草地与农牧交错带退化生态系统重建及防治途径

草地不仅是草地畜牧业的基地，而且在生态环境保护与建设方面的作用尤为重要。草原与农牧交错带，即不同于西部牧区，也不同于东部农区。根据它在地理、气候、农林牧产业结构、生态、经济、文化、社会等方面具有自己独特地位的实际情况，因地制宜提出了相应之对策，为国家在西部大开发和草地与农牧交错带生态环境的恢复提供科学依据。     

Telomeres and meiosis in health and disease

Meiotic dysfunction increasingly afflicts women as they age, resulting in infertility, miscarriage and handicapped offspring. How aging disrupts meiotic function in women remains unclear, but as women increasingly delay childbearing, this issue becomes urgent. Telomeres, which mediate aging in mitotic cells, may also mediate aging during meiosis. Telomeres shorten during DNA replication. In mammals, oocytes remain quiescent, but their precursors replicated during fetal oogenesis. Moreover, eggs ovulated from older women entered meiosis later during fetal oogenesis than eggs ovulated when younger, and therefore underwent more replications. Telomeres also shorten from reactive oxygen, which triggers a DNA repair response, so the prolonged interval between fetal oogenesis and ovulation in some women would further shorten telomeres. Mice normally do not exhibit age-related meiotic dysfunction (interestingly, their telomeres are manyfold longer than telomeres in women), but genetic or pharmacologic shortening of mouse telomeres recapitulates the reproductive aging phenotype of women. This has led to a telomere theory of age-related meiotic dysfunction in women, and underlined the importance to human health of a mechanistic understanding of telomeres and meiosis.     

Models and structures: Phenomenological and partial

In a recent paper, Suárez and Cartwright (2008) return to the example of London and London's construction of a model for superconductivity and raise a number of concerns against the account of this construction presented in French and Ladyman (1997) and elsewhere. In this discussion note, we examine the challenge they raised and offer our responses.     

Telomeres and meiosis in health and disease

The aim of this review is threefold. First, we want to report on recent observations on the role of telomeres in the alignment of homolog and non-homologues in the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe and the relationship of early telomere clustering to later recombination events. Second, we compare the similarities and differences between synaptic and asynaptic yeasts. Third, we report on the increasing evidence of the effect of meiosis on telomeric sequences that suggest an induction of a specific form of recombination processes termed telomere rapid deletion.     

Contrasting tail and other responses to morphine and reserpine in rats and mice

Zusammenfassung Charakteristisch verschiedene Schwanzstellungen zeigen Albino-Ratten und -Mäuse als Morphium- bzw. Reserpinreaktion. Verstärkte Schwanzreaktionen erhält man bei der Maus nach Morphium, bei der Ratte nach Reserpin. Methylphenidat erweist sich bei der Ratte antagonistisch gegen Reserpin, während im Mäuseversuch nach Reserpin injiziertes Morphium kompetitiv zu wirken scheint.

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This work was aided by a grant from the Medical Research Council.     

Linear and threshold forecasts of output and inflation using stock and housing prices

This study examines whether simple measures of Canadian equity and housing price misalignments contain leading information about output growth and inflation. Previous authors have generally found that the information content of asset prices in general, and equity and housing prices in particular, are unreliable in that they do not systematically predict future economic activity or inflation. However, earlier studies relied on simple linear relationships that would fail to pick up the potential nonlinear effects of asset price misalignments. Our results suggest that housing prices are useful for predicting GDP growth, even within a linear context. Meanwhile, both stock and housing prices can improve inflation forecasts, especially when using a threshold specification. These improvements in forecast performance are relative to the information contained in Phillips‐curve type indicators for inflation and IS‐curve type indicators for GDP growth. Copyright © 2008 John Wiley & Sons, Ltd.     

Telomeres and meiosis in health and disease

Telomeres are important segments of chromosomes that protect chromosome ends from nucleolytic degradation and fusion. At meiosis telomeres display an unprecedented behavior which involves their attachment and motility along the nuclear envelope. The movements become restricted to a limited nuclear sector during the so-called bouquet stage, which is widely conserved among species. Recent observations suggest that telomere clustering involves actin and/or microtubules, and is altered in the presence of impaired recombinogenic and chromosome related functions. This review aims to provide an overview of what is currently known about meiotic telomere attachment, dynamics and regulation in synaptic meiosis.     

Telomeres and meiosis in health and disease

Beyond their role in replication and chromosome end capping, telomeres are also thought to function in meiotic chromosome pairing, meiotic and mitotic chromosome segregation as well as in nuclear organization. Observations in both somatic and meiotic cells suggest that the positioning of telomeres within the nucleus is highly specific and believed to be dependent mainly on telomere interactions with the nuclear envelope either directly or through chromatin interacting proteins. Although little is known about the mechanism of telomere clustering, some studies show that it is an active process. Recent data have suggested a regulatory role for telomere chromatin structure in telomere movement. This review will summarize recent studies on telomere interactions with the nuclear matrix, telomere chromatin structure and factors that modify telomere chromatin structure as related to regulation of telomere movement.     

Telomeres and meiosis in health and disease

Telomeres are important segments of chromosomes that protect chromosome ends from nucleolytic degradation and fusion. At meiosis telomeres display an unprecedented behavior which involves their attachment and motility along the nuclear envelope. The movements become restricted to a limited nuclear sector during the so-called bouquet stage, which is widely conserved among species. Recent observations suggest that telomere clustering involves actin and/or microtubules, and is altered in the presence of impaired recombinogenic and chromosome related functions. This review aims to provide an overview of what is currently known about meiotic telomere attachment, dynamics and regulation in synaptic meiosis.     

Hyperbaric oxygen and testicular damage and fertility

Zusammenfassung Männliche Ratten zeigen nach einmaliger oder wiederholter stark erhöhter O₂-Zufuhr (3–5 at) Krämpfe und Lungenschäden und zum Teil Absterben. Schädigungen der Spermatogenese oder der Fertilität traten nicht auf.     

Structure and function of desmosomal proteins and their role in development and disease

Desmosomes represent major intercellular adhesive junctions at basolateral membranes of epithelial cells and in other tissues. They mediate direct cell-cell contacts and provide anchorage sites for intermediate filaments important for the maintenance of tissue architecture. There is increasing evidence now that desmosomes in addition to a simple structural function have new roles in tissue morphogenesis and differentiation. Transmembrane glycoproteins of the cadherin superfamily of Ca²⁺-dependent cell-cell adhesion molecules which mediate direct intercellular interactions in desmosomes appear to be of central importance in this respect. The complex network of proteins forming the desmosomal plaque associated with the cytoplasmic domain of the desmosomal cadherins, however, is also involved in junction assembly and regulation of adhesive strength. This re-view summarizes the structural features of these desmosomal proteins, their function during desmosome assembly and maintenance, and their role in development and disease.Received 5 February 2003; received after revision 14 March 2003; accepted 1 April 2003     

Space and Time in Particle and Field Physics

Textbooks present classical particle and field physics as theories of physical systems situated in Newtonian absolute space. This absolute space has an influence on the evolution of physical processes, and can therefore be seen as a physical system itself; it is substantival. It turns out to be possible, however, to interpret the classical theories in another way. According to this rival interpretation, spatiotemporal position is a property of physical systems, and there is no substantival spacetime. The traditional objection that such a relationist view could not cope with the existence of inertial effects and other manifestations of the causal efficacy of spacetime can be answered successfully. According to the new point of view, the spacetime manifold of classical physics is a purely representational device. It represents possible locations of physical objects or events; but these locations are physical properties inherent in the physical objects or events themselves and having no existence independently of them. In relativistic quantum field theory the physical meaning of the spacetime manifold becomes even less tangible. Not only does the manifold lose its status as a substantival container, but also its function as a representation of spacetime properties possessed by physical systems becomes problematic. ‘Space and time’ become ordering parameters in the web of properties of physical systems. They seem to regain their traditional meaning only in the non-relativistic limit in which the classical particle concept becomes approximately applicable.     

The metabolism and function of sphingolipids and glycosphingolipids

Sphingolipids and glycosphingolipids are emerging as major players in many facets of cell physiology and pathophysiology. We now present an overview of sphingolipid biochemistry and physiology, followed by a brief presentation of recent advances in translational research related to sphingolipids. In discussing sphingolipid biochemistry, we focus on the structure of sphingolipids, and their biosynthetic pathways – the recent identification of most of the enzymes in this pathway has led to significant advances and better characterization of a number of the biosynthetic steps, and the relationship between them. We then discuss some roles of sphingolipids in cell physiology, particularly those of ceramide and sphingosine-1-phosphate, and mention current views about how these lipids act in signal transduction pathways. We end with a discussion of sphingolipids and glycosphingolipids in the etiology and pathology of a number of diseases, such as cancer, immunity, cystic fibrosis, emphysema, diabetes, and sepsis, areas in which sphingolipids are beginning to take a central position, even though many of the details remain to be elucidated. Received 13 February 2007; received after revision 19 April 2007; accepted 26 April 2007     

Hyaluronan synthesis and degradation in cartilage and bone

Hyaluronan (HA) is a large but simple glycosaminoglycan composed of repeating D-glucuronic acid, β1–3 linked to N-acetyl-D-glucosamine β1–4, found in body fluids and tissues, in both intra- and extracellular compartments. Despite its structural simplicity, HA has diverse functions in skeletal biology. In development, HA-rich matrices facilitate migration and condensation of mesenchymal cells, and HA participates in joint cavity formation and longitudinal bone growth. In adult cartilage, HA binding to aggrecan immobilises aggrecan, retaining it at the high concentrations required for compressive resilience. HA also appears to regulate bone remodelling by controlling osteoclast, osteoblast and osteocyte behaviour. The functions of HA depend on its intrinsic properties, which in turn rely on the degree of polymerisation by HA synthases, depolymerisation by hyaluronidases, and interactions with HA-binding proteins. HA synthesis and degradation are closely regulated in skeletal tissues and aberrant synthetic or degradative activity causes disease. The role and regulation of HA synthesis and degradation in cartilage, bone and skeletal development is discussed. Received 5 August 2007; received after revision 19 September 2007; accepted 20 September 2007