• No results found

Revised model for inflorescence development in pea

Genetic control of inflorescence development in pea

Genetic control of inflorescence development in pea

... Historically, pea has been a popular model legume for studies of flowering, often through the characterisation of flowering and inflorescence ...study, pea genes with an apparent or putative ...

19

Genetic control of inflorescence development in pea

Genetic control of inflorescence development in pea

... 4.1.1 A forward genetics approach Prior to the molecular era, a genetic approach was adopted to investigate the influence of natural variation and induced mutations on flowering behaviour in pea. In more recent ...

396

VEGETATIVE1 is essential for development of the compound inflorescence in pea

VEGETATIVE1 is essential for development of the compound inflorescence in pea

... in inflorescence architecture is important to understanding how the huge diversity in plant form has been ...primary inflorescence axis, and compound, as in legumes, where they are formed at secondary or ...

14

Dissection of genetic regulation of compound inflorescence development in Medicago truncatula

Dissection of genetic regulation of compound inflorescence development in Medicago truncatula

... Schultz and Haughn, 1991). UNI is involved in the regulation of I 1 meristem identity in pea as uni mutant plants terminate with the formation of a stub at the apical meristem (Singer et al., 1999; Berbel et al., ...

13

Genetic control of inflorescence architecture in legumes

Genetic control of inflorescence architecture in legumes

... of inflorescence development is best known, has a simple inflorescence, where the primary inflorescence meristem directly produces the flowers, which are thus borne in the main ...

14

Quantitative Trait Loci for Inflorescence Development in Arabidopsis thaliana

Quantitative Trait Loci for Inflorescence Development in Arabidopsis thaliana

... The amount of phenotypic variance explained by QTL interaction effects relative to QTL main effects was evaluated by comparing type III sums of squares of interaction and main effects of markers to the total type III ...

20

Development of the ammonia emission inventory in Finland : revised model for agriculture

Development of the ammonia emission inventory in Finland : revised model for agriculture

... 4 Uncertainties Animal numbers for the years 1990–2007 are from agricultural statistics and are relatively reliable (Statistics Finland 2007, p. 148). Animal number projections for the future are less sure because there ...

63

Wheat Inflorescence Architecture

Wheat Inflorescence Architecture

... simple model whereby a weak floral signal facilitates slightly delayed conversion of inflores- cence axillary meristems to spikelet meristems, so that a short branch comprising a lateral (secondary) and terminal ...

218

CREEP TEST AND DEVELOPMENT OF KELVIN’S MODEL FOR GREEN PEA KERNELS SUBJECTED TO UNIAXIAL COMPRESSIVE LOADING

CREEP TEST AND DEVELOPMENT OF KELVIN’S MODEL FOR GREEN PEA KERNELS SUBJECTED TO UNIAXIAL COMPRESSIVE LOADING

... A rectangular wooden box provided with a cylinder cavity to firmly hold the PVC cylinder at the bottom. A stand was provided to facilitate mounting of scale for measurement of downward movement of cover plate inside the ...

11

Mechanisms regulating inflorescence development and flowering traits in Arabis alpina, an alpine perennial

Mechanisms regulating inflorescence development and flowering traits in Arabis alpina, an alpine perennial

... great model plant for uncovering molecular basis for reproductive development and has allowed the transfer of knowledge gained to several other ...perennial model species for the study of flowering ...

165

A revised model of platelet aggregation

A revised model of platelet aggregation

... ences between these two proteins. A key issue for future investigation will be to determine the relative contribu- tion of the platelet and plasma pools of both vWf and fibrinogen in supporting the various stages of ...

10

Genotype-Environment Interactions at Quantitative Trait Loci Affecting Inflorescence Development in Arabidopsis thaliana

Genotype-Environment Interactions at Quantitative Trait Loci Affecting Inflorescence Development in Arabidopsis thaliana

... regulation model explains most plastic- ity and GEI, then QTL for environmental sensitivity scores ...cence development were identified in the Ler ⫻ Col no expectation of positional overlap with QTL ...

14

CONCEPTUAL MODEL (Revised November 2012)

CONCEPTUAL MODEL (Revised November 2012)

... View of the Educational Process The Department of Occupational Therapy is aligned with that of the AOTA’s Philosophy of Education (AOTA, 2007), Purpose and Value of Fieldwork Education (AOTA, 2009), and its Philosophical ...

13

Inflorescence branching in maize: A quantitative genetics approach to identifying key players in the inflorescence development pathway

Inflorescence branching in maize: A quantitative genetics approach to identifying key players in the inflorescence development pathway

... obscured once crossed to B73. This was not surprising since natural modifiers of ra1 are known to be present in B73 and efforts to map them are currently underway (Chapter 3). However, the difficulty in mapping these ...

119

THE GROWTH AND DEVELOPMENT OF WHEAT INFLORESCENCE: THE EFFECT OF PRE-ANTHESIS NITROGEN TREATMENT ON FERTILITY AND ASSIMILATE CONCENTRATION OF THE INFLORESCENCE

THE GROWTH AND DEVELOPMENT OF WHEAT INFLORESCENCE: THE EFFECT OF PRE-ANTHESIS NITROGEN TREATMENT ON FERTILITY AND ASSIMILATE CONCENTRATION OF THE INFLORESCENCE

... In both control and nitrogen treated conditions; the concentrations of soluble carbohydrates and amino acids decHned in a curvilinear fashion upto day 52, the time o[r] ...

9

Inflorescence: Mapping the Development of Interdisciplinal Studies on the Sago Palm in the University of the Philippines

Inflorescence: Mapping the Development of Interdisciplinal Studies on the Sago Palm in the University of the Philippines

... Reporting on the results of their research team’s study in chapters 6 and 9, Nikko Laorden and Th addeus Acuña, respectively, determined that while there is no robust value chain of sago products at present, there is ...

14

Barren inflorescence1 Functions in Organogenesis During Vegetative and Inflorescence Development in Maize

Barren inflorescence1 Functions in Organogenesis During Vegetative and Inflorescence Development in Maize

... P.M. thanks Sarah Hake for her mentorship early in the develop- ment of the barren inflorescence project. We thank Tony Omeis, W. Scott Harkcom, and Bob Oberheim for plant care in the Department of Biology ...

13

Leaf and seed development in pea (Pisum sativum L )

Leaf and seed development in pea (Pisum sativum L )

... Strong alleles of the uni mutant change the multiple leaflets and tendrils of a wild-type leaf into a single leaf blade with basal stipules (Fig. 2.4) and seem to merge the proximal an[r] ...

164

Development of Pea Breeding Lines with Resistance to Orobanche crenata Derived from Pea Landraces and Wild Pisum spp.

Development of Pea Breeding Lines with Resistance to Orobanche crenata Derived from Pea Landraces and Wild Pisum spp.

... adapted pea background through sexual crossing and yearly field ...the development of a number of advanced pea breeding lines resistant to broomrape infection that are described here and that are ...

7

A Multicountry Econometric Model (Revised)

A Multicountry Econometric Model (Revised)

... The positive effect is a direct one: interest rates appear as explanatory variables in the price equa- tion (equation 5). The first negative effect is the negative Indirect effect of int[r] ...

83

Show all 10000 documents...

Related subjects