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1. The impact of land-claim on the intertidal areas of the Forth estuary, eastern Scotland is described. It is shown that in recent times almost 50% of the intertidal area has been destroyed for a variety of purposes, including agriculture, harbours and industrial development. 2. The loss of infaunal invertebrate biomass and production from the intertidal habitat has been calculated for each part of the estuary, and by summation for the whole estuary. The loss is discussed in relation to the total biomass and production, both intertidally and subtidally, of the estuary. It is shown that proportionately more biomass and production may have been lost than area. 3. The impact of land-claim on estuarine fish is calculated. Land-claim has removed 24% of the natural fish habitats in the Forth estuary, and thereby removed 40% of their food supply. 4. The impact of habitat loss on birds was observed for one area where observations continued throughout a period of land-claim. For individual bird species at Torry Bay, land-claim had consequences ranging from neutral to substantially negative. Significant declines were found for overwintering populations of dunlin and bar-tailed godwit. Comparisons of pre- and post-land-claim bird feeding usage of this area, showed that the impact of land-claim on local bird populations differed between species. The large scale loss of habitat on the Forth seems likely to have reduced the size of some shorebird populations which overwinter on the estuary. 5. It is concluded that when considering the impact of land-claim on estuaries that, as found in some previous studies, a simple consideration of area lost may be inadequate to describe the effects of land-claim, and the consequences for animals living within the estuary may differ considerably amongst themselves and from area to area.  相似文献   
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Pseudomonads were isolated from the roots of winter wheat plants. Plants produced from direct-drilling of seeds into plots where crop residues had been burnt were larger and appeared healthier than those from plots where crop residues remained. Tests showed that roots from the plants direct-drilled into the plots where crop residues had been burnt were colonized by fewer pseudomonads which could inhibit plant growth than those from plants produced from plots where crop residues remained. The tests were performed by inoculating wheat seedlings with individual bacterial isolates and measuring root growth. When several wheat cultivars were bioassayed against each of two of the inhibitory pseudomonads, they differed greatly in susceptibility to the adverse effects of the bacteria.  相似文献   
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Congenital dyserythropoiesis with dyskeratosis is a slow, progressive, and often fatal disease in Polled Hereford calves. Affected calves have a macrocytic normochromic anemia with a mild reticulocytosis. Studies indicate that calves are hyperferremic with increased saturation of serum total iron binding capacity, which rules out iron deficiency as a cause. Other secondary causes of dyserythropoiesis, including cobalamin and folate deficiencies, are unlikely because serum cobalamin and folate levels of affected calves were normal. Virus isolation was negative, and failure to identify bovine retroviral antigens or antibodies from several calves suggested that viral agents were not involved. Bone marrow cytologic findings were similar to those in congenital hereditary dyserythropoiesis in humans and included occasional multinucleate cells, internuclear chromatin bridging between nuclei of partially divided cells, and, more frequently, irregular nuclear shapes and chromatin patterns. DNA content and cell cycle distribution of erythroid cells appeared normal, and no electrophoretic abnormalities were detected in erythrocyte membrane proteins. The Polled Hereford syndrome is similar in many ways to type I congenital dyserythropoiesis in humans and may be an appropriate biomedical model for studying erythroid proliferation during dyserythropoiesis.  相似文献   
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In the polymerase chain reaction (PCR), two specific oligonucleotide primers are used to amplify the sequences between them. However, this technique is not suitable for amplifying genes that encode molecules where the 5' portion of the sequences of interest is not known, such as the T cell receptor (TCR) or immunoglobulins. Because of this limitation, a novel technique, anchored polymerase chain reaction (A-PCR), was devised that requires sequence specificity only on the 3' end of the target fragment. It was used to analyze TCR delta chain mRNA's from human peripheral blood gamma delta T cells. Most of these cells had a V delta gene segment not previously described (V delta 3), and the delta chain junctional sequences formed a discrete subpopulation compared with those previously reported.  相似文献   
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