The system signature is a useful tool for studying coherent systems. For a given coherent system, various methods have been proposed in the literature to compute its signature. However, when any system signature is given, the literature does not address how to construct the corresponding coherent system(s). In this article we propose an algorithm to address this research gap. This algorithm enables the validation of whether a provided probability vector qualifies as a signature. If it does, the algorithm proceeds to generate the corresponding coherent system(s). To illustrate the applicability of this algorithm, we consider all three and four-dimensional probability vectors, verify if they are signatures, and finally obtain 5 and 20 coherent systems, respectively, which coincides with the literature (Shaked and Suarez-Llorens 2003).

Preservation of stochastic orders through the system signature has captured the attention of researchers in recent years. Signature-based comparisons have been made for the usual stochastic order, hazard rate order, and likelihood ratio orders. However, for the mean residual life (MRL) order, it has recently been proved that the preservation result does not hold true in general, but rather holds for a particular class of distributions. In this paper, we study whether or not a similar preservation result holds for the mean inactivity time (MIT) order. We prove that the MIT order is not preserved from signatures to system lifetimes with independent and identically distributed (i.i.d.) components, but holds for special classes of distributions. The relationship between these classes and the order statistics is also highlighted. Furthermore, the distribution-free comparison of the performance of coherent systems with dependent and identically distributed (d.i.d.) components is studied under the MIT ordering, using diagonal-dependent copulas and distorted distributions.

Fall armyworm, Spodoptera frugiperda (J. E. Smith) is a polyphagous and highly destructive invasive insect pest of many crops. It was recently introduced into India and widely reported in almost all parts of India. Development of a temperature-based phenology model for predicting its rate of development and distribution will help in understanding the establishment and further spread of introduced invasive insect pests. Development, survival and reproduction parameters of S. frugiperda at six constant temperature conditions (15, 20, 25, 27, 30 and 35°C) were investigated and further validated with data generated under fluctuating temperature conditions. The estimated lower developmental threshold temperatures were 12.1°C for eggs, 11°C for larvae, 12.2°C for pupae, 15.13°C for males and 12.66°C for females. Degree-day (DD) requirements for the development of the different stages of S. frugiperda were 50, 250 and 200 DD for egg, larva and pupa, respectively. The best-fitted functions were compiled for each life stage to yield a phenology model, which was stochastically simulated to estimate the life table parameters. The developed phenology model predicted temperature ranges between 27 and 30°C as favourable for S. frugiperda development, survival and reproduction. The results revealed that maximum net reproductive rate (215.66 females/female/generation) and total fecundity (981.08 individuals/female/generation) were attained at 30°C constant temperature. The mean length of generations decreased from 74.29 days at 15°C to 38.74 days at 30°C. The maximum intrinsic rate of increase (0.138 females/female/day) and shortest doubling time (4.9 days) were also observed at 30°C. Results of simulated life table parameters showed high temperature-dependent development of S. frugiperda and complete development within all the tested constant temperature ranges (15–35°C). Simulated life table parameters for predicting risk indices of S. frugiperda in India indicated a significant increase in activity indices and establishment risk indices with a higher number of generations during future (2050 and 2070) climatic change scenarios compared to present conditions. Our results indicate that India will be highly suitable for the establishment and survival of S. frugiperda in future time periods.

Fluorine-rich prismatine, (□,Fe,Mg)(Mg,Al,Fe)5Al4(Si,B,Al)5O21(OH,F), with F/(OH+F) = 0.36–0.40 and hercynite are major constituents of a Fe-Al-B-rich lens in ultrahigh-temperature granulite-facies quartz-sillimanite-hypersthene-cordierite gneisses of the Eastern Ghats belt, Andhra Pradesh, India. Hemo-ilmenite, sapphirine, magnetite, biotite and sillimanite are subordinate. Lithium, Be and B are concentrated in prismatine (140 ppm Li, 170 ppm Be, and 2.8 –3.0 wt.% B2O3). Another Fe-rich lens is dominantly magnetite, which encloses fine-grained zincian ferrohögbomite-2N2S, (Fe2+,Mg,Zn,Al)6 (Al,Fe3+,Ti)16O30(OH)2, containing minor Ga2O3 (0.30 –0.92 wt.%). Fe-Al-B-rich lenses with prismatine (or kornerupine) constitute a distinctive type of B-enrichment in granulite-facies rocks and have been reported from four other localities worldwide. A scenario involving a tourmalineenriched lateritic precursor affected by dehydration melting is our preferred explanation for the origin of the Fe-Al-B-rich lenses at the five localities. Whole-rock analyses and field relationships at another of these localities, Bok se Puts, Namaqualand, South Africa, are consistent with this scenario. Under granulite-facies conditions, tourmaline would have broken down to give kornerupine-prismatine (±other borosilicates) plus a sodic melt containing H2O and B. Removal of this melt depleted the rock in Na and B, but the formation of ferromagnesian borosilicate phases in the restite prevented total loss of B.

A new occurrence of awaruite, from India, is reported in the ultramafic units of the Dras area which form part of the Indus Suture ophiolites in Kashmir Himalaya. Its formation in these rocks suggests a low-temperature process of serpentinization. Ni and Fe released from olivine and/or pyroxene must have formed awaruite peragenetically next to magnetite and pentlandite.

Analyses are given of four pairs of coexisting pyroxenes; their Kp ranges from 1.282 to 1.369, suggesting equilibration temperatures as high as 1200 °C and pressures of the order of 8 to 9 kb.

Agriculture and livestock production systems are two major emitters of greenhouse gases. Methane with a GWP (global warming potential) of 21, and nitrous oxide (N2O) with a GWP of 300, are largely emitted from animal production agriculture, where livestock production is based on pasture and feed grains. The principal biological processes involved in N2O emissions are nitrification and denitrification. Biological nitrification inhibition (BNI) is the natural ability of certain plant species to release nitrification inhibitors from their roots that suppress nitrifier activity, thus reducing soil nitrification and N2O emission. Recent methodological developments (e.g. bioluminescence assay to detect BNIs in plant root systems) have led to significant advances in our ability to quantify and characterize the BNI function. Synthesis and release of BNIs from plants is a highly regulated process triggered by the presence of NH4+ in the rhizosphere, which results in the inhibitor being released precisely where the majority of the soil-nitrifier population resides. Among the tropical pasture grasses, the BNI function is strongest (i.e. BNI capacity) in Brachiaria sp. Some feed-grain crops such as sorghum also have significant BNI capacity present in their root systems. The chemical identity of some of these BNIs has now been established, and their mode of inhibitory action on Nitrosomonas has been characterized. The ability of the BNI function in Brachiaria pastures to suppress N2O emissions and soil nitrification potential has been demonstrated; however, its potential role in controlling N2O emissions in agro-pastoral systems is under investigation. Here we present the current status of our understanding on how the BNI functions in Brachiaria pastures and feed-grain crops such as sorghum can be exploited both genetically and, from a production system's perspective, to develop low-nitrifying and low N2O-emitting production systems that would be economically profitable and ecologically sustainable.

Precision X-ray powder-diffraction data of pure solid C70 is reported. C70 prepared by slow evaporation of C70-in-toluene solution adopts an hcp structure (space group P63/mmc) with lattice parameters a=10.5934(10)Å and c=17.262(2)Å.

The structure of K3H(SO4)2 is found to be monoclinic with space group C2/c based on analogy of the powder X-ray diffraction pattern with that of the Rb3H(SO4)2. The lattice parameters are a=14.6984(7), b=5.6840(2), c=9.7834(5) Å, and β=103.004(5)°, Vol=796.39(5); Dx=2.589 gcm−3, Z=4, and I/Icor=1.30.

A new and improved sample holder for use with powder X-ray diffractometry has been developed. This holder is made from a semiconductor grade silicon single crystal cut perpendicular to the [911] axis, i.e., Si (911). This crystal meets most of the basic requirements of an ideal zero background plate, with practically no interference lines. The pattern obtained, by using this crystal as background plate, is very clean, and even very low-intensity Bragg reflections of samples can be detected easily.

X-ray powder diffraction data of CoSi are reported. The sample was prepared by an arc melting process and has a cubic structure (space group P213, space group No. 198) with lattice parameter a=4.4427 Å, Dx=6.591 gcm−3, Z=4, and I/Ic=1.03.

The conglutinating complement absorption test (CCAT) has been used to detect Cysticercus tenuicollis (Taenia hydatigena cysticercus) infection in sheep and goats. Sera from naturally infected sheep and goats showing a titre above 1:40 were considered positive for cysticercosis. Experimentally infected lambs gave a higher antibody response than sheep and goats.

The relationship between chromosome pairing and chromosome fragmentation has been studied in a gene controlled mutant of pearl millet (2n = 14). Premeiotic mitosis, premeiotic cell development and early prophase I are normal without any fragments, which first appear at pachytene. The extent of fragmentation varies from zero to very extreme with two discrete classes of plants, namely those with partial fragmentation and those with multiple fragmentation. A quantitative analysis of bivalent distribution and the distribution of AI bridges in desynaptic and fragmented cells show all of them to be nonrandom events. We suggest that in cells showing partial fragmentation the bridges and fragments result from U-type exchanges at pachytene. The reduced frequency of AII bridges indicates relatively low sister chromatid reunion at pachytene. In multiple fragmented plants numerous minute fragments were seen from pachytene. Despite these anomalies most PMCs complete meiosis but subsequently abort at the pollen grain stage. The mutant gene also causes disturbances in the sequence of meiotic development in the ear and in the synchronous development of PMCs within an anther. It has no effect on the tapetum or on the physiological development of the anther.