Note on the methods for determination of chromic oxide in shrimp feeds.

Chromic oxide is used as an inert marker to measure apparent digestibility of feeds in insects, terrestrial, and aquatic animals. Quantitative determination of chromic oxide content in the sample requires the oxidation of water insoluble trivalent chromic oxide to its water-soluble hexavalent form. The two commonly used oxidizing agents are 70% perchloric acid or a mixture of sodium molybdate, sulfuric, and perchloric acid. Chromic oxide content of the oxidized solution is then measured against known standards either directly by spectrophotometry in the visible range at 350, 370, or 440 nm or after forming a colored complex with diphenylcarbazide (DPC) by colorimetry at 540 nm. This study compared the two methods of oxidation followed by spectrophotometry at the three wavelengths and by DPC colorimetry. DPC colorimetry gave precise results than the direct measurement of dichromate ion, irrespective of the method of oxidation used. Ash from samples oxidized by perchloric acid and quantified by DPC colorimetry gave a better measure of actual chromic oxide content as compared to the other methods tested.     

Genetic manipulation for enhancing calcium content in potato tuber

Increased calcium (Ca) in potatoes may increase the production rate by enhancing tuber quality and storability. Additionally, increased Ca levels in important agricultural crops may help ameliorate the incidence of osteoporosis. However, the capacity to alter Ca levels in potato tubers through genetic manipulations has not been previously addressed. Here we demonstrate that potato tubers expressing the Arabidopsis H+/Ca2+ transporter sCAX1 (N-terminal autoinhibitory domain truncated version of CAtion eXchanger 1) contain up to 3-fold more Ca than wild-type tubers. The increased Ca appears to be distributed throughout the tuber. The sCAX1-expressing potatoes have normally undergone the tuber/plant/tuber cycle for three generations; the trait appeared stable through successive generations. The expression of sCAX1 does not appear to alter potato growth and development. Furthermore, increased Ca levels in sCAX1-expressing tubers do not appear to alter tuber morphology or yield. Given the preponderance of potato consumption worldwide, these transgenic plants may be a means of marginally increasing Ca intake levels in the population. To our knowledge, this study represents the first attempts to use biotechnology to increase the Ca content of potatoes.     

Rabbiteye blueberry plant response to nitrogen and phosphorus

Acid, sandy soils selected for blueberry production are usually deficient in plant available phosphorus. Fertilizer addition at planting has not been a recommended practice. This research was designed to evaluate potted blueberry (Vaccinium ashei Reade) plant growth response to P applied at establishment and interacted with N applied during the growing season. Four liter containerized ‘Tifblue’ rabbiteye blueberry plants were transplanted into 4.4 kg of 1:1 v/v loamy sand:peat mixture in an 8‐liter container. Preplant P was incorporated into the mixture at 0, 20, 40, 60, and 80 kg/ha rates. Nitrogen was split‐applied post‐plant four times at 60‐day intervals beginning 30 days after blueberry bushes were transplanted. Total N rates were equivalent to 0, 112, 224, or 336 kg/ha. Plants were harvested 270 days after transplanting. Phosphorus at the 60 and 80 kg/ha rates increased plant growth 40 and 31%, respectively. Plant growth responded linearly to increasing N rate. Leaf and stem weight increases contributed to this linear response while root weight was not affected by fertilizer N. Total plant dry weight was increased by N rates at the 60 and 80 kg/ha P levels. Phosphorus applications increased leaf P levels, but did not increase soil test P. Leaf redness, caused by cool temperatures, was reduced by high N rates. The optimum P rate for fertilization of the soilrpeat mixture in the planting hole under conditions of this experiment was the equivalent of 60 kg/ha.     

Atmospheric mercury concentrations above mercury contaminated mill tailings in the Carson River Drainage Basin,NV

During processing of the historic Comstock Ore, Virginia City, NV, an estimated 5.5 × 10⁹ g of metallic mercury (Hg) were released into the Carson River Drainage Basin. The Bessels Mill site is one of at least 75 locations where Hg was used to amalgamate the gold and silver from the ore. Although the mill is no longer standing, Hg contaminated tailings attest to its past location. Mercury concentrations in samples of tailings from the Bessels Mill site are as high as 1570 μg/g. Mercury concentrations vary spatially over the site. Total Hg concentrations in air measured directly over the site are well above regional background levels (1 to 7.1 ng/m³). The highest average atmospheric Hg concentration measured at the site was 240 ng/m³ for October 1993. The estimated range of Hg flux to the atmosphere from the site was 37 to 500 ng/m² hr. Atmospheric Hg concentrations varied seasonally, diurnally and spatially. Atmospheric Hg concentrations varied as a function of Hg concentration, soil and air temperature, wind speed and surface morphology.     

Genetic relationships within Vigna unguiculata (L.) Walp. based on isozyme analyses

Summary Isozyme analyses of genetic diversity in Vigna unguiculata were performed to determine genetic relationships and level of genetic diversity between wild and cultivated cowpea. Thirty-four cultivated accessions of V. unguiculata, 56 wild accessions of V. unguiculata, and six accessions representing five related wild Vigna species were analyzed. Ten enzyme systems were polymorphic within Vigna unguiculata: AAT, ACO, G6PDH, DIAP, LAP, MUE, ME MDH, PRX, and SOD. Fourteen of 24 putative loci (58%) were polymorphic within wild V. unguiculata, but only one locus (4%) was polymorphic within cultivated cowpea; when five related Vigna species were examined, 21 of the 24 bands of activity showed polymorphisms (88%) adding 33 alleles to the 48 identified within V. unguiculata. In one F₂ population of 68 plants (UCDVg 36 × UCDVg 21) a loose linkage was indicated between Diap-2 and G6pd-1 (² = 15.39; p = 0.004) with an estimated distance of 36.0 cM ± 5.02 (recombination (r) = 0.31). Also in another F₂ population of 38 plants (CB 88 × UCDVg 21) a loose linkage was indicated between Lap-1 and Prx (\gC² = 9.62; p = 0.047) with an estimated distance of 39.8 cM ± 7.0 (r = 0.33). Total genetic diversity (H_T) was 0.085 over all of the accessions including the one classified as V. nervosa. Within accession diversity (H_s) approached zero and between accession diversity (D_si) was responsible for all of the genetic diversity present. Therefore the coefficient of gene differentiation (G_ST = D_STII_T) approached 1. Absolute gene differentiation (D_m) was 0.087. Two of the nine segregations in this study were skewed. In general, results of this study concurred with the taxonomic classification within V. unguiculata and provided a strong indication that a severe genetic bottleneck occurred during the domestication process of cowpea.Abbreviations AAT aspartate amino-transferase - ACO aconitase - ALD aldolase - AUS Australia - BDI Burundi - BWA Botswana - CHN China - CMR Cameroon - DIAP diaphorase - DZA Algeria - ETH Ethiopia - G6PDH glucose-6-phosphate dehydrogenase - GDH glutamate dehydrogenase - GHA Ghana - GUY Guyana - IDH isocitrate dehydrogenase - IND India - KEN Kenya - LAO Laos - LAP leucine aminopeptidase - MDH malate dehydrogenase - ME malic enzyme - MEX Mexico - MOZ Mozambique - MUE methylumelliferyl-esterase - MWI Malawi - MYS Malaysia - NER Niger - NGA Nigeria - PRX peroxidase - RBSC ribulose-bisphosphate carboxylase - SEN Senegal - SLE Sierra Leone - SOD superoxide dismutase - TGO Togo - TZA Tanzania - USA United States of America - XDH xanthine dehydrogenase - ZAF South Africa - ZAR Zaire - ZIM Zimbabwe - ZMB Zambia     

The effect of footrot on body weight and wool growth of sheep

Body weight and traits associated with production of wool were measured over a 2-year period between 1985 and 1987 in south-western New South Wales in a flock of Merino wethers experimentally infected with footrot. The disease was allowed to spread freely amongst 150 of the flock but kept at very low prevalence in the remaining 50 by preventive footbathing during transmission periods. Severe, underrunning footrot had a significant adverse effect on body weight, for each year of the trial. Body weight was most severely reduced at times of the year when footrot was spreading among animals and lesions were severe. The mean body weight of the infected group at the end of the 2 years of observation was 7.3 kg (11.6%) below that of the control group. Footrot also depressed wool growth, with the mean clean fleece weight of the infected group being 0.4 kg (8%) lighter than that of the controls at each of the 2 annual shearings. There were no consistent differences between the groups for the other wool characteristics measured.