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Effects of Restricted Feed Intake On Heat Energy B
Effects of Restricted Feed Intake On Heat Energy B
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ABSTRACT: Sixteen Boer goat doelings, 16 Spanish ly]. Equations describing the temporal pattern of HE
doelings, and 8 Angora doelings and 8 wethers, 283, (kJ/kg of BW0.75 per day), expressed as a percentage of
316, and 330 d of age initially (SEM = 5.0), respective- the wk-0 value and corrected for corresponding breed
ly, were used to evaluate effects of nutrient restriction × week CONT means, in phase 1 were 95.8 ± 2.43 –
on heat energy (HE). During the first and second 10-wk (8.18 ± 1.144 × week) + (0.655 ± 0.1098 × week2) for
phases, 8 animals of each breed were fed a 50% concen- Angora (R2 = 0.58), 95.3 ± 2.63 – (4.34 ± 1.237 × wk)
trate pelletized diet at a level adequate for maintenance + (0.271 ± 0.1187 × wk2) for Boer (R2 = 0.41), and
and moderate energy accretion (CONT). Other animals 97.4 ± 2.21 − (4.69 ± 1.068 × wk) + (0.282 ± 0.1021
were fed approximately 50% of these amounts in phase × wk2) for Spanish (R2 = 0.53). Phase 2 equations were
1 relative to initial BW, followed by the greater level of 78.9 ± 2.22 + (8.74 ± 1.036 × wk) − (0.608 ± 0.0095
feeding in phase 2 based on initial or actual BW when × wk2) for Angora (R2 = 0.60), 77.5 ± 2.10 + (3.30 ±
greater (REST). Average daily gain was 43, −20, 16, 0.978 × wk) − (0.153 ± 0.0942 × wk2) for Boer (R2 =
−78, 8, and −48 g in phase 1 (SEM = 5.0) and 26, 44, 0.39), and 80.6 ± 2.50 + (4.50 ± 1.165 × wk) − (0.208
50, 65, 27, and 32 g in phase 2 (SEM = 3.5) for An- ± 0.1122 × wk2) for Spanish (R2 = 0.43). These equa-
gora-CONT, Angora-REST, Boer-CONT, Boer-REST, tions indicate that changes in HE in response to nutri-
Spanish-CONT, and Spanish-REST, respectively. Total ent restriction and realimentation were more rapid and
HE was greater for CONT vs. REST in both phases of greater magnitude in Angora vs. Boer and Spanish.
(P < 0.001), greater in phase 1 for Angora than for The temporal pattern of decline in HE by Boer and
Boer (P < 0.01) and Spanish (P < 0.01), and greatest Spanish during restriction was similar, but the subse-
(P < 0.01) in phase 2 among breeds for Angora [481, quent rise with realimentation was slower and smaller
347, 430, 356, 424, and 338 kJ/kg of BW0.75 per day in for Boer. In conclusion, most appropriate methods of
phase 1 (SEM = 11.1), and 494, 479, 445, 397, 444, and predicting change in the maintenance energy require-
406 kJ/kg of BW0.75 per day in phase 2 (SEM = 11.3) ment during and after periods of limited feed intake
for Angora-CONT, Angora-REST, Boer-CONT, Boer- may differ among breeds of goats.
REST, Spanish-CONT, and Spanish-REST, respective-
Key words: energy, feed intake, goat
©2011 American Society of Animal Science. All rights reserved. J. Anim. Sci. 2011. 89:4175–4187
doi:10.2527/jas.2011-3907
4175
4176 Helal et al.
smaller value for a BCS of 1. Sahlu et al. (2004) pro- quirement for ADG was 23.1 and 19.8 kJ/g of ADG for
posed that the MEm of goats be adjusted similarly for Boer and Spanish, with ADG targets of 25 and 17.5 g,
decreased BCS, with smaller adjustments applied with respectively. Requirements for tissue and clean mohair
advancing time (i.e., linear). The NRC (2007) subse- fiber growth were 37.2 and 157 kJ/g, respectively, and
quently recommended this method for goats. anticipated tissue and clean mohair fiber growth for
The NRC (2007) adjustment of MEm for low planes Angora were 12.5 and 7.5 g/d, respectively. However,
of nutrition was not based on actual data with goats ADG of CONT animals was less than expected, result-
and has not been evaluated. There are reports sug- ing in increased feeding in wk 6 to 10 (i.e., to support
gesting that reductions of MEm might be greater than 50 and 35 g of ADG for Boer and Spanish and 20 and 5
20% depending on severity of restriction in ME intake g/d of tissue and clean mohair fiber growth for Angora,
(Brosh et al., 1986; Silanikove, 1986, 1987; Choshniak respectively). When BW did not markedly increase or
et al., 1995; Asmare et al., 2006). However, there have declined, the amount of feed offered was not changed.
not been meaningful comparisons of goat breeds, and With increasing BW in wk 6 to 8 for CONT animals,
linearity of change in MEm during realimentation has feed amounts were increased slightly in wk 9 and 10.
not been evaluated. Hence, the objectives of this exper- The same feeding rates were employed in phase 2 for
iment were to determine effects of restricted feed intake the CONT treatment, with amounts offered increasing
on HE by Angora, Boer, and Spanish goats during and as BW rose. These rates were used for the REST treat-
after limited feed intake. ment in phase 2, except that only a partial increase
was imposed in wk 11 to avoid potential digestive upset
MATERIALS AND METHODS and feeding continued to be based on initial BW when
greater than actual BW. A 50% concentrate pelleted
The protocol for the experiment was approved by the diet (Table 1) was used, with a ME concentration of
Langston University Animal Care Committee. 9.4 MJ/kg of DM used, as determined by Ngwa et al.
(2007a). During a 4-wk preliminary period, this same
Animals and Treatments diet was fed at the CONT level.
Item Trt Brd Int Phase CONT REST CONT REST CONT REST SEM Breed2
BW, kg
Initial, wk 0 0.92 <0.01 0.89 13.7 13.9 21.4 21.5 19.5 19.0 0.82 Angora < Spanish < Boer
End of phase 1 <0.01 <0.01 0.34 16.5 12.8 22.7 16.9 20.1 16.4 0.78 Angora < Boer, Spanish
End of phase 2 <0.01 <0.01 0.39 18.6 15.9 26.5 21.3 22.5 18.8 0.86 Angora < Spanish < Boer
BCS3
Initial, wk 0 0.57 <0.01 0.50 2.66 2.71 3.12 3.05 3.07 3.02 0.055 Angora < Boer, Spanish
End of phase 1 <0.01 0.79 0.05 2.78b 2.25a 3.16c 2.04a 3.03bc 2.04a 0.119
End of phase 2 <0.01 0.12 <0.01 2.66a 2.50a 3.22b 2.39a 3.16b 2.39a 0.115
DMI, g/d <0.01 <0.01 0.17 1 476 234 514 259 441 219 8.9 Spanish < Angora < Boer
<0.01 <0.01 0.62 2 505 435 581 497 486 426 12.2 Angora, Spanish < Boer
ADG, g <0.01 <0.01 <0.01 1 43e −20c 16d −76a 8d −48b 5.0
<0.01 <0.01 0.15 2 26 44 50 65 27 32 3.5 Angora, Spanish < Boer
BCS change <0.01 <0.01 0.07 1 0.12 −0.46 0.03 −1.01 −0.04 −0.97 0.103 Boer, Spanish < Angora
<0.01 0.12 0.67 2 −0.13 0.25 0.06 0.36 0.13 0.34 0.088
<0.01 0.14 <0.01 1–2 −0.01bc −0.21b 0.10c −0.66c 0.09c −0.63a 0.095
Tissue gain, g/d <0.01 <0.01 <0.01 1 33.1e −27.7c 12.9d −77.7a 4.1d −50.4b 4.99
<0.01 <0.01 0.11 2 17.7 37.2 48.1 63.8 24.9 29.8 3.50 Angora, Spanish < Boer
Unwashed fiber growth, g/d <0.01 <0.01 0.67 1 9.6 7.7 3.0 2.0 3.6 2.3 0.50 Boer, Spanish < Angora
<0.01 <0.01 0.04 2 8.2c 6.5b 2.2a 1.7a 2.5a 2.3a 0.31
Clean mohair growth, g/d 0.08 1 6.70 5.33 0.513
0.02 2 6.63b 5.37a 0.350
Restricted intake for different goat breeds
Mid-side patch fiber yield, % 0.03 0.61 0.28 1 70.1 69.3 73.1 57.0 72.4 63.9 4.69
0.21 <0.01 0.03 2 80.6a 82.8a 91.6bc 89.7b 93.5c 90.6b 1.00
Fiber diameter, µm <0.01 <0.01 0.30 1 24.3 22.4 27.5 26.3 25.1 21.5 0.78 Angora, Spanish < Boer
0.21 <0.01 0.36 2 26.2 23.6 36.5 37.6 36.7 32.5 1.85 Angora < Boer, Spanish
a–e
Means in a row without a common superscript letter differ (P < 0.05).
1
Trt = treatment (CONT = intake for moderate energy accretion in 10-wk phases 1 and 2; REST = 50% of CONT intake in phase 1 relative to initial BW, followed by the greater level of feeding
in phase 2 based on initial or actual BW when greater); Brd = breed; Int = interaction between treatment and breed.
2
< indicates P < 0.05 for breed main effect means when the interaction was nonsignificant (P > 0.05).
3
Scores: 1 to 5, with 1 and 5 = extremely thin and obese, respectively.
4179
4180 Helal et al.
Item Trt Brd Int Phase CONT REST CONT REST CONT REST SEM Breed2
BW, kg 0.01 <0.01 0.86 1 14.8 12.9 21.3 18.5 19.4 16.9 0.78 Angora < Boer, Spanish
<0.01 <0.01 0.38 2 17.3 14.1 24.1 18.7 20.9 17.3 0.80 Angora < Spanish < Boer
HE:HR, kJ/kg of BW0.75 per beat
Mean 0.92 <0.01 0.85 4.92 4.90 5.60 5.66 5.60 5.52 0.119 Angora < Boer, Spanish
Before experiment 0.90 <0.01 0.76 4.95 4.95 5.59 5.68 5.56 5.42 0.129
After experiment 4.88 4.85 5.61 5.65 5.63 5.63
ME intake, MJ/d <0.01 <0.01 0.17 1 4.47 2.20 4.84 2.43 4.14 2.06 0.084 Spanish < Angora < Boer
<0.01 <0.01 0.62 2 4.74 4.09 5.46 4.67 4.57 4.01 0.114 Angora, Spanish < Boer
ME intake, kJ/kg of BW0.75 <0.01 <0.01 <0.01 1 597f 328c 490e 277b 449b 249a 4.8
0.02 <0.01 0.35 2 561 568 503 523 467 473 5.3 Spanish < Boer < Angora
HE
Total HE, MJ/d <0.01 <0.01 0.71 1 3.64 2.34 4.26 3.12 3.91 2.82 0.130 Angora < Spanish < Boer
<0.01 0.06 0.24 2 4.20 3.47 4.84 3.56 4.34 3.45 0.160
Total HE, kJ/kg of BW0.75 <0.01 0.02 0.03 1 481c 347a 430b 356a 424b 338a 11.1
<0.01 0.01 0.33 2 494 479 445 397 444 406 11.3 Boer, Spanish < Angora
Maintenance from tissue, MJ/d <0.01 0.01 <0.01 1 0.00a 0.27b 0.00a 0.69b 0.00a 0.75b 0.062
0.84 0.17 0.71 2 0.00 0.00 0.00 0.00 0.01 0.00 0.004
Maintenance from the diet, MJ/d <0.01 <0.01 0.02 1 2.44c 1.36a 4.10d 2.43c 3.82d 2.06b 0.125
<0.01 <0.01 0.10 2 3.18 2.45 4.37 2.94 4.08 3.15 0.163 Angora < Boer, Spanish
Total of maintenance, MJ/d <0.01 <0.01 0.75 1 2.44 1.63 4.10 3.12 3.82 2.82 0.146 Angora < Boer, Spanish
<0.01 <0.01 0.11 2 3.18 2.45 4.37 2.94 4.08 3.15 0.164 Angora < Boer, Spanish
Total of maintenance, kJ/kg of BW0.75 <0.01 <0.01 0.73 1 321 238 414 353 415 338 13.2 Angora < Boer, Spanish
<0.01 <0.01 0.29 2 372 338 402 328 417 370 12.6 Angora, Boer < Spanish
Tissue gain,3 MJ/d <0.01 <0.01 <0.01 1 0.31d 0.00a 0.16c 0.00a 0.09b 0.00a 0.027
<0.01 <0.01 0.17 2 0.14 0.30 0.47 0.62 0.26 0.30 0.032 Angora, Spanish < Boer
Mohair fiber growth, MJ/d 0.08 1 0.89 0.71 0.068 Angora, Spanish < Boer
0.02 2 0.88b 0.72a 0.047
Restricted intake for different goat breeds
RE
Total RE, MJ/d <0.01 <0.01 0.21 1 0.83 −0.15 0.57 −0.69 0.23 −0.75 0.089 Spanish < Boer < Angora
<0.01 <0.01 0.15 2 0.54 0.63 0.62 1.11 0.23 0.56 0.107
Tissue gain,3 MJ/d <0.01 <0.01 <0.01 1 0.21d 0.00a 0.11c 0.00a 0.06b 0.00a 0.018
<0.01 <0.01 0.17 2 0.10 0.20 0.32 0.42 0.18 0.21 0.022 Angora, Spanish < Boer
Mohair fiber growth, MJ/d 0.08 1 0.16 0.13 0.012
0.02 2 0.16b 0.13a 0.008
ME use
Tissue gain,3 MJ/d <0.01 <0.01 <0.01 1 0.52d 0.00a 0.27c 0.00a 0.15b 0.00a 0.045
<0.01 <0.01 0.17 2 0.24 0.50 0.80 1.04 0.43 0.51 0.053 Angora, Spanish < Boer
Mohair fiber growth, MJ/d 0.08 1 1.05 0.84 0.080
0.02 2 1.04b 0.84a 0.055
a–f
Means in a row without a common superscript letter differ (P < 0.05).
1
Trt = treatment (CONT = intake for moderate energy accretion in 10-wk phases 1 and 2; REST = 50% of CONT intake in phase 1 relative to initial BW, followed by the greater level of feeding
in phase 2 based on initial or actual BW when greater); Brd = breed; Int = interaction between treatment and breed.
2
< indicates P < 0.05 for breed main effect means when the interaction was nonsignificant (P > 0.05).
3
Scores: 1 to 5, with 1 and 5 = extremely thin and obese, respectively.
4181
4182 Helal et al.
Table 4. Equations for regressions of heat energy (HE) by different goat breeds expressed as a percentage of HE
in wk 0 for animals subjected to restricted feed intake, corrected for HE of corresponding animals on a constant
plane of nutrition adequate for maintenance and moderate energy accretion, against length of restriction (wk) in
phase 1 or time after restriction ended in phase 2 (HE%CH, MJ/d; HEMBW%CH, kJ/kg of BW0.75)
HE%CH HEMBW%CH
Phase 1
Angora Intercept 97.0 2.05 0.01 0.76 95.8 2.43 0.01 0.58
Week −10.23 0.966 0.01 −8.18 1.144 0.01
Week2 0.801 0.0928 0.01 0.655 0.1098 0.01
Boer Intercept 96.9 2.18 0.01 0.76 95.3 2.63 0.01 0.41
Week −6.39 1.025 0.01 −4.34 1.237 0.01
Week2 0.334 0.0984 0.01 0.271 0.1187 0.03
Spanish Intercept 99.0 1.88 0.01 0.79 97.4 2.21 0.01 0.53
Week −7.03 0.907 0.01 −4.69 1.068 0.01
Week2 0.415 0.0867 0.01 0.282 0.1021 0.01
Phase 2
Angora Intercept 73.4 2.49 0.01 0.71 78.9 2.22 0.01 0.60
Week 9.49 1.160 0.01 8.74 1.036 0.01
Week2 −0.526 0.1115 0.01 −0.608 0.0995 0.01
Boer Intercept 65.1 2.21 0.01 0.63 77.5 2.10 0.01 0.39
Week 3.83 1.03 0.01 3.30 0.978 0.01
Week2 −0.074 0.0992 0.46 −0.153 0.0942 0.11
Spanish Intercept 72.4 2.37 0.01 0.57 80.6 2.50 0.01 0.43
Week 4.74 1.103 0.01 4.50 1.165 0.01
Week2 −0.164 0.1062 0.13 −0.208 0.1122 0.07
of previous studies indicate that the nature of nutrient accurate evaluation of nutrient partitioning to mohair
intake restriction (e.g., length, magnitude) will influ- fiber growth.
ence comparisons of Boer goats and indigenous or local The decline in mohair fiber growth for REST vs.
genotypes with decreased growth potential. CONT in phase 2, which was of similar magnitude to
Greater ADG in phase 2 for Boer vs. Spanish and that in phase 1, is in accordance with a carryover effect
Angora suggests that the period of time after nutri- of restricted feed intake reported by Sahlu et al. (1999)
ent restriction with low HEm relative to MEI for Boer when later consumption was ad libitum. However, the
goats was long compared with Spanish. Greater ADG change in tissue gain noted by Sahlu et al. (1999) was
for Boer compared with Angora and Spanish on the fully compensatory for limited ADG earlier. In accor-
CONT intake treatment in phase 2, in fact greater dance with no effect of different levels of intake during
than in phase 1, also implies an ability of Boer goats the period of restricted feeding, Puchala et al. (2011)
to adapt over time to a moderate nutrient restriction found similar mohair fiber growth by yearling Ango-
for subsequent efficient nutrient use in tissue accretion. ras later with ad libitum consumption. Findings of the
present study along with those of Sahlu et al. (1999)
Fiber and Puchala et al. (2011) indicate that if feed intake
restriction retards real-time mohair fiber growth, sub-
The negative effect of the REST intake treatment sequent fiber growth also will be slowed but to a magni-
on clean mohair fiber growth in phase 1 agrees with tude no greater than during the restriction period. Re-
a small decrease in mohair fiber growth by Angoras sults of Sahlu et al. (1999) regarding compensation in
14 mo of age, in addition to limited tissue gain, ob- tissue growth during realimentation, but with contin-
served by Sahlu et al. (1999). Conversely, Puchala et ued decreased mohair fiber growth, and tissue gain 19.5
al. (2011) noted relatively constant clean mohair fiber g/d greater for REST vs. CONT during phase 2 of the
growth by 6-mo-old Angoras subjected to 6 levels of present experiment indicate that nutrient restriction
restricted feed intake. Nutrient partitioning to mohair has relatively long-term effects on follicle metabolism.
fiber growth neither can be truly confirmed nor refuted Further research would be required to fully character-
in the present experiment or that of Sahlu et al. (1999). ize influences of the length and magnitude of nutrient
That is, nutrient restriction decreased mohair fiber intake restriction on subsequent mohair fiber growth.
growth, but it is unknown if the magnitude of change Even though unwashed fiber growth was consider-
was minimized at the expense of nonfiber tissue gain. ably greater for Angora than for Boer and Spanish,
Studies with multiple levels of feed intake, such as that intake restriction in phase 1 still decreased fiber growth
of Puchala et al. (2011), can potentially provide more by Boer and Spanish, which was due at least in part
Restricted intake for different goat breeds 4185
was deemed inappropriate given substantial differences
in HE and BW among weeks within phases. Weekly HE
was expressed relative to that in wk 0 so that any pre-
diction methods developed could be readily incorporat-
ed into nutrient requirement calculation systems [e.g.,
web-based for goats of Langston University available at
http://www2.luresext.edu, applying recommendations
of Sahlu et al. (2004) and NRC (2007)]. Adjustment of
REST values for mean change of the different breeds at
each measurement time partially corrected for factors
such as procedural variability and increased reflection
of true change in MEm relative to that of animals on a
continual plane of nutrition adequate for maintenance
and moderate tissue and fiber gain. In this regard, for
the CONT intake treatment in phase 1, effects of breed,
week, week2, week × breed, and week2 × breed were
nonsignificant for both HE%CH and HEMBW%CH. In
phase 2 for the CONT treatment, effects were noted for
breed and week in HE%CH and for week and week2 in
HEMBW%CH.
Magnitudes of change in HE%CH for REST were
greater than in HEMBW%CH because of the adjust-
ment for BW0.75 at measurement times with the latter
but not former expression. For most appropriate poten-
Change in HE
Figure 6. Prediction of heat energy (HE) by different goat breeds
expressed as a percentage of HE in wk 0 for animals subjected to
Change in total HE with advancing time during restricted feed intake, corrected for HE of corresponding animals on
phases 1 and 2 was addressed rather than MEm be- a constant plane of nutrition adequate for maintenance and moder-
cause measurement of MEm involved estimates for en- ate energy accretion at different times in phase 2 after restriction
ended (panel A = HE%CH, MJ/d; panel B = HEMBW%CH, kJ/kg
tire phases. Total HE in specific weeks could have been of BW0.75). Weeks 10 to 20 are wk 0 to 10 after change in level of feed
partitioned into HEm based on phase averages, but this intake. Equations are given in Table 4.
4186 Helal et al.
tial application or incorporation of any methods of pre- wk while on a constant adequate plane of nutrition.
diction developed into nutrient requirement calculation Even with an initial BCS of 1, only a 20% decrease in
systems, use of HEMBW%CH is preferable and will be MEm was recommended by NRC (2007), with sequen-
addressed below. tial weekly increases of 2% of MEm for 10 wk while on
From equations in Table 4, the pattern and mag- a constant adequate plane of nutrition. For develop-
nitude of decline in HEMBW%CH for REST during ment of preferable means, extensive experimentation
phase 1 was almost identical for Boer and Spanish, with multiple levels and lengths of nutrient restriction
with average linear and quadratic regression coeffi- and realimentation would be required.
cients of −4.52 and 0.277%/wk, respectively. For both
breeds, HEMBW%CH reached a minimum in wk 6 to
Conclusions
7 at approximately 78% of the wk-0 value, with little
change thereafter through wk 10. Conversely, for Ango-
Although nutrient partitioning cannot be ruled out,
ra HEMBW%CH decreased with advancing time dur-
mohair fiber growth by Angora goats decreased during
ing phase 1 much more rapidly (i.e., linear regression
a 10-wk intake restriction period and the subsequent
coefficient of −8.2%/wk), with the minimum of 70%
10 wk with greater intake. Nutrient intake restriction
at wk 6. Then, HEMBW%CH increased rapidly to wk
resulted in greater BW loss for Boer vs. Spanish goats,
10 to reach nearly 80% in wk 10. Therefore, a differ-
but ADG was greatest for Boer goats in a realimenta-
ent method of adjusting real-time MEm of Angora vs.
tion period. Heat energy by Angora goats decreased
Boer and Spanish goats for a limited nutritional plane
more rapidly and to a greater extent than that by Boer
seems warranted. Reasonably accurate prediction for
and Spanish, although eventually levels converged rela-
Boer and Spanish goats could be achieved through use
tive to values before restricted intake. Likewise, the
of a linear decrease until wk 6, with steady HE thereaf-
speed and magnitude of rise in HE by Angora goats
ter. For Angora goats, inclusion of a quadratic regres-
when intake was increased after restriction was greater
sion coefficient is advisable. However, it is not known
than for Boer and Spanish. The pattern of change in
if similar regression coefficients would be applicable to
HE with increasing length of nutrient restriction was
various magnitudes and lengths of intake restriction or
similar between Boer and Spanish goats, although the
animals of different ages. In general agreement with the
magnitude of increase when feed intake was increased
prediction system suggested by Sahlu et al. (2004) and
was less for Boer, which may have accounted for the
NRC (2007), for each breed final HEMBW%CH was
difference in ADG. Most appropriate methods of pre-
near 80%.
dicting change in HEm during and after periods of lim-
In contrast to phase 1, in phase 2 patterns of change in
ited feed intake may differ among breeds of goats.
HEMBW%CH differed between Boer and Spanish. The
rate of increase for Spanish was greater than for Boer
(i.e., linear regression coefficients of 3.30 and 4.50%/ LITERATURE CITED
wk for Boer and Spanish, respectively). As in phase
1, change in HEMBW%CH for Angora with advanc-
AFRC. 1998. The Nutrition of Goats. CAB Int., New York, NY.
ing week was much greater than for Boer and Spanish AOAC. 1990. Official Methods of Analysis. 15th ed. Assoc. Off.
(i.e., linear regression coefficient of week for Angora of Anal. Chem., Arlington, VA.
8.74%/wk). Likewise, HEMBW%CH peaked in wk 16 Asmare, A., R. Puchala, R. C. Merkel, T. Sahlu, and A. L. Goetsch.
to 18 and declined in wk 19 and 20 (quadratic regres- 2006. Changes in energy expenditure by meat goats with vary-
sion coefficient of −0.608%/wk). Mean values in wk 20 ing levels of feed intake near maintenance and below. J. Appl.
Anim. Res. 29:81–89.
for Angora and Spanish were similar at approximately ASTM. 1988. Standard Tests Method D584: Wool content of wool-
105%, both considerably greater than between 94 and laboratory scale. In Annual Book of ASTM Standards. Am.
95% for Boer. Patterns of change in HEMBW%CH for Soc. Testing Materials, Philadelphia, PA.
Angora goats in both phases imply less stringent or Berhan, T., R. Puchala, A. L. Goetsch, and R. C. Merkel. 2006.
tight regulation of HE and MEm compared with meat Effects of walking speed and forage consumption on energy ex-
penditure and heart rate by Alpine does. Small Rumin. Res.
goat breeds of Boer and Spanish. 63:119–124.
To potentially adjust MEm of goats during a reali- Brosh, A. 2007. Heart rate measurements as an index of energy ex-
mentation period, these results suggest that different penditure and energy balance in ruminants: A review. J. Anim.
methods should be considered both for Angora than for Sci. 85:1213–1227.
meat goat breeds such as Boer and Spanish and also Brosh, A., A. Shkolnik, and I. Choshniak. 1986. Metabolic effects
of infrequent drinking and low-quality feed on Bedouin goats.
for different meat goat breeds. Furthermore, results of Ecology 67:1086–1090.
this experiment are not in close accordance with recom- Brouwer, E. 1965. Report of sub-committee on constants and fac-
mendations of Sahlu et al. (2004) and NRC (2007) for tors. Pages 441–443 in Energy Metabolism: Proceedings of the
adjusting MEm of goats for previous low planes of nutri- 3rd Symp. K. L. Blaxter, ed. EAAP Publ. No. 11. Academic
tion. For example, with an initial BCS of 2 after a low Press, London, UK.
Choshniak, I., N. Ben-Kohav, C. R. Taylor, D. Robertshaw, R. J.
plane of nutrition, the NRC (2007) adjustment of MEm Barnes, A. Dobson, V. Belkinb, and A. Shkolnik. 1995. Meta-
for all goat breeds is a 10% reduction in wk 1, followed bolic adaptations for desert survival in the Bedouin goat. Am.
by sequential weekly increases of 1.67% of MEm for 6 J. Physiol. 268:R1101–R1110.
Restricted intake for different goat breeds 4187
Downes, A. M., and L. F. Sharry. 1971. Measurement of wool growth and energy expenditure in Alpine, Angora, Boer and Spanish
and its response to nutritional changes. Aust. J. Biol. Sci. goat wethers goats consuming different quality diets at level
24:117–130. of intake near maintenance or fasting. Small Rumin. Res.
Drochner, W., G. Flachowsky, J. Pallauf, E. Pfeffer, M. Rodehu- 70:183–193.
tscond, and W. Staudacher. 2003. Recommendations for the Puchala, R., I. Tovar-Luna, T. Sahlu, H. C. Freetly, and A. L.
Supply of Energy and Nutrients to Goats. DLG-Verlag, Frank- Goetsch. 2009. The relationship between heart rate and energy
furt, Germany. expenditure in growing crossbred Boer and Spanish wethers. J.
Freetly, H. C., J. A. Nienaber, K. A. Leymaster, and T. G. Jenkins. Anim. Sci. 87:1714–1721.
1995. Relationships among heat production, body weight, and Reis, P. J., and D. A. Tunks. 1976. The influence of abomasal sup-
age in Suffolk and Texel ewes. J. Anim. Sci. 73:1030–1037. plements of zein and some amino acids on wool growth and
Galbraith, H. 2000. Protein and sulphur amino acid nutrition of hair plasma amino acids. J. Agric. Sci. 86:475–482.
fibre-producing Angora and Cashmere goats. Livest. Prod. Sci. Restall, B. J., H. Restall, M. Restall, and A. Perry. 1994. Seasonal
64:81–93. production of cashmere and environmental modification in Aus-
Ivey, D. S., F. N. Owens, T. Sahlu, T. H. Teh, P. L. Claypool, and A. tralian Cashmere goats. Pages 63–74 in Hormonal Control of
L. Goetsch. 2000. Growth and cashmere production by Spanish Fibre Growth and Shedding. J. P. Laker and D. Allain, ed.
goats consuming ad libitum diets differing in protein and energy European Fine Fibre Network, Vol. 2. Macaulay Land Use Re-
levels. Small Rumin. Res. 35:133–139. search Institute, Aberdeen, Scotland.
Joemat, R., A. L. Goetsch, G. W. Horn, T. Sahlu, R. Puchala, Russel, A. J. F. 1995. Current knowledge on the effects of nutrition
B. R. Min, and J. Luo. 2004. Growth of yearling meat goat on fibre production in nutrition and grazing ecology of special-
doelings with changing plane of nutrition. Small Rumin. Res. ity fibre-producing animals. Pages 3–21 in Hormonal Control of
52:127–135. Fibre Growth and Shedding. J. P. Laker and A. J. F. Russel,
Littell, R. C., G. A. Milliken, W. W. Stroup, and R. D. Wolfinger. ed. European Fine Fibre Network, Vol. 3. Macaulay Land Use
1996. SAS® Systems for Mixed Models. SAS Inst. Inc., Cary, Research Institute, Aberdeen, Scotland.
NC. Sahlu, T., A. L. Goetsch, J. Luo, I. V. Nsahlai, J. E. Moore, M.
Luo, J., A. L. Goetsch, I. V. Nsahlai, T. Sahlu, C. L. Ferrell, F. N. L. Galyean, F. N. Owens, C. L. Ferrell, and Z. B. Johnson.
Owens, M. L. Galyean, J. E. Moore, and Z. B. Johnson. 2004. 2004. Energy and protein requirements of goats: Developed
Prediction of metabolizable energy and protein requirements equations, other considerations and future research to improve
for maintenance, gain and fiber growth of Angora goats. Small them. Small Rumin. Res. 53:191–220.
Rumin. Res. 53:339–356. Sahlu, T., S. P. Hart, and A. L. Goetsch. 1999. Effects of level
Nagorcka, B. N. 1977. The description and analysis of wool growth. of feed intake on body weight, body components, and mohair
Aust. J. Agric. Res. 28:737–746. growth in Angora goats during realimentation. Small Rumin.
Negesse, T., A. K. Patra, L. J. Dawson, A. Tolera, R. C. Merkel, T. Res. 32:251–259.
Sahlu, and A. L. Goetsch. 2007. Performance of Spanish and Sainz, R. D., and B. E. Bentley. 1997. Visceral organ mass and cel-
Boer × Spanish doelings consuming diets with different levels lularity in growth-restricted and refed beef steers. J. Anim.
of broiler litter. Small Rumin. Res. 69:187–197. Sci. 75:1229–1236.
Ngwa, A. T., L. J. Dawson, R. Puchala, G. Detweiler, R. C. Merkel, Shargal, E., A. Brosh, and I. Choshniak. 2001. Heart rate as measure
I. Tovar-Luna, T. Sahlu, C. L. Ferrell, and A. L. Goetsch. of energy expenditure and energy intake in the black Bedouin
2007a. Effect of initial body condition of Boer × Spanish year- goat. Abstract ID number 1975 on CD in Proc. 34th Int. Congr.
ling goat wethers and level of nutrient intake on body composi- Physiol. Sci. Int. Union Physiol. Sci., Christchurch, NZ.
tion. Small Rumin. Res. 73:13–26. Silanikove, N. 1986. Interrelationships between feed quality, digest-
Ngwa, A. T., L. J. Dawson, R. Puchala, G. Detweiler, R. C. Merkel, ibility, feed consumption, and energy requirements in desert
I. Tovar-Luna, T. Sahlu, C. L. Ferrell, and A. L. Goetsch. (Bedouin), and energy requirements in desert (Bedouin) and
2007b. Urea space and body condition score to predict body non-desert (Saanen) goats. J. Dairy Sci. 69:2157–2162.
composition of meat goats. Small Rumin. Res. 73:27–36. Silanikove, N. 1987. Effect of imposed reduction in energy intake on
Ngwa, A. T., L. J. Dawson, R. Puchala, G. D. Detweiler, R. C. resting and fasting heart production in the black Bedouin goat.
Merkel, Z. Wang, K. Tesfai, T. Sahlu, C. L. Ferrell, and A. L. Nutr. Rep. Int. 35:725–731.
Goetsch. 2009. Effects of breed and diet on growth and body Tovar-Luna, I., A. L. Goetsch, R. Puchala, T. Sahlu, G. E. Carstens,
composition of crossbred Boer and Spanish wether goats. J. H. C. Freetly, and Z. B. Johnson. 2007a. Effects of moderate
Anim. Sci. 87:2913–2923. feed restriction on energy expenditure by 2-year-old crossbred
NRC. 1981. Nutrient Requirements of Goats: Angora, Dairy, and Boer goats. Small Rumin. Res. 72:25–32.
Meat Goats in Temperate and Tropical Countries. Natl. Acad. Tovar-Luna, I., A. L. Goetsch, R. Puchala, T. Sahlu, G. E. Carstens,
Press, Washington, DC. H. C. Freetly, and Z. B. Johnson. 2007b. Efficiency of energy
NRC. 2000. Nutrient Requirements of Beef Cattle (Update 2000). use for maintenance and gain by growing crossbred Boer and
Natl. Acad. Press, Washington, DC. Spanish goats consuming diets differing in forage level. Small
NRC. 2007. Nutrient Requirements of Small Ruminants. Sheep, Rumin. Res. 67:20–27.
Goats, Cervids, and New World Camelids. Natl. Acad. Press, Tovar-Luna, I., R. Puchala, T. Sahlu, H. C. Freetly, and A. L.
Washington, DC. Goetsch. 2011. Effects of level of feeding on energy utilization
Puchala, R., A. Patra, A. L. Goetsch, G. Animut, and T. Sahlu. by Angora goats. J. Anim. Sci. 89:142–149.
2011. Effects of feed restriction and subsequent realimentation Wester, T. J., R. A. Britton, T. J. Klopfenstein, G. A. Ham, D. T.
on tissue and mohair fiber by growing Angora goats. Livest. Hickok, and C. R. Krehbiel. 1995. Differential effects of plane of
Sci. 138:180–186. protein or energy nutrition on visceral organs and hormones in
Puchala, R., I. Tovar-Luna, A. L. Goetsch, T. Sahlu, G. E. Carstens, lambs. J. Anim. Sci. 73:1674–1688.
and H. C. Freetly. 2007. The relationship between heart rate