Weaning weight records of 24 758 Bonsmara calves produced by 503 sires in 30 herds, from 1980 to 1993, were used to examine the importance of the inclusion of herd-year-season by sire interaction in the estimation of genetic parameters. Three separate models were used in the DFREML analysis of the data. In the first, permanent maternal environment was included as an additional random factor, while in the second, herd-year-season by sire interaction was included, also as an additional random factor. Both these factors were included as additional random factors in the third model. The estimates of the (co)variance components and heritabilities for direct additive (a), maternal additive (m) and additional random factor (c) for the three models analysed, were as follows: Q'u, 138.04, 65.23, 67.46; (o'..nr 84.77,143.80, 66.8*3; (oa.., (o'p"r..nt 73.72, 71.01; (o'Hysxs:41.79,+1.39; (o'":251.31,274.78,265.97; (ozo: 490.37,497.35,490.74',hza'.0.28,0.13,0.14; h',n: 0.17,0.29,0.14. The results indicate the importance of both permanent maternal environment and herdyear-season by sire interaction in the estimation of the genetic parameters. The exclusion of herd-year-season by sire interaction could lead to a serious overestimation of the direct additive components. The same applies for permanent maternal environment. The exclusion of this factor could lead to a serious overestimation of the maternal components. Both these factors should therefore be included in the across-herd weaning weight analysis of Bonsmara cattle.Speengewig rekords van 24 758 Bonsmarakalwers, die nageslag van 503 bulle uit 30 kuddes gebore vanaf 1980 tot 1993, is gebruik om die invloed van die insluiting van kudde-jaar-seisoen by vaar interaksie op die beraming van die genetiese parameters te ondersoek. Drie aparte modelle is gebruik in die DFREML analise van die data. In die eerste is permanente maternale omgewingseffekte ingesluit as 'n addisionele toevallige effek. Permanente maternale omgewingseffekte is in die tweede model vervang met kudde-jaar-seisoen by vaar interaksie. In die derde model is beide die faktore as addisionele toevallige effekte ingeluit. Die beramings van die (ko)variansie komponente en oorerflikhede vir direk additief (a), maternaal additief (m) en addisionele toevallige effekte vir die drie modelle gebruik in die analise was soos vo^lg: (o2": 138.04,65.23, 67.46; (o2r: 84.77,143.8b, 66.83; (o2per ^: 73.72, 71 .01; (o2Hvsrsi 41 .79, 41 .39; (o2": 251 .31',"274.78, 265.97; (o'o: 490.37,497.35,490.74;h'^:0.28,0.13, 0.14;h'^:0.17,0.29,0.14. Die resultate dui op die belangrikheid van beide die twee addisionele toevallige effekte in die beraming van die genetiese parameters. Die uitsluiting van kudde-jaar-seisoen by vaar interaksie kan lei tot 'n ernstige oorberaming van die direk additiewe komponente. Dieselfde geld vir permanente maternale omgewing. Die uitsluiting van die effek kan weer op sy beurt lei tot 'n oorberaming van die maternaal additiewe komponente, Beide die effekte behoort dus ingesluit te word in die tussen-kudd...