, which is not efficiently removed using vapor acidification techniques.

Isotopic and Geochemical Tracers for U(VI) Reduction and U Mobility at an in Situ Recovery U Mine

In situ recovery (ISR) uranium (U) mining mobilizes U in its oxidized hexavalent form (U(VI)) by oxidative dissolution of U from the roll-front U deposits. Postmining natural attenuation of residual U(VI) at ISR mines is a potential remediation strategy. Detection and monitoring of naturally occurring reducing subsurface environments are important for successful implementation of this remediation scheme. We used the isotopic tracers (238)U/(235)U (δ(238)U), (234)U/(238)U activity ratio, and (34)S/(32)S (δ(34)S), and geochemical measurements of U ore and groundwater collected from 32 wells located within, upgradient, and downgradient of a roll-front U deposit to detect U(VI) reduction and U mobility at an ISR mining site at Rosita, TX, USA. The δ(238)U in Rosita groundwater varies from +0.61‰ to -2.49‰, with a trend toward lower δ(238)U in downgradient wells. The concurrent decrease in U(VI) concentration and δ(238)U with an ε of 0.48‰ ± 0.08‰ is indicative of naturally occurring reducing environments conducive to U(VI) reduction. Additionally, characteristic (234)U/(238)U activity ratio and δ(34)S values may also be used to trace the mobility of the ore zone groundwater after mining has ended. These results support the use of U isotope-based detection of natural attenuation of U(VI) at Rosita and other similar ISR mining sites.

Quantifying uncertainty in stable isotope mixing models

Mixing models are powerful tools for identifying biogeochemical sources and determining mixing fractions in a sample. However, identification of actual source contributors is often not simple, and source compositions typically vary or even overlap, significantly increasing model uncertainty in calculated mixing fractions. This study compares three probabilistic methods, Stable Isotope Analysis in R (SIAR), a pure Monte Carlo technique (PMC), and Stable Isotope Reference Source (SIRS) mixing model, a new technique that estimates mixing in systems with more than three sources and/or uncertain source compositions. In this paper, we use nitrate stable isotope examples (δ15N and δ18O) but all methods tested are applicable to other tracers. In Phase I of a three-phase blind test, we compared methods for a set of six-source nitrate problems. PMC was unable to find solutions for two of the target water samples. The Bayesian method, SIAR, experienced anchoring problems, and SIRS calculated mixing fractions that most closely approximated the known mixing fractions. For that reason, SIRS was the only approach used in the next phase of testing. In Phase II, the problem was broadened where any subset of the six sources could be a possible solution to the mixing problem. Results showed a high rate of Type I errors where solutions included sources that were not contributing to the sample. In Phase III some sources were eliminated based on assumed site knowledge and assumed nitrate concentrations, substantially reduced mixing fraction uncertainties and lowered the Type I error rate. These results demonstrate that valuable insights into stable isotope mixing problems result from probabilistic mixing model approaches like SIRS. The results also emphasize the importance of identifying a minimal set of potential sources and quantifying uncertainties in source isotopic composition as well as demonstrating the value of additional information in reducing the uncertainty in calculated mixing fractions.

Smoke signals from corals: isotopic signature of the 1997 Indonesian ‘haze’ event

Abstract From September to November 1997, most of Indonesia was covered by a dense blanket of haze, originating from fires on Sumatra and Borneo. Specimens of Porites lobata were collected from two locations, i.e. the Riau Archipelago, south of Singapore, where the haze was most dense, and the Karimunjawa Islands, north of Central Java, where the effects were less severe. All corals exhibited strong Kinetic Isotope Effects (KIE). On plots of δ 18 O vs. δ 13 C, shifts in coral metabolism associated with the haze event could be estimated from the distance individual values are positioned from the theoretical KIE line. Skeletons of corals affected by the haze showed decreased δ 13 C values, perhaps produced by a shift to a more heterotrophic mode of feeding. These results suggest that wildfires and major forest fire events on tropical coastlines may be recorded in nearby corals, as could temporal variation in frequency of major fires. Moreover, information on coral metabolism may be determined by examining shifts of coral skeletal values in C–O space.