ALBERT

Description: The late Palaeocene Thermal Maximum (LPTM) was a brief interval at c. 55 Ma characterized by a −2.5 to −3‰ shift in the δ13C of global carbon reservoirs. The geochemical perturbation probably represents a massive input of 12C-rich carbon to the exogenic carbon cycle. Largely unresolved issues concerning this carbon injection during the LPTM are the rates of carbon input and removal. Simple expressions are developed here to describe a δ13C excursion in the exogenic carbon cycle after carbon input. A change in global δ13C (dδEx/dt) can be explained to a first approximation by a set of parameters: the initial mass and isotopic composition of the global carbon cycle (MEx(o), δEx(o)), and the fluxes and isotopic compositions of external carbon inputs, outputs and injected carbon (FIn, δIn, FOut, δOut, FAdd, δAdd). In general, for a given exogenic carbon cycle, a large FAdd or low δAdd results in a larger δ13C excursion. Likewise, for a given negative δ13C excursion, a large MEx or low δEx requires a greater input of 12C. Differences in FIn, δIn, FOut and δOut cause changes in the response of δEx over time. For a negative δ13C excursion of given magnitude, a greater FIn requires a greater input of 12C and lessens the time for δEx to return to initial conditions. A decrease in δOut (caused by an increase in the relative output of organic matter and carbonate) has a similar effect. Variable dMAdd/dt produces transients in δEx that are related to the source function but modified by carbon removal. In theory, a well-dated and representative global δ13C excursion could be used to derive the carbon inputs and ouputs. Ocean Drilling Program (ODP) Site 1051 has an expanded early Palaeogene section, and recent work at this location has provided a well-dated δ13C record across the LPTM. This δ13C record contains transient variations of apparently global nature. These observed transients are best explained by a pulsed injection of CH4 into an exogenic carbon cycle with a greater carbon throughput or enhanced burial of organic matter after carbon addition.

Description: Deep Sea Drilling Project Site 577 on Shatsky Rise (North Pacific Ocean) recovered a series of cores at three holes that contain calcareous nannofossil ooze of latest Cretaceous (late Maastrichtian) through early Eocene age. Several important records have been generated using samples from these cores, but the stratigraphy has remained outdated and confusing. Here we revise the stratigraphy at Site 577. This includes refining several age datums, realigning cores in the depth domain, and placing all stratigraphic markers on a current time scale. The work provides a template for appropriately bringing latest Cretaceous and Paleogene data sets at old drill sites into current paleoceanographic literature for this time interval. While the Paleocene Eocene Thermal Maximum (PETM) lies within core gaps at Holes 577* and 577A, the sedimentary record at the site holds other important events and remains crucially relevant to understanding changes in oceanographic conditions from the latest Cretaceous through early Paleogene.

Description: It contains three tables that correspond to the supplementary information of the article mentioned above. Tables S1 and S2 can be found within the Supplementary Information document. Table S3 contains the characteristic remanent magnetisation (ChRM) directions (with associated sample position and confidence angle) used for the magnetostratigraphic correlation. Table S4 lists the calcareous nannofossil abundance for each rock sample expressed in number of specimens per squared millimetre. Table S5 is the foraminifera distribution chart.

Description: Sediment cores collected from the Eastern Equatorial Pacific Ocean display a clear positive second-order relationship between wet bulk density (WBD) and carbonate content. This has long interested the paleoceanography community because detailed Gamma Ray Attenuation Porosity Evaluator (GRAPE) measurements, which approximate WBD, might be used to determine records of carbonate content at very high temporal resolution. Although general causes for the relationship are known, they have not been presented and discussed systematically on the basis of first principles. In this study, we measure the mass and carbonate content of 50 sediment samples with known WBD from Site U1338, before and after rinsing with de-ionized water; we also determine the mass related proportion of coarse (〉 63 µm) material. Samples exhibit clear relationships between WBD, carbonate content, mass loss upon rinsing, and grain size. We develop a series of mathematical expressions to describe these relationships, and solve them numerically. As noted by previous workers, the second-order relationship between WBD and carbonate content results from the mixing of biogenic carbonate and biogenic silica, which have different grain densities and different porosities. However, at high carbonate content, a wide range in WBD occurs because samples with greater amounts of coarse carbonate have higher porosity. Moreover compaction impacts carbonate particles more than biogenic silica particles. As such, a single two-component equation cannot be used to determine carbonate content accurately across depth intervals where both the porosity and type of carbonate vary. Instead, the WBD-carbonate relationship is described by an infinite series of curves, each which represents mixing of multiple sediment components with different densities and porosities. Dissolved ions also precipitate from pore space during sample drying, which adds mass to the sediment. Without rinsing samples, simple empirical relationships between WBD and carbonate content are further skewed by salt dilution.

Description: The Palaeocene/Eocene thermal maximum represents a period of rapid, extreme global warming approx ~55 million years ago, superimposed on an already warm world (Zachos et al., 2003, doi:10.1126/science.1090110; Bowen et al., 2004, doi:10.1038/nature03115; Thomas et al., 2002, doi:10.1130/0091-7613(2002)030〈1067:WTFFTF〉2.0.CO;2). This warming is associated with a severe shoaling of the ocean calcite compensation depth **4 and a 〉2.5 per mil negative carbon isotope excursion in marine and soil carbonates (Zachos et al., 2003, doi:10.1126/science.1090110; Bowen et al., 2004, doi:10.1038/nature03115; Thomas et al., 2002, doi:10.1130/0091-7613(2002)030〈1067:WTFFTF〉2.0.CO;2; Zachos et al., doi:10.1126/science.1109004). Together these observations indicate a massive release of 13C-depleted carbon (Zachos et al., doi:10.1126/science.1109004) and greenhouse-gas-induced warming. Recently, sediments were recovered from the central Arctic Ocean (Backman et al., 2006, doi:10.2204/iodp.proc.302.2006), providing the first opportunity to evaluate the environmental response at the North Pole at this time. Here we present stable hydrogen and carbon isotope measurements of terrestrial-plant- and aquatic-derived n-alkanes that record changes in hydrology, including surface water salinity and precipitation, and the global carbon cycle. Hydrogen isotope records are interpreted as documenting decreased rainout during moisture transport from lower latitudes and increased moisture delivery to the Arctic at the onset of the Palaeocene/Eocene thermal maximum, consistent with predictions of poleward storm track migrations during global warming (Backman et al., 2006, doi:10.2204/iodp.proc.302.2006). The terrestrial-plant carbon isotope excursion (about ~4.5 to ~6 per mil) is substantially larger than those of marine carbonates. Previously, this offset was explained by the physiological response of plants to increases in surface humidity (Bowen et al., 2004, doi:10.1038/nature03115). But this mechanism is not an effective explanation in this wet Arctic setting, leading us to hypothesize that the true magnitude of the excursion - and associated carbon input - was greater than originally surmised. Greater carbon release and strong hydrological cycle feedbacks may help explain the maintenance of this unprecedented warmth.of this unprecedented warmth.