Call number: LD2668 .T4 1962 Y8

Call number: LD2668 .T4 1966 H798 / Master of Science

Call number: LD2668 .T4 1979 H667 / Master of Science

Call number: LD2668 .T4 1953 D6 / Master of Science

This item was digitized as part of the Million Books Project led by Carnegie Mellon University and supported by grants from the National Science Foundation (NSF). Cornell University coordinated the participation of land-grant and agricultural libraries in providing historical agricultural information for the digitization project; the University of Arizona Libraries, the College of Agriculture and Life Sciences, and the Office of Arid Lands Studies collaborated in the selection and provision of material for the digitization project.

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M. Tech. Agriculture / Herbs are a rich source of active phytochemicals (flavonoids, phenols, antioxidants, ascorbic acid, carotenoids, mineral salts and terpenoids. They are an ancient source of flavouring, aromatic compounds and medicine. Herbs have always constituted an important component of the human diet, adding variation and flavour to staple foods, as well as being used for food preservation. They are mostly processed because of the perishable nature of its leaves. The quality of herbs therefore can be improved by the manipulation of light quality during production and also by sheltering them from environmental hazards such as excessive solar radiation, wind and flying pests. In this study the effect of photo-selective netting technology (ChromatiNet™) (red, pearl and yellow) with 40% shading and commercial black net with 25% shading used as a control were investigated on herbs. Three herbs (coriander, marjoram and oregano) were planted. The aim of the present study was to evaluate the responses of the three photo-selective nets (red, pearl and yellow) and the black net (control) on quality parameters and bioactive compounds in herbs (in this study, coriander, marjoram and oregano).

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Thesis (MScAgric)--University of Stellenbosch, 2000. / ENGLISH ABSTRACT: The objective of this study was to obtain more information regarding the characterisation of Afrikaner (A), Hereford (H) and Simmentaler (S) breeds in an initial crossbreeding programme and subsequent composite development. This involves the estimation of breed additive effects, breed maternal, individual heterotic effects and maternal heterotic effects in the initial crossbreeding phase and the estimation of genetic parameters and prediction of breeding values in later generations for birth weight (BW), weaning weight (WW) and cow efficiency (CE; WW/dam weight" 75 x 100) in an intensive environment under high stocking rates. In the analysis of the initial crossbreeding phase, the S breed direct effects, expressed as deviation from the general mean, were positive (P :s; 0.01) for both BW and WW. Hereford and A breed direct effects were negative (P :s; 0.01) for both BW and WW. Afrikaner direct maternal effects were positive (P :s; 0.01) for both BW and WW. The H direct maternal effect was negative (P :s; 0.05) (- 2.8%) for WW. Simmentaler maternal effect was negative (P :s; 0.01) for BW but non-significant (P ;:::0:.05) for WW. Individual heterotic effects for BW were significant (P:S; 0.01) in H x S (3.5%) and S x A (11.0%) only. Individual heterotic effects were positive (P :s; 0.01) for WW, with that of the H x A (9.8%) and S x A (6.7%) crosses exceeding the H x S (3.1%) cross. Maternal heterotic effects were non-significant (P ;:::0:.05) for both BW and WW. Investigations of the contributions of the A, Hand S during composite development in later generations, respectively, were made to estimate direct heritabilities (h2 a) and maternal heritabilities (h2 m) for BW and WW of the calf and CE of the dam. Calves were born between 1968 and 1993 (n = 52628). Calves of this composite population had varying levels of A, Hand S genes ranging from o to 75%, 0 to 100% and 0 to 96.9%, with an average of 4.3,19.3 and 33.4%, respectively. For the A, direct heritabilities fitting unitrait models were 0.67, 0.53 and 0.19 for BW, WW and CE, respectively, with corresponding estimates of h2mbeing 0.22, 0.36 and 0.58. Genetic correlations between direct and maternal effects (ram)were negative for all three traits, varying from -0.32 to - 0.62. Direct breeding values for BW increased and reached a maximum value at 0.11 proportion of A. The maternal breeding values for BW decreased linearly between 1.6 to 37.5% A proportion and increased linearly between 37.5 to 75% A proportion. For WW, the direct breeding values decreased linearly with increasing A proportion, while the maternal breeding values were not affected by proportion of A. Cow efficiency was unaffected by an increase in proportion of A. For the H, direct heritabilities fitting unitrait models were 0.67,0.52 and 0.21 for BW, WW and CE, respectively, with corresponding estimates of h2mbeing 0.22, 0.36 and 0.60. Genetic correlations between direct and maternal effects (ram)were negative for all three traits, varying from -0.32 to - 0.64. Direct breeding values and maternal breeding values for BW and WW decreased with increasing proportion of H. Direct breeding value for CE increased, while the maternal breeding value for CE reached minimum value at 0.62 proportion ofH. For the S, direct heritabilities fitting unitrait models were 0.66, 0.53 and 0.21 for BW, WW and CE, respectively, with corresponding estimates of h2m being 0.22, 0.36 and 0.59. Genetic correlations between direct and maternal effects (ram)were negative for all three traits, varying from -0.32 to - 0.63. Direct breeding values for BW and WW decreased and maternal breeding values increased with increasing proportion of S. Cow efficiency was unaffected by an increase in proportion of S. The study suggests that in the initial crossbreeding phase, purebred S breeding seems to be the best breeding practice for this environment and that during composite development, high A and H contributions could lead to low BW and WW (except the maternal contribution of the A for BW and WW). The advantage of the S lies more in the maternal contribution than in the direct contribution suggesting that the S is a large-framed maternal line rather than a terminal sire line. / AFRIKAANSE OPSOMMING: 'N WAARDEBEP ALING VAN DIE BYDRAE VAN DIE AFRIKANER, SIMMENTALER EN HEREFORD TYDENS KOMPOSIETE RASONTWIKKELING BY VLEISBEESTE: Die doel van die studie was om inligting aangaande die karakterisering van die Afrikaner (A), Hereford (H) en Simmentaler (S) rasse tydens die oorspronklike aanvangsfase van kruisteling en daaropvolgende komposiet ontwikkeling te verkry. Dit het die beraming van direkte additiewe, individuele heterose, direkte materne en materne heterotiese effekte tydens die aanvangsfase van die kruisteeltprogram, die beraming van genetiese parameters en die voorspelling van die teeltwaardes in latere generasies behels. Die eienskappe wat ingesluit is, is geboortegewig (BW), speengewig (WW) en koeidoeltreffendheid (CE; WW/koeigewigo.75 ). Hierdie kudde is in 'n intensiewe maar onder 'n hoë weidingsdruk omgewing aangehou. Tydens die ontleding van die eerste kruisteeltfase is die direkte additiewe effekte vir die S, uitgedruk as afwyking van die algemene gemiddelde, vir beide BW en WW positief (P ~ 0.01). Direkte additiewe effekte vir die H en A was vir beide BW en WW negatief (P ~ 0.01). Afrikaner materne effekte was vir beide BW en WW (P ~ 0.01) positief. Die H direkte materne effekte was negatief (-2.8%) (P ~ 0.05) vir WW. Simmentaler maternal effekte was ook vir BW negatief (P ~ 0.01), maar nie-betekenisvol (P 20.05) vir WW. Individuele heterose was slegs betekenisvol (P ~ 0.01) vir kombinasies van H x S (3.5%) en S x H (11.0%) vir BW. Individuele heterose was positief (P ~ 0.01) vir WW waar H x A (9.8%) en S x A (6.7%) kruisings dié van die H x S (3.1%) kruising oortrefhet. Materne heterose was vir beide BW en WW nie-betekenisvol (P 2 0.05). Die relatiewe bydraes van die A, H en S is ook tydens komposiet-ontwikkeling bereken. Direkte additiewe oorerflikhede (h2 a) en materne oorerflikhede (h2m) is vir BW en WW van die kalf en CE van die koei beraam. Kalwers in die komposiet kudde, gebore tussen 1968 en 1993 (n = 52628), het variërende vlakke van A, H en S gene. Die samestelling het gevarieer van 0 - 75%, 0 - 100% en 0 - 96.9%, met 'n gemiddeld van 4.3, 19.3 en 33.4%. Vir die A was die direkte erfbaarhede (h2 a), soos deur die passing van 'n enkeleienskapmodel beraam, 0.67, 0.53 en 0.19 vir onderskeidelik BW, WW en CE, met ooreenstemmende beramings van 0.22, 0.36 en 0.58 vir h2 rn- Genetiese korrelasies tussen direkte en mateme effekte (ram)was almal negatief en het tussen -0.32 en -0.62 gewissel. Direkte teelwaardes vir BW het met toenemende A-bydrae gestyg en het 'n maksimum waarde by 0.11 bereik. Die mateme teelwaardes vir BW het lineêr gedaal tussen 1.6 en 37.5% A-bydrae en het weer lineêr tussen 37.5 en 75% Abydrae gestyg. Vir WW het die direkte teelwaardes lineêr met toenemende A-bydrae gestyg, terwyl die mateme teelwaardes nie deur A-bydrae beïnvloed was nie. Koeidoeltreffendheid was nie deur 'n toename in A-bydrae beïnvloed nie. Vir die H was die direkte erfbaarhede (h2 a), soos deur die passing van 'n enkeleienskapmodel beraam 0.67, 0.52 en 0.21 vir onderskeidelik BW, WW en CE, met ooreenstemmende beramings van 0.22, 0.36 en 0.60 vir h2 rn- Genetiese korrelasies tussen direkte en mateme effekte (ram)was almal negatief en het tussen -0.32 en -0.64 gewissel. Direkte teelwaardes en mateme teelwaardes vir BW en WW het met toenemende H-bydrae gedaal. Direkte teelwaarde vir CE het ook met toenemende If-bydrae gedaal, terwyl die mateme teelwaarde 'n minimum waarde by 0.62 H-bydrae bereik het. Vir die S was die direkte erfbaarhede (h2a), soos deur die passing van 'n enkeleienskapmodel beraam 0.66, 0.53 en 0.21 vir onderskeidelik BW, WW en CE, met ooreenstemmende beramings van 0.22, 0.36 en 0.59 vir h2 m- Genetiese korrelasies tussen direkte en mateme effekte (ram)was almal negatief en het tussen -0.32 en -0.63 gewissel. Direkte teelwaardes vir BW en WW het gedaal, terwyl die mateme teelwaardes met toenemende S-bydrae gestyg het. Koeidoeltreffendheid was nie deur 'n toename in S-bydrae beïnvloed nie. Die bevinding was dat tydens die ontleding van die eerste kruisteeltfase die teling van suiwer S aanbeveel word en dat tydens komposiete-ontwikkeling toenemende A- en H-bydraes neig om aanleiding te gee tot afnames in BW en WW (behalwe die mateme bydrae van die A vir BW en WW). Die S-bydrae se voordeel is meer in die mateme bydrae as in die direkte bydrae geleë en dui dus aan dat die S as 'n mateme grootraam lyn i.p.v. as 'n terminale bullyn gebruik moet word.