The biological half life and distribution of 125Iodide and radioiodinated protein in the imported fire ant, Solenopsis invicta

The radioisotope ¹²⁵Iodide, a gamma emittor, was used in two different forms, as ¹²⁵I mixed with egg yolk and as ¹²⁵I covalently attached to egg albumin and mixed with egg yolk, to study food flow in the imported fire ant, Solenopsis invicta Buren. The biological half life of ¹²⁵I-albumin in egg yolk powder was determined to be 96 hr in isolated workers, 108 hr in individuals held with small groups of unlabelled workers, and 1,008 hr in workers held in colonies exposed to labelled food for 48 hr. In contrast, the biological half life of free ¹²⁵I mixed with egg yolk powder was 22 hr, 20 hr, and 40 hr, respectively.The internal distribution of radioactivity was checked after 24,48, and 380 hr. There was a significant difference in distribution of ¹²⁵I in ants fed either free ¹²⁵I or ¹²⁵I-albumin. Most of the free ¹²⁵I was rapidly excreted. A high percentage of ¹²⁵I-albumin was assimilated, apparently through protein digestion pathways with eventual storage in or below the cuticle. There was no evidence of gland involvement in food flow to either larvae or queens with the radio-iodinated protein.

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Résumé L'utilisation de l'iode radio-actif (¹²⁵I) a permis d'étudier le cheminement de la nourriture chez Solenopsis invicta Buren (Myrmicinée). Deux formes différentes de l'isotope ont été étudiées. L'iode 125 a été fixé d'une manière covalente à la tyrosine dans l'albumine des oeufs en utilisant la méthode chloramine T pour ioder les protéines. L'albumine marquée a été mangée ensuite à du jaune d'oeuf en poudre.La seconde forme contenait de l'iode 125 mélangé au jaune d'oeuf en poudre en absence de tout catalyseur, ce qui empêche la fixation chimique. La demi-vie biologique (T_biol) des deux formes a été déterminée chez des ouvrières isolées, chez des individus gardés avec de petits groupes d'ouvrières non-marquées, et chez des ouvrières gardées dans des colonies exposées à la nourriture radio-active pendant 48 h. La demi-vie biologique de l'albumine marquée était de 96 h, 108 h, et 1.008 h. En contraste, la demi-vie de l'iode 125 était de 22 h, 20 h, et 40 h. L'effet de groupe créé par des échanges répétés de nourriture entre les individus était négligeable avec la nourriture protéique. L'échange répété de nourriture entre les larves et les ouvrières a beaucoup augmenté la demi-vie de l'albumine marquée à I 125. Cet effet n'était pas aussi clair avec l'iode 125 par suite de son élimination rapide.La distribution de la radio-activité a été examinée chez des ouvrières au bout de 24, 48 et 380 h après les avoir nourries avec de l'albumine marquée à I 125 et de l'iode 125. Il y avait une différence considérable de distribution, avec un haut pourcentage d'albumine assimilé, sans doute par les voies de digestion de protéines. Le radio-isotope a été ensuite conservé sous forme d'iode 125 ou d'iodotyrosine, dans (ou sous) la cuticule de l'ensemble du corps. Les fourmis ont rapidement excrété l'iode 125 libre avec 5% de la radioactivité résiduelle après 380 h, peut-être fixée aux protéines cellulaires, et ensuite transportée vers la cuticule. Les différences considérables entre les demi-vies biologiques et la distribution interne de la radioactivité chez les fourmis nourries avec de l'iode 125 ou à l'albumine marquée à I 125, soulignent le danger de croire que le cheminement de la nourriture peut être définitivement étudié en utilisant des radio-isotopes qui ne sont pas fixés chimiquement à la substance étudiée.

     

Ultrastructural observations on the cell surface of the intestinal epithelium of the nematode,Ascaris suum

Summary The intestinal epithelium of Ascaris suum consists of a single layer of tall columnar epithelial cells that rest on a thick basal membrane in contact with the pseudocoelomic cavity. Experiments were conducted on glutaraldehyde-fixed tissue to ascertain the nature of the electronegative charges associated with both the apical microvillar surface and basal membrane.A strong electronegative charge was demonstrated on the microvillar surface and basal membrane with ruthenium red and cationic ferritin staining. The ionic nature of ferritin binding was demonstrated with poly-L-lysine, a polycation that interacts with anionic groups on the membrane and thus blocks the subsequent binding of ferritin. Tissue thus treated was devoid of reaction product. Methylation with diazomethane completely abolished staining. Since the stronger acidic groups of sulfates or phosphates would not be protonated under the conditions employed in this study, and therefore susceptible to methylation, staining by ferritin is thought to be due to its interaction with carboxyl groups. Prior enzymatic treatment of tissue with neuraminidase or phospholipase C had no effect on subsequent ferritin binding. Tissue exposed to colloidal iron at various pH values showed maximal reactivity at a pH of 2.5 or above. Above pH 2.5, the dissociation of protons from free carboxyl groups of protein-bound amino-acid residues with pK's of 3.8 and 4.2 would be maximal, and the ionized carboxyl groups are then available to interact with iron micelles. These results suggest the presence of weaker acidic groups, such as the carboxyl groups of acidic amino acids or uronic acid residues. The stronger acidic groups of sialic acid and the esterified sulfate groups, if present, contribute only minimally to overall staining. These results demonstrate that a high electronegative charge density exists, despite the apparent lack of sialic acid. Staining is believed to be due to carboxyl groups of acidic amino acids and/or carboxyl groups or uronic acid residues.Part of this work was conducted at the Department of Zoology, Louisiana State University, Baton Rouge, Louisiana     

DIFFERENTIAL ENRICHMENT OF CELLS FROM EMBRYONIC RAT CEREBRA BY CENTRIFUGAL ELUTRIATION

—Centrifugal elutriation was used to obtain different populations of cells dissociated from 16-day-old rat embryo cerebra. The cell populations recovered were viable and could be maintained for several weeks in vitro. Sterile conditions were maintained throughout a preparation. Rat pups were removed by Caesarean section, the cerebra dissected and the cells dissociated by brief exposure to trypsin (0.125%, 6 min). An equivalent volume of elutriation medium (Dulbecco's medium containing 1% fetal calf serum, sodium bicarbonate, penicillin and streptomycin, EDTA, and deoxyribonuclease) was added to the trypsin-cell suspension, the dissociated cells pelleted, resuspended in elutriation medium and counted. Up to 4 x 10⁸ cells were injected into the previously sterilized elutriator. Seven fractions were usually recovered from a preparation. The first fraction contained primarily red blood cells and cell debris, which could not be maintained in vitro. Upon culture, fraction 2 consisted of predominantly non-neuronal cells, while fractions 3–6 contained neuronal and non-neuronal cells. The morphological characteristics of the neurons differed in these fractions. Fraction 7 contained cells that had reaggregated during the elutriation procedure and exhibited a variety of cell types in vitro.     

Seasonal patterns of CO2 and water vapor exchange of three salt marsh succulents

Summary Diurnal carbon dioxide exchange patterns of three salt marsh succulents, Borrichia frutescens, Batis maritima and Salicornia virginica, were determined on a seasonal basis in the marsh at Sapelo Island, Georgia. Year-round photosynthetic activity was observed in these species though winter rates of CO₂ exchange were reduced. Net primary productivity, estimated using gas exchange techniques, agreed with previously reported harvest data. The role of light and temperature in the control of seasonal photosynthetic changes was investigated. A similar variation in light utilization with season was found in all three species, while seasonal temperature acclimation was species dependent. Less than 20% of fixed CO₂ was lost through dark respiration in any of the species.Water use in the salt marsh succulents was found to be relatively inefficient. High rates of transpiration were observed both summer and winter in the succulents.The succulents were judged to be C₃ plants on the basis of several criteria.Contribution No. 391 from the University of Georgia Marine Institute     

Identifying human cells capable of metabolizing various classes of carcinogens

Human cells that appear capable of metabolizing various classes of carcinogens have been identified using one of two methods: metabolism of tritiated benzo(a)pyrene to aqueous-acetone soluble forms or inhibition of cellular DNA synthesis. Each of the assay systems was optimized and the results on 15 human epithelial cell lines were compared. One or more cell lines were found to activate each of four classes of carcinogens examined: polycyclic hydrocarbons, aromatic amines, heterocyclic hydrocarbons, and nitrosamines. Cells that appeared capable of metabolizing polycyclic hydrocarbons or aromatic amines by these methods were also found to produce metabolites which were cytotoxic to cocultivated human xeroderma pigmentosum fibroblasts after a 48-hr exposure to the carcinogen.     

Lethal white foals in matings of overo spotted horses

Overo is a variable pattern of white coat color spotting which occurs in several breeds of horses in the United States. Occasionally, when overos are crossed inter se white foals are born which die soon after birth. Both intestinal tract abnormalities and isoerythrolysis have been reported in these foals. This report presents data which show that neonatal isoerythrolysis (NI) is not involved in the death of the white foals. Further research is needed to define the nature of the lethal anomaly, as well as the genetics, of overo and lethal white foals.     

The second polar lobe of theSabellaria cementarium embryo plays an inhibitory role in apical tuft formation

Summary The embryo ofSabellaria cementarium (Polychaeta) forms a polar lobe at each of the first two cleavage divisions which becomes absorbed into one of the blastomeres at the end of the division. Lobe removal experiments show that the polar lobe preceding first cleavage is necessary for the development of the apical tuft and the posttrochal region of the trochophore larva. The polar lobe preceding second cleavage is smaller than the first polar lobe and is necessary only for post-trochal region development. In blastomere isolation experiments, isolates containing the C but not the D blastomere form apical tufts. Isolates containing the D but not the C blastomere do not form apical tufts. When the polar lobe preceding second cleavage is removed and the C and D blastomeres are separated and raised in isolation, each can form an apical tuft. When the second cleavage is equalized with sodium dodecyl sulfate (SDS) such that both the C and the D blastomeres receive second polar lobe material, no apical tuft is formed. These results suggest that apical tuft determinants are distributed to both the C and D blastomeres at second cleavage but that the second polar lobe contains an inhibitor for apical tuft formation which is shunted to the D blastomere after the completion of second cleavage.     

The identification of dimethylphenylarsine as a microbial metabolite using a simple method of chemofocusing

Candida humicola acts on benzenearsonic acid to produce dimethylphenylarsine, which was identified by mass spectroscopy following the chemofocusing of the volatile metabolite onto a mercuric chloride impregnated filter. The same technique established that trimethylarsine is the volatile metabolic product obtained from C. humicola treated with 4-NH₂-2-OHC₆H₃AsO(OH)₂ and (CH₃)₃AsO. Arsanilic acid, 4-NH₂C₆H₄AsO(OH)₂, is not metabolized to a volatile arsine.     

Heterochromatin accumulation,disposition and diversity in Gibasis karwinskyana (Commelinaceae)

C-banding differences within Gibasis karwinskyana (Roem & Schult.) Rohw. were reassessed using dual fluorochrome staining. Pronounced differences in C-band pattern between two subspecies with identical basic karyotypes were due to different chromosomal locations of AT-rich and GC-rich heterochromatin. The AT-rich component had an equilocal distribution in the karyotype and has evidently been accumulated at telomeres, as shown by its prevalence in supernumerary segments and B chromosomes. The GC-rich component also varied in amount, but was limited to nucleolus organizing regions (NORs) and centromeres. Centromeres and telomeres are suggested to constitute separate, although perhaps interdependent, centres of heterochromatin amplification. The possible role of nuclear architecture in determining the accumulation, distribution and spread of these sequences is discussed.Abbreviations H Hoechst 33258 - CMA chromomycin A3 - NOR nucleolus organizing region - SS supernumerary segment - Q quinacrine dihydrochloride - H⁺ H etc. indicate enhanced (+) and quenched (-) fluorescence with the stated fluorochrome by H.C. Macgregor