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At least 19 recordsLinked to original sources

[Effect of nitrogen fertilization and square loss on cotton aphid population, cotton leafhopper population and cotton yield].

The study on the effects of nitrogen fertilization (0-450 kg x hm(-2)) and square loss (0-12 x plant(-1)) on cotton aphid population, cotton leafhopper population and cotton yield showed that there were no significant differences in cotton aphid population, cotton leafhopper population, and numbers of effective bolls between transgenic Bt cotton and non-transgenic cotton. Cotton aphid populations on the two cottons were significantly influenced by nitrogen fertilization and by the interaction of nitrogen fertilization and square loss, while leafhopper populations were not significantly influenced by them. Nitrogen fertilization at squaring and flowering stage was one of important factors affecting cotton yield. There was a positive correlation between the application rate of nitrogen fertilizer and cotton yield, but a negative correlation between the number of lost square per plant and the yield of the two cottons.

Animals↗

Endothelial cell cytotoxicity of cotton bracts tannin and aqueous cotton bracts extract: tannin is the predominant cytotoxin present in aqueous cotton bracts extract.

Using an in vitro cytotoxicity assay based on the release of 51Cr from cultured porcine thoracic aortic and pulmonary arterial endothelial cells, we have demonstrated that cotton bracts tannin is a potent endothelial cell cytotoxin. It produces dose-dependent lethal injury to both types of endothelial cells with the aortic cells being somewhat more sensitive to tannin-mediated injury than the pulmonary arterial cells. Cytotoxic injury to the cells was biphasic. During the first 3 hr of exposure to tannin, no lethal injury was detected. However, during this period, profound changes in morphology were observed suggesting sublethal injury to the cells preceded the ultimate toxic damage. Comparison of the cytotoxicity dose curves for aqueous bracts extracts with those for tannin demonstrated that tannin was the major cytotoxin present in bracts.

Animals↗

[Ultrastructure differences of in vitro cotton fiber and native cotton fiber].

Native cotton fiber and in vitro cotton fiber that was induced from cotton ovule callus by suspension culture were observed using transmission electron microscope and scanning electron microscope. The ovule surface on the first day preanthesis was quite smooth. On the anthesis, it had a lot of protuberances. Two kinds of callus, smooth and rough were found. The microfibrils of callus was vertical to the cell long axis and they changed their orientations with the development of the in vitro cotton fiber: from the vertical to shallow spiral and then to parallel to the cell long axis. So was the native cotton fiber. It suggests that in vitro cotton fiber and native cotton fiber have similar development process. Compared with the ovule surface cell, most callus cells had smaller nuclear. During the development of the fiber, the plasm of native cotton fiber was denser than that of in vitro fiber, and it has more cellular organ than in vitro fiber. The cell wall of native cotton fiber was thicker and denser than that of the in vitro cotton fiber too. It suggests that the physiological activity of in vitro cotton fiber was less active than native cotton fiber.

Cotton Fiber↗

[Response of parasitic wasps of cotton bollworm to different cotton varieties with transgenic Bacillus thringienthsis genes].

The relationship between the parasitic wasp population number of cotton bollworm (Helicoverpa armigera) and the varieties of cotton was studied by releasing and collecting the eggs and larvae of cotton bollworm on transgenic and non-transgenic cottons. The research results from 2000 to 2003 showed that the parasitic rates of the eggs and larvae of cotton bollworm were notably lower in transgenic cotton field than in non-transgenic cotton field. At the same time, the effect of transgenic and non-transgenic cottons on the selection behavior of the parasitic wasp Microplitis mediatar of the larvae of cotton bollworm was studied by using "Y" olfactometer. The results showed that the selection response about the parasitic wasp Microplitis mediatar of cotton bollworm on non-transgenic cotton was prior to the transgenic cotton.

Animals↗

Bollgard II cotton: compositional analysis and feeding studies of cottonseed from insect-protected cotton (Gossypium hirsutum L.) producing the Cry1Ac and Cry2Ab2 proteins.

Bollgard II cotton event 15985 producing the Cry1Ac and Cry2Ab2 proteins has been developed by genetic modification to broaden the spectrum of insects to which the plant is tolerant and to provide an insect resistance management tool to impede the onset of resistance. The purpose of this study was to evaluate the composition and nutrition of Bollgard II cotton, relative to the use for food and animal feed, compared to that of conventional cotton varieties. Compositional analyses were conducted to measure proximate, fiber, amino acid, fatty acid, gossypol, and mineral contents of cottonseed from a total of 14 U.S. field sites over two years. Compositional analysis results showed that the cottonseed and cottonseed oil from Bollgard II cotton were comparable in their composition to those of the conventional control cotton line and other commercial varieties. The composition data are supported by nutritional safety studies conducted with dairy cows, catfish, and quail. Results from these studies showed that Bollgard II performed similarly to the conventional control cotton varieties. These data demonstrate that Bollgard II cotton is compositionally and nutritionally equivalent to conventional cotton varieties. These data support the conclusion that Bollgard II cotton is as safe and nutritious as conventional cotton for food and feed use.

Amino Acids↗

Characterization of airborne cotton dust concentrations in the non-textile cotton industry.

Workers in the "non-textile" cotton industry breathe a dust which is similar to the dust in the cotton spinning and weaving or "textile" industry. This exposure prompts the question of byssinosis prevalence and other respiratory disease in the non-textile cotton industry. NIOSH has completed a cross-sectional medical and environmental study evaluating the prevalence of byssinosis in five segments of the non-textile cotton industry. A total of 92 non-textile cotton facilities were evaluated, including cotton gins, cotton classing offices, cottonseed oil mills, cotton compress-warehouses, and waste utilization plants. This paper presents the results of the measurements of cotton dust levels and particle size distributions in these segments. Average elutriated dust concentrations for individual plants ranged from 101 to 2050 micrograms per cubic meter of air (micrograms/m3) in 35 cotton gins, 81 to 376 micrograms/m3 in 13 classing offices, 502 to 2041 micrograms/m3 in 18 cottonseed oil mills, 39 to 831 micrograms/m3 in 13 compress-warehouses, and 237 to 3968 micrograms/m3 in 13 waste utilization facilities. Results tend to be lower than those reported in the literature for non-textile operations.

Dust↗

Cotton alpha-globulin promoter: isolation and functional characterization in transgenic cotton, Arabidopsis, and tobacco.

Globulins are the most abundant seed storage proteins in cotton and, therefore, their regulatory sequences could potentially provide a good source of seed-specific promoters. We isolated the putative promoter region of cotton alpha-globulin B gene by gene walking using the primers designed from a cotton staged embryo cDNA clone. PCR amplified fragment of 1108 bp upstream sequences was fused to gusA gene in the binary vector pBI101.3 to create the test construct. This was used to study the expression pattern of the putative promoter region in transgenic cotton, Arabidopsis, and tobacco. Histochemical GUS analysis revealed that the promoter began to express during the torpedo stage of seed development in tobacco and Arabidopsis, and during cotyledon expansion stage in cotton. The activity quickly increased until embryo maturation in all three species. Fluorometric GUS analysis showed that the promoter expression started at 12 and 15 dpa in tobacco and cotton, respectively, and increased through seed maturation. The strength of the promoter expression, as reflected by average GUS activity in the seeds from primary transgenic plants, was vastly different amongst the three species tested. In Arabidopsis, the activity was 16.7% and in tobacco it was less than 1% of the levels detected in cotton seeds. In germinating seedlings of tobacco and Arabidopsis, GUS activity diminished until it was completely absent 10 days post imbibition. In addition, absence of detectable level of GUS expression in stem, leaf, root, pollen, and floral bud of transgenic cotton confirmed that the promoter is highly seed-specific. Analysis of GUS activity at individual seed level in cotton showed a gene dose effect reflecting their homozygous or hemizygous status. Our results show that this promoter is highly tissue-specific and it can be used to control transgene expression in dicot seeds.

Alpha-Globulins↗

Probabilistic risk assessment of cotton pyrethroids: III. A spatial analysis of the Mississippi, USA, cotton landscape.

Estimates of potential aquatic exposure concentrations arising from the use of pyrethroid insecticides on cotton produced using conventional procedures outlined by the U.S. Environmental Protection Agency's Office of Pesticide Programs Environmental Fate and Effects Division seem unrealistically high. Accordingly, the assumptions inherent in the pesticide exposure assessment modeling scenarios were examined using remote sensing of a significant Mississippi, USA, cotton-producing county. Image processing techniques and a geographic information system were used to investigate the number and size of the water bodies in the county and their proximity to cotton. Variables critical to aquatic exposure modeling were measured for approximately 600 static water bodies in the study area. Quantitative information on the relative spatial orientation of cotton and water, regional soil texture and slope, and the detailed nature of the composition of physical buffers between agricultural fields and water bodies was also obtained. Results showed that remote sensing and geographic information systems can be used cost effectively to characterize the agricultural landscape and provide verifiable data to refine conservative model assumptions. For example, 68% of all ponds in the region have no cotton within 360 m and 92% of the ponds have no cotton within 60 m. Only 2% of ponds have cotton present in all directions around the ponds and within 120 m. These are significant modifications to conventional pesticide risk assessment exposure modeling assumptions and exemplify the importance of using landscape-level risk assessments to better describe the Mississippi cotton agricultural landscape. Incorporating spatially characterized landscape information into pesticide aquatic exposure scenarios is likely to have greater impact on the model output than many other refinements.

Animals↗

[Genetic diversity analysis of brown cotton and green cotton].

Genetic diversity analysis of brown cotton Xincai 1 and Xincai 2 and green cotton Xincai 3 and Xincai 4 and other 47 color cottons was conducted by the random amplified polymorphism DNA (RAPD) techniques, using 6 random primers. Cluster and similarity analysis of these cottons showed that the differences in genetic relationship and similarity among the brown cottons, green cottons and brown-green cottons are not remarkable. The results also reflect that the genetic bases of the brown and green cottons are narrow, and they are at the same genetic diversity level. These results are probably due to the same basic germplasms, the same breeding aims and the similar breeding approaches.

Cluster Analysis↗

Additive effect of smoking and cotton dust exposure on respiratory symptoms and pulmonary function of cotton textile workers.

One hundred and sixty-nine and 175 cotton textile workers (CTWs) were enrolled in the first (1991) and second (1996) surveys to investigate the prevalence of byssinosis. The synergistic effect of smoking on cotton dust exposure was also evaluated. Although the difference in prevalence of abnormal pulmonary function between the first (38.5%) and second study (38.9%) was not statistically significant, smokers had significantly higher frequency than nonsmokers in both surveys. A significant trend existed between the cotton dust levels and the frequency of abnormal lung function. The significant trend was also noted in both smokers and nonsmokers. The frequency of respiratory symptoms and the prevalence of severe byssinosis in the second survey (14.9% and 12.6%, respectively) were significantly lower than that in the first survey (39.7% and 21.9%, respectively). The reduction of symptoms was due to remodeling of this old cotton mill. The prevalences of respiratory symptoms and byssinosis in smokers being significantly higher than in nonsmokers only found in the first survey, but not found in the second survey. These results indicate that smoking potentiates the effect of cotton dust exposure on respiratory symptoms and byssinosis. The second study reveals high prevalence of byssinosis still existed in Taiwanese cotton mill, although the prevalence was declining. Smoking was found to show an additive effect on cotton dust exposure. Anti-smoking campaign, occupational health program to reduce the dust exposure, and periodical medical examination are measures to prevent from byssinosis.

Adult↗

Potential for transport of boll weevils (Coleoptera: Curculionidae) to the cotton gin within cotton modules.

There is concern that cotton gins located in boll weevil, Anthonomus grandis grandis Boheman, eradication zones serving customers in adjacent infested zones may serve as a site for boll weevil reintroductions if weevils are transported alive inside cotton modules. We surveyed fields in three distinct areas of Texas and found that weevils can be present in large numbers in cotton fields that have been defoliated and desiccated in preparation for harvest, both as free adults and as immatures inside unopened bolls. Harvested cotton taken from module builders indicated that approximately = 100-3700 adult boll weevils were packed inside modules constructed at the sampled fields. Marked weevils were forced through a laboratory field cleaner (bur extractor) commonly mounted on stripper-harvesters, and 14% were recovered alive in the seed cotton fraction and lived at least to 24 h. Survival of weevils placed inside modules declined over time up to 7 d, but the magnitude of the decline varied with experimental conditions. In one experiment, 91% of the weevils survived to 7 d, whereas under harsher environmental conditions, only 11% survived that long. Together, our results indicate that when cotton is harvested in an infested area, boll weevils likely will be packed alive into cotton modules, and many will still be alive by the time the module is fed into the gin, at least up to 7 d after the module's construction.

Agriculture↗

Clones of cotton leaf curl geminivirus induce symptoms atypical of cotton leaf curl disease.

The causative agent of cotton leaf curl disease has previously been shown to be transmissible by the whitefly Bemisia tabaci (Gennadius) and a begomovirus (Geminiviridae) was shown to be associated with the disease. This virus was provisionally called cotton leaf curl virus (CLCuV) although no causal relationship between virus and disease was shown. In the present study full-length clones of CLCuV, equivalent to the DNA A component of bipartite begomoviruses, were obtained. The clones of CLCuV were systemically infectious to both Nicotiana benthamiana and cotton. Infected plants did not exhibit symptoms characteristic of cotton leaf curl disease, producing mild leaf curling, yellowing and some stunting. Efforts to identify a second genomic component were not successful. These findings suggest that the begomovirus, CLCuV, is not or not the sole cause of cotton leaf curl disease. The transmission of cotton leaf curl disease by B. tabaci, however, may indicate that the begomovirus plays a part in the transmission of the disease. The implications of these findings are discussed.

Blotting, Southern↗

Smoking and cotton dust effects in cotton textile workers.

Cotton textile workers have an increased prevalence of both obstructive and restrictive lung function patterns compared with control subjects. Similar abnormal patterns may occur with respiratory diseases of other etiologies, notably those associated with cigarette smoking. The shape of the maximum expiratory flow volume (MEFV) curve has been used to characterize patterns of lung function abnormality. To better evaluate the respiratory effects of cotton dust exposure and to contrast them with those of cigarette smoking, we defined a new functional parameter (angle beta) related to the shape of the MEFV curve. We compared 477 cotton textile workers, both current smokers and never smokers, 45 years and older, with 932 similarly aged control subjects from three communities. Smokers, regardless of their occupational exposure or sex, have smaller beta values than nonsmokers. Cotton textile workers, despite a greater prevalence of abnormal lung function, have beta values that do not differ from those of persons without occupational exposure to cotton dust. We suggest that morphologic patterns of flow volume curves reflect separate effects of cotton dust exposure and smoking and may be related to different sites of airway injury.

Aged↗

[Effect of plumular axis-cutted cotton on growth and development of cotton bollworm].

The method of plumular axis cutting was used to induce the resistance of cotton plants to cotton bollworms(Heliothis armigera). The bollworm was cultured in the laboratory, and the effect of induced cotton on the duration of larval development and weights of larvae and pupae was studied. In the treatments of infection and control, the lengths of larval period were delayed by 3 days and 0.5 days, the weights of larvae were decreased by 19.60% and 11.45%, and the pupae weights were decreased by 10.81% and 6.54%, respectively. After the 8 days old larvae were reared with induced cotton leaves for 3 days, the infected and uninfected cutted plants resulted in a decrease of the relative growth rates of larvae by 22.9% and 17.2% respectively, and in a decrease of the relative feeding rates by 26.1% and 21.4% respectively. It is suggested that plumular axis cutting could induce the resistance of cotton plants to bollworm, and influence the growth and development speed of bollworms through retarding their feeding and digestion. Combining with the treatment of Pseudomona gladioli D-2251 strain could obviously increase the insect-resistance of cotton plants.

Animals↗

The cotton kinesin-like calmodulin-binding protein associates with cortical microtubules in cotton fibers.

Microtubules in interphase plant cells form a cortical array, which is critical for plant cell morphogenesis. Genetic studies imply that the minus end-directed microtubule motor kinesin-like calmodulin-binding protein (KCBP) plays a role in trichome morphogenesis in Arabidopsis. However, it was not clear whether this motor interacted with interphase microtubules. In cotton (Gossypium hirsutum) fibers, cortical microtubules undergo dramatic reorganization during fiber development. In this study, cDNA clones of the cotton KCBP homolog GhKCBP were isolated from a cotton fiber-specific cDNA library. During cotton fiber development from 10 to 21 DPA, the GhKCBP protein level gradually decreases. By immunofluorescence, GhKCBP was detected as puncta along cortical microtubules in fiber cells of different developmental stages. Thus our results provide evidence that GhKCBP plays a role in interphase cell growth likely by interacting with cortical microtubules. In contrast to fibers, in dividing cells of cotton, GhKCBP localized to the nucleus, the microtubule preprophase band, mitotic spindle, and the phragmoplast. Therefore KCBP likely exerts multiple roles in cell division and cell growth in flowering plants.

Amino Acid Sequence↗