Performance differences in Pinus radiata progeny with differing site nutrient availability

2004 ◽  
Vol 34 (12) ◽  
pp. 2410-2423 ◽  
Author(s):  
S D Carson ◽  
M F Skinner ◽  
A T Lowe ◽  
M O Kimberley
Keyword(s):  
Nutrient Availability ◽  
Pinus Radiata ◽  
Nutrient Concentration ◽  
Radiata Pine ◽  
Substantial Improvement ◽  
Treatment Combination ◽  
Control Seed ◽  
Foliar Nutrient ◽  
Selection For ◽  
Selection Of

Two intensive harvesting trials with contrasting nutrient capital were examined for genetic × environment interactions to age 5 years after planting. Treatments included differences in removal of organic matter and in site preparation and weed control, with each treatment having both fertilized and nonfertilized plots. Three harvest treatments (both fertilized and nonfertilized) were common to both sites, with two additional treatments at one site. There were four replicate plots of each treatment combination at each site, with two trees from each of three control seed lots and 47 open-pollinated families chosen to represent the range of performance for growth planted in each plot. Large differences among sites and among treatments in both growth and foliar nutrient concentration were observed. Genetic × site interactions and genetic × treatment within site interactions were seldom significant. Significant interactions did not appear to be related to changes in rankings of families, but rather to the differences in variance among families in different treatments. This study suggests that selection of specific radiata pine (Pinus radiata D. Don) families for better growth performance on nutrient-deficient sites in New Zealand would not result in substantial improvement over selection for growth on all sites disregarding nutrient availability.

Inheritance of spiral grain in the juvenile core of Pinus radiata

2007 ◽  
Vol 37 (1) ◽  
pp. 116-127 ◽  
Author(s):  
Washington Gapare ◽  
Adrian Hathorn ◽  
Dominic Kain ◽  
Colin Matheson ◽  
Harry Wu
Keyword(s):  
Pinus Radiata ◽  
Genetic Gain ◽  
Radiata Pine ◽  
Correlated Response ◽  
Lower Grade ◽  
Tangential Plane ◽  
Individual Tree ◽  
Spiral Grain ◽  
Grain Angle ◽  
Selection For

Spiral grain is the angular arrangement of fibres in a tangential plane with reference to the pith or vertical tree axis. Spiral grain angles exceeding 5° can cause wood to twist, which may result in a considerable amount of waste and degrade. We assessed spiral grain at breast height in two related progeny tests of radiata pine (Pinus radiata D. Don) aged 8 and 9 years established at two different sites in Australia. Radial trends for grain angle at the two sites were similar. Mean spiral grain (MSG) across the two trials was 4.3° with a standard deviation of 1.5° and a range of 0.8–10°. Estimates of individual tree heritabilities on a single-site basis for individual rings and MSG suggested that spiral grain is lowly to highly inherited (h2 = 0.11 ± 0.08 to 0.66 ± 0.21 for individual rings and 0.44 ± 0.12 for MSG). Additive genotypic correlations between individual rings grain angle and MSG were generally high, above 0.71, suggesting a favourable expected correlated response of mean grain angle in the juvenile wood to selection for grain angle of individual rings. Selection to reduce spiral grain on any of rings 2–4 (at a selection intensity of 1.755, i.e., selecting the best 10% of trees) would result in a predicted correlated genetic gain in MSG of 1.0°. Our results suggest that selection could be performed in any of the individual rings 2, 3, or 4 (equivalent to ages 4–6) and still achieve at least 75% of the genetic gain possible from selection on the mean of all rings 1–5 (MSG). This suggests that there is an optimum stage (rings 2–4) in which selection for this trait should take place. Our results suggest that a reduction in spiral grain angle in the juvenile core is one strategy to reduce the amount of lower grade timber owing to twist.

scholarly journals Genetic Parameters and Strategies for Genetic Improvement of Stiffness in Radiata Pine

2006 ◽  
Vol 55 (1-6) ◽  
pp. 77-84 ◽  
Author(s):  
S. Kumar ◽  
H. S. Dungey ◽  
A. C. Matheson
Keyword(s):  
Pinus Radiata ◽  
Genetic Improvement ◽  
Genetic Parameters ◽  
Growth Ring ◽  
Genetic Correlations ◽  
Radiata Pine ◽  
Core Sample ◽  
Standing Tree ◽  
Coefficients Of Variation ◽  
Selection For

Abstract The two main objectives of this study were: (1) to determine how early is it possible to undertake selection to improve the stiffness of corewood; (2) to determine if the selection based on corewood stiffness could also improve outerwood stiffness, and vice versa. Breastheight data from two progeny trials of Pinus radiata D. Don were used. In the first trial (age 30 years), data on Silviscan predicted stiffness (MoE) was obtained for each growth ring on each core sample from 50 open-pollinated families. In the second trial (age 14 years), data on static-bending MoE was obtained using clearwood sticks (300 × 20 × 20 mm) cut from each tree from 18 control-pollinated families. MoE varied from 3.5 GPa in rings 1-5 to about 17 GPa in rings 21-25. Coefficients of variation of corewood and outerwood MoE were about 20-30% and 15-20% respectively. Estimates of narrowsense heritability for MoE were generally higher (0.50-0.70) in the corewood compared with the outerwood (0.15-0.30). Early selection for MoE could yield substantial gain in corewood MoE but only small gains, if any, in outerwood MoE (especially for rings 21-30). Estimated genetic correlations between density and stiffness appeared moderate in the corewood zone, but high in the outerwood zone. Selection based on density (using 5-mm cores) and acoustic stiffness (using standing tree tools), assessed at age 6-7 years, appeared to be a good option to improve both corewood and outerwood stiffness.

Identifying Measurement Invariant Item Sets in Cross-Cultural Settings Using an Automated Item Selection Procedure

Methodology ◽  
2018 ◽  
Vol 14 (4) ◽  
pp. 177-188 ◽  
Author(s):  
Martin Schultze ◽  
Michael Eid
Keyword(s):  
Measurement Invariance ◽  
Optimal Solution ◽  
Selection Procedure ◽  
Cross Cultural ◽  
Item Selection ◽  
Ant System ◽  
Item Quality ◽  
Ant System Algorithm ◽  
Selection For ◽  
Selection Of

Abstract. In the construction of scales intended for the use in cross-cultural studies, the selection of items needs to be guided not only by traditional criteria of item quality, but has to take information about the measurement invariance of the scale into account. We present an approach to automated item selection which depicts the process as a combinatorial optimization problem and aims at finding a scale which fulfils predefined target criteria – such as measurement invariance across cultures. The search for an optimal solution is performed using an adaptation of the [Formula: see text] Ant System algorithm. The approach is illustrated using an application to item selection for a personality scale assuming measurement invariance across multiple countries.

ESTIMASI NILAI HERITABILITAS BOBOT IKAN MAS VARIETAS PUNTEN DALAM PROGRAM SELEKSI INDIVIDU

2016 ◽  
Vol 11 (3) ◽  
pp. 217
Author(s):  
Estu Nugroho ◽  
Budi Setyono ◽  
Mochammad Su’eb ◽  
Tri Heru Prihadi
Keyword(s):  
Body Weight ◽  
Selection Response ◽  
Base Population ◽  
Breeding Programs ◽  
Male And Female ◽  
Body Weight Trait ◽  
Population Selection ◽  
Selection For ◽  
Weight Trait ◽  
Selection Of

Program pemuliaan ikan mas varietas Punten dilakukan dengan seleksi individu terhadap karakter bobot ikan. Pembentukan populasi dasar untuk kegiatan seleksi dilakukan dengan memijahkan secara massal induk ikan mas yang terdiri atas 20 induk betina dan 21 induk jantan yang dikoleksi dari daerah Punten, Kepanjen (delapan betina dan enam jantan), Kediri (tujuh betina dan 12 jantan), Sragen (27 betina dan 10 jantan), dan Blitar (15 betina dan 11 jantan). Larva umur 10 hari dipelihara selama empat bulan. Selanjutnya dilakukan penjarangan sebesar 50% dan benih dipelihara selama 14 bulan untuk dilakukan seleksi dengan panduan hasil sampling 250 ekor individu setiap populasi. Seleksi terhadap calon induk dilakukan saat umur 18 bulan pada populasi jantan dan betina secara terpisah dengan memilih berdasarkan 10% bobot ikan yang terbaik. Calon induk yang terseleksi kemudian dipelihara hingga matang gonad, kemudian dipilih sebanyak 150 pasang dan dipijahkan secara massal. Didapatkan respons positif dari hasil seleksi berdasarkan bobot ikan, yaitu 49,89 g atau 3,66% (populasi ikan jantan) dan 168,47 g atau 11,43% (populasi ikan betina). Nilai heritabilitas untuk bobot ikan adalah 0,238 (jantan) dan 0,505 (betina).Punten carp breeding programs were carried out by individual selection for body weight trait. The base population for selection activities were conducted by mass breeding of parent consisted of 20 female and 21 male collected from area Punten, eight female and six male (Kepanjen), seven female and 12 male (Kediri), 27 female and 10 male (Sragen), 15 female and 11 male (Blitar). Larvae 10 days old reared for four moths. Then after spacing out 50% of total harvest, the offspring reared for 14 months for selection activity based on the sampling of 250 individual each population. Selection of broodstock candidates performed since 18 months age on male and female populations separately by selecting based on 10% of fish with best body weight. Candidates selected broodstocks were then maintained until mature. In oder to produce the next generation 150 pairs were sets and held for mass spawning. The results revealed that selection response were positive, 49.89 g (3.66%) for male and 168.47 (11.43%) for female. Heritability for body weight is 0.238 (male) and 0.505 (female).

Evaluation of Large-Sunflower Lines of Sunflower on Quantitative Morphological Traits

2020 ◽  
pp. 46-55
Keyword(s):  
Fertility Restoration ◽  
Morphological Characters ◽  
Direct Selection ◽  
Oilseed Crops ◽  
Turkish Origin ◽  
Self Pollination ◽  
Special Area ◽  
Pericarp Color ◽  
Selection For ◽  
Selection Of

Confectionery sunflower - a special area of use of sunflower, which requires the creation of marketable seeds quality features. One of the possible ways to create large-fruited sunflower is to create production hybrids and lines. Objective: to evaluate the created new large-fruited sunflower lines by a complex of morphological characters and determine the best lines for use as large-seeds hybrids as parent components or source material. In 2016-2019 years on the basis of the Institute of Oilseed Crops NAAS a study was conducted to assess the economic characteristics of large-fruited sunflower lines. We studied a collection of 27 lines of large-seeds sources. The lines were created by direct selection or crossing and sampling: Reyny of Argentinean origin, Zaporizhzhya confectionery variety, confectionery hybrid with striped pericarp color of Israeli origin, white seed of Turkish origin, synthetic population - donor of complex resistance. To study from the collection, lines were drawn that went through at least 7 generations with selection for seed size. Experience has shown that the shortest growing season for lines 174d and KP11 was 99 days, and the longest for lines I2K670 was 109 days. In the studied collection, the greatest mass of 1000 seeds has the KP11-146.47g line, which is the mother component and does not have branching. The second by weight of 1000 seeds (109 g) stood out line 168v, which also had branches and pollen fertility restoration genes and will be used as the paternal form. The third largest is also one basket line ZKN51-100. The collection included lines originating from the same combination, but with a different morphotype for the presence and absence of branching. So, based on the combination of KP11 x Zaporizhzhya Confectionery, three lines were obtained. A mass of 1000 seeds was observed in 98-86 g, with the branching line having the largest mass of 1000 seeds. The lines created with one combination VK678 x ZKN32: with a branch 168a had a mass of 1000 seeds 95g, and a line 168b - without a branch 109 g. Of the two lines obtained from the descendants of the combination KP11 x the striped hybrid both had branches, but the seeds were much smaller (weight of 1000 seeds 59 and 79 g). The collection also studied samples created on the basis of varieties and populations 160c, 174, 175b, the mass of 1000 seeds of which turned out to be more acceptable for large-fruited use from 83 to 99 g. Summing up the results of studying the collection of newly created lines, we can highlight the lines 162d, 168v, 175b, KP11 that are potentially promising for use in hybrids. The selections showed that large-fruited lines can be obtained from large-fruited varieties, self-pollination of large-fruited hybrids and crossing lines with hybrids and varieties. Self-pollination and selection of large-fruited lines in several generations does not provide the necessary variability for positive changes in selections. The result of the selection by weight of 1000 seeds in the offspring from crosses and from populations creates opportunities for new large-seeds sunflower.

scholarly journals Regulating the Regulators: Mechanisms of Substrate Selection of the O-GlcNAc Cycling Enzymes OGT and OGA

Glycobiology ◽  
2021 ◽  
Author(s):  
Hannah M Stephen ◽  
Trevor M Adams ◽  
Lance Wells
Keyword(s):  
Nutrient Sensing ◽  
Substrate Selection ◽  
Disease States ◽  
Dynamic Modification ◽  
Selection For ◽  
Outstanding Question ◽  
Glcnac Transferase ◽  
Future Work ◽  
Partner Proteins ◽  
Selection Of

Abstract Thousands of nuclear and cytosolic proteins are modified with a single β-N-acetylglucosamine on serine and threonine residues in mammals, a modification termed O-GlcNAc. This modification is essential for normal development and plays important roles in virtually all intracellular processes. Additionally, O-GlcNAc is involved in many disease states, including cancer, diabetes, and X-linked intellectual disability. Given the myriad of functions of the O-GlcNAc modification, it is therefore somewhat surprising that O-GlcNAc cycling is mediated by only two enzymes: the O-GlcNAc transferase (OGT), which adds O-GlcNAc, and the O-GlcNAcase (OGA), which removes it. A significant outstanding question in the O-GlcNAc field is how do only two enzymes mediate such an abundant and dynamic modification. In this review, we explore the current understanding of mechanisms for substrate selection for the O-GlcNAc cycling enzymes. These mechanisms include direct substrate interaction with specific domains of OGT or OGA, selection of interactors via partner proteins, posttranslational modification of OGT or OGA, nutrient sensing, and localization alteration. Altogether, current research paints a picture of an exquisitely regulated and complex system by which OGT and OGA select substrates. We also make recommendations for future work, toward the goal of identifying interaction mechanisms for specific substrates that may be able to be exploited for various research and medical treatment goals.

Selection for rate and efficiency of lean gain in Hereford cattle 1. Selection pressure applied and direct responses

1990 ◽  
Vol 51 (1) ◽  
pp. 23-34 ◽  
Author(s):  
R. A. Mrode ◽  
C. Smith ◽  
R. Thompson
Keyword(s):  
Genetic Parameters ◽  
Control Line ◽  
Correlated Responses ◽  
Direct Response ◽  
Lean Growth ◽  
Hereford Cattle ◽  
Frozen Semen ◽  
Phenotypic Standard Deviation ◽  
Selection For ◽  
Selection Of

ABSTRACTSelection of bulls for rate and efficiency of lean gain was studied in a herd of Hereford cattle. There were two selection lines, one selected for lean growth rate (LGR) from birth to 400 days and the other for lean food conversion ratio (LFCR) from 200 to 400 days of age, for a period of 8 years. A control line bred by frozen semen from foundation bulls was also maintained. Generation interval was about 2·4 years and average male selection differentials, per generation were 1·2 and — 1·1 phenotypic standard deviation units for LGR and LFCR respectively.Genetic parameters and responses to selection were estimated from the deviation of the selected lines from a control line and by restricted maximum likelihood (REML) techniques on the same material. Realized heritabilities were 0·40 (s.e. 0·12) for LGR and 0·40 (s.e. 0·13) for LFCR using the control line. Corresponding estimates from REML were 0·42 (s.e. 0·10) and 0·37 (s.e. 0·14). The estimate of the genetic correlation between LGR and LFCR was about — 0·69 (s.e. 0·12) using REML.The estimates of direct annual genetic change using deviations from the control were 3·6 (s.e. 1·3) g/day for LGR and — 0·14 (s.e. 0·07) kg food per kg lean gain for LFCR. Corrsponding estimates from REML were similar but more precisely estimated. The correlated responses for LFCR in the LGR line was higher than the direct response for LFCR.

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