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101.
高寒地区多年生禾草混播草地种间竞争效应分析 总被引:16,自引:5,他引:11
从高寒地区3组分禾草混播草地群落的种问竞争机制出发,建立了适合高寒地区3组分禾草混播草地群落种间竞争机制的Lotka—Volterra竞争效应模型,并对该模型所描述的竞争进行了计算机模拟试验。模拟结果表明,试验所选的3种高寒地区3组分禾草混播草群的种间相容性分为两种类型,即不稳定的群落:多叶老芒麦 无芒雀麦 垂穗披碱草和垂穗披碱草 多叶老芒麦 扁穗冰草,其竞争结局是:群落内多叶老芒麦和垂穗披碱草二者共同表现为优势种群,无芒雀麦或扁穗冰草与优势植物的竞争结果将导致其从群落中消失,多叶老芒麦和垂穗披碱草种群将能稳定共存;不稳定-稳定过渡群落:无芒雀麦 多叶老芒麦 扁穗冰草,在没有多叶老芒麦种群的时候,无芒雀麦和扁穗冰草种群可以共存,但是如果多叶老芒麦种群加入无芒雀麦和扁穗冰草所占的区域,它将导致无芒雀麦和扁穗冰草种群趋于灭绝。通过对3个混播试验组计算机模拟竞争模型的竞争效应分析,其结果与方法对科学建植同类型的多年生混播人工草地具有一定的指导意义。 相似文献
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Regional land-cover change affects biodiversity, hydrology, and biogeochemical cycles at local, watershed, and landscape scales.
Developing countries are experiencing rapid land cover change, but assessment is often restricted by limited financial resources,
accessibility, and historical data. The assessment of regional land cover patterns is often the first step in developing conservation
and management plans. This study used remotely sensed land cover and topographic data (Landsat and Shuttle Radar Topography
Mission), supervised classification techniques, and spectral mixture analysis to characterize current landscape patterns and
quantify land cover change from 1985 to 2003 in the Altiplano (2535–4671 m) and Intermediate Valley (Mountain) (1491–4623 m)
physiographic zones in the Southeastern Bolivian Andes. Current land cover was mapped into six classes with an overall accuracy
of 88% using traditional classification techniques and limited field data. The land cover change analysis showed that extensive
deforestation, desertification, and agricultural expansion at a regional scale occurred in the last 20 years (17.3% of the
Mountain Zone and 7.2% of the Altiplano). Spectral mixture analysis (SMA) indicated that communal rangeland degradation has
also occurred, with increases in soil and non-photosynthetic vegetation fractions in most cover classes. SMA also identified
local areas with intensive management activities that are changing differently from the overall region (e.g., localized areas
of increased green vegetation). This indicates that actions of local communities, governments, and environmental managers
can moderate the potentially severe future changes implied by the results of this study. 相似文献
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杂柑类新品种——建阳橘柚的选育 总被引:1,自引:0,他引:1
建阳橘柚是从国外引进的橘柚品种中通过芽变选育成的杂柑类新品种。该品种果实扁圆形或圆球形,平均单果质量为171g,果面亮黄色,有蜡质光泽,油胞较突出,果皮较厚,较耐贮藏,果肉橙黄色,无核,肉质细嫩,多汁,兼有橘和柚的风味,可溶性固形物14.0%,12月上中旬果实成熟,果实生育期220~230d。该品种具有品质优,风味独特,适应性广,抗逆性强等特点,适宜在福建省温州蜜橘种植区推广。 相似文献
109.
A. Omrani-Sabbaghi M. Shahriari M. Falahati-Anbaran S.A. Mohammadi A. Nankali M. Mardi B. Ghareyazie 《Scientia Horticulturae》2007
To study the genetic variation in Iranian olive collections and some foreign olive cultivars, 47 accessions of 18 local cultivars from 6 olive collections of Iran (Roudbar, Zanjan, Ahvaz, Dezful, Kazeroon and Shiraz), were analyzed along with 30 imported cultivars using 16 microsatellite primer pairs. All the used microsatellite loci revealed polymorphism in the studied genotypes, except GAPU14 and GAPU113 markers. Fourteen microsatellite primers amplified 126 polymorphic alleles in the 87 selected olive accessions. The average number of alleles per locus was 9, ranging from 3 to 14. Polymorphic information content (PIC) was 0.85. The genetic similarity based on Jaccard coefficient ranged from 0.15 to 1. The genetic relationships among accessions were investigated using cluster analysis and principal component analysis (PCA). Most of the accessions with the same name were grouped together; some exceptions were also observed. As expected, close relationship was observed among accessions within same cultivar. Most of the Iranian olive accessions were clustered to a main distinct group. Two-dimensional scatter plot of principal component analysis revealed a clear separation of most of the Iranian olives from Syrian and other introduced cultivars. These suggest that Iranian cultivars have different origin related to West Mediterranean basin cultivars and have evolved independently from the others. Between and within Iranian and foreign cultivars (cultivars including three or more accessions) genetic diversity was analyzed using analysis of molecular variance (AMOVA). AMOVA revealed higher within cultivar genetic variation (62.76%) as compare to that between cultivar variations (37.24%). The intra- and inter-cultivar variance tested by permutation test showed significant genetic variation at both levels. The high level within cultivar genetic variance could be due to mislabeling and presence of homonyms in cultivars produced by vegetative propagation from original plants. 相似文献
110.
To obtain the basic information on fruit set regulation, effects of several RNases including S-RNase on pollen tube growth and RNA degradation in the tube were studied in the pear. Purified S-RNase from the Japanese pear ‘Kosui’ (S4S5) predominantly inhibited the growth of ‘Kosui’ pollen tubes (self) in vitro at 0.28 unit μL−1, but it inhibited ‘Chojuro’ (S2S3) pollen (cross) only slightly. The same unit of RNase T1 (EC 3.1.27.3) clearly inhibited the pollen tube growth, but the action was significantly weaker than that of the S-RNase against the self-pollen. Inhibitory effect of RNase T2 (EC 3.1.27.1) and RNase A (EC 3.1.27.5) was only slight. The proteins other than the S-RNase extracted from pear style did not have any inhibitory action, though they possessed RNase activity 3.8 times higher than S-RNase. Thus, RNases tested here could not substitute for the S-RNase in specific inhibition against the self-pollen tube growth. Total RNA degradation by each RNase occurred in the pollen tubes as following order; S-RNase (self) ≥T1 > T2 ≥ A > S-RNase (cross). Degradation degree of 28S and 18S rRNA was as follows; S-RNase (self) > A > T1 > T2 > S-RNase (cross). The degradation of 5.8S and 5S rRNA was; S-RNase (self) > S-RNase (cross) > A > T2 > T1. The degree of rRNA degradation was, thus, not always in parallel with the degree of pollen growth inhibition. The S-RNase may degrade not only rRNA but also mRNA essential for pollen tube growth, and may be specifically adapted to inhibit the growth of self-pollen tubes. Therefore, controlling S-RNase amount in the style will produce self-thinning cultivars efficiently, which are unnecessary not only for hand-pollination but fruit-thinning practices in the pear. Practically, cultivar with weak self-incompatibility and small amount of S-RNase, such as ‘Okusankichi’, may be an expecting candidate for breeding self-thinning cultivars. 相似文献