Arkansas - Agricultural Communication Services - University of ...
Arkansas - Agricultural Communication Services - University of ...
Arkansas - Agricultural Communication Services - University of ...
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<strong>Arkansas</strong> Animal Science Department Report 2001<br />
which created differences in the spontaneous heating characteristics<br />
<strong>of</strong> these bales. A total <strong>of</strong> 20 bales from each harvest<br />
year were selected for evaluation <strong>of</strong> rumen escape N. Initial<br />
moisture concentrations <strong>of</strong> the treatment bales ranged from<br />
17.8 to 32.5% in 1998 (Coblentz et al., 2000) and 21.9 to<br />
30.2% in 1999.<br />
Temperature data. Internal bale temperatures were<br />
monitored by inserting single thermocouple wires into the<br />
center <strong>of</strong> the bales. Bale temperatures were recorded at 0700<br />
and 1600 h for the first 10 d after baling and once daily (at<br />
1600 h) thereafter, until the end <strong>of</strong> the 60-d storage period.<br />
All temperature data were obtained with an Omega 450 AKT<br />
Type K thermocouple thermometer (Omega Engineering,<br />
Stamford, CT). For purposes <strong>of</strong> analysis, the mean internal<br />
bale temperature for a given day was considered the same as<br />
the observed temperature, except during the first 10 d, when<br />
the mean <strong>of</strong> the two observations was used.<br />
Forage Preparation and Analysis. After the storage<br />
period, at least two cores (Star Quality Samplers, Edmonton,<br />
AB, Canada) were taken from the ends <strong>of</strong> each bale (35-cm<br />
depth). Core samples were dried to constant weight under<br />
forced air at 122°F. Dry forage samples were ground through<br />
a Wiley mill (Arthur H. Thomas, Philadelphia, PA) equipped<br />
with a 1-mm screen prior to analysis. Total plant N was determined<br />
using a macro-Kjeldahl procedure (Kjeltec Auto 1030<br />
Analyzer, Tecator, Inc., Herndon, VA). The procedures used<br />
to determine estimates <strong>of</strong> rumen escape N utilized a preparation<br />
<strong>of</strong> Streptomyces griseus protease (P-5147; Sigma<br />
Chemical Co., St. Louis, MO) and were similar to those<br />
described by Coblentz et al. (1999). Estimates <strong>of</strong> rumen<br />
escape N were expressed on the basis <strong>of</strong> total plant N and<br />
DM. All forty samples <strong>of</strong> bermudagrass hay were evaluated<br />
in each <strong>of</strong> three separate runs; therefore, estimates <strong>of</strong> rumen<br />
escape N are the means <strong>of</strong> three individual evaluations.<br />
Statistical Analysis. Estimates <strong>of</strong> rumen escape N were<br />
regressed linearly (PROC REG; SAS Inst., Inc., Cary, NC) on<br />
two indices <strong>of</strong> spontaneous heating; these included maximum<br />
internal bale temperature, and the average internal bale temperature<br />
over the first 30 d <strong>of</strong> storage. For purposes <strong>of</strong> analysis,<br />
bale temperatures were averaged over the initial 30 d <strong>of</strong><br />
storage because little evidence <strong>of</strong> heating occurred beyond<br />
this time interval in previous studies. An independent test <strong>of</strong><br />
homogeneity (PROC GLM) was included to determine if<br />
a common line could be used to describe the data from<br />
both years.<br />
Results and Discussion<br />
For our test forages, the mean concentration <strong>of</strong> N was<br />
2.24 ± 1.3% in 1998 and 2.06 ± 1.2% in 1999 (14.0 and<br />
12.9% CP, respectively). Concentrations <strong>of</strong> rumen escape N<br />
for bermudagrass hays harvested in 1998 exhibited a range <strong>of</strong><br />
11.3 percentage units when expressed on a total N basis and<br />
0.41 percentage units when expressed on a DM basis (Fig. 1<br />
and 2, respectively). Slightly smaller ranges were observed<br />
for bales harvested in 1999 (9.0 and 0.37 percentage units,<br />
respectively), which can probably be explained on the basis<br />
<strong>of</strong> the narrower range <strong>of</strong> heating characteristics in these bales.<br />
Mean concentrations <strong>of</strong> rumen escape N were numerically<br />
greater for hay harvested in 1999 than in 1998 (57.1 vs. 44.6<br />
% <strong>of</strong> total N or 1.18 vs. 0.99% <strong>of</strong> DM). Estimates <strong>of</strong> rumen<br />
escape N for warm-season grasses can exceed 50% <strong>of</strong> the<br />
total N pool, and concentrations <strong>of</strong> rumen escape N for both<br />
harvest years were consistent with those determined for other<br />
warm-season grasses by various enzymatic and in situ<br />
methodologies (Coblentz et al., 1999).<br />
Both indices <strong>of</strong> spontaneous heating (maximum and<br />
30-d average temperature) positively affected (P < 0.0001)<br />
concentrations <strong>of</strong> rumen escape N; this was true when rumen<br />
escape N was expressed as a percentage <strong>of</strong> total N (Fig. 1) or<br />
DM (Fig. 2). In each <strong>of</strong> these cases, there was no difference<br />
(P ≥ 0.416) between slopes for hays made in 1998 and 1999,<br />
thereby suggesting that heat affected concentrations <strong>of</strong> rumen<br />
escape N consistently across years. Across the entire range <strong>of</strong><br />
spontaneous heating, estimates <strong>of</strong> rumen escape N were generally<br />
greater in 1999 than in 1998, and intercepts were dissimilar<br />
(P < 0.0001) for these regression lines; therefore, no<br />
single line could be used to describe the relationship between<br />
rumen escape N and indices <strong>of</strong> spontaneous heating in any<br />
case. The r 2 statistics for these relationships were substantially<br />
greater for hays harvested in 1998 (range = 0.597 to 0.706)<br />
than in 1999 (range = 0.294 to 0.439); it remains unclear why<br />
these relationships were weaker for hay harvested in 1999.<br />
These data clearly suggest that rumen escape N is<br />
increased in bermudagrass hay in response to spontaneous<br />
heating during bale storage. The rate <strong>of</strong> increase in this fraction<br />
was similar (P > 0.05) across years, implying that this<br />
response may be consistent across some storage environments.<br />
Other work has shown similar rates <strong>of</strong> increase with<br />
heat for alfalfa hay (Coblentz et al., 1997). These increases in<br />
rumen escape N are likely to occur as a greater proportion <strong>of</strong><br />
the total N pool is associated with the cell wall; these relationships<br />
with spontaneous heating have been observed commonly<br />
in bermudagrass and other forages. Although our data<br />
is based on only two harvests, is also clear that estimates <strong>of</strong><br />
rumen escape N for bermudagrass can be affected by other<br />
factors; an incomplete list could potentially include forage<br />
variety, climate, fertilization, frequency <strong>of</strong> contaminant<br />
species, and maturity at harvest. One or more <strong>of</strong> these factors<br />
may explain the numerically higher estimates <strong>of</strong> rumen<br />
escape N observed across all increments <strong>of</strong> spontaneous heating<br />
during the 1999 harvest year. In this study, the proportions<br />
<strong>of</strong> N from bermudagrass that would likely escape the<br />
rumen intact are considerably higher than those <strong>of</strong>ten reported<br />
for cool-season grasses and legumes; however, our estimates<br />
<strong>of</strong> rumen escape N for these bermudagrass hays are<br />
consistent with similar estimates for numerous other warmseason<br />
grasses.<br />
Implications<br />
Rumen escape N for the 40 hays ranged from 40.7 to<br />
61.3% <strong>of</strong> total N and increased linearly with all indices <strong>of</strong><br />
spontaneous heating in both 1998 and 1999. These data sug-<br />
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