11 research outputs found
A computer program to process data from a direct current plasma emission spectrometer
This program processes data from a Spectraspan IIB spectrometer retrofitted
with a Spectrajet III plasma excitation source (Spectrametrics, Inc .,
Andover, MA). The spectrometer is operated manually and can determine only
one element at a time. Accordingly, the program treats data for each element
individually.
Two of the spectrometer's performance characteristics tend to change
gradually during normal operation: average blank count and analytical
sensitivity. The program compensates for these variations. For the program
to process data from the spectrometer, a reagent blank and a high standard
(in this order) should be aspirated first; then the high standard and blank
(in this order) should be run again after every six or fewer samples .
The program, moreover, causes all data to be converted to logarithmic
form before being used in computation. This makes possible the calculation
of statistically valid confidence limits about predicted analyte concentrations.
The program consists of a main section, DCPEOES, and three external
sub-routines: BASELINE, SENSITIV, and XLNSQFT. BASELINE compensates for
any change in the average blank count, and SENSITIV corrects for any
variation in analytical sensitivity. XLNSQFT governs all correlation and
prediction functions and has two interchangeable versions: one for first-order;
the other for second-order, correlation.Prepared for the United States Department of Energy under
Contract DE A102-81EV10694 and for the National Science
Foundation under Grant OCE 81-19056
The accumulation of barium by marine phytoplankton grown in culture
Marine phytoplankton have been implicated as potentially important vectors for the vertical transport of barium in the oceans. To better assess the extent to which phytoplankton can influence the geochemical cycling of barium, its bioconcentration was studied in 21 clones of 19 species of marine phytoplankters belonging to 9 algal classes. Barium levels in the ash ranged from less than 2 μg g–1 for the coccolithophore Emiliania huxleyi and the red alga Porphyridium cruenturn to 589 μg g–1 for the flagellate Tetraselmis levis. Concentrations ≥4000 μg g–1, previously reported for certain samples of diatom ash were not encountered in this study. Concentration factors on a volume basis (VCF) ranged from 0 to 3.2 × 104; the geometric mean VCF for all species was 225. Diatoms and coccolithophores generally had lower VCFs (geometric means of 90 and 12, respectively) than did other species; dinoflagellates had a geometric mean VCF of 490. Experiments with the diatom Thalassiosira pseudonana indicated that Ba cell–1 increased linearly with ambient Ba concentration. Experiments to localize the site of Ba deposition in diatom cells indicated that most of the Ba was associated with the frustules rather than with the organic fraction. Dinoflagellates and several other algae not only concentrated Ba to relatively high levels, but also accumulated Si when grown in Si-enriched medium, although they grew at least as well without added Si as with it. Ba and Si accumulation were generally negatively correlated
The determination of rare earth elements in marine sediments by ion-exchange separation and ICP emission spectrometry
A method has been developed to measure rare-earth elements (REE) in
gram-sized marine sediment samples. A strong acid digestion technique
followed by ion-exchange chromatography is used to solubilize, separate, and
purify the REE from other matrix components. Instrumental detection is by
inductively coupled plasma-atomic emission spectrometry (ICP-AES). Excellent
precision and accuracy were proved by analyses of unknown sediment replicates
and standard reference rock samples. Blanks and empirically determined
detection limits are discussed in relation to measured REE concentrations in
sediments. Direct evidence is given for the co-precipitation and fractionation
of the REE by precipitates formed as a result of the acid digestion
with HF. A technique for dissolving these is then presented.Funding was provided by the National Science Foundation
under grant Number OCE 84-17910; and the United
States Department of Energy under grant Number
DE-AC02-76EV03566