Effects of restricted feed intake on blood constituent concentrations in Dorper, Katahdin, and St. Croix sheep from different regions of the USA.

Forty-six Dorper, 47 Katahdin, and 41 St. Croix female sheep (initial BW = 62, 62, and 51 kg, respectively, SEM = 1.43; 3.8 ± 0.18 yr) from farms in Midwest, Northwest, Southeast, and central Texas regions of the USA were used to evaluate effects of feed restriction on blood constituent levels. The amount of feed offered varied in the first 4 wk to achieve stable BW, and that in wk 5-10 was 55% of intake in wk 3-4. Blood was sampled at the end of wk 3, 4, 6, 8, and 10. There were relatively few effects and interactions involving region and no breed × time interactions. Breed affected the concentration of a small number of constituents, including urea N (14.0, 13.7, and 15.4 mg/dl; SEM = 0.31) and creatinine (0.945, 0.836, and 0.809 mg/dl for Dorper, Katahdin, and St. Croix, respectively; SEM = 0.0253). Also, the concentration of triglycerides in wk 4 and 10 was lowest for St. Croix (29.8, 29.5, and 26.7 mg/dl for Dorper, Katahdin, and St. Croix, respectively; SEM = 0.88). There was a trend for a difference (P = 0.051) between wk 4 and 10 in the glucose concentration (51.9 and 54.2 mg/dl; SEM = 0.90), and there were differences (P < 0.05) in lactate (23.9 and 20.3 mg/dl; SEM = 0.89), urea N (16.4 and 13.0 mg/dl; SEM = 0.25), creatinine (0.808 and 0.919 mg/dl; SEM = 0.0165), triglycerides (31.8 and 25.5 mg/dl; SEM = 0.63), and cholesterol (67.5 and 74.7 mg/dl, respectively; SEM = 1.66). In conclusion, similar responses in blood constituent levels of different hair sheep breeds to feed restriction is in accordance with comparable effects on the maintenance energy requirement.

Effects of water restriction on feed intake, digestion, and energy utilization by mature female St. Croix sheep.

Eleven St. Croix ewes (46.9 ±â€¯1.59 kg BW and 3.6 ±â€¯0.67 yr age) were used in a crossover design to evaluate effects of restricted drinking water availability on intake of a 50% concentrate diet, digestion, and energy utilization. After 2 wk to determine ad libitum water consumption, there were two 4-wk periods, with measures in metabolism cages during wk 4. One treatment was water offered at the ad libitum level (CONT) and the other entailed a 25% reduction in wk 1 and 50% thereafter (REST). Although, some water was refused in wk 4, with intake of 2556 and 1707 g/day for CONT and REST, respectively (SEM=170.9). Digestibility of gross energy was greater (P = 0.034) for REST than for CONT (66.5 vs. 62.4%; SEM=1.16); however, because of a numerical difference (P = 0.448) in energy intake (15.79 and 14.66 MJ/day for CONT and REST, respectively; SEM=1.426 MJ/day), digested energy intake was similar between treatments (P = 0.870). Urinary energy was greater (P = 0.023) for CONT vs. REST (0.62 and 0.52 MJ/day; SEM=0.038) and methane energy did not differ (P = 0.213) between treatments (0.76 and 0.89 MJ/day; SEM=0.084), resulting in similar (P = 0.665) ME intake (8.50 and 8.01 MJ/day for CONT and REST, respectively; SEM=0.855). Both heat (8.60 and 8.33 MJ/day; SEM=0.437) and recovered energy (-0.10 and -0.30 MJ/day for CONT and REST, respectively; SEM=0.623) were similar between treatments (P ≥ 0.880). In conclusion, increased digestibility appears an important adaptive response to limited availability of drinking water.

Across and within breed differences in the relationship between packed cell volume and fecal egg count in growing meat goat and hair sheep males naturally and artificially infected with gastrointestinal nematodes.

The relationship between packed cell volume (PCV) and fecal egg count (FEC) in different breeds of meat goats and hair sheep infected with gastrointestinal nematodes, including Haemonchus contortus, was characterized. Growing males from eight commercial and two research farms (one Kiko, Spanish, Dorper, and St. Croix; three Boer; four Katahdin) in the southcentral United States were evaluated in a central performance test with ad libitum intake of a 50% concentrate pelleted diet. There were 84 Boer, 55 Kiko, and 57 Spanish goats and 52 Dorper, 129 Katahdin, and 49 St. Croix sheep. During adaptation, animals were dewormed then dosed with 10,000 infective H. contortus larvae. PCV and FEC were determined before deworming (i.e., natural infection potentially with multiple internal parasites) and 21, 28, 35, 42, and 49 days after artificial infection. Effects of species, breed, and year were analyzed with mixed effects models including day of sampling post dosing as a repeated measure and FEC and FEC × breed as covariates. Moreover, differences in correlation coefficients between PCV and logarithmic FEC (lnFEC) among species, breed, year, and day of sampling were evaluated. Breed affected (P ≤ 0.001) PCV in goats (24.8, 27.2, and 26.0% for Boer, Kiko, and Spanish, respectively; SEM = 0.42) and sheep (29.8, 26.7, and 31.0% for Dorper, Katahdin, and St. Croix, respectively; SEM = 0.28). There were effects of FEC × breed (P ≤ 0.029) on PCV for Boer, Kiko, Dorper, Katahdin, and St. Croix (-0.31, -0.33, -0.46, -0.46, and - 0.49% per 1000 eggs, respectively) but not for Spanish goats (P = 0.451). With all data, PCV and lnFEC with natural infection were highly correlated (P < 0.001) for Boer and Kiko goats and Dorper and Katahdin sheep (r = -0.59, -0.67, -0.77, and - 0.84, respectively) but not for Spanish goats or St. Croix sheep (P ≥ 0.323). Correlation coefficients for artificial infection with H. contortus were significant (P ≤ 0.002) except for Spanish goats, although values were lower (-0.40, -0.21, -0.23, -0.47, and - 0.28 for Boer, Kiko, Dorper, Katahdin, and St. Croix, respectively) compared with natural infection. In conclusion, PCV was not related to FEC in Spanish goats infected either naturally or artificially, and the nature of the relationship varied among breeds of goats and sheep. Based on the magnitude of the FEC × breed coefficient, sheep incurred a relatively greater reduction in PCV as FEC increased, and correlation coefficients indicate stronger relationships with natural than artificial infection.

Effect of Ovar-DRA and Ovar-DRB1 genotype in small ruminants with haemonchosis.

The effect of Ovar-DRA and Ovar-DRB1 genotypes on faecal egg count (FEC) was determined in sheep and goats infected with Haemonchus contortus. One hundred and forty-three sheep from 3 different breeds (St. Croix, Katahdin and Dorper) and 150 goats from three different breeds (Spanish, Boer and Kiko) were used. Parasitological (FEC), haematological (packed cell volume) and immunological (IgA, IgG and IgM) parameters were measured. Sheep populations showed a higher FEC and humoural response than goat breeds. Genotypes were determined by high-resolution melting assays and by conventional PCR. For Ovar-DRA, sheep and goats carrying the AA genotype showed significant lower FEC than AG and GG genotypes. The additive effect was found to be 115.35 less eggs per gram of faeces for the A allele for goats. For Ovar-DRB1, only in sheep, the GC genotype was associated with low FEC. The additive effect was 316.48 less eggs per gram of faeces for the G allele, and the dominance effect was 538.70 less eggs per gram of faeces. The results indicate that single nucleotide polymorphisms within Ovar-DRA and Ovar-DRB1 could be potential markers to be used in selection programmes for improving resistance to Haemonchus contortus infection.

Effects of level of brackish water on feed intake, digestion, heat energy, and blood constituents of growing Boer and Spanish goat wethers.

Twenty Boer (6.1 mo old and 21.3 kg) and 20 Spanish (6.6 mo old and 19.7 kg) goat wethers were used to determine effects of brackish water on feed intake, digestion, heat energy, and blood constituents. Brackish water had 6,900 mg/L total dissolved salts, 1,885 mg/L Na, 75 mg/L Mg, 1,854 mg/L chloride, 2,478 mg/L sulfate, and 9 mg/L boron. Water treatments were 100% tap water (control), 100% of a brackish water source (100-BR), 33% control and 67% brackish water (67-BR), and 67% control and 33% brackish water (33-BR). Water and a moderate-quality grass hay (8.5% CP and 68% NDF) were offered free choice. The experiment consisted of 14 d of adaptation, 5 d for metabolizability measures, and 2 d for determining gas exchange and heat energy. There were no interactions ( > 0.05) between breed and water treatment. Water intake (931, 942, 949, and 886 g/d [SE 59.1] for the control, 33-BR, 67-BR, and 100-BR, respectively) and DM intake (525, 556, 571, and 527 g/d [SE 31.0] for the control, 33-BR, 67-BR, and 100-BR, respectively) were similar among treatments ( = 0.876 and = 0.667, respectively). Urinary water was greater for brackish water treatments than for the control ( = 0.003; 211, 317, 319, and 285 g/d [SE 25.6] for the control, 33-BR, 67-BR, and 100-BR, respectively) and fecal water content was similar among treatments ( = 0.530; 247, 251, 276, and 257 g/d [SE 19.0] for the control, 33-BR, 67-BR, and 100-BR, respectively), implying less water loss by other means such as evaporation when brackish water was consumed. Total tract OM digestibility was lower ( = 0.049) for treatments with brackish water than for treatments without brackish water (64.2, 61.5, 58.6, and 59.3% [SE 1.86] for the control, 33-BR, 67-BR, and 100-BR, respectively), although ME intake was similar among treatments ( = 0.940; 4.61, 4.57, 4.60, and 4.31 MJ/d [SE 0.394] for the control, 33-BR, 67-BR, and 100-BR, respectively). Daily heat energy in kilojoules per kilogram BW was less with brackish water than without brackish water ( = 0.001; 474, 436, 446, and 445 kJ/kg BW [SE 7.7] for the control, 33-BR, 67-BR, and 100-BR, respectively), although values in megajoules were similar among treatments ( = 0.588; 4.36, 4.12, 4.22, and 4.18 MJ [SE 0.124] for the control, 33-BR, 67-BR, and 100-BR, respectively). Body weight of wethers consuming brackish water decreased less than that of wethers consuming the control water ( = 0.006; -37, -14, -7, and -16 g [SE 7.2] for the control, 33-BR, 67-BR, and 100-BR, respectively), but recovered energy was similar among treatments ( = 0.923; 0.25, 0.45, 0.38, and 0.13 MJ/d [SE 0.356] for the control, 33-BR, 67-BR, and 100-BR, respectively). In conclusion, brackish water inclusion in drinking water had a number of effects, but it does not appear that consumption of this source would adversely impact performance of growing meat goats.

Effects of conditions of an experimental model to evaluate methods of electric-fence strand addition to barbed-wire fence to contain goats.

Growing meat goats of 4 types (Boer and Spanish of both wethers and doelings) were used to evaluate conditions for a method of testing efficacy of electric-fence strand additions to barbed-wire fence used for cattle to also contain goats. Animals were allocated to 8 sets, with each set consisting of 5 groups. There was 1 goat of each of the 4 types in a group. One side of five 2.4- × 3.7-m evaluation pens consisted of barbed-wire strands at 30, 56, 81, 107, and 132 cm from the ground. Evaluation pens were adjacent to a pasture with abundant vegetation. Fence treatments (FT) were electrified strands (6 kV) at 15- and 43- (LowHigh), 15- and 23- (LowMed), 15- (Low), 23- (Med), and 43-cm (High), where Low, Med, and High abbreviations are for low, medium, and high heights from the ground, respectively. For adaptation, there were 4-wk and sequential exposures to evaluation pens: wk 1, no electric strands; wk 2, 1 strand at 0 kV; wk 3, LowHigh; and wk 4, LowHigh. There were 6 periods for measurements, each separated by 1 wk. During the 1-wk intervals on pasture, sets were exposed to 1 interval treatment without and another with 2 electric strands (6 kV) positioned next to supplement troughs, to potentially affect familiarity with electrified strands and influence subsequent behavior. All animal sets were used for measurements in period 1 in a completely randomized design (CRD). Four sets were also used in 4-wk subsequent measurement periods for a 5 × 5 Latin square (LS). All animal sets were exposed to the same FT in period 6 as in period 1. Behavior in evaluation pens was observed for 1 h with a video surveillance system in the 6 periods. There were no effects of gender and few and minor effects of preliminary and interval treatments. The percentage of animals that exited evaluation pens differed (P < 0.05) among FT, with the CRD approach in period 1 (25%, 47%, 38%, 66%, and 84%; SEM = 8.0) and with repeated measures in periods 1 and 6 (6%, 22%, 22%, 63%, and 81% for LowHigh, LowMed, Low, High, and Med, respectively; SEM = 4.9), and between breeds in periods 1 (34% and 70%) and 1 and 6 (28% and 50% for Boer and Spanish, respectively). For the LS approach, FT affected exit (31%, 23%, 16%, 35%, and 30%; SEM = 5.3) and breeds differed (P < 0.05), as well (12% and 43%). Exit decreased as period advanced (60%, 35%, 23%, 10%, and 8%, for 1, 2, 3, 4, and 5, respectively; SEM = 5.3). In conclusion, breed should be considered in the model being developed. A LS approach was not suitable, but a CRD experiment after these adaptation procedures appears promising.

Effects of different fresh-cut forages and their hays on feed intake, digestibility, heat production, and ruminal methane emission by Boer x Spanish goats.

Twenty-four yearling Boer × Spanish wethers were used to assess effects of different forages, either fresh (Exp. 1) or as hay (Exp. 2), on feed intake, digestibilities, heat production, and ruminal methane emission. Treatments were: 1) Sericea lespedeza (SER; Lespedeza cuneata), a legume high in condensed tannins (CT; 20% and 15% in fresh forage and hay, respectively), 2) SER supplemented with polyethylene glycol (SER-PEG; 25 g/d), 3) alfalfa (Medicago sativa), a legume low in CT (ALF), and 4) sorghum-sudangrass (Sorghum bicolor), a grass low in CT (GRASS). Experiments were 22 d, which included 16 d for acclimatization followed by a 6-d period for fecal and urine collection, and gas exchange measurement (last 2 d). Intake of OM was 867, 823, 694, and 691 g/d (SEM = 20.1) with fresh forage, and 806, 887, 681, and 607 g/d with hay for SER, SER-PEG, ALF, and GRASS, respectively (SEM = 46.6). Apparent total tract N digestion was greater for SER-PEG vs. SER (P < 0.001) with fresh forage (46.3%, 66.5%, 81.7%, and 73.2%; SEM = 1.71) and hay (49.7%, 71.4%, 65.4%, and 54.8% for SER, SER-PEG, ALF, and GRASS, respectively; SEM = 1.57). Intake of ME was similar among treatments with fresh forage (8.24, 8.06, 7.42, and 7.70 MJ/d; SEM = 0.434) and with hay was greater for SER-PEG than ALF (P < 0.03) and GRASS (P < 0.001) (8.63, 10.40, 8.15, and 6.74 MJ/d for SER, SER-PEG, ALF, and GRASS, respectively; SEM = 0.655). The number of ciliate protozoa in ruminal fluid was least for SER with fresh forage (P < 0.01) (9.8, 20.1, 21.0, and 33.6 × 10(5)/ml; SEM = 2.76) and hay (P < 0.02) (6.3, 11.4, 13.6, and 12.5 × 10(5)/ml for SER, SER-PEG, ALF, and GRASS, respectively; SEM = 1.43). Methane emission as a percentage of DE intake was lower (P < 0.01) for SER vs. ALF and GRASS with fresh forage (6.6, 8.3, 9.4, and 9.2%; SEM = 0.64) and hay (4.3, 4.9, 6.4, and 6.7% for SER, SER-PEG, ALF, and GRASS, respectively; SEM = 0.38). In summary, methane emission in this short-term experiment was similar between a legume and grass low in CT as fresh forage and hay. The CT in SER markedly decreased N digestibility and elicited a moderate decline in ruminal methane emission. Supplementation with PEG alleviated the effect of CT on N digestibility but not ruminal methane emission, presumably because of different modes of action. In conclusion, potential of using CT-containing forage as a means of decreasing ruminal methane emission requires further study, such as with longer feeding periods.

Effects of restricted feed intake on heat energy by different goat breeds.

Sixteen Boer goat doelings, 16 Spanish doelings, and 8 Angora doelings and 8 wethers, 283, 316, and 330 d of age initially (SEM = 5.0), respectively, were used to evaluate effects of nutrient restriction on heat energy (HE). During the first and second 10-wk phases, 8 animals of each breed were fed a 50% concentrate pelletized diet at a level adequate for maintenance and moderate energy accretion (CONT). Other animals were fed approximately 50% of these amounts 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 (REST). Average daily gain was 43, -20, 16, -78, 8, and -48 g in phase 1 (SEM = 5.0) and 26, 44, 50, 65, 27, and 32 g in phase 2 (SEM = 3.5) for Angora-CONT, Angora-REST, Boer-CONT, Boer-REST, Spanish-CONT, and Spanish-REST, respectively. Total HE was greater for CONT vs. REST in both phases (P < 0.001), greater in phase 1 for Angora than for Boer (P < 0.01) and Spanish (P < 0.01), and greatest (P < 0.01) in phase 2 among breeds for Angora [481, 347, 430, 356, 424, and 338 kJ/kg of BW(0.75) per day in phase 1 (SEM = 11.1), and 494, 479, 445, 397, 444, and 406 kJ/kg of BW(0.75) per day in phase 2 (SEM = 11.3) for Angora-CONT, Angora-REST, Boer-CONT, Boer-REST, Spanish-CONT, and Spanish-REST, respectively]. Equations describing the temporal pattern of HE (kJ/kg of BW(0.75) per day), expressed as a percentage of the wk-0 value and corrected for corresponding breed × week CONT means, in phase 1 were 95.8 ± 2.43 - (8.18 ± 1.144 × week) + (0.655 ± 0.1098 × week(2)) for Angora (R(2) = 0.58), 95.3 ± 2.63 - (4.34 ± 1.237 × wk) + (0.271 ± 0.1187 × wk(2)) for Boer (R(2) = 0.41), and 97.4 ± 2.21 - (4.69 ± 1.068 × wk) + (0.282 ± 0.1021 × wk(2)) for Spanish (R(2) = 0.53). Phase 2 equations were 78.9 ± 2.22 + (8.74 ± 1.036 × wk) - (0.608 ± 0.0095 × wk(2)) for Angora (R(2) = 0.60), 77.5 ± 2.10 + (3.30 ± 0.978 × wk) - (0.153 ± 0.0942 × wk(2)) for Boer (R(2) = 0.39), and 80.6 ± 2.50 + (4.50 ± 1.165 × wk) - (0.208 ± 0.1122 × wk(2)) for Spanish (R(2) = 0.43). These equations indicate that changes in HE in response to nutrient restriction and realimentation were more rapid and of greater magnitude in Angora vs. Boer and Spanish. The temporal pattern of decline in HE by Boer and Spanish during restriction was similar, but the subsequent rise with realimentation was slower and smaller for Boer. In conclusion, most appropriate methods of predicting change in the maintenance energy requirement during and after periods of limited feed intake may differ among breeds of goats.

Effects of level of feeding on energy utilization by Angora goats.

Twelve mature Angora does were used in a replicated 3 × 3 Latin square to determine effects of feeding level on energy utilization. Fiber growth and change in tissue (nonfiber) mass were determined in the first 4 wk of 6-wk periods, preceded by 14 or 18 d of adaptation. Determination of ME intake and gas exchange measures occurred in wk 4, followed by feeding near maintenance, then fasting in wk 5 and 6 to determine the ME requirement for maintenance (ME(m)). A 60% concentrate diet was fed at levels to approximate 100, 125, and 150% of assumed ME(m) [low, medium (med), and high, respectively]. Digestibilities and diet ME/GE were not affected by treatment with different amounts of feed offered and subsequent intake near ME(m). Heat energy during fasting (261, 241, and 259 kJ/kg of BW(0.75); SEM = 8.7) and efficiency of ME used for maintenance (71.6, 69.6, and 69.2%; SEM = 2.29) were similar among treatments, although ME(m) differed (P < 0.04) between med and high (365, 344, and 377 kJ/kg of BW(0.75) for low, med, and high, respectively; SEM = 10.3). Tissue gain was less (P < 0.01) for low than for the mean of med and high (MH; -0.6, 23.7, and 29.8 g/d), although clean fiber growth only tended (P < 0.09) to differ between low and MH (5.60, 6.57, and 7.36 g/d for low, med, and high, respectively; SEM = 0.621). Intake of ME was greater (P < 0.01) for MH than for low (6.87, 8.22, and 8.41 MJ/d for low, med, and high, respectively). Total heat energy was less (P < 0.02) for low vs. MH and tended (P < 0.07) to be greater for high than for med (6.03, 6.31, and 6.77 MJ/d); mobilized tissue energy was low but greater (P < 0.02) for low vs. MH (0.16, 0.01, and 0.04 MJ/d for low, med, and high, respectively). Efficiency of ME use for fiber growth was similar among treatments (17.2, 16.3, and 17.7% for low, med, and high, respectively; SEM = 1.61). In conclusion, efficiency of ME use for fiber growth was similar to the NRC recommendation regardless of feeding level, although ME(m) was decreased perhaps because of experimental conditions used. Energy appeared partitioned to fiber growth, but preferential usage was not complete possibly because energy metabolism for tissue accretion reached a plateau with the greatest feeding level.

Effects of stage of lactation and dietary concentrate level on energy utilization by Alpine dairy goats.

Twenty-four lactating and 13 nonlactating Alpine goats were used to determine effects of stage of lactation and dietary concentrate level on energy utilization. Diets comprising 60 or 20% concentrate (60%C and 20%C, respectively) were consumed ad libitum by lactating animals and at a level of intake near maintenance by nonlactating animals. Measurement periods were d 25 to 31 (early), 87 to 94 (mid), and 176 to 183 (late) of lactation. Eleven observations were made in early and mid lactation for each diet, and 8 and 7 were made in late lactation for the 60%C and 20%C diets, respectively. Efficiency of metabolizable energy (ME) use for maintenance (66.9, 71.4, and 61.1% for early, mid, and late lactation, respectively) and the maintenance ME requirement (479, 449, and 521 kJ/kg of BW(0.75) for early, mid, and late lactation, respectively) determined with nonlactating animals differed among stages of lactation. The efficiency of ME use for maintenance was similar between diets, but the maintenance requirement tended to be greater for the 60%C than for the 20%C diet (504 vs. 463 kJ/kg of BW(0.75)). The latter difference may have involved greater ME intake for the 60%C diet, resulting in a slightly greater difference between ME intake and total heat energy for the 60%C compared with the 20%C diet (11 vs. -8 kJ/kg of BW(0.75)). Intake of ME by lactating goats was greater for the 60%C than for the 20%C diet (18.6 vs. 16.3 MJ/d). Recovered energy in lactation from mobilized tissue tended to be greater for the 60%C than for the 20%C diet (8.44 vs. 6.55 MJ/d) and differed among stages of lactation (2.60, 1.59, and 1.13 MJ/d in early, mid, and late lactation, respectively). Recovered energy in tissue gain was similar among stages of lactation and between diets and was not different from 0. Efficiency of use of dietary ME for lactation differed among stages of lactation (59.5, 51.9, and 65.4% for early, mid, and late lactation, respectively) and tended to be greater for the 60%C than for the 20%C diet (64.2 vs. 54.9%). The efficiency of use of dietary ME for maintenance and lactation was similar among stages of lactation and was greater for the 60%C compared with the 20%C diet (64.3 vs. 60.9%). Predicted milk yield from National Research Council requirements was reasonably accurate. In conclusion, using data of nonlactating goats to study energy utilization for maintenance in lactation has limitations. Efficiency of energy use by lactating dairy goats consuming diets high in concentrate appears greater than that by goats consuming diets low in concentrate. Despite differences in nutrient requirement expressions, observations of this study support National Research Council recommendations of energy requirements of lactating dairy goats.

Effects of stage of lactation and level of feed intake on energy utilization by Alpine dairy goats.

Thirty-six lactating Alpine does were used to determine effects of stage of lactation and level of feed intake on energy utilization. Twelve does were assigned to measurement periods in early, mid, and late lactation (wk 5, 13, and 27, respectively). For 6 does of each group, after ad libitum consumption of a 60% concentrate diet, feed intake was restricted to near the metabolizable energy (ME) requirement for maintenance (ME(m)) for 8 d followed by fasting for 4 d. For other does, fasting immediately followed ad libitum consumption. Intake of ME was similar among stages of lactation with ad libitum intake (22.1, 22.1, and 19.8 kJ/d in early, mid, and late lactation, respectively). The efficiency of ME use for maintenance determined with does fed near ME(m) averaged 81%. Fasting heat energy was greater for ad libitum consumption than for near ME(m) consumption [368 vs. 326 kJ/kg of body weight (BW)(0.75)] and was numerically lowest among stages in late lactation with near ME(m) intake (334, 350, and 295 kJ/kg of BW(0.75) in early, mid, and late lactation, respectively) and ad libitum consumption (386, 384, and 333 kJ/kg of BW(0.75) in early, mid, and late lactation, respectively). The efficiency of use of dietary ME for lactation was greater for consumption near ME(m) than for consumption ad libitum (67.9 vs. 58.6%) and with ad libitum consumption tended to decrease with advancing stage of lactation (63.9, 57.3, and 54.5% for early, mid, and late lactation, respectively). Estimated ME(m) was greater for ad libitum intake than for near ME(m) intake and was lowest during late lactation (429, 432, and 358 kJ/kg of BW(0.75) for near ME(m) intake and 494, 471, and 399 kJ/kg of BW(0.75) for ad libitum intake in early, mid, and late lactation, respectively). However, because of increasing BW as the experiment progressed, ME(m) (MJ/d) was similar among stages of lactation with both levels of intake. The efficiency of ME use for maintenance and lactation was similar among stages of lactation and greater with near ME(m) intake than ad libitum intake (77.1 vs. 67.7%). In conclusion, the ME(m) requirement (kJ/kg of BW(0.75)) of does in late lactation was less than in early and mid lactation. A marked effect of restricted feed intake subsequent to ad libitum consumption on estimates of efficiency of energy use for maintenance and lactation was observed compared with use of nonlactating animals. Level of feed intake can have substantial effect on estimates of energy utilization by lactating dairy goats.

Invited review: feeding behavior of goats.

Factors influencing the feeding behavior of goats include grazing management practices, type of vegetation and season, breed and stage of production, group size, and properties of diets fed in confinement. Considerable information has been gathered from visual observation during daylight. However, tools are now available to characterize the feeding behavior of goats while grazing and while in confinement throughout the day. Global positioning system collars can be used to assess horizontal and vertical distances traveled, up or down position of the head, and movement within pasture or rangeland areas. A commercially available leg activity monitor allows estimation of the number of steps and time spent standing, lying, and moving rapidly without grazing. However, these measurements do not directly determine grazing. Therefore, prediction equations based on visual observation must be developed. Classification tree analysis is a robust method in developing these equations because the decision tree can be pruned or expanded to provide the best fit. Another equipment system determines time spent eating, ruminating, and remaining idle from the pattern of jaw movement. In addition to use of n-alkanes as internal markers to estimate digestibility, their profile can provide an indication of the botanical composition of the selected diet. Automated feeding systems for confined goats permit determinations such as number of feeder visits and meals, eating time, and rate and pattern of feed intake. Heart rate measured while goats are in normal production settings can be used to predict total energy expenditure through multiplication by energy expenditure per heartbeat of individual animals. To partition the activity energy cost, an estimate of ME intake or measures of changes in body energy status and milk energy yield are needed to determine other sources of heat to be subtracted from total energy expenditure. These methods create the opportunity to gain a fuller understanding of factors influencing the feeding behavior of goats and the relationships with levels and efficiencies of production.

Effects of stage of lactation and dietary forage level on body composition of Alpine dairy goats.

Multiparous Alpine does (42) were used to determine how stage of lactation and dietary forage level affect body composition. The feeding and body composition portion of the study had a 2 x 3 factorial arrangement of treatments. Eighteen does were fed a 40% forage diet (40F) and 18 received a diet with 60% forage (60F) for approximately 2, 4, or 6 mo of lactation (59 +/- 1.3, 116 +/- 1.0, and 184 +/- 1.4 d, respectively), followed by determination of body composition (6 does per diet at each time of slaughter). Does were assigned sequentially to treatments as kidding occurred. The 60F diet had 20% more dehydrated alfalfa pellets than the 40F diet, with higher levels of corn and soybean meal and inclusion of supplemental fat in the 40F diet. Initial body composition measures were made with 6 other does a few days after kidding (0 mo; 4 +/- 0.6 d). Before parturition, does were fed a 50% concentrate diet free choice. Intake of dry matter was greater for 60F than for 40F, average daily gain tended to be affected by an interaction between diet and month (0, 24, 121, -61, 46, and 73 g), and 4% fat-corrected milk was less in mo 5 to 6 than earlier. Internal fat mass was greatest among times at 6 mo and greater for 40F than for 60F. Mass of the gastrointestinal tract was less for 40F than for 60F and decreased with increasing time in lactation. Concentrations of fat in the carcass (13.8, 13.1, 16.5, 11.2, 11.5, and 14.4%), noncarcass tissues (18.6, 24.2, 33.3, 14.3, 16.5, and 24.5%), and empty body (16.5, 18.7, 25.2, 12.9, 14.1, and 19.5% for 40F at 2 mo, 40F at 4 mo, 40F at 6 mo, 60F at 2 mo, 60F at 4 mo, and 60F at 6 mo, respectively) were affected by stage of lactation and diet. Based on daily change in tissue mass and energy, energy concentration in tissue mobilized or accreted was 16, 20, and 32 MJ/kg in 1 to 2, 3 to 4, and 5 to 6 mo of lactation, respectively. In conclusion, based on tissue mass, more energy was expended by the gastrointestinal tract with 60F than with 40F. Considerable internal fat appeared to be mobilized in early lactation, particularly with the diet moderate to high in forage, with more rapid and a greater magnitude of repletion by does consuming the diet lower in forage. The concentration of energy in tissue mobilized or accreted varied with stage of lactation, being considerably greater at 5 to 6 mo of lactation than earlier.

Effects of breed and diet on growth and body composition of crossbred Boer and Spanish wether goats.

Sixty growing 3/4 Boer x 1/4 Spanish (BS) and Spanish (SP) wethers were used to determine influences of diet and breed on growth and body composition. A pelleted 50% concentrate diet (CD) and a diet based on grass hay (HD) were fed for ad libitum intake. Six wethers of each breed were slaughtered at 0 wk (total of 12). Six wethers of each diet-breed combination were slaughtered at 14 and 28 wk (24 per time) after consumption of the CD or HD. Initial BW of fed wethers were 21.6 and 18.8 kg for BS and SP, respectively (SEM = 0.7). Average daily gain during the entire experiment was influenced by an interaction (P < 0.05) between breed and diet (199, 142, 44, and 50 g/d for BS:CD, SP:CD, BS:HD, and SP:HD, respectively). Carcass mass was greater (P < 0.05) for CD vs. HD (56.2, 56.2, 53.2, and 54.0% of empty BW for BS:CD, SP:CD, BS:HD, and SP:HD, respectively). Mass of the liver (2.11, 1.92, 2.00, and 1.98% of empty BW; SEM = 0.05) and gastrointestinal tract (5.50, 4.83, 8.43, and 8.36% of empty BW for BS:CD, SP:CD, BS:HD, and SP:HD, respectively; SEM = 0.16) tended (P < 0.07) to be influenced by an interaction between breed and diet. Mass of internal fat (12.2, 12.1, 3.4, and 3.4% empty BW for BS:CD, SP:CD, BS:HD, and SP:HD, respectively; SEM = 0.3) differed (P < 0.05) between diets. Energy in the carcass (320, 236, 87, and 79 MJ), noncarcass tissues (318, 237, 77, and 72 MJ), and empty body (638, 472, 164, and 150 MJ) ranked (P < 0.05) BS:CD > SP:CD > BS:HD and SP:HD. Empty body concentration of protein was 18.3, 17.5, 18.3, and 19.7% (SEM = 0.3) and of fat was 24.0, 23.4, 10.8, and 10.3% for BS:CD, SP:CD, BS:HD, and SP:HD, respectively (SEM = 0.6). Energy concentration in accreted tissue was 17.0, 18.7, 16.3, and 6.4 MJ/kg for CD:wk 1 to 14, CD:wk 15 to 28, HD:wk 1 to 14, and HD:wk 15 to 28, respectively (SEM = 1.4). In conclusion, relatively high growth potential of growing Boer crossbred goats with a moderate to high nutritional plane does not entail a penalty in realized growth when the nutritional plane is low. Body composition of growing Boer and Spanish goats is fairly similar regardless of growth rate. For growing meat goats other than with a prolonged limited nutritional plane, an average energy concentration in accreted tissue is 17.3 MJ/kg.

Technical Note: The relationship between heart rate and energy expenditure in growing crossbred Boer and Spanish wethers.

Eight Boer (75%) x Spanish (BS) and 8 Spanish (S) wethers (155 +/- 8 d of age and 19.2 +/- 2.3 kg of BW initially) were used in a replicated crossover design with a 2 x 2 factorial arrangement of treatments to determine effects of genotype, diet quality, and time of day on energy expenditure (EE), heart rate (HR), and EE:HR with ad libitum, near maintenance, and fasting levels of feed intake. Diets were 65% concentrate or coarsely ground alfalfa hay. Energy expenditure was ranked (P < 0.05) ad libitum > maintenance > fasting (500, 390, and 270 kJ/kg of metabolic BW). Heart rate did not differ between genotypes when fasting and with maintenance intake, but was greater (P < 0.05) for S than for BS when intake was ad libitum (BS: 55, 71, and 92; S: 52, 72, and 100 beats/min for fasting, maintenance, and ad libitum, respectively, SEM = 2.0). There was an interaction in EE:HR (P < 0.05) between level of feed intake and genotype (BS: 5.31, 5.59, and 5.00; S: 5.07, 5.57, and 5.22 kJ/kg of metabolic BW:beat/min for ad libitum, maintenance, and fasting, respectively, SEM = 0.13), without an effect of diet. The effect of time on EE, HR, and EE:HR differed among levels of intake (P < 0.05). General patterns of change in EE and HR as time of day advanced did not differ, but increases near meals followed by decreases were of slightly greater magnitude for maintenance than for ad libitum intake. The ratio of EE:HR was greater for the maintenance level of feed intake than for ad libitum intake at most times. These results indicate similar potential for use of HR to predict EE of different genotypes of growing meat goats and that establishing EE:HR with different diets or levels of intake may not be crucial. Magnitudes of difference among hours suggest that when EE:HR is used to predict EE of confined goats from full-day measurement of HR, EE:HR should be determined over an extended period of time, such as 24 h.

ASAS Centennial Paper: Impact of animal science research on United States goat production and predictions for the future.

Goat research in the United States has increased but at a rate less than that in production. Research on goat meat includes nutritional quality, packaging, color, sensory characteristics, and preslaughter management. Goat skins have value for leather, but quality of goat leather has not been extensively studied. Research in the production, quality, antibiotic residues, and sensory characteristics of goat milk and its products has aided development of the US dairy goat industry. Limited progress has been made in genetic improvement of milk or meat production. There is need to explore applications of genomics and proteomics and improve consistency in texture and functionality of goat cheeses. New goat meat and milk products are needed to increase demand and meet the diverse tastes of the American public. Despite research progress in control of mohair and cashmere growth, erratic prices and sale of raw materials have contributed to further declines in US production. Innovative and cooperative ventures are needed for profit sharing up to the consumer level. Internal parasites pose the greatest challenge to goat production in humid areas largely because of anthelmintic resistance. Study of alternative controls is required, including immunity enhancement via nutrition, vaccination, pasture management such as co-grazing with cattle, and genetic resistance. Similarly, the importance of health management is increasing related in part to a lack of effective vaccines for many diseases. Nutrition research should address requirements for vitamins and minerals, efficiencies of protein utilization, adjusting energy requirements for nutritional plane, acclimatization, and grazing conditions, feed intake prediction, and management practices for rapid-growth production systems. Moreover, efficient technology transfer methods are needed to disseminate current knowledge and that gained in future research.

Technical Note: Effects of tethering on herbage selection, intake and digestibility, grazing behavior, and energy expenditure by Boer x Spanish goats grazing high-quality herbage.

Twenty-four yearling Boer x Spanish goats were used in a crossover experiment to determine the effects of tethering on herbage selection, intake and digestibility, grazing behavior, and energy expenditure (EE) with high-quality herbage. Four 0.72-ha paddocks of wheat (Triticum aestivum) and berseem clover (Trifolium alexandrium) were grazed in the spring. Each paddock hosted 6 animals, 3 with free movement and 3 attached to a 3-m tether that was moved daily and provided access to an area of 28.3 m(2). One animal of each treatment and paddock was used to determine herbage selection, fecal output, or grazing behavior and EE. Herbage DM mass in tethered areas before grazing averaged 2,649 and 2,981 kg/ha in periods 1 and 2, respectively. The CP concentration in ingesta was greater (P < 0.05; 23.1 and 20.3 +/- 0.82%) for free vs. tethered animals, although in vitro true DM digestion (75.7 and 76.5 +/- 1.20%, respectively) did not differ (P > 0.05) between treatments. Intake of ME based on in vitro true DM digestion and fecal output was greater (P < 0.05) for free vs. tethered animals (12.7 and 10.4 +/- 0.89 MJ/d). No treatment effects were observed (P > 0.05) for time spent ruminating or grazing (405 and 366 +/- 42.5 min/d, respectively), although mean EE was greater (P < 0.05) for free vs. tethered animals (633 and 512 +/- 27.4 kJ/kg of BW(0.75) for free and tethered, respectively), with differences (P < 0.05) between treatments at each hour of the day. Tethering animals may be acceptable to model those with free movement for some measures such as ingesta composition but appears inappropriate for others, such as energy metabolism.

The effect of a condensed tannin-containing forage on methane emission by goats.

The objective of this study was to compare methane emission by goats consuming the condensed tannin-containing forage sericea lespedeza (Les-pedeza cuneata) or a mixture of crabgrass (Digitaria ischaemum) and Kentucky 31 tall fescue (Festuca arundinacea). Two groups of 12 Angora does (initial average BW = 41.5 +/- 2.7 kg) that previously grazed a pasture of sericea lespedeza or crabgrass/tall fescue for approximately 4 mo were used. After 1 wk of adaptation to metabolism cages, gas exchange was measured for 24 h in an open-circuit respiration calorimetry system with four head boxes. Forage harvested daily from the previously grazed pastures was consumed ad libitum. Crude protein concentration was 10.3 and 13.0%, IVDMD was 64.5 and 75.3%, and the level of condensed tannins was 17.7 and 0.5% for sericea lespedeza and crabgrass/tall fescue, respectively. Dry matter intake (1.11 vs. 0.67 kg/d) and digestible DMI (estimated from IVDMD; 0.71 vs. 0.51 kg/d) were greater (P < 0.01) for sericea lespedeza than for crabgrass/tall fescue. Ruminal ammonia N (3.7 and 9.9 mg/dL; P < 0.001) and plasma urea-N concentrations (16.7 and 20.9 mg/dL; P = 0.07) were lower for sericea lespedeza than for crabgrass/tall fescue. Concentrations of individual and total VFA and the acetate-to-propionate ratio in ruminal fluid did not differ between treatments (P > 0.19). Despite higher DMI by goats fed sericea lespedeza, daily energy expenditure (409 vs. 431 kJ/kg BW(0.75)), heart rate (70 vs. 73 beats/min), and the ratio of energy expenditure to heart rate (5.82 vs. 5.94) did not differ between sericea lespedeza and crabgrass/tall fescue, respectively (P > 0.13). Methane emission expressed as both quantity per day or relative to DMI was lower (P <0.001) for sericea lespedeza than for crabgrass/tall fescue (7.4 vs. 10.6 g/d and 6.9 vs. 16.2 g/kg DMI). Substantial differences between the forages in condensed tannins concentration and methane emission by Angora goats suggest that condensed tannins decreased methane emission.

Effects of prolactin administered to a perfused area of the skin of Angora goats.

It is suspected that prolactin may affect mohair growth; therefore, effects of infusing prolactin on mohair growth were investigated using a skin perfusion technique. Seven Angora wethers (average body weight, 30 +/- 3 kg) were implanted bilaterally with silicon catheters into the superficial branches of the deep circumflex iliac artery and vein. For the first 14 d of the experiment, animals were infused (2.4 mL/h) with prolactin (one side) or control (other side) into the deep circumflex iliac arteries. The infusion rate of prolactin was 2.21 mg/d and was calculated to triple prolactin blood concentration in the perfused region. The area of skin supplied by the deep circumflex iliac artery was approximately 240 cm2. Two weeks after the cessation of infusions, 100-cm2 areas within the perfused regions were shorn to determine mohair growth. Greasy and clean mohair production was decreased (P < 0.05) by prolactin compared with control (3.79 vs 4.62 and 3.02 vs 3.67 g/[100 cm2 x 28 d], respectively). Oxygen satura tion in blood hemoglobin from the deep circumflex iliac veins was greater (P < 0.02) on the side infused with prolactin than on the control side (75.1 vs 68.2%). Higher concentrations of methionine, lysine, valine, isoleucine, and leucine were observed in blood of the deep circumflex iliac vein on the side infused with prolactin vs that infused with control (P < 0.05). In conclusion, direct skin infusion with prolactin decreased mohair fiber synthesis by the skin and may have concomitantly lessened oxygen consumption. Thus, effects of increasing prolactin concentration approximately two-fold in the skin on mohair fiber growth may not be limited to simple competition for nutrients between skin and other tissues such as the mammary gland.

Effects of small peptides or amino acids infused to a perfused area of the skin of Angora goats on mohair growth.

The effect of infusing dipeptides or their amino acids on mohair growth of Angora goats was investigated using a skin perfusion technique. Seven Angora wethers (average BW 24 +/- 2.5 kg) were implanted bilaterally with silicon catheters into the superficial branches of the deep circumflex iliac artery and vein and carotid artery. The experiment consisted of three 28-d phases. In the first 14 d of Phases 1 and 3, saline was infused into deep circumflex iliac arteries supplying skin and in Phase 2 a mixture of dipeptides (methionine-leucine [Met-Leu], lysine-leucine [Lys-Leu]) was infused into the artery on one side, and free amino acids were administered on the other side. Infusion rates of peptides were 0.85 mg/h Met-Leu and 0.85 mg/h Lys-Leu in 2.4 mL saline. Infusion rates of amino acids were 0.474 mg/h Lys, 0.483 mg/h Met, and 0.743 mg/h Leu in 2.4 mL saline. A 100-cm2 area within the perfused region was used to determine mohair growth. Two weeks after the cessation of infusions, perfused areas were shorn. Clean mohair production from the dipeptide- and amino acids-perfused regions were similar (4.21 vs 4.35 g/[100 cm2 +/- 28 d], respectively; P > 0.05). However, clean mohair production during dipeptides and amino acids infusions was greater (P < 0.01) than that observed during saline infusions (3.63 g/[100 cm2 +/- 28 d]). There were no significant differences between dipeptides and free amino acids in concentrations of various hormones and metabolites in blood from deep circumflex iliac veins (P > 0.05). In conclusion, the studied small dipeptides and amino acids similarly increased mohair fiber growth, presumably through supplying limiting amino acids directly to the fiber follicle.