Genetic control of flowering time and its component processes in subterranean clover (Trifolium subterraneum L.)

Euphytica ◽  
1987 ◽  
Vol 36 (3) ◽  
pp. 887-902 ◽  
Author(s):  
P. A. Salisbury ◽  
Y. Aitken ◽  
G. M. Halloran
Keyword(s):  
Flowering Time ◽  
Genetic Control ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Component Processes

Flowering time in subterranean clover

1956 ◽  
Vol 7 (5) ◽  
pp. 388 ◽  
Author(s):  
FHW Morley ◽  
CI Davern
Keyword(s):  
Plant Breeding ◽  
Flowering Time ◽  
Natural Habitat ◽  
Strain Differences ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Relative Importance

Genotype-environment interactions have been observed in the flowering times of a number of varieties of subterranean clover (Trifolium subterraneum L.) grown in different locations. These interactions are interpreted in terms of the effects of photoperiod and temperature on flowering. Sensitivity to photoperiod may be independent of sensitivity to temperature. Flowering times of some strains, although simultaneous in one environment, may differ in another environment. This is due to variation in the relative importance of different components of the environment in controlling flowering time. These strain differences in flowering-time physiology are shown to be related to the climate of the strain's natural habitat. The importance of a knowledge of flowering physiology, and the recognition of the existence of genotype - environment interactions, are discussed in relation to plant breeding and introduction.

The inheritance of flowering time in Trifolium subterraneum L

1957 ◽  
Vol 8 (2) ◽  
pp. 121 ◽  
Author(s):  
CI Davern ◽  
JW Peak ◽  
FHW Morley
Keyword(s):  
Genetic Variation ◽  
Flowering Time ◽  
Intraclass Correlation ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Diallel Analysis ◽  
Genetic Effects ◽  
Breeding Behaviour ◽  
Variable Factor ◽  
Additive Genetic Effects

The inheritance of flowering time in subterranean clover, using a number of strains and hybrids among them, was investigated on autumn-sown material at Canberra. Heterosis and dominance were not found, and genetic variation was polygenic. An F1 diallel analysis and F2 two-way analysis showed that approximately 90 per cent. of the total variance was attributable to additive genetic effects. An estimate of the repeatability of strain performance over two seasons showed that small but significant strain-year interactions were occurring. Strain repeatability, as measured by intraclass correlation, was 86 per cent. A breeding test involving F2 selections and their progeny gave a mean parent-offspring regression of 0.86 over the six crosses studied, which is well in accord with expectations of breeding behaviour based on the above analyses. The results are discussed in relation to other studies on flowering time, especially with reference to the problem of interpreting results based on the threshold expression of a character dependent on the value of a continuously variable factor.

Evolution in sown populations of subterranean clover (Trifolium subterraneum L. ) in South Australia

1992 ◽  
Vol 43 (7) ◽  
pp. 1583 ◽  
Author(s):  
PS Cocks
Keyword(s):  
Natural Selection ◽  
Flowering Time ◽  
Mediterranean Basin ◽  
South Australia ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Sole Source ◽  
Selection For ◽  
The Mediterranean ◽  
The Mediterranean Basin

The seed banks of three pastures at Kingscote, Parndana and Waterloo, S.A., were sampled to determine the frequency of divergent genotypes in subterranean clover, and the direction of natural selection. The seeds were grown in nursery rows at Adelaide, and the resulting plants classified into one of the commercial cultivars, or as divergent genotypes. The divergent genotypes from one locality, Kingscote, were described in terms of 17 variables, and compared with strains collected from southern Australia and the Mediterranean basin. At each locality there was more genetic diversity than had been sown, both in terms of additional cultivars and the presence of divergent genotypes. The percentage of divergent genotypes appeared to be proportional to the age of the pasture, and was greatest at Kingscote, where it reached 67% of the population. The Kingscote genotypes were genetically related to Mt Barker and Dwalganup, only five out of 283 genotypes having leaf markings that differed from both cultivars. The 17 variables fell between the values recorded for Mt Barker and Dwalganup, and there was evidence of directional selection. For example, formononetin content was less, and genistein more than would be expected in the absence of natural selection. Mean flowering time was about equal to that of Seaton Park, and closer to Mt Barker than to Dwalganup. Flowering time was related to elevation above the lowest point in the paddock, the latest genotypes tending to inhabit sites at the foots of slopes, and the earliest genotypes sites on the tops. Seed and burr weight were slightly larger than expected. Hybridization was the most important, but not the sole source of genetic divergence at Kingscote, whereas contamination was the main source at Waterloo. It is likely that only a minority of the divergent genotypes was generated by mutation. The Australian subterranean clovers were as diverse as those from the Mediterranean. Those from Kingscote were also diverse, but, on the whole, had longer peduncles, shorter internodes and were taller than strains from other parts of Australia and from the Mediterranean basin.

Effect of cultivar and grazing intensity in spring on shear and compression energies of dry mature subterranean clover (Trifolium subterraneum L.)

1997 ◽  
Vol 48 (8) ◽  
pp. 1199 ◽  
Author(s):  
Y. J. Ru ◽  
J. A. Fortune
Keyword(s):  
Flowering Time ◽  
Large Range ◽  
Grazing Intensity ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Plant Materials ◽  
Leaf Petiole ◽  
Dry Matter Digestibility ◽  
Highly Correlated ◽  
Shear Energy

Twenty-six cultivars of subterranean clover were divided into 3 maturity groups according to the flowering time and sown in 2 blocks with 4 replicates. The plots were grazed under 2 intensities (hard and lax) during the growing season. The proportions of leaf, petiole, stem, and burr before senescence, dry matter digestibility (DMD), herbage availability, and seed yield in summer were measured. The energies required to shear and compress the resultant dry mature plant materials were determined using an Instron material testing instrument. The results showed a large range for shear (11·3-18·2 kJ/m2) and compression energies (2·8-4·6 kJ/kg DM) among the 26 cultivars. Grazing intensity in spring did not affect shear energy (P > 0·05) but increased the compression energy of dry mature subterranean clover by 0·2 units (P < 0·05). The energy required to shear or compress plant materials was highly correlated with herbage availability, flowering time, proportions of leaf and petiole in the sward, and fibre content of the plant materials, with the relationships being modified by grazing intensity in spring. Compression energy was related to DMD of plants (r = -0·7) and shear energy did not account for a significant amount of variation in DMD.

Genetic control of flowering time in subterranean clover

1985 ◽  
Vol 36 (2) ◽  
pp. 275 ◽  
Author(s):  
BH Tan
Keyword(s):  
Flowering Time ◽  
Regression Coefficient ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Diallel Analysis ◽  
Diallel Cross ◽  
Quantitative Inheritance ◽  
Dominance Model ◽  
Degree Of Dominance ◽  
Asymmetrically Distributed

The quantitative inheritance of flowering time in autumn-sown subterranean clover (Trifolium subterraneum L. ssp. subterraneum) was studied in a 13 x 13 diallel cross in a Mediterranean-type environment. Flowering time was shown to be highly heritable with a low average degree of dominance, which was predominantly in the direction of earliness. Covariance/variance ( Wr/Vr) regression analysis indicated early flowering to be conditioned mostly by dominant alleles, and lateness mostly by recessives. The alleles were slightly asymmetrically distributed among the parents, with recessives marginally in excess. Inadequacy of the additive-dominance model, on which the Birmingham diallel analysis is based, was detected by a significant departure from unity of the joint regression coefficient and the heterogeneity among arrays of (Wr Vr) values, which could be ascribed to and overcome by omitting two late-flowering parents from the diallel cross.

Competition among seedlings of perennial grasses, subterranean clover, white clover, and annual ryegrass in replacement series mixtures

2000 ◽  
Vol 51 (3) ◽  
pp. 377 ◽  
Author(s):  
G. M. Lodge
Keyword(s):  
White Clover ◽  
Plant Competition ◽  
Perennial Grass ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Perennial Grasses ◽  
Maximum Likelihood Estimates ◽  
Annual Ryegrass ◽  
Replacement Series ◽  
Successful Establishment

Seedlings of 3 perennial grasses, Danthonia linkii Kunthcv. Bunderra, D. richardsonii Cashmore cv. Taranna(wallaby grasses), and Phalaris aquatica L. cv. Sirosa,were each grown in replacement series mixtures with seedlings ofTrifolium repens L. (white clover),Trifolium subterraneum L. var. brachycalycinum (Katzn.et Morley) Zorahy & Heller cv. Clare (subterraneanclover), and Lolium rigidum L. (annual ryegrass). Plantswere sown 5 cm apart in boxes (45 by 29 by 20 cm) at a density of 307plants/m2. Maximum likelihood estimates were usedto derive parameters of a non-linear competition model using the dry matterweights of perennial grasses and competitors at 3 harvests, approximately 168,216, and 271 days after sowing. Intra-plant competition was examined inmonocultures of each species, grown at plant spacings of 2, 5, and 8 cm apartwith plants harvested at the above times.Competition occurred in all perennial grass–competitor mixtures, exceptin those of each perennial grass with white clover and thephalaris–subterranean clover mixture (Harvest 1) and those withD. richardsonii and phalaris grown with white clover(Harvest 2). For D. richardsonii (Harvests 1 and 2) andD. linkii (Harvest 1 only) grown with white clover andthe phalaris–subterranean clover (Harvest 1), the two species in themixture were not competing. In the phalaris–white clover mixture, eachspecies was equally competitive (Harvests 1 and 2). These differences incompetition and aggressiveness reflected differences in individual plantweights in monocultures where there was an effect (P < 0.05) of species ondry matter weight per box, but no significant effect of plant spacing.These data indicated that for successful establishment,D. richardsonii and D. linkiishould not be sown in swards with either subterranean clover or white clover,or where populations of annual ryegrass seedlings are likely to be high.Phalaris was more compatible with both white clover and subterranean clover,but aggressively competed with by annual ryegrass.

scholarly journals Host plant recognition by the root feeding clover weevil, Sitona lepidus (Coleoptera: Curculionidae)

2004 ◽  
Vol 94 (5) ◽  
pp. 433-439 ◽  
Author(s):  
S.N. Johnson ◽  
P.J. Gregory ◽  
P.J. Murray ◽  
X Zhang ◽  
I.M. Young
Keyword(s):  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Plant Roots ◽  
Grass Species ◽  
Movement Rates ◽  
Sitona Lepidus ◽  
Macro Scale ◽  
Significant Difference ◽  
Invasive Techniques ◽  
Root Feeding

AbstractThis study investigated the ability of neonatal larvae of the root-feeding weevil, Sitona lepidus Gyllenhal, to locate white clover Trifolium repens L. (Fabaceae) roots growing in soil and to distinguish them from the roots of other species of clover and a co-occurring grass species. Choice experiments used a combination of invasive techniques and the novel technique of high resolution X-ray microtomography to non-invasively track larval movement in the soil towards plant roots. Burrowing distances towards roots of different plant species were also examined. Newly hatched S. lepidus recognized T. repens roots and moved preferentially towards them when given a choice of roots of subterranean clover, Trifolium subterraneum L. (Fabaceae), strawberry clover Trifolium fragiferum L. (Fabaceae), or perennial ryegrass Lolium perenneL. (Poaceae). Larvae recognized T. repens roots, whether released in groups of five or singly, when released 25 mm (meso-scale recognition) or 60 mm (macro-scale recognition) away from plant roots. There was no statistically significant difference in movement rates of larvae.

The influence of seed size and depth of sowing on pre-emergence and early vegetative growth of subterranean clover (Trifolium subterraneum L.)

1956 ◽  
Vol 7 (2) ◽  
pp. 98 ◽  
Author(s):  
JN Black
Keyword(s):  
Leaf Area ◽  
Seed Size ◽  
Vegetative Growth ◽  
Dry Matter ◽  
Relative Rate ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Dry Weight ◽  
Total Leaf Area ◽  
Pot Culture

Changes in the pre-emergence distribution of dry matter in subterranean clover (Trifolium subterraneum L.) variety Bacchus Marsh were followed at 21°C, using three sizes of seed and three depths of sowing, ½, 1¼, and 2 in. Decreasing seed size and increasing depth of sowing both reduce the weight of the cotyledons a t emergence. Seed of the three sizes were sown a t three depths in pot culture a t staggered intervals so that emergence was simultaneous. Dry weight in the early vegetative stage was proportional to seed size, and total leaf area and leaf numbers showed similar trends. Plants of each seed size grew at the same relative rate. No effect of depth of sowing could be detected, and this was shown to be due to the cotyledon area a t emergence being constant for any given seed size, regardless of varying depth of sowing and hence of cotyledon weight. It was concluded that seed size in a plant having epigeal germination and without endosperm is of importance: firstly, in limiting the maximum hypocotyl elongation and hence depth of sowing, and secondly, in determining cotyledon area. Cotyledon area in turn influences seedling growth, which is not affected by cotyledon weight. Once emergence has taken place, cotyledonary reserves are of no further significance in the growth of the plants.

CANTERBURY EXPERIENCE WITH SUBTERRANEAN CLOVER (Trifolium subterraneum)

1935 ◽  
pp. 64-68
Author(s):  
H. Neave ◽  
C.H. Hewlett
Keyword(s):  
Personal Experience ◽  
Subterranean Clover ◽  
Trifolium Subterraneum

The information contained in this paper is principally first-hand knowledge extending over a period of six years gained from personal experience from our own "Oakleigh" farm.

Varietal reactions of Trifolium subterraneum L. to Phaseolus virus 2 Pierce.

1954 ◽  
Vol 5 (4) ◽  
pp. 598 ◽  
Author(s):  
EM Hutton ◽  
JW Peak
Keyword(s):  
Trypan Blue ◽  
Continuous Distribution ◽  
Systemic Infection ◽  
Subterranean Clover ◽  
Trifolium Subterraneum ◽  
Epidermal Cells ◽  
Severe Strain ◽  
Resistant Varieties ◽  
Lethal Reaction ◽  
The Mean

A number of varieties of subterranean clover (Trifolium subterraneum L.) were tested with a severe strain of Phaseolus virus 2 Pierce. Northam First Early, Dwalganup, and Pink Flowered gave lethal necrotic reactions while the rest developed mottles and chlorosis of different degrees of intensity. Reductions in the mean fresh weights of plants of five subterranean clover varieties ranged from 26.1 to 76.7 per cent. Epidermal cells of mottled leaves contained irregular aggregates of viroplasts stained by treatment with phloxine-trypan blue. Viroplasts in young tip leaves did not stain if the plants were held at temperatures below 44.6°F while those in mature basal leaves were not so affected. The lethal-reactors Northam First Early, Dwalganup, and Pink Flowered were resistant in the field to Phaseolus virus 2. With hand inoculation in the glass-house an average of 10 per cent. of plants of these varieties remained free from systemic infection, whereas all the plants of mottle-reacting varieties became systemically infected. The virus had a discontinous distribution in plants of lethal-reactors, compared with a continuous distribution in those of mottle-reactors such as Mount Barker. The lethal reaction is heritable in a dominant fashion in most crosses, so that the development of desirable new virus- resistant varieties is possible.

Sign in / Sign up

Export Citation Format

Share Document