Sea surface ichthyoplankton off southeastern New Zealand,summer 1977–78

Plankton samples from the Chatham Rise, Pukaki Rise, and Campbell Plateau provided information on the young stages of a number of poorly known New Zealand fish species, and on the presence of a large spawning area of barracouta, Thyrsites atun, over the Mernoo Bank, The Chatham Rise was more important as a spawning area than the areas further south.     

Comparing an estimate of seabirds at risk to a mortality estimate from the November 2004 Terra Nova FPSO oil spill

On 21 November 2004, about 1000 barrels of crude oil were accidentally released from the Terra Nova FPSO (floating production, storage and offloading) onto the Grand Banks, approximately 340 km east-southeast of St. John's, Newfoundland. We estimated the number of vulnerable seabirds (murres (Uria spp.) and dovekies (Alle alle)) at risk from this incident by multiplying observed densities of seabirds with the total area covered by the slick, estimated at 793 km(2). A mean density of 3.46 murres/km(2) and 1.07 dovekies/km(2) on the sea surface was recorded during vessel-based surveys on 28 and 29 November 2004, with a mean density of 6.90 murres/km(2) and 13.43 dovekies/km(2) combining those on the sea and in flight. We calculated a mean of 9858 murres and dovekies were at risk of being oiled, with estimates ranging from 3593 to 16,122 depending on what portion of birds in flight were assumed to be at risk. A mortality model based on spill volume was derived independently of the risk model, and estimated that 4688 (CI 95%: 1905-12,480) birds were killed during this incident. A low mortality estimate based strictly on spill volume would be expected for this incident, which occurred in an area of relatively high seabird densities. Given that the risk and mortality estimates are statistically indistinguishable, we estimate that on the order of 10,000 birds were killed by the Terra Nova spill.     

Dust transport near electron beam impact and shadow boundaries

When the moon enters the plasma sheet of the earth, high energy electron fluxes are incident upon the lunar surface. Some regions are in the shadow of these fluxes due to topographic features. Large electric fields were found at similar shadow boundaries created by the electron beams incident upon an obstacle in the laboratory. Potentials on the beam-illuminated surface follow beam energies and were negative relative to potentials on the shadowed surface. Charged dust particles in the beam-illuminated region were observed to move into the shadow due to these electric fields. The oblique incidence of the electron fluxes upon craters can lead to a portion of the crater surface in the beam-illumination and another portion in the shadow. Dust particles on the slopes of the craters can thus experience large electric fields and transport downhill to fill the bottom of the craters. This mechanism may contribute to the formation of dust ponds observed by the NEAR-Shoemaker spacecraft at Eros, and might be at work on the lunar surface as well. In the laboratory, we used electron fluxes with energies up to 90 eV to bombard an insulating half-pipe. An angle of incidence was chosen so that the impact occurred on farside of the slope and left the bottom and the nearside slope in the shadow. Dust particles on the beam-illuminated slope moved down along the surface toward the bottom of the half-pipe and hopped to the bottom as well, while particles on the shadowed slope remained at rest.     

DXL: a sounding rocket mission for the study of solar wind charge exchange and local hot bubble X-ray emission

The Diffuse X-rays from the Local galaxy (DXL) mission is an approved sounding rocket project with a first launch scheduled around December 2012. Its goal is to identify and separate the X-ray emission generated by solar wind charge exchange from that of the local hot bubble to improve our understanding of both. With 1,000 cm² proportional counters and grasp of about 10 cm² sr both in the 1/4 and 3/4 keV bands, DXL will achieve in a 5-min flight what cannot be achieved by current and future X-ray satellites.     

Iron oxides in comet 81P/Wild 2

Abstract– We have used synchrotron Fe‐XANES, XRS, microRaman, and SEM‐TEM analyses of Stardust track 41 slice and track 121 terminal area slices to identify Fe oxide (magnetite‐hematite and amorphous oxide), Fe‐Ti oxide, and V‐rich chromite (Fe‐Cr‐V‐Ti‐Mn oxide) grains ranging in size from 200 nm to ～10 μm. They co‐exist with relict FeNi metal. Both Fe‐XANES and microRaman analyses suggest that the FeNi metal and magnetite (Fe₂O₃FeO) also contain some hematite (Fe₂O₃). The FeNi has been partially oxidized (probably during capture), but on the basis of our experimental work with a light‐gas gun and microRaman analyses, we believe that some of the magnetite‐hematite mixtures may have originated on Wild 2. The terminal samples from track 121 also contain traces of sulfide and Mg‐rich silicate minerals. Our results show an unequilibrated mixture of reduced and oxidized Fe‐bearing minerals in the Wild 2 samples in an analogous way to mineral assemblages seen in carbonaceous chondrites and interplanetary dust particles. The samples contain some evidence for terrestrial contamination, for example, occasional Zn‐bearing grains and amorphous Fe oxide in track 121 for which evidence of a cometary origin is lacking.     

A computational chemical study of penetration and displacement of water films near mineral surfaces

A series of molecular dynamics simulations have been performed on organic–water mixtures near mineral surfaces. These simulations show that, in contrast to apolar compounds, small polar organic compounds such as phenols can penetrate through thin water films to adsorb on these mineral surfaces. Furthermore, additional simulations involving demixing of an organic–water mixture near a surfactant-covered mineral surface demonstrate that even low concentrations of adsorbed polar compounds can induce major changes in mineral surface wettability, allowing sorption of apolar molecules. This strongly supports a two-stage adsorption mechanism for organic solutes, involving initial migration of small polar organic molecules to the mineral surface followed by water film displacement due to co-adsorption of the more apolar organic compounds, thus converting an initial water-wet mineral system to an organic-covered surface. This has profound implications for studies of petroleum reservoir diagenesis and wettability changes.