首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 0 毫秒
1.
2.
3.
A successful protocol was developed for mass propagation of Lawsonia inermis Linn., an important medicinal plant. Multiple shoots were induced in apical and axillary meristems derived from mature explants of L. inermis on Murashige and Skoog (1962) medium supplemented with 0.25 mg/l 6-benzylaminopurine (BA), 0.25 mg/l Kinetin (Kn), 0.5 mg/l ascorbic acid and 3% (w/v) sucrose. The rate of multiplication was higher when the cultures were incubated under continuous light rather than the 14 hr photoperiod. Rooting was readily achieved upon transferring the microshoots onto MS basal semi-solid medium supplemented with 0.25 mg/l indole-3-butyric acid (IBA) after ten days of culture. Micropropagated plantlets were acclimatized and successfully grown in soil.  相似文献   

4.
5.
6.
7.
GRAHAM, S. A., CRISCI, J. V. & HOCH, P. C, 1993. Cladistic analysis of the Lythraceae sensu lato based on morphological characters. The Lythraceae s. I. comprise 31 mostly highly distinctive genera distributed worldwide. Cladistic analyses of the family were undertaken using 26 characters from anatomy, floral morphology, pollen, and seed morphology. Of four outgroup hypotheses, the Onagraceae offered the best heuristic assessment, generating 3746 trees with a tree length of 83 and consistency index and (C.I.) of 0.41. A strict consensus tree from the 3746 trees produced a basal monophyletic group of five genera (Sonneratia, Duabanga, Punka, Lagerstroemia, Lawsonia) characterized by anthotelic (determinate) inflorescences and wet stigmas, and a second clade with blastotelic (indeterminate) inflorescences, dry stigmas, and reduced carpel number. Successive weighting with Onagraceae as outgroup generated five most parsimonious trees with a tree length of 164 and C.I. of 0.75. Internal branches are weakly supported by only seven non-homoplasious characters. Significant results of the analysis include: (1) recognition of the two major clades and a total of seven monophyletic groups within the family; (2) the paraphyly of subfamily Lythroideae (Lythraceae s. s .); and (3) indication that genera endemic to the New World have been derived from more than one ancient Old World evolutionary line. The current taxonomic classification of the family is not closely correlated with results of the cladistic analysis.  相似文献   

8.
Fossil Algae     
J. Niklas 《Brittonia》1977,29(4):433-433
  相似文献   

9.
10.
Style morph frequencies (shortmidlong) were determined for a total of n = 11 918 plants in 16 Minnesota populations of Lythrum salicaria L. Nine populations were in the establishment phase, with population sizes ranging from n = 56 to n = 2 192. Most of these populations exceeded previously reported population sizes in the native European habitat. A nonparametric statistical test, the chi-square (2), can be used to determine if populations are at isoplethic equilibrium (111, shortmidlong); a 2 value >5.99 is significant at the 5% level. Only one established population (White Bear Lake, n = 1991, 2 = 3.0) fitted the null hypothesis for isoplethy, although all established populations contained all three style morphs. Pooled values for these populations indicated an excess of mids and longs, with shorts being deficient. Colonizing populations had a higher percentage of mids (54%) when compared to established populations (33.7%). Short styles were almost nonexistent (8%) in colonizing populations. Five out of the seven populations lacked at least one style morph. A review of the literature reporting style morph frequencies in tristylous L. salicaria revealed that no statistical analysis for isoplethy has been performed. Darwin originally assumed that all populations would be isoplethic, possessing equal numbers of all three style morphs, but concluded, without statistical analysis, that, instead, populations were anisoplethic. Since tests for statistical deviations from the expected frequencies (111) have not been used, 2 analysis was performed. Several of these populations were at isoplethic equilibrium (Nadder su2 = 1.7, Blelham 2 = 1.69, Potsdam 2 = 1.5, Vestfold 2 = 0.4, Buskerud 2 = 5.62, Kilchberg 2 = 0.35, Lausanne 2 = 3.32, Canberra 2 = 5.29, Massachusetts 2 = 3.13), suggesting that the general conclusion of anisoplethy in tristylous L. salicaria is inappropriate.This is Scientific Journal Series Paper Number 19 128 of the Minnesota Agricultural Experiment Station  相似文献   

11.
Fossil Macroscelidea   总被引:1,自引:0,他引:1  
  相似文献   

12.
The Brazilian genus Diplusodon is the second largest genus within Lythraceae. Their 85 species occupy diverse habitats within the ‘cerrado’ vegetation, and range from shrubs and treelets to dwarf, xylopodium-bearing subshrubs. A comparative-morphological survey of their inflorescence structures using Trollian typology is here presented, as well as some evolutionary considerations drawn from mapping inflorescence characters onto a preliminary phylogeny. The inflorescences of Diplusodon are mostly polytelic, ranging from single racemes to more or less complex double-, triple-, and multiple-racemes. Frondose, compound racemes are plesiomorphic within the genus. Nevertheless, an array of derived features has been found among their species, including production of lateral cymes, proliferation of the main axis, diverse patterns of internode elongation, reduction of subtending leaves to bracts, development of accessory branches, paedomorphic flowering, and, in three species, reversion to monotely.  相似文献   

13.
14.
Heterostyly typically involves reciprocal polymorphism in stamen and style lengths, physiological self- and intramorph-incompatibility, and a set of associated polymorphisms of pollen and stigma characters. This study examined floral morphology and compatibility relationships in the monotypic, herbaceous perennial Decodon verticillatus (Lythraceae). There have been conflicting reports on the occurrence of tristyly in the species, probably because of frequent loss of style morphsm from populations in parts of the species' range. Floral morphology was examined using material collected from natural populations throughout the range. Detailed floral measurements revealed discrete trimorphism in style length and anther positioning in three populations. Data from two dimorphic populations showed similar patterns of floral polymorphism, except that both were missing the mid-styled morph. In one dimorphic population, there was evidence for modification in the length of mid-level stamens. Measurements in three populations indicated pronounced floral variability, including high frequencies of modified phenotypes with reduced stigma-anther separation. Pollen size was only weakly differentiated among anther levels, and there were no differences in pollen production among anther levels or morphs. In contrast, stigma size and papilla length showed a strong negative correlation with style length; a pattern opposite to most heterostylous species. Experimental crosses performed under glasshouse conditions on plants from two populations showed a high degree of both self- and intramorph-compatibility. A comparative analysis of floral morphology showed that D. verticillatus is not unusual in terms of the precision and reciprocity of organ positioning compared with 13 other tristylous species.  相似文献   

15.
Inference of past and present global biodiversity requires enough global data to distinguish biological pattern from sampling artifact. Pertinently, many studies have exposed correlated relationships between richness and sampling in the fossil record, and methods to circumvent these biases have been proposed. Yet, these studies often ignore paleobiogeography, which is undeniably a critical component of ancient global diversity. Alarmingly, our global analysis of 481,613 marine fossils spread throughout the Phanerozoic reveals that where localities are and how intensively they have been sampled almost completely determines empirical spatial patterns of richness, suggesting no separation of biological pattern from sampling pattern. To overcome this, we analyze diversity using occurrence records drawn from two discrete paleolatitudinal bands which cover the bulk of the fossil data. After correcting the data for sampling bias, we find that these two bands have similar patterns of richness despite markedly different spatial coverage. Our findings suggest that i) long-term diversity trends result from large-scale tectonic evolution of the planet, ii) short-term diversity trends are region-specific, and iii) paleodiversity studies must constrain their analyses to well-sampled regions to uncover patterns not driven by sampling.  相似文献   

16.
Cuphea luteola is described from cerrado vegetation in Noel Kempff Mercado National Park, eastern Bolivia. It is assigned to sectionEuandra subsectionOidemation and is distinguished by yellow flowers, linear uninerved leaves, and the inner surface of the floral tube pilose and without vesicles. Several species of the subsection share one or more characters withC. luteola, but none are closely similar.  相似文献   

17.
New microsatellite loci for pomegranate, Punica granatum (Lythraceae)   总被引:1,自引:0,他引:1  
? Premise of the study: A new set of pomegranate microsatellites was selected and characterized to assess the level of genetic diversity among cultivars and wild genotypes. ? Methods and Results: Nine Simple Sequence Repeat (SSR) markers were obtained using the Microsatellite-AFLP technique and were successfully amplified in 34 genotypes belonging to Italian, Spanish, and Turkish germplasm collections. The number of alleles per locus ranged from 1 to 5, and the total number of alleles was 22. ? Conclusions: Because only a few codominant markers are available for this species, the newly identified SSRs will facilitate genetic diversity studies, fingerprinting, and mapping. In addition, the 9 loci successfully amplified in P. granatum var. nana. No cross transferability was observed for Cuphea micropetala and Lagerstroemia indica (Lythraceae).  相似文献   

18.
Described as new areCuphea flavovirens (sect.Heterodon), C. dibrachiata (sect.Leptocalyx), andC. ownbeyi (sect.Diploptychia).  相似文献   

19.
20.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号