Operations and performance of the PACS instrument 3He sorption cooler on board of the Herschel space observatory

A ³He sorption cooler produced the operational temperature of 285 mK for the bolometer arrays of the Photodetector Array Camera and Spectrometer (PACS) instrument of the Herschel Space Observatory. This cooler provided a stable hold time between 60 and 73 h, depending on the operational conditions of the instrument. The respective hold time could be determined by a simple functional relation established early on in the mission and reliably applied by the scientific mission planning for the entire mission. After exhaustion of the liquid ³He due to the heat input by the detector arrays, the cooler was recycled for the next operational period following a well established automatic procedure. We give an overview of the cooler operations and performance over the entire mission and distinguishing in-betweenthe start conditions for the cooler recycling and the two main modes of PACS photometer operations. As a spin-off, the cooler recycling temperature effects on the Herschel cryostat ⁴He bath were utilized as an alternative method to dedicated Direct Liquid Helium Content Measurements in determining the lifetime of the liquid Helium coolant.     

A detailed pyrolysis-GC/MS analysis of a black carbon-rich acidic colluvial soil (Atlantic ranker) from NW Spain

Despite the potentially large contribution of black carbon (BC) to the recalcitrant soil organic matter pool, the molecular-level composition of aged BC has hardly been investigated. Pyrolysis-GC/MS, which provides structural information on complex mixtures of organic matter, was applied to the NaOH-extractable organic matter of an acidic colluvial soil (Atlantic ranker) sampled with high resolution (5 cm) that harbours a fire record of at least 8.5 ka. Additionally, 5 charcoal samples from selected soil layers were characterised using pyrolysis-GC/MS for comparison. Pyrolysis-GC/MS allowed distinguishing between BC and non-charred organic matter. It is argued that a large proportion of the polycyclic aromatic hydrocarbons (PAHs), benzenes and benzonitrile in the pyrolysates of the extractable organic matter, together accounting for 21–54% of total identified peak area, derived from BC. In charcoal samples, these compounds accounted for 60–98% of the pyrolysis products. The large quantity of BC in almost all samples suggested a key role of fire in Holocene soil evolution. The high C content of the soil (up to 136 g C kg⁻¹ soil) may be attributed to the presence of recalcitrant organic C as BC, in addition to the sorptive preservation processes traditionally held responsible for long-term C storage in acid soils. Interactions between reactive Al hydroxides and BC could explain the longevity of BC in the soil. This work is the first thorough pyrolysis-GC/MS based study on ancient fire-affected organic matter.     

Chemical fractionation of zinc versus cadmium among other metals nickel, copper and lead in the northern North Sea

Concentrations of dissolved Ni, Cu, Zn, Cd and Pb were measured in water samples collected during a cruise with R.V Pelagia (29-6/14-7-1993) in the northern North Sea and N.E. Atlantic Ocean. At least six depths (0–90 m) were sampled with modified Go-Flo samplers from a rubber zodiac. In the study area, the first 25 m were well mixed and stratification occurred below this depth. The local bloom of Emiliania huxleyi hardly affected the trace metals concentration, except for some removal of Cd as seen from its correlation with nitrate. The mean dissolved concentrations were for Ni (3.66 nM), Cu (1.61 nM), Zn (4.5 nM), Cd (48 pM) and Pb (108 pM). These concentrations are among the lowest reported for the North Sea and are of similar magnitude to those found in the eastern North Atlantic at the same latitude. Zn was the only exception with values 10 times higher compared to those in the Atlantic Ocean, suggesting external inputs, mainly atmospheric and possibly from surrounding land masses. The observed ratio Zn:Cd in the North Sea and estuaries is in between the high ratio 600–900 for continental sources and the low ratio 5–10 for oceanic waters. Latter low ratio is consistent with the 21-fold stronger inorganic complexation of Cd in seawater which, in combination with the preferential biological uptake of Zn, may lead to the observed about hundredfold fractionation of Zn versus Cd in the marine system. Other processes may play a role but would need further investigation. The dissolved Pb values tend to be lower than found before in the North Sea, indicating decreasing inventories due to reduced anthropogenic emissions.     

Recognition of Space Weather Impact on the Isophot Detectors

The effects of changes in the space environment on the ISOPHOT photoconductivedetectors over the whole ISO mission were studied using the complete setof responsivity check measurements taken after the curing of the detectors.We found that the responsivity of the Ge-based, low bias voltage far-infrared detectors (P3, C100, and C200) is sensitive to the conditions of the Space Weather.We present evidence that an increased responsivity level (20% – 50%) after curing of the detectors is linked to the onset of geomagnetic storms. TheSi-based, high bias voltage detectors P1, P2 and PHT–SS show only small changesin their responsivity. An exception is the PHT–SL array which shows a similar,but less pronounced behaviour as the FIR detectors. While these relationshave been demonstrated by our study, a detailed physical understanding is still outstanding. The Space Weather dependent scatter of the responsivity,being the photometric scaling factor (conversion from measured photo currentto inband power on the detector), justifies the observing mode design to include frequent monitoring of its actual level.     

Cyclic channel-shoal dynamics at the Ameland inlet: the impact on waves,tides, and sediment transport

Ocean Dynamics - Ebb-tidal deltas are shallow features seaward of tidal inlets, acting as a wave filter for the nearby barrier island and a source of sediment for the landward tidal basin. On many...     

Calcification rate and temperature effects on Sr partitioning in coccoliths of multiple species of coccolithophorids in culture

Five common placolith-bearing coccolithophorid algae—Gephyrocapsa oceanica, Coccolithus pelagicus, Calcidiscus leptoporus, Umbilicosphaera sibogae (var. sibogae and var. foliosa), and Emiliania huxleyi—were cultured to investigate controls on Sr partitioning in coccolith calcite. For identical temperature and media composition, Sr partitioning varies by more than 30% in exponential phase cultures of the five species and is linearly related to rates of calcite production/cell (ρ=0.91). Exponential phase culture experiments with three strains of C. leptoporus and six strains of G. oceanica at varying temperatures show variations in Sr partitioning of 20% and 30%, respectively. With C. leptoporus, Sr partitioning is equally correlated with temperature and calcification rate (ρ=0.8), which themselves are highly correlated; the slope of the relationship between D_Sr and calcification rate is comparable to that observed in all species at constant temperature. However, in G. oceanica, increased temperature appears to enhance Sr incorporation by up to 2% to 1.6% °C⁻¹ in the range of 15 to 30 °C. The strong influence of calcification rate on Sr partitioning may be useful for inferring past variations in coccolithophorid productivity from Sr partitioning in coccolith sediments if the influence of temperature on Sr partitioning can be resolved. Because the relationship between calcite production and Sr partitioning is linear, a proportional change in calcification should be expressed much more strongly in the Sr/Ca ratio of large species with rapid calcite production than in smaller species, which produce calcite more slowly. Consequently, it may be possible to separate temperature and calcification influences on coccolith Sr/Ca by separately analyzing Sr/Ca in species that produce calcite rapidly and those that produce calcite slowly, if both undergo comparable relative changes in calcification rates.     

The Herschel PACS photometer calibration

We present a flux calibration scheme for the PACS chopped point-source photometry observing mode based on the photometry of five stellar standard sources. This mode was used for science observations only early in the mission. Later, it was only used for pointing and flux calibration measurements. Its calibration turns this type of observation into fully validated data products in the Herschel Science Archive. Systematic differences in calibration with regard to the principal photometer observation mode, the scan map, are derived and amount to 5 ? 6 %. An empirical method to calibrate out an apparent response drift during the first 300 Operational Days is presented. The relative photometric calibration accuracy (repeatability) is as good as 1 % in the blue and green band and up to 5 % in the red band. Like for the scan map mode, inconsistencies among the stellar calibration models become visible and amount to 2 % for the five standard stars used. The absolute calibration accuracy is therefore mainly limited by the model uncertainty, which is 5 % for all three bands.     

Influence of atmospheric inputs on the iron distribution in the subtropical North-East Atlantic Ocean

Aerosol (soluble and total) iron and water-column dissolved (DFe, < 0.2 μm) and total dissolvable (TDFe, unfiltered) iron concentrations were determined in the Canary Basin and along a transect towards the Strait of Gibraltar, in order to sample across the Saharan dust plume. Cumulative dust deposition fluxes estimated from direct aerosol sampling during our one-month cruise are representative of the estimated deposition fluxes based on near surface water dissolved aluminium concentrations measured on board. Iron inventories in near surface waters combined with flux estimates confirmed the relatively short residence time of DFe in waters influenced by the Saharan dust plume (6–14 months). Enhanced near surface water concentrations of DFe (5.90–6.99 nM) were observed at the Strait of Gibraltar mainly due to inputs from metal-rich rivers. In the Canary Basin and the transect towards Gibraltar, DFe concentrations (0.07–0.76 nM) were typical of concentrations observed in the surface North Atlantic Waters, with the highest concentrations associated with higher atmospheric inputs in the Canary Basin. Depth profiles showed that DFe and TDFe were influenced by atmospheric inputs in this area with an accumulation of aeolian Fe in the surface waters. The sub-surface minimum of both DFe and TDFe suggests that a simple partitioning between dissolved and particulate Fe is not obvious there and that export may occur for both phases. At depths of around 1000–1300 m, both regeneration and Meddies may explain the observed maximum. Our data suggest that, in deep waters, higher particle concentrations likely due to dust storms may increase the scavenging flux and thus decrease DFe concentrations in deep waters.