Ocean surface layer carbon dioxide (CO2) data collected in the Gulf of Maine from 2004 to 2008 are presented. Monthly shipboard observations are combined with additional higher-resolution CO2 observations to characterize CO2 fugacity (fCO(2)) and CO2 flux over hourly to interannual time scales. Observed fCO(2) and CO2 flux dynamics are dominated by a seasonal cycle, with a large spring influx of CO2 and a fall-to-winter efflux back to the atmosphere. The temporal results at inner, middle, and outer shelf locations are highly correlated, and observed spatial variability is generally small relative to the monthly to seasonal temporal changes. The averaged annual flux is in near balance and is a net source of carbon to the atmosphere over 5 years, with a value of +0.38 mol m(-2) yr(-1). However, moderate interannual variation is also observed, where years 2005 and 2007 represent cases of regional source (+0.71) and sink (-0.11) anomalies. We use moored daily CO2 measurements to quantify aliasing due to temporal undersampling, an important error budget term that is typically unresolved. The uncertainty of our derived annual flux measurement is +/- 0.26 mol m(-2) yr(-1) and is dominated by this aliasing term. Comparison of results to the neighboring Middle and South Atlantic Bight coastal shelf systems indicates that the Gulf of Maine exhibits a similar annual cycle and range of oceanic fCO(2) magnitude but differs in the seasonal phase. It also differs by enhanced fCO(2) controls by factors other than temperature-driven solubility, including biological drawdown, fall-to-winter vertical mixing, and river runoff.

Concentrated separator by-product (CSB) is produced when beet molasses goes through an industrial desugaring process. To investigate the nutritional value of CSB as a supplement for grass hay diets (12.5% CP; DM basis), 4 ruminally and duodenally cannulated beef steers (332 +/- 2.3 kg) were used in a 4 x 4 Latin square with a 2 x 2 factorial arrangement of treatments. Factors were intake level: ad libitum (AL) vs. restricted (RE; 1.25% of BW, DM basis) and dietary CSB addition (0 vs. 10%; DM basis). Experimental periods were 21 d in length, with the last 7 d used for collections. By design, intakes of both DM and OM (g/kg of BW) were greater (P < 0.01; 18.8 vs. 13.1 +/- 0.69 and 16.8 vs. 11.7 +/- 0.62, respectively) for animals consuming AL compared with RE diets. Main effect means for intake were not affected by CSB (P = 0.59). However, within AL-fed steers, CSB tended (P = 0.12) to improve DMI (6,018 vs. 6,585 +/- 185 g for 0 and 10% CSB, respectively). Feeding CSB resulted in similar total tract DM and OM digestion compared with controls (P = 0.50 and 0.87, respectively). There were no effects of CSB on apparent total tract NDF (P = 0.27) or ADF (P = 0.35) digestion; however, apparent N absorption increased (P = 0.10) with CSB addition. Total tract NDF, ADF, or N digestion coefficients were not different between AL- and RE-fed steers. Nitrogen intake (P = 0.02), total duodenal N flow (P = 0.02), and feed N escaping to the small intestine (P = 0.02) were increased with CSB addition. Microbial efficiency was unaffected by treatment (P = 0.17). Supplementation with CSB increased the rate of DM disappearance (P = 0.001; 4.9 vs. 6.9 +/- 0.33 %/h). Restricted intake increased the rate of in situ DM disappearance (P = 0.03; 6.4 vs. 5.3 +/- 0.33 %/h) compared with AL-fed steers. Ruminal DM fill was greater (P = 0.01) in AL compared with RE. Total VFA concentrations were greater (P = 0.04) for CSB compared with controls; however, ammonia concentrations were reduced (P = 0.03) with CSB addition. At different levels of dietary intake, supplementing medium-quality forage with 10% CSB increased N intake, small intestinal protein supply, and total ruminal VFA.

In Exp. 1, 4 ruminally and duodenally cannulated beef steers (444.0 +/- 9.8 kg) were used in a 4 x 4 Latin square with a 2 x 2 factorial treatment arrangement to evaluate the effects of forage type (alfalfa or corn stover) and concentrated separator byproduct (CSB) supplementation (0 or 10% of dietary DM) on intake, site of digestion, and microbial efficiency. In Exp. 2, 5 wethers (44 +/- 1.5 kg) were used in a 5 x 5 Latin square to evaluate the effects of CSB on intake, digestion, and N balance. Treatments were 0, 10, and 20% CSB (DM basis) mixed with forage; 10% CSB offered separately from the forage; and a urea control, in which urea was added to the forage at equal N compared with the 10% CSB treatment. In Exp. 1, intakes of OM and N (g/kg of BW) were greater (P < 0.01) for steers fed alfalfa compared with corn stover. Steers fed 10% CSB had greater (P < 0.08) OM and N intakes (g/kg of BW) compared with 0% CSB-fed steers. Total duodenal, microbial, and nonmicrobial flows of OM and N were greater (P < 0.01) for steers fed alfalfa compared with corn stover. Steers fed 10% CSB had increased (P = 0.02) duodenal microbial flow (N and OM) compared with 0% CSB-fed steers. Forage x CSB interactions (P < 0.01) existed for total tract N digestibility; alfalfa with or without CSB was similar (67.4 vs. 69.5), whereas corn stover with CSB was greater than corn stover without CSB (31.9 vs. -23.9%). True ruminal OM digestion was greater (P < 0.09) in steers fed alfalfa vs. corn stover (73.0 vs. 63.1%) and in steers fed 10 vs. 0% CSB (70.3 vs. 65.8%). Microbial efficiency was unaffected (P > 0.25) by forage type or CSB supplementation. In Exp. 2, forage and total intake increased (linear; P < 0.01) as CSB increased and were greater (P < 0.04) in 10% CSB mixed with forage compared with 10% CSB fed separately. Feeding 10% CSB separately resulted in similar DM and OM apparent total tract digestibility compared with 10% CSB fed mixed. Increasing CSB led to an increase (linear; P < 0.02) in DM, OM, apparent N digestion, and water intake. Nitrogen balance (g and percentage of N intake) increased (linear; P < 0.08) with CSB addition. Feeding 10% CSB separately resulted in greater (P < 0.01) N balance compared with 10% CSB fed mixed. Using urea resulted in similar (P = 0.30) N balance compared with 10% CSB fed mixed. Inclusion of CSB improves intake, digestion, and increases microbial N production in ruminants fed forage-based diets.

The objective of this study was to compare fatty acid weight percentages and cholesterol concentrations of longissimus dorsi (LD), semitendinosus (ST), and supraspinatus (SS) muscles (n = 10 for each) of range bison (31 mo of age), feedlot-finished bison (18 mo of age), range beef cows (4 to 7 yr of age), feedlot steers (18 mo of age), free-ranging cow elk (3 to 5 yr of age), and chicken breast. Lipids were analyzed by capillary GLC. Total saturated fatty acids (SFA) were greater (P < 0.01) in range bison than in feedlot bison and were greater (P < 0.01) in SS of range beef cattle than in feedlot steers. Muscles of elk and range bison were similar (P > 0.05) in SAT. In LD, polyunsaturated fatty acids (PUFA) were highest (P < 0.01) for elk and range bison and lowest (P < 0.01) for feedlot steers within each muscle. Range bison and range beef cows had greater (P < 0.01) PUFA in LD and ST than feedlot bison or steers, respectively. Range-fed animals had higher (P < 0.01) n-3 fatty acids than feedlot-fed animals or chicken breast. Chicken breast n-6 fatty acids were greater (P < 0.01) than for muscles from bison, beef, or elk. Elk had higher (P < 0.01) n-6 fatty acids than bison or beef cattle; however, range-fed animals had higher (P < 0,01) n-6 fatty acids than feedlot-fed animals in ST. Conjugated linoleic acid (CLA, 18:2cis9, trans-11) in LD was greatest (P < 0.01) for range beef cows (0.4%), and lowest for chicken breast and elk (mean = 0.1%). In ST, CLA was greatest (P < 0.01) for range and feedlot bison and range beef cows (mean = 0.4%) and lowest for elk and chicken breast (mean = 0.1%). Also, SS CLA was greatest (P < 0.01) for range beef cows (0.5%) and lowest for chicken breast (0.1%). Mean total fatty acid concentration (g/100 g tissue) for all muscles was highest (P < 0.01) for feedlot bison and feedlot cattle and lowest (P < 0.01) for range bison, range beef cows, elk, and chicken. Chicken breast cholesterol (mg/100 g tissue) was higher (P < 0.01) than LD and ST cholesterol, which were lowest (P < 0.01; 43.8) for range bison and intermediate for the other species. Cholesterol in SS was highest (P < 0.01) for feedlot bison and steers, which were similar to chicken breast (mean = 61.2 vs 52.8 for the mean of the other species). We conclude that lipid composition of bison muscle varies with feeding regimen, and range-fed bison had muscle lipid composition similar to that of forage-fed beef cows and wild elk.