Printer Friendly

Seasonal production performance of Angora rabbits under sub-temperate Himalayan conditions.

INTRODUCTION

Angora rabbit wool production in a particular area, under conventional rearing system, is influenced greatly by climatic conditions, nutrition and management other than germplasm. An ideal ambient temperature for Angora rabbit rearing ranges between 15-25[degrees]C and a small fluctuation between maximum and minimum temperature could disturb their growth performance (Chiericato et al., 1992) and the wool yield and quality (Rochambeau and Thebault, 1990). Around 25-28[degrees]C of ambient temperature, rabbits required more digestible energy with decreased feed consumption (Lebas, 1983). The feed consumption reported to decrease by 30% at 30[degrees]C along with body growth (Matheron and Martial, 1981). Angora rabbits are reported to have special requirements with regard to avoidance of temperature stress, which involved a lack of heat protection after shearing on one hand and difficulty to lose the waste heat of metabolism due to long fleece on the other hand (Schlolaut, 1986). High temperature restrict food intake in Angora rabbits, which leads to reduction in hair growth and ultimately poor fiber yield. Where as, in cooler season, the fiber yield was higher due to increased density and length of fibers. Warmer climatic conditions favored for Angora rabbit production improves the balance between feeding costs and fiber value (Stephen et al., 1979), however, the best productive performances have been achieved with a temperature between 15-20[degrees]C (Casamassima et al., 1988). Low environmental temperature affected the body fat deposition adversely as most of the energy was used for maintaining temperature homeostasis (Stephen, 1980). Temperate grasses compositionally with less lignification had better digestibility and higher nutritive values than the tropical grasses (Cheeke, I987). Under sub-temperate Himalayan conditions, winter was found to be the best season for broiler rabbit production (Bhatt et al., 2002). However, information on the effect of different seasons on the biological performance of Angora rabbits under conventional rearing system, in sub-temperate Himalayan conditions are lacking and the present experiment was, therefore, undertaken using German Angora rabbits.

MATERIALS AND METHODS

An experiment was undertaken with sixteen adult Angora male rabbits to assess the effect of three major seasons on their body weight, wool production, wool quality and nutrient utilization. Three major seasons categorized were--winter (October-March), summer (April-June) and rainy (July-September). Daily meteorological data viz. minimum and maximum temperature ([degrees]C), rainfall (mm) and relative humidity (%) were recorded during the experimental period. Rabbit were kept individually, under similar housing and management conditions, in all wire mash cages of standard size inside the house having asbestos roof and wall made up to asbestos and chicken wire mesh. Each rabbit was fed a mash concentrate at 150 g/d consisting of maize-20, rice-phak-25, barley-20, sunflower cake-6, mustard cake-6, groundnut cake-6, soyaflakes-6, fish meal-4, molasses-5, mineral mixture-1 and salt-1. Seasonal grasses fed ad lib were mainly a mixture of Festuca arundinacea, Lolium perenae, Trifolium repens, Paspalum spp., Puereria thunbergiana, Panicum spp. and Setaria spp. Roughage samples were collected fortnightly, dried and stored for their composition. The body weight and wool yield of rabbits were recorded at the time of shearing. Each animal was sheared manually, with scissors, by the same person, at 75 d of experimental feeding, during each season, and wool samples from dorsal region of rabbit were collected for quality evaluation. Wool samples were analyzed for staple length, fiber diameter, medulation, pure fiber and guard hair using Ermascope (Erma India, Chandigarh). At the 70th day of feeding, a digestibility trial of five days duration was conducted on four representative rabbits during each season. Feed, fodder and faeces were analyzed for proximate principles (AOAC, 1990) and fiber fraction (Goering and Van Soest, 1984). Statistically, the data generated were analyzed for analysis of variance (ANOVA) as per the method of Snedecor and Cochran (1994) and presented as mean [+ or -]standard error.

RESULTS AND DISCUSSION

Meteorological attributes

The monthly minimum and maximum average temperatures during winter, summer and rainy seasons during the experiment ranged from 1.5 to 29.7[degrees]C, 9.5 to 32.8[degrees]C and 17.1 to 34.5[degrees]C, respectively. The average temperature during winter, summer and rainy season were 13.8 [+ or -] 2.9, 23.2 [+ or -] 3.0 and 24.3 [+ or -] 3.3[degrees]C respectively. The average relative humidity and total rainfall during these periods were 69.5 [+ or -] 3.0 percent and 73.5 [+ or -] 22.2 mm; 58.1 [+ or -] 1.5 percent and 25.7 [+ or -] 5.7 mm; and 73.1 [+ or -] 0.04 percent and 146.0 [+ or -] 21.0 mm, respectively.

Chemical composition of concentrate and roughages

The chemical composition of grasses fed to rabbits during different season is given in Table 1. The dry matter content of grasses fed during winter was highest (63.23 [+ or -] 2.57%) due to the high proportion of dry hay, while it was lowest (47.23 [+ or -] 4.31%) during summer season due to the availability of succulent lush grasses. The protein content of the roughage was highest (9.88%) during winter followed by summer (7.27%) and lowest (6.55%) during rainy season. Composition of concentrate (Table 1) revealed 17.76% crude protein, 10.21% crude fiber, 3.36% ether extract, 8.8% total ash, 59.87% nitrogen free extract, 24.7% acid detergent fiber, 19.3% cellulose and 5.4% lignin. All the nutrients present in the diet (concentrate+roughage) were within the permissible limits (NRC, 1977).

Biological performance and wool quality

The initial and final body weights and change in rabbit weights during different seasons are presented in Table 2. Significant (p [less than or equal to] 0.05) difference among seasons was observed for all body weight in rabbits. The increase in body weight of rabbits was due to fattening, which occurred after attaining the reproductive age and was significantly (p[less than or equal to] 0.05) higher during rainy than summer and winter seasons. This could be due to the reason that during winter the body fat reserves were used much for maintaining temperature homeostasis as compared to summer and rainy seasons. Contrary to these observations, Stephen (1980) reported decreased gain at higher (30[degrees]C) as compared to lower (5[degrees]C) environmental temperature. This difference could have been due to the reasons that fluctuation in environmental temperature was very high in former as compared to constant temperature in later experiment. The productive performance reported to improve in some way at 25[degrees]C and even a small fluctuation between maximum and minimum temperature disturbed the growth performance of rabbits (Chiericato et al., 1992). Bhatt et al. (2002) found winter season appropriate for the best feed: gain in broiler rabbit under sub-temperate Himalayan conditions. Significant (p[less than or equal to]0.05) differences were also observed in the wool yield per shearing of rabbits during different seasons (Table 2). The wool yield during winter was significantly (p[less than or equal to]0.05) higher than rainy followed by the summer season. These observations were in agreement with Rochambeau (1988), who reported winter harvest more productive than summer ones. Xu et al. (1992) reported that with an increase or decrease of ambient temperature by 1[degrees]C, the wool output of Angora rabbits reduce or increase by 4.244 g. Schlolaut (1987) also reviewed low wool yield in Angora rabbits at 30[degrees]C as compared to 5[degrees]C with elucidation that low feed intake at high temperature reduces hair growth and consequently decreased wool yield. However, it was not the case in this experiment as the total dry matter intake during different seasons was almost equal. Temperature, relative humidity and rainfall appeared to be the major variables, but not much of the differences were observed in roughage sources fed during these periods. Rochambeau and Thebault (1990) reported maximum wool production for autumn and winter, and minimum for summer season and these variations in coat growth are reported to regulate by photoperiodism (Allain and Thebault, 1988). Wool quality attributes (Table 3) revealed non-significant differences for staple length, fiber diameter, medulation percent, pure fiber and guard hair during different seasons. However, fiber diameter and pure fiber were lower in winter and increased during summer and rainy seasons. Herrmann et al. (1996) reported that Angora fiber yield and quality are influenced by environmental conditions. Doppler et al. (1984) observed lower wool yield in Angora rabbits at higher environmental temperature and was related to the higher fiber density and the longer fiber in colder climates compared to warmer ones. However, the extent of dependence of this effect on the temperature alone or on other environmental components was unknown (Herrmann et al., 1996). Rochambeau and Thebault (1990) reported longer bristles and dawn during winter than summer clipping. Allain and Thebault (1988) reported seasonal variation with thick, long coat in autumn and winter and thin flat coat in summer.

Plane of nutrition

Plane of nutrition revealed significant (p[less than or equal to]0.05) differences among seasons for concentrate and roughage intake. The daily concentrate intake was highest during winter and lowest in rainy season whereas the opposite trend was observed for roughage with lowest intake during winter and highest during summer followed by rainy season. Therefore, the differences in total dry matter intake were non-significant among three seasons. The highest concentrate intake with lowest roughage intake during winter months was possibly due to feeding of dry hay having low palatability. Minimum requirement of dietary fiber is no doubt of importance in maintaining the health status and growth performance of rabbits (Ying et al., 2007). Palatability of grasses remains highest in early succulent stage and reported to decrease with the maturity of grasses (Church, 1986). The higher roughage intake during summer and rainy months was due to feeding green succulent roughage having higher palatability. Bhatt et al. (2002) observed similar trends in broiler rabbits under sub-temperate conditions. Digestibility coefficients of nutrients in Angora rabbits are presented in Table 4. Significant (p=0.05) effect of season on the digestibilities of crude protein, crude fiber, ether extract, acid detergent fiber and cellulose was observed. The digestibility of crude protein was highest during winter than summer and rainy seasons. It was due to high intake of concentrate having highest nutritive value. The observations were in agreement to those reported in broiler rabbits (Bhatt et al., 1996) that decreased level of concentrate decrease protein digestibility. The digestibilities of crude fiber, ether extract, acid detergent fiber and cellulose were lowest during winter and highest during rainy season. The results indicate that during winter rabbit satisfied its energy needs by consuming much of concentrate and could not utilize roughage efficiently due to poor nutritive value. Rabbit satisfies its requirement mostly from non-fiber component of diet as the digestive tract of the rabbit is adapted to the utilization of fibrous feeds but not to the use of fiber itself (Cheeke, 1983). Grasses fed during summer and rainy season were either premature or partially mature and therefore, had better digestibilities of crude fiber, acid detergent fiber and cellulose. The higher digestibility during rainy season as compared to summer season was due to the differences in composition of roughage consumed during these two seasons. Supharoek et al. (2008) also reported significant effect of foliage sources on the digestibility of nutrients in broiler rabbits. The roughages during summer had higher crude fiber, acid detergent fiber, cellulose and lignin and therefore, low digestibilities as compared to rainy season. Xiccato (1998) reported that in non fat added diet the fat was strictly associated with cell walls and therefore, the digestibility of fat was related with the digestion of cell walls means fiber digestibility and possibly holds true in our findings as well. The digestibilities of acid detergent fiber and cellulose had trend similar to the crude fiber. The acid detergent fiber and cellulose digestibilities were higher during rainy season due to low contents of acid detergent fiber, cellulose and lignin in roughage. Similar results were reported earlier in broiler rabbits (Bhatt et al., 2002). Xiccato and Cinetto (1988) also reported low fiber digestibility at high nutritive level, which were confirmed in broiler rabbits (Bhatt et al., 2005). No significant difference for the digestibility of dry matter was observed.

CONCLUSIONS

From this study it can be concluded that under sub-temperate Himalayan conditions, seasons significantly affect the forage composition. Also significant effects of seasons on wool yield and concentrate intake in Angora rabbit were observed. Digestibility of crude protein was higher whereas that of crude fiber, ether extract, acid detergent fiber and cellulose was lower during winter season and was influenced significantly by different seasons. Total dry matter intake, NFE digestibility and wool quality attributes were not affected significantly by different seasons. Dry matter used for producing 100 g of wool was lower during winter than other two seasons indicating winter as the best season for Angora rabbit wool production under conventional management system in sub-temperate Himalayan conditions.

ACKNOWLEDGMENT

The authors are thankful to the Director, Central Sheep and Wool Research Institute, Avikanagar for providing facilities to conduct this experiment.

REFERENCES

Allain, D. and R. G. Thebault. 1988. Effect of various melatonin treatments on summer wool production in Angora rabbits. 4th World Rabbit Congress (Hungary) 2:441-447.

AOAC. 1990. Official methods of analysis (15th Ed). Association of official analytical chemists, Washington, DC.

Bhatt, R. S., V. Bhasin and D. R. Bhatia. 1996. Growth patterns in Soviet Chinchilla weaners fed four levels of robinia leaves. In: Proceedings of 6th World Rabbit Congress, Toulouse, France. pp. 93-96.

Bhatt, R. S., S. R. Sharma, U. Singh, D. Kumar and V. Bhasin. 2002. Effect of different seasons on the performance of Grey Giant Rabbits under Sub-temperate Himalayan conditions. Asian-Aust. J. Anim. Sci. 15:812-820.

Bhatt, R. S., S. R. Sharma, D. Kumar, U. Singh and K. S. Risam. 2005. Effect of concentrate levels of the production performance of Soviet Chinchilla rabbits. Indian J. Anim. Sci. 75:312-315.

Casamassima, D., C. Manera and M. G. Scarascia. 1988. Influenza del microclima sulla productivita del coniglio. Rivista di Coniglicoltura, 25:28-41.

Chiericato, G. M., L. Bailoni and C. Rizzi. 1992. The effect of environmental temperature on the performance of growing rabbits. J. Appl. Rabbit Res.15:723-731.

Cheeke, P. R. 1983. The significance of fiber in rabbit nutrition. J. Appl. Rabbit Res. 6:103-107.

Cheeke, P. R. 1987. Rabbit feeding and nutrition. Hartcourt Brace Jovanovich Publishers Academic Press, Inc.

Church, D. C. 1986. Livestock Feeds and feeding (2nd Ed) Prentice-Hall, Englewood cliffs, New Jersey, USA.

Doppler, W., K. Lange, L. Koliger, S. Paufler, W. Schlolaut and E. Zimmermann. 1984. "Kompendium der Kaninchenproduktion unter Berucksichtigung der verhaltnisse in der dritten welt," GTZ schriftenreihe 134-137.

Goering, H. K. and P. J. Van Soest. 1984. Forage fiber analysis. Agricultural Handbook No. 379, ARS, USDA, Washington, DC.

Herrmann, S., G. Wortmann and F. J. Wortmann. 1996. Characteristics of Angora rabbit fiber 2- the influence of the methionine content in feed and of the environmental temperature on fiber and medulla diameter in angora wool. World Rabbit Sci. 4:155-158.

Lebas, F. 1983. Small scale rabbit rearing in developing country. World Rev. 46:10-17.

Matheron, G and J. P. Martial. 1981. Growth and feed consumption of rabbit does from weaning to 4 months of age in different ambient temperature and humidities. Zootechniques of Physiologiques. ENSA. Rennes.

NRC. 1977. Nutrients requirement of rabbit (2nd Ed) National Acad. Sci. Washington, DC.

Rochambeau, H. de. 1988. Genetics of the rabbit for wool and meat production. In: Proceedings of the 4th Congress of the World Rabbit Science Association, Budapest, Hungary. pp. 168.

Rochambeau, H. de and R. G. Thebault. 1990. Genetics of the rabbits for wool production. Animal Breeding Abstract 58:1-15.

Schlolaut, W. 1986. "Beitrage zur Angorakaninchen-Wollproduktion", Referiert am 23 und 24.4, 1986. Universidad de Chile, Santiago, unveroffentlichtes Manuskript.

Schlolaut, W. 1987. Angora rabbit housing and management. J. Appl. Rabbit Res.10:164-169.

Snedecor, G. W. and W. G. Cochran. 1994. Statistical methods (6th Ed). Oxford and IBH publishing Co. Calcutta.

Stephen, E. 1980. The influence of environmental temperatures on meat rabbit of different breeds. J. Appl. Rabbit Res. 3:25-27.

Stephen, E., W. Schlolaut and W. Lange. 1979. Schurleistung, futter-und wasseraufnahme bei mannlichen angorakaninchen unter verschiedenen temperaturbedingungen. III. Arb. Tag. Vet. Med. Ges. Celle.

Supharoek, N., M. Choke and L. Inger. 2008. Effect of feeding head lettuce, water spinach, ruzi grass or Mimosa pigra on feed intake, digestibility and growth in rabbits. Asian-Aust. J. Anim. Sci. 21:1171-1177.

Xicatto, G. and M. Cinetto. 1988. Effect of nutritive level and of age on feed digestibility and nitrogen balance in rabbits. In: Proceedings of the 4th Congress of the World Rabbit Science Association, Budapest, Hungary. pp. 96-104.

Xiccato, G. 1998. Fat digestion cited in the nutrition of the rabbit (Ed. C. De Blas and J. Wiseman). CABI Publication University Press Cambridge.

Xu, L., C. Z. Chen and Y. Ye. 1992. Studies on the effect of ambient temperature and relative humidity on feed intake and wool output of angora rabbits. J. Appl. Rabbit Res. 15:1672-1675.

Ying, C., Q. Yinghe, X. Yiqiang, D. Yuchuan and M. Qingxiang. 2007. Response of growth performance, cecal fermentation traits and in vitro gas production to substitution of soyhulls for lignified fiber in rabbit diets. Asian-Aust. J. Anim. Sci. 20:45-51.

R. S. Bhatt * and S. R. Sharma

North Temperate Regional Station, Central Sheep and Wool Research Institute Garsa Via Bhuntar, Kullu (H.P.) 175 141, India

* Corresponding Author: R. S. Bhatt. Tel: +91-1437-220143,

Fax: +91-1437-220163 , E-mail: bhatt_rs@yahoo.com

Received May 24, 2008; Accepted September 30, 2008
Table 1. Chemical composition of concentrate and roughage(s)
in different seasons

 Roughage

Composition Concentrate Winter

DM 90.00 63.23 [+ or -] 2.57
CP 17.76 9.88
CF 10.21 27.33
EE 3.36 2.70
Total Ash 8.8 7.41
NFE 59.87 52.67
ADF 24.70 39.40
Cellulose 19.30 36.06
Lignin 5.4 4.20

 Roughage

Composition Summer Rainy

DM 47.91 [+ or -] 4.31 52.35 [+ or -] 2.35
CP 7.27 6.55
CF 28.19 21.05
EE 2.29 2.91
Total Ash 9.40 11.14
NFE 52.84 51.80
ADF 41.05 36.06
Cellulose 35.51 31.93
Lignin 5.54 4.13

Dietary composition- maize-20, barley-20, rice-phak-25, sunflower
cake-6, mustard cake-6, groundnut cake-6, soyaflakes-6, fish
meal-4, molasses-5, mineral mixture-1 and salt- 1%.

Table 2. Body weight, wool yield and plane of nutrition during
different seasons

 Winter
Parameters October-March

Initial body weight (kg) 2.68 [+ or -] 0.08 (a)
Final body weight (kg) 2.82 [+ or -] 0.08 (a)
Gain/day (g) 0.94 [+ or -] 0.04 (a)
Wool yield (g per shearing) 140.4 [+ or -] 10.0 (c)
Wool yield (g/kg [W.sup.0.75]) 63.5 [+ or -] 2.4
Plane of nutrition
 Concentrate intake (g/d) 124.4 [+ or -] 2.6 (b)
 Roughage intake (g/d) 24.0 [+ or -] 1.5 (a)
 Dry matter intake (g/d) 148.4 [+ or -] 4.0
 Proportion of concentrate (%) 83.8
 Proportion of roughage (%) 16.2
 Dry matter used/100 g wool produced (kg) 7.92

 Summer
Parameters March-July

Initial body weight (kg) 2.82 [+ or -] 0.08 (b)
Final body weight (kg) 2.97 [+ or -] 0.05 (b)
Gain/day (g) 1.0 [+ or -] 0.05 (a)
Wool yield (g per shearing) 108.5 [+ or -] 6.9 (a)
Wool yield (g/kg [W.sup.0.75]) 47.9 [+ or -] 2.1
Plane of nutrition
 Concentrate intake (g/d) 86.8 [+ or -] 8.9 (a)
 Roughage intake (g/d) 71.3 [+ or -] 8.1 (b)
 Dry matter intake (g/d) 158.1 [+ or -] 16.9
 Proportion of concentrate (%) 54.9
 Proportion of roughage (%) 45.1
 Dry matter used/100 g wool produced (kg) 10.93

 Rainy
Parameters July-October

Initial body weight (kg) 2.97 [+ or -] 0.05 (c)
Final body weight (kg) 3.23 [+ or -] 0.03 (c)
Gain/day (g) 3.47 [+ or -] 0.10 (b)
Wool yield (g per shearing) 123.3 [+ or -] 5.2 (b)
Wool yield (g/kg [W.sup.0.75]) 48.9 [+ or -] 1.9
Plane of nutrition
 Concentrate intake (g/d) 80.7 [+ or -] 11.8 (a)
 Roughage intake (g/d) 69.5 [+ or -] 5.9 (b)
 Dry matter intake (g/d) 150.2 [+ or -] 17.6
 Proportion of concentrate (%) 53.7
 Proportion of roughage (%) 46.3
 Dry matter used/100 g wool produced (kg) 9.14

Values with different superscripts in a row differ
significantly (p=0.05).

Table 3. Wool attributes during different seasons

Parameters Winter Summer

Staple length (cm) 5.18 [+ or -] 0.12 5.10 [+ or -] 0.12
Fiber diameter (micron) 13.50 [+ or -] 0.35 13.96 [+ or -] 0.30
Medulation (%) 90.10 [+ or -] 0.84 89.39 [+ or -] 0.87
Pure fiber (%) 6.28 [+ or -] 0.87 7.06 [+ or -] 0.97
Guard hair (%) 3.67 [+ or -] 0.55 3.33 [+ or -] 0.43

Parameters Rainy

Staple length (cm) 5.37 [+ or -] 0.13
Fiber diameter (micron) 14.30 [+ or -] 0.27
Medulation (%) 88.55 [+ or -] 1.23
Pure fiber (%) 7.78 [+ or -] 1.46
Guard hair (%) 3.72 [+ or -] 0.44

Table 4. Digestibility coefficients (%)of nutrients in different
seasons

Nutrient Winter Summer

DM 64.1 [+ or -] 1.5 58.7 [+ or -] 2.4
CP 77.8 [+ or -] 1.1 (b) 67.2 [+ or -] 2.2 (a)
CF 12.5 [+ or -] 3.5 (a) 31.7 [+ or -] 5.5 (b)
EE 54.3 [+ or -] 3.9 (a) 59.4 [+ or -] 1.7 (a)
NFF 73.7 [+ or -] 1.4 69.0 [+ or -] 1.7
ADF 37.9 [+ or -] 3.1 (a) 39.8 [+ or -] 2.4 (a)
Cellulose 35.3 [+ or -] 2.4 (a) 39.7 [+ or -] 3.4 (a)

Nutrient Rainy

DM 66.8 [+ or -] 3.3
CP 71.1 [+ or -] 2.9 (a)
CF 45.0 [+ or -] 7.4 (c)
EE 70.4 [+ or -] 6.7 (b)
NFF 75.0 [+ or -] 2.2
ADF 47.8 [+ or -] 4.7 (b)
Cellulose 51.9 [+ or -] 4.5 (b)

Values with different superscripts in a row differ
significantly (p=0.05).
COPYRIGHT 2009 Asian - Australasian Association of Animal Production Societies
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2009 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Bhatt, R.S.; Sharma, S.R.
Publication:Asian - Australasian Journal of Animal Sciences
Article Type:Report
Geographic Code:9INDI
Date:Mar 1, 2009
Words:3679
Previous Article:Effect of self-photoperiod on live weight, carcass and growth traits in quails (Coturnix coturnix Japonica).
Next Article:Effect of dietary inclusion of medicinal herb extract mix in a poultry ration on the physico-chemical quality and oxidative stability of eggs.
Topics:


Related Articles
To each his own ... breed of rabbit, and raising methods!
Wool on four feet.
Angora rabbits.
In love with angora rabbits.
Raising dual-purpose rabbits.
Genetic and phenotypic parameter estimates of body weight at different ages and yearling fleece weight in Markhoz goats.
Boom time for rabbit breeders in Uttarakhand.

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters