Strategic and tactical modeling: cotton-spider mite agroecosystem management

We discuss the development of two simulation models, a mechanistic cotton crop model and a spider mite population model. In a strategic mode, the simulation models are used to address basic hypotheses involving the interaction of cotton with its environment, and with the spider mite population, and to develop general strategies for managing the crop and its herbivores. In a tactical mode, these models are used to provide estimates of the anticipated severity of a spider mite population. Tactical modelling is made possible by using a statistically-based adaptive interface. The departure of simulated patterns of growth from observed patterns is used to adapt several crop parameters including rate of photosynthesis, rate of vegetative growth, and metabolite allocation priority for fruit. For the spider mite population model, fecundity, predator-mediated mortality, and acaricide-induced mortality are adapted to specific field conditions.     

Growth ofClostridium thermoaceticum on H2/CO2 or CO as energy source

The type strain Fontaine ofClostridium thermoaceticum proliferated on H₂/CO₂ as energy source and was culturally adapted to grow on 100% CO in the headspace. The doubling times at 55°C on CO or H₂/CO₂ were 16 and 18 h, respectively. Under these conditions, the substrate-product transformation stoichiometries observed were: 4H₂+2.1CO₂→0.9 acetate and 4CO→2CO₂+1.1 acetate. It is concluded thatC. thermoaceticum has a single carbon growth physiology.     

Catabolic enzymes of the acetogen Butyribacterium methylotrophicum grown on single-carbon substrates.

When grown on formate, formate-CO, and methanol-CO, Butyribacterium methylotrophicum contained high levels of tetrahydrofolate (H4folate) and required enzymes, carbon monoxide dehydrogenase, formate dehydrogenase, and hydrogenase. The activities of methylene-H4folate reductase were comparable to other H4 folate activities (which ranged from 0.55 to 9.28 mumol/min per mg of protein) when measured by an improved procedure. The H4folate activities in formate-grown cells were twice those found in formate-CO-grown cells. This result correlated with a growth yield on formate that was one-half that on formate-CO. The stoichiometry of the formyl-H4folate synthetase reaction was 1 mol of ATP per 1 mol of formate. The methylene-H4folate dehydrogenase was NAD+ dependent. We conclude that B. methylotrophicum utilizes these enzymes in homoacetogenic catabolism.     

Regulation of rat ovarian cell growth and steroid secretion

A cultured rat ovarian cell line (31 A-F(2)) was used to study the effect of growth factors (epidermal growth factor [EGF] and fibroblast growth factor [FGF]), a survival factor (ovarian growth factor [OGF]), a hormone (insulin), and an iron-binding protein (transferring) on cell proliferation and steroid production under defined culture conditions. EGF and insulin were shown to be mitogenic (half-maximal response at 0.12 nM and 0.11 muM, respectively) for 31A-F(2) cells incubated in serum-free medium. EGF induced up to three doublings in the cell population, whereas insulin induced an average of one cell population doubling. FGF, OGF, and transferrin were found not to have any prominent effect on cell division when incubated individually with 31A-F(2) cells in serum-free medium. However, a combination of EGF, OGF, insulin, and transferrin stimulated cell division to the same approximate extent as cells incubated in the presence of 5 percent fetal calf serum. EGF or insulin did not significantly affect total cell cholesterol levels (relative to cells incubated in serum-free medium) when incubated individually with 31A-F(2) cells. However, cell cholesterol levels were increased by the addition of OGF (250 percent), FGF (370 percent), or a combination of insulin and EGF (320 percent). Progesterone secretion from 31A-F(2) cells was enhanced by EGF (25 percent), FGF (80 percent), and insulin (115 percent). However, the addition of a mitogenic mixture of EGF, OGF, insulin, and transferrin suppressed progesterone secretion 150 percent) below that of control cultures. These studies have permitted us to determine that EGF and insulin are mitogenic factors that are required for the growth of 31A-F(2) cells and that OGF and transferrin are positive cofactors that enhance growth. Also, additional data suggest that cholesterol and progesterone production in 31A-F(2) cells can be regulated by peptide growth factors and the hormone insulin.     

Divalent cations mimic the inhibitory effect of extracellular ionised calcium on bone resorption by isolated rat osteoclasts: further evidence for a "calcium receptor".

Osteoclast activity is thought to be regulated by calcitonin, as well as by the level of ionised calcium generated locally as a result of bone resorption. The exposure of isolated osteoclasts to elevated ambient calcium levels has been shown to lower resorptive activity and to reduce rates of enzyme release. We have attempted to determine whether these effects are mediated by a divalent cation-sensitive "calcium receptor," as has been reported for the parathyroid chief cells. Thus, we compared the effect of alkaline earth metal cations on osteoclast function using a morphometric measure of bone resorption and a spectrophotometric method for measuring the activity of the released enzyme, acid phosphatase. The exposure of resorbing osteoclasts to between 5 and 20 mM extracellular ionised calcium ([Ca2+]e) inhibited bone resorption and enzyme release to an extent similar to that seen with 0.1 to 10 microM ionomycin. The effect of combining submaximal concentrations of [Ca2+]e (15 mM) and ionomycin (0.1 microM) resulted in additivity, suggesting that the influence of [Ca2+]e on bone resorption was mediated by elevated intracellular calcium levels ([Ca2+]i). The other cations studied (Mg2+, Ba2+) were effective and elicited similar effects, although some required higher concentrations. Thus, whilst Ca2+ and Mg2+ were effective at 10 to 15 mM levels, Ba2+ was effective only at high (20 mM) concentrations. These findings are consistent with an influence of [Ca2+]e on osteoclast activity through an action on a surface membrane "calcium receptor" that can also bind other divalent cations, rather than by passive changes of [Ca2+]i with [Ca2+]e elevation.     

Native seeds incorporated into activated carbon pods applied concurrently with indaziflam: a new strategy for restoring annual‐invaded communities?

Reestablishing native perennial vegetation in annual grass‐invaded rangelands is critical to restoring ecosystems. Control of exotics, often achieved with preemergent herbicides, is essential for successful restoration of invaded rangelands. Unfortunately, desirable species cannot be seeded simultaneously with preemergent herbicide application due to nontarget damage. To avoid this, seeding is commonly delayed at least 1 year. Delaying seeding increases the likelihood that annual grasses will begin reestablishing and compete with seeded species. Activated carbon (AC) can provide preemergent herbicide protection for seeded species because it adsorbs and deactivates herbicides. Previous studies suggest that a cylindrical herbicide protection pod (HPP), containing AC and seeds, allows desired species to be seeded simultaneously with the application of the preemergent herbicide imazapic. Unfortunately, imazapic is only effective at controlling annual grasses for 1–2 years. Indaziflam is a new preemergent herbicide which exhibits longer soil activity, with which HPPs may be useful. To assess this possibility, we evaluated seeding two native species (Wyoming big sagebrush [Artemisia tridentata Nutt ssp. wyomingensis] and bluebunch wheatgrass [Pseudoroegneria spicata (Pursh) Á. Löve]), both incorporated into HPPs and as bare seed, at four application rates of indaziflam in a grow room study. HPPs protected seeded species at low, mid, and high rates of indaziflam. The abundance and size of plants was greater in HPPs compared to bare seed treatments. These results suggest that HPPs can be used to seed native grasses and shrubs simultaneously with indaziflam application.     

Comparative proteomics analysis of Barrett metaplasia and esophageal adenocarcinoma using two-dimensional liquid mass mapping

Esophageal adenocarcinoma, currently the seventh leading cause of cancer-related death, has been associated with the presence of Barrett metaplasia. The malignant potential of Barrett metaplasia is evidenced by ultimate progression of this condition to invasive adenocarcinoma. We utilized liquid phase separation of proteins with chromatofocusing in the first dimension and nonporous reverse phase HPLC in the second dimension followed by ESI-TOF mass spectrometry to identify proteins differentially expressed in six Barrett metaplasia samples as compared with six esophageal adenocarcinoma samples; all six Barrett samples were obtained from the identical six patients from whom we obtained the esophageal adenocarcinoma tissue. Approximately 300 protein bands were detected by mass mappings, and 38 differentially expressed proteins were identified by microLC-MS/MS. The false positive rates of the peptide identifications were evaluated by reversed database searching. Among the proteins that were identified, Rho GDP dissociation inhibitor 2, alpha-enolase, Lamin A/C, and nucleoside-diphosphate kinase A were demonstrated to be up-regulated in both mRNA and protein expression in esophageal adenocarcinomas relative to Barrett metaplasia. Candidate proteins were examined at the mRNA level using high density oligonucleotide microarrays. The cellular expression patterns were verified in both esophageal adenocarcinomas and in Barrett metaplasia by immunohistochemistry. These differentially expressed proteins may have utility as useful candidate markers of esophageal adenocarcinoma.