The n-alkane method was developed in temperate areas as a tool to estimate voluntary intake (VI) at pasture. The present study aimed to investigate the performance of n-alkanes as markers for estimating VI of steers (mean live weight 213 kg) offered a range of tropical grass hays and lucerne. Tropical and temperate forages have different n-alkane profiles and little is known about the issues which affect the accuracy of the method under tropical conditions. In two pen experiments (no. = 20 and no. = 24) n-alkanes were dosed using intraruminal controlled-release devices. Actual mean voluntary dry matter intakes for the diets ranged from 3·12 to 4·60 kg/day and actual mean dry-matter digestibility varied between 439 and 620 g/kg. n-Alkane profiles (C30 to C36) of the diets and the faeces for each animal were determined using gas chromatography. The recovery of each n-alkane was determined for each animal. Recoveries of n-alkanes were highly variable and generally varied between diets and between experiments. When adjacent n-alkanes were used to estimate VI (ratio method), agreement with actual VI was often poor. Despite this, where the recoveries of n-alkane pairs were similar, group mean VI were accurately estimated. From these data, it is concluded that estimation of VI in cattle offered tropical grass hays or lucerne hay, requires measured recoveries of both dosed and natural plant n-alkanes. The dosed and natural n-alkane pairs having the most similar recoveries should be used in the ratio method to estimate VI.

Drugs that activate beta 2-adrenoceptors (beta-agonists) are known to have profound effects on growth, body composition, and meat quality. Physiologically, these adrenoceptors are activated and regulated by the hormone adrenaline. Because the response to a drug or hormone is dependent partly on the density of the tissue receptors, the potential for predicting growth, carcass quality, or meat quality from knowing beta 2-adrenoceptor density in three disparate sample sites in cattle was examined. Cell membrane fragments were prepared using samples of longissimus muscle, semitendinosus muscle, or ear obtained within 30 min of death from 48 steers. Beta 2-Adrenoceptor density (Bmax) was measured in these membrane preparations by saturating them with the radioligand [125I]iodocyanopindolol. There was no correlation between Bmax values measured in ear samples, longissimus muscles, or semitendinosus muscles. Bmax measured in samples of ear did not correlate with any growth or carcass traits, including weight gain, carcass weight, fat depth, or eye muscle area. Bmax measured in longissimus muscle only correlated weakly with meat color, and Bmax measured in semitendinosus muscle only correlated with carcass weight. We conclude that beta 2-adrenoceptor density is not a useful predictor of growth, carcass quality, or meat quality in cattle.

An experiment was conducted to determine if molasses could be successfully used to administer dotriacontane (C32) and hexatriacontane (C36) n-alkane markers to steers and to compare this method with a commercially available intra-ruminal controlled release device (CRD). The experiment was conducted over two similar periods (runs) using 24 Brahman crossbred steers in each run to study the effect of marker delivery methods and tropical grass hay diets in a randomized complete block design with three replicates. All steers were housed individually in partially covered pens, received one of two buffel-grass hays (B20: 20-week regrowth; 0·72 g nitrogen (N) per 100 g and B8: 8-week regrowth; 1·11 g N per 100 g) and one of four marker delivery treatments (control: no marker; 200 mg/day of C32 and C36 n-alkanes from a CRD or offered three times (Ms ✕ 3) or five times (Ms ✕ 5) a day in molasses). Voluntary intake (VI) and dry matter digestibility (DMD) for diets differed (P < 0·001) with B8 greater than B20. There was no difference among marker treatments for VI but the control treatment had greater, unexplained and possibly spurious, DMD than the Ms ✕ 3 marker treatment. Although the recovery of n-alkanes was variable (0·84 to 1·05) adjacent odd- and even-chain n-alkanes were similar with no differences (P > 0·05) due to marker treatment or diet. The CRD supplied a consistent marker dose between 6 and 18 days after insertion. Deviation from the 24-h mean faecal concentration seldom varied more than 0·03 for the individual markers and 0·05 for C31/C32 and C33/C32 ratios for all treatments. Over all the n-alkanes studied, the between-day variation was less than the within-day variation. For instance, the average of subsamples taken at 06:00 h and 18:00 h was within proportionately 0·05 of the 10-day mean concentration for 0·38 and 0·25 of records for C32 and C36 markers, respectively. It was concluded that molasses containing C32 and C36 n-alkane markers and given either three or five times daily was as accurate as the commercial CRD in administering n-alkane markers to steers and provides a method of delivering n-alkanes over an extended period in grazing studies.