Methane seepage along the Hikurangi Margin of New Zealand : geochemical and physical data from the water column, sea surface and atmosphere

The concentration and carbon isotope values of dissolved methane were measured in the water column at Rock Garden, Omakere Ridge and Wairarapa areas in the first dedicated cold seep investigation along the Hikurangi Margin of New Zealand. These measurements provide a high resolution impression of the methane distribution in the water column and show that these seep sites are actively venting methane with varying intensity. The highest concentrations (up to 3500 nM) measured in water samples obtained from Conductivity–Temperature–Depth (CTD) operations were at Faure Site of Rock Garden. Here, seafloor bubble release was observed by ROV. The Omakere Ridge area is actively venting over almost its entire length (not, vert, similar 25 km), in particular at Bear's Paw, a newly discovered seep site. In the Wairarapa area another new seep site called Tui was discovered, where methane measurements often exceeded 500 nM. No evidence was obtained from water column or sea surface measurements along the Hikurangi Margin to indicate that methane from seeps is reaching the sea surface. In fact, a consistent upper boundary was observed at a density of 26.85 kg/m3, which occurs at about 500 m below sea surface, above which methane decreased to background concentrations. No obvious oceanographic feature is associated with this 500 m CH4 boundary. Bubble dissolution calculations show that about 500 m was also the model-derived maximum bubble rise height. A wide range of δ13CCH4 values from − 71 to − 19‰ (VPDB) were measured, with the highest CH4 concentrations having the lowest δ13CCH4 values of about − 71 to − 68‰. Simple mixing and isotope fractionation calculations show that changes of δ13CCH4 values are predominantly caused by the dilution of seep fluids with the seawater, with some anaerobic oxidation also occurring

A portable and autonomous mass spectrometric system for on-site environmental gas analysis

We developed a portable mass spectrometric system (“miniRuedi”) for quantificaton of the partial pressures of He, Ne (in dry gas), Ar, Kr, N2, O2, CO2, and CH4 in gaseous and aqueous matrices in environmental systems with an analytical uncertainty of 1−3%. The miniRuedi does not require any purification or other preparation of the sampled gases and therefore allows maintenance- free and autonomous operation. The apparatus is most suitable for on-site gas analysis during field work and at remote locations due to its small size (60 cm × 40 cm × 14 cm), low weight (13 kg), and low power consumption (50 W). The gases are continuously sampled and transferred through a capillary pressure reduction system into a vacuum chamber, where they are analyzed using a quadrupole mass spectrometer with a time resolution of ≲1 min. The low gas consumption rate (<0.1 mL/min) minimizes interference with the natural mass balance of gases in environmental systems, and allows the unbiased quantification of dissolved-gas concentrations in water by gas/water equilibration using membrane contractors (gasequilibrium membrane-inlet mass spectrometry, GE-MIMS). The performance of the miniRuedi is demonstrated in laboratory and field tests, and its utility is illustrated in field applications related to soil-gas formation, lake/atmosphere gas exchange, and seafloor gas emanations

A 500,000-year-long sediment archive drilled in eastern Anatolia

Sedimentary archives host a wealth of information that can be used to reconstruct paleoclimate as well as the tectonic and volcanic histories of specific regions. Long and continuous archives from the oceans have been collected in thousands of locations by scientific ocean drilling programs over the past 40 years. In contrast, suitable continental archives are rare because terrestrial environments are generally nondepositional and/or subject to erosion. Lake sediments provide ideal drilling targets to overcome this limitation if suitable lakes at key locations have existed continuously for a long time

Noble gas based temperature reconstruction on a Swiss stalagmite from the last glacial–interglacial transition and its comparison with other climate records

Here we present the results of a first application of a “Combined Vacuum Crushing and Sieving (CVCS)” system to determine past (cave / soil) temperatures from dissolved noble gas concentrations in stalagmite samples grown under ‘cold’ climatic conditions (e.g. close to freezing point of water) during the last glacial-interglacial transition. To establish noble gas temperatures (NGTs) also for stalagmites grown in cold regions, we applied the CVCS system to samples from stalagmite M2 precipitated in the Milandre Cave, located in the Swiss Jura Mountains. The investigated stalagmite M2 covers the Allerød – Younger Dryas – Holocene transitions. Noble gas temperatures are determined by using a new algorithm based on noble gas and water abundances and not from concentrations. Noble gas results indicate annual mean temperatures in the Milandre Cave were 2.2 ± 1.8 °C during the late stages of the Allerød, then dropping to 〖0 〗_((-))^( +) 2.6 °C at the onset of the Younger Dryas. Such temperatures indicate conditions near to the freezing point of water during the first part of the Younger Dryas. During the last part of the Younger Dryas, the temperature increased to 6.3 ± 2.3 °C. No early Holocene temperature could be determined due the non-detectable water abundances in these samples, however one late Holocene sample indicates a cave temperature of 8.7 ± 2.7 °C which is close to the present day annual mean temperature. NGTs estimated for the Allerød – Younger Dryas – Holocene are in good agreement with paleo-temperature reconstructions from geochemical and biological proxies in lake sediments. The observed deviations between the different paleo-temperature reconstructions are minor if the according temperatures are rescaled to annual mean temperatures and are primarily attributed to the chronological tuning of the different records. As in other stalagmites, NGT reconstructions of the recently precipitated stalagmite (‘young’) samples again are biased, most likely due to diffusive gas loss during sample processing. We speculate that a reduced retentivity of noble gases during experimental sample processing is a general feature of recently precipitated stalagmite fabrics. Therefore, the recently precipitated stalagmite samples do not allow the reliable NGT determination given the currently available experimental methods. Nevertheless, this study makes the case that noble gas thermometry can be applied to stalagmites for physically based paleo-temperature reconstruction, also for stalagmites grown during cold climatic conditions