Maataloustieteellinen Aikakauskirja Vol. 60: 566—575, 1988 Reproduction and adaptation characteristics in D’man sheep A. LAHLOU-KASSI, S. BENLAMLIH, R. BOUKLIQ, A. TIBARY and E BOUJENANE Hassan II Agronomic and Veterinary Medicine Institute, P. O. Box 6202, Rabat-Instituts, Morocco Abstract. D’man breed (D) is found in the oasis of the subsaharian regions of Morocco and reared usually in sedentary type of management with small flocks (< 10 ewes). Prelimi- nary field surveys showed that D is early maturing, prolific and aseasonal. Hence, a multidis- ciplinary research programme on D was started in 1974. This paper reports the findings of these studies and describes the approach used to (1) characterize and evaluate the performances of D in field and station, (2) study the physiologi- cal mechanism involved in its peculiar reproduction and production, (3) study the genetic ba- sis of reproduction parameters, and (4) evaluate use of D in crossbreeding schemes to improve the productivity of other Moroccoan breeds. Results show that D is one of the rare breeds that is simultaneously early maturing, highly prolific and completely aseasonal. However, studies on water turnover and nitrogen recycling show that D is not well adapted to hot climate and poor nutrition. Its reproduction parameters are relatively independent of photoperiod and related to a low sensitivity to negative oestrogen feedback. D male is characterized by high libido and can be used for synchronizing oestruses through the »ram effect». Crossbreeding experiments with non-prolific sheep confirm the heritability of reproduc- tive parameters. However, the genetic basis for these is not yet well known. Index words: D’man, reproduction, adaptation, crossbreeding, early maturity, libido 1. Introduction Early work undertaken on D’man (D) breed both in station and on the field showed reproductive characteristics of this breed which are different from those of other Moroccan breeds: precocious puberty (219—229 d), a short postpartum anestrus (34—64 d), non seasonality of breeding and high prolificacy (2.86) (7, 17, 19, 20). With an ovulation rate (OR) of 2.85 (17), D ewe is considered among the most prolific breeds as this OR approaches that of other prolific breeds (Romanov 2.86, Boorola 2.68, Finn- 566 JOURNAL OF AGRICULTURAL SCIENCE IN FINLAND https://www.c-info.fi/en/info/?token=GM1iFuRvJSR9aQBE.24UDBVW5DmjU9wVHfLr52A.wvDX5Cef5A8PAfy_WWL1hD4vPvX7UTwj95IiCU50IU48RodnZt4cPi1tMkvjGwwbMU65_9AwF3hbC4CfVPfwXnXyfkbPTVTaoRw88Yq8-pUgBLXyYhXYm46Vll9-HV5USgL7RbNMjSdvr2vtBBAp3sng50MfMq-XAbN-RiRMmNv6FnzbfdUoHGrUqFz2zgp2ANYYHC1IzQCUhoa5pbyTN0DNd4O4lsslKFTO29KIOzYMdg sheep 3.31) (30) and is higher than that of oth- er Moroccan breeds (Beni-Hsen 1.25, Timah- dite (T) 1.1, Beni-Guil 1.1, Sardi (S) 1.1). Prolificacy in D varies from 2 to 2.6 compared to that of Beni-Hsen (1.18), T (1.0), S (1.0) and Beni-Guil (1.0) (4, 8, 17). Experiments were designed to try to deter- mine the physiologic mechanism and genetic components which are behind these charac- teristics; these esperiments can be summarized as follows: Studies of litter size (LS), OR and embryo survival (ES). Determination of endocrine regulation of multiovulation. Determination of photoperiod and genet- ic involvement in the expression of sexual activity. Studies on adaptation of D to harsh en- vironment and its possible use for inten- sification of sheep production through crossbreeding with local meat breed like Sardi. 2. Litter size and its components 2.1 Litter size From the analysis of 1852 performances gathered in two stations at Ziz valley, Bouje- nane et al. (6) reported an average LS of 2.09, ranging from 1.77 in ewes of less than 12 months old to 2.32 in ewes for which age was between 30 and 42 months (Table 1). Moreover, LS varied from 1 to 3 in ewe lambs and from 1 to 7 in ewes older than 42 months. In a crossbreeding experiment involving D and S purebreeds, Boujenane et al. (6) reported that the average LS were 1.80, 1.20 and 1.55 in D, S and D X S ewes. These results which are in agreement with those of Bradford al. (9) (Table 2) shows that LS var- ied from 1 to 6 in D, 1 to 3 in S and 1 to 4 in D x S ewes. It seems from these that LS has an additive inheritance, since heterosis was small (1.4 %). This result agrees with several other studies (10, 22, 28). 2.2 Ovulation rate From Table 3, OR in adult D ewes (3.18) is signifantly higher than in 1-year old ewe lambs (1.9 to 2.3). It ranged from 1 to 7 and from 1 to 4 for adult and young females, respectively. The mode of the OR distribution is 3 and 2 for both groups. Seasonal variation of OR is not significant. Repeatability of OR as determined through simple correlation of OR on 2 successives cy- cles in 15 D ewes was 0.59 (20). However, it ranged only from 0.2 to 0.37 when calculat- ed, through simple correlation between pairs of data for 3 seasons (9). In comparing OR of D, S and their crossbred ewes, Boujenane et al. (5) found averages of 2.56, 1.23 and 1.92 respectively. Moreover, OR ranged from 1 to 8, 1 to 3, and 1 to 4 in D, S and D x S ewes (Table 4). It is essential to point out that as the mean OR increases, the proportion of single births decreases while that of multiple births in- creases. High repeatability of OR in this breed in- dicates the possibility of presence of a major gene comparable to the Boorola gene report- ed by Piper and Bindon (26). On the other hand, individual heterosis for OR was small and negative (—0.5 %) (6). This result shows that OR is controlled by additive genes and it is in agreement with those of Land et al. (22) and Ricordeau et al. (28). 2.3 Embryo survival ES reported in D (Table 5) is as high as that of Romanov (28) and Javanese (12). This trait is influenced by age. OR and LS were respec- tively (2.89, 2.07) and (2.27, 1.35) for adult ewes and ewes lambs giving an ES rate of 0.72 and 0.59 for these age groups. This suggest that LS is more correlated to OR in adult ewes than in ewelambs. In addition, averages of ES were 68.3 %, 83.7 % and 95.4 °7o in D, D x S and S ewes which ovulated respectively. The effect of breed group for the same number of corpora 567 lutea was not significant (P > .05). The only effect on embryo mortality was the number of ova shed. Thus, when the number of cor- pora lutea were 1,2, 3 and 4or greater, ES was 81.2 %, 86.8 %, 79.2 % and 66.3 % respectively. An equation similar to that of Table 1. Least squares means and distribution of litter size in D’man ewes by age class. Age Number Least Stan- Frequency (%) class of squares dard ' " ' " " " ~ iv l 12 3 4 5 6/(months). obs. means error < 12 48 1.77 .13 43.8 45.8 10.4 12 to 18 395 2.02 .05 30.4 47.8 18.7 2.8 .3 18 to 24 267 2.12 .06 28.1 42.3 23.6 4.9 .7 .4 24 to 30 292 2.21 .05 22.6 44.5 26.7 4.5 1.7 30 to 42 356 2.32 .05 18.0 44.6 27.0 9.0 1.1 .3 >42 494 2.13 .05 28.9 39.5 24.3 6.3 .6 .2 .2 All ages 1852 2.09 .03 26.4 43.6 23.5 5.4 .8 .2 .1 Table 2. Variability in litter size of Sardi, D’man and FI ewes. (9). Breed Age at Total no. Mean litter Frequency (%) mating litters size ~ ~ ~ 1 2 3 4 5 6 Sardi 20 mo 136 1.11 73.8 9.6 10 mo 20 1.00 100 D'man 20 mo 12 2.17 41.7 16.7 33.3 8.3 10 mo 33 1.58 42.4 51.5 6.1 DxS 20 mo 42 1.79 35.7 50.0 14.3 10 mo 91 1.26 73.6 26.4 Table 3. Variation of ovulation rate with age and season in D’man ewes (9). Age at Season Number of 9 Mean Number of 9 joining number endo wthC.L , n , 1 2 3 4 5 6 7of C.L Adult Nov— Dec 38 34 2.82 4 9 11 9 1 May— Jun 36 32 3.81 5 8 13 2 2 2 March 41 39 2.97 4 9 15 7 3 1 115 105 3.18 8 23 34 29 6 3 2 21—22 May—Jun 16 15 3.40 14 3 3 3 1 months II Nov—Dec 14 11 2.27 2 5 3 1 months March 29 25 1.92 8 12 4 1 Table 4. Least squares means and distribution of ovulation type by breed group. Breed Number Least Stan- Frequency (%) Group of squares dard ~ . 12345678obs. means error D'man 179 2.56 .07 14.7 32.9 27.1 17.1 5.0 2.1 1.3 .4 Sardi 411 1.23 .05 74.2 25.5 .3 DxS 191 1.92 .09 45.1 40.7 12.8 .8 568 Table 5. Embryo survival in D’man dynumber of ovula- tions. AuthorsOvulation rate 1 2 3 4 5,6,7 90 82 69 58 (9)Embryo Survival (%) 90 78 71 49 (20) 88 87 79 67 (5) Hankahan (15) was derived for all ewes which ovulated: Y = 1.198 X—.116 X 2 where X and Y indicate OR and LS respec- tively. This equation shows that the highest LS of 2.65 corresponds to an OR of 4.78. ES of crossbred ewes was better than the average of parental breeds; heterosis was 14.6 %. This result shows that ES is a heterotic trait. 3. Endocrine mechanism of multiovulation Comparative studies on folliculogenesis in D and Timahdite around birth and in the adult indicate that D has more large follicles and less atretic follicles which is mainly due to high lev- el of FSH (19, 21). In recent studies, D sen- stivity to estrogen negative feed-back and to gonadotrophins was tested. Results summarized in table 6 and table 7 indicates that the D had a greater OR after PMSG than did the non-prolific breeds either in adult and ewe-lambs. This is in agreement with results of other experiments (3, 11) show- ing greater gonadotrophin responsiveness in animals with higher natural OR. However, when the response to PMSG is expressed as a multiple natural OR, the non-prolific breed seems to be more responsive than the D. The relative increase in OR when the dose of PMSG increased from 250 to 500 was 43 % and 92 °/o for D and T ewes, respectively (31). On the other hand, estrogen negative feed- back is more marked in T than in D ewes. This was shown in ovariectomized ewes fitted with estrogen implants. In these animals, the lev- els of FSH and LH were singificantly higher in D than in T (Lahlou-Kassi, unpubl. data). It was concluded that D ewes are less sensi- tive to estrogen feedback mechanism. Multiovulation seems to be a resultant from higher level of FSH allowing growth of more follicles that are in last stages of development and a higher sensitivity of follicles to gonadotrophins probably due to higher con- centration of FSH and LH receptors. This hypothesis is under investigation (Lahlou- Kassi, unpubl. data). 4. Photoperiod effect on breeding season in D’man 4.1 In the female Total seasonal anestrus is absent in this breed, even in ewes out of their natural in- Table 6. Induced ovulation rate by using PMSG and HCG in D’man and Sardi ewe-lambs. (Lahlou-Kassi et al., unpubl. data). Croup n Age Weight PMSG HCG Number of C.L (days) (kg) m (|ii) 1 2 3 4 S 6 7 8 910 II D'man 7 95.4111.9 9.7 + 2.1 400 500 13— 1 1 1 (7 4.14±3.36) D'man 7 96.6± 7.6 11.4 + 3.9 200 500 1 1 2 (4 2.25 + 0.83) D'man 6 87.5+11.6 9.811.9 500 1 1 (2 2.5 +0.5 ) Sardi 7 103.1+ 4.9 13.0 + 3.4 400 500 3 11 (5 1.6 10.8 ) Sardi 7 97.81 6.2 12.812.4 200 500 2 1 (3 1.3310.47) 569 habitat. Maximum estrus activity occurs around summer and winter solstices, and a minimum activity occurs in October and around March. However, the percentage of ewes in estrus is never lower than 50 % (7, 17). These results suggest that D breed is less sen- sitive to photoperiod. This hypothesis was tested on 20 D maintained under an artificial photoperiod corresponding to that of Eat : Table 7. Ovulation rate after treatment with different doses of PMSG. Dose Ovulation rate Authors of PMSG - 7ZD man Timandite 0 1.5610.2 1.02±0.0 (27) 250 2.90+1.26 1.36±0.75 (32) 375 2.40±0.4 1.57 + 0.2 (27) 400 3.03 + 1.88 (24) 500 4.16± 1.95 2.62 ±1.57 (32) 750 6.72 ±1.2 4.58+1.1 (27) 1500 11.01 ±1.3 6.93 ±l.O (27) 570 56°N (Edinburgh, Scotland). Estrus and ovar- ian activity of these ewes was compared to a control group (Eat : 32°N, Tadla, Morocco). Results of this experiment (Table 8) show that estrous behaviour was affected by Scottish photoperiod in D. Number of ewes showing estrus was low during the Sept—Dec period in the first year of the experiment and between July and Dec in the second year. This was not clearly shown in S ewes of which breeding sea- son is centered around the winter solstice. However, ovarian activity determined by plas- ma progesterone levels was not affected in D (18). This pleads in favour of a lower sensi- tivity of this breed to photoperiod variation. 4.1. In the male In the male, a study on characteristics of semen from 5 rams collected by artificial va- gina weekly for 2 years showed that volume, gross motility and individual motility were Fig. I. Weight gain per animal and per Kg of body weight in genotypes S, S x D, and D placed in shade (SH) or exposed to the sun (SN) during winter and during summer. relatively constant. However, concentration was affected by season and decreased between May and August, may be due to poor nutri- tional level. The D ram seems to reach exhaus- tion earlier than S rams as concentration of semen decreasedrapidly by rank of ejaculate (32). The libido in D ram seems to be higher than Table 8. Ovarian activity of D’man and Sardi ewes as monitored by changes in plasma progesterone level and by detection of oestrus under two photoperiods during a period of 682 days. Group Theoretical Observed Observed Mean no. of no. of no. of efficiency ovul. or est. ovul. estrus. of est. exp. D'man Control 351 314 211 67.2% 34.8±3.9 23.4±4.2 Experimental 779 736 345 46.9 % 36.8± I.9ns 17.3 + s.9*** Sardi Control 442 271 230 84.5 to 22.5±3.5 19.2±4.2 Experimental 664 418 287 68.7 % 23.3±3.6ns 15.3 ±6.3* Fig. 2. Plasma thyroxine (T4) and triodothyronon (T3) in genotypes S, S x D, and D placed in shade (SH) or ex posed to the sun (SN) during winter and during summer. 571 in other breeds. In Tadla experimental farm, breeding record indicates a possible high male effect of ram from this breed, but this hypoth- esis was not thoroughly investigated. 5. Adaptation of D’man sheep to environmental constraints The production of sheep is influenced by genetic potential of the breed (growth rate, fertility) and its adaptation to the environmen- tal stress (heat, solar radiation, water and food restriction). Because of its high prolificacy, there is a rising interest to use the D outside its original habitat either as a pure breed or more than often in cross breeding. The most advanced program is the crossbreeding with the S in the Tadla region. The D is originally reared in the shade of the oasis where it is watered permanently and fed with a high nitrogen ration composed with alfa-alfa. The S is grazing in the Tadla region. During the hot season, this breed is fed on the stubble which are poor in nitrogen and high in fiber. In addition, it is exposed to solar radi- ation and subjected to unfrequent watering. The production under this environment de- pends on the ability of the animals to econo- mize water and nitrogen and to minimize the effect of heat stress. Comparative studies have been made on water turnover, urea recycling and reactions to heat stress in Sardi, D’man and FI. 5. 1. Water turnover and urea recycling Water turnover which expresses the water needs was measured during the critical phases of the production cycle such as pregnancy, lac- tation, and the growth period using tritiumas tracer. Table 9 shows that water turnover un- der thermoneutral conditions is higher in S than in D and FI. These differences were sig- nificant during pregnancy and growth. In ruminants, it is well established that en- dogenously produced urea is partly degraded to ammonia in the digestive tract and partly excreted in the urine. The ammonia produced in the rumen can be used for microbial pro- tein synthesis (14). The proportion of urea degraded in the digestive tract (= urea recy- cling) increases when the diet becomes poor in nitrogen. In addition, it was reported that the ability to recycle the urea is influenced by the genotype (25). When fed with a low pro- tein diet, S and the FI show a higher urea re- cycling rate than D and this effect was more pronounced during pregnancy than during lac- tation (Table 9). The low water turnover and high urea recy- cling rate seen in S can be related to the adap- tation to the stress of low nitrogen intake and unfrequent drinking observed during the sum- mer in the Tadla region. 5.2. Seasonal heat stress and growth Berger et al. (2) reported that the post weaning growth is depressed when it occurs during the summer period. To elucidate this seasonal difference in growth, a comparative study was conducted in growing lambs (3 to 6 months age) during the summer and during the winter with a similar nutrition level. The animals from 3 genotypes (D, S and FI) were divided in 2 groups, one exposed to the sun and the other having access to the shade. The results in the Table 10 confirm that the post weaning growth is depressed in the summer, but mainly when the animals are exposed to the sun. This effect was not caused by a de- crease in food intake, but by a decrease in food conversion efficiency. When growth was compared in the 3 geno- types, S and FI showed the highest absolute growth in comparison with S. Since the 3 genotypes do not have the same mature weight, the relative growth rate was used to compare the 3 breeds. It appeared that the D and the FI have a much higher (28 %) rela- tive growth rate as compared to the S. In ad- dition, the relative growth rate was depressed during summer in D and FI but not in the S. It is known that the level of thyroid hor- mones are influencedby ambient temperature and genetic background and that there is a 572 Table 9. Water turnover and urea recycling rate in D’man, Sardi and FI during pregnancy, lactation and growth. Water turnover Urea recycling T l/a (h) (ml/kg 77d) (mmol/kg'Vd) % Pregnancy D'man 131+ 3 228+ 8 5.7 + 0.9 71+2 Sardi 217+15 161 + 17 9.4 + 0.7 80±4 F, 153± 8 201110 8.3+1.2 76 + 3 Lactation D'man 98+ 7 306+14 5.0 + 0.4 74±4 Sardi 115+ 6 285+15 5.5+1.3 77 + 4 F, 101 ± 7 307+17 6.1 + 1.1 76±4 Growth D'man 1031 3 260110 Sardi 1271 5 229113 F, 106+ 3 279+10 Table 10. Absolute growth rate and food efficiency coefficient during the winter and during the summer in lambs (3 to 6 months age). The animals were divided in 2 groups, one exposed to the sun and the other having access to the shade. Winter Summer Shade Sun Shade Sun Growth (g/day) 160+11 154± 10 13916 118±9 Food efficiency 13.7 14.0 16.0 18.7 (Meal ME/kg gain) relationship between thyroid activity and growth rate (1, 13). A related question is the possible role that thyroid function (known to be depressed by environmental heat) played in the observed reduced growth rate during the summer and in the difference in growth be- tween breeds. In fact, it has been shown in this study that thyroxine (T4) and triiodothyronin (T3) were depressed during summer in all the 3 genotypes. On the other hand, the D showed higher levels of T 4 and T, than S with inter- mediate levels for the F,. 6. Conclusion Results obtained by different authors sug- gest that prolificacy in D may be related to other parameters (low age at puberty, non seasonality, ...). All these components of reproductive efficiency may have the same basic mechanism. The low sensitivity of pro- lific breeds to estrogen negative feed-back (22) and the role of this feed-back in seasonality (23) may explain the relationship between reproductive parameters. Results from the study on genetic support of prolificacy in D shows that the presence of a major gene controlling this trait is controver- sial. The existence of this type of gene will al- low a selection for two strains, one with a LS < 2 and one with a LS > 3. This selection offers possibility of controlling LS and use of D by farmers for cross-breeding with non-pro- lific ewes according to their goals and their specific production system. D shows, in addition to its high prolifica- cy, a high potential for fast growth which can be efficiently used in cross-breeding. This characteristic is associated with high water turnover and high levels of blood thyroid hor- mones. However, D appears to be more suceptible to the effect of environmental stress of the summer period than the S. 573 Aknow lodgements:The authors would like to record their appreciation of the support provided for this work by the Title XII Small Ruminant CRSP, Grant No. AID/ DSAN/XII/G-0049, by the lAEA, Projects MOR/5/015 and 3159/IG and by IFS grant B/464. References 1. Baccari, F., Johnson, H.D. & Lerory Hann, G. 1983. Proc. Soc. Experim. Biol. Med. 173, 312. 2. Berger, Y.M., Bradford, G.E., Essaadi, A., John- son, D.W., Bourfia, M. & Lahlou-Kassi, A. 1988. Performance of D’man and Sardi breeds of sheep in purebred and crossbred matings on an accelerat- ed lambing schedule. 111. Lamb mortality, growth and production per ewe. Submitted to Small Ruminant Research. 3. Bindon, 8.M., Thimonier, J. & Piper. L.R. 1978. Timing of pre-ovulatory LH discharge in high fecun- dity sheep. Proc. Aust. Soc. Reprod. Biol., 10, 82 (Abstr.). 4. Bouix, J., Kadiri, M. & Chari, A. 1974. 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