Expert system application for prioritizing preventive actions for shift work: shift expert

Introduction. Shift patterns, work hours, work arrangements and worker motivations have increasingly become key factors for job performance. The main objective of this article is to design an expert system that identifies the negative effects of shift work and prioritizes mitigation efforts according to their importance in preventing these negative effects. The proposed expert system will be referred to as the shift expert. Methods. A thorough literature review is conducted to determine the effects of shift work on workers. Our work indicates that shift work is linked to demographic variables, sleepiness and fatigue, health and well-being, and social and domestic conditions. These parameters constitute the sections of a questionnaire designed to focus on 26 important issues related to shift work. The shift expert is then constructed to provide prevention advice at the individual and organizational levels, and it prioritizes this advice using a fuzzy analytic hierarchy process model, which considers comparison matrices provided by users during the prioritization process. An empirical study of 61 workers working on three rotating shifts is performed. After administering the questionnaires, the collected data are analyzed statistically, and then the shift expert produces individual and organizational recommendations for these workers.     

Distribution patterns of larval myctophid fishes in the transition region of the western North Pacific

We examined the species composition and horizontal distribution of myctophid fish larvae in the transition region of the western North Pacific during the early summer. In total, 4,760 myctophid larvae were collected at 44 stations; 18 species of myctophids from 15 genera were collected, and the 8 most abundant species accounted for >95% of larvae. The distribution patterns of these larvae were well defined by the hydrographic structures of the study area including the Oyashio and Kuroshio fronts, the Subarctic Boundary, and a warm core ring. The horizontal distribution patterns of the eight dominant species were categorized into three groups: northern transition water (Stenobrachius nannochir, Tarletonbeania taylori, and Lampanyctus jordani), southern transition water (Symbolophorus californiensis, Diaphus theta, and Nannobrachium regale), and Kuroshio (Myctophum asperum and Diaphus garmani). The Subarctic Boundary defined the distributions of the northern and southern transition-water groups. The importance of areas of western North Pacific transition water as spawning and nursery grounds for subarctic, transitional, and subtropical myctophid fishes was indicated by the relationship between the horizontal distribution patterns of larvae, juveniles, and adults and the physical oceanographic structures.Communicated by T. Ikeda, Hakodate     

Teil 1: PCDD/F in Böden,Vegetation und Kuhmilch

Soil samples were taken from residential gardens, grasslands and forests at 22 locations in Marsberg, North Rhine-Westphalia, and analyzed for PCDD/F. Sampling was concentrated on the vicinity of a former copper smelter where copper waste material (calledKieselrot) was deposited and emissions from former stacks contaminated a large land area. Maximum PCDD/F-concentrations were 407 ng TE GBA/kg dm in garden soil (0–30 cm depth), 98 ng TE BGA/kg dm in agricultural grassland (0–10 cm depth), 227 ng TE BGA/kg dm in wasteland, and up to 8073 ng TE BGA/kg dm in forest soils. PCDD/F-levels in soil decreased with increasing distance from the former sources providing a large historic emission problem, apart from the still existing kieselrot waste site. Ash residues from former flue gas duct showed up to 2,4 mg TE BGA/kg dm. PCDD/F-concentrations in vegetable samples from highly contaminated garden soils and grass from agricultural grassland were found to be relatively low in relation to soil values. PCDD/F-levels in salad showed a mean of 2,2 ng TE BGA/kg dm while grass concentrations were <6 ng TE BGA/kg dm. Thus, no correlation was found between soil and vegetation values with the exception for carrot roots where obviously a small transfer of PCDD/F between the two media took place. PCDD/F-content in grass taken over the vegetation period showed a tendency to increase toward the end of the growing season, which is probably related to changes in the dry matter yield over the season. No correlation was found in general between soil, grass and milk PCDD/F contents when all samples were taken from the same grassland. PCDD/F-concentrations in milk ranged between 0,6 and 1,1 pg TE BGA/g milkfat and were thus in the same range as consumer milk in the Federal Republic of Germany. PCDD/F in needles from conifers showed a clear relationship with respect to distance from the former waste site. The relatively high levels in conifer needles [36 ng TE BGA/kg dm] were obviously due to sporting activities (i.e. motocross racing where contaminated material was resuspended and deposited on surrounding trees).     

Growth and reproduction of Pycnogonum litorale (Pycnogonida) under laboratory conditions

The complete life cycle of Pycnogonum litorale Ström was observed under laboratory conditions. At 15?°C and a 16?h light:8?h dark photocycle, the duration of embryonic development from oviposition to egg-hatching varied from 32 to 111?d. The onset of egg hatching ranged from 32 to 81?d after oviposition in different egg batches, and the period between the first and the last hatch within a single egg batch varied between 16 and 57?d. The larval period, consisting of five larval instars, lasted between 66 and 113?d. Juvenile development required seven (exceptionally 8 or 9) moults and lasted between 263 and 400?d. The average interval between successive moults in juveniles increased with increasing size from 24 to 82?d. Though females did not moult more often than their male conspecifics, they reached a size from 8.5 to 11.0?mm (average 10.1?mm) while adult males measured only 7.0 to 8.5?mm (average 7.7?mm). At low temperatures (2?°C) moulting was almost completely inhibited. After raising the temperature to 6?°C, the moulting frequency increased to a rate almost as high as at a constant temperature of 15?°C. Moulting was also retarded by starvation and accelerated by subsequent feeding. Adults lived for up to 9?years without further moults, with several periods of mating and oviposition at irregular intervals. In combination with previous long-term field observations, the present results provide a more complete picture of the life cycle of P. litorale in a natural habitat. The great variation in the duration of the different developmental stages, the ability to survive periods of cold and starvation, and the longevity of the adults are important for the survival of pycnogonid populations under changing environmental conditions.     

Are naked and common mole-rats eusocial and if so, why?

Eusociality in mammals is defined in the present paper by the following criteria: reproductive altruism (which involves reproductive division of labor and cooperative alloparental brood care), overlap of adult generations, and permanent (lifelong) philopatry. We argue that additional criteria such as the existence of castes, colony size, reproductive skew, and social cohesion are not pertinent to the definition of eusociality in mammals. According to our definition of mammalian eusociality, several rodent species of the African family Bathyergidae can be considered eusocial, including the naked mole-rat (Heterocephalus glaber), Damaraland mole-rat (Cryptomys damarensis), and several additional, if not all, species in the genus Cryptomys. Furthermore, some species of social voles (like Microtus ochrogaster) may also fulfill criteria of mammalian eusociality. Understanding the evolution of eusociality in mole-rats requires answers to two primary questions: (1) What are the preconditions for the development of their eusocial systems? (2) Why do offspring remain in the natal group rather than dispersing and reproducing? Eusociality in mammals is by definition a special case of monogamy (more specifically: monogyny one female breeding), involving prolonged pair bonding for more than one breeding period. We argue that eusociality in mole-rats evolved from a monogamous mating system where cooperative brood care was already established. A tendency for group living is considered to be an ancestral (plesiomorph) trait among African bathyergid mole-rats, linking them to other hystricognath rodents. A solitary lifestyle seen in some genera, such as Bathyergus, Georychus, and Heliophobius, is assumed to be a derived trait that arose independently in different lineages of bathyergids, possibly as a consequence of selective constraints associated with the subterranean environment. In proximate terms, in eusocial mole-rats either puberty is assumed to be developmentally delayed so that under natural conditions most animals die before dispersal is triggered (e.g., in the case of Heterocephalus) or dispersal is induced only by an incidental encounter with an unfamiliar, yet adequate sexual partner (e.g., in the case of Cryptomys). Ultimately, a combination of strategies involving either dispersal and/or philopatry can be beneficial, especially in a highly unpredictable environment. If genetic relatedness among siblings is high (e.g., a coefficient of relatedness of 0.5 or more), then philopatry would not invoke an appreciable loss of fitness, especially if the cost of dispersing is higher than staying within the natal group. High genetic relatedness is more likely in a monogamous mating system or a highly inbred population. In this paper, we argue that the preconditions for eusociality in bathyergid mole-rats were a monogamous mating system and high genetic relatedness among individuals. We argue against the aridity food-distribution hypothesis (AFDH) that suggests a causal relationship between cooperative foraging for patchily distributed resources and the origin of eusociality. The AFDH may explain group size dynamics of social mole-rats as a function of the distribution and availability of resources but it is inadequate to explain the formation of eusocial societies of mole-rats, especially with respect to providing preconditions conducive for the emergence of eusociality.