An in situ study was conducted on four rumen-cannulated wethers to determine (using 15 N infusion techniques) the microbial contamination (mg bacterial DM or crude protein (CP)/100 mg DM or CP) and the associated error on the effective degradability of fourteen feeds: barley and maize grains, soyabean and sunflower meals, full-fat soyabean, maize gluten feed, soyabean hulls, brewers dried grains, sugarbeet pulp, wheat bran, lucerne and vetch-oat hays, and barley and lentil straws. The DM or CP contamination in residues (M) fitted to single exponential or sigmoid) was proposed to match this fit. Asymptotic values (m) varied from 2·84 % to 13·3 % and from 2·85 % to 80·9 % for DM and CP, respectively. Uncorrected results underestimated the effective degradability of both DM (P,0·05) and CP (P, 0·01). For CP, this underestimation varied from 0·59 % to 13·1 %, with a higher but unascertainable error for barley straw. Excluding maize grain, the microbial contamination of both DM and CP, and the associated underestimation of the effective degradability of CP, were positively related to the cellulose content of the feed. The error in the effective degradability of CP was also negatively related to the CP content and its apparent effective degradability (R 2 0·867). This equation allows easier and more accurate estimates of effective degradability, needed to improve protein-rationing systems. The current systems of protein rationing for ruminants require an accurate knowledge of the quantity of the microbial and feed proteins that reach the post-ruminal tract. The magnitude of both protein fractions is influenced by the rumen degradation of feeds included in the ration. In situ methods are the most common way to obtain estimates of effective degradability (ED). However, adherent micro-organisms that colonise and degrade feed particles simultaneously contaminate them. The resultant underestimate of the ED of crude protein (CP) or amino acids in vegetable feeds may be important as a consequence of the high N content in micro-organisms, although feed characteristics determining microbial adherence and the development and persistence of the micro-organisms may also influence this underestimate.In spite of these errors, uncorrected ED values are commonly employed in current systems, because the estimation of microbial contamination is a laborious, complex and expensive procedure. Although microbial attachment has been the subject of many types of research, quantitative and systematic in situ studies across a wide range of feeds are scarce (Michalet-Doreau & Ould Bah, 1989), and in most cases these have focused only on the effects of N contamination on ED estimates. Studies on microbial colonisation may, however, also contribute to a better knowledge of factors affecting feed degradation (McAllister et al. 1994) and microbial protein supply associated with feed particles, which represents an important contribution to the nutrition of the ruminant (Merry & McAllan, 1983, Rodríguez et al. 2003. The objectives of the present...