Deriving a preliminary breeding objective for commercial ostriches: an overview

2008 ◽  
Vol 48 (10) ◽  
pp. 1247 ◽  
Author(s):  
S. W. P. Cloete ◽  
A. Engelbrecht ◽  
J. J. Olivier ◽  
K. L. Bunter

Ostrich farmers rely on skins and meat as their most important sources of revenue, with feathers being of secondary importance. This paper provides a summary of parameter estimates (heritabilities and genetic correlations) estimated from the resource flock held at the Oudtshoorn Research Farm. Traits considered were egg production, chick production, mature liveweight, offspring slaughter weight and skin traits. Feather weight of mature breeding birds was not included, as revenue received for this commodity is comparatively low, and mostly reliant on quality. All the traits considered were moderately to highly heritable, and reproduction traits in particular were highly variable. No substantial unfavourable genetic correlations were noted, and worthwhile gains in all traits appear to be achievable within a selection objective based on economic principles. Economic weights for key traits were obtained from a bio-economical input–output simulation model that was prepared for the industry. A simple preliminary selection index including chick production (as a hen reproductive trait) and slaughter weight (as a measure of growth) appears to be adequate for the present needs, given the limited availability of routinely recorded traits. A key performance trait that is currently missing from the economic assessment is chick survival, which is known to be low and highly variable among ostrich flocks. Further information will be added as it becomes available.

2001 ◽  
Vol 26 (1) ◽  
pp. 237-249 ◽  
Author(s):  
J.E. Pryce ◽  
R.F. Veerkamp

AbstractIn recent years there has been considerable genetic progress in milk production. Yet, increases in yield have been accompanied by an apparent lengthening of calving intervals, days open, days to first heat and a decline in conception rates, which appears to be both at the genetic and phenotypic level. Fertility has a high relative economic value compared to production traits such as protein, making it attractive to include in a breeding programme. To do this there needs to be genetic variance in fertility. Measures of fertility calculated from service dates have a small genetic compared to phenotypic variance, hence heritability estimates are small, typically less than 5%, although coefficients of genetic variance are comparable to those of production traits. Heritabilities of commencement of luteal activity determined using progesterone profiles are generally higher, and have been reported as being from 0.16 to 0.28, which could be because of a more precise quantification of genetic variance, as management influences such as delaying insemination and heat detection rates are excluded. However, it might not be the use of progesterone profiles alone, as days to first heat observed by farm staff has a heritability of 0.15. The most efficient way to breed for improved fertility is to construct a selection index using the genetic and phenotypic parameter estimates of all traits of interest in addition to their respective economic values. Index traits for fertility could include measures such as calving interval, days open, days to first service, or days to first heat but there may also be alternative measures. Examples include traits related to energy balance, such as live weight and condition score (change), both of which have higher heritabilities than fertility measures and have genetic correlations of sufficient magnitude to make genetic progress by using them feasible. To redress the balance between fertility and production, some countries already publish genetic evaluations of fertility including: Denmark, Finland, France, Germany, Israel, The Netherlands, Norway and Sweden.


Author(s):  
Eser Kemal Gurcan ◽  
Dogan Narinc ◽  
Selcuk Kaplan

This study aimed to determine the phenotypic values of the slaughter and carcass traits in the flocks of quails obtained when a flock of parent quails were at 12, 16, and 20 weeks of age and to estimate the heritabilities and the genetic correlations for these traits. For this purpose, a total of 1,346 Japanese quails were slaughtered at 8 weeks of age, and their slaughter weights as well as carcass, breast, leg, and abdominal fat weights and ratios were determined. Differences in all traits were detected between female and male quails (P<0.05). The averages of many important traits, primarily slaughter weight, carcass weight, and breast weight, increased with the increase in the breeder age. On the contrary, the carcass yield decreased (P<0.05). There were no significant variations in the phenotypic and genetic variances for the slaughter and carcass traits in the flocks obtained when the breeder flock was at different ages. The heritabilities for slaughter weight, carcass weight, and abdominal fat weight were estimated to be moderate, and the genetic correlations among them were estimated to be positive and high. In conclusion, it is possible to state that positive results might be obtained by using the carcass ratio as the criterion for selection in quails. Besides, the breeder age was discovered to have had no significant effect on the genetic parameter estimations.


1998 ◽  
Vol 49 (8) ◽  
pp. 1195 ◽  
Author(s):  
M. V. Benavides ◽  
A. P. Maher ◽  
M. J. Young ◽  
P. R. Beatson ◽  
T. C. Reid

The potential for the reduction of wool yellowing susceptibility (YPC) in Corriedale sheep via selection was examined. The heritabilities of YPC and greasy fleece weight (GFW) and clean fleece weight (CFW), yield percentage (Yield), mean fibre diameter (MFD), and subjective greasy wool colour assessment (Visual), and phenotypic and genetic correlations among these traits were estimated from records on 1492 progeny of 53 sires of a Corriedale flock by using restricted maximum likelihood procedures using an average information algorithm. The heritability of YPC was 0·27 ± 0·06. Genetic correlations between YPC and GFW, CFW, Yield, MFD, and Visual were 0·20 ± 0·14, 0·11 ± 0·14, –0·15 ± 0·13, 0·24 ± 0·14, and 0·95 ± 0·06, respectively. Phenotypic correlations were low between these traits and YPC. Visual had a heritability of 0·30 ± 0·06 and medium-high genetic correlations with all traits, except CFW. Heritability estimates of GFW, CFW, Yield, and MFD were 0·55 ± 0·07, 0·52 ± 0·07, 0·51 ± 0·07, and 0·52 ± 0·07, respectively. The expected correlated responses to selection against YPC are likely to cause reductions in CFW and MFD. Correlated responses from the reduction of Visual are predicted to be greater for all production traits than those from the reduction of YPC. Responses in YPC are predicted to be slightly higher when selection is on Visual (–0·21 score/year) than when selection is on YPC itself (–0·19 score/year). A selection index, including CFW, MFD, and YPC as aggregate breeding and breeding objective traits, calculated at I = +3·26CFW – 0·14MFD + 0·03YPC, predicted a YPC increase, worsening the problem.


2000 ◽  
Vol 51 (2) ◽  
pp. 191
Author(s):  
M. V. Benavides ◽  
A. P. Maher

The potential for improvement of clean wool colour (CWC) in Corriedale sheep via selection was examined. The heritability, and phenotypic and genetic correlations, of CWC, brightness (Y), greasy (GFW) and clean (CFW) fleece weights , yield percentage (Yield), mean fibre diameter (MFD), and visual colour score were estimated from 440 progeny of 19 sires of a Corriedale flock using restricted maximum likelihood (REML) procedures with average information algorithm (AIREML). The heritability of CWC was estimated at 0.27±0.13. Clean wool colour showed strong positive genetic correlations with CFW and MFD. Visual colour score and CWC were also positively genetically correlated. As expected, direct selection criteria against MFD, CWC, or visual colour score would reduce CWC; however, direct selection against MFD would improve clean wool colour with negligible reductions on CFW, thus resulting in small economic gains. Several selection indices were calculated having either CFW, MFD, and CWC or CFW and MFD as selection criteria. The b-values of an unrestricted index were estimated at I1 = + 1.15 CFW + 0.13 MFD + 0.43 CWC, with positive correlated responses for all 3 breeding objective traits (CFW, MFD, and CWC). A second index, where CFW was restricted to nil genetic change, was estimated at: I2 = + 0.14 CFW − 0.02 MFD + 0.01 CWC. This index was expected to cause a negligible genetic gain for CWC (−0.04 Y–Z units/head.year). To avoid economic losses with the reduction on CFW, a third selection index was calculated where CWC was restricted to nil change. The index was estimated at I3 = +0.61 CFW − 0.07 MFD + 0.02 CWC with expected increases in CFW and decreases in MFD. Selection indices with (a) CFW and MFD (I4) and (b) CFW, MFD, and visual colour score (I5) as selection criteria would increase CFW, MFD, and CWC at the same rates observed in I1.


1985 ◽  
Vol 15 (3) ◽  
pp. 488-493 ◽  
Author(s):  
G. Sam Foster ◽  
Robert K. Campbell ◽  
W. Thomas Adams

Variation in 1st-year height (HT) of western hemlock (Tsugaheterophylla (Raf.) Sarg.) rooted cuttings was partitioned into environmental and genetic components. C effects, a unique type of environmental effect, was highly significant and made up 8% of the total variation. Much of the variation (21%) resulted from genetic control of HT, producing a broad-sense heritability of 0.81. As reported in a previous paper, initial rooting ability of the rooted cuttings affected the 1st-year height growth of the trees. Genetic correlations between HT and the five rooting traits ranged from 0.37 to 0.59. Using a selection index (assuming 33% selection intensity) containing both HT and a rooting trait (VOL) would result in gains of 8–10% for HT and 20–34% for VOL, depending on relative economic weights for the two traits.


1994 ◽  
Vol 45 (2) ◽  
pp. 427 ◽  
Author(s):  
LD Brash ◽  
NM Fogarty ◽  
AR Gilmour

Reproductive performance of ewes in a large Dorset stud flock is reported. The data included 2488 ewes with 10016 joining records over 25 years. Average performance for reproductive traits were: fertility 92%, litter size 1.31, neonatal lamb survival 91%, lamb survival to weaning 85%, with overall lambs born 1.20 and lambs weaned 1.02 per ewe joined. Differences between breeds (Poll Dorset and Dorset Horn), season of birth (spring and autumn) and season of joining (spring and autumn) were significant for most reproduction traits. Linear and quadratic regressions for age of ewe at joining were highly significant for all traits (P < 0.001) with maximum performance between three and six years of age. Estimates of heritability for ewe reproductive traits were: 0.062 � 0-02 for number of lambs born and 0.04 � 0.01 for number of lambs weaned per ewe joined, and component traits, 0.02 �0 -01 for fertility, 0 08 � 0 -02 for litter size and 0.00 � 0.01 for lamb survival. Estimates of repeatability were less than 0.14 for all the reproduction traits, which resulted in substantially higher predicted heritabilities when repeated records were used. Heritability estimates for average ewe lifetime performance, with approximately four records, were 0.08 � 0 06 for lambs born, 0.12 � 0.05 for lambs weaned, 0.08 � 0.04 for fertility, 0.l9 � 0 -04 for litter size and zero for lamb survival. The genetic correlations between litter size and lambs born and weaned were close to unity, whereas those for fertility were lower and declined from lambs born (0.6l � 0.22) to lambs weaned (0-45 � 0.30). The estimated heritability for ewe longevity, defined as the number of years the ewe remained in the breeding flock, was 0.00 � 0.03. The potential for genetic improvement in reproductive rate is discussed in relation to other reports in the literature and in the context of the roles of the Dorset breed in the Australian lamb industry. Increased reproductive rate in Dorset flocks impacts on stud profitability and the rate of genetic improvement from selection for other traits such as liveweight. The parameter estimates derived will be used in compiling breed-specific parameter sets for genetic evaluation in LAMBPLAN.


1985 ◽  
Vol 65 (1) ◽  
pp. 21-29
Author(s):  
B. B. ALLAN ◽  
G. M. WEISS ◽  
H. T. FREDEEN

Two-trait selection indexes comprising average daily gain (G) and adjusted average backfat depth (F) were constructed utilizing several permutations of economic and genetic parameters. In these permutations the ratio of economic weights employed (value per kg G: value per mm F) ranged from 5:1 to 75:1, the ratios of heritabilities (G:F) ranged from 0.625:1 to 1:1 and the genetic and phenotypic correlations ranged from zero to 0.25. The relative merits of these indexes were evaluated by comparing the expected genetic merit of progeny produced by the top 10% of the boars identified by each index as applied to a population of 590 boars station tested under the Canadian Record of Performance (ROP) system. Responses were estimated for each component trait (G,F), for feed conversion (FC) and the aggregate genetic response (G + F + FC) in standard deviation units. The net economic value of the aggregate genetic response was calculated as the sum of the values of the genetic responses for the individual traits weighted by their economic values. Variation in the economic and genetic parameters influenced the expected genetic response for the component traits but the aggregate response and its economic value varied little over the range of parameters employed. Indeed, an index constructed from estimates of the actual genetic, phenotypic and economic parameters gave net returns that were only $0.04 per hog greater than an index based on equal economic weights, equal heritabilities and zero correlations. This index, of course, is the simple phenotypic index which leads to the conclusion that results of selection based on a phenotypic index will be fully comparable to those of a highly sophisticated genotypic index. Key words: Selection index sensitivity to parameter variation, genotypic selection index, phenotypic selection index, effectiveness of index selection


2012 ◽  
Vol 57 (No. 4) ◽  
pp. 160-170 ◽  
Author(s):  
L. Vostrý ◽  
J. Přibyl ◽  
P. Šimeček

The estimated genetic parameters were used for selection of important conformation traits and reduction in the number of the described characteristics. For reduction in the number of described traits from the original 36 to 24, the traits were selected according to: measure of genetic similarity (cluster analysis), measure of uncertainty multidimensional quantity, value of the variance of aggregate genotype, value of the variance of selection index and correlation of trait to the first principal component of the genetic matrix. Reduction in the number of the described traits was based on the value of heritability coefficient and genetic correlations matrix. The reliabilities of selection indexes were estimated between 0.41 and 0.53. Among the three multivariate analysis methods evaluated in this study, the variance of selection index had the highest reliabilities of selection indexes. The estimation of selection index variance which omitted traits with low heritability coefficient and high genetic correlation was the most suitable for the traits selection. This procedure would enable the breeders to reduce field costs (e.g. time, labour) required for obtaining the genetic parameter estimates necessary for a specific breeding programme. &nbsp;


Genetics ◽  
1996 ◽  
Vol 143 (3) ◽  
pp. 1409-1416 ◽  
Author(s):  
Kenneth R Koots ◽  
John P Gibson

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.


Sign in / Sign up

Export Citation Format

Share Document