Structure of indole-3-acetic acid myoinositol esters and pentamethyl-myoinositols

GC-MS properties of three isomeric esters of indole-3-acetic acid and myoinositol, three esters of indole-3-acectic acid and myoinositol arabinoside and three esters of indole-3-acetic acid and myoinositol galactoside are presented. MS fragmentation patterns for the four possible pentamethyl myoinositols are also shown. These data indicated that the arabinose, and galactose of the glycosides were in the pyranose form and that C-1 of the sugar was linked to the 5 hydroxyl of myoinositol. Homologies in fragmentation patterns for the esters and the glycoside esters, together with knowledge of the properties of 2-O-indole-3-acetyl-myoinositol, permitted identification of one of the arabinosides as 5-O-l-arabinopyranosyl-2-O-indole-3-acetyl-myoinositol and one of the galactosides as 5-O-d- galactopyranosyl-2-O-indole-3-acetyl-myoinositol. The remaining two GLC peaks observed for the arabinoside were then, most likely, the two mixtures of diastereoisomers 1 d- and 1 l-5-O-l-arabinopryranosyl-1-O-indole-3-acetyl myoinositol and 1 d- and 1 l-5-O-l-arabinopyranosyl-4-O-indole-3-acetyl-myoinositol. The remaining two GLC peaks observed for the galactoside would then be the 1 d and 1 l-5-O-d-galactopyranosyl-1-O-indole-3-acetyl-myoinositol and 1 d- and 1 l-5-O-d- galactopyranosyl-4-O-indoleacetyl-myoinositol.     

Comparative demography of a laboratory and a wild strain of the oriental fruit fly, Dacus dorsalis

Host-specific development and survival rates were measured and population parameters computed for both a wild and a laboratory strain of the oriental fruit fly (Dacus dorsalis Hendel) in Hawaii. Gross fecundities of the wild and laboratory strains were 241 and 1551 eggs per female, respectively. Egg to eclosion developmental rates were 27 days for the wild strain and 24 days for the laboratory strain. The preovipositional period of the wild strain was 19 days compared to 9 days in the laboratory strain.Differences of this magnitude in fecundity and developmental rates between laboratory and wild strains have not been observed in other recent demographic studies of tephritids. The results suggest that the laboratory strain of the oriental fruit fly may have undergone more intense selection than laboratory strains of the other species.

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Résumé Pour deux souches, l'une sauvage, l'autre de laboratoire, de D. dorsalis de Hawaï, les mesures ont porté sur la durée de développement et le taux de survie, les paramètres caractéristiques de la population ont été traités sur ordinateur. Pour les souches sauvage et de laboratoire, les fécondités brutes ont été respectivement de 241 et 1551 oeufs par femelle. Les durées de développement larvaire et nymphal ont été de même de 27 jours pour la souche sauvage et de 24 j pour celle de laboratoire; les périodes de latence avant la ponte ont été de 19 j pour la souche sauvage contre 9 j pour celle de laboratoire.Jamais de telles différences de fécondités et de durées de développement entre souches sauvages et de laboratoire n'avaient été observées lors des études récentes sur des téphritidae. Ces résultats suggèrent que la sélection subie par la souche de laboratoire de D. dorsalis été plus intense que celles subies par d'autres espèces.

     

The use of life tables to assess varietal resistance of cotton to spider mites

Life tables of Tetranychus urticae Koch were used to assess resistance to spider mites in five varieties of cotton in the southern San Joaquin Valley of California. Experiments were conducted during midseason and again in mid- to late season. The most resistant variety was Pima S-5 and the most susceptible was Acala SJ-2. Resistance of S-5 was expressed primarily as lower mite survivorship and fecundity. Developmental rates were similar on all 5 varieties. Although differences in the net reproductive rate (R_o) were large, there were only slight differences in the intrinsic rate of increase (r). Comparisons of the data in the first and second experiment, showed that resistance to spider mites increased as the plants matured. It is hypothesized that increased resistance associated with plant maturation results from a decrease in available nutrients in the leaves of older plants.

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Résumé Les tables de vie de T. urticae Koch ont servi à la mise en évidence de la résistance de cinq variétés de coton dans la partie méridionale de la vallée de San Joaquin en Californie. Les expériences ont eu lieu à la mi-saison et à nouveau de la mi à la fin saison. La variété la plus résistante a été Pima S-5 et la plus sensible Acala SJ-2. La résistance de S-5 s'est traduite d'abord par une diminution de la survie et de la fécondité des acariens. Les taux de développement ont été les mêmes sur les cinq variétés. Bien que les différences entre les taux de reproduction nets (R_o) aient été importants, il n'y a eu que de légères différences entre les taux intrinsèques d'accroissement (r). La comparaison des résultats des lère et 2ème expériences a montré que la résistance aux acariens a augmenté quand les plantes ont mûri. L'hypothèse est émise d'un accroissement de la résistance lié à la maturation par suite d'une diminution de la quantité de'éléments nutritifs dans les feuilles des plantes âgées.

     

Demography of a native strain of the melon fly, Dacus cucurbitae, from Hawaii

Preadult development and survival rates for a wild strain of melon fly in Hawaii were examined when reared on six common hosts at 25°C. These data were combined with information gathered on adult survival, fecundity and fertility in order to construct life tables.The duration of the egg stage was slightly over 1 day for this species. Depending on host, larval-to-adult development and survival rates were 17–20 days and 35–85%, respectively. Gross fecundity (total eggs) was 1293 eggs/ while net fertility (total fertile eggs weighted by hatch and adult survival) was 518 fertile eggs/. The finite rate of increase () for the species was conditional on the host on which it was reared and ranged from 1.08 to 1.12. The percent of adults in the stable age distribution averaged around 14% over all hosts.

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Démographie d'une souche de Dacus cucurbitae Coquillet, originaire d'Hawaii

Résumé Le développement préimaginal et les taux de survie d'une souche sauvage de D. cucurbitae de Hawaí sur six hôtes courants ont été examinés à 25°C. Ces résultats ont été combinés aux informations récoltées sur la survie des adultes, la fécondité et la fertilité pour réaliser des tables de vie.La durée du stade oeuf est légèrement supérieure à un jour pour cette espèce. La durée de développement de l'éclosion de l'oeuf à l'imago et les taux de survie ont été respectivement de 17 à 20 jours et de 35 à 85% suivant les hôtes. La fécondité brute (ponte totale) a été de 1293 oeufs par femelle, tandis qui la fertilité (nombre total d'oeufs fertiles pondéré par les taux d'éclosion et de survie des adultes) était de 518 oeufs fertiles par femelle.Le taux d'accroissement () variait de 1,08 à 1,12 suivant l'hôte sur lequel D. cucurbitae a été élevé. La proportion d'adultes dans une distribution en âge stable était d'environ 14% sur tous les hôtes.

     

Demographic trends and biological status of historic populations from Central Poland: the Ostrów Lednicki microregion

The microregion of Ostrów Lednicki in the province of Wielkopolska was the center of the formation of the Polish State in Early Middle Ages. The analysis of skeletal remains and parish records from the region documented the biological status of inhabitants and its changes over a millennium. The study material comprised 424 human skeletons from an Early Medieval burial ground on Lake Lednica, records of 2,704 deaths from the registers of the Roman Catholic parish of Dziekanowice, made between 1818-1903, data on the deaths of 929,192 inhabitants of rural areas all over the province Wielkopolska obtained from Prussian statistical materials for the years 1865-1900, and comparative data from the literature. Assuming both a stationary population model and a stable population model with nonzero natural increase, parameters of life tables and measures of opportunity for natural selection (Crow's index I(m), potential gross reproductive rate R(pot), and the biological state index I(bs)) were calculated for the Early Middle Ages and for the two periods of the 19th century which were characterized by different laws of land ownership and thus different rural economies. In the first period, peasants were tenants, whereas in the second, they were given freehold of the land they cultivated. Causes of death were also analyzed. A distinct increase in longevity from the early Middle Ages to the end of the 19th and the beginning of the 20th century was found. This was related to a higher level of demographic development in the parish of Dziekanowice during the 19th century, which was achieved earlier than in other areas of Poland. This was confirmed by genetic measures: coefficients of exogamy and coefficients of kinship. The reasons were related to the historical prominence of this region and to its proximity to the first two capitals of the Polish state, Gniezno and Poznań.     

Nonparametric adjustment techniques for binary covariates

Though a variety of reasons are often articulated for adjusting analyses for covariates, these reasons often fall into one of two general objectives, specifically to increase precision or to decrease bias. In practice, one does not generally choose between these objectives, because the methods that address one tend to address the other, as well. Because of this, no distinction is made in the methods used to correct for a baseline imbalance with respect to a prognostic covariate versus to ensure a fair comparison across treatment groups by making the comparisons within the levels of a prognostic covariate. Yet the literal translation of these two uses of covariate adjustment will lead to two distinct adjustment methods. We illustrate this divergence in the simplest case of a single binary covariate, a binary outcome, and two treatments, and we note that it is possible to combine the two approaches to derive yet a third approach. Each of these approaches is nonparametric and exact, and so it is the precise reason for adjusting that should dictate which would be used in any given situation.     

Life tables and intrinsic rate of natural increase ofPediobius furvus [Hym.: Eulophidae] onChilo partellus [Lep.: Pyralidae]

In the present studies, life table data and intrinsic rate of natural increase (r_m) of the eulophid pupal parasitoid,P. furvus (Gahan) were obtained fromChilo partellus (Swinhoe) at a constant temperature of 26.7±0.6°C, 52.3±2.7% RH in the laboratory. Development of immature stages took 19.1±0.3 days; adult females lived for 7.9±3.3 (range, 2–13) days and produced a mean of 91.9±22.4 progeny per female, with a sex ratio of 1:2.9 (♂:♀). The intrinsic rate of natural increase (rm) was 0.2558/female/day; the net reproductive rate (R₀), 237.25; the capacity for increase (r_c) of 0.252; and the finite rate of increase (λ) of 1.29/female/day; thus, each female contributed 231.42 individuals to the population in a mean generation time of 21.38 days.      

Reducing Gaseous Emissions and Resource Consumption Embodied in French Final Demand: How Much Can Waste Policies Contribute?

This study investigates the benefits of waste management policies on gaseous emissions and resource consumption caused by the final demand, in the specific case of France and in a context of economic growth. Waste input‐output analysis is implemented to compare three scenarios, depicting and combining the upward trend of final demand from 2008 to 2020, the increase in recycling rates by 2020 (encompassing the achievement of recycling objectives set by European Union Directives), and the simultaneous larger implementation of best available techniques (BAT) for waste incineration. Hybrid monetary physical input‐output tables are initially derived from balanced physical supply and use tables and further complemented with process inventory data on waste treatment technologies. A dramatic reduction in the demand for primary metals (by a factor of 2.0) and for primary mining and quarrying products for construction (by a factor of 1.9) is observed in 2020, as compared to 2008, in the case of the scenario “recycling,” despite the competition induced by the evolution of the final demand. On the contrary, considering energy requirements and fossil carbon dioxide, sulfur dioxide, and nitrogen oxide emissions caused by the French final demand, the combined improvements in recycling and incineration performances by 2020 would only limit the rise induced by the evolution of the final demand. On the basis of these results, the potential contribution of waste management policies to the decoupling of resource consumption and gaseous emissions from final demand's growth is finally discussed.     

A Supply‐Use Approach to Waste Input‐Output Analysis

In this article, we extend Namakura and Kondo's waste input‐output (WIO) framework by incorporating a supply‐use formalism, resulting in waste supply‐use tables (WSUTs). We present the theoretical underpinnings of the WSUT and, in particular, the transition from Nakamura and Kondo's WIO form to the new WSUT form. Further, we offer a mathematical proof of the equivalence of WIO and WSUT multipliers. We illustrate the workings of the WSUT calculus using economic and waste data for the Australian economy in 2008–2009.