Upload
mga
View
214
Download
0
Embed Size (px)
Citation preview
Wear Science 61i982) 285-.-"94
G R O W T H A N D D E V E L O P M E N T O F W A T E R B U F F A L O A N D F R I E S I A N C R O S S B R E D C A T T L E , W I T H S P E C I A L R E F E R E N C E T O T H E ' E N T I R E ' A N D ' B O N E L E S S ' C U T S
O. Y. AIIDAI..LAlt, KARIMA A. SHAHIN ,Ik M. G. A. LXTtF
Department of Animal Production, Faculty of Agriculture, Ain Shams University. Shoubra El-Kheima, Cairo, Egypt
(Received: 25 February. 1981)
SUMMARY
Tweh'e buffaloes, nine Friesian x Baladi and nine Friesian x ( Friesian x Baladi) bulls were slaughtered over the live weight ranges 161-560kg for buffaloes and 176-448 k g for cattle. Right sides of all carcasses were jointed and dissected and the increase in the weight of'entire' and'boneless" cuts and cut groups (i.e. pistol; BLRC) relative to the "entire" and 'boneless' side weights, respectively, were examined using covariance analyses.
Increasing distoproximal and dorsoventral growth gradients were found in both species. Most noticeably, the sticking was early developing in buffaloes and late developing in cattle, whereas the shortloin dereloped approximately at an arerage rate in buffaloes and at a lower rate in cattle. Statistically significant but relatively slight differences were recorded between buffaloes and cattle in the adjusted means of the 'entire' and "boneless' hind shank, sirloin (favouring buffaloes) and brisket (favouring cattle). Buffaloes were superior to cattle in weight o f pistol. At an equal side weight o f 73 kg buffaloes had significantly higher weight o f pistol (maximum difference = 1"4 kg). A t a ! 15 kg side weight, the maximum difference in 'entire' and "boneless" pistol reached 3"58 and 5"04 kg, respectively.
INTRODUCTION
A detailed study of the composition of the carcass in terms of its component tissues in buffaloes and Friesian crossbred bulls has been described previously (Abdallah et al., 198 I). At 73 kg dissected side weight, buffaloes, compared with half Friesian and three-quarter Friesian crosses, had less muscle (47.88; 50.70; 50.36 kg, respectively), more bone (12-45; I1.11; I 1-57 kg, respectively) and more fat (7.35; 5.63; 5-94kg, respectively). The assessment of the composition of the carcass in terms of its component marketable cuts in this series of animals is of interest from several points of view.
285 Meat Science 0309-1740/82/0006-0285/$02.75 ~ Applied Science Publishers Ltd, England, 1982 Printed in Great Britain
286 O . Y . ABDALLAH, KARIMA A. SHAHIN, M. G. A. LATIF
A knowledge of the percentage yield of various carcass cuts ensures more efficient pricing of such carcasses (Caroil, 1972). A more or less accurate knowledge with regard to the pattern of growth of carcass cuts is of interest in deciding, from the point of view of desirable conformation, the optimum marketable carcass weight (Harrington & Pomeroy, 1959). Experiments designed to determine the yield of wholesale cuts of slaughter animals varying greatly in conformation have been conducted to specify to what extent visual assessment may be a good indicator of yields of cuts in the carcass (Cole et al., 1964; McAllister et al., 1976). The present study was undertaken to look at data from carcasses of buffaloes and Friesian crossbred cattle from these points of view.
MATERIALS AND METHODS
In an experiment to compare growth patterns of body components and carcass tissues of water buffalo and Friesian crossbred cattle, twelve buffalo, nine half Friesian (3 Friesian x 2 Baladi, Egyptian native cattle) and nine three-quarter Friesian (3 Friesian x ~ half Friesian) bulls were randomly chosen, individually penned and fed from weaning to slaughter on cubed concentrates and green roughage and wheat straw. Details of the feeding regime adopted, management and slaughter procedures were given in a previous paper (Abdallah et al., 1981). The animals were slaughtered over the body ranges 161-560kg, 176-440kg and 186-448 kg for buffaloes, half Friesians and three-quarter Friesians, respectively.
After slaughter, each dressed carcass was chilled at 2 °C for approximately 24 h, after which the right side of each carcass was taken and jointed according to the Chicago style of cutting described by Levie (1963). The kidney and kidney and channel fat were removed from the sides before jointing. The cuts in the Chicago style (Fig. 1) are (i) in the hindquarter: hind shank, buttock, sirloin, shortloin. tenderloin and flank; (ii) in the forequarter: 7 x 10 rib, plate, brisket, foreshank, chuck-plus-shoulder and sticking. Two groups of cuts were made to represent the high price cuts in the carcass. (i) The combination of the hind shank, buttock, loin and 7 x 10 rib represents the Egyptian pistol and (ii) thecombination ofthe buttock, loin, 7 x 10 rib and chuck-plus-shoulder is referred to as BLRC.
All cuts were dissected into muscle, fat, bone and 'other tissues'. For each cut, the total weight of muscle, bone, fat and 'other tissues' was referred to as the 'entire' cut and the total weight of muscle, fat and 'other tissues' was referred to as the 'boneless" cut. Weights of the "entire" cuts were analysed each relative to the 'entire' side weight (total weight of 'entire' cuts) and weights of the 'boneless' cuts relative to 'boneless" side weight (total weight of "boneless' cuts). One-way analysis of cowmance was applied using the following model.
log Y0 = Ao + G, + blogX 0 + (Gb) , logX , j + e o
GROWTH OF BUFFALO AND CATTLE CARCASS CUTS 287
Wl,nk
Wo~er.t~a~Jc
lb
.~Loulder
Fig. I. Side cuts according to the Chicago style.
where: Y,~ = weight in kilograms of the 'entire" or "boneless" cut o f the ith animal; A o = intercept: G, = fixed effect o f the ith genotype group; X, = total weight in kilograms of the "entire" side or "boneless" side o f the ith animal; b = regression coefficient for Y on X: (Gb), = adjustment to slope b due to the ith genotype group and e,, = e r r o r . assumed to be N I D (0, a~).
In cases where the individual regressions were not different, the c o m m o n regressions were used to adjust the genotype g roup means to the geometric mean of the "entire" side or the 'boneless" side. Duncan 's multiple range test, as modified by Kramer (1956). was used to compare each group mean with every other group mean whenever a significant Fva lue was obtained for the difference between adjusted means. According to the cowtriance concept, compar ison of adjusted means is not legitimate if the individual regressions are significantly different. Therefore, adjusted means in such cases were calculated merely for completeness but have not been statistically compared.
RESULTS AND DISCUSSION
Unadjusted means and standard deviations for weights of fasted body, carcass, "entire' and "boneless' sides and "entire' individual cuts and cut groups are given in Table I. Overall means and standard deviations are also given in the same Table. It
288 o . Y . ABDALLAH, KARIMA A. SHAHIN, M. G. A. LATIF
TABLE I UNADJUSTED MEANS IN KILOGRAMS ( +-STANDARD DEVIATION) FOR WEIGHTS OF FASTED BODY (FBW)o COLD
CARCASS (CCW), 'ENTIRE' SIDE, "BONELESS" SIDE AND "ENTIRE" INDIVIDUAL CUTS AND CUT GROUPS
Buffaloes Half Friesians Three-quarter Friesians Overall
FBW 348 + 145-6 299 + 92.6 313 + 97-8 320 + 116.0 CCW 180-7 + 68.91 157. I + 60.62 157.3 _+ 56.33 166.6 + 96.92 'Entire" side 85.1 _.+ 38-43 74.9 __. 27.02 76.3 _+ 26.94 79.7 _+ 31-33 "Boneless" side 71.4 + 33.44 64.3 + 23.90 64.8 __. 23.82 67.3 + 27-43 Hind shank 5-62 + 1-912 4-70 + 1.343 4.81 + 1.170 5-10 + 1-561 Buttock 19.95 + 8'653 17-63 __. 6-326 17.23 + 5.385 18-44 + 7.004 Sirloin 6.81 _.+ 3.164 5-45 + 1.857 5-51 + 1.932 6-01 + 2.493 Tenderloin i.03 + 0.472 1-01 __. 0.436 1-08 + 0.359 1-04 + 0.413 Shortloin 5.04 + 2.504 4.38 + 1.391 4-29 + 1.333 4.62 + 1.874 Flank 2.57 + 1.514 2.47 __. 1-246 2.65 + i.163 2-56 _.+ 1.291 7 x 10 rib 6.95 + 2-993 6-25 + 2.070 6.43 + 2. i 13 6.58 + 2.434 Plate 5-17 + 3-076 3-85 + 1.654 4-09 __. 2.033 4.45 + 2.424 Brisket 3.70 + 2.093 3.50 __. 1.473 3.54 + 1.452 3-59 + 1.693 Fore shank 3.28 + I. 184 2-87 + 0.812 2-95 + 0-800 3.05 + 0.692 Chuck+shoulder 17.98+_8.352 15.87+-5.691 16.31+6.232 16.85_.+6.851 Sticking 6.01 + 2.648 6.75 + 2-802 6.56 + 2.821 6-39 + 2.670 Pistol 45.41 +- 19.563 39-36+ 13-320 39.40+- 12.151 41.79 + 15.622 BLRC 57.77 + 25-992 50.55 + 17.672 51.23 +- 17.582 53.64 +- 20.964 Hindquarter 41.03 +- 17.984 35.61 __. 12.493 35.61 _+ 11.193 37.78 +- 14.405 Forequarter 44.06 +- 20.421 39.84 __. 14.524 40.71 _+ 15.372 41.80 +- 16.893
appeared that the buttock was the greatest con t r ibu to r to the side weight (23 o~) followed by the chuck-plus-shoulder (21.2 ~/o). The pistol accounted for 52-4 ~ and the BLRC for 67-3 ~ of the side weight. The h indquar te r : fo requar te r ratio was
1 : 1-1 in the 'ent ire ' sides.
Table 2 gives the analyses o fcovar iance for the weight of each cut taken as 'entire" and "boneless' with, respectively, the 'entire" side weight and the 'boneless ' side weight as the independent variate. Table 3 gives corresponding analyses of covariance for the hind- and forequarters and expensive cuts. The buffaloes, half
Friesians and three-quarter Friesians did not differ significantly in the relative rate of increase (b value) of the weight of the 'entire ' and 'boneless ' hind shank, sirloin, 7 x 10 rib, brisket, foreshank and chuck-plus-shoulder . There were no differences
(P > 0.05) between groups in the relative growth of the 'ent i re ' tenderloin, flank (cuts without bone) and buttock or in the relative growth of the 'boneless ' plate. However, there were significant differences (P < 0-05) between groups in the relative rate of increase of the 'entire ' and 'boneless ' shor t lo in and sticking, the 'entire' plate and the 'boneless ' but tock (Table 2). The rates of increase in the 'boneless" pistol and BLRC, those of the combined forequarter 'ent i re ' cuts and of the combined h indquar ter 'entire ' and 'boneless ' cuts were significantly different between genotypes (Table 3).
A striking result in both the 'entire ' and "boneless' analyses was the inconsistency of the individual genotype group slopes both for 'entire ' and the 'boneless" short loin and sticking. The growth coefficient of the short loin was significantly less than 1 (b = 0-81-0.85) in the Friesian crossbred groups and did not differ significantly
TA
BL
E 2
F_
~TIM
AT
ES
OF
P
AR
AM
ET
ER
S O
F A
LI.
OM
ET
RIC
RE
GR
ES
SIO
N A
ND
AD
JUS
TE
D M
EA
NS
FO
R
WE
IGH
T O
F '
EN
TIR
E'
CU
TS
AN
D "
B(I
NE
I.F
-~'
cu
rs
WIT
II
CO
RR
ES
PO
ND
ING
W|!
IGII
I O
F
rOT
AL
C
UT
S A
S T
HE
IN
DE
PE
ND
EN
T V
AR
IAT
E (
X)
Dep
cade
nt
Bu~'
al,~
es
Hal
l Fr
lesl
ans
Thre
e-6l
'~ar
ler
.l~'rl
esgl
n$
Com
mon
R
estd
ual
.4d/
uste
d m
¢¢l//
Is.~
Sq
cmhc
am'e
la
rglt
e .
..
..
..
..
..
..
..
..
('
|/
Ult
ti/U
R Y
fO
fllqF
ted
I0
u'u
II/
dl~e
rem
clo
t 11
o R Y
) A
o
h"
SE
A
o
b S
E
A o
b
~,'L
" A
o
b S
'¢"
(".)
o
f te
om
etr
lc
mea
n o
/X
- -
-
..
..
..
..
..
..
..
B
etw
ttll
B
etw
ttP
l B
" ]
f ~F
s/
oil
s ad
lust
ed
rise*
ms
Ifin
dsh
an
k E
ntir
e -0
55
8
0-69
8 0
03
-0
74
6
07
58
0
02
-0
61
4
0691
0
05
B
onel
ess
-09
25
0
7"1
9
00
7
-09
99
0
77
7
00
6
-08
79
0
7i7
0
08
B
utto
ck
Ent
src
- 0
577
0:97
3 0
02
-
0-64
5 i ~
7
00
3
- 0
471
0-¢~
10-8
- 0'
03
Bon
eles
s -0
58
6
09
88
0-
02
-06
34
10
08
00
3
-04
51
0
90
0
0'03
S
irlo
in
Ent
ire
- 1.
155
1,02
9 0-
04
- 1.
069
0.96
2 0.
04
- 1.
157
1.00
8 0.
03
Bon
eles
s -
I 05
5 0
983
00
4
- 10
26
0-94
1 0,
05
- 1,
142
1.00
6 0,
03
Ten
derl
oin
Ent
ire
- 1.
931
1.00
7 0-
05
- 2.
094
I.I
14
0.08
-
1-60
a 0-
872
0.10
S
hort
ioin
E
ntsr
e -
I 36
1 10
66
OO
S -O
95
2
08
~0
0
'06
-0
-96
2
O'8
.$0
00
3
Bon
¢lc~
s -I
35
3 1
061
00
5
• 0
92
1
()~
23
00
7
-09
08
0-
80~/
" 0
03
Fl
ank
Entire
- 1972
1-226
0 09
- 2269
i 40
8 0
I0
- 1852
1204
0 08
7x
1
0r,
b
lint,
re
-09
99
0-
959
00
3
-09
09
U
SO
9"
00
4
-09
96
0
95
8
0'03
H
~mel
ess
-10
70
0
97
6
00
3
-09
55
0
91
9
00
4
-09
67
0
93
0
0,05
P
late
E
ntir
e -
I 97
2 I
380
O0-
4 -
1531
1.
124
00
7
- I
721
1232
0'
13
Hon
cles
s -1
73
5
1278
0
04
-1
41
4
1083
0
07
-1
50
6
1"14
3 0'
13
Bris
ket
[!nt
*re
- I
962
I 30
~-
0 08
-
I 86
1 12
76
0 10
-
1 69
0 1'
186
011
Bon
ek~s
s -
1 88
4 1"
287
00
7
- 1"
793
1"2~
" 0
08
-
16
10
1"
163
0"11
F
~e
sha
nk
Ent
ire
-09
60
0-
769
0-03
-O
92
1
0"73
6 0.
06
- 1.
002
07
84
0"
05
Bon
eles
s -1
19
4
08
13
0
04
-0
90
7
06
43
0'
14
-I.2
30
0'
840
00
5
Chuck +s
houl
der
Enti
re
-0653
I ()2-9
001
-0653
()-9
-87"
002
-0"810
I'073 0"05
Bon
eles
s -0
71
2
1.01
9 0
02
-0
65
7
09
85
0
02
-0
76
1
IO42
0
07
S
licki
ng
E
ntir
e -0
87
6
08
87
0
05
-1
20
9 I
108
00
4
- 13
70
1.18
6 0
05
Boneless
-0 811
0 ~
0
00
5
- 1-193
I -I [6"
0'04
- 1"
298
i:l-
6f
0"05
t G
row
th c
o~l~
:*en
ts u
ndef
linoc
l w
ere
$ism
fica
mly
dzl
Tere
nt
fro
m
1 at
P <
00
5
- 0
64
2
0 71
1 0-
02
46
7
08"
6 36
* 6
49*
NS
"*
* -
0'9
50
0
766
00
4
10.1
4
8U"
40
2*
4
'I 3
* N
S
***
-0'5
76
0
96
9
00
1
31
23
73
2
34
3
22
88
N
S
NS
-0
-57
5
0 96
7 0"
01
3'7
24 8
2 24
"08
23'5
3 *
-1"1
43
1'
009
0"02
5
'0
7-98
" 7-
29 j
7'23
* N
S
***
- 1-
075
0.97
7 0
02
5
5 8
22
j 7
43*
7-40
* N
S
***
-1-8
96
1
-00
7
00
4
103
I 21
" I
31 "~
1
43
' N
S
**
- 1.
182
0"97
1 0
04
8"
1 5
83
5.92
5
78
* -I
161
0954
00
4
96
57
4
582
57
3
-2007
1"226
006
12 8
2-81"
3.10
"*
339*
NS
**
-0974
0944
0-02
45
8-30
838
8.~0
NS
NS
-I018
0953
002
54
77
5
7-99
810
NS
NS
- 1.
820
1-2
88
0-
05
10"4
5
48
5'07
5-
17
* -1
61
6
1.204
004
10
5
581
545
563
NS
NS
-I-8
72
I
273
00
6
II 7
40
1 °
4 53
* 4
56
* N
S
* -
1.79
6 1'
257
0"05
11
'4
4-27
" 4"
806
4'82
~ N
S
* -0
'96
2
0"76
4 0"
02
3"4
4"09
3'
88
3 95
N
S
NS
-
1.31
0 0'
777
00
5
11.7
3"
05
2'87
2,
98
NS
N
S
-07
27
10
27
0-02
3
6
21'0
5 21
"16
21-2
6 N
S
NS
-0
-71
0
1"0
15
0'
02
4 7
20 66
20.8
2 21
O0
NS
NS
- I '
036
0.999
0 04
8 4
8'33
881
949
* -0
'985
0'981
004
9 5
8-66
I0 33
9-92
* ..........................
Ad
just
me
nt t
o 8c
orn¢
t r;
c m
ean
of'
en
tire
' si
de w
l .
72.9
6 k
s an
d'bo
mel
c~s'
sid
e w
t =
61 2
2 kg
alo
ng
the
slop
e o
f co
mm
on
rcg
ress
aon
line
B =
buf
falo
: ~F
-
ha
lf F
rics
lan
; ,JF
~ t
hree
-qua
rter
Frl
¢~,a
n N
un,'~
fals
in th
e f.
lm¢
row
bca
fln 8
dll|
¢ren
t su
pcr~
crlp
~ d
dFcr
sis
nlh
can
lly a
t P
< 0
05
?t
NS
no
ss
gniti
cant
(P
>0
05
) *
P<
00
5;
**P
<0
OO
l;
***P
<0
OO
I
TA
BL
E
3 I.
S ! I
MA
I I
S O
1'
PA
RA
MI
I liR
S O
F
AI.
I.O
MI:
1 R
IC
I(I:
(,;R
F.S.
~;IO
N A
ND
AI)
JU.~
I I!
i)
MI:
AN
S F
OR
W
EI(
;III
O
F "
I:.N
'IIR
E'
AN
D "
IH)N
I:I.
F.S.
~'
('O
MI|
INI~
I)
I IIG
II-P
RI(
'Id
),
IIIN
IH~
UA
H I
I'R
A
NI)
Dep
ende
nt
la.a
tc
11,,~
¢ Y]
FO
RE
QU
AR
TE
R C
UIS
W
ITH
('
OR
RE
SP
ON
I)IN
G
WE
I(3
H]
OF
1
OR
AL
CU
TS
AS
TH
E I
ND
EP
EN
DE
NT
VA
RIA
TE
(X
)
Buffa
loe~
H
alf
Fr~
esi~
ms
Thre
e-qu
arte
t F
.esi
ans
Co
mm
on
Re
sadu
al
Adl
uUed
mea
lts,~
.
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
('
V
am
iloK
Y ¢
~m
l~tt
cd t
. o,
,
A o
b
' S
E
A o
b
' S
'£
A u
b
SE
A
u
b S
E
(')
uJ x
eo
.~u
, m
ean
.J X
a 1~
,'+
F~,io
l ls
m.c
-0
-17
8
09
52
00
1 -U
]73
0'
942
OO
I -0
-08
9
08
96
0
02
-0
-16
2
09
39
0
01
2
1
5426
" 52
66'
52
38'
B
onel
c~
-0.2
06
0.
964
001
-0
190
()94
7 0
02
-0
09
9
()8~
/4
00
2
-0
185
09
46
00
1 2.
4 53
.90
51
90
51
63
BL
RC
E
nhfe
-0
17
2 I
002
00
1
-0
127
09
75
00
1 -0
15
0 0.
988
00
2
-0.1
57
0~99
3 -
0O
I 1
6
6811
6
74
9
67
48
B
onel
e~,s
-O
-163
I-0
(30
O01
-0
12
1 09
72"
001
-00
90
0-
952
00
2
-01
41
0
98
4
00
1
19
6
90
8
67-6
8 6
70
4
}{m
dqua
rlcr
E
n|il'¢
-0
-25
3
09
68
00
1 -0
28
6
09
79
0
01
-0
-15
5
09
07
0.
02
-0.2
45
0
95
9
00
1
2-2
47
29
4
74
6
47
29
/~
on<l
e~s
-02
63
0
97
6
OO
l -0
2~
9 O
9)1
1
00
2
-0
154
09
05
0.
02
-0.0
52
0.
963
00
! 2
5 49
53
47
7i
47-5
8 F
orc
qu
a.e
r E
n.re
-0
3.1
7
IO31
00
1 -0
30
8
I 01
6 0
02
-0
42
6
I 08
1 0
02
-0
35
0
I 03
7 00
1 2-
1 51
-57
5298
53
0"/
Bo
ncl
¢~
-0
33
9 -1
02
3
0O
I -0
32
1 I
022
00
I -0
396
I
063
0 03
-0
.34
3
1-0
31
0
01
2
5
~O 7
4"
52 4
9*
52
.28
' .
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
..
.
Sixn
i/~ur
u¢
.J #
t/Jc
re~
¢Jt
t
~lw
¢¢
n
J~l w
ren
Jh,p
¢~
adlu
Jtcd
nw
unJ
NS
""
NY
J N
S
NS
**
t, :
. tt
A.
cxpl
d*nc
d in
T~b
l~ 2
GROWTH OF BUFFALO AND CATTLE CARCASS CUTS 291
from 1 in buffaloes (b = 1.01-1.07) whereas the coefficient for the sticking was significantly less than l in buffaloes (b = 0.86-0-89)and significantly greater than 1 in Friesian crosses (b = 1-I !-1.19). Literature data on the growth of shortloin and sticking cuts are non-existent. Berg et al. (I 978) found the growth coefficient of the muscles of the loin in cattle bulls to be significantly less than 1 and that of the neck significantly greater than 1. The results of Ragab et al. (1966) on buffalo bulls showed that, as carcass weight increased, the proportion of the loin increased and that of the neck decreased. These findings are in support of the present results.
The results of the present study agree with reported results on cattle bulls and steers (Joubert. 1959) and on buffalo bulls and steers (Ragab et al . , 1966) in that the hind shank is the earliest developing cut in the carcass and the fore limb cuts (fore shank and shoulder; the shoulder common b + SE was 1.021 + 0.02 for 'entire" and 1-011 +0.03 for 'boneless' cuts) have higher relative growth rates than the corresponding hind limb cuts. This probably reflects the fact that the hind limb does not have to support so much weight as the fore limb, with the increase of the animal weight anterior-wise.
The present results on bulls were in agreement with published results on heifers and steers (Harrington & Pomeroy, 1959; Luitingh, 1962) in that the ventral cuts in the trunk are late-developing and had higher relative growth rates than the corresponding dorsal cuts, indicating that buffalo and cattle on the one hand, and bulls, heifers and steers, on the other, are alike in that respect. This can be explained on the basis of the weight-supporting r61e of the ventral region of the thorax in quadrupeds (Dukes, 1955) and the increase in the rigidity of the ribs and the development of the abdominal wall as the thoracic and abdominal organs increase in weight (Fowler, 1968).
The last stages of development were found to occur in the loin cut in lambs (Hammond, 1932) and between the neck and chuck (the hump cut) (Joubert, 1959) and in the chuck cut (Luitingh, 1962) in cattle. In the present study the relative growth of the loin (sirloin, tenderloin, shortloin) and of the chuck-plus-shoulder was similar to the total side weight. This difference may be due to the different jointing techniques employed in the studies. Butterfield (1963), Seebeck & Tulloh (1968) and Kempster et al. (I 976) suggested that the late maturity of the loin joint reported by Hammond (1932) was a reflection of the late developing abdominal muscles included in the loin joint. These authors showed that the muscles of the anatomical loin region develop at the same rate as the total side muscle.
The present results showed remarkable similarity in the growth patterns of the bone-in and the bone-out forms of the same cut compared for the same genotype group. This suggests that the growth of a cut follows the same law as governs the development of the non-bone tissues.
After adjustment using the common regression equations given in Tables 2 and 3, the "entire" buttock, the 'boneless' plate and the 'entire" and "boneless" 7 x 10 rib, fore shank and chuck-plus-shoulder cuts occupied similar proportions in the buffalo and
EO
TA
BL
E
4 E
ST
IMA
IED
ME
AN
S A
ND
P
ER
CE
NTA
GE
S
OF
"EN
TIR
E'
AN
D '
BO
NE
LES
S'
CO
MB
INE
D H
IGH
-PR
ICE
D,
HIN
DQ
UA
RT
ER
A
ND
FO
RE
QU
AR
TER
C
UT
S A
T F
IVE
DIF
FE
RE
NT
.O
W
EIG
HT
S O
F C
OR
RE
SP
ON
DIN
G T
OT
AL
CU
TS
"<
(Yet
ght
Cut
W
eJX
bt a
nd p
erce
ntag
e oJ
the
cut
gro
up i
n th
e er
a(re
~id
es o
f.
Wei
gh!
~ pe
rcen
tage
of
the
~t
grou
p m
the
boc
lele
ss s
oles
of
W
oJ t
otal
gr
oup
....
..
cuts
B
uffa
loes
H
alf
Frl
esm
nJ
Thr
ee.~
artt
r FF
tesJ
ans
Buf
falo
ej
Hal
( F
riej
~uu
Thre
e.qu
arte
~ Fr
l¢~i
ans
)"
l'(-g}
/~g
¢'~
k 8
~g
~,
kg
?~
kg
%
k&
~/.
["
>
35
I~,to
l 19
59
(560
I i9
15
(.~4
7)
19 7
0 (~
,'3)
1918
(~
4-8)
18
.70
(534
) 19
'12
(546
) B
LR
C
23 7
0 (6
77}
23 9
4 (6
8 4)
23
73
(67.
8)
24-0
9 (6
88)
2398
(6
85)
24 0
2 (5
8 6)
H
indq
uart
er
1742
(4
98)
1681
(4
80)
1764
(5
0.4)
17
"53
(50"
13
1684
(4
8.13
17
-51
(500
) ~b
, Fo
requ
arte
r 17
.58
(50'
2)
1823
(5
2 i)
17
-43
(498
3 17
.47
(49-
9)
18.0
9 (5
173
17.6
1 (5
0 3)
55
P~
slol
30
12
(54
8)
29 3
3 (5
3 3(
29
54
(557
) 29
66
(53
9)
2868
(5
2-13
28
"63
(52.
1)
~'
BLR
C
37 2
7 (6
7 8I
37
20
(676
3 37
0~
(67,
4)
37.8
7 (6
88J
37.2
2 (6
7 7)
36
.94
(67.
2)
~"
H*n
dqua
rlet
26
98
(491
) 26
17
(47
5)
26 5
8 (4
&3I
27
-22
(495
) 26
"23
(477
) 26
35
(47"
9)
~,
I'ore
quaT
lcr
28 O
( (5
0 9)
28
86
(52
53
28 4
2 (5
1.73
27
76
(50.
5)
28"7
1 (5
2'2)
28
48
(51
'8)
75
P~Io
( 40
46
153"
93
39 2
8 15
2 4)
39
'00
(52
0)
4000
(5
33)
38'4
7 (5
1 '3
) 37
"78
(504
) B
LR
C
5085
(6
78)
5035
(6
71l
5038
(6
72)
51"6
4 (6
5"9)
50
'31
(67-
15
4960
(6
61)
~,
Hin
dqua
rter
36
42
(486
) 35
46
147
3)
35 2
2 14
70)
3685
(4
9-13
35
.55
(47-
4)
]4-8
9 (4
65)
~l"
):oT
cqua
rtcr
38
56
(51.
4)
3956
(5
27)
39 7
4 (5
30)
38-1
3 (5
08)
39.4
2 (5
26)
39-6
1 (5
2 8)
.~
95
Pt
~lol
50
66
(53
J)
4908
(5
1 7)
48
19
(.~J.
7J
50.2
4 (5
29)
4811
(5
061
46,6
7 (4
9 I,~
-
BI.
RC
64
44
(67
8)
63 4
0 (6
6 7)
63
63
(67
O)
65 4
1 (6
8 9)
63
31
(666
) 62
17
(65
4)
~'
)hnd
quar
ter
45 7
8 (4
8.23
.11
4 69
(47
0(
43 6
4 (4
5.9)
46
41
(48
8)
44 ~
4 (4
7 2)
43
-21
(455
) (-
ore(
outle
t 49
20
15! 8
) 50
30
(52
9)
51 3
( (5
40)
48 5
7 (5
1-7)
50
.19
(32
8)
50.9
2 (5
3-6)
C
~ I I
5
Pis
tol
60 7
7 (5
38)
58 7
7 (5
11)
57 1
9 (4
9'7)
60
-40
(525
) 57
65
(50
l)
5536
(4
8"I)
B
LRC
78
03
(67
9)
76 3
9 (6
6 4)
76
85
(668
3 79
19
(68.
9)
76-2
4 (6
633
74 5
8 (6
4 9)
~
' lh
ndqu
artc
T 55
07
147
9)
53 8
9 (4
6 9l
51
90
(45
i I
55.9
1 (4
8 6)
54
(~
(470
) 51
-37
(44
7)
F'
I"or¢
quar
tct
5991
15
213
61 0
8 (5
3 l)
63
08
(349
1 59
07
(5|.
4)
61.0
1 (5
31)
62-3
9 (5
43)
~'
• L)
cr,v
ed fr
om r
c~rC
~lon
cqu
atlo
n~ E
lven
in T
able
3; ~
clsh
ls I
hcn
con~
trtcd
to p
crcc
nlai
¢~
~q
GROWTH OF BUFFALO AND CATTLE CARCASS CUTS 293
cattle carcass sides. However, buffaloes had higher proportions of 'entire' and 'boneless" hind shank and sirloin and of 'entire' pistol but lower proportions of 'entire" and 'boneless' brisket and 'boneless' forequarter than the Friesian crossbred groups which did not differ from each other (P > 0.05). The proportions of the tenderloin and flank also differed between genotype groups. In the two cuts the three-quarter Friesians were superior (P < 0.05) to buffaloes whereas the half Friesians did not differ from both groups (P > 0.05).
The coefficients of residual variation recorded in the present study (Tables 2 and 3) indicate very low variability in the weight of cut groups (expensive groups and hind- and forequarters) and individual cuts of relatively high yield (buttock and chuck- plus-shoulder). The variability in the weight of a cut tended to increase with the decrease of its contribution to the side weight. The remarkable lack of variability for cut groups and heavy cuts, which was also reported in previous work (Le Guelte et
al., 1964; McAIlister et al. , 1976) was apparent in spite of the great variation in fatness reported for the present animals by Abdallah et al. (1981).
The individual genotype group allometric equations shown in Tables 2 and 3 permitted the comparison in weights ofexpensive cuts and hind- and forequarters to be made at 'entire" and 'boneless' side weights of 35, 55, 75, 95 and I 15 kg (Table 4). For all genotypes, as the side weight increased, the proportion of the pistol and hindquarter decreased whereas the proportion of the forequarter increased. The proportion of the BLR.C decreased in both Friesian crosses but showed practically no change in buffaloes. At all side weights the estimated percentages of pistol, BLRC and hindquarter were higher and the percentages of forequarter were lower in the buffaloes than in the Friesian crosses. The largest estimated difference was 5.04 kg (at 115 kg side weight) in the "boneless' pistol. In a previous study (Abdailah et al., 1981) on the same animals used in the present study, the carcass composition has been estimated at the above-mentioned side weights (i.e. 35kg up to 115kg). Buffaloes had a lower ratio of muscle to bone, a lower percentage of muscle and higher percentages of fat and bone than Friesian crosses. These findings, combined with those obtained in the present work, permit one to conclude that the com- position of the carcass in buffaloes is inferior in terms of its component tissues but slightly superior in terms of its component desirable cuts to that of Friesian crosses.
ACKNOWLEDGEMENT
This study was one aspect of a project supported in part by grants from the Research Development Fund of Ain Shams University.
REFERENCES
ABDALLAH, O. Y., SHAHII'4, K. A. • LATIF, M. G. A. 0980. J. Agric. Sci., Camb., 97, 205. BERG, R. T., ANDER.~N, B. B. & LlaORIUSSEN, T. (1978). Anita. Prod., 27, 51.
294 O.Y. ABDALLAH, KARIMA A. SHAHIN, M. G. A. LATIF
BUTTERFIELD. R. M. (1963). In: Syrup. Carcase Composition and Appraisal of Meat Animals. (Tribe, D. E. (Ed.)), CSIRO, Melbourne.
CAROLL, M. A. 0972). In: Syrup. Aspects of Carcass Eraluation. Proc. Br. Soc. Anita. Prod.. p. 123. COLE, J. W., R^MSEY. C. B., HOBaS. C. S. & TEMPLE, R. S. (1964). J. Anita. Sci.. 23. 71. DUKES. H. H. 0955). The physiology of domestic animals (seventh edition). London. Ballicr¢. Tindall &
Cox. FOWLER. V. R. (1968). In: Growth anddeL'elopment ofmammab. ( Lodge. E. A. & Lamming. G. E. (Eds)).
London, Butterworths. HAMMOND. J. (1932). In: Growth and the de~'elopment of mutton qualities in the sheep. (Crew, F. A. E. &
Culter, D. W. (Eds)). Edinburgh, Oliver & Boyd. HARRINGTO.~. G. & POMEROY. R. W. (1959). J. Agric. Sci., Camb.. 53, 64. JOb'BERT, D. M, (1959). S. Aft. J. Sci.. 55. 139. KEMPS'r~R, A. J., Ct,'TffBEaTSO~. A.. SMITH. R. J. (1976). J. Agric. Sci., Camb., 87, 533. KRA.~ER. C. W. (1956). Biota., 12, 307. LE Gt;ELTE, P.. DU~OST. B. L. & AFtNOUX, J. (1964). Ann. Zootech.. 13, 255. LEVJE, A. (1963). The meat handbook. Connecticut. The Avi Publishing Company. Inc. LUlTINGff. H. C. (1962). J. Agric. Sci., Camb., 58. I. McALUSTER. T. J., WILSON. L. L.. ZIEGLER, J. H. & SINK. J. D. (1976). J. Anita. Sci.. 42, 324. RAG^g, M. T.. DAll.WlSI-I, M. T. H. & M^LEK. A. G. A. (1966). J. Anita. Prod., U.A.R., 6, 31. SEEBECK. R. M. & TULLOff. N. M. 0968). Aust. J. Agric. Res.. 19. 673.