Jens Fiebig

Daily Growth Rates in Shells of Arctica islandica: Assessing Sub-seasonal Environmental Controls on a Long-lived Bivalve Mollusk

Abstract Shells of the extremely long-lived bivalve mollusk Arctica islandica (Linnaeus 1767) provide century-long, multi-proxy records of inter-annual environmental variability in middle- to high-latitude marine settings. Reliable interpretation of these climate archives, however, requires exact knowledge of the length and timing of the growing season and which environmental parameters control shell growth rate during the year. Here, intra-annual growth microstructures, δ18O-derived ambient water temperatures, and δ13C from A. islandica shells collected from the southern and central North Sea are studied. Such data were analyzed in conjunction with observational sea-surface temperature and primary productivity data. Arctica islandica produces circadian growth increments in its shell (on average 31.5 μm per day during age four, measured along the outer shell surface), which allow assignment of calendar dates to each shell portion. The growing season of A. islandica in the upper mixed layer of the ocean (here 25 m water depth) is not continuous over an eight-month period as previously suggested. Rather, it is interrupted during spawning between early September and mid-November. In addition, shell production ceases or is strongly retarded due to food scarcity between mid-December and mid-February. Water temperatures derived from oxygen-isotope ratios are in good accord with observed sea-surface temperatures. In specimens at 25 m water depth, abrupt changes in shell δ18O-derived temperature (Tδ18O) were interpreted to represent vertical displacements of the seasonal thermocline. Daily shell growth is controlled by temperature and food availability. Up to 58% of the variation in daily growth rate is explained by these environmental parameters. This study demonstrates that A. islandica can provide seasonal to subseasonal, precisely dated proxies of environmental variables. Such data are of increasing importance for climate models.

Clumped isotope analysis of carbonates: comparison of two different acid digestion techniques

RATIONALE The kinetic nature of the phosphoric acid digestion reaction enables clumped isotope analysis of carbonates using gas source isotope ratio mass spectrometry (IRMS). In most laboratories acid digestions are performed at 25°C in sealed vessels or at 90°C in a common acid bath. Here we show that different Δ47 results are obtained depending on the digestion technique employed. METHODS Several replicates of a biogenic aragonite and NBS 19 were reacted with 104% H3 PO4 in sealed vessels at 25°C and at 90°C using a common acid bath. The sample size varied between 4 mg and 14 mg. Purification methods that are standard for clumped isotope analyses were applied to the evolved CO2 before measuring the abundances of masses 44 to 49 relative to a reference gas by IRMS. RESULTS A systematic trend to lower and more consistent Δ47 values is observed for reactions at 25°C if the sample size is increased. We suggest that secondary re-equilibration of evolved CO2 or reaction intermediates with free water molecules preferentially occurs for relatively small samples (4-7 mg), finally yielding elevated Δ47 values compared with >7 mg aliquots. In contrast, no such sample size effect on Δ47 values is observed for carbonates that are digested at 90°C using the common acid bath. CONCLUSIONS The determination of Δ47 values of carbonate samples smaller than 7 mg becomes more precise and accurate if digestions are performed at 90°C. Based on our results we propose that the difference in phosphoric acid fractionation factor between 25°C and 90°C is 0.07‰ for both calcite and aragonite.

Excess methane in continental hydrothermal emissions is abiogenic

Thermogenic hydrocarbons entirely deriving from the thermal degradation of organic matter usually exhibit methane to ethane plus propane ratios smaller than 100. We present hydrocarbon distribution data of continental hydrothermal gases, whose methane has been independently identified to derive from the abiogenic reduction of CO2. We find that excess amounts of methane with respect to thermogenic hydrocarbon distributions are characteristic for the investigated gases. A similar pattern is observed for well discharges whose temperatures are too high to support any microbially mediated methanogenesis. These findings strongly suggest that abiogenic methane production in continental-hydrothermal systems is a more widespread process than previously assumed. The maximum contribution of such emissions to the modern atmospheric CH4 budget is estimated at ~1%.

A 1500-Year Holocene Caribbean Climate Archive from the Blue Hole, Lighthouse Reef, Belize

Abstract Sediment cores (up to 6 m in length) from the bottom of the Blue Hole, a 125 m deep Pleistocene sinkhole located in the lagoon of Lighthouse Reef Atoll, Belize, consist of undisturbed, annually layered biogenic carbonate muds and silts with intercalated coarser grained storm beds. The sedimentation rate of the layered sections is 2.5 mm/y on average, and the long cores span the past 1500 years. Oxygen isotopes of laminated sediment provide a late Holocene climate proxy: A high-resolution δ18O time series traces the final Migration Period Pessimum, the Medieval Warm Period, the Little Ice Age, and the subsequent temperature rise. Carbon isotopes (δ13C) decrease up core and show the impacts of the decline of the Mayan culture and the Suess effect. Time series analyses of δ18O and δ13C content reveal 88-, 60-, 52-, and 32-year cyclicities, and suggest solar forcing. Storm event beds are most common during AD 650–850, around AD 1000, during AD 1200–1300, and AD 1450–1550. Major storm beds are rare during the past 500 years BP.

No causal link between terrestrial ecosystem change and methane release during the end-Triassic mass extinction

Profound changes in both marine and terrestrial biota during the end-Triassic mass extinction event and associated successive carbon cycle perturbations across the Triassic-Jurassic boundary (T-J, 201.3 Ma) have primarily been attributed to volcanic emissions from the Central Atlantic Magmatic Province and/or injection of methane. Here we present a new extended organic carbon isotope record from a cored T-J boundary succession in the Danish Basin, dated by high-resolution palynostratigraphy and supplemented by a marine faunal record. Correlated with reference C-isotope and biotic records from the UK, it provides new evidence that the major biotic changes, both on land and in the oceans, commenced prior to the most prominent negative C-isotope excursion. If massive methane release was involved, it did not trigger the end-Triassic mass extinction. Instead, this negative C-isotope excursion is contemporaneous with the onset of floral recovery on land, whereas marine ecosystems remained perturbed. The decoupling between ecosystem recovery on land and in the sea is more likely explained by long-term flood basalt volcanism releasing both SO2 and CO2 with short- and long-term effects, respectively.

Reliability of Multitaxon, Multiproxy Reconstructions of Environmental Conditions from Accretionary Biogenic Skeletons

Evaluation and quantification of climate change require data on subseasonal to daily environmental extremes from those periods before instrumental records were available. This study employs a high‐resolution, multitaxon, multiproxy approach and analyzes how faithfully accretionary biogenic skeletons record environmental extremes. Six specimens of two bivalve mollusks (Chione fluctifraga, Mytella guyanensi) and one barnacle species (Chthamalus fissus) from a single habitat (northern Gulf of California, Mexico) were collected. Contemporaneous shell portions from these specimens were analyzed for shell growth rates (sclerochronology) and stable isotopes (δ18O, δ13C) and were compared to instrumental records. The results of these analyses included some significant observations. First, shell δ18O values overestimate winter temperatures and underestimate summer temperatures. Second, the actual diurnal temperature range is not recorded in the biogenic skeletons. Third, skeletal growth is biased toward a species‐specific optimum growth temperature (24°–30.9°C). Therefore, higher sampling resolution will not necessarily capture actual environmental extremes. Despite measured temperature extremes of 37.8° and 4.5°C, none of the studied species recorded temperatures above 30.9° or below 12.2°C. Duration and timing of the annual growing period is species specific as well. Faster shell growth occurred at higher temperatures. Up to 58% (C. fissus) of the variability in shell growth can be explained by water temperature during growth. Contemporaneous trends in shell δ13C show a weak correlation with pigment concentration ( \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage[OT2,OT1]{fontenc} \newcommand\cyr{ \renewcommand\rmdefault{wncyr} \renewcommand\sfdefault{wncyss} \renewcommand\encodingdefault{OT2} \normalfont \selectfont} \DeclareTextFontCommand{\textcyr}{\cyr} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document} \landscape

Excimer laser isotope-ratio-monitoring mass spectrometry for in situ oxygen isotope analysis

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Hydrothermal alteration of biotite and plagioclase as inferred from intragranular oxygen isotope- and cation-distribution patterns

\end{document} ). Higher levels of chlorophyll appear to increase shell production rates. Our study highlights the difficulties inherent in using biogenic skeletons for the reconstruction of paleoenvironmental extremes and demonstrates the power and utility of multiproxy and multitaxon approaches.