GENETIC CONTROL OF THE GROWTH HABIT OF APPLE TREES

2004 ◽  
pp. 397-400 ◽  
Author(s):  
V. Djouvinov
1982 ◽  
Vol 62 (2) ◽  
pp. 513-518
Author(s):  
B. J. PARLIMAN ◽  
C. STUSHNOFF

Beacon apple tree (Malus domestica Borkh.) variants derived from gamma-irradiated scionwood on Columbia Crab seedling (CC) rootstocks were compared to both standard Beacon/clonal rootstocks, standard Beacon/CC rootstocks and Columbia Crab seedling trees. Stem or root measurements of trees classed as induced spur-type dwarf variants/CC rootstocks had larger bark to xylem ratios than trees from other growth habit classes. Stem and root bark to xylem ratios have the potential to be used as juvenile selection criteria in screening for spur-type dwarf variants in irradiation-exposed apple tree populations.


HortScience ◽  
1991 ◽  
Vol 26 (8) ◽  
pp. 1074-1075 ◽  
Author(s):  
Yonatan Elkind ◽  
Arie Gurnick ◽  
Nachum Kedar

The objective of this study was to elucidate the genetic control of the semideterminate growth habit in tomato (Lycopersicon esculentum Mill.). A semideterminate tomato line was crossed with determinate and indeterminate lines; their F1, F2, and backcrosses were grown; and the growth habit recorded and analyzed. Plants with six or more inflorescences on the main stem were defined as semideterminate, while those with fewer were defined as determinate. The F2 and backcross to determinate were bimodal, indicating a single recessive gene for semideterminate, which was denoted as sdt. The goodness-of-fit chi square for a single recessive gene model was 88% and 69% for F2 and backcross generations, respectively. In the cross between semideterminate and indeterminate types, the results indicated control by two genes, sp and sdt, with the sp+ indeterminate type epistatic over semideterminate. The goodness-of-fit to this model was 70% and 82% for F2 and backcross generations, respectively.


HortScience ◽  
1991 ◽  
Vol 26 (10) ◽  
pp. 1266-1267 ◽  
Author(s):  
John Warner

`Sturdeespur Delicious', `MacSpur`, `Summerland McIntosh', `Idared', and `Empire' apple trees (Malus domestics Borkh.) planted in 1986 on various size-controlling rootstock were used to determine the effect of rootstock on primary scaffold branch crotch angle. There were differences in crotch angle depending on rootstock. Rootstock effects were more pronounced with the upright growing `Sturdeespur Delicious' than with `Idared' and `Empire', which have a spreading growth habit. Ottawa 8 rootstock had a tendency to produce primary branches with wider crotch angles than other semidwarf to standard rootstock.


2002 ◽  
Vol 127 (2) ◽  
pp. 254-261 ◽  
Author(s):  
Ralph Scorza ◽  
Daniele Bassi ◽  
Alessandro Liverani

A study was conducted to determine genetic control of the columnar or pillar (PI) growth habit, and to evaluate the effects of interactions of various genes that influence peach [Prunus persica (L.) Batsch (Peach Group)] growth habit. The PI habit (brbr) examined in this study was inherited as a monogenic trait expressing incomplete dominance. The heterozygous Brbr derived from crosses between standard (ST) and PI genotypes was recognized as an upright (UP) tree with narrower branch angles than ST trees but wider than PI trees. The combination of brbr and brachytic dwarf (DW) (dwdw) produced dwarf-pillar (DWPI) trees. The effects of the heterozygous Brbr in combination with dw and/or compact (CT) (Ct) could not be recognized by visual observation. Compact pillar (CTPI) trees resulted from the expression of Ct_ brbr. These trees were distinguished from globe-shaped (GL) trees (Ct_Brbr) by the more upright growth habit of the CTPI trees. This genetic study highlights the genetic plasticity of tree growth habit in peach. The investigation of novel growth habits extends our concept of the peach tree. Some growth habits such as PI may have commercial potential for high-density peach production systems. Others, such as DWPI and CTPI may have potential as ornamentals.


HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 478g-479
Author(s):  
E.M.K. Koinange ◽  
S.P. Singh ◽  
P. Gepts

Cultivated plants and their wild progenitors show marked phenotypic differences regarding seed dormancy, the ability to disperse seeds, growth habit, phenology, photoperiod sensitivity, etc. We have used RFLP mapping to investigate the genetic control of these differences in a recombinant inbred population derived from across between a snap bean and a wild bean. Traits were scored either at Davis or in Colombia. Our results suggest that the genetic control is relatively simple. In particular, most of the phenotypic variation (>60%) in the population could be accounted for in genetic terms for all but two traits. The genetic control of many traits involved genes with major effect (>30%). Some regions of the genome had major effects on several traits. Our results suggest that evolution can proceed by macromutations, domestication could have taken place fairly rapidly and introgression of additional genetic diversity could be itrogressed relatively easily from wild beans into the cultivated bean gene pool.


Genome ◽  
1989 ◽  
Vol 32 (1) ◽  
pp. 19-23 ◽  
Author(s):  
A. L. Brule-Babel ◽  
D. B. Fowler

Rye (Secale cereale L.) is recognized as the most cold-tolerant winter cereal species. However, little is known of the genetic control of cold hardiness and its interaction with vernalization requirement in rye. In the present study, the modes of inheritance of cold hardiness and vernalization requirement were investigated in crosses among one spring and two winter rye cultivars that represented a wide range of winter survivability. Differences in growth habit were found to be determined by a single dominant gene for the spring growth habit. Multiple alleles, or modifiers, for this major gene may also have been present. Cold hardiness was controlled by genes with mainly additive effects, but other factors may also have been involved. Cytoplasmic effects were not detected. Broad-sense heritability estimates were generally high (48–82%), indicating that selection for cold hardiness should be effective in breeding programs.Key words: Secale cereale L., dominance, additive gene action, heritability, cytoplasmic effects.


HortScience ◽  
2004 ◽  
Vol 39 (3) ◽  
pp. 475-476 ◽  
Author(s):  
Shawn A. Mehlenbacher ◽  
Maxine M. Thompson

The style color of standard hazelnut (Corylus avellana L.) cultivars ranges from pink to dark purple. Styles with an unusual yellow color were first noted in seedlings of the progeny `Goodpasture' × `Compton', and the ratio was ≈3 red: 1 yellow. Controlled crosses were made to investigate the genetic control of style color. The same 3:1 ratio was observed in four additional crosses in which both parents had red styles. Two crosses of a red and a yellow parent gave ≈50% yellow styles, while a cross of two selections with yellow styles gave only seedlings with yellow styles. These segregation ratios indicate control by a single locus, with yellow style color recessive to red. Seedlings with yellow styles have green buds and catkins and a more upright growth habit than their siblings with red styles. Inspection of the pedigrees of these progenies shows that `Daviana', `Willamette', `Butler', `Compton', `Goodpasture', and `Lansing #1' are heterozygous. `Daviana' appears to be the original source of the allele for yellow styles, as it is a known or suspected parent or ancestor of the others. Ratios in a progeny segregating simultaneously for growth habit (normal vs. contorted) and style color indicated independence of the traits. However, in a progeny segregating simultaneously for leaf color (red vs. green) and style color, no redleaf seedlings had yellow styles. The S-alleles of eight genotypes with yellow styles were determined, and indicate a possible linkage between the yellow style locus and the S locus that controls pollen-stigma incompatibility. One explanation is that the yellow style trait is conferred by an allele (ays) at the anthocyanin (A) locus that controls leaf color. A second explanation is that there is a yellow style locus closely linked to the A locus. The A locus is known to be loosely linked to the S locus.


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