Energy spectra of cosmic ray nuclei: 4≤Z≤26 and 0.3≤E≤2 GeV amu−1

Energy spectra of cosmic ray nuclei in the charge range 5Z26 have been derived from the response of an acrylic plastic erenkov detector. Data were obtained using a balloon-borne detector and cover the energy range 320E2200 MeV amu^–1. Spectra are derived from a formal deconvolution using the method of Lezniak (1975). Relative spectra of different elements are compared by observing the charge ratios. Secondary-primary ratios are observed to decrease with increasing energy, consistent with the effect previously observed at higher energy. Primary-to-primary ratios are constant for 6Z10 and 14Z26 but vary for 10Z14. This data is found to be consistent with existing data, where comparable, and lends strong support to the idea of two separate source populations contributing to the cosmic ray composition.Work supported by University of Maryland Grant NGR 21-002-316.     

Hα coronagraph observations of a flare spray,March 1, 1969

An H solar prominence with the characteristics of a spray was ejected in association with a bright limb flare. Knots of material were observed to a distance of more than one solar radius above the west limb of the Sun. The optical event was followed by 80 MHz emission from a type IV source which was observed moving out through several solar radii.Coronagraph observations have been used to determine the trajectories and velocities of the knots in directions perpendicular to the line of sight. After some early deceleration velocities increase to 300–500 km/sec and slowly decline with variations depending on the initial direction of outflow. We suggest that the magnetic field over the spot group is deformed by the energy of the mass motions of material fragments, some of which then continue to move outward from the Sun.     

Physical and numerical modeling of reflections from interfaces and thin layers

Basic models for understanding the reflection of seismic waves by the seafloor or the sublayering consist of isolated interfaces and isolated thin layers. An isolated interface model is used to demonstrate a reasonable agreement between physical modeling and two numerical solutions of the elastic wave equation. An isolated thin-layer model is used to show that reflections from it can be regarded as a scattered wavefield caused by three secondary sources proportional toDeltaM,-Deltamu, and,Deltarhoat each element of the layer, whereDelta, indicates the difference between the layer and the surroundings,Mis the compressional wave modulus,muis the shear wave modulus, andrhois the density. This viewpoint leads to a simple explanation of the observed variations in amplitude and phase of the reflected waves as the offset distance from source to receiver increases.     

Statistical techniques for the classification of chromites in diamond exploration samples

A database of 1267 quality-screened major- and trace-element analyses of chromites (s.l.) from kimberlites, lamproites, ultramafic lamprophyres (UMLs) and crustal sources (‘greenstones’, including ophiolites, gabbros, basalts and komatiites) has been subjected to statistical analysis, in order to derive discriminants for use in diamond exploration. The techniques used included nearest-neighbour analysis, CART (classification and regression trees) and MARS (multivariate adaptive regression splines). The results show that both CART and MARS approaches can correctly discriminate kimberlite/lamproite chromites from UML/‘greenstone’ chromites at levels near 90%. Discrimination into the four classes separately is achieved at levels of ca. 80% by MARS and > 70% by CART; much of the misclassification is between the kimberlite and lamproite classes. These results probably represent the maximum probable level of discrimination on chemical criteria, given that ascending magmas may sample both mantle and crustal rocks. The CART approach produces a classification tree that requires no further computation to classify a given grain; the MARS approach requires the use of a simple software package. Tests on known samples illustrate the high level of accuracy of the methods in an exploration context, as well as the useful petrogenetic conclusions that can be drawn from some ‘misclassifications’.     

Market access,population density,and socioeconomic development explain diversity and functional group biomass of coral reef fish assemblages

There is overwhelming evidence that many local-scale human activities (e.g. fishing) have a deleterious effect on coral reef fish assemblages. Our understanding of how broad social phenomena (e.g. socioeconomic development) affect the diversity and function of coral reef fish assemblages however, is still poor. Here, we use structural equation models to reveal how human population density, socioeconomic development, and market access affect fishing pressure and coral cover to, in turn, explain the diversity and biomass of key functional groups of reef fish assemblages within Solomon Islands. Fishing pressure is predominantly driven by both market access and local population density, and has a clear negative effect on the diversity and function of coral reef fishes. The strong positive effect of market access on fishing pressure makes clear the importance of understanding social-ecological linkages in the context of increasingly connected societies. This study highlights the need to address broad social phenomena rather than focusing on proximate threats such as fishing pressure, to ensure the continued flow of coral reef goods and services in this time of rapid global social and environmental change.     

Scales of nutrient-limited phytoplankton productivity in Chesapeake Bay

The scales on which phytoplankton biomass vary in response to variable nutrient inputs depend on the nutrient status of the plankton community and on the capacity of consumers to respond to increases in phytoplankton productivity. Overenrichment and associated declines in water quality occur when phytoplankton growth rate becomes nutrient-saturated, the production and consumption of phytoplankton biomass become uncoupled in time and space, and phytoplankton biomass becomes high and varies on scales longer than phytoplankton generation times. In Chesapeake Bay, phytoplankton growth rates appear to be limited by dissolved inorganic phosphorus (DIP) during spring when biomass reaches its annual maximum and by dissolved inorganic nitrogen (DIN) during summer when phytoplankton growth rates are highest. However, despite high inputs of DIN and dissolved silicate (DSi) relative to DIP (molar ratios of N∶P and Si∶P>100), seasonal accumulations of phytoplankton biomass within the salt-intruded-reach of the bay appear to be limited by riverine DIN supply while the magnitude of the spring diatom bloom is governed by DSi supply. Seasonal imbalances between biomass production and consumption lead to massive accumulations of phytoplankton biomass (often>1,000 mg Chl-a m^?2) during spring, to spring-summer oxygen depletion (summer bottom water <20% saturation), and to exceptionally high levels of annual phytoplankton production (>400 g m^?2 yr^?1). Nitrogen-dependent seasonal accumulations of phytoplankton biomass and annual production occur as a consequence of differences in the rates and pathways of nitrogen and phosphorus cycling within the bay and underscore the importance of controlling nitrogen inputs to the mesohaline and lower reaches of the bay.     

Transport of Crustacean Larvae Between a Low-Inflow Estuary and Coastal Waters

The effectiveness of larval behavior in regulating transport between well-mixed, low-inflow estuaries and coastal waters in seasonally arid climates is poorly known. We determined the flux of an assemblage of benthic crustacean larvae relative to physical conditions between a shallow estuary and coastal waters on the upwelling coast of northern California (38°18′N, 123°03′W) from 29 to 31 March 2006. We detected larval behaviors that regulate transport in adjacent coastal waters and other estuaries for only two taxa in the low-inflow estuary, but they were apparent for taxa outside the estuary. Vertical mixing in the shallow estuary may have overwhelmed larvae of some species, or salinity fluctuations may have been too slight to cue tidal vertical migrations. Nevertheless, all larval stages of species that complete development in nearshore coastal waters were present in the estuary, because they remained low in the water column reducing seaward advection or they were readily exchanged between the estuary and open coast by tidal flows. Weak tidal flows and gravitational circulation at the head of the estuary reduced seaward transport during development for species that completed development nearshore, whereas larval release during nocturnal ebb tides enhanced seaward transport for species that develop offshore. Thus, nonselective tidal processes dominated larval transport for most species back and forth between the low-inflow estuary and open coastal waters, whereas in adjacent open coastal waters, larval behavior in the presence of wind-induced shear was more important in regulating migrations between adult and larval habitats along this upwelling coast.