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1.
The objective of this study was to produce durum wheat doubled haploid (DH) plants through the induction of microspore embryogenesis.
The microspore culture technique was improved to maximize production of green plants per spike using three commercial cultivars.
Studies on factors such as induction media composition, induction media support and the stage and growth of donor plants were
carried out in order to develop an efficient protocol to regenerate green and fertile DH plants. Microspores were plated on
a C17 induction culture medium with ovary co-culture and a supplement of glutathione plus glutamine; 300 g/l Ficoll Type-400 was
incorporated to the induction medium support. Donor plants were fertilized with a combination of macro and microelements.
With the cultivars ‘Ciccio’ and ‘Claudio’ an average of 36.5 and 148.5 fertile plants were produced, respectively, from 1,000
anthers inoculated. This technique was then used to produce fertile DH plants of potential agronomic interest from a collection
of ten F1 crosses involving cultivars of high breeding value. From these crosses 849 green plants were obtained and seed was harvested
from 702 plants indicating that 83% of green plants were fertile and therefore were spontaneously DHs. No aneuploid plant
was obtained. The 702 plants yielded enough seeds to be field tested. One of the DH lines obtained by microspore embryogenesis,
named ‘Lanuza’, has been sent to the Spanish Plant Variety Office for Registration by the Batlle Seed Company. This protocol
can be used instead of the labor-intensive inter-generic crossing with maize as an economically feasible method to obtain
DHs for most crosses involving the durum wheat cultivars grown in Spain. 相似文献
2.
Summary Callus was initiated from in vitro-grown plants of Gladiolus cultivars ‘Jenny Lee’ and ‘Florida Flame.’ The age of callus used for regeneration of plants was either 9 mo. old or 8 yr
old from ‘Jenny Lee,’ and 4 mo. old from ‘Florida Flame.’ Regeneration medium consisted of Murashige and Skoog’s basal salts
medium supplemented with 2.0 mg/l (9.3 μM) kinetin. This medium was supplemented with various concentrations of either bialaphos (Meiji Seika, Tokyo, Japan) or phosphinothricin
(Hoechst-Roussell, Frankfurt, Germany). Bialaphos was more effective than phosphinothricin at stimulating plant regeneration.
Plants regenerated from 8-yr-old callus of ‘Jenny Lee’ only when the regeneration medium was supplemented with 0.10 mg/l bialaphos.
A bialaphos concentration of 0.01 mg/l stimulated regeneration from 9-mo.-old callus of cultivar ‘Jenny Lee’ and 4-mo.-old
callus of ‘Florida Flame.’ 相似文献
3.
Jolanta Biesaga-Kocielniak Janusz Kocielniak Maria Filek Anna Janeczko 《Plant Cell, Tissue and Organ Culture》2008,94(2):139-147
The aim of this study was to produce suspension cultures of winter wheat directly from immature embryos bypassing the callus
stage, and to determine their capacity for growth and regeneration in comparison to suspension cultures produced from callus.
The study was carried out using Polish winter wheat varieties: ‘Grana’ and ‘Rosa’. Immature embryos were isolated, homogenized
and transferred directly to liquid medium supplemented with 2,4-D. Actively dividing cell cultures were obtained within 2 months
after the cultures were started. Suspension cultures from callus of immature embryos was also produced. With both cultivars,
faster growth was observed in the suspension cultures produced directly from embryos than in the suspensions produced from
callus. Metabolic activity was higher in the suspension culture produced directly from embryos than in the suspension derived
from callus only in ‘Grana’. The production of 1-amiocyclopropane-1-carboxylic acid (ACC), an ethylene precursor, was lower
in the suspension cultures produced directly from embryos than in the suspensions produced from callus. Morphogenic capacity
was significantly higher in aggregates derived directly from embryos than in aggregates derived from callus. With ‘Rosa’,
about one third of the aggregates derived directly from embryos regenerated shoots. Production of ACC was lower in ‘Rosa’
cell culture that regenerated then in other cell cultures that did not. Photosystem II reactions were more efficient in dark
green aggregates than in light green or pale green aggregates which were unable to regenerate. With the method presented,
wheat cell suspension cultures with a regeneration potential can be produced in 2 or 3 months less time than with traditional
methods. 相似文献
4.
M. L. Ruíz J. Rueda M. I. Peláez F. J. Espino M. Candela A. M. Sendino A. M. Vázquez 《Plant Cell, Tissue and Organ Culture》1992,28(1):97-101
In vitro culture of immature embryo and young leaf tissues was carried out with five cultivars of barley, Hordeum vulgare. Two cultivars (Albacete and Porthos) responded poorly from both types of explants, while the three others (Dissa, Golden Promise and Ingrid) produced a high frequency of embryogenic callus from these explants (25–60%). For Dissa and Ingrid, young leaf explants were slightly better than immature embryo explants for embryogenic callus induction, while immature embryo cultures of Golden Promise responded better than young leaf explants. Thus, there appears to be a significant genotype × explant interaction in the initiation of embryogenic callus in barley.Some phenotypic variants were detected among the regenerated plants of Golden Promise and Ingrid, most originating by epigenetic changes. Only in one case was the variant phenotype heritable, probably due to a mutation in the chloroplast DNA. Mitotic alteractions were not detected. Consequently, somaclonal variation did not appear to be a very frequent event in plants regenerated from 1- to 6- month-old cultures of barley. 相似文献
5.
We used four cultivars ofCapsicum annuum L.—Sweet Banana, California Wonder, Yolo Wonder, and Ace—to reexamine the critical factors influencing somatic embryogenesis
from zygotic embryo explants, as reported in the literature. When we followed the protocol of Buyukalaca and Mavituna (1996),
which had induced somatic embryogenesis from mature zygotic embryos of cv. Ace, only callus was formed without embryogenesis
from our mature zygotic embryo expiants. Using the procedures of Harini and Lakshmi Sita (1993) and Binzel et al. (1996),
with some modifications, we were able to induce somatic embryogenesis in all four cultivars. Rates of conversion were significantly
reduced, from 75% and 65% to 40% and 28% in ’Sweet Banana’ and ’California Wonder’, respectively, when the immature zygotic
embryo expiants were held on the induction medium for longer than two weeks. Likewise, somatic embryogenesis of ’Yolo Wonder’
was not observed if the induction medium was supplemented with 10% glucose or fructose, or without 10% sucrose. For somatic
embryo induction and eventual plantlet conversion in Yolo Wonder’, maltose could adequately replace sucrose. In all four cultivars,
somatic embryos were initiated from immature zygotic explants on media with or without coconut water, under both light and
dark conditions. 相似文献
6.
Alonzo G. Saiano F. Tusa N. Fatta Del Bosco S. 《Plant Cell, Tissue and Organ Culture》2001,66(1):31-34
Volatile compounds released from callus and nucellar embryo tissues of ‘Valencia late’ and ‘Washington Navel’ sweet oranges
(Citrus sinensis, L. Osbeck) were collected/concentrated by head space solid phase micro extraction and analysed by gas chromatography-mass
spectrometry. Friable, white embryogenic cultures released a number of volatile compounds, including some essential oils.
Different samples of the same embryogenic culture showed variability, possibly related to the presence of tissues undergoing
differentiation. Analyses of the somatic embryos permitted the identification of several components, including limonene and
methyl anthranilate. Considering the simplicity and the very small sample required (0.3 g of fresh tissue) head space solid
phase micro extraction is suitable for studies and comparisons of volatile metabolites released from in vitro Citrus tissue cultures suggesting its potential in Citrus biochemical, genetic and breeding research.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
7.
Effects of growth regulators and incubation period on in vitro regeneration of adventitious shoots from gerbera petioles 总被引:4,自引:0,他引:4
Orlikowska Teresa Nowak Elzbieta Marasek Agnieszka Kucharska Danuta 《Plant Cell, Tissue and Organ Culture》1999,59(2):95-102
An effective system for in vitro regeneration of adventitious shoots from callus for the transformation or mutation of gerbera was developed. Callus was produced
from petioles of the youngest 3–4 leaves detached from auxillary shoots produced in vitro. Induction medium, on which leaves were incubated over 3 or 6 days, contained 2.3 μM thidiazuron and 0.53 μM α-naphthaleneacetic
acid. Explants were than transferred to one of three regeneration media with lower levels of growth regulators. Regeneration
was quantified over four (4-weeks each) passages at the time of explant transfer to fresh medium. Direct shoot regeneration
occurred during the first 4 weeks, and after these shoots were discarded a semi-compact organogenic callus was produced. Effectiveness
of shoot regeneration depended on four criteria: the cultivar (three cultivars were tested), the sequence of passage on regeneration
medium, the growth regulators in regeneration medium and the duration of the induction period. Regeneration potential from
calli of all cultivars increased from the first to the fourth passage. Duration of the incubation period on induction medium
(3 or 6 days) influenced regeneration to varying degrees, depending on the cultivar used and the regeneration medium contents.
There were no differences between two of the regeneration media – B, containing 2.2 μM 6-benzyladenine and 0.3 μM indole-3-acetic
acid and C, containing 4.4 μM 6-benzyladenine, 4.6 μM zeatin and 0.6 μM indole-3-acetic acid. Cultivar Mariola was the most
productive and regenerated more than seven shoots per callus in the fourth passage. Regeneration on medium B was further evaluated
on four additional gerbera cultivars.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
8.
A reliable protocol for plant regeneration from mature embryo derived calli of nine barley (Hordeum vulgare) cultivars has been developed. The auxins 2,4-dichlorophenoxyacetic acid, picloram and dicamba proved effective in inducing
callus from mature embryos of most of the barley cultivars. The induced primary callus was loose, friable and translucent.
It ultimately yielded creamy white and compact callus after 2 - 3 transfers on fresh medium of the same composition. Callus
induction and regeneration capacity were highly cultivar dependent. Addition of a high concentration of picloram (4 mg dm-3) promoted regeneration in 3 cultivars (Tallon, Grimmett and Sloop). In cv. Arapiles, abscisic acid and betaine were crucial
in generating morphogenic callus from the mature embryos. Plants regenerated from these calli were hardy and developed roots
readily when transferred to hormone free medium.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
9.
V. R. Bommineni P. P. Jauhar T. S. Peterson R. N. Chibbar A. B. Almouslem 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1997,95(5-6):757-763
The objective of this study was to detect the presence of alien chromatin in intergeneric hybrids of durum wheat (Triticum turgidum, 2n=4x=28; AABB genomes) with the perennial grass Thinopyrum junceiforme (2n=4x=28; J1J1J2J2) using RAPD markers. The first step was to identify amplification of species-specific DNA markers in the parental grass species
and durum wheat cultivars. Initially, the genomic DNA of five grass species (Thinopyrum junceiforme, Th. bessarabicum, Lophopyrum elongatum, Leymus karataviensis and Elytrigia pycnantha) and selected durum cultivars (‘Langdon’, ‘Durox’, ‘Lloyd’, ‘Monroe’, and ‘Medora’) was screened with 40 oligonucleotide
primers (nano-mers). Three oligonucleotides that amplified DNA fragments specific to a grass species or to a durum cultivar
were identified. Primer PR21 amplified DNA fragments specific to each of the five durum cultivars, and primers PR22 and PR23
amplified fragments specific to each of the grass species. Intergeneric hybrids between the durum cultivars ‘Langdon’, ‘Lloyd’
and ‘Durox’ and Th. junceiforme, and their backcross (BC) progeny were screened with all 40 primers. Six primers amplified parent-specific DNA fragments
in the F1 hybrids and their BC1 progeny. Three primers, PR22, PR23 and PR41, that amplified Th. junceiforme DNA fragments in both F1 and BC1 were further analyzed. The presence of an amplified 1.7-kb Th. junceiforme DNA fragment in the F1 hybrids and BC1 progeny was confirmed using Southern analysis by hybridization with both Th. junceiforme genomic DNA and Th. junceiforme DNA amplified with primer PR41. With the exception of line BC1F2 no. 5, five selfed progeny of BC1 and a BC2 of line 3 (BC1F2 no. 3בLloyd’) from a cross of ‘Lloyd’×Th. junceiforme showed the presence of the 1.7-kb DNA fragment. All selfed BC1 and BC2 lines retained the 600-bp fragment that was confirmed after hybridization with Th. junceiforme DNA amplified with primer PR22. Other experiments using RFLP markers also showed the presence of up to seven Th. junceiforme DNA fragments in the F1 hybrids and their BC progeny after hybridization with Th. junceiforme DNA amplified with primer PR41. These studies show the usefulness of molecular markers in detecting alien chromatin/DNA fragments
in intergeneric hybrids with durum wheat.
Received: 21 November 1996 / Accepted: 21 March 1997 相似文献
10.
G. A. Moore M. J. Miller Kenneth Cline 《In vitro cellular & developmental biology. Plant》1988,24(12):1205-1208
Summary The effects of the antibiotics methotrexate and chloramphenicol on somatic embryogenesis inCitrus were evaluated. Relatively low levels (0.1 to 1.0 μg/ml) of these antibiotics did not inhibit embryo production from undeveloped
ovules of ‘Key’ lime [C. aurantifolia) (Christm.) Swing.]. Surprisingly, both antibiotics induced the formation of embryogenic callus in these cultures. This is
usually a rare event in cultures of undevelopedCitrus ovules, and ‘Key’ lime is especially recalcitrant. The effects of these antibiotics on embryogenic callus appeared to be
limited to the induction stage, because there was no consistent effect, either stimulatory or inhibitory, on established,
lines of embryogenic callus.
Florida Agricultural Experiment Station Journal Series No. 8958. This research was supported in part by a grant to Moore and
Cline from the Competitive Grants Office of the SEA, USDA (85-CRCR-1-1623). 相似文献
11.
Summary Turfgrass, like other major crop species, is recalcitrant to manipulation in vitro. To perform efficient genetic transformation of turfgrass, it is necessary to optimize tissue culture conditions. In most
reports, plant tissue culture techniques have been applied to propagate a single cultivar or several cultivars in one species
of turfgrass. In this experiment, four turfgrass genera were used, namely common bermudagrass, Cynodon dactylon [L.] Pers. (California origin); red fescue, Festuca rubra L. var. rubra ‘Shadow’; perennial ryegrass, Lolium perenne L. ‘Barbal’; and Kentucky bluegrass, Poa pratensis L. ‘Merion.’ Mature seeds were surface-sterilized and cultured on basal Murashige and Skoog (MS) media supplemented with
30–250 μM 2,4-dichlorophenoxyacetic acid (2,4-D) for callus induction. Regeneration media consisted of MS supplemented with 5–10 μM 6-benzyladenine (BA). Among the genera, Poa had the higest callus induction percentage (CIP) regardless of 2,4-D concentration, followed by Cynodon, Lolium, and Festuca, respectively. Cynodon and Lolium had the highest callus regeneration percentage (CRP) and overall regeneration rate (ORR). Festuca had a poor CIP, CRP, and ORR compared to other studied genera. Cynodon produced the highest shoot number per explant. Based on the results of the present study, MS medium supplemented with 60
μM 2,4-D (for callus induction) and 7.5 μM BA (for regeneration) can be used in multi-generic transformation studies with the genera used. 相似文献
12.
Summary An in vitro protocol has been developed for callus indiction, somatic embryogenesis, and plant regeneration from stigma-style culture
of grapevine. Four different grapevine cultivars (Vitis vinifera L.: cvs. ‘Bombino Nero’, ‘Greco di Tufo’, ‘Merlot’, and ‘Sangiovese’) were tested. Exlants were cultured on Nitsch and Nitsch
medium (NN) supplemented with various combinations of 6-benzylaminopurine (BA: 4.5 and 9.0 μM) and β-naphthoxyacetic acid (NOA; 5.0 and 9.9 μM). Sucrose (88 mM) was used as the carbon source. Somatic embryogenesis was induced within 3–7 mo. after culture initiation. Even though explants
of different origin (unfertilized ovules and anthers) regenerated somatic embryos, the higher embryogenic potential was observed
in stigma and style explants, with the exception of ‘Merlot’, which regenerated somatic embryos only from unfertilized ovules.
The percentages of stigma-style explants producing somatic embryos was 7% in ‘Bombino Nero’ (cultured on NN medium supplemented
9.0 μM BA and 9.9 μM NOA). 14% in ‘Greco di Tufo’ (4.5 μM BA and 9.9 μM NOA), and 8% in ‘Sangiovese’ (9.0 μM BA and 9.9 μM NOA). The presence of growth regulators (BA and NOA) in the medium was essential for induction of somatic embryogenesis.
Plants were regenerated on hormone-free NN medium containing 88 mM sucrose. 相似文献
13.
Breeding linseed (Linum usitatissimum L.) using haploid techniques allows breeders to develop new cultivars in a shorter time period. Many research groups successfully
created new linseed genotypes through anther culture; however ovary culture has been the subject of only a few earlier studies.
In the present study, the effect of genotype and growth regulators combination on callus induction and shoots regeneration
in ovary culture of nine commercially important linseed cultivars was investigated. Ovaries were cultured on modified MS medium
supplemented with three different combinations of plant growth regulators. Variable callogenic responses were expressed by
all of the genotypes tested on different induction media. The results suggested that specific combination of growth regulators
for callus induction must be designed for each genotype. Shoot regeneration from ovary derived callus is a critical phase
of the whole gynogenetic process. Differences in adventitious shoot formation frequency among genotypes were demonstrated
and four responsive genotypes have been selected. Ovary derived callus from cultivar ‘Mikael’ manifested the highest adventitious
shoot formation frequency with a high number of shoots per explant. The optimum ratio of growth regulators for shoot regeneration
was shown to depend on the genotype. Cultivars ‘Linola’, ‘Mikael’ and ‘Szaphir’ showed the highest shoot regeneration frequency
when callus had originated on induction medium supplemented with 2 mg L−1 BAP and 2 mg L−1 NAA, while combination of 1 mg L−1 BAP and 2 mg L−1 IAA promoted shoot formation in ovary-derived callus of ‘Barbara’. The highest rate of shoots per explant has been obtained
in second subculture. 相似文献
14.
Ying Li Yuping Song Gongjun Shi Jianjun Wang Xilin Hou 《Acta Physiologiae Plantarum》2009,31(1):155-162
Changes in ascorbic acid content and antioxidant enzyme activities were investigated in non-heading Chinese cabbage (Brassica campestris ssp. chinensis Makino) leaves of ‘Wutacai’ and ‘Erqing’ exposed to excess copper (Cu). Cu treatment reduced the fresh weight of shoot and
root by 57% and 46% in ‘Wutacai’, and 60 and 54% in ‘Erqing’, respectively. The accumulation of copper in leaves was higher
in ‘Wutacai’ than that in ‘Erqing’. Compared to the control, ascorbic acid (AsA) contents were significantly decreased after
copper treatment in both cultivars, while they were higher in ‘Wutacai’ than in ‘Erqing’, which may explain the higher copper-tolerance
of ‘Wutacai’ with higher copper accumulation. The higher AsA contents of ‘Wutacai’ resulted from their lower activities of
degrading enzymes, such as ascorbate oxydase (AAO) and ascorbate peroxidase (APX), as well as the increasing activity of dehydroascorbate
reductase (DHAR) after copper treatment compared with ‘Erqing’. Copper stimulated superoxide dismutase (SOD) activity in both
cultivars, but for catalase (CAT), there was little difference between both cultivars. Peroxidases (POD) activity was decreased
after copper treatment in ‘Erqing’, while in ‘Wutacai’, it was significantly increased at 14 days, and POD activity was higher
in ‘Wutacai’ than that in ‘Erqing’ at 21 and 28 days. Therefore, the induced increasing activity of POD in ‘Wutacai’ also
played an important role in its copper tolerance. 相似文献
15.
We evaluated the efficiency of callus induction and plantlet regeneration from hypocotyl explants of broccoli (Brassica oleracea var. italica). The cultivars were ‘Marathon’, ‘Greenbelt’, and ‘Shogun’. Transformation success was not affected by the presence
of tobacco feeder-cell layers on the culture media. The frequency of shoot regeneration was greater from 10-d-old hypocotyls
than from 14-d-old hypocotyls. Both ‘Marathon’ and ‘Greenbelt’ had higher potentials for tissue regeneration than did ‘Shogun’.
We found that for transformation selection, the optimum concentration was either 50 mg/L kanamycin or 100 mg/L genetkin. 相似文献
16.
Kathryn Kamo Janet Chen Roger Lawson 《In vitro cellular & developmental biology. Plant》1990,26(4):425-430
Summary Inflorencence stalks from greenhouse-grownGladiolus plants of the cultivars ‘Blue Isle’ and ‘Hunting Song’ cultured on a Murashige and Skoog basal salts medium supplemented
with 53.6 μM 1-napthaleneacetic acid formed a compact, not friable type of callus that regenerated plantlets. Cormel slices and intact
plantlets of three cultivars (‘Peter Pears’, ‘Rosa Supreme’, ‘Jenny Lee’) propagated through tissue culture formed a friable
type of callus when cultured on Murashige and Skoog basal salts medium supplemented with 2,4-dichlorophenoxyacetic acid. This
friable callus readily formed a cell suspension when the callus was placed in a liquid medium. Plants were regenerated from
two-month-old suspension cell cultures of the commercial cultivar ‘Peter Pears’ after the suspension cells had been cultured
on solid medium. 相似文献
17.
Margarita Pérez-Jiménez Antonio Carrillo-Navarro José Cos-Terrer 《Plant Cell, Tissue and Organ Culture》2012,108(1):55-62
Somatic peach plants were regenerated from callus derived from the base of stem explants of the scion cultivars ‘UFO-3’, ‘Maruja’,
‘Flariba’ and ‘Alice Bigi’, and the peach × almond rootstocks ‘Garnem’ and ‘GF677’. A protocol for organogenic plant regeneration
was developed using three culture media containing different concentrations of 6-benzyladenine (BA) and indolebutyric acid
to produce organogenic calli. Shoots were obtained from sliced calli after their transfer to a differentiation culture medium
containing 2 mg l−1 BA and 1 mg l−1 α-naphthalene acetic acid. Using this procedure, up to 29 regenerated plants per callus were obtained. The highest regeneration
rate was obtained with the peach × almond rootstocks. This work provides an effective protocol that could be utilized for
peach transformation research. 相似文献
18.
In an attempt to optimize somatic embryo formation in Oncidium ‘Gower Ramsey’, the effects of five auxins (2,4-D, IAA, IBA, NAA and picloram) and five cytokinins (2iP, BA, kinetin, TDZ
and zeatin), used alone, was tested in vitro using root-derived callus. In general, kinetin (0.5 and 2 mg l−1) and zeatin (0.5 mg l−1) were found to be more effective than other auxin and cytokinin treatments to induce somatic embryogenesis from root-derived
callus. 相似文献
19.
Summary This study is mainly concerned with some parameters contributing to growth as indicators of difference in drought resistance
and salt tolerance of wheat and barley cultivars. Parameters made use of are: transpiration efficiency (‘dry matter/transpiration’
ratio), ‘leaf/root’ ratio, chlorophyll content, chlorophyll stability to heat and anatomical modifications. The results revealed
that transpiration efficiency is much higher in mexican ‘super-x’ wheat than in the egyptian ‘Giza-155’ cultivar under reduced
soil water matric- or osmotic potentials. Chlorophyll content increased in super-x with decreasing soil water potential while
chlorophyll heat stability decreased. The reverse is true in Giza-155 cultivar. Decreased leaf/root ratio in super-x is interpretted
in favour of more beneficial water balance in this cultivar. Development of more sclerenchyma in its stems supports this judgement.
Of barley cultivars tested, Borg El-Arab is favoured for drought resistance and Giza-117 for salt tolerance. re]19751014 相似文献
20.
Maria Karadimova Galina Djambova 《In vitro cellular & developmental biology. Plant》1993,29(4):180-182
Summary Callus cultures were initiated from immature embryos of oneTriticum aestivum and threeT. durum cultivars. Growing morphogenic calli were exposed to different concentrations of NaCl (0, 0.3, 0.5, and 0.7%) added to the
culture medium during two subsequent subcultures (4 wk each). The growth rate of the calli was determined by the relative
fresh weight callus growth (RFWCG). The callus growth of all investigated genotypes was slightly changed in the presence of
0.3 and 0.5% NaCl, but strongly inhibited by 0.7% NaCl. Selected NaCl-tolerant clones were isolated and plants were regenerated
on MS-based regeneration medium without NaCl. The regeneration capacity of the selected calli was highly reduced compared
to the control. The highest number of regenerants was scored for cv. Gladiator (T. aestivum). All regenerated plants were morphologically normal and many developed to maturity and set seeds. Seedlings from the R1 generation of selected and control plants were treated with 0.5% NaCl in vivo in liquid cultures for 6 wk. Salt tolerance
of the progenies of selected plants appeared in all cultivars, but those derived from calli grown on medium with 0.7% NaCl
showed the highest survival rate.T. aestivum showed higher tolerance to NaCl salinity thanT. durum. 相似文献