Trenbolone chemical structureFinaplix Gold, Manufactured by Valopharm
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Trenbolone

Trenbolone is an anabolic steroid used by veterinarians on livestock to increase muscle growth and appetite. To increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate (Finaplix Gold from Valopharm USA, TREMBLONA QV75from Quality Vet, Mexico), or trenbolone cyclohexylmethylcarbonate (Parabolan from Laboratoires NEGMA until 1997). Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor. more...

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No trenbolone compounds have been approved by the FDA for human use, due to a lack of clinical applications and considerable negative side-effects. It is classified as a Schedule III drug under the Controlled Substances Act. However, bodybuilders have been known to use the drug illicitly in order to increase body mass more effectively than by weight training alone.

Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5α-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure and increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. The use of the drug over extended periods of time can lead to kidney damage and sterility for both sexes. The kidney toxicity has not yet been proven.

A normal body-building dosage can range from 200mgs/week up to 500 plus mgs/week. Due to it's relatively short metabolic half-life, dosages should commonly be split into injections at least once every two days.

Trenbolone cyclohexymethylcarbonate has effects identical to those of trenbolone acetate as they produce the same active metabolite, but has a significantly longer elimination half-life: up to a week rather than one or two days.

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Effects of Feed Intake Restriction on Performance and Carcass Characteristics of Finishing Beef Steers1,2
From Professional Animal Scientist, 6/1/04 by Drager, C D

Abstract

Crossbred steers (n = 264, 311 ± 1.6 kg initial BW) were blocked by BW, randomly assigned to one of four treatments (28 pens, 7 pens per treatment), and fed a common 90% concentrate diet to determine the effects of the severity of caloric restriction on animal performance and carcass characteristics. Treatments were 1) ad libitum access to feed for 151 d (AL100); 2) 75% of DMI by AL100 for 65 d, 95% of DMI by AL100 for 65 d, and ad libitum access to feed for 21 d (AL85); 3) 80% of DMI by AL100 for 65 d, 100% of DMI by AL100 for 65 d, and ad libitum access to feed for 21 d (AL90); and 4) 85% of DMI by AL100 for 65 d, 105% of DMI by AL100 for 65 d, and ad libitum access to feed for 21 d (AL95). Feed was offered for AL85, AL90, and AL95 based on DMI by AL100 the previous week. All steers were fed a similar quantity of DM for 4 d prior to initial, interim, and final BW determinations to minimize gastrointestinal fill differences. Overall DMI was greater (P0.10) between AL100 and the average of the remaining treatments. Overall ADG and ADG:DMI (carcass-adjusted) responded quadratically (P

(Key Words: Caloric Restriction, Restricted Feeding, Limit Feeding.)

Introduction

Evidence suggests that maximum feed intake by feedlot cattle may not support maximum gain efficiency (Meissner et al., 1995; Ferrell and Jenkins, 1998). Numerous methods of offering feedlot cattle less feed than could be consumed by offering ad libitum access have been developed (Galyean, 1999) as strategies to increase animal performance, simplify bunk management, or both. Execution of these methods generally imposes either continuous DMI restriction to a constant degree throughout the feeding period, DMI restriction to a constant degree for a fraction of the feeding period followed by a period of ad libitum access to feed, or DMI restriction to various degrees for various durations during the feeding period followed by a final period of ad libitum access to feed.

Previous data indicate that using the latter approach of programming intake by steers to support an increasing rate of gain can increase gain efficiency 8 to 9% without altering ADG, days on feed, or carcass quality (Knoblich et al. 1997; Loerch and Fluharty, 1998). In the work by Knoblich et al. (1997) and Loerch and Fluharty (1998), dietary CP was increased as DMI restriction increased to provide a similar quantity of CP daily. Rossi et al. (2000; Exp. 1) reported that animal performance did not differ between steers fed either 14 or 12% CP diets at an average of 84% of ad libitum for 150 d of a 184-d feeding period compared with steers allowed ad libitum access to a 12% CP diet for 170 d. Further data describing the effects of incremental DMI increases on performance by finishing steers fed a common diet for an equal number of total days on feed are not available. In addition, Wilson and Osbourn (1960) suggested that the duration of the period of restriction and the pattern of re-alimentation are important determinants of the extent of growth compensation. The objective of the present study was to evaluate the effects of the severity of caloric restriction, independent of duration, on performance and carcass characteristics of steers.

Materials and Methods

Animals and Diets. Two hundred seventy-six crossbred steers were received from Oklahoma and Kansas at the West Texas A&M Research Feedlot over 8 d in june 2000. all procedures used were reviewed and approved by the Amarillo-Area Cooperative Research, Education, and Extension Triangle Animal Care and Use Committee (protocol number 2000 - 09). Animais were processed on the morning following arrival. Processing included individual identification with a numbered ear tag in the left ear (Allflex®; Brussels Agri Services, Brussel, Ontario, Canada), individual BW determination, vaccination against viral antigens (IBR, PI^sub 3^, BRSV, BVD; Reliant 4®; Merial Animal Health, Iselin, NJ) and clostridial organisms (Vision 7®; Bayer Animal Health, Shawnee Mission, KS), treatment for internal and external parasites (Dectomax®; Pfizer Animal Health, Exton, PA), and excision of previous implant(s). all BW measurements taken during the experiment were acquired using a single animal scale. Scale accuracy was verified before BW determination using twenty 22.67-kg certified weights; the scale was calibrated as needed. Twelve steers were determined to be ineligible for the study because of health problems or lack of conformity with BW of the remaining steers.

Cattle were fed a common 65% concentrate diet (Table 1) at 1.5% of BW for 4 d to minimize fill differences before beginning the study. Two hundred sixty-four steers were individually weighed, implanted (36 mg of zeranol; RaIgro®; Schering-Plough, Union, NJ), blocked by BW, and randomly assigned to one of four treatments (7 pens per treatment) on june 19, 2000. Study pens (6.1 m × 27.4 m) were soil-surfaced, contained an individual water tank, allowed 16.7 to 18.5 m^sup 2^ of pen space per animal, and allowed 31 to 34 cm of bunk space per animal. Cattle were re-implanted with Revalor-S® (28 mg of estradiol + 120 mg of trenbolone acetate; Hoechst Roussel Vet, Warren, NJ) on d 56.

Treatments. Based on previous data (Knoblich et al., 1997), the experiment was designed to include a final period of ad libitum access to feed for 28 d (Period 3). The remainder of the projected feeding period was divided into two DMI restriction periods of equal length (Periods 1 and 2), and the magnitude of increased DMI from Periods 1 to 2 was similar across treatments. In addition, a review of six feedlot studies (unpublished observations) employing at least one interval of DMI restriction followed by a final period of ad libitum access to feed suggested that an expected compensatory DMI increase following a period of restriction may be approximately 2 to 10% greater than DMI by cattle allowed ad libitum access. The final period in the present study was abbreviated to 21 d because DMI and ADG were greater than initially projected. Therefore, treatments were as follows 1) ad libitum access to feed for 151 d (ALlOO); 2) 75% of DMI by ALlOO for 65 d, 95% of DMI by ALlOO for 65 d, and ad libitum access to feed for 21 d (AL85); 3) 80% of DMI by ALlOO for 65 d, 100% of DMI by ALlOO for 65 d, and ad libitum access to feed for 21 d (AL90); and 4) 85% of DMI by ALlOO for 65 d, 105% of DMI by ALlOO for 65 d, and ad libitum access to feed during Period 3 (AL95).

All steers were adapted to a common 90% concentrate diet by feeding 65, 75, and 82.5% concentrate diets (Table 1) for 6 d each, including a 3-d transition period between diets. Diet transitions were made by offering equal NE8 on d 1 of the new diet. During the adaptation period, DMI by AL85, AL90, and AL95 treatments was increased at a rate similar to ALlOO steers until ALlOO steers refused feed or until assigned pens reached 75% (AL85), 80% (AL90), or 85% (AL95) of predicted overall feed intake. Thereafter, DMI by AL85, AL90, and AL95 was adjusted weekly based on DMI the previous week by ALlOO. Feed was offered at approximately 110% of ad libitum for steers on ALlOO, and orts were weighed weekly and DM determined. Increases in feed offered between periods were accomplished by offering an additional 0.2 kg of DM/d until the desired DMI was achieved. Potential differences in gastrointestinal fill prior to determining ending BW of Periods 1, 2, and 3 were minimized by feeding all steers 75, 90, and 90%, respectively, of DMI the previous week by ALlOO steers for 4 d.

Carcass Evaluation. Steers were shipped to a commercial slaughter facility (IBP, Amarillo, TX) to be harvested after an average of 151 d of feeding. hot carcass weight was determined immediately after slaughter, and carcasses were evaluated after chilling for approximately 48 h for longissimus area; fat thickness over the 12th rib; percentage kidney, pelvic, and heart fat; yield grade; marbling score; and quality grade (USDA, 1997) by the Beef Carcass Research Center personnel of West Texas A&M University.

Laboratory Procedures. Weekly diet samples were composited gravimetrically within 4-wk intervals and were ground in a Wiley mill to pass a 1-mm screen. These samples and samples of orts were analyzed for DM (100°C for 24 h). Following digestion of diet samples in a block digester, digested samples were analyzed for N and P using automated procedures (Technicon, 1977).

Statistical Analyses. Carcass-adjusted final BW of all steers was calculated as hot carcass weight divided by overall mean dressing percentage. Overall performance on a live basis is not presented because hides contained a noticeable amount of mud at the end of Period 3. Data were analyzed as a randomized complete block design. The distribution of the number of carcasses grading Choice, Prime + Choice, Select, and Select + Standard were analyzed by Chi-square using CATMOD procedures of SAS® (SAS Inst., Inc., Cary, NC). Liver abscess score and number of carcasses grading Prime and Standard were not analyzed because of a limited number of observations.

Remaining data were analyzed using the MIXED procedures of SAS® (SAS Inst., Inc.) with pen as the experimental unit. Performance data were not analyzed as repeated measures because all periods were not of equal length. The fixed effect of treatment and the random effect of block were included in the model. Actual overall DMI during the restriction periods were 92.9, 89.9, and 86.4% of DMI by steers allowed ad libitum access for AL95, AL90, and AL85, respectively. Therefore, contrast coefficients for these unequally spaced treatments were determined using IML procedures of SAS( (SAS Inst., Inc.). Orthogonal contrasts were used to separate means and were as follows: 1) ALlOO v.v the average of AL85, AL90, and AL95; 2) linear effects among AL85, AL90, and AL95; and 3) quadratic effects among AL85, AL90, and AL95. The significance level for all analyses was set at 0.10.

Results and Discussion

Period 1. Four steers died during the study for reasons unrelated to treatment: one steer from treatment AL95, two steers from AL90, and one steer from AL85. Feed DM consumed by deceased steers was adjusted based on average pen DMI. An additional AL90 steer was removed after the study started because of marked BW loss unrelated to treatment (hardware). Only the DMI to meet NE^sub m^ (NRC, 1996) was deducted for this steer because estimates of NE^sub m^ derived from mobilized tissue for growing animals are lacking and gut fill was not quantified. Performance data (Table 2) are presented with deceased animals removed.

As designed, Period 1 DMI was greater (P0.54) among treatments.

Steers in the present study were restricted to 75, 80, or 85% of ad libitum during Period 1. Previous data support our observations of less DMI resulting in reduced ADG (Rossi et al., 2000; Rossi and Loerch, 2001; Rossi et al., 2001) compared with allowing ad libitum access to feed. Steers in the present study were fed a common diet throughout finishing. With the exception of Rossi et al. (2000) and Rossi et al. (2001; Exp. 1), formulated dietary CP concentration in previous studies has generally been increased as feed intake restriction has increased. Thus, changes in BW gain efficiency from feed intake restriction in the majority of previous data include a small dietary NE dilution from replacement of grain with protein sources.

The lack of an effect of feed intake restriction on gain efficiency has been reported for steers restricted to 80 (Loerch and Fluharty, 1998; Exp. 2) or 81% of ad libitum (Rossi et al., 2001; Exp. 2) for approximately 60 to 70 d. In contrast, Rossi and Loerch (2001; Exp. 2) reported that gain efficiency was increased 5% for steers restricted to 76% of ad libitum for approximately 65 d. Gain efficiency has more commonly been decreased by feed restriction early in the overall feeding period; gain efficiency has been decreased (numerically or statistically) 4 to 8% when steers were restricted from 71 to 80% of ad libitum for approximately 30 to 95 d (Knoblich et al., 1997; Loerch and Fluharty, 1998; Rossi et al., 2000; Rossi et al., 2001). These data suggest that restricting steer DMI >20% of ad libitum may adversely affect gain efficiency. Sainz (1995) reviewed the literature and indicated that feed intake restriction >15% of ad libitum decreased gain efficiency. Present data suggest that gain efficiency is not adversely affected when steer DMI of an isoclaoric diet is restricted to 75% of ad libitum.

Period 2. The DMI in Period 2 by AL90 did not equal DMI by ALlOO nor did DMI by AL95 exceed ALlOO as expected, suggesting that the restriction in Period 1 might have been of insufficient severity, duration, or both to translate into a subsequent feed intake response. Thus, steers assigned to treatments AL95 and AL90 actually had ad libitum access to feed during Period 2. Steer DMI was approximately 3% greater (P0.30) among treatments, and ADG:DMI was 3.5% greater (P

The inability of AL90 and AL95 to consume the targeted quantities of DM was unexpected. Although gastrointestinal organ weight of sheep was reduced by DMI restriction (Burrin et al., 1990; McLeod and Baldwin, 2000), the data of Wright and Russel (1991) indicated that gastrointestinal organ weight of cattle restricted to 71% of ad libitum for approximately 200 d was comparable with that of unrestricted cattle after 35 d of refeeding. The improvement in gain efficiency in the second restriction period in the present study was considerably less than observed in previous studies in which duration of restriction (i.e., length of Periods 1 and 2) varied by approximately 5 to 25 d.

Rossi and Loerch (2001) increased steer DMI from 80 to 98% of ad libitum and reported that ADG was numerically 6% greater and ADG:DMI was 9% greater than steers allowed ad libitum access to feed. In a second study (Rossi and Loerch, 2001), ADG was similar, and ADG:DMI was 12% greater, when steer DMI was increased from 76 to 91% of ad libitum than when steers were allowed ad libitum access to feed. Rossi et al. (2001) indicated that ADG:DMI was 20, 20, and 26% greater as steer DMI was increased from 74 to 90, 76 to 91, and 81 to 95% of ad libitum, respectively. Knoblich et al. (1997; Exp. 1) increased steer DMI from 76 to 92% and 75 to 85% of ad libitum and observed that ADG:DMI was 28 to 30% greater than steers allowed ad libitum access, whereas increasing DMI from 74 to 80% of ad libitum resulted in 17% greater ADG:DMI. Rossi et al. (2000; Exp. 1) indicated that ADG:DMI was 16% greater when steer DMI was increased from 77 to 91% or from 78 to 90% of ad libitum. Perhaps the greater magnitude of increased DMI by AL85, AE90, and AE95 from Period 1 to Period 2 in the present study and(or) equal duration of restriction used across treatments compared with previous studies precluded a more marked increase in gain efficiency.

Period 3. Period 3 DMI did not differ (P>0.39) among treatments, whereas Period 3 ADG was less (P

The DMI response of restricted steers in Period 3 was in contrast to that reported by Rossi and Eoerch (2001; Exp.l), where steers consumed approximately 18% more during a period of ad libitum access to feed following a pattern of restriction similar to that in the present study (80 and 98% of ad libitum for approximately 70 and 80 d, respectively) than steers allowed ad libitum access. Eoerch and FIuharty (1998; Exp. 2) fed steers 80 and 98% of ad libitum in consecutive periods (70 and 56 d, respectively) and indicated that DMI during a final period of ad libitum access to feed did not differ between previously restricted steers and steers allowed ad libitum access to feed. In the present study, AL85, AL90, and AL95 steers gained an average of 13% more BW/d when allowed ad libitum access to feed (Period 3) than control steers. Average daily gain for the previously restricted steers of Loerch and FIuharty (1998; Exp. 2) was numerically increased by approximately 9%, whereas Rossi and Loerch (2001) indicated that ADG by previously restricted steers was either increased (25%; Rxp. 2) or numerically increased approximately 16% (Exp. 1).

Overall Performance. Overall DMI was greater (P0.49) between ALlOO and the average of remaining treatments. Overall ADG:DMI responded quadratically (73

The increase in DMI by previously restricted cattle when allowed ad libitum access to feed agrees with previously reported data for steers that were prescribed to incremental increases in DMI and ADG (Knoblich et al.,1997; Rossi and Loerch, 2001; Rossi et al., 2001). Steers in several previous studies were fed to a common BW endpoint, allowing a longer duration in interim and final periods in which ADG for restricted steers was greatest. Gain efficiency has been increased 4 to 9% for restricted steers fed O to 2 d longer overall than unrestricted steers [Knoblich et al., 1997 (Exp. 1); Loerch and Fluharty, 1998 (Exp. 2); Rossi et al., 2001]. The 6% greater gain efficiency by AL90 than remaining treatments in the present study seems to agree with these data and suggests that gain efficiency of finishing steers may be improved by restricting DMI to 80% of ad libitum for 65 d of a 151-d feeding period. However, steer ADG under these conditions was numerically less.

Carcass Characteristics. hot carcass weight (Table 3) was heavier (/MIOl) for ALlOO than for the average of remaining treatments and responded quadratically (P0.34) between ALlOO and remaining treatments; however, fat thickness decreased linearly (P0.34).

Earlier investigations into incremental increases in BW gain through previous feed restriction have reported little influence on carcass characteristics (Knoblich et al., 1997; Loerch and Fluharty, 1998) or decreased fat thickness and marbling score (Rossi et al., 2000) when cattle were fed to the same final BW. However, cattle in the present study were fed a similar number of days. The hot carcass weight response across treatments was approximately twice the magnitude of decreased hot weight computed from previous studies in which restricted and unrestricted cattle were fed a similar number of days [Knoblich et al., 1997 (Exp. 1); Loerch and Fluharty, 1998 (Exp. 2); Rossi et al., 2001]. Eongissimus area seemed to mirror the response observed for hot carcas weight, which supports data regarding the relationship between longissimus area and BW (Price, 1977; Yambayamba et al., 1996).

According to Berg and Butterfield (1976), there is a tendency during re-alimentation for cattle to replenish intermuscular fat before rebuilding the subcutaneous depot. Measures of intermuscular fat mass were not obtained in the present study, whereas fat thickness was similar between the averages of AE95, AL90, and AL85 and AElOO. Restricting DMI more than an average of 90% of ad libitum over 130 d of the 151-d feeding period was necessary to reduce fat thickness markedly, whereas measures of perirenal and intramuscular fat were generally reduced by all DMI restriction treatments. The combination of the tendency for lesser carcass quality when DMI was restricted and the numeric shifts in yield grade distribution would be expected to have practical economic implications to a feeder. Average carcass prices tabulated from actual quality and yield grade data (excluding carcasses that were dark, heavy, light, bloodshot, or >3.99 yield grade) were $2.59, $2.60, $2.61, and $2.57/kg for AElOO, AE95, AE90, and AE85, respectively.

Implications

Gain efficiency by finishing yearling steers was neither improved nor adversely affected by restricting feed intake up to 75% of ad libitum for the initial 65 d of the feeding period, and steers fed 75 to 85% of ad libitum during this time were not able to subsequently consume more DM than steers allowed ad libitum access to feed. When duration of caloric restriction and length of the feeding period were controlled, programmed feeding to attain graded increases in feed intake by finishing yearling steers generally resulted in slower overall daily BW gain, lower marbling score, and carcasses that were lighter and leaner than yearling steers allowed ad libitum access to feed.

1 THe authors gratefully acknowledge support provided through product donation by Schering-Plough Animal Health, Pfizer Animal Health, Roche Vitamins, and Elanco Animal Health.

2 This manuscript, approved as publication number AREC 03-49, reports research partially supported by the Texas Agricultural Experiment Station, The Texas A&M Universitv Svstem.

Literature Cited

Berg, R. T., and R. M. Buttcrfleld. 1976. New Concepts of Cattle Growth. Sydney University Press, Sydney, Australia.

Burrin, D. G., C. L. Ferrell, R. A. Britton, and M. Bauer. 1990. Level of nutrition and visceral organ size and metabolic acivity in sheep. Br. J. Nutr. 64:439.

Ferrell, C. L., and T. G. Jenkins. 1998. Body composition and energy utilization by steers of diverse genotypes fed a high-concentrate diet during the finishing period: II. Angus, Boran, Brahman, Hereford, and TuIi sires. J. Anim. Sei. 76:647.

Galyean, M. L. 1999. Review: Restricted and programmed feeding of beef cattle-definitions, application and research results. Prof. Anim. Sei. 15:1.

Knoblich, H. V., F. L. Fluharty, and S. C. Loerch. 1997. Effects of programmed gain strategies on performance and carcass characteristics of steers. J. Anim. Sei. 75:3094.

Loerch, S. C., and F. L. Fluharty. 1998. Effects of programming intake on performance and carcass characteristics of feedlot cattle. J. Anim. Sei. 76:371.

McLeod, K. R., and R. L. Baldwin, VI. 2000. Effects of forage:concentrate ratio and metabolizablc encregy intake on visceral organ growth and in vitro oxidative capacity of gut tissues in sheep. J. Anim. Sei. 78:760.

Meissner, H. H., M. Smutz, and D. V. Paulsmeler. 1995. The relationship between feed Intake, dally gain, and feed efficiency in fast-growing feedlot steers. In: Symposium: Intake by Feedlot Cattle P-492, p 49. Oklahoma Agric. Exp. Stn., Stillwater.

NKC. 1996. Nutirtional Requirements for Beef Cattle. (7th ed.). National Academy Press, Washington, DC.

Price, M. A. 1977. The effects of severe feed restriction on bulls and steers. 11. Carcass composition. Aust. J. Agrlc. Res. 28:529.

Kossi, J. E., and S. C. Loerch. 2001. Proportion of corn silage in diets of feedlot steers fed to achieve stepwise increases in growth. J. Anim. Sei. 79:1402.

Rossi, J. E., S. C. Loerch, and F. L. Fluharty. 2000. Effects of crude protein concentration in diets of feedlot steers fed to achieve stepwise increases in rate of gain. J. Anim. Sei. 78:3036.

Rossi, J. E., S. C. Loerch, S. J. Moeller, and J. P Schoonmaker. 2001. Effect of programmed growth rate and days fed on performance and carcass characteristics of feedlot steers. J. AnIm. Sei. 79:1394.

Sainz, R. D., 1995. Why does feed restriction improve feed efficiency? In Symposium: Intake by Feedlot Cattle P-942. p 175. Oklahoma Agric. Exp. Stn., Stillwater.

Technicon. 1977. Individual/simultaneous determination of nitrogen and/or phosphorus in BD acid digests. Tech n icon Autoanalyzcr II Industrial Method No. 320-74W/B. Technicon, Tarrytown, NY.

USDA. 1997. Official U. S. Standards for Grades of Carcass Beef. AMS, USDA, Washington, DC.

Wilson, P. N., and D. F. Osbourn. 1960. Compensatory growth after undernutrition in mammals and birds, liiol. Rev. 35:324.

Wright, I. A., and AJ F. Russel. 1991. Changes in the composition of beef cattle during compensatory growth. Anim. Prod. 52:105.

Yambayamba, E.S.K, M. A. Price, and S.D.M. Jones. 1996. Compensatory growth of carcass tissues and visceral organs In beef heifers. Livest. Prod. Sci. 46:19.

C. D. DRAGER3, M. S. BROWN, PAS, M. B. JETER, and P. F. DEW

Division of Agriculture, West Texas A&M University, Canyon and Texas Agricultural Experiment Station, Amarillo

3 To whom correspondence should be addressed: msbrown@mail.wtamu.edu

Copyright American Registry of Professional Animal Scientists Jun 2004
Provided by ProQuest Information and Learning Company. All rights Reserved

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