Absorption and translocation of 14C fosamine by three woody plant species

Absorption and translocation of ¹⁴C fosamine (ethyl hydrogen (aminocarbonyl) phosphonate) and/or fosamine metabolites were monitored in intermediately susceptible seedling black cherry (Prunus serotina Ehrh.) and resistant seedling rhododendron (Rhododendron sp.) and magnolia (Magnolia sp.). The mid two-thirds of the third leaf below the apical bud of each plant was treated with 0·5 μCi ¹⁴C fosamine (carbonyl carbon labelled). Plants were harvested 3, 7 and 14 days following treatment. In black cherry the majority of ¹⁴C absorption and translocation occurred during the second week following treatment, while magnolia and rhododendron translocated and absorbed most of the ¹⁴C within 3 days after treatment. Retention of ¹⁴C in the treated portion of the treated leaf did not differ between species. However, total translocated ¹⁴C was greatest in black cherry, less in magnolia, und minimal in rhododendron. Magnolia translocated ¹⁴C basipetally, while black cherry translocated acropetally, as well as basipetally. Absorpiion et migration de la fosamine ¹⁴C chez trois espèces de plantes ligneuses L'absorptlon et la migration de La ¹⁴C fosamine ((amino carbonyl) phosphonate d'éthyle hydrogène) et/ou de ses métabolites, ont étéétudiées chez des plantules moyennement sensibles de Prunus serotina (Ehrh.) et chez des plantules résistantes de rhododendron (Rhododendron sp.) et de magnolia (Magnolia sp). Les deux tiers moyens de la troisième feuille en-dessous du bourgeon apical de chaque plant ont été traités avec 0.5 Ci ¹⁴C de fosamine (marquée sur le carbone du carbonyl). Les plantes ont été récoltées 3, 7 et 14 jours après le traitement. Chez P. serotina, la plus grande partie de l'absorption et de la migration du ¹⁴C a eu lieu durant la deuxième semaine après le traitement, alors que chez le magnolia et le rhododendron, le maximum d'adsorption et de migration s'est situé dans les trois jours qui ont suivi le traitement. La rétention du ¹⁴C dans la partie traitée n'a pas variè d'une espèce à l'autre. Toutefois, la quantité totale de ¹⁴C qui a migré a été plus grande chez P. serotina, moindre chez le magnolia et minimaie chez le rhododendron. Chez le magnolia, la migration du ¹⁴C s'opere dans le sens basipète, alors que chez le P. serotina. elle s'effectue aussi bien dans le sens acropète que dans le sens basipète. Aufnahme- und Trunstokaiion von ¹⁴C-Fosaminc bei drei Gehölzpflanzen Es wurde die Aufnahme und die Translokation von ¹⁴C Fosamine (O-Äthyl-aminocarbonylphosphonsäure) und/oder seiner Abbauprodukte bei drei Gehölzarten beobachtet. Verwendet wurden Sämlinge der Traubenkirsche (Prunus serotina Ehrh.), die eine mittlere Empfindlichkeit zeigt und Sämlinge des resistenten Rhododendron (Rhododendron sp.) und der ebenfalls resistenten Magnolie (Magnolia sp.). Die mittleren zwei Drittel des dritten Blattes unterhalb der Endknospe wurden bei jeder Pflanze mit 0.5 μCi ¹⁴C-Fosamine (markiert am Carbonylkohlenstoff) behandelt. Die Pflanzen wurden nach 3, 7 und 14 Tagen nach der Behandlung geerntet. Bei der Traubenkirsche wurde während der zweiten Woche am meisten ¹⁴C aufgenommen und transloziert, während dies bei der Magnolie und dem Rhododendron bereits innerhalb der ersten drei Tage der Fall war. Bezüglich der Retention von ¹⁴C in der behandelten Blattfläche unterschieden sich die drei Arten nicht. In der Traubenkirsche wurde aber am meisten ¹⁴C transloziert, weniger in der Magnolie und am wenigsten im Rhododendron. Die Magnolie translozierte das ¹⁴C basipetal, während die Traubenkirsche akropetal wie basipetal translozierte.     

Effect of canopy cover,seeding depth,and soil moisture on emergence of Centaurea maculosa and C. diffusa*

The effects of canopy cover, seeding depth, and soil moisture on emergence of Centaurea maculosa Lam. and C. diffusa Lam. were studied. Canopy cover had no effect on ermergence rate (seedlings/day/100 seeds) of either species. Seeds of both species emerged faster when placed on the soil surface. Emergence rate decreased as seeding depth increased. Both species required more than 55% initial soil moisture to initiate emergence, with 65–70% being optimum. Percentage emergence followed exactly the same trend as emergence rate. C. maculosa had better emergence characteristics over a wider range of conditions than C. diffusa, possibly being some of the reasons for the former having a wider geographical distribution in the United States and Canada.     

The use of immunochemically purified anti-brucella antibody in a direct fluorescent antibody test for Brucella abortus

Antibodies specific for Brucella abortus were purified from the serum of hyperimmunized sheep using immunochemical procedures. They were conjugated to fluorescein isothiocyanate and used in a fluorescent antibody (FA) test for B. abortus. The conjugate did not stain any heterologous bacterial or fungal species tested and background fluorescence associated with its use on smears and sections of abortion materials was particularly low. Of 239 cases of abortion examined fluorescent microscopy demonstrated B. abortus in all 12 cases in which the organism was isolated. A few areas of fluorescence typical of B. abortus were also seen in 3 cases from which the organism was not cultured. B. abortus was demonstrated in lymph nodes from 6 of 36 Brucella reactor cows by culture and 7 by the FA test. However, only very low numbers of B. abortus were isolated or seen and sampling errors would have been significant. Use of the FA test allows diagnosis of Brucellosis to be made in 2 hours, compared to 6 days by the usual cultural procedures.     

Precocene II metabolism: Comparative in vivo studies among several species of insects,and structure elucidation of two major metabolites

Several species of insects, exhibiting varying responsiveness to the juvenile hormone antagonist precocene II (6,7-dimethoxy-2,2-dimethylchromene), were challenged topically with a tritiated preparation of the title compound. Metabolism of [³H]precocene II was subsequently examined by withdrawing hemolymph samples from treated animals at appropriate time intervals and characterizing the extractable radiolabel chromatographically. Quantitative (or qualitative) differences observed between the respective metabolic profiles were found not correlative with specimen sensitivity to precocene. Production of two heretofore unreported metabolites, identified by spectral and chemical means as O-β-glucosides of 6- and 7-monodemethylated precocene II, was demonstrated in both sensitive and insensitive species. No evidence for the presence of a hemolymphborne, biologically effective “activated metabolite” produced in vivo by precocene-susceptible insects could be found. The latter finding may well argue for in situ bioactivation of precocene at the target tissue(s) by these sensitive insects.     

Evaluation of reconstitution of immunodeficient mice by partially purified thymic extracts.

Partially purified thymus products were used to evaluate the maturation of T lymphocytes in immunodeficient mice. Three different bovine thymic extracts, designated thymic extracts A, B, and C, were successful in increasing the longevity of conventionally raised nude mice. Daily injection of bovine thymic extracts A, B, and C and mouse thymus extracts failed to mature a population of T lymphocytes and restore the capacity to reject heart allografts. Preincubation of normal syngeneic bone marrow with thymic extract B in vitro before injection into nude mice also failed to reconstitute the host's ability to reject heart grafts. The number of antibody plaque-forming cells of sheep red blood cells in lethally irradiated, bone marrow-reconstituted mice could be increased by preincubating the bone marrow cells with bovine thymic extract fraction B before injection followed by daily injections. A similar but less marked increase in plaque-forming cells was obtained by the daily injection of bovine thymic extract fraction C. Complete functional maturation of T lymphocytes in immunodeficient animals appears to require more than thymic extract stimulation of bone marrow cells or pre-T lymphocytes.