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PRODUCTION, MODELING, AND EDUCATION |



* Iowa State University, Ames 50011;
University of Maryland, College Park 20742;
Rose Acres Farms, Seymour, IN 47274; and
Purdue University, West Lafayette, IN 47907
1 Corresponding author: wpowers{at}iastate.edu
| ABSTRACT |
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Key Words: hen air emission diet ammonia hydrogen sulfide
| INTRODUCTION |
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| MATERIALS AND METHODS |
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The experiment was designed with 2 treatments. During each experimental phase, a total of 640 hens (initial BW = 1.36, 1.47, and 1.52 kg in trials 1, 2, and 3, respectively) were allocated randomly to 1 of 8 chambers (indirect calorimeters) that were built to allow for continuous monitoring of emissions from livestock. In each chamber, 80 birds were divided among 4 2-cage units (10 birds/cage, 355 cm2 of cage space/bird). Diets were assigned randomly to each of the 8 chambers (4 chambers/diet), with the chamber constituting the experimental unit.
Diets and Management
All diets were formulated to meet NRC (1994) nutrient requirements for laying hens. Feed (approximately 95, 97, and 99 g/hen per d in trials 1, 2, and 3, respectively) was offered twice daily (0600 and 1600 h) in a mash form, and feed intake was recorded weekly on a 2-cage unit basis (20 birds/unit). Samples of diets were retained weekly for determination of nutrient content. Composition of experimental diets is shown in Table 1
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Bird Measures
Hens were weighed at the beginning and end of each age period. Body weight change (BWC) within each chamber was calculated by subtracting the average chamber BW at the beginning of each trial from the average chamber BW at the end of each trial. Average daily feed intake (ADFI) of each chamber was calculated based on that weeks total feed consumption, divided by 7 d and the number of birds present. Eggs were collected daily from each 2-cage unit, and egg weight and number were recorded daily. Excreta production was determined at the end of each age phase, and a subsample was collected for compositional analysis. Average daily egg weights (ADEW), average daily egg production (ADEP), ADFI, and BWC over the study period were calculated at the end of each trial.
Measurements of Gaseous Concentrations
Eight chambers (2.14 x 3.97 x 2.59 m) were designed to continuously measure incoming and exhaust concentrations of NH3, H2S, NO, NO2, CO2, CH4, and NMTHC. Ammonia and NO were measured using a chemiluminescence NH3 analyzer (model 17C, Thermal Environmental Instruments, Franklin, MA), which is a combination of an NH3 converter and NO-NO2-NOx analyzer. Hydrogen sulfide was analyzed using pulsed fluorescence H2S-SO2 analyzer (model 450C, Thermal Environmental Instruments). Carbon dioxide was monitored using the BINOS 100 2M dual gas detector (Rosemount Analytical Inc., Orrville, OH). Methane and NMTHC were measured by flame ionization detector (model 200, VIG Industries Inc., Anaheim, CA). During trial 1, NMTHC data were not available due to the absence of calibration gases. Through software control, gaseous concentration monitoring of each chamber occurred in a sequential manner, beginning first with incoming air for 20 min, then through each of the 8 chambers exhaust airs for 15 min, with all gases measured simultaneously within a sample stream. Airflow rates into and out of each chamber were measured accurately using orifice plates, calibrated for each chamber under specific ranges of conditions. Cumulative NH3, H2S, NO, NO2, CO2, CH4, and NMTHC emissions from each chamber were calculated daily by averaging all recordings for that day (10 to 11 daily observations per chamber). Based on light periods, daytime and nighttime emissions were determined. The average daily gaseous emissions in each chamber were expressed as emission rate (mg/min), cumulative total mass (mg), daytime mass (mg), nighttime mass (mg), milligrams per kilogram of BW, and milligrams per hen.
Statistical Analyses
Performance data were analyzed using a GLM procedure, and emissions data were analyzed using a MIXED procedure of SAS (SAS Institute, 1990). For ADEW, ADEP, ADFI, and BWC variables, the model included the fixed effects of chamber and diet (CM and RE diets), the interaction between chamber and diet. For emissions data, the model tested the fixed effects of diet, age, and the interaction of diet and age on emission. Date was treated as a random variable. Significant differences among the means were declared at P
0.05.
| RESULTS AND DISCUSSION |
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Across ages, birds fed both the CM and RE diets performed similarly to the performance outlined for Hy-Line W-36 laying hens (Hy-Line International, 2003). Our findings were similar to work conducted by Keshavarz (2003), who reported ADEW of 51.5, 56.2, and 59.7 g; ADEP of 81.2, 73.9, and 69.3%; and ADFI of 91.1, 91.5, and 96.0 g at 20 to 35, 36 to 51, and 52 to 63 wk of age, respectively.
NH3 Emissions
Across ages, the RE diet reduced the daily mass of NH3 emitted (mg/hen) by 39% (Table 3
). Daily emissions of NH3 from hens fed the RE diet (185.5, 312.2, and 333.5 mg/hen) were significantly less than from hens fed the CM diet (255.1, 560.6, and 616.3 mg/hen) in the 21-, 38-, and 59-wk trials, respectively. Feeding the RE diet decreased the daily emission rate of NH3 emitted from all 3 age groups (16.3 vs. 26.9 mg/min, Table 3
). The RE diet also reduced the cumulative NH3 emission mass (mg) over the 3 ages studied by 39% (22,628 compared with 37,269 mg, Table 3
). Daily emission of NH3 adjusted for total live weight from hens fed the RE diet (203.4 mg/kg of BW) was less than daily emissions of NH3 from hens fed the CM diet (334.1 mg/kg of BW).
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Heber et al. (2004) measured emissions from a modern high-rise egg laying house using a chemiluminescence method along with multipoint extractive gas sampling and found that the average daily means of NH3 concentrations were 2.4, 16.1, and 43.3 mg/m3 for inlet, cage, and exhaust air, respectively, and the net NH3 emission rate was 387 ± 25 kg/d or 1.57 ± 0.10 g/d per hen. Liang et al. (2005) reported an annual average NH3 emission rate of 0.87 ± 0.29 g/d per hen for the high-rise houses, 0.094 ± 0.062 g/d per hen for the manure-belt houses with semiweekly manure removal, and 0.054 ± 0.026 g/d per hen for the manure-belt houses with daily manure removal. In the current study, NH3 emissions were determined in chambers over a 3-wk period with manure accumulation for the duration of the test period. Average NH3 emission was 0.47 ± 0.03 g/d per hen when fed a CM diet, which was lower than the value reported by Liang et al. (2005) for high-rise houses but greater than reported values for houses employing a manure belt. This suggests that had the experimental period been longer than 3 wk, average daily NH3 emissions may have been more similar to emissions reported from high-rise housing.
H2S Emissions
Daily H2S emissions from hens fed the RE diet (1.6, 7.1, and 3.7 mg/hen) were greater than from hens fed the CM diet (0.5, 1.9, and 0.8 mg/hen) at 21, 38, and 59 wk of age, respectively (Table 4
). Feeding the RE diet also increased the cumulative H2S emission mass 3-fold across all 3 age groups (322.8 vs. 104.9 mg). Daily H2S emission adjusted for total live weight from hens fed the RE diet (2.9 mg/kg of BW) was more than that from hens fed the CM diet (0.9 mg/kg of BW). Lim et al. (2003) reported H2S emissions from high-rise laying hen houses of 0.432 mg/kg of BW, which is about half of the emission observed in the current study when hens were fed the CM diet. Differences are likely due to the amount of time that excreta had been stored. Although H2S emissions increased 3-fold as a result of feeding the RE diet, the increase was not to the extent that most laying hen operations would trigger federal reporting requirements. Over 10 million hens would be needed on a single site for those reporting requirements to be exceeded.
Whitney et al. (1999) found that a mean reduction of 23% in the S concentration of nursery pigs diets during a 5-wk period tended to reduce H2S emissions from the stored manure, although this tendency was not significant. It was shown by J. Shurson, M. Whitney, and R. Nicolai (Univ. Minnesota, St. Paul, personal communication) that S excretion was reduced by 30%, by selecting low-S feed ingredients, without affecting their growth. In the current study, CaSO4, a S-containing compound, was added to the diet as an acidifying agent. This additional dietary S combined with the acidifying effect of the CaSO4 likely caused the increased H2S production. Because feed is ultimately the major source of manure S, 1 method of mitigating manure H2S emissions is to reduce dietary S. This can be done by reducing excess nutrients, selecting low-S ingredients, or including additives that improve digestive efficiency or alter the microflora in the large intestine (Clark et al., 2005). In addition, a reduction in pH from pH 7.0 to 6.0 has been shown to result in a doubling of the proportion of molecular H2S (Xue et al., 1998). Use of a dietary acidulant in the current study contributed to increased S emissions, suggesting that alternative acidulants should be considered to avoid exacerbating sulfurous emissions.
CH4 Emissions
Across ages, feeding the RE diet reduced daily CH4 emission (mg/hen) by 17% (Table 5
). Daily emissions from hens fed the RE diet (66.4 mg/hen) were less than emissions from hens fed the CM diet (80.2 mg/hen). Across ages, the RE diet decreased the daily emission rate of CH4 emitted (3.8 and 4.6 mg/min for RE and CM diets, respectively; Table 5
). The RE diet also reduced the cumulative CH4 emission mass (5,272 vs. 6,394 mg/d for RE and CM diets, respectively; Table 5
). Daily emission adjusted for total live weight of hens housed in each chamber from hens fed the RE diet (47.1 mg/kg of BW) was less than daily emission from hens fed the CM diet (57.1 mg/kg of BW). Twenty-one-week-old hens produced greater emissions of CH4 than did 38- and 59-wk-old hens when CH4 emissions are expressed on a per bird and per kilogram of BW basis. Although the reason for this is not evident, it does follow the same pattern as NH3 emissions, except that in the case of CH4, concentration is greater for the 21-wk old hens compared with both the 38- and 59-wk-old hens. No data are available to support differences in cecal fermentation patterns among hens of different ages, but differences, if they did exist, could explain the effect on CH4 production.
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CO2 Emissions
Daily CO2 emissions from hens fed the RE diet (74,548 mg/hen) were less than from hens fed the CM diet (78,432 mg/hen; Table 6
), as was daily emission adjusted for total live weight in the chamber (53,013 mg/kg of BW and 55,900 mg/kg of BW for hens fed the RE diet and the CM diet, respectively; Table 6
).
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NO and NMTHC
Daily NO emissions from hens fed the RE diet (0.2 mg/hen) were less than NO emissions from hens fed the CM diet (0.4 mg/hen; Table 7
). No age effects were observed (Table 7
). No diet or age effects on emissions of NO2 (Table 8
) and NMTHC (Table 9
) were observed in the current study. No data for these emissions were found in the literature for comparative purposes.
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| ACKNOWLEDGMENTS |
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Received for publication June 19, 2006. Accepted for publication August 22, 2006.
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