排序方式: 共有32条查询结果,搜索用时 18 毫秒
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T. Winkel H. D. Bertero P. Bommel J. Bourliaud M. Chevarría Lazo G. Cortes P. Gasselin S. Geerts R. Joffre F. Léger B. Martinez Avisa S. Rambal G. Rivière M. Tichit J. F. Tourrand A. Vassas Toral J. J. Vacher M. Vieira Pak 《Journal of Agronomy and Crop Science》2012,198(4):314-319
Reviewing the situation of quinoa production in southern Bolivia, Jacobsen (2011, J. Agron. Crop Sci. 197: 390) argues that the booming export market has a negative effect on the environment and on the home consumption of quinoa, thereby leading to an environmental disaster in the region. In view of the scarcity of scientific knowledge on the rapid social and environmental dynamics in the region, we consider that Jacobsen’s review misrepresents the situation of quinoa production in southern Bolivia. Specifically, we argue that (i) the data presented by Jacobsen (2011, J. Agron. Crop Sci. 197: 390) do not support any drop in quinoa crop yield supposed to reflect soil degradation and (ii) his demonstration regarding home consumption of quinoa is ill‐founded from both a nutritional and a cultural point of view. We suggest that the diffusion of the arguments exposed by Jacobsen (2011, J. Agron. Crop Sci. 197: 390), because of their flaws, might have strong negative impacts on those concerned with sustainable food production and fair‐trade with developing countries. We conclude that, rather than reinforced agro‐technical controls on local farmers, the rising competition in the international quinoa market requires a shift towards an ethical economy and ethical research cooperation with quinoa producers. 相似文献
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Monotelodisomics of chromosome arms 2RL and 6RL were observed in progenies of rye trisomics. The monotelodisomic of chromosome arm 6RL (2n = 13 + 6RL) is vital and is well transmitted through the pollen. In the progeny of monotelodisomic 2RL. (2n = 13 + 2RL) no monotelodisomic but one monotelotrisomic of chromosome arm 2RS (2n = 14 + 2RS), one trisomic with an aberrant chromosome consisting (if chromosome arm IRS and a part of chromosome arm 2RL (2n = 14 + 2RSL) and one double telotrisomic of chromosome 2R (2n = 13 + 2RS + 2RL) have been identified. 相似文献
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Bright Spots, Structure, and Magmatism in Southern Tibet from INDEPTH Seismic Reflection Profiling 总被引:8,自引:0,他引:8
LD Brown W Zhao KD Nelson M Hauck D Alsdorf A Ross M Cogan M Clark X Liu J Che 《Science (New York, N.Y.)》1996,274(5293):1688-1690
INDEPTH seismic reflection profiling shows that the decollement beneath which Indian lithosphere underthrusts the Himalaya extends at least 225 kilometers north of the Himalayan deformation front to a depth of approximately 50 kilometers. Prominent reflections appear at depths of 15 to 18 kilometers near where the decollement reflector apparently terminates. These reflections extend north of the Zangbo suture to the Damxung graben of the Tibet Plateau. Some of these reflections have locally anomalous amplitudes (bright spots) and coincident negative polarities implying that they are produced by fluids in the crust. The presence of geothermal activity and high heat flow in the regions of these reflections and the tectonic setting suggest that the bright spots mark granitic magmas derived by partial melting of the tectonically thickened crust. 相似文献
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This article addresses the German debate on the issue of the common welfare designation of public forests. In the first part,
drawing on two case studies, the political discourse on the issue is introduced. Two major competing ‘story lines’ can be
made out that are both based on a long tradition of controversially discussed concepts of regulatory forest policy. While
they both emphasise that common welfare services in forestry run counter to profit orientation, they fundamentally differ
with regard to the consequences for forest policy, e.g., considering the degree of state intervention. Afterwards, an overview
on the scientific debate on common welfare in the German context is given, and different concepts of common welfare determination
are distinguished. Existing approaches of common welfare determination in German forest policy are related to these concepts
and discussed. It is argued that the common welfare designation of the public forest is only insufficiently implemented by
the actual governance arrangements. Based on this consideration, eventually, the implementation of a procedural concept of
common welfare operationalisation in Germany’s public forests at the local level is proposed. While such a concept will not
solve all complex problems related to the determination of common welfare in public forestry, it would notably contribute
to a more operational definition of common welfare in public forestry and a more informed public debate on the issue. 相似文献
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Extract Myophosphorylase deficiency (glycogen storage disease Type V) has been diagnosed in Charolais calves in New Zealand. It is manifested as exercise intolerance and recumbency, usually at several weeks of age, due to an inability to mobilise glucose, as glucose phosphate, from glycogen. Affected calves may rise and walk after a rest to again become affected on further exercise. There is rhabdomyolysis and after repeated or severe attacks the calf may remain recumbent and need to be euthanised. The mutant phosphorylase gene has been described. We have established a PCR-RFLP test based on a published method, and have confirmed the diagnosis in affected calves and heterozygous status of sires, dams and other related individuals belonging to an extended family. In addition, several other non-related heterozygotes have been identified in that and another herd. There appears to have been importations of the gene from both England and America. 相似文献
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AC Johnstone KD McSporran JE Kenny IL Anderson GR MacPherson RD Jolly 《New Zealand veterinary journal》2013,61(6):404-408
AIM: To describe a disease of muscle in Charolais calves and confirm the putative diagnosis of inherited myophosphorylase deficiency. METHODS: Variously stained paraffin sections of muscle prepared from affected calves were used to describe the lesions. A polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) test was developed and applied to affected calves, their sires, dams and other individuals. RESULTS: The lesions were those of rhabdomyolysis of skeletal muscles and sub-sarcolemmal spaces in normal fibres. The PCR-RFLP test confirmed the expected mutation for phosphorylase deficiency of Charolais cattle in two affected calves. In addition, sires, dams and other closely-related individuals of four affected calves tested as heterozygous for the mutation. Other apparently unrelated animals also tested as heterozygous. CONCLUSIONS: The diagnosis of myophosphorylase deficiency was confirmed. The PCR-RFLP test is suitable for use in controlling this recessively-inherited disorder as it can diagnose heterozygous individuals that are otherwise clinically normal. 相似文献
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