Effect of whole and fractionated dietary alfalfa meal on zearalenone toxicosis and metabolism in rats and swine

Experiments were conducted to determine the mechanism by which dietary alfalfa can protect against zearalenone toxicosis. Female weanling rats were fed semipurified diets containing whole alfalfa meal, fractionated alfalfa meal (fiber, solvent extract, and water extract), and purified components of alfalfa (coumestrol, saponin, lignin, coumestrol + lignin, and saponin + lignin) with and without 250 mg zearalenone/kg of diet. All ingredients were provided for 2 weeks at levels corresponding to those found in diets containing 15 and 25% alfalfa. Yorkshire gilts were fed 15 and 25% alfalfa meal with and without 10 mg zearalenone/kg of diet for 4 weeks. The feeding of zearalenone to rats reduced growth and food consumption but this was overcome by 25% alfalfa. Zearalenone also increased the activity of hepatic 3 alpha-hydroxysteroid dehydrogenase (3 alpha-HSD), the enzyme believed to metabolize zearalenone to alpha- and beta-zearalenols. Dietary alfalfa did not overcome this effect. Alfalfa fiber was the only fraction to partially overcome the growth-depressing effects of zearalenone while the other fractions had no beneficial effects and 3 alpha-HSD was not affected by diet. None of the purified components affected growth parameters or 3 alpha-HSD. The enzyme was also not affected by zearalenone or alfalfa in swine diets. Coumestrol, alpha-zearalenone, and beta-zearalenone were shown to be competitive inhibitors of 3 alpha-HSD in rat liver. It was concluded that the fiber fraction of alfalfa protects against zearalenone toxicity, and that this effect is not dependent on coumestrol or saponin and is not likely mediated through 3 alpha-HSD.     

The ability of dehydrated hamster and human sperm nuclei to develop into pronuclei.

To determine whether the nuclei of mature mammalian spermatozoa are resistant to dehydrated conditions, nuclei of hamster and human spermatozoa were freeze-dried or treated with various dehydrating agents before injection into hamster oocytes. Freeze-dried nuclei remained capable of developing into pronuclei even after 12 mo of storage at 4 degrees C. The level of DNA synthetic activity in the sperm (male) pronucleus was comparable to that in the egg (female) pronucleus. Sperm nuclei that had been stored in 100% ethanol, 100% methanol, or chloroform-methanol (2:1) mixture for 20 days were also capable of developing into pronuclei. Even the nuclei that had been dehydrated ("fixed") with Carnoy's fluid could develop into morphologically normal pronuclei. However, the level of DNA synthesis in the pronuclei derived from these chemically dehydrated nuclei was generally lower than that in the female pronuclei. Although the genetic integrity of the dehydrated sperm nuclei is yet to be determined, nuclei of mature hamster and human spermatozoa appear to be fairly resistant to dehydrated conditions.     

Influence of nutrient and energy deprivation on cellular response to single and fractionated heat treatments

The effect of hypoglycemia and hypoxia on cell survival following single and fractionated 44 degrees C heat treatments was investigated. These studies show that short-term glucose deprivation or oxygen deprivation does not increase sensitivity to single or fractionated heat treatments compared to normal nutrient conditions. However, simultaneous hypoglycemia and hypoxia leads to an increased sensitivity to single heat treatments, and to an even greater increase in sensitivity to fractionated heat treatments. Sensitivity to heat treatment under nutrient-deprived conditions correlates with intracellular ATP levels at the time of treatment. These data indicate that it is not nutrient concentration per se, but rather the effect of nutrient level on intracellular ATP concentration that affects thermal sensitivity.     

Experimental testing of dynamic energy budget models

1. Dynamic energy budget (DEB) models describing the allocation of assimilate to the competing processes of growth, reproduction and maintenance in individual organisms have been applied to a variety of species with some success. There are two contrasting model formulations based on dynamic allocation rules that have been widely used (net production and net assimilation formulations). However, the predictions of these two classes of DEB models are not easily distinguished on the basis of simple growth and fecundity data.
2. It is shown that different assumptions incorporated in the rules determining allocation to growth and reproduction in two classes of commonly applied DEB models predict qualitatively distinct patterns for an easily measured variable, cumulative reproduction by the time an individual reaches an arbitrary size.
3. A comparison with experimental data from Daphnia pulex reveals that, in their simplest form, neither model predicts the observed qualitative pattern of reproduction, despite the fact that both formulations capture basic growth features.
4. An examination of more elaborate versions of the two models, in which the allocation rules are modified to account for brief periods of starvation experienced in the laboratory cultures, reveals that a version of the net production model can predict the qualitative pattern seen for cumulative eggs as a function of mass in D. pulex . The analysis leads to new predictions which can be easily tested with further laboratory experiments.     

Optimization models for the force and energy in competitive running

 In [2] the author has developed an optimization model for the force and energy in competitive running. In this paper the energy processes in the muscle were described by a three-compartment hydraulic model. Here this is reviewed briefly and applied to the current world records in order to determine the key parameters, maximal force, energy reserves and oxygen uptake. These values agree well with those given in the literature and those obtained by other means. The velocity profiles for 100 m sprints are described equally well. The model is then applied to older world records to deduce a relation between the force and energy by linear regression. Finally the fully parameterized model is used to compute the effects of adverse wind and altitude. Inasmuch as there are data available, there is a good agreement. Received 19 July 1995; received in revised form 27 February 1996     

Conversion of the energy of a high-current REB into electromagnetic wave energy

Results are presented from a theoretical investigation and quantitative analysis of the physical processes that govern the efficiency of a coaxial device aimed at converting the energy of a relativistic electron beam into the energy of a TEM wave (a wave in a circular cylindrical coaxial waveguide). The key diffractional problem is solved exactly using a simplified theoretical model, which makes it possible to understand the mechanisms for the formation of a TEM wave and determine how the beam parameters and the design parameters of the converter affect the relative fractions of the kinetic energy of a relativistic electron beam and the energy of its own magnetic and electric fields that are transferred into the energy of the TEM wave field. The results obtained are analyzed quantitatively, and prospects for further theoretical and experimental research in this area are outlined.     

紫花苜蓿的花蜜量和访花蜜蜂数量对种子产量的影响

对10个紫花苜蓿品种的花萼直径、花蜜量、访花蜜蜂数量和种子产量进行了研究,结果表明,紫花苜蓿的单位面积花蜜量与访花蜜蜂数量呈极显著正相关(r=0.93**),访花蜜蜂数量与种子产量呈显著正相关(r=0.87*);紫花苜蓿的花蜜量与花萼直径呈极显著正相关(r=0.99**);紫花苜蓿品种赛特(Sitel)和德宝(Derby)在兰州地区能获得高产、优质的种子。     

A generalization of the clonal survival models: Equations for the families of curves obtained with fractionated irradiation

Summary The survival curves obtained when cellular recovery follows various first radiation dose deliveriesDI seem, when semi-logarithmically plotted, to be translated from the part of the curve corresponding to an unfractionated irradiation beyond a doseDR. A possible assumption consistent with such experimental observations is proposed which allows the generalization of any survival modelS = f(D). The derived equationS = f(DR + D - DI)f(DI)/f(DR) is convenient for the whole family of experimental survival curves involving cellular damage repairs when the first radiation doses vary. All the parameters of the family equation can be simultaneously fitted so that their reliability is increased. The generalized equations are given for the four following models: two-hits targets, Chadwick and Leenhouts, Green and Burki, Wideröe. As an example, the Chadwick and Leenhouts generalized model parameters are fitted to a family of experimental survival curves concerningChlorella cells exposed to fractionated and continuous gamma irradiation. The fittings are presented with their confidence limits and are briefly discussed.     

Mechanical models for insect locomotion: active muscles and energy losses

 We extend the analysis of simple, energy-conserving models for the dynamics of insect locomotion in the horizontal plane developed in Schmitt and Holmes (2000a,b, 2001), where gaits characteristic of steady cockroach running and turning were evoked. In this paper, we include dissipation and energy inputs via active “muscles” in three forms: via prescribed torques at the “hip” pivot, via an active spring element of variable length, and via a pair of Hill-type muscle models representing an extensor/flexor system. Due to mechanical feedback of passive elastic forces, the stable gaits of the conservative models are preserved, and now energy input and absorption balances to additionally stabilize a preferred speed, with only modest neural sensing and feedback being required. However, these bipedal models still cannot simultaneously match observed moment-yaw magnitudes and fore-aft dynamics. Received: 17 September 2001 / Accepted: 20 February 2003 / Published online: 20 May 2003 Correspondence to: P. Holmes (e-mail: pholmes@math.Princeton.EDU) Acknowledgements. This work was supported by DARPA/ONR: N00014-98-1-0747 and DoE: DE-FG02-95ER25238. John Schmitt was partially supported by a DoD Graduate Fellowship, a Wu Fellowship of the School of Engineering and Applied Science, and a George Van Ness Lothrop Honorific Fellowship of the Graduate School at Princeton University. We thank Kenneth Meijer for allowing us to use his muscle model in Sect. 4 and Bob Full and Dan Koditschek for numerous helpful suggestions.     

Theoretical models of adaptive energy management in small wintering birds

Many small passerines are resident in forests with very cold winters. Considering their size and the adverse conditions, this is a remarkable feat that requires optimal energy management in several respects, for example regulation of body fat reserves, food hoarding and night-time hypothermia. Besides their beneficial effect on survival, these behaviours also entail various costs. The scenario is complex with many potentially important factors, and this has made 'the little bird in winter' a popular topic for theoretic modellers. Many predictions could have been made intuitively, but models have been especially important when many factors interact. Predictions that hardly could have been made without models include: (i) the minimum mortality occurs at the fat level where the marginal values of starvation risk and predation risk are equal; (ii) starvation risk may also decrease when food requirement increases; (iii) mortality from starvation may correlate positively with fat reserves; (iv) the existence of food stores can increase fitness substantially even if the food is not eaten; (v) environmental changes may induce increases or decreases in the level of reserves depending on whether changes are temporary or permanent; and (vi) hoarding can also evolve under seemingly group-selectionistic conditions.     

Flow analysis sensitivities for models of energy or material flow

Sensitivity analyses have been used to examine the flow structure of two hypothetical ecosystem models. These analyses have results which relate to important aspects of ecosystem theory. Cycles are shown to increase the sensitivity of the network, while increased throughflow is shown to decrease the sensitivity. Such results indicate that several factors can be modified to decrease the sensitivity of ecosystems to environmental stress.