Am. J. Bot. Subscribe to E-TOCs
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via ISI Web of Science (27)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Xie, Z.-w.
Right arrow Articles by Li, F.-z.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Xie, Z.-w.
Right arrow Articles by Li, F.-z.
Agricola
Right arrow Articles by Xie, Z.-w.
Right arrow Articles by Li, F.-z.
(American Journal of Botany. 2001;88:1058-1064.)
© 2001 Botanical Society of America, Inc.

Population Biology

Clonality in wild rice (Oryza rufipogon, Poaceae) and its implications for conservation management1

Zhong-wen Xie2, Yan-qin Lu3, Song Ge2,4, De-yuan Hong2 and Fa-zen Li3

2Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, P. R. China 3Biology Department, Shandong Normal University, Jinan 250014, P. R. China

Received for publication March 30, 2000. Accepted for publication October 20, 2000.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 LITERATURE CITED
 
Correlations were examined between habitat characters and clonal structures determined by the RAPD (random amplified polymorphic DNA) assay in five populations of Oryza rufipogon in China. Nine of 175 decameric primers were used in the study because they reproducibly amplified polymorphisms. The extent of clonality together with the clonal and sexual reproductive strategies varied greatly among the five populations and correlated with the habitats where they occur. The populations under serious disturbance or seasonal drought tended to have small clones with relatively high clonal diversity caused by sexual reproduction, whereas the populations with little disturbance and sufficient supply of water were prone to have large clones with relatively low clonal variation and low sexual reproduction. Therefore, the dynamics of sexual vs. clonal reproduction of this species depended mainly on environmental factors, such as external disturbance and water supply, rather than latitudes indicated by previous study. These results have important implications for in situ conservation of O. rufipogon. Adequate external disturbance and water supply control are essential for maintaining high clone diversity of in situ conserved populations. According to the extent of clonality of the populations examined, we recommend that an interval of >12 m should be required for collecting samples for ex situ conservation and for population genetic studies to capture possible genetic diversity for O. rufipogon in China.

Key Words: clonal diversity • clonal structure • conservation • Oryza rufipogon • Poaceae • population • wild rice


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 LITERATURE CITED
 
Clonal reproduction is a common phenomenon in plants. Most perennials possess a capacity for asexual reproduction by either vegetative propagation or the formation of asexual seeds (Abrahamson, 1980 ; Richards, 1986 ). In most species, asexual reproduction is facultative and mingled with some capacity for sexual reproduction (Stebbins, 1950 ). Recently, the genetic and evolutionary consequences of clonal species have been addressed frequently (Ellstrand and Roose, 1987 ; Eckert and Barrett, 1993 ; Sydes and Peakall, 1998 ; Esselman et al., 1999 ), and studies have shown that reproductive mode commonly varied among species and among populations within a species (Ellstrand and Roose, 1987 ; Barbier, 1989 ; Eckert and Barrett, 1993 ; Widen, Cronberg, and Widen, 1994 ). The occurrence of clonality in rare and threatened plants has several important implications for their conservation (Sipes and Wolf, 1997 ; Sydes and Peakall, 1998 ). First, vegetative reproduction in clonal species may lead to difficulties in estimating the actual population size because a population may consist of numerous intermingled ramets belonging to only a few genets or comprise many distinct genets with each genet producing a small cluster of ramets (Ellstrand and Roose, 1987 ). In such cases, a census based on recognizable individuals would overestimate the number of genets. Consequently, the genetic vulnerability of particularly clonal plants may be undetected and a heavy loss of genetic variation may occur before the endangered status of species is apparent (Sydes and Peakall, 1998 ). Second, the size and longevity of individual are of great importance because large and/or long-lived individuals may contribute a disproportionate number of offspring, reducing the effective population size (Richards, 1986 ). Therefore, the genetic structure of a population may be greatly influenced by the largest genet because size and age are frequently correlated in plants (Ayres and Ryan, 1997 ). Finally, if the extent and patterns of clonality cannot be predicted, the general strategies for in situ conservation or ex situ collections of clonal plants would be inappropriate (Coates, 1988 ). Furthermore, in self-compatible plants, pollen transfers within clones may increase the level of inbreeding (Peakall and Beattie, 1991 ). Hence, an understanding of clonality is critical for the implementation of the most appropriate conservation management of threatened clonal plants.

Oryza rufipogon Griff. is a perennial that is widely distributed in the tropics and subtropics of monsoon Asia (Vaughan, 1994 ). As the progenitor of cultivated rice O. sativa, this species has been proven to be a valuable gene pool for rice genetic improvement and thus plays a critical role in rice breeding in the future (Chang, 1984 ). Oryza rufipogon has been found in eight provinces and autonomous regions of China (Gao, 1997 ). However, our recent field surveys indicated that this species was at the edge of extinction (Xie et al., unpublished data) and would be entirely extinct in China in the next 10–15 yr if no proper strategies were taken to conserve it (Hong, 1995 ). Therefore, it was listed as a threatened plant in China (Fu, 1992 ). Oryza rufipogon reproduces by both seeds and horizontal stems. In Thailand, it propagates mainly by asexual means (ratooning), with much investment in vegetative growth, and has a high competitive ability (Oka and Morishima, 1967 ; Sano and Morishima, 1982 ; Barbier, 1989 ). Based on our field observations, horizontal stems in this species extended in water or underground for up to 5 m, forming new stems and adventitious roots. In addition, physical connections between parent and daughter ramets often decay, thereby obscuring the genetic relatedness of ramets within a clone and leading to intermixed dense stems from different clones. This makes it difficult to estimate clonality in the field. Until now, little has been known about clonality in Oryza rufipogon.

The genetic markers developed recently make it possible for more accurate determination of genetic individuals. Of them, allozyme technique is the most commonly used approach (McClintock and Waterway, 1993 ; Widen, Cronberg, and Widen, 1994 ; Sipes and Wolf, 1997 ; Ge, Wang, and Dong, 1999 ). However, a problem with the application of enzyme electrophoresis for clonal identification is the low number of polymorphic loci available in many studies (Ellstrand and Roose, 1987 ; Esselman et al., 1999 ; Wang, Ge, and Dong, 1999 ). The random amplified polymorphic DNA (RAPD) technique (Williams et al., 1990 ) has been successfully used for characterizing clones and detecting clonal diversity in plants (Wilde, Waugh, and Powell, 1992 ; Neuhaus et al., 1993 ; Hsiao and Rieseberg, 1994 ; Stiller and Denton, 1995 ; Waycott, 1995 ; Van de Ven and McNicol, 1995 ; Ayres and Ryan, 1997, 1999 ; Graham et al., 1997 ; Sydes and Peakall, 1998 ). In the present paper, the extent of clonality in O. rufipogon was investigated using the RAPD technique; the level of clonality was determined in populations subject to different levels of disturbance. We were particularly interested in whether clonal structure varies within and among populations and in the impacts of abiotic and biotic factors on the diversity and pattern of clones in O. rufipogon. Such information could then be used to facilitate conservation and management of the genetic resources of this crop.


   MATERIALS AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
RESULTS AND DISCUSSION
 LITERATURE CITED
 
Study populations and sampling sategies
During the 1997 field survey, 18–35 individuals were randomly chosen, and their leaves were collected from each of five populations studied according to the population sizes. These populations are typical of O. rufipogon in China and located at different ecological sites from the north to south of its distribution area in China (Fig. 1). The Taoshuxia population (P02) in Dongxiang Country, Jiangxi Province, is the most northern population in the entire distribution region of this species. In contrast, the Sanjia population (P49) in Dongfang Country, Hainan Province, is one of the southern marginal populations of this species in China (Gao, 1997 ). The Jiuqujiang population (P41) is in Qionghai Country, Hainan Province, and the Boluo (P07) and Chengxi (P36) populations are both in Guangdong Province. The Taoshuxia (P02) and Jiuqujiang (P41) populations existed in wetland and marsh habitats, respectively. For these two populations, sampling was made in a grid pattern, usually with an interval of 3 m between adjacent samples. The shape of the grids varied depending on the shape of the patches. In the Boluo (P07), Chengxi (P36), and Sanjia (P49) populations where the plants were distributed along a small river or the shoreline of a pond, leaves were sampled at 3-m intervals along one or two transects. Because the individuals were scattered irregularly in some populations, the adjacent samples were 2–5 m apart within the row and line (Fig. 2).



View larger version (23K):
[in this window]
[in a new window]
  		Fig. 1. Map of China showing locations of the five populations studied. Population numbers correspond to those in Table 1

 


View larger version (39K):
[in this window]
[in a new window]
  		Fig. 2. Maps of clonal structure at the sampling populations. Each circled number represents a sampled individual, and larger circles uniting individuals indicate putative clones. Population numbers correspond to those in Table 1

 
RAPD analysis
For RAPD analyses, harvested leaves were preserved with silica gel in the fields. The methods for leaf preservation and DNA extraction were described by Xie, Ge, and Hong (1999) . In order to select a set of suitable primers, eight template DNAs from population P36, including two samples from one clone and six from different clones based on field observation, were initially screened with 175 10-mer primers (Kit B, Kit T to Kit Z, and Kit J-1-15, Operon Technologies, Alameda, California, USA). A subset of nine primers was selected for further analyses using 130 samples based on the following criteria: (1) strong and reproducible amplified bands; (2) exactly the same RAPD profiles of two samples representing a single clone; and (3) polymorphic fragments across six other samples of unknown genetic background.

The RAPD PCR was run on the RapidcyclerTM (Idaho Technology, Idaho Falls, Idaho, USA) in a reaction volume of 10 µL containing 1.2 µL mol/L primer, 10 ng DNA template, 50 mmol/L Tris-HCl (pH 8.3), 0.5 µg/µL BSA, 2 mmol/L MgCl2, 0.5 units of Tag DNA polymerase, 200 µmol/L dNTPs, 0.75% Ficoll, and 1 mol/L Tartrazine. The initial two amplification cycles were carried out with 1 min at 94°C, 10 s at 35°C, and 20 sec at 72°C. The subsequent 45 cycles were run with the program: 2 s at 94°C, 10 sec at 35°C, and 1 min at 72°C, and a final 4 min extension at 72°C followed. A negative control, in which template DNA was omitted, was included with every run in order to verify the absence of contamination. DNA samples were run with each primer at least twice to check the reproducibility of the bands scored for the analysis.

The amplification products were electrophoresed through 1.4% agarose gel (Promega Corporation, Madison, Wisconsin, USA) containing 0.5 µL/mL ethidium bromide and were visualized and photographed on an UV transilluminator. The molecular mass of RAPD fragments was estimated by using a 100 bp DNA Ladder (Pharmacia Biotech, SE-751 84, Uppsala, Sweden).

We defined a clone to be a repeatable combination of polymorphic amplified bands.

Clonal diversity analysis
The mean clone size (N/G) was calculated for each population by dividing sample size (N) by the number of genotypes (G) detected (McClintock and Waterway, 1993 ). A modified version of the Simpson's diversity index (D) (Pielou, 1969 ) was calculated for each population as D = 1 – {Sigma} [Nj(Nj – 1)/N(N – 1)], where Nj is the number of samples of the jth genotype, and N is the sample size. This index was originally developed as a measure of species diversity and evenness and has also been employed to measure the clonal diversity within a population (Parker, 1979 ; Ellstrand and Roose, 1987 ; Eckert and Barrett, 1993 ; McClintock and Waterway, 1993 ; Ge, Wang, and Dong, 1999 ). Because the D value depends in part on the total number of clones identified in a population, Fager's (1972) E value was also calculated as E = (D – Dmin)/(Dmax – Dmin), where Dmin = (G – 1) (2N – G)/N(N – 1), Dmax = (G – 1)N/G(N – 1). This statistic describes uniformity of distribution of genotypes within a population. The D and E values vary between 0 and 1.


   RESULTS AND DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
LITERATURE CITED
 
Clonal diversity and the extent of clonality
The mean clone size (N/G) and values for Simpson's diversity index (D) and the uniformity of clonal distribution within the populations (E) are listed in Table 1. Over the five populations, the mean clone sizes ranged from 1.06 to 1.94, and the means of clonal diversity and evenness were 0.96 and 0.62, respectively. A total of 70 genotypes were identified for all the populations using nine selected primers.


View this table:
[in this window]
[in a new window]
  		Table 1. Clonal diversity and distributional uniformity in five populations of Oryza rufipogon.

 
The spatial pattern of clones varied greatly among the five populations studied. Population P02 occupied a small and isolated wetland with an area of 300 m2 and <150 individuals in total. Based on 14 polymorphic loci, a total of 13 clones were revealed in this population. The largest clone consisted of three adjacent samples (6, 15, and 17), and three other multisample clones were composed of two adjacent samples. Each of these multisample clones spread at maximum ~5 m long (Fig. 2: P02). The remaining samples were all distinct clones. According to our field observations, it seemed that horizontal stems of O. rufipogon stretched from dry to wet habitats in the dry season, and new ramets might be produced in the areas of deep water. As a result, all the multisample clones were located between shallow and deep water of small puddles. Handel (1985) and Schmid and Harper (1985) indicated that clonal plants could extend by rhizomes to more favorable environments or for water or mineral resources in response to environmental heterogeneity. We infer that there might be ~100 actual genets in the P02 population.

Population P07 was distributed along the river ~100 m long and grew vigorously. Twenty-five polymorphic bands were generated (Table 2). These identified 18 clones among the 35 samples shown in Fig. 3. Two large clones, each consisting of seven samples, were identified along the river. One (samples 20–26) covered ~11 x 4 m2 area, and the other (samples 29–35) extended an area of ~12 x 5 m2 along the river. In addition, samples 1 and 2, samples 6 and 7, samples 8, 9, and 10, and samples 18 and 19 belonged to four distinct clones, respectively. Each of these multisample clones comprised two or three neighboring samples, suggesting that the direction of clonal stretch was consistent with that of water flow. Accordingly, water flow may be an important factor that affects clone formation and distribution (Fig. 2: see clone distribution of P07). Twenty-four polymorphic loci were produced to identify clones in population P36. Of 32 samples, 19 clones were detected. Interestingly, mosaic clonal distribution was found in this population. For example, the clone of samples 1 and 4 interspersed with clone 3, while the clone of samples 8, 10, and 16 occurred between clones 12 and 14 (Fig. 2: P36). Furthermore, these mosaic clones extended from 6 m to >12 m in distance. Population P36 existed in a large pond with high density and horizontal stems woven closely. The water level in the pond fluctuated seasonally 1–2 m in different years. In the dry season, the crawling stems or stolons sprawled across other individuals when the water level decreased severely. We observed in the field that buds and roots were generated from the nodal parts of crawling stems or stolons, which further could develop new ramets. Therefore, mosaic pattern of clone distribution observed is not unexpected in this population.


View this table:
[in this window]
[in a new window]
  		Table 2. Polymorphic nonoverlapping fragments useful for distinguishing different clones in the P07 population

 


View larger version (78K):
[in this window]
[in a new window]
  		Fig. 3. RAPD profile using the template DNAs of P07 population with the primers of OPZ10. Arrows show the polymorphic bands scored. The numbers 1 to 36 are sampled individuals of P07, while 1' belongs to another population

 
Population P41 was distributed in a marsh adjacent to a river and was frequently disturbed by grazing, mowing, and digging. Therefore, most of the plants were short with few scrambling stems. Sixteen polymorphic bands were amplified and used for recognizing 17 clones from 18 samples (Fig. 2: P41). Samples 16 and 18 belonged to one clone, which was the only one multisample clone in this population. This population was the most disturbed one compared with the other four populations examined. The severe disturbance may result in its high clone diversity. In population P49, plants were scattered in a river and the neighboring tableland. Of 27 samples, 23 clones were identified by 30 polymorphic fragments (Fig. 2: P49). In the river, O. rufipogon plants exhibited lush growth with long and scrambling stems. Therefore, one mosaic clone consisting of samples 1, 3, and 4 was identified along the river. In contrast, in the tableland, plants were short and small with slender crawling stems because the water supply was not sufficient from October to April of the next year. That we identified only two small multisample clones (samples 20 and 21 and samples 26 and 27) is reasonable in these disturbed habitats.

Clonal diversity and structure in populations of clonal species vary greatly. Some endangered species, especially those with little or no sexual reproduction, such as Taraxacum obliquum (Van Oostrum, Sterk, and Wusman, 1985 ; Ellstrand and Roose, 1987 ) and Haloragodendron lucasii (Sydes and Peakall, 1998 ), have only one or a few genets. For several species, the number of genets varies greatly among populations with some populations consisting of only one genet but others of many (Aspinwall and Christian, 1992 ; Eckert and Barrett, 1993 ; Ayres and Ryan, 1997 ). For those species with both asexual and sexual reproductions, populations usually consisted of a number of genets (Ellstrand and Roose, 1987 ; Eckert and Barrett, 1993 ; Eriksson and Bremer, 1993 ; Ayres and Ryan, 1999 ; Ge, Wang, and Dong, 1999 ). In the present study, all five populations of O. rufipogon sampled comprised multiple genets. This is consistent with the reproductive strategy of O. rufipogon (Oka and Morishima, 1967 ; Gao, 1997 ). Moreover, clonal structures of four of the five populations (with the exception of population P41) were similar to those of the majority of 21 clonal plants summarized in Ellstrand and Roose (1987) . That is they were neither dominated by a single genotype nor consisted of numerous genotypes in roughly equivalent frequencies. However, the proportion of distinguishable genotypes (i.e., the number of clones identified divided by the sample size) ranged from 0.51 to 0.94 and was 0.54 across all the five populations in the present study. This value is much higher than the average value (0.17) for clonal populations (Ellstrand and Roose, 1987 ). The following reasons may apply. First, O. rufipogon has a certain degree of sexual reproduction (Ge et al., 1999 ) and thereby maintains high genetic diversity in wild populations. In contrast, approximately half of the clonal plants described by Ellstrand and Roose (1987) were dominated by asexual reproduction through apogamety or agamospermy or by some mechanism of permanent translocation heterozygotes. Second, RAPD assays can yield abundant polymorphic loci and thus allow more precise identification of clones (Stewart and Porter, 1995 ; Esselman et al., 1999 ). In the present study, the numbers of polymorphic loci used for discriminating clones varied from 14 (P02) to 30 (P49), which were higher than the average number of polymorphic loci used for allozymes (Ellstrand and Roose, 1987 ). Thus, many more clones could be detected for O. rufipogon populations by RAPD markers. On the other hand, genotypic diversity (as measured by D and E) may have been overestimated in natural populations of O. rufipogon because of the coarse spatial scale of sampling (~3-m intervals).

Implications for conservation management
Oryza rufipogon is a perennial with mixed sexual and asexual reproductive strategies (Barbier, 1989 ; Gao, 1997 ). The allocation of asexual vs. sexual reproduction may vary among populations in different habitats (Barbier, 1989 ). In the present study, population P41 was frequently disturbed, while population P49 grew under harsh conditions such as drought. Thus, it is difficult for them to produce large dominant clones. The high clone diversity and small clone sizes indicated that sexual reproduction might be more important than clonal reproduction for these two populations. Oka and Morishima (1967) and Barbier (1989) also demonstrated that wild rice (O. rufipogon) populations growing in disturbed habitats produced many seeds and promoted seed propagation. In contrast, populations P07 and P36 existed in pond or river with sufficient water supply and little disturbance. They grew luxuriantly and formed large clones through stretching of sprawling stems enhanced by water flow or seasonal fluctuation of water level. Consequently, these two populations have relatively low clone diversities. Investment for clonal reproduction might be high in both populations. Gao (1997) studied variation in the breeding system of O. rufipogon and found an increased allotment to sexual reproduction over clonal reproduction when going from lower to higher latitudes in China. According to our results, the recruitment of sexual vs. clonal progeny depends mainly on environmental factors, such as external disturbance and water condition, rather than on the latitude. These results have important implication for conservation of O. rufipogon in situ. Moderate disturbance and reduction of the water supply, gradually from sufficient to wet and finally to dry, at the stage of vegetative growth (from April to September of a year in China) could be helpful for maintenance of genetic diversity of natural populations of O. rufipogon. As indicated by the present study, the extent of clonality varies from 3 to 12 m in the five populations of O. rufipogon examined, suggesting that an interval of 12 m or more in sampling would probably result in collection of completely distinct genotypes from a population in most cases. Therefore, we recommend that an interval of ~12 m be used for comparative studies on population genetics in O. rufipogon as well as for sampling for ex situ conservation of this species in the future.


   FOOTNOTES
 
1 The authors thank Dr. Wei Qian for his great help in the field and Miss Yingxue Sun for laboratory assistance. This research was supported by the Key Project of Chinese Academy of Sciences (KZ951-B1-102) and the Grant for Biological Science and Technology (STZ-1-10). Back

4 Author for reprint requests (Tel: +86-10-62591431-6097; FAX: +86-10-62590843; e-mail: gesong{at}ns.ibcas.ac.cn or song_ge{at}hotmail.com ). Back


   LITERATURE CITED
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 LITERATURE CITED
 
Abrahamson W. G. 1980 Demography and vegetative reproduction. In O. T. Solbrig [ed.], Demography and evolution in plant populations, 89–106. Blackwell, Oxford, UK

Aspinwall N. andT. Christian 1992 Clonal structure, genotypic diversity, and seed production in populations of Filipendula rubra (Rosaceae) from the northcentral United States. American Journal of Botany 79: 294-299[CrossRef][ISI]

Ayres D. R. andF. J. Ryan 1997 The clonal and population structure of a rare endemic plant, Wyethia reticulata (Asteraceae): allozyme and RAPD analysis. Molecular Ecology 6: 761-772[CrossRef][ISI]

———, and ———. 1999 Genetic diversity and structure of the narrow endemic Wyethia reticulata and its congener W. Bolanderi (Asteraceae) using RAPD and allozyme techniques. American Journal of Botany 86: 344-353[Abstract/Free Full Text]

Barbier P. 1989 Genetic variation and ecotypic differentiation in the wild rice Oryza rufipogon. I. Population differentiation in life-history traits and isozymes. Japanese Journal of Genetics 64: 259-271

Chang T. T. 1984 Conservation of rice genetic resources: luxury or necessity. Science 224: 251-256[Free Full Text]

Coates D. J. 1988 Genetic diversity and population genetic structure in the rare chittering grass wattle Acacia anomola Court. Australian Journal of Botany 36: 22-27

Eckert C. G. andS. C. H. Barrett 1993 Clonal reproduction and patterns of genotypic diversity in Decodon verticillatus (Lythraceae). American Journal of Botany 80: 1175-1182[CrossRef][ISI]

Ellstrand N. C. andM. L. Roose 1987 Patterns of genotypic diversity in clonal plant species. American Journal of Botany 74: 123-131[CrossRef][ISI]

Eriksson O. andB. Bremer 1993 Genet dynamics of the clonal plant Rubus saxatilis.. Journal of Ecology 81: 533-542[CrossRef]

Esselman E. J. L. Jianqiang D. J. Crawford J. L. Windus andA. D. Wolfe 1999 Clonal diversity in the rare Calamagrostis porteri ssp. insperata (Poaceae): comparative results for allozymes and random amplified polymorphic DNA (RAPD) and intersimple sequence repeat (ISSR) markers. Molecular Ecology 8: 443-451[CrossRef][ISI]

Fager E. W. 1972 Diversity: a sample study. American Naturalist 106: 293-310[CrossRef][ISI]

Fu L. G. 1992 Endangered plants in China, ser. 1, 314–316. Science Press, Beijing, P. R. China

Gao L. Z. 1997 Studies on genetic variation of three wild rice (Oryza spp.) in China and their conservation biology. Ph.D. Dissertation, Institute of Botany, Chinese Academy of Sciences, Beijing, P.R. China

Ge S. G. C. X. Oliveira B. A. Schaal L. Z. Gao andD. Y. Hong 1999 RAPD variation within and between natural population of wild rice Oryza rufipogon from China and Brazil. Heredity 82: 638-644

———,K. Q. Wang andM. Dong 1999 Genetic diversity and clonal structure of Hedysarum laeve in Mo Us Sandland. Acta Botanica Sinica 41: 301-306 (in Chinese).[ISI]

Graham J. G. R. Squire B. Marshall andR. E. Harrison 1997 Spatially dependent genetic diversity within and between colonies of wild raspberry Rubus idaeus detected using RAPD markers. Molecular Ecology 6: 1001-1008[CrossRef]

Handel S. N. 1985 The intrusion of clonal growth patterns on plant breeding systems. American Naturalist 125: 367-384[CrossRef][ISI]

Hong D. Y. 1995 Rescuing germplasm resources of wild rices in China. Bulletin of Chinese Academy of Sciences 10: 325-326 (in Chinese).

Hsiao J. Y. andL. H. Rieseberg 1994 Population genetic structure of Yushania niitakayamensis (Bambusoideae, Poaceae) in Taiwan. Molecular Ecology 3: 201-208

Hutchinson G. E. 1975 A treatise on limnology, vol. 3, Limnological botany. John Wiley and Sons, New York, New York, USA

McClintock K. A. andM. J. Waterway 1993 Patterns of allozyme variation and clonal diversity in Carex lasiocarpa and C. Pellita (Cyperaceae). American Journal of Botany 80: 1251-1263[CrossRef][ISI]

Neuhaus D. H. Kuhl J. G. Kuhl P. Dorfel andT. Borner 1993 Investigation on the genetic diversity of Phragmites stands using genomic fingerprinting. Aquatic Botany 45: 357-364[CrossRef]

Oka H. I. andH. Morishima 1967 Variation in the breeding systems of a wild rice, Oryza perennis.. Evolution 21: 249-258[CrossRef][ISI]

Parker E. D., Jr. 1979 Ecological implications of clonal diversity in parthenogenetic morphospecies. American Zoology 19: 753-762

Peakall R. andA. J. Beattie 1991 Genetic consequences of worker ant pollination in a self-compatible, clonal orchid. Evolution 45: 1837-1848[CrossRef][ISI]

Pielou E. C. 1969 An Introduction to mathematical ecology. Wiley-Interscience, New York, New York, USA

Richards A. J. 1986 Plant breeding systems. George Allen and Unwin, London, UK

Sano Y. andH. Morishima 1982 Variation in resources allocation and adaptative strategy of a wild rice, Oryza perennis Moench. Botanical Magazine 143: 518-543

Schmid B. andJ. L. Harper 1985 Clonal growth in grassland perennials. I. Density and pattern-dependent competition between plants with referent growth forms. Journal of Ecology 73: 793-808[CrossRef]

Silander J. A., JR. 1985 Microevolution in clonal plants. In J. B. C. Jackson, L. W. Buss, and R. E. Cook [eds.], Population biology and evolution of clonal organisms, 107–152. Yale University Press, New Haven, Connecticut, USA

Sipes D. S. andP. G. Wolf 1997 Clonal structure and patterns of allozyme diversity in the rare endemic Cycladenia humilis var. jonesii (Apocynaceae). American Journal of Botany 84: 401-409[Abstract]

Stebbins G. L. 1950 Variation and evolution in plants. Columbia University Press, New York, New York, USA

Stewart C. N. andD. M. Porter 1995 RAPD profiling in biological conservation: an application to estimating clonal variation in rare and endangered plants. Biological Conservation 74: 135-142[CrossRef][ISI]

Stiller J. W. andA. L. Denton 1995 One hundred years of Spartina alterniflora (Poaceae) in Willapa Bay, Washington: random amplified polymorphic DNA analysis of an invasive population. Molecular Ecology 4: 355-363[ISI]

Sydes M. A. andR. Peakall 1998 Extensive clonality in the endangered shrub Haloragodendron lucasii (Haloragaceae) revealed by allozymes and RAPDs. Molecular Ecology 7: 87-93[CrossRef]

Van Den Ven W. T. G. andR. J. Mcnicol 1995 The use of RAPD markers for the identification of Sitka spruce (Picea sitchensis) clones. Heredity 75: 126-132[ISI]

Van oostrum H. A. A. Sterk andH. J. W. Wusman 1985 Genetic variation in agamospermous microspecies of Taraxacum sect. Erythrosperma and sect. Obliqua.. Heredity 55: 223-228[ISI]

Vaughan D. A. 1994 The wild relatives of rice: a genetic resources handbook. International Rice Research Institute, Philippines

Wang K. Q. S. Ge andM. Dong 1999 Allozyme variance and clonal diversity in the rhizomatous grass Psammochloa villosa (Gramineae). Acta Botanica Sinica 41: 537-540 (in Chinese).[ISI]

Waycott M. 1995 Assessment for genetic variation and clonality in the seagrass Posidonia australis using RAPD and allozyme analysis. Marine Ecology and Progress, Series 116: 289-295

Widen B. N. Cronberg andM. Widen 1994 Genotypic diversity, molecular markers and spatial distribution of genets in clonal plants, a literature survey. Folia Geobotanica and Phytotaxonomica 29: 245-263

Wilde J. R. Waugh andW. Powell 1992 Genetic fingerprinting of Theobroma clones using randomly amplified polymorphic DNA markers. Theoretical and Applied Genetics 83: 871-877[ISI]

Williams J. G. K. A. R. Kubelik K. J. Livak J. A. Rafalski andS. V. Tingey 1990 DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Research 18: 6531-6535[Abstract/Free Full Text]

Xie Z. W. S. Ge andD. Y. Hong 1999 Preparation of DNA from silica gel dried mini-amount of leaves of Oryza rufipogon for RAPD study and total DNA bank construction. Acta Botanica Sinica 41: 807-812[ISI]





This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via ISI Web of Science (27)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Xie, Z.-w.
Right arrow Articles by Li, F.-z.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Xie, Z.-w.
Right arrow Articles by Li, F.-z.
Agricola
Right arrow Articles by Xie, Z.-w.
Right arrow Articles by Li, F.-z.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS