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Genetic parameters of some growth and egg production traits in laying Brown Tsaiya (Anas platyrynchos)
C. Tai, R. Rouvier, J.P. Poivey
To cite this version:
C. Tai, R. Rouvier, J.P. Poivey. Genetic parameters of some growth and egg production traits in
laying Brown Tsaiya (Anas platyrynchos). Genetics Selection Evolution, BioMed Central, 1989, 21
(3), pp.377-384. �hal-00893809�
Original article
Genetic parameters of some growth and egg
production traits in laying Brown Tsaiya
(Anas platyrynchos)
C. Tai R. Rouvier J.P. Poivey 2
1
Taiwan
Livestock Research InstituteDepartment of
AnimalBreeding,
Tainan 71210,Taiwan, Republic of China;
2
lnstitut
National de la RechercheAgronomique,
station d’am6liorationg6n6tique
des animaux, centre de recherches deToulouse,
BP 27, F 31326Castanet-Tolosan,
France(received
4 November1987, accepted
22 December1988)
Summary - Five hundred and
thirty
seven female ducks from the native BrownTsaiya
in
Taiwan,
derived from 156dams,
40 sires, 4 locations(sire origin),
from five hatcheswere used in
study.
Fifteen traits were recorded.Average
values of traits measured werethe
following:
adult(30
weeks ofage) body weight,
1397 f 120 g; age at first egg, 121± 11
days;
egg numbers up to245,
280 and 360days
of age, 107 t13,
139 f 15, 207±
26, respectively;
egg shellstrength,
3.8 t 0.5kg/cm2;
egg shellthickness,
0.37 t 0.02mm; egg
weight
at 30 and 40 weeks of age, 64.2 ! 4.3 g and 67.8 t 4.3 g. Genetic parameters were calculated:heritability
estimate from the sire variance component(hs),
dam variance component
(hd). Body weights
at8, 16, 20, 30,
40 weeks of age showedhigh
additivegenetic
variation(h.
= 0.36 to0.61).
For eggweight
at 30 and 40 weeks of age,h,
= 0.32 andh,
= 0.24. For traits related to eggnumber, h. values
were lowand increased with age,
being 0.02,
0.12 and 0.14respectively
for245,
280 and 360days
of age. But the
respective
heritabilities calculated from dam variance components werehigher, being 0.32,
0.17 and 0.26. The non-additivegenetic
variation of these traits andperhaps
the existence of maternalgenetic
variance indicate thepossibility
ofconducting
within line selection and
cross-breeding
between lines of the same breed.laying duck - Brown Tsaiya - economical trait - genetic parameter
Résumé - Paramètres génétiques de quelques caractères de croissance et de pro- duction d’oeufs chez la cane pondeuse Tsaiya Brune
(Anas
platyrynchos).Cinq
cent trente-septfemelles
de la race locale de caneTsaiya
Brune àTaiwan,
issues de 156mères, 40 pères, l, régions
de Taiwan(origine
despères),
nées dans 5 lotsd’éclosion,
sont utiliséesdans cette
étude,
15 caractères sont étudiés. Lespoids
des adultes(âge :
30semaines)
sontde 1397 ± 120 g. Les valeurs moyennes des caractères mesurés sont les suivantes :
âge
au leT
oeuf,
126 :L 11j.
Pour les nombresd’ceufs pondus
auxâges
de245,
280 et 360jours,
on arespectivement
107 :L 13, 139 t 15, 207 f 26. Pourl’épaisseur
de lacoquille 0,37 t
0,02 mm et pour sasolidité, 3,8 :L
0,5kg/em 2 .
Lespoids
del’œuf, respective-
ment aux
âges
de 30 et!,0
semaines sont64,2
t,!,3
g et67,8
iLl!,3
g. Lesparamètres
génétiques
ont été calculés: estimation des héritabilités àpartir
des composantespère (hs)
et mère
(hd)
de la variance. Lespoids corporels
auxâges
de8, 16,
20, 30 et !,0 semainesprésentent
une variabilitégénétique
additiveforte (hs
= 0,360,61).
Pour lepoids
de1’oeuf
à 30 et
!!0
semainesd’âge, hs
=0,32
et0,24.
Pour les caractères deproduction d’œufs,
lesvaleurs de
h s
sontfaibles
et s’accroissent avecl’âge : hs
= 0,02,0,12, 0,14.
Par contre leshéritabilités calculées à
partir
des composantes mères de la variance sontsignificatives : hd
2=
0,32,
0,17, 0,25. L’existence d’une variabilitégénétique
non additive pour ces caractères conduira àenvisager
une sélection de souches et leur croisement.cane pondeuse - Tsaiya brune - caractère économique - paramètre génétique INTRODUCTION
The estimation of
genetic parameters
foreconomically
related traits has two mainobjectives:
betterunderstanding
of the nature ofgenetic
variation of these traits andoptimization
selection methods for theirimprovement.
Few studies have been concerned with the estimation ofgenetic parameters
inlaying ducks, although
Hutt
(1952) pointed
out that ducks have ahigh potential
for eggproduction.
Duck
production
is animportant
branch in the livestockindustry
ofTaiwan,
withproduces including
muleducks, processed
eggs,exported partially
incubated eggs and frozen meat(Tai, 1985a).
The native breedTsaiya (Anas Platyrynchos
var.domestica)
is themajor
breed oflaying
duck. Before1970, Tsaiya
was also theonly
dam line for atwo-way
cross mule duck(Muscovy
male xTsaiya female).
Forcenturies,
selection in BrownTsaiya
was carried outonly by
duck farmers. The Duck Research Center of Taiwan Livestock Research Institute(TLRI)
started abreeding project
oflaying
ducks in 1984(Tai, 1985b).
The
genetic improvement
oflaying
traits in ducks can includetwo components:
egg
production
or meatproduction
in a dam line. The purpose of thestudy reported
in this paper is to estimate and to discuss the
genetic parameters
of somegrowth
and
laying
traits of BrownTsaiya
in Taiwan.MATERIALS AND METHODS Ducks
Two hundred
Tsaiya
ducksand
60Tsaiya
drakes from four different locations around Taiwan were collected in 1984 and divided into four sireorigins.
Five hatches derived from 156 ducks and 40 drakes were used in thisstudy.
Thegenetic parameter
estimates were obtained from theperformance
data of 537 femaleducklings.
Withineach sire
origin,
10 sires were mated to 2 to 5 dams and each dam had 3 to 5daughters,
with a few cases ofonly
1 or 2daughters.
The total number of dams for eachof the
sireorigins
was36, 41, 39,
40 and thecorresponding
number ofdaughters
was
118 ; 140, 139, 140, respectively.
Hence with damsbeing
nested withinsires,
thegenetic relationship
structure was hierarchical. While sires were nested within sireorigins they were cross-classified
with hatches.Management
tDucklings
were raised in brooders until 4 weeks of age, after whichthey
were movedto floor houses with
swimming pools (3
x9m 2 ).
After 16 weeks of age, ducks from the first and second hatches were raised in individual cages with a dimension of(33
x 33 x 33cm),
while those from theremaining
hatches werekept
in floor pens(20
ducks perpen).
From 4 to 16 weeks of age,ducklings
were fed lowprotein
diets
(12%)
in order todelay
the age at first egg and thus reduce the number of small eggs. From 16 weeks of age ducks were fed apelleted
dietcontaining 19.2%
protein
and 2 765 kcal metabolizable energy perkg.
Water and feed wereprovided
ad libitum
throughout
theexperimental period. Light intensity
was very low in the floor house tokeep
the ducks fromlaying
eggs on theplayground
orswimming pool.
The same
intensity
oflight
wasgiven
to the cage house.Traits measured
Fifteen traits were recorded on each individual. Growth traits were
body weights
at
8, 16, 20,
30 and 40 weeks of age. Thelength
of the fourthprimary
feather wasmeasured at 8 and 16 weeks of age.
Egg
numbers were recorded from the age at first egg up to245, 280,
and 360days
of age.Egg
shell thickness andstrength
weremeasured for at least 3 eggs at 30 weeks of age,
using
FHK(Fujihira
IndustrialCo., Ltd)
shell thickness andstrength
meters. Five eggs, laid over consecutivedays,
were
weighed
at 30 and 40 weeks of agerecording
the averageweight.
Statistical
computations
Statistical
parameters
The
following parameters
were calculated for each trait: mean,variance,
standarddeviation,
coefficient of variation. The data were tested fornormality.
Estimates of
genetic parameters
for female duck traitsThe
following
model was usedwhere
Y ijkl m
observation p meanhi (i
= 1 to5)
hatcheffect,
fixedf
j
(j
= 1 to4)
sireorigin effect,
fixed s!!; sire withinorigin effect,
random(0, o- 2 ) d
jkl
dam withinsire,
random(0, U2 )
e!!A.!,r,.
residual,
random(0, oe 2 ).
Variance
components
due to sires and dams within sires were estimatedby
Restricted Maximum Likelihood Estimation
(REML) using
the SASprocedure
forunivariate
analysis (SAS
InstituteInc., 1985).
Theasymptotic
covariance matrix of estimates was obtained.The heritabilities were calculated from
paternal
half sib(hs),
dam half sib(hd)
and from maternal full sib.
(hs+!)
correlations(Falconer, 1960).
The standard errors of these
heritability
estimates were calculatedaccording
toKendall & Stuart
(1969).
The variance of the ratio of random variableX l
and!2
is
given by
for
example,
RESULTS
Table I
gives
the statisticalparameters
for the 15 traits measured. Featherlength stopped growing
at 16 weeks of age, butbody weights
increased after the ageat first egg
(126 days),
until 30 weeks of age. Means and standard deviations for egg number up to245,
280 and 360days
of age were 107 f13,
139 !15,
207 26.
Corresponding
values were 3.8 t 0.5kg/cm 2
for egg shellstrength
and0.37 0.02 mm for egg shell thickness at 30 weeks of age. For egg
weight
at 30and 40 weeks of age values were 64.2 t 4.3 g and 67.8 ! 4.3 g,
respectively.
Asmeasured
by
coefficient ofvariation,
featherlength
washighly
variable at 8 but not16 weeks of age.
Variability
of 8 weeksbody wieght
washigher
than that forbody weights
at the older ages, and variation of egg number an egg shellstrength
wassimilar.
Variation of age at first egg was
moderately
low as was that of egg shell thickness and eggweight. According
to the calculated values of the skewness and kurtosis coefficients(data
notshown),
most of the traits werenormally
distributed.Only
feather
length
at 16 weeks showed ahighly positive
kurtosis and the egg number at 360days
wasskewly
distributed.Heritability
estimates with standard errors are summarized in Table II. Values forbody weights
weregenerally greater
than those for egg numbers.Comparisons
between
paternal
and maternal half sib estimates showed the former to begenerally larger
forbody weight
and smaller for egg numbers than the latter.DISCUSSION
Chinese farmers have raised
Tsaiya
ducks for centuries. These ducks exhibited considerable variation inplumage
colorranging
from solid black to pure white. Dueto the farmers’
preference,
ducks withlight
brownplumage
were selected andkept
as the
major variety
ofTsaiya.
Thus &dquo;BrownTsaiya&dquo;
became a common name for the localTsaiya
duck(Tai, 1985b).
Thebody weight
of BrownTsaiya
at 30 weeksof age
( 1 397 g)
which could be taken as an adultbody weight,
was similar to thoseof White
Tsaiya (Huang
etal., 1983).
Thisweight, however,
was less than that of nativelaying
duck in Indonesia(Hetzel, 1984). Tsaiya
appears to be thelightest
in
body weight
and thehighest
in eggproduction
of small ducks under intensivefeeding. Although
the recordsanalysed
werestopped
at 360days
of age in order tostudy part
records and to shorten thegeneration interval,
these ducks canlay
onaverage 240 and 300 eggs per
caged
bird up to 58 and 69 weeks of agerespectively (Rouvier unpublished data).
These values are similar to thosereported
forAlabio, Bali, Tegal
and KhakiCampbell
ducks under intensivemanagement (Hetzel, 1985).
Compared
to the Pekin andMuscovy breeds, Tsaiya
ducks mature at a young age(average
126days)
and havehigh
eggproduction
to 360days
of age(average
207eggs).
It should be remembered that the Pekin andMuscovy
are meatbreeds,
while the BrownTsaiya
in an egglaying
breed.According
to the coefficients of variation there washomogeneity
of the traitsexcept
forbody weight
and featherlength
at 8 weeks of age, which were measuredduring
thegrowing period.
The veryhigh
coefficient of kurtosis value for featherlength
at 16 weeks indicates that most of the values of this trait are the same.The
negative
skewness andpositive
kurtosis values for egg number indicated thehigh
average egglaying
rate(88%
up to 360days
ofage)
and the limitation ofthe
period
of observation on eggproduction.
The duck eggs aremainly
consumedin
processed
form such as salted eggs andthousand-years
eggs andpayment
isby
number in
Taiwan,
thus eggs of medium size(66-67 g)
are most welcomedby
eggdealers,
and farmers have selected for this trait for many years. Thismight explain
the low coefficient of variation in egg
weight.
Estimates of heritabilities for
body weight
were moderate tohigh.
Values ofh’
ranged
from 0.36 t 0.15 to 0.61 ! 0.19 and ofha ranged
from 0.30 ! 0.16 to 0.55! 0.18. This indicated the existence of considerable additive
genetic
variation forthese traits and the absence of maternal effects. Values of
hs
wereslightly higher
than
h!,
which could be due to some additivegenetic
variation for sex linked genes.Body weight
at 30 weeks of age which could beregarded
as adultbody weight
hada
high heritability (hs +d
= 0.44 t0.11).
These results were not consistent with those of Sochocka &Wezyk (1971)
who foundhigher h! values
thanh2 values
forgrowth
traits in Pekin females. On thewhole,
additivegenetic
variation for eggweights
waslow, except
forweight
at 30 weeks of age withheritability
estimates ofh2
= 0.32 ! 0.15 andh!+d
= 0.27t 0.10. Thisimplies
thatbody weight
and eggweight
traits could beimproved easily by predicting breeding
values andselecting
on a within line basis. It is
interesting
to note that there was no noticeablegenetic
variation for egg shell
strength
and featherlength
at 16 weeks of age. For featherlength
at 8 weeks of age, that isduring
feathergrowth, h s +d
was 0.31 f 0.10.For
laying
traits(egg number),
dam variancecomponents (Q!)
werehigher
thansire variance
components (a 2).
Whilehs estimates
werelow, h!+d
values weresignificant, being respectively
for egg numbers up to245,
280 and 360days
ofage,
h 2 +d
= 0.17 !0.08;
0.15 ! 0.08 and 0.20 ! 0.09. Twoexplanations
could begiven.
If we suppose no maternalgenetic
effects and no effects of sex linked genes,ad - 0&dquo;; can
be written(Falconer, 1960)
asHere
VpXA! VAXAXA! VAXD! VDXD!
areepistatic genetic
variances due to thegene interactions among additive x
additive,
additive x additive xadditive,
additive xdominance,
and dominance x dominanceeffects,
V
D
is the dominancegenetic variance,
andV
ac
is the variance of common environment. This could be reduced to a minimumaccording
to theexperimental design.
But a small maternal effect linked to the eggweight
could exist.The presence of non-additive
genetic
variation for egglaying
traits observed inthis
study suggests
that these traits aresignificantly
associated with fitness for this breed. This could be also due to thelong
term mass selection of this breedby
Chinese farmers.
According
to thisinterpretation,
non-additivegenetic
variation(dominance
andepistasis)
exists. Thereforecrossbreeding
of lines should beapplied
to
improve
thelaying ability
ofTsaiya.
If maternal
genetic
effects doexist,
in the case of additive and dominancegenetic
variation,
forexample,
where
V Am
is additivegenetic
variance for maternaleffects, V D &dquo;,
is dominancegenetic variance, CovA o A&dquo;,
is covariance between direct and maternal additivegenetic
effects.Although CovA o A&dquo;,
could benegative,
ifV Am
exists that could make17! higher
than1 7;.
In that case, within line selection couldproduce
furthergenetic improvement
for thelaying
traits.CONCLUSION
Considerable additive gene action existed for
growth
rate up tomaturity
and eggweight
in thelaying
duck BrownTsaiya.
Thus these traitsmight
beeasily
controlledby
selection.Body weight
at sexualmaturity
and in adults could be indicatedby
the
body weight
at 30 weeks of age whereheritability
islarger
than at 20 weeksof age.
Egg weight
could be measured at 30 weeks of ageaccording
to itsgenetic
variation at that age. There were considerable non-additive
genetic
variations and maternalgenetic
variation for eggproduction
traits.Additivity
was not evidentfor egg number up to 245
days
of age and appearsonly
after 280days
of age, as in the results from Tai(1985b)
with WhiteTsaiya.
The lack of additivegenetic
variation may be due to the
history
of this breed which was selected forincreasing
egg
production
for centuriesby
Chinese farmers. The rate of eggproduction
washigh
whencompared
to other duck breeds. Furtherimprovements
could begot by
within line selection
and/or crossbreeding
between lines of the BrownTsaiya
breed.It would be useful to
study
egg number up to 280days
or 360days
oflaying.
ACKNOWLEDGEMENT
This
study
is madeaccording
to acooperative
researchproject
between theDepartment
of AnimalBreeding,
Taiwan Livestock ResearchInstitute,
and the Station d’Am6liorationG6n6tique
desAnimaux,
INRA.Our thanks go to Mr S.R. Lee and Ms M.F. Tsai of the Duck Research
Center,
Taiwan Livestock Research Institute for their very efficient
management
and record-keeping
for the ducks in thisstudy.
We are indebted to Professor H.H.Huang
ofthe Council of
Agriculture,
ExecutiveYuen, R.O.C,
for hisarrangement
for thiscooperative
researchproject.
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(1960)
An introduction toquantitative genetics.
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London
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KhakiCampbell
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(1985)
Duckbreeding strategies.
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(1952)
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S.(1971)
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