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Literature review
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January and February, 1997 |
Performance, carcass, and meat quality advantages of boars over barrows:
A literature review
JinLiang Xue, DVM, PhD; Gary D. Dial, DVM, PhD, MBA; James E. Pettigrew,
PhD
JLX, GDD: Department of Clinical and Population Sciences, College of
Veterinary Medicine; JEP: Department of Animal Science; 385 Animal Science/Veterinary
Medicine, 1988 Fitch Ave, University of Minnesota, St. Paul, Minnesota 55108
Citation: Xue JL, Dial GD, Pettigrew JE. Performance, carcass,
and meat quality advantages of boars over barrows: A literature review.
Swine Health Prod. 1997;1:21-28.
Copyright (C) 1997 American Association of Swine Practitioners.
Also available in PDF format.
Summary
This paper reviews the literature comparing growth performance, carcass,
and meat quality data between barrows and boars. Compared with barrows,
boars have reduced feed intake, improved feed efficiency, less backfat,
higher nitrogen retention, and leaner carcasses. Growth rate of boars will
be higher than that of barrows if adequate dietary amino acids are supplied.
The improved growth performance and carcass characteristics of boars are
primarily due to the anabolic effects of androgens and estrogen produced
in the testis. However, administering manufactured anabolic agents, androgens,
and estrogens to barrows has not yet been shown to improve growth and carcass
in swine.
Keywords: swine, boars, carcass, meat, growth
Received: September 17, 1996
Accepted: December 27,1996
Increased consumer demands for lean pork and heightened awareness of
production efficiency have stimulated the pork industry to investigate new
strategies to improve lean accretion in pigs being raised to slaughter.
Repartitioning agents such as porcine somatotropin or growth hormone (GH),
ractopamine, and cimaterol can greatly improve growth rate and feed efficiency,
increase lean tissue, and decrease fat deposition.1-3 However,
there are some problems with GH. Studies that treated pigs with GH have
reported a significant decrease in the tenderness, juiciness, and flavor
of pork chops.4-5 Also, pigs treated with GH have increased incidence
of pale, soft, and exudative (PSE) pork.6-8 Joint strength and
joint soundness is reduced in pigs treated with GH,9 and increased
incidence and severity of osteochondrosis has been reported.10
Furthermore, meat tenderness has been reported to decrease in pigs treated
with certain b-adrenergic repartioning agents, such as cimaterol.11
Traditionally in most areas of the world, male piglets are castrated
shortly after birth despite the fact that intact males are widely reported
to have improved feed efficiency and lean accretion over castrated males.
Castrating male farm animals is an ancient custom dating back almost as
far as human domestication of animals,12 first recorded between
the 16th and 11th century BCE in the Chinese Shang Dynasty.13
Several countries, such as Denmark, Britain, Spain, Australia, and New
Zealand, currently raise entire males for pork. The European Economic Community
(EEC) has passed a regulation (64/433/EEC, 1993) that allows intact male
pigs to be reared to 80 kg (176 lb) carcass weight throughout the union
countries.14 Carcasses above 80 kg (176 lb) must be tested for
odor or taint. In most other countries (including the United States), however,
all male pigs not destined for breeding are usually castrated at a young
age.
In this review, we discuss the literature comparing growth performance,
carcass characteristics, and meat quality of boars and barrows. We also
review the other benefits of rearing boars over barrows.
Improved growth performance of intact
male pigs
The relative feed efficiency of boars and barrows reported in the literature
has been consistent (Table 1).
In general, boars appear to use feed more efficiently than their barrow
littermates. Compared with barrows, feed efficiency improvements in boars
range from 2.6%-32.1% under various rearing conditions, thus saving 1.8-27
kg (4-60 lb) of feed during the grow-finish period compared to barrows.
The findings on growth rate of boars relative to barrows have been inconsistent.
Some researchers found that boars grew faster.15-19 Others did
not observe a difference in growth rate between boars and barrows,20-25
and some observed that boars had a lower growth rate than barrows.26-28.
Several factors can influence growth rate in swine and thus should be
taken into consideration when the growth rate is compared between boars
and barrows. These factors include dietary levels of protein and amino acids,
energy intake, age at castration, slaughter weight, and management. The
inconsistency of findings in the literature is undoubtedly due at least
in part to variability among these factors across studies.
Dietary levels of protein and amino acids
Current literature indicates that boars need more nutrient-dense diets
than littermate barrows to achieve improved growth. Current NRC requirements29
are established for barrows and gilts. Increased concentrations of dietary
protein over these NRC requirements favor boars, especially at a heavier
weight.30 Daily weight gain of boars was reported to be the same
as that of barrows on a conventional diet, but boars grew faster than barrows
on a higher-protein diet.31 Many experiments have been conducted
to determine influences of various dietary protein levels on the growth
rate of boars and barrows. The average daily gain (ADG) of boars increased
linearly with increasing dietary protein levels ranging from 14%-22% in
the growing period up to 55 kg (14 lb) liveweight and from 14%-18% in the
finishing period up to 100 kg (220 lb), followed by a decline in gain at
24% or higher protein levels.20,32-35
Lysine is the first limiting amino acid for growing pigs fed corn-soy
diets. Boars require a higher level of dietary lysine than barrows.30-32,36
Significant reductions in growth rate, feed efficiency, and nitrogen
retention are evident in boars fed low-lysine diets (0.47%-0.60%). When
bodyweight is between 25-55 kg (55-124 lb), there is a linear increase in
the growth rate and improved feed:gain ratio (F:G) as dietary lysine concentrations
increase from 0.75% to 1.11%.21,35,36 The concentration of lysine
required to achieve maximum gain in boars is about 11.8 g per kg (25 g per
lb) when bodyweight is between 25-55 kg (55-124 lb). Barrows and
gilts require lower lysine concentrations when in the same range of bodyweight.37
During the 50-90 kg (110-198 lb) liveweight phase of growth in boars, there
is a linear response for the growth rate, F:G, and carcass lean proportions
when lysine concentrations are increased up to 9.1 g per kg (20 g per lb)
with a daily lysine intake of 22.9 g per kg (50 g per lb) for boars.38
It is important to remember that amino acid requirements vary among boars
as well as among barrows due to differences in genetic lines, health status,
environment, etc.
An excessive protein intake may also result in depressed boar growth
performance.32,35,39,40 Besides the reduced voluntary feed intake,
the growth-decreasing effect of high-protein diets is partly due to the
reduced energy value of diets with increased protein concentrations.41,42
Excess protein intake causes a high rate of protein turnover, increased
muscle respiration43 and increased visceral organ mass,44,45
which contribute to increased heat production.46 It appears that
a supply of protein in excess of requirements reduces the net energy available
to animals, which in turn depresses the rates of deposition of protein and
water, and to a lesser extent, the deposition of fat.35,40 The
same effect has been observed in castrated male pigs given high protein
diets ad libitum.47
Energy intake
When fed ad libitum, barrows consumed more feed than boars and exhibited
a liveweight gain similar to that of boars.48 When energy intake
was restricted, boars grew faster than barrows from 45-90 kg (100-200 lb)
liveweight.48 It is clear that boars grow faster than barrows
when fed restricted diets, and barrows grow faster than boars when fed ad
libitum.49,50 The association of growth rate with feeding patterns
is probably related to appetite. Several researchers have reported that
barrows have greater appetites than boars,15,20,26,50 i.e., they
have increased daily feed intake compared to boars when animals are given
free access to feed. The difference in appetites is profound from 55 kg
(121 lb) liveweight onwards.21 A dramatic increase in backfat
thickness of barrows from 56 kg (123 lb) liveweight (120 days old) has been
reported, but this increase did not occur in entire males.28
Further research needs to be conducted to determine whether the differences
in body composition between boars and barrows are due to feed intake, or
vice versa.
Age at castration
Age at castration may affect growth performance of barrows. It seems
that superior muscle growth in entire males is manifested only when animals
are approaching puberty. Castration did not affect liveweight or total soft
tissue protein content when performed at 1, 2, or 4 weeks of age.51
In barrows that had been castrated at 15 and 40 kg (33 and 88 lb) bodyweight,
skeletal muscle protein accretion did not differ from that of boars 5 weeks
after castration. There was no difference in ADG among barrows castrated
at birth or at 6, 12, 16, and 20 weeks of age52 and at 3-4, 9-10,
and 15-16 weeks of age.53 Average feed intake of barrows castrated
at 16 and 20 weeks of age was decreased compared with those castrated at
birth or at 6 and 12 weeks of age.52 In contrast, postpubertal
boars had greater muscle protein accretion rates than barrows that were
castrated at 75 kg (165 lb) liveweight.54
Slaughter weight
In many European countries, 90-100 kg (198 - 220 lb) liveweight has been
regarded as the optimal slaughter weight. In the United States, however,
slaughter weights tend to be heavier, and slaughter at 120-130 kg (264-286
lb) is not uncommon. In a Swedish study of two genetic lines (Landrace
and Yorkshire),55 boars reached slaughter weights of 90, 110,
and 130 kg (198, 242, and 286 lb) earlier than barrows and gilts. The
magnitude of the differences in age to attain a given slaughter weight are
greater between barrows and boars as bodyweight increases. Boars
attained a slaughter weight of 110 kg (242 lb) 10 days sooner than barrows.55
When fed to higher slaughter weights (e.g., 130 kg/286 lb), boars had
10% higher ADG than barrows. Boars had better feed efficiency than
barrows from 70-130 kg (154-286 lb) bodyweight. The ADG of barrows reached
a maximum from 70 to 90 kg (154 to 198 lb) liveweight, after which their
ADG decreased. In boars, ADG peaked at a bodyweight 10 kg (22 lb)
heavier than for barrows, and the magnitude of the subsequent decrease in
ADG was smaller in boars compared to barrows after that weight.15,55
In a similar study in the United States,24 ADG of barrows
was slightly greater than boars until 76 kg (167 lb) liveweight (17 weeks
old), when it plateaued. Boars reached the maximum rate of gain at 87 kg
(192 lb) (20 weeks old). Thus, the bodyweight at which ADG peaked was 11
kg (24 lb) heavier for boars than for barrows.
Rates of nitrogen deposition also appear to differ between barrows and
boars. The rate at which nitrogen was deposited responded quadratically
over time for both boars and barrows as they gained weight, reaching a maximum
for boars at a liveweight of 60 kg (132 lb) and for barrows at 55 kg (121
lb).56 The difference in weight/age of maximum growth rate and
nitrogen deposition between boars and barrows is another explanation for
the inconsistencies of growth rate found in the literature.
Management
Floor space and group size affect the growth rate of pigs. The ADG of
pigs with a floor space of 0.34 m2 (3.7 ft2) per pig
was reduced compared to pigs that had 0.68 or 1.01 m2 (7.3 or
10.9 ft2) per pig.57 Meunier-Salaun, et al.,57
determined the optimal range of floor space to ensure optimal performance.
We speculated that pig density may have been a primary factor causing reduced
ADG of boars compared to barrows in some studies.28 Aggressive
behavior increases when group size and pig density increase.58
Swine with higher concentrations of salivary androstenone are more aggressive
than those with lower concentrations.59 Group size (40 pigs per
pen)28 may influence growth rate of boars because they have higher
concentrations of androstenone than barrows.
No management problems were reported when boars and gilts were raised
together up to bodyweights of 81, 93, and 110 kg (178, 205, and 242 lb).
At heavier weights, growth performance was slightly reduced for the boar/gilt
groups compared to mixed barrows and gilts.60,61
Carcass comparison
Reports in the literature of carcass comparisons between boars and barrows
are consistent (Table 2). Boars
have less backfat,16,20 longer carcass length,24,62
and a larger longissimus muscle area than do barrows.21,22,30
Barrows tend to have a higher dressing percentage compared with their contemporary
intact males, due partly to the higher genitalia weight of boars.20,60-64
Boar carcasses have more lean meat, less fat, more bone, and more skin
compared to barrows (Table 3).
The carcass composition of gilts is intermediate between boars and barrows.
Ratio of bone:muscle is relatively constant at between 1:5.4 and 1:5.6
in boars and barrows.20 Boar carcasses contain more water
and protein and less fat than those of barrows (Table 4).
Lean meat
Boars retain a higher percentage of nitrogen intake and of digested nitrogen
than barrows when they are given a diet with concentrations of amino acids
that support the higher nitrogen retention.36,40 Castration reduced
the ceiling for protein deposition in one study by 30%, from 128 to 85 g
(4.5 to 3.0 oz) per day.48 Castrated male pigs have an inherently
lower capacity for protein deposition and a higher rate of fat accretion,
and thus require less dietary protein and amino acids to support maximum
growth than entire males.20,34,36-38,65
Proportions of lean meat and adipose tissue in the carcass are affected
by the interaction between gender and amino acid levels. The amino acid
requirements for lean accretion is higher for boars than for barrow littermates.30,31
Dressing percentage decreases at a similar rate for both boars and barrows
as dietary protein increases.63,66,67
With an adequate protein and lysine diet, protein deposition of boars
increased linearly with increased energy intake up to 7.9 mcal DE per day,
and then remained constant when feed intake was at 120 g per day thereafter.
The response in barrows was similar to that of boars, but protein deposition
in barrows reached a maximum value of only 85 g per day.48
Rearing pigs to heavier slaughter weights results in a lower percentage
of lean meat in carcasses. The effect of slaughter weight on lean percentage
is, however, not the same in barrows, gilts, and boars. Lean percentage
in barrows and gilts is more influenced by weight at slaughter, while in
boars slaughter weight is less of a factor in lean percentage.55
At 90 kg (200 lb) liveweight, each Landrace boar produced 3.7 kg (8.1 lb)more
lean meat than did a 90-kg (200-lb) barrow. The magnitude of the difference
between boars and barrows increased as slaughter weight increased. At 130
kg (286 lb) liveweight, boars had 7 kg (15.4 lb) more lean meat than barrows.
With a higher lean meat content in boar carcasses, the content of fat in
boars is lower than that in barrows.49,55 For all traits, gilts
were intermediate between barrows and boars. As liveweight of boars increased
from 105 to 145 kg (230 to 320 lb), carcass length, tenth rib backfat thickness,
longissimus muscle area, and longissimus weight increased linearly. Proportion
of moisture and protein in the soft tissue decreased while ether extract
increased as liveweight increased in boars (Table
5).
Fat tissue
Boars have been reported to have softer fat than barrows.68,69
Soft fat fails to "set" properly after chilling, as tissue separates
between the fat-fat or fat-muscle interfaces.70 Edwards, et al.,71
reported that the gender effects on soft fat are not evident when fat hardness
is adjusted for fat thickness. However, Dransfield and Kempster72
observed that boars have softer fat than gilts and barrows even after adjusting
for fat thickness. Leaner pigs have softer fat, but castration had no effect
on fat hardness in pigs at 68 kg (150 lb).73
Backfat from intact males, compared with barrows and gilts, has a relatively
higher proportion of unsaturated fatty acids, mainly linoleic acid.52,74
The highest proportion of saturated acids are observed in barrows, mainly
due to a higher palmitic acid content. Gilts are intermediate between barrows
and boars.70,75,76 It has been suggested that this difference
may result in a softer backfat and marbling of boars. In all sexes, palmitic,
stearic, oleic, and linoleic acids are the major fatty acids and amount
to over 90% of the total fatty acids in the backfat.77
Bone and skin
Boars have heavier bones than barrows at the same slaughter weights.
The difference in bone content between boars and barrows is approximately
the same at several slaughter weights.55,78,79 With increasing
weight, the percentage of bone decreases. The greater proportion of bone
may be due, at least in part, to the anabolic effect of sexual hormones,
such as testosterone, on the growth rate of specific bones and body components.
Boars have thicker skin than barrows.17,18,80,81 The dermis
above the first lumbar vertebra in boars was 0.82 mm (0.03 inches) thicker
than that in barrows (3.76 versus 2.94 mm, 0.15 versus 0.12 inches) at 90
kg (200 lb) liveweight in the Landrace genotype.80 In addition
to the difference in thickness, the dermis of barrows has a finer structure
than that of boars. Sebaceous glands in barrows are poorly developed.80
Meat quality
Weight loss through exudate or drip is an economically important meat
quality trait in pigs.82 Carcass pH values at 45 minutes (pH45)
and 24 hours (pHu) post slaughter are widely used as indirect
measurements of incidence of PSE and dark, firm, and dry (DFD) meat quality
defects. Abnormally low pH45 values are associated with PSE while
abnormally high pHu values typically occur in DFD meat. Pork
with a pH45 < 6.1 has higher water drip while pork with a
pH45 > 6.1 has improved water holding capacity and less water
drip.83 Boars have been reported to have higher pHu
values than barrows.84 In boars held overnight after transport
before slaughter, pH values and DFD frequency were higher compared with
barrows.85,86 During preslaughter holding, physical activity
is associated mainly with aggressive behavior. Entire males tend to be more
aggressive than barrows. There is no difference in DFD and PSE frequencies
between boars and barrows when less than 4 hours elapse from farm to slaughter.75
Other advantages of rearing intact males
Genetic selection
Because most male pigs are castrated at young ages, breeding stock must
be selected at an early age before their true genetic potential can be accurately
assessed and only a limited number of boars are tested for genetic improvement.
If boars were reared for meat, genetic companies would have larger populations
for genetic selection.
Castration and animal welfare
Raising boars removes labor input for castration. Castration is believed
to be stressful and painful to the animals, which raises ethical and welfare
concerns.87 Legal restrictions on animal welfare are already
in place in some European countries.88
Efficiency of nutrient use
Swine farm waste and related odor are becoming serious issues in the
swine industry, particularly in the top pig production states, such as Iowa
and North Carolina.89,90 It was recognized that animal production
causes almost 90% of the total NH3 emission.91 In
Denmark, nitrogen content in manure has been used for determining the amount
of manure applied per hectare of land.92 Since boars have improved
feed efficiency and nitrogen retention compared with barrows,36,40,56
avoiding castration would improve nitrogen utilization in swine production
systems.
Financial return
Packers pay a much lower price for boar carcasses than carcasses from
barrows. In recent upper Midwest markets, packers paid approximately $0.22
per kg ($0.10 per lb) of carcass weight less for boars than barrows produced
from the same genetic company, indicating that producers will receive $22-$28
less for a boar than a barrow--a considerable economic loss for producers.
If boars were sold at the same price as barrows, based on our data,28
each boar would net $5-$20 more than a barrow because of improved feed efficiency
and lean proportion in carcasses.
Anabolic effect of gonadal steroids
The superior performance and carcasses of boars relative to barrows are
explained by the anabolic effect of gonadal steroids. Anabolic agents
used in beef cattle result in increased feed intake, daily weight gain,
and carcass lean proportion, and decreased F:G.93,94 However,
when administered after castration, manufactured anabolic agents, exogenous
androgens or/and estrogens had negligible effects on growth performance
in pigs in some studies,95-104 and positive effects on growth
performance in other studies.105 The reason for interspecies
variation in the effects of anabolic agents is not yet determined.
Implications
- Intact male pigs have improved feed efficiency and a higher proportion
of lean tissue than castrated males.
- Intact males grow faster than barrows when diets with adequate concentrations
of protein and amino acids are supplied.
- Producers will receive a higher net financial benefit from rearing
intact male pigs than that from barrows if boars and barrows were sold
at the same price.
References
1. Chung CS, Etherton TD, Wiggins JP. Stimulation of swine growth performance
by porcine growth hormone. J Anim Sci. 1985; 60:118-130.
2. Etherton TD, Sorensen MT, Coleman ME, Chaudhuri S. Mechanisms by which
somatotropin alters muscle growth and adipose tissue accretion. Proc
Recip Meats Conf. 1989;42:83-89.
3. Boyd RD, Bauman DE, Fox DG, Scanes CG. Impact of metabolism modifiers
on protein accretion and protein and energy requirements of livestock. J
Anim Sci. 1991;69 (Suppl. 2):56-75.
4. Boles JA, Parrish FC, Jr Shaggs CL, Christian LL. Effect of porcine
somatotropin, stress susceptibility and final end point of cookery on the
sensory, physical, and chemical properties of pork loin chops. J Anim
Sci. 1991;69:2865-2870.
5. Boles JA, Parrish FC, Jr Shaggs CL, Christian LL. Sensory, physical,
and chemical properties of pork loin chops from somatotropin-treated pigs
of three stress classifications. J Anim Sci.1992; 70:3066-3070.
6. Solomon MB, Campbell RG, Steele NC, Capema TJ, McMurtry JP. Effect
of feed intake and exogenous porcine somatotropin on longissimus muscle
fiber characteristics of pigs weighing 55 kilograms liveweight. J Anim
Sci.1988;66:3279-3284.
7. Soloman MB, Campbell RG, Steele NC, Caperna TJ. Effects of exogenous
porcine somatotropin administration between 30 and 60 kilograms on longissimus
muscle fiber morphology and meat tenderness of pigs growth to 90 kilograms.
J Anim Sci.1989;67(Suppl. 1):153(Abstr).
8. Solomon MB, Campbell RG, Steele NC. Effect of sex and exogenous porcine
somatotropin on longissimus muscle fiber characteristics of growing pigs.
J Anim Sci.1990;68:1176-1181.
9. He P, Aherne FX, Nam DS, Schaefer AL, Thompson JR, Nakano T. Effects
of recombinant porcine somatotropin (rpST) on joint cartilage and axial
bones in growing and finishing pigs. Can J Anim Sci.1994;74:257-263.
10. He P, Aherne FX, Schaefer AL, Thompson JR, Nakano T, Jones SDM. Differentiation
of the effects of somatotropin and enhanced growth rate on the occurrence
of osteochondrosis in pigs. Can J Anim Sci.1994.74:251-255.
11. Jones RW, Easter RA, McKeith FK, Dalrymple RH, Maddock HM, Bechtel
PJ. Effect of the b-adrenergic agonist cimaterol (CL 263,780) on the growth
and carcass characteristics of finishing swine. J Anim Sci.1985;61:905-913.
12. Turton JD. The effect of castration on meat production and quality
in cattle, sheep and pigs. Anim Breed Abstr.1962;30:447-456.
13. Zhang ZG, Li BT, Chen XH, et al. Pig Breeds in China. Shanghai
Scientific & Technical Publishers, Shanghai, China.1986; p. 1-6.
14. Willeke H. Possibilities of breeding for low 5b-androstenone content
in pigs. Pig News Info. 1993;14:31N-33N.
15. Blair R, English PR. The effect of sex on growth and carcass quality
in the bacon pig. J Agric Sci Camb.1965;64:169-176.
16. Wong WC, Boylan WJ, Stothers SC. Effects of dietary protein level
and sex on swine performance and carcass traits. Can J Anim Sci.1968;48:383-388.
17. Allen P, Riordan PB, Hanrahan TJ, Joseph RL. Production and quality
of boar and castrate bacon. I. Pig production, in-factory processing and
carcass value. Ir J Food Tech.1981;5:93-104.
18. Wood JD, Riley JE. Comparison of boars and castrates for bacon production.
1. Growth data, and carcass and joint composition. Anim Prod.1982;35:55-63.
19. Nicholls LL, Price MA. A comparison of boars and barrows for growth
and carcass characteristics at four slaughter weights. Agric Forestry Bulletin,
Univ of Alberta, Special Issue 65th Annual Feeders' Day Rep.1986;120-122.
20. Newell JA, Boland JP. Performance, carcass composition, and fat composition
of boars, gilts and barrows fed two levels of protein. Can J Anim Sci.1972;52:543-551.
21. Pay MG, Davies TE. Growth, food conversion, and carcass characteristics
in castrated and entire male pigs fed three different dietary protein levels.
J Agric Sci Camb.1973;81:65-68.
22. Fortin A, Friend DW, Sarkar NK. A note on the carcass composition
of Yorkshire boars and barrows. Can J Anim Sci.1983;63:711-714.
23. Castell AG, Strain JH. Influence of diet and sex-type (boar, castrate
or gilt) on live and carcass measurements of self-fed pigs from two breed
lines differing in growth rates. Can J Anim Sci.1985; 65:185-195.
24. Knudson BK, Hogberg MG, Merkel RA, Allen RE, Magee WT. Developmental
comparisons of boars and barrows: I. Growth rate, carcass and muscle characteristics.
J Anim Sci.1985;61:789- 796.
25. Friend DW, Fortin A, Butler G, Poste LM, Kramer JKG, Burrow VD. Naked
oats (Avena nuda) with and without lysine supplementation, for boars
and barrows: Growth, carcass and meat quality, energy and nitrogen metabolism.
Can J Anim Sci.1989;69:765-778.
26. Castell AG, Cliplef RL, McKay RM. Effects of diet, litter, and sex
type on the performance (from 22 to 90 kg liveweight) and carcass measurements
of crossbred pigs. Can J Anim Sci.1985;65:821-834.
27. Squires EJ, Adeola O, Young G, Hacker RR. The role of growth hormones,
b-adrenergic agents and intact males in pork production: A review. Can
J Anim Sci.1993;73:1-23.
28. Xue JL, Dial GD, Schuiteman J, Kramer A, Fisher C, Marsh WE, Morrison
RB, Squires JE. Evaluation of growth, carcass, and compound concentrations
related to boar taint in boars and barrows. Swine Hlth Prod.1995;3:155-160.
29. National Research Council. Nutrient Requirements of Swine.
National Academy Press, 1988; Washington, D.C. 1988.
30. Prescott JHD, Lamming GE. The influence of castration on the growth
of male pigs in relation to high levels of dietary protein. Anim Prod.1967;9:535-545.
31. Creswell DC, Wallace HD, Combs GE, Palmer AZ, West RL. Lysine and
tryptophan in diets for boars and barrows. J Anim Sci.1975;40:167
(Abstr).
32. Luce WG, Johnson RK, Walters LE. Effects of levels of crude protein
on performance of growing boars. J Anim Sci.1976;42:1207-1210.
33. Reinhard MK, Mahan DC, Workman BL, Cline JH, Fetter AW, Grito AP
Jr. Effect of increasing dietary protein level, calcium and phosphorus on
feedlot performance, bone mineralization and serum mineral values with growing
swine. J Anim Sci.1976;43:770-780.
34. Taverner MR, Campbell RG, King RH. The relative protein and energy
requirements of boars, gilts and barrows. Austr J Exp Agric Anim Husb.1977;17:574-580.
35. Tyler RW, Luce WG, Johnson RK, Maxwell CV, Hintz RL, Walters LE.
The effects of level of crude protein on performance of growing boars.
J Anim Sci.1983;57:364-372.
36. Williams WD, Cromwell GL, Stahly TS, Overfield JR. The lysine requirement
of the growing boar versus barrow. J Anim Sci.1984;58:657-665.
37. Yen HT, Cole DJA, Lewis D. Amino acid requirements of growing pigs.
7. The response of pigs from 25 to 55 kg liveweight to dietary ideal protein.
Anim Prod.1986;43:141-154.
38. Yen HT, Cole DJA, Lewis D. Amino acid requirements of growing pigs.
8. The response of pigs from 50 to 90 kg liveweight to dietary ideal protein.
Anim Prod.1986;43:155-165.
39. Cooke R, Lodge GS, Lewis D. Influence of energy and protein concentration
in the diet on the performance of growing pigs. 3. Response to differences
in levels of both energy and protein. Anim Prod.1972;14:219-228.
40. Holmes CW, Carr JR, Pearson G. Some aspects of the energy and nitrogen
metabolism of boars, gilts and barrows given diets containing different
concentrations of protein. Anim Prod.1980;31:279- 289.
41. Just A. The net energy value of crude (catabolized) protein for growth
in pigs. Livest Prod Sci. 1982;9:349-360.
42. Henry Y, Colléaux Y, Sève B. Effects of dietary level
of lysine and of level and source of protein on feed intake, growth performance,
and plasma amino acid pattern in the finishing pig. J Anim Sci. 1992;70:188-195.
43. Adeola O, Young LG. Dietary protein-induced changes in porcine muscle
respiration, protein synthesis and adipose tissue metabolism. J Anim
Sci.1989;67:664-673.
44. Sugahara M, Baker DH, Harmon BG, Jensen AH. Effect of excess levels
of dietary crude protein on carcass development in swine. J Anim Sci.1969;29:598-601.
45. Pond WG, Varel VH, Dickson JS, Haschek WM. Comparative response of
swine and rats to high-fiber or high-protein diets. J Anim Sci.1989;67:716-723.
46. Fuller MF, Cadenhead A, Mollison G, Sève. Effects of the amount
and quality of dietary protein on nitrogen metabolism and heat production
in growing pigs. Br J Nutr.1987;58:277-285.
47. Campbell RG, Taverner MR, Curic DM. The effects of sex and liveweight
on the growing pig's response to dietary protein. Anim Prod.1988;46:123-130.
48. Campbell RG, Taverner MR. Genotype and sex effects on the relationship
between energy intake and protein deposition in growing pigs. J Anim
Sci.1988;66:676-686.
49. Kroeske D. Value of boars in fattening compared to hogs and gilts.
Report at the Commission on Pig Production, EAAP-Meeting. Dublin,
1968.
50. Walstra P. Experiments in the Netherlands on the effect of castration
of pigs in relation to feeding level. Meat production from entire male
animals. DN Rhodes, J & A Churchill Ltd, London. 1969;p129-141.
51. Skjaerlund DM, Mulvaney DR, Bergen WG, Merkel RA. Skeletal muscle
growth and protein turnover in neonatal boars and barrows. J Anim Sci.1994;72:315-321.
52. Charette LA. The effects of sex and age of male at castration on
growth and carcass quality of Yorkshire swine. Can J Anim Sci. 1961;41:30-39.
53. Bates RO, Zumbrunnen C, Jesse GW. Effect of age at castration on
swine. J Anim Sci.1992; 70(Suppl 1):49 (Abstr).
54. Mulvaney DR. Effects of castration and administration of androgens
to castrated male pigs upon growth and carcass composition. PhD Dissertation.1984;Michigan
State University, East Lansing.
55. Hansson I. Effect of sex and weight on growth, feed efficiency and
carcass characteristics of pigs. 1. Growth rate and feed efficiency of boars,
barrows and gilts. Swed J Agric Res.1974:209-218.
56. Hansen BC, Lewis AJ. Effects of dietary protein concentration (corn:soybean
meal ratio) on nitrogen balance of growing boars, barrows, and gilts: mathematical
descriptions. J Anim Sci.1993;71:2110-2121.
57. Meunier-Salaun MC, Vantrimponte MN, Raab A, Dantzer R. Effect of
floor area restriction upon performance, behavior and physiology of growing-finishing
pigs. J Anim Sci.1987;64:1371-1377.
58. Simonsen HB. Behavior and distribution of fattening pigs in the multi-activity
pen. Appl Anim Behav Sci.1990;27:311-324.
59. Booth WD. Endocrine and exocrine factors in the reproductive behavior
of the pig. Symp Zool Soc London.1980;45:289-311.
60. Bonneau M, Desmoulin B. Evolution de la teneur en androsténone
du tissu adipeux dorsal chez la porc mâle entier de type Large White:
variation selon les conditions d'élevage. Reprod Nutr Dév.
1980;20:1429-1437.
61. Patterson RLS, Lightfoot AL. Effect of sex grouping during growth
on 5b-androstenone development in boars at three commercial slaughter weights.
Meat Sci.1984;10:253-263.
62. Froseth JA, Matin EL, Hill JK. Effects of limited feeding, sex and
liveweight on porcines. J Anim Sci.1973;37:262(Abstr).
63. Hansen BC, Lewis AJ. Effects of dietary protein concentration (corn:soybean
meal ratio) on the performance and carcass characteristics of growing boars,
barrows, and gilts: mathematical descriptions. J Anim Sci.1993;71:2122-2132.
64. Hansson I, Lundström K, Malmfors B. Effect of sex and weight
on growth, feed efficiency and carcass characteristics of pigs. 2. Carcass
characteristics of boars, barrows and gilts, slaughtered at four different
weights. Swed J Agric Res.1975;5:69-80.
65. Campbell RG, Taverner MR. Effects of strain and sex on protein and
energy metabolism in growing pigs. In: PW Moe, HF Tyrrell, PJ Reynolds (Ed.)
Energy Metabolism of Farm Animals. 1985;p78 Eur Assoc Anim Prod Publ
No 32 Rowan and Littlefield, USA
66. Wilson GD, Burnside JE, Bray RW, Phillips PH, Grummer RH. Pork carcass
value as affected by protein level and supplementation with aureomycin and
vitamin B12. J Anim Sci.1953;12:291- 296.
67. Greeley MG, Meade RJ, Hanson LE, Nordstrom J. Energy and protein
intakes by growing swine. II Effects on rate and efficiency of gain and
on carcass characteristics. J Anim Sci.1964;23:816-822.
68. Sather AP, Jones SDM, Joyal S. Feedlot performance, carcass composition
and pork quality from entire male and female Landrace and Large White market-weight
pigs. Can J Anim Sci. 1991;71:29- 42.
69. Sather AP, Jones SDM, Robertson WM, Zawadski S. Sex effects on fat
hardness mater reading of market weight pigs. Can J Anim Sci.1995;75:509-515.
70. Wood JD. Fat quality in pig meat - UK. In: JD Wood (ed), Meat
Research Institute Special Report No.2. A Workshop in CEC Program of Coordination
of Research on Animal Husbandry, Brussels.1984;p9-14.
71. Edwards SA, Wood JD, Moncrieff CB, Porter SJ. Comparison of the Duroc
and Large White as terminal sire breeds and their effect on pigmeat quality.
Anim Prod. 1992;54:289-297.
72. Dransfield E, Kempster ANJ. Incidence of soft fat in British pigs.
Anim Prod. 1988;88:502(abstr).
73. Wood JD, Enser M. Comparison of boars and castrates for bacon production.
Anim Prod. 1982;35:65-74.
74. Malmfors B, Lundström K, Hansson I. Fatty acid composition of
porcine back fat and muscle lipids as affected by sex, weight and anatomical
location. Swed J Agric Res.1978;8:25-38.
75. Barton-Gade PA. Meat and fat quality in boars, castrates and gilts.
Livest Prod Sci.1987;16:187- 196.
76. Nicholls LL, Price MA. A comparison of boars and barrows for meat
quality characteristics and steroid concentrations at four slaughter weights.
Agric Forestry Bulletin, Univ of Alberta, Special Issue 66th Annual Feeders'
Day Rep.1987;30-32.
77. Smithard RR, Smith WC, Ellis M. A note on the fatty acid composition
of backfat from boars in comparison with gilts and barrows. Anim Prod.1980;31:217-219.
78. Buck SF. A comparison of pigs slaughtered at three different weights.
I. Carcass quality and performance. J Agric Sci Camb.1963;60:19-26.
79. Emerson JA, Pearson AM, Hoefer JA, Magee WT, Bratzler LJ. Effect
of slaughter weight upon the processing characteristics, quality and consumer
acceptability of pork carcasses and cuts. J Anim Sci.1964;23:436-443.
80. Vold E, Moen RA. A note on the effect of castration upon the development
of the skin in the pig. Anim Prod.1972;14:253-254.
81. Knudson BK, Hogberg MG, Merkel RA, Allen RE, Magee WT. Developmental
comparisons of boars and barrows: II. Body composition and bone development.
J Anim Sci.1985;61:797-801.
82. Lundström K, Nilsson H, Malmfors B. Interrelationships between
meat quality characteristics in pigs. Acta Agric Scand Supp.1979;l
21:71-80.
83. Warriss PD. The relationship between pH45 and drip in
pig muscle. J Food Tech.1982;17:573- 578.
84. Tarrant PV, Gallwey WJ, McGloughlin P. Carcass pH values in Irish
Landrace and Large White pigs. Ir J Agric Res.1979;18:167-172.
85. Moss BW, Robb JD. The effect of pre-slaughter lairage on serum thyroxine
and cortisol levels at slaughter, and meat quality of boars, hogs and gilts.
J Sci Food Agric.1978;29:689-696.
86. Ellis M, Smith WC, Clark JBK, Innes N. A comparison of boars, gilts
and castrates for bacon manufacture. 1. On farm performance, carcass and
meat quality characteristics and weight loss in the preparation of sides
for curing. Anim Prod.1983;37:1-9.
87. Rose M, Adams D. Evidence for pain and suffering in other animals.
In: Langley G (ed.) Animal Experimentation. Chapman & Hall, New
York.1989.
88. Jackson WT. On-farm animal welfare law in Europe - using the law.
Appl Anim Behav Sci. 1988;20:165-173.
89. McMahon, K. Iowa manure bill has 'something for everyone to hate'.
National Hog Farmer. 1996;41(No.1):12-13.
90. McMahon, K. North Carolina tightens manure regulations. National
Hog Farmer.1996; 41(No.4):28.
91. Anonymous. Paper on acidification. Ministry of Housing, Physical
Planning and Environment/Ministry of Agriculture and Fisheries, The Hague,
the Netherlands.1984;p59.
92. Anonymous. Bekendt gørelse om husdyrgødning og ensilage
m.v. Miljoministeriets bekendtgørelse.1988;nr.568.
93. Sawyer GJ, Barker DJ. Growth promotants in cattle in Australia. Austr
Vet J.1988;65:101-108.
94. Hancock DL, Wagner JF, Anderson DB. Effects of estrogens and androgens
on animal growth. In Pearson AM, Dutson TR (ed), Advances in Meat Research.
Vol 7 Growth Regulation in Farm Animals. Elservier Applied Science Publisher,
Essex, UK.1991;p255-297.
95. Woehling HL, Wilson GD, Grummer RW, Bray RW, Casida LE. Effects of
stilboestrol and testosterone pellets implanted into growing-fattening pigs.
J Anim Sci.1951;10:889-892.
96. Pearson AM, Combs GE, Wallace HD, Sleeth RB, Stroud JW, Shepherd
JM, Koger M. The effects of stilboestrol implants on swine of different
sexes. J Anim Sci.1952;11:251-260.
97. Sleeth RB, Pearson AM, Wallace HD, Voropf DH, Koger M. Effect of
injection of testosterone, estradiol and a combination of the two upon growing-fattening
swine. J Anim Sci.1953;12:322-330.
98. Bidner TD, Merkel RA, Miller ER. Effect of a combination of diethylstilbestrol
and methyltestosterone on performance, carcass traits, serum and muscle
characteristics of pigs. J Anim Sci.1972;35:525-533.
99. Lucas LE, Peo ER, Jr, Svajgr AJ. Effect of a combination of diethylstilbestrol
and methyltestosterone and protein level in the diet on performance and
carcass traits in an unselected line of swine. J Anim Sci.1973;36:1094-1098.
100. DeWilde RO, Lauwer H. The effect of parenteral use of estradiol,
progesterone, testosterone and trenbolone on growth and carcass composition
in pigs. J Anim Sci.1984;59:1501-1509.
101. Denzer LE, Thompson LH, McKeith FK, Parrett DF, Thomas DL. Evaluation
of growth, carcass traits and reproductive organs of young boars in response
to zeranol implantation. J Anim Sci.1986;62:1164-1171.
102. Kluber EF, III, Minton JE, Stevenson JS, Hunt MC, Davis DL, Hoagland
TA, Nelssen JL. Growth, carcass traits, boar odor and testicular and endocrine
functions of male pigs fed a progestogen, altrenogest. J Anim Sci.1988;66:470-478.
103. Sheridan PJ, Austin FH, Bourke S, Roche JF. The effect of anabolic
agents on growth rate and reproductive organs of pigs. Livest Prod Sci.1990;26:263-275.
104. Martinez M, López-Bote C, Sancho G, Ventanas J. Effects of
trenbolone acetate on swine carcass characteristics and backfat composition.
Can J Anim Sci.1992;72:969-972.
105. Hancock DL, Wagner JF, Anderson DB. Effects of estrogens and androgens
on animal growth. In Pearson AM, Dutson TR, eds. Advances in Meat Research.
Volume 7: Growth Regulation in Farm Animals. Elsevier Applied Science
Publishers: Essex, England. 1991. 255-297.
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