USGS Science⌕ Search

Geology topics

J. L. Allen

Publications and source records attributed to J. L. Allen.

At least 19 recordsLinked to original sources
USGS2020

Gas chromatographic separation and quantitative estimation of barbiturate mixtures in solid dosage forms

A gas chromatographic method has been described for the analysis of mixed barbiturates in solid dosage forms. Analysis on a 10% SE-30 column gave good separations for butabarbital, amobarbital, secobarbital, pentobarbital, and/or phenobarbital; amobarbital is not separated adequately from pentobarbital. An internal standard, mephobarbital, is used to minimize injection errors. The method gives both good quantitative and qualitative results on the barbiturates investigated. Two synthetic tablet mixtures were analyzed by this procedure and recoveries were 98—103%. It is recommended that the method be subjected to collaborative study.

Journal of the Association of Official Analytical ↗
USGS2020

GLC determination of quinaldine residue in fish

A procedure for the determination of quinaldine residue in various fish tissues is described. Homogenized tissues are extracted with hexane-ethyl ether, the extracts are concentrated by partitioning through 0.1N sulfuric acid, and the residues are measured by alkali flame ionization gas chromatography. Muscle tissues containing from 0.01 to 10.0 ppm quinaldine were successfully analyzed with recoveries from 75 to 100%.

Journal of the Association of Official Analytical ↗
USGS2020

UV identification and quantitative measurement of quinaldine residues in fish

A method for the confirmatory analysis of quinaldine residue in fish is described. The method utilizes the same extraction and cleanup procedure as the GLC method reported previously. The lower limit of sensitivity for quinaldine residue in fish muscle is 0.01 ppm. Identification is accomplished by comparing the UV spectra of the sample and a standard solution of quinaldine.

Journal of the Association of Official Analytical ↗
USGS2020

Liquid-chromatographic determination of rotenone in fish, crayfish, mussels, and sediments

An analytical procedure is described for determining residues of rotenone in fish muscle, fish offal, crayfish, freshwater mussels, and bottom sediments. Tissue samples were extracted with ethyl ether and extracts were cleaned up by gel permeation chromatography and silica gel chromatography. Sediment samples were extracted with methanol, acidified, partitioned into hexane, and cleaned up on a silica gel column. Rotenone residues were quantitated by liquid chromatography, using ultraviolet (295 nm) detection. Recoveries from sediment samples fortified with rotenone at 0.3 μg/g were 80.8%, whereas recoveries from tissue samples fortified with 0.1 μg/g ranged from 87.7 to 96.8%. Samples fortified with 0.3 μg/g and stored at - 10°C for 6 months before analysis had recoveries ranging from 83.2 to 90.5%. Limits of detection were 0.025 μg/g for sediments and 0.005 μg/g for tissue samples.

Journal of the Association of Official Analytical ↗
USGS2020

Determination of malachite green and its leuco form in water

Liquid chromatographic (LC) analysis can detect malachite green residues in water at less than 10µg/L. Water samples were concentrated on disposable diol columns, eluted with 0.05M p-toluenesulfonic acid in methanol, and determined by reversed- phase LC. When combined with a lead oxide postcolumn reactor, the LC method can simultaneously determine both leuco and chromatic forms of malachite green. Recoveries averaged 95.4% for the chromatic form and 57.3% for the leuco form of malachite green oxalate and leuco malachite green in spiked pond water samples. Recoveries of the carbinol form of malachite green (an equilibrium product of the dye in water) from spiked tap water samples averaged 98.6%. Recoveries of leuco malachite green were low and pH-dependent.

Journal of AOAC International↗
USGS2009

Metabolism and elimination of benzocaine by rainbow-trout, Oncorhynchus mykiss

1. Branchial and urinary elimination of benzocaine residues was evaluated in adult rainbow trout, oncorhynchus mykiss, given a single dorsal aortic dose of c-14-benzocaine hydrochloride.^2. Branchial elimination of benzocaine residues was rapid and accounted for 59.2% Of the dose during the first 3 h after dosing. Renal elimination of radioactivity was considerably slower; the kidney excreted 2.7% Dose within 3 h and 9.0% Within 24 h. Gallbladder bile contained 2.0% Dose 24 h after injection.^3. Of the radioactivity in radiochromatograms from water taken 3 min after injection, 87.3% Was benzocaine and 12.7% Was n-acetylated benzocaine. After 60 min, 32.7% Was benzocaine and 67.3% Was n-acetylated benzocaine.^4. Of the radioactivity in radiochromatograms from urine taken 1 h after dosing, 7.6% Was para-aminobenzoic acid, 59.7% Was n-acetylated para-aminobenzoic acid, 19.5% Was benzocaine, and 8.0% Was n-acetylated benzocaine. The proportion of the radioactivity in urine changed with time so that by 20 h, 1.0% Was para-aminobenzoic acid and 96.6% Was n-acetylated para-aminobenzoic acid.^5. Benzocaine and a more hydrophobic metabolite, n-acetylated benzocaine, were eliminated primarily through the gills; renal and biliary pathways were less significant elimination routes for benzocaine residues.

Xenobiotica↗
USGS2006

Renal excretion in channel catfish following injection of quinaldine sulphate or 3-trifluoromethyl-4-nitrophenol

Channel catfish, Ictalurus punctatus Rafinesque, injected intraperitoneally with 2-methyl-quinoline sulphate (QdSO 4 ) or 3-trifluoromethyl-4-nitrophenol (TFM) eliminate most of the dose of these compounds by extra-renal routes. Patterns of renal excretion of Na + , K + , Ca 2+ , Mg 2+ , and Cl - (pEq kg -1 h -1 ) appeared to be associated with the 'stress' of the urine collection technique rather than with the elimination of either compound. Concentrations of Na + , K + , Ca 2+ , Mg 2+ , and Cl - (mEq/1) were determined in urine, plasma and gall bladder bile.

Journal of Fish Biology↗
USGS2006

Stand and landscape level effects of a major outbreak of spruce beetles on forest vegetation in the Copper River Basin, Alaska

From 1989 to 2003, a widespread outbreak of spruce beetles (Dendroctonus rufipennis) in the Copper River Basin, Alaska, infested over 275,000 ha of forests in the region. During 1997 and 1998, we measured forest vegetation structure and composition on one hundred and thirty-six 20-m ?? 20-m plots to assess both the immediate stand and landscape level effects of the spruce beetle infestation. A photo-interpreted vegetation and infestation map was produced using color-infrared aerial photography at a scale of 1:40,000. We used linear regression to quantify the effects of the outbreak on forest structure and composition. White spruce (Picea glauca) canopy cover and basal area of medium-to-large trees [???15 cm diameter-at-breast height (1.3 m, dbh)] were reduced linearly as the number of trees attacked by spruce beetles increased. Black spruce (Picea mariana) and small diameter white spruce (<15 cm dbh) were infrequently attacked and killed by spruce beetles. This selective attack of mature white spruce reduced structural complexity of stands to earlier stages of succession and caused mixed tree species stands to lose their white spruce and become more homogeneous in overstory composition. Using the resulting regressions, we developed a transition matrix to describe changes in vegetation types under varying levels of spruce beetle infestations, and applied the model to the vegetation map. Prior to the outbreak, our study area was composed primarily of stands of mixed white and black spruce (29% of area) and pure white spruce (25%). However, the selective attack on white spruce caused many of these stands to transition to black spruce dominated stands (73% increase in area) or shrublands (26% increase in area). The post-infestation landscape was thereby composed of more even distributions of shrubland and white, black, and mixed spruce communities (17-22% of study area). Changes in the cover and composition of understory vegetation were less evident in this study. However, stands with the highest mortality due to spruce beetles had the lowest densities of white spruce seedlings suggesting a longer forest regeneration time without an increase in seedling germination, growth, or survival. ?? 2006 Elsevier B.V. All rights reserved.

Forest Ecology and Management↗
USGS2002

Residues of isobornyl thiocyanoacetate (Thanite) and a metabolite in fish and treated ponds

Isobornyl thiocyanoacetate (Thanite) is an insecticide that induces a surfacing response in fish and therefore has been considered to have potential as a fish collection agent. Analyses for residues of Thanite in carp (Cyprinus carpio) and largemouth bass (Micropterus salmoides) exposed to chemical yielded only a trace of the parent compound. A metabolite, isobornyl a-(methylthio)acetate, was isolated and indentified by GC-MS,and a reference standard for the metabolite was synthesized. Residues of the metabolite were present in largemouth bass muscle tissue within 1 h after exposure to Thanite. The metabolite was also observed in the muscle, blood plasma, and bile of carp. Residues of the metaboliteare rapidly elimanated after the fish are transferred to Thanite-free water. Residues of Thanite in water, algae, and from soil from ponds treated with Thanite declined to undetectable levels within 28 days after treatment.

Journal of Agricultural and Food Chemistry↗
USGS1996

Uptake, tissue distribution, and metabolism of malachite green in the channel catfish (Ictalurus punctatus)

The disposition of malachite green was determined in channel catfish ( Ictalurus punctatus ) after intravascular dosing (0.8 mg . Kg -1 ) or waterborne exposure (0.8 mg . L -1 for 1 h). After intravascular dosing, mean plasma concentrations of the parent compound exhibited a triphasic decline with a terminal elimination half-life of 6.2 h. Malachite green was rapidly absorbed and concentrated in the tissues during waterborne exposure. The rate of accumulation was directly related to pH of the exposure water. After waterborne exposure, elimination of the parent compound from plasma also was triphasic with a terminal half-life of 4.7 h. In muscle, the half-life of the parent compound was approximately 67 h. Malachite green and its metabolites were widely distributed in all tissues. In fish exposed to C-14-labeled malachite green, total drug equivalent concentrations were highest in abdominal fat and lowest in plasma. Malachite green was rapidly and extensively metabolized to its reduced form, leucomalachite green, which was slowly eliminated from the tissues. Leucomalachite green is an appropriate target analyte for monitoring exposure of channel catfish to this drug.

Canadian Journal of Fisheries and Aquatic Sciences↗
USGS1991

Post-column reaction for simultaneous analysis of chromatic and leuco forms of malachite green and crystal violet by high-performance liquid chromatography with photometric detection

The chromatic and leuco forms of malachite green and crystal violet were readily separated and detected by a sensitive and selective high-performance liquid chromatographic procedure. The chromatic and leuco forms of the dyes were separated within 11 min on a C 18 column with a mobile phase of 0.05 M sodium acetate and 0.05 M acetic acid in water (19%) and methanol (81%). A reaction chamber, containing 10% PbO 2 in Celite 545, was placed between the column and the spectrophotometric detector to oxidize the leuco forms of the dyes to their chromatic forms. Chromatic and leuco malachite green were quantified by their absorbance at 618 nm; and chromatic and leuco Crystal Violet by their absorbance at 588 nm. Detection limits for chromatic and leuco forms of both dyes ranged from 0.12 to 0.28 ng. A linear range of 1 to 100 ng was established for both forms of the dyes.

Journal of Chromatography↗
USGS1988

Residues of benzocaine in rainbow trout, largemouth bass, and fish meal

Residues of the anesthetic benzocaine in muscle tissue of rainbow trout ( Salmo gairdneri ) and largemouth bass ( Micropterus salmoides ) were determined after exposure of the fish to 50 mg benzocaine/L for 15 min and withdrawal times of 0–24 h. The mean concentration of benzocaine residues in fish sampled immediately after exposure was 14.0 μg/g in rainbow trout and 10.6 μg/g in largemouth bass. Residues were below the control value after 8 h of withdrawal in largemouth bass and near the control value after 4 h of withdrawal in rainbow trout. Although residues of benzocaine were high in fish immediately after exposure, the concentration declined rapidly when the fish were held in flowing fresh water. Fish meal prepared from Pacific salmon ( Oncorhynchus sp.) that had been anesthetized with benzocaine or trieaine (MS‐222) contained residues of 45.1 μg benzocaine/g or 47.7 μg trieaine/g.

Progressive Fish-Culturist↗
USGS1987

Elimination of super(14)C-bisazir residues in adult sea lamprey (Petromyzon marinus)

Bisazir (P.P-bis(1-aziridinyl)-N-methylphosphinothioic amide), a chemosterilant, was administered to sea lampreys (Petromyzon marinus ) by intraperitoneal injection of 100 mg/kg or by immersion for 2 h in a 100- mg/L aqueous solution of the chemical. Whole body analysis of the injected lampreys showed that total residue concentrations decreased to 4.65 in males and 10.07 in females during the first day after injection, and to 1.46 in males and 3.74 in females after 10 days of withdrawal. Lampreys exposed by bath immersion contained residues of about 25 mu g/g of tissue immediately after exposure. The concentration ( mu g/g) decreased to 1.02 in males and 2.11 in females after 1 day of withdrawal and to 0.51 in males and 0.85 in females after 10 days.

Technical Report↗