EAM会议专刊辑述评——气候变化下旱区农业生态系统的可持续性

农业生产是将自然资源不断转化为农产品的过程。简单的说就是将阳光、空气、水和土壤等无机资源转化为可以供人类消费的有机产物。农业生态系统必须对全球气候变化、市场竞争、自然环境的恶化、经济等政策法规和人民的需求等因素做出灵活的应对策略,同时还要保证自然生态系统的稳定性。在发展中国家,有超过20亿的人口每天收入低于2美元,他们收入中绝大部分都用于解决温饱。这些人大部分生活在干旱、半干旱地区,并以农业生产作为生活的主要来源。由于这些地区水资源匮乏、土壤贫瘠,粮食安全问题一直是该地区人类生存的关键。中澳两国都把干旱、半干旱地区的农牧业发展作为研究的重点。两国的专家都致力于恢复和维护干旱半干旱地区脆弱的农业生态系统。气候变化正在使农业生态系统可持续发展面临严峻挑战。因此,迫切需要农学,生态学,环境学,社会经济学等多学科的共同发展和融合解决这一问题。2010年7月20—25日在兰州大学举办了以“气候变化和旱区农业生态系统管理”为主题的“第二届生态系统评估与管理（EAM）国际会议”。国内外众多知名专家参与了此次会议,并共同讨论在全球气候变化背景下如何提高干旱半干旱地区脆弱农业生态系统生产力与可持续性。本次会议的议题是：(1）半干旱地区旱作雨养农业生态系统评估与管理,(2）干旱地区绿洲农业生态系统评估与管理。此次会议由兰州大学和澳大利亚西澳大学联合主办,中国科学院生态环境研究中心协办,由国家教育部和国家外专局联合支持、兰州大学干旱与草地生态教育部重点实验室承担的“旱寒生态学”学科创新引智基地和西澳大学农业研究院、FAO属下的叙利亚国际旱地农业研究中心(ICARDA)联合提供资金支持。会议期间,25位专家就干旱、半干旱地区植物土壤互作关系作了报告。另外还有18位在干旱半干旱地区科研一线工作的青年学者汇报了研究进展,并与专家进行了广泛交流。报告会之后,大会组织专家分别对典型旱区农业进行了考察,分别是兰州大学黄土高原旱地农业生态实验站(榆中)和甘肃武威市民勤绿洲农业生态系统。此次大会遴选出35篇学术论文,以专刊的形式发表于《生态学报》第31卷第9期。会议遴选出的其它英文文章将于2011年在《Plant and Soil》和《Crop and Pasture Science》上发表,敬请期待。我们相信,本专刊的出版将会对气候变化背景下旱区农业生态系统的研究和发展产生重要的推动作用。     

Wild relatives of wheat: <Emphasis Type="Italic">Aegilops</Emphasis>–<Emphasis Type="Italic">Triticum</Emphasis> accessions disclose differential antioxidative and physiological responses to water stress

Wild relatives of wheat are an outstanding source of resistance to both abiotic and biotic stresses. In the present study, we evaluated the activity of four antioxidant enzymes—superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and guaiacol peroxidase (GPX)—along with photosynthetic pigments and shoot biomass in 12 Aegilops–Triticum accessions with different genomic constitutions and two tolerant and sensitive control varieties under well-watered (WW; 90% FC), moderate (MS; 50% FC) and severe (SS; 25% FC) water stress treatments. The analysis of variance for measured traits indicated highly significant effects of the water stress treatments, accessions, and their interactions. The 12 domesticated and wild relatives of wheat exhibited more variability and greater activity in the expression of antioxidative enzymes than cultivated wheats. While domesticated forms of wheat, T. aestivum (AABBDD) and T. durum (AABB) seem to have a functionally active antioxidant mechanism, other accessions with alien genomes—Ae. umbellulata (UU), Ae. crassa (MMDD), Ae. caudata (CC), Ae. cylindrica (DDCC) and T. boeoticum (A^bA^b)—respond to water stress by increasing enzymatic antioxidants as the dominant mechanism that contributes to the retention of oxidative balance in the cell. Furthermore, abovementioned accessions with alien genomes had higher photosynthetic pigment contents (chlorophyll a, chlorophyll b, total chlorophyll, and carotenoid) under water stress than well-watered conditions. Hence, these accessions could be used in future breeding programs to combine beneficial stress-adaptive characters of alien genomes into synthetic hexaploid wheat varieties in the field, even at limited water supply.     

Identification and validation of QTL and their associated genes for pre-emergent metribuzin tolerance in hexaploid wheat (<Emphasis Type="Italic">Triticum aestivum</Emphasis> L.)

Background

Herbicide tolerance is an important trait that allows effective weed management in wheat crops. Genetic knowledge of metribuzin tolerance in wheat is needed to develop new cultivars for the industry. Here, we evaluated metribuzin tolerance in a recombinant inbred line (RIL) mapping population derived from Synthetic W7984 and Opata 85 over two consecutive years to identify quantitative trait loci (QTL) contributing to the trait. Herbicide tolerance was measured by two chlorophyll traits, SPAD chlorophyll content index (CCI) and visual senescence score (SNS). The markers associated with major QTL from Synthetic W7984, positively contributing to reduced phytotoxic effects under herbicide treatment were validated in two F_3/4 recombinant inbred populations developed from crosses of Synthetic W7984?×?Westonia and Synthetic W7984?×?Lang.

Results

Composite interval mapping (CIM) identified four QTL, two on chromosome 4A and one each on chromosomes 2D and 1A. The chromosomal position of the two QTL mapped on 4A within 10 cM intervals was refined and validated by multiple interval mapping (MIM). The major QTL affecting both measures of tolerance jointly explained 42 and 45% of the phenotypic variation by percentage CCI reduction and SNS, respectively. The identified QTL have a pure additive effect. The metribuzin tolerant allele of markers, Xgwm33 and Xbarc343, conferred lower phytotoxicity and explained the maximum phenotypic variation of 28.8 and 24.5%, respectively. The approximate physical localization of the QTL revealed the presence of five candidate genes (ribulose-bisphosphate carboxylase, oxidoreductase (rbcS), glycosyltransferase, serine/threonine-specific protein kinase and phosphotransferase) with a direct role in photosynthesis and/or metabolic detoxification pathways.

Conclusion

Metribuzin causes photo-inhibition by interrupting electron flow in PSII. Consequently, chlorophyll traits enabled the measure of high proportion of genetic variability in the mapping population. The validated molecular markers associated with metribuzin tolerance mediating QTL may be used in marker-assisted breeding to select metribuzin tolerant lines. Alternatively, validated favourable alleles could be introgressed into elite wheat cultivars to enhance metribuzin tolerance and improve grain yield in dryland farming for sustainable wheat production.

     

Analysis of copia sequence variation within and between Drosophila species

The sequences of the 5' long-terminal repeat (LTR) and adjacent leader regions of 27 full-length copia elements isolated from natural populations of Drosophila melanogaster, D. simulans, and D. mauritiana are presented. Phylogenetic analyses indicate that although D. melanogaster copia elements are distinct from those of D. simulans and D. mauritiana, the elements of these latter two species are not distinguishable from one another. LTRs and adjacent 5' leader regions of elements isolated from D. simulans and D. mauritiana are structurally similar to one another and carry substantial deletional variation mapping to regions previously identified as being of potential importance for copia expression.      

Salt tolerance of Beta macrocarpa is associated with efficient osmotic adjustment and increased apoplastic water content

The chenopod Beta macrocarpa Guss (wild Swiss chard) is known for its salt tolerance, but the mechanisms involved are still debated. In order to elucidate the processes involved, we grew wild Swiss chard exposed to three salinity levels (0, 100 and 200 mm NaCl) for 45 days, and determined several physiological parameters at the end of this time. All plants survived despite reductions in growth, photosynthesis and stomatal conductance in plants exposed to salinity (100 and 200 mm NaCl). As expected, the negative effects of salinity were more pronounced at 200 mm than at 100 mm NaCl: (i) leaf apoplastic water content was maintained or increased despite a significant reduction in leaf water potential, revealing the halophytic character of B. macrocarpa; (ii) osmotic adjustment occurred, which presumably enhanced the driving force for water extraction from soil, and avoided toxic build up of Na⁺ and Cl^– in the mesophyll apoplast of leaves. Osmotic adjustment mainly occurred through accumulation of inorganic ions and to a lesser extent soluble sugars; proline was not implicated in osmotic adjustment. Overall, two important mechanisms of salt tolerance in B. macrocarpa were identified: osmotic and apoplastic water adjustment.     

A single base deletion from the C1-inhibitor gene causes type I hereditary angio-oedema.

RFLP analysis, the polymerase chain reaction and nucleotide sequencing have been used to characterise a C1-inhibitor gene mutation responsible for type I hereditary angio-oedema (HAE). A single base deletion (C-16698) from the eighth exon of the C1-inhibitor gene alters the reading frame of the exon and generates a premature translation termination codon. This represents the first report of this form of C1-inhibitor gene mutation in type I HAE.     

The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2

Sensitivity to nonmodified poliovirus infection is an autosomal dominant trait, specific to primates. The gene for poliovirus sensitivity (PVS) is encoded on human chromosome 19. In order to sublocalize the PVS gene, we infected rodent-human hybrid cell lines that divide human chromosome 19 into four regions with poliovirus 1 and/or 3. When infected, these hybrid cell lines showed the typical cytopathic effect of poliovirus infection only if they contained 19q12----q13.2 as the smallest region of overlap. Appropriate negative and positive controls were used. PVS may be of relevance to myotonic dystrophy (DM) and the inherited motor neuron diseases: to DM because it localizes to the same region of chromosome 19 and to the inherited motor neuron diseases because it encodes a cell-surface receptor expressed on motor neurons.     

Exclusion of the expansion of CAG/CTG repeats at thirteen loci on chromosome 12 as a candidate genetic mutation in scapuloperoneal spinal muscular atrophy with anticipation

Scapuloperoneal spinal muscular atrophy (SPSMA) is a neuromuscular disorder characterized by weakness in the distribution of shoulder girdle and peroneal muscles. We have previously described a large New England kindred with autosomal dominant SPSMA and have subsequently linked this family trait to 12q24.1-q24.31. In this family, disease expression becomes more severe and progressive in successive generations, suggesting genetic anticipation. Accordingly, we have investigated the thirteen known CAG/CTG repeat loci on chromosome 12 that could be tested by using the polymerase chain reaction as candidate genetic mutations in SPSMA. None of these loci is expanded. Received: 12 June 1996 / Revised: 24 January 1997