Calculation of the heritability of spinning fineness from phenotypic and genetic parameters of the mean and CV of fibre diameter

1992 ◽  
Vol 43 (6) ◽  
pp. 1441 ◽  
Author(s):  
KL Butler ◽  
M Dolling
Keyword(s):  
Genetic Correlation ◽  
Coefficient Of Variation ◽  
Selection Criteria ◽  
Genetic Parameters ◽  
Genetic Correlations ◽  
Fibre Diameter ◽  
Diameter Distribution ◽  
The Mean

In sheep selection programmes where fibre diameter distribution measurements are available, such as when using the FDA method of assessing fibre diameter, spinning fineness (as defined by Anderson, S.L. (1976), J. Text. Inst., 67, 175-80) might be preferable to using mean fibre diameter as a sheep selection criteria. This paper uses a Taylor's expansion to obtain an approximation to the heritability of spinning fineness when the phenotypic and genetic parameters of only the mean and the coefficient of variation of fibre diameter are available. The approximation assumes that the mean and coefficient of variation of fibre diameter are both phenotypically and genetically independent. Approximations are also obtained for the genetic correlation between spinning fineness and mean fibre diameter, and between spinning fineness and coefficient of variation. Using the approximations, estimates of heritability of spinning fineness and of the two genetic correlations are calculated for published studies.

Inclusion of skin follicle traits in selection indices in breeding programs improves genetic gain in Australian fine-wool Merinos

2007 ◽  
Vol 58 (9) ◽  
pp. 921 ◽  
Author(s):  
M. Asadi Fozi ◽  
J. H. J. Van der Werf ◽  
A. A. Swan
Keyword(s):  
Body Weight ◽  
Coefficient Of Variation ◽  
Genetic Parameters ◽  
Genetic Correlations ◽  
Fibre Diameter ◽  
Selection Criterion ◽  
Breeding Programs ◽  
Breeding Objectives ◽  
Staple Strength ◽  
Fleece Weight

Genetic parameters for skin follicle traits, wool traits, body weight, and number of lambs weaned per ewe joined were estimated for 5108 10-month-old Australian fine-wool Merinos born between 1990 and 1996. These animals were descended from 261 sires and 2508 dams. The skin follicle number index that is based on skin surface area, and primary, secondary, or total follicle density were introduced as possible early-age selection criteria estimated at 6 months of age. Heritability estimates for total, secondary, and primary follicle number index were 0.45 ± 0.04, 0.46 ± 0.04, and 0.38 ± 0.04, respectively. The genetic correlations of total follicle number index with clean fleece weight, mean fibre diameter, staple strength, coefficient of variation of fibre diameter, body weight, and number of lambs weaned were 0.16, –0.67, 0.00, 0.03, 0.22, and 0.22, respectively. Responses to selection on indices including and excluding follicle traits were calculated based on the genetic parameters estimated, and with annual responses calculated using an optimised age structure. On average, 10% greater response was predicted when total follicle number index was used as an additional selection criterion in different micron premium scenarios. In comparison, skin follicle density had a smaller effect on genetic improvement. The extra response was ~1%. Similar index responses were obtained when total follicle number index was used as a replacement selection criterion for clean fleece weight, mean fibre diameter, and coefficient of variation of fibre diameter for breeding objectives with low emphasis on fibre diameter. In objectives with high emphasis on fibre diameter, unfavourable correlated responses in staple strength and CV of fibre diameter limited the effectiveness of using total follicle number index as a selection criterion. Although the use of total follicle number index as an additional selection criterion can be favourable for some breeding objectives, measuring this trait is currently cost prohibitive to inclusion in Merino breeding programs.

scholarly journals Use of part records in Merino breeding programs — the inheritance of wool growth and fibre traits during different times of the year to determine their value in Merino breeding programs

2005 ◽  
Vol 45 (4) ◽  
pp. 347
Author(s):  
J. C. Greeff ◽  
B. Paganoni ◽  
R. P. Lewer
Keyword(s):  
Genetic Correlation ◽  
Coefficient Of Variation ◽  
Selection Criteria ◽  
Fibre Diameter ◽  
Indirect Selection ◽  
Mediterranean Environment ◽  
Breeding Programs ◽  
Wool Growth ◽  
Heritability Estimates ◽  
Fibre Traits

Fibre diameter can vary dramatically along a wool staple, especially in the Mediterranean environment of southern Australia with its dry summers and abundance of green feed in spring. Other research results have shown a very low phenotypic correlation between fibre diameter grown between seasons. Many breeders use short staples to measure fibre diameter for breeding purposes and also to promote animals for sale. The effectiveness of this practice is determined by the relative response to selection by measuring fibre traits on a full 12 months wool staple as compared to measuring them only on part of a staple. If a high genetic correlation exists between the part record and the full record, then using part records may be acceptable to identify genetically superior animals. No information is available on the effectiveness of part records. This paper investigated whether wool growth and fibre diameter traits of Merino wool grown at different times of the year in a Mediterranean environment, are genetically the same trait, respectively. The work was carried out on about 7 dyebanded wool sections/animal.year, on ewes from weaning to hogget age, in the Katanning Merino resource flocks over 6 years. Relative clean wool growth of the different sections had very low heritability estimates of less than 0.10, and they were phenotypically and genetically poorly correlated with 6 or 12 months wool growth. This indicates that part record measurement of clean wool growth of these sections will be ineffective as indirect selection criteria to improve wool growth genetically. Staple length growth as measured by the length between dyebands, would be more effective with heritability estimates of between 0.20 and 0.30. However, these measurements were shown to have a low genetic correlation with wool grown for 12 months which implies that these staple length measurements would only be half as efficient as the wool weight for 6 or 12 months to improve total clean wool weight. Heritability estimates of fibre diameter, coefficient of variation of fibre diameter and fibre curvature were relatively high and were genetically and phenotypically highly correlated across sections. High positive phenotypic and genetic correlations were also found between fibre diameter, coefficient of variation of fibre diameter and fibre curvature of the different sections and similar measurements for wool grown over 6 or 12 months. Coefficient of variation of fibre diameter of the sections also had a moderate negative phenotypic and genetic correlation with staple strength of wool staples grown over 6 months indicating that coefficient of variation of fibre diameter of any section would be as good an indirect selection criterion to improve stable strength as coefficient of variation of fibre diameter for wool grown over 6 or 12 months. The results indicate that fibre diameter, coefficient of variation of fibre diameter and fibre curvature of wool grown over short periods of time have virtually the same heritability as that of wool grown over 12 months, and that the genetic correlation between fibre diameter, coefficient of variation of fibre diameter and fibre curvature on part and on full records is very high (rg >0.85). This indicates that fibre diameter, coefficient of variation of fibre diameter and fibre curvature on part records can be used as selection criteria to improve these traits. However, part records of greasy and clean wool growth would be much less efficient than fleece weight for wool grown over 6 or 12 months because of the low heritability of part records and the low genetic correlation between these traits on part records and on wool grown for 12 months.

Direct and maternal genetic (co)variances for hogget liveweight and fleece traits in Western Australian Merino sheep

2002 ◽  
Vol 53 (3) ◽  
pp. 271 ◽  
Author(s):  
S. W. P. Cloete ◽  
J. C. Greeff ◽  
R. P. Lewer
Keyword(s):  
Genetic Correlation ◽  
Coefficient Of Variation ◽  
Genetic Correlations ◽  
Fibre Diameter ◽  
Phenotypic Variance ◽  
Selection For ◽  
Fleece Weight ◽  
Variance Estimates ◽  
Western Australian ◽  
Australian Merino

(Co)variance estimates for hogget liveweight, greasy fleece weight, clean fleece weight, clean yield, fibre diameter, and the coefficient of variation of fibre diameter were obtained for a Western Australian Merino resource flock. The flock encompassed 16 medium wool bloodlines and data were available for the period 1982–93. Direct additive genetic variances (h2) — expressed as a ratio of the total phenotypic variance within bloodlines — were estimated at 0.52 for hogget liveweight, 0.44 for greasy fleece weight, 0.42 for clean fleece weight, 0.63 for clean yield, 0.71 for fibre diameter, and 0.62 for coefficient of variation of fibre diameter. Maternal genetic variance estimates were significant (P < 0.05) only in hogget liveweight and fibre diameter, but components within bloodlines were low (0.05 for liveweight and 0.02 for fibre diameter). Direct within-bloodline genetic correlations of hogget liveweight as well as greasy and clean fleece weight with fibre diameter were positive (0.17, 0.31, and 0.31, respectively), suggesting that selection for bigger and heavier cutting sheep would generally lead to a broader fibre diameter. Liveweight was unrelated to clean yield and negatively related to coefficient of variation of fibre diameter (–0.17). Greasy fleece weight was negatively related to clean yield (–0.20). The genetic correlation of clean fleece weight with clean yield was positive (0.37). Wool quantity was, in general, positively related to coefficient of variation of fibre diameter, although the estimated genetic correlations were low (0.12 for greasy fleece weight and 0.07 for clean fleece weight). The genetic correlation between fibre diameter and coefficient of variation of fibre diameter was negative, and fairly low (–0.10). These results are discussed with reference to sheep breeding.

scholarly journals Realized Sampling Variances of Estimates of Genetic Parameters and the Difference Between Genetic and Phenotypic Correlations

Genetics ◽  
1996 ◽  
Vol 143 (3) ◽  
pp. 1409-1416 ◽  
Author(s):  
Kenneth R Koots ◽  
John P Gibson
Keyword(s):  
Genetic Correlation ◽  
Genetic Parameters ◽  
Genetic Parameter ◽  
Genetic Correlations ◽  
Phenotypic Correlation ◽  
Parameter Estimates ◽  
Sampling Variance ◽  
Phenotypic Correlations ◽  
Genetic And Phenotypic Correlations ◽  
Heritability Estimates

Abstract A data set of 1572 heritability estimates and 1015 pairs of genetic and phenotypic correlation estimates, constructed from a survey of published beef cattle genetic parameter estimates, provided a rare opportunity to study realized sampling variances of genetic parameter estimates. The distribution of both heritability estimates and genetic correlation estimates, when plotted against estimated accuracy, was consistent with random error variance being some three times the sampling variance predicted from standard formulae. This result was consistent with the observation that the variance of estimates of heritabilities and genetic correlations between populations were about four times the predicted sampling variance, suggesting few real differences in genetic parameters between populations. Except where there was a strong biological or statistical expectation of a difference, there was little evidence for differences between genetic and phenotypic correlations for most trait combinations or for differences in genetic correlations between populations. These results suggest that, even for controlled populations, estimating genetic parameters specific to a given population is less useful than commonly believed. A serendipitous discovery was that, in the standard formula for theoretical standard error of a genetic correlation estimate, the heritabilities refer to the estimated values and not, as seems generally assumed, the true population values.

HERITABILITIES AND GENETIC CORRELATIONS FOR ULTRASONIC BACKFAT MEASUREMENTS, GROWTH AND CARCASS TRAITS IN SWINE

1982 ◽  
Vol 62 (3) ◽  
pp. 665-670 ◽  
Author(s):  
D. C. JEFFRIES ◽  
R. G. PETERSON
Keyword(s):  
Key Words ◽  
Genetic Correlation ◽  
Genetic Parameters ◽  
Average Daily Gain ◽  
Genetic Correlations ◽  
Phenotypic Correlation ◽  
Ultrasonic Measurements ◽  
Yorkshire Pigs ◽  
Daily Gain ◽  
Season Interaction

Genetic parameters were estimated for 2403 purebred Yorkshire pigs over a 2-yr period, representing 21 sires. The traits studied included average daily gain, age adjusted to 90 kg, ultrasonic measurements of backfat at the mid-back and loin positions, total and adjusted total ultrasonic backfat and corresponding carcass backfat measurements. Least squares analyses were used to estimate and adjust for the effects of sex, year-season and sex by year-season interaction. Heritabilities and genetic correlations were calculated for all traits using both half- and full-sib estimates. Adjusted age and adjusted total ultrasonic backfat measurements were found to have the highest heritabilities of the live traits in this study. Estimates of heritability for adjusted age and adjusted total ultrasonic backfat were 0.24 ± 0.10 and 0.26 ± 0.10 based on half-sib and 0.56 ± 0.07 and 0.41 ± 0.06 from full-sib analyses. The genetic correlation between these two traits was −0.07 ± 0.28 based on the half-sib method. The total phenotypic correlation was −0.01 ± 0.02. Key words: Swine, ultrasonic backfat, heritabilities, genetic correlations

scholarly journals Genetic parameters of production and reproduetive traits in on a farm tested Danish Large White and Landrace swine in Greece

2000 ◽  
Vol 43 (3) ◽  
pp. 287-298
Author(s):  
J. Bizelis ◽  
A. Kominakis ◽  
E. Rogdakis ◽  
F. Georgadopoulou
Keyword(s):  
Maximum Likelihood ◽  
Genetic Correlation ◽  
Genetic Parameters ◽  
Genetic Correlations ◽  
Production Traits ◽  
Likelihood Methods ◽  
Large White ◽  
Reproduction Traits ◽  
Maximum Likelihood Methods ◽  
Genetic And Phenotypic Correlations

Abstract. Production and reproduetive traits in Danish Landrace (LD) and Large White (LW) swine were analysed by restricted maximum likelihood methods to obtain heritabilities as well as genetic and phenotypic correlations. Production traits were: age, backfat thickness (BT), muscle depth (MD) and the ratio BT/MD, adjusted to Standard bodyweight of 85 kg. Reproduction traits were: number of pigs born (NB) and number of pigs weaned (NW) per sow and parity. Heritabilities for age, BT, MD and BT/MD were 0.60, 0.44, 0.51 and 0.42 for LD and 0.36, 0.44, 0.37 and 0.45 for LW, respectively. Genetic correlations between age and BT were −0.22 in LD and – 0.44 in LW. The genetic correlation between age and MD was close to zero in both breeds. Genetic correlation between BT and MD were −0.36 and −0.25 in LD and LW, respectively. Heritabilities for NB were 0.25 in LD and 0.13 in LW while heritabilities for NW were close to zero in both breeds. Genetic correlation between NB and NW was 0.46 and 0.70 in LD and LW, respectively.

scholarly journals PSVIII-38 Late-Breaking Abstract: Estimating genetic parameters of feed efficiency traits in American mink

2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 347-347
Author(s):  
Pourya Davoudi ◽  
Duy Ngoc Do ◽  
Guoyu Hu ◽  
Siavash Salek Ardestani ◽  
Younes Miar
Keyword(s):  
Body Weight ◽  
Genetic Correlation ◽  
Feed Intake ◽  
Feed Efficiency ◽  
Fixed Effects ◽  
Genetic Parameters ◽  
American Mink ◽  
Genetic Correlations ◽  
Final Body Weight ◽  
Selection For

Abstract Feed cost is the major input cost in the mink industry and thus improvement of feed efficiency through selection for high feed efficient mink is necessary for the mink farmers. The objective of this study was to estimate the heritability, phenotypic and genetic correlations for different feed efficiency measures, including final body weight (FBW), daily feed intake (DFI), average daily gain (ADG), feed conversion ratio (FCR) and residual feed intake (RFI). For this purpose, 1,088 American mink from the Canadian Center for Fur Animal Research at Dalhousie Faculty of Agriculture were recorded for daily feed intake and body weight from August 1 to November 14 in 2018 and 2019. The univariate models were used to test the significance of sex, birth year and color as fixed effects, and dam as a random effect. Genetic parameters were estimated via bivariate models using ASReml-R version 4. Estimates of heritabilities (±SE) were 0.41±0.10, 0.37±0.11, 0.33±0.14, 0.24±0.09 and 0.22±0.09 for FBW, DFI, ADG, FCR and RFI, respectively. The genetic correlation (±SE) was moderate to high between FCR and RFI (0.68±0.15) and between FCR and ADG (-0.86±0.06). In addition, RFI had low non-significant (P &gt; 0.05) genetic correlations with ADG (0.04 ± 0.26) and BW (0.16 ± 0.24) but significant (P &lt; 0.05) high genetic correlation with DFI (0.74 ± 0.11) indicating that selection for lower RFI will reduce feed intake without adverse effects on the animal size and growth rate. The results suggested that RFI can be implemented in genetic/genomic selection programs to reduce feed intake in the mink production system.

Genetic parameter estimations and genomic insights for teat and udder structure in young and mature Canadian Angus cows

2021 ◽  
Author(s):  
K Devani ◽  
J J Crowley ◽  
G Plastow ◽  
K Orsel ◽  
T S Valente
Keyword(s):  
Animal Model ◽  
Genetic Correlation ◽  
Genetic Parameters ◽  
Genetic Parameter ◽  
Genetic Correlations ◽  
Age Groups ◽  
Morbidity And Mortality ◽  
Parameter Estimations ◽  
Angus Cattle ◽  
Genetic Evaluations

Abstract Poor teat and udder structure, frequently associated with older cows, impact cow production and health, as well as calf morbidity and mortality. However, producer culling, for reasons including age, production, feed availability, and beef markets, creates a bias in teat and udder scores assessed and submitted to the Canadian Angus Association for genetic evaluations towards improved mammary structure. In addition, due to the infancy of the reporting program, repeated scores are rare. Prior to adoption of genetic evaluations for teat and udder scores in Canadian Angus cattle, it is imperative to verify that teat and udder scores from young cows are the same trait as teat and udder scores estimated on mature cows. Genetic parameters for teat and udder scores from all cows (n=4,192), and then from young cows (parity 1 and 2) and from mature cows (parity ≥ 4) were estimated using a single trait animal model. Genetic correlations for the traits between the two cow age groups were estimated using a two-trait animal model. Estimates of heritability (PSD) were 0.32 (0.07) and 0.45 (0.07) for young teat and udder score, and 0.27 (0.07) and 0.31 (0.07) for mature teat and udder score, respectively. Genetic correlation (PSD) between the young and mature traits was 0.87 (0.13) for teat score and 0.40 (0.17) for udder score. GWAS were used to further explore the genetic and biological commonalities and differences between the two groups. Although there were no genes in common for the two udder scores, 12 genes overlapped for teat score in the two cow age groups. Interestingly, there were also 23 genes in common between teat and udder scores in mature cows. Based on these findings, it is recommended that producers collect teat and udder score on their cow herd annually.

scholarly journals Estimation of Genetic Parameters for Peak Yield, Yield and Persistency Traits in Murciano-Granadina Goats Using Multi-Traits Models

Animals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 411
Author(s):  
Judith C. Miranda ◽  
José M. León ◽  
Camillo Pieramati ◽  
Mayra M. Gómez ◽  
Jesús Valdés ◽  
...  
Keyword(s):  
Multivariate Analysis ◽  
Selection Criteria ◽  
Genetic Parameters ◽  
Genetic Correlations ◽  
Multiple Trait ◽  
Lactation Curve ◽  
Derivative Free ◽  
Selection For ◽  
Estimated Breeding Values ◽  
Estimation Of Genetic Parameters

This paper studies parameters of a lactation curve such as peak yield (PY) and persistency (P), which do not conform to the usual selection criteria in the Murciano-Granadina (MG) breed, but are considered to be an alternative to benefit animal welfare without reducing production. Using 315,663 production records (of 122,883 animals) over a period of 24 years (1990–2014), genetic parameters were estimated with uni-, bi- and multivariate analysis using multiple trait derivative free restricted maximum likelihood (MTDFREML). The heritability (h2)/repeatability (re) of PY, yield (Y) and P was estimated as 0.13/0.19, 0.16/0.25 and 0.08/0.09 with the uni-trait and h2 of bi- and multi-traits analysis ranging from 0.16 to 0.17 of Y, while that of PY and Y remained constant. Genetic correlations were high between PY–Y (0.94 ± 0.011) but low between PY–P (–0.16 ± 0.054 to –0.17 ± 0.054) and between Y–P (–0.06 ± 0.058 to –0.05 ± 0.058). Estimates of h2/re were low to intermediate. The selection for Y–PY or both can be implemented given the genetic correlation between these traits. PY–P and Y–P showed low to negligible correlation values indicating that if these traits are implemented in the early stages of evaluation, they would not be to the detriment of PY–Y. The combination of estimated breeding values (EBVs) for all traits would be a good criterion for selection.

Genetic parameters for egg weight v. age curve, and other egg production and egg weight traits, in synthetic lines of chickens

1983 ◽  
Vol 34 (1) ◽  
pp. 85 ◽  
Author(s):  
BH Yoo ◽  
BL Sheldon ◽  
RN Podger
Keyword(s):  
Standard Deviation ◽  
Genetic Correlation ◽  
Egg Production ◽  
Genetic Parameters ◽  
Genetic Correlations ◽  
Egg Mass ◽  
Control Line ◽  
Egg Weight ◽  
Egg Number ◽  
Selection For

An exponential curve, W = P-Qexp(- Rt), where W is egg weight at age t, was fitted to egg weights of individual pullets, and genetic parameters were estimated for P, Q and R, the residual standard deviation and other egg weight and egg production characters. The data consisted of records collected over six generations on more than 4000 pullets in two selection lines and a control line which originated from a synthetic gene pool of White Leghorn x Australorp crosses. The half-sib and offspring-on-parent regression estimates of heritability pooled over the lines were 0.23 and 0.33 for P, 0.14 and 0.20 for Q, and 0.14 and 0.25 for R. Genetic correlations were estimated to be -0.10 between P and Q, -0.46 between P and R, and 0.90 between Q and R. These estimates suggest that the egg weight v. age curve may be modified to increase the proportion of eggs in desirable weight grades and reduce the incidence of oversized eggs later in the production year. The genetic correlation between mean weight of first 10 eggs and egg weight at 62 weeks of age was estimated to be 0.68, further suggesting that early egg weight may be improved partly independently of late egg weight. The heritability estimates of egg mass output were not higher than those of egg number in spite of the highly heritable average egg weight being an important component of egg mass, probably because of the negative genetic correlation (r = -0.49) between egg number and average egg weight. The standard deviation of individual pullet's egg weights was moderately heritable and genetically correlated positively with egg weight characters and negatively with egg production; these estimates were consistent with the responses to selection for reduced egg weight variability observed elsewhere

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