Nitrogen and calcium nutrition of Petunia × hybrida ‘Coral Sea’

The effects of N and Ca nutrition on plant growth and shoot elemental content of Petunia × hybrida Hort. Vilm. - Andr. ‘Coral Sea’ were evaluated. Nitrogen and Ca were applied separately or in combination in three experiments: (1) N at 0, 100, 200 or 400 mg l^?1; (2) Ca at 0, 75, 150 or 300 mg l^?1; (3) N at 0 or 100 mg l^?1 and Ca at 0 or 150 mg l^?1 combined factorially. Shoot and root dry weights, branch length and flower number were highest when plants received 100 mg l^?1 N. Plants treated with 150 mg l^?1 Ca had the highest shoot and root dry weights. Branch length was maximal at 300 mg l^?1 Ca.Nitrogen and Ca interacted to increase shoot dry weights, branch number and length, leaf area and flower number. Increasing N concentrations increased N and decreased P, Mn and Zn shoot contents. Calcium content of shoots increased while N, P and Mg decreased in response to increasing applications of Ca to petunia plants. Minimal N and Ca tissue concentrations for optimal P. × hybrida growth were 3.3 and 0.67%, respectively.     

In vitro metabolism of ovarian steroids by bovine whole blood and plasma

Experiments were conducted to evaluate the effects of time and temperature on the potential of bovine whole blood (WB) or plasma (PL) to metabolize the ovarian steroids progesterone, estradiol-17β and testosterone. During a radioimmunoassay study (Experiment 1), we observed a temperature and time-dependent reduction (P<0.001) of plasma progesterone concentrations in samples incubated as WB at 5, 15, 25, or 35C for up to 48 hr. Most notable was the observation that 27% of progesterone present in controls was lost when WB was incubated at 5C for 48 hr and a 17% reduction was observed when PL samples were incubated at 35C for 48 hr. Immunoreactive estradiol-17β concentrations (Experiment 2) in PL and WB incubates were not affected by time or temperature. However, immunoreactive testosterone concentrations increased more than 3-fold by 48 hr in WB incubates held at 35C. To examine the latter observation further, ³H-progesteone was incubated with WB at 35C, followed by extraction and thin-layer chromatography (Experiment 3). Results generally supported RIA findings and revealed the presence of significant 17α-hydroxylase, 17–20 lyase and aromatase activity. Heretofore this has not been considered to occur outside major steroid metabolizing organs.     

Swine trichinosis in mid-atlantic slaughterhouses: Possible relationship to hog marketing systems

Digests of diaphragms from 33 482 hogs slaughtered in the mid-atlantic states were examined for the presence of Trichinella spiralis larvae. The samples were obtained from 7 slaughterhouses, ranging in slaughter capacity from less than 50 per day to more than 4000 per day. The sources of the hogs varied from “backyard” operations, raising hogs for home use, to commercial farms. The means by which hogs were brought to the slaughterhouse also differed; the larger slaughterhouses often purchased directly from the producer while the smaller slaughterhouses (1000 hogs per day or less) usually purchased through dealers or brokers. Infected hogs were detected more frequently than was expected from previously-published prevalence studies; overall, 0.58% of samples examined contained T. spiralis larvae. All of the infected hogs were marketed through the smaller slaughterhouses (less than 1000 per day) and nearly all were marketed through brokers. The mean number of larvae per gram of diaphragm, determined by slaugterhouses type, ranged from 0.5 to 74.6; most infections were light although 5 had counts of 1000–2480.Most of the positive samples were obtained from one slaughterhouse, the data from which exhibited marked differences in the frequency of infection by day of the week; 128 positive samples of the total of 190 found were obtained on Fridays, although only 10% of all samples were obtained on that day. Analysis of the geographic origin of shipments containing infected hogs revealed that most originated in New Jersey and Pennsylvania, although the hogs shipped from the latter state might originated in New England or Maryland. Attempts to trace back infected hogs for further epidemiological investigation were largely futile, owing to the absence of an identification system.     

浅谈秋季造林

根据多年各季节效果的总结,论述了采用秋季造林的优点、秋季造林的技术要求及秋季造林方法。     

一款老人助力起身智能马桶研究

研究一款能在现有旧式马桶基础上,通过加装助力起身智能马桶盖,实现助力起身和智能冲洗的结合,简化操作动作,适应老人使用的设备.     

浅谈森林生态用水

当前,研究森林生态功能时,人们较多地关注森林涵养水源功能,即森林对生态建设的贡献,却较少研究培育森林、维系森林生态还需要水分,森林的生存和发展都需要水,森林是水分循环的主要载体.文章阐明森林能涵水、提供水分,同时森林的形成也需要水分这个新理念,并从宏观上提出森林生态用水的策略,与同行探讨.     

Insecticidal activity and microsomal metabolism of biooxidizable lindane analogs

The insecticidal activity of lindane analogs, in which some chlorine atoms were replaced by other groups susceptible to microsomal oxidative metabolism, was determined against mosquitos, house flies, and German cockroaches. When tested with a synergist, piperonyl butoxide, one of the methylthio analogs was as active as lindane, whereas several others were also highly active. By examining the ratio of synergized and unsynergized LD₅₀ values (synergistic ratio value), the highly insecticidal methylthio, methoxy, and methyl analogs appear to undergo metabolic detoxication effectively in house flies. By means of in vitro metabolism experiments using microsomal fraction from house fly abdomen, the methoxy, ethoxy, and methylthio analogs were shown to be metabolized rapidly at similar rates. The synergized insecticidal activities of these compounds against various insect species relate linearly with each other, suggesting that the oxidative degradation is inhibited by the synergist to a similar extent and that the transport process to the site of action is not a limiting factor in determining the relative insecticidal activity.     

The mechanism of resistance to lindane and hexadeuterated lindane in the Third Yumenoshima strain of house fly

The factors which cause lindane resistance in the Third Yumenoshima strain, a strain of house flies highly resistant to insecticides, were studied using hexadeuterated lindane. Hexadeuterated lindane has the same physicochemical properties as lindane, but the former is much less biodegradable than the latter. The LD₅₀ ratio of lindane to hexadeuterated lindane in this strain, deuterium isotope effect on LD₅₀ values, was larger than that in S_NAIDM, a susceptible (nonresistant) strain. The penetration rates of labeled and nonlabeled lindane through the insect cuticle were about the same for both strains. Thus, penetration rate does not cause resistance. The metabolic degradation of lindane in the resistant strain in vivo occurred much faster than in the susceptible strain. This was also the case for lindane degradation processes in vitro such as microsomal oxidation and glutathione conjugation. In both strains, significant isotope effects were observed in the degradation rates in vitro of labeled and nonlabeled lindane. Therefore, principal biodegradation and detoxication pathways should include reactions which cleave the CH bonds. When the much less biodegradable d₆ counterpart of lindane was applied to both strains, the susceptible strain became much more highly intoxicated than the other within 20 to 30 min. This indicates that a combination of both greater degradability and probably lower sensitivity at the action site are the main factors underlying resistance in the Third Yumenoshima strain.     

Effects of herbicides and herbicide analogs on [14C]leucine incorporation by suspension-cultured Solanum nigrum cells

Assays of [¹⁴C]leucine incorporation were used to measure effects of herbicides on suspensioncultured heterotrophic Solanum nigrum cells. Most herbicidal vs. nonherbicidal chemicals in a set of 47 compounds could be distinguished from each other based on their extent of inhibition of leucine incorporation by S. nigrum cells. Herbicides which failed to inhibit leucine incorporation were photosynthetic inhibitors. Both phytotoxic and nonphytotoxic thiocarbamate analogs (as determined by whole-plant studies) tended to inhibit leucine incorporation. It was concluded that the leucine incorporation screen could detect a majority of compounds tested which are herbicidal, and that it may also be useful to detect compounds which have cellular toxicity which is not observed in the whole plant.     

In vitro effects of malathion and O,O,S-trimethyl phosphorothioate on cytotoxic T-lymphocyte responses

Oral administration of O,O,S-trimethyl phosphorothioate (OOS), an impurity present in technical formulations of malathion, has been shown to be associated with a high incidence of pneumonia in rats and to be highly immunosuppressive in mice. Based on these findings, an in vitro model was established to study the effect of this and other organophosphorus compounds on murine cytotoxic T-lymphocyte (CTL) responses. The organophosphorus compounds were tested for their ability to block in vitro generation of CTL responses to alloantigen and/or the expression of these cytotoxic responses. Responses were generated in C57Bl/6 (H-2^b) spleen cells to mitomycin C-blocked P815 (H-2^d) tumor cells. The cytotoxicity of the cultured splenocytes to P815 target was measured using a 4-hr chromium release assay. These data demonstrated that malathion was able to block the ability of splenocytes to sensitize to P815 at concentrations as low as 25 μg/ml, but was not able to block the expression of cytotoxicity by mature killer T cells. The same was true for OOS which had been activated by preincubation with rat liver postmitochondrial supernatant (PMS). Activated OOS blocked the generation of CTL responses at concentrations as low as 75 μg/ml while having no effect on mature cytotoxic cells. In fact, both malathion and activated OOS were no longer able to suppress CTL responses if treatment was performed as early as 24 hr after exposure to antigen. Additionally, it was demonstrated that when malathion was preincubated with PMS it was no longer suppressive and that OOS without activation failed to suppress CTL responses.