{"id":{"repo_id":"the-open-u","oai_identifier":"oai:oro.open.ac.uk:54878"},"canonical_url":"https://search.dev.ndltd.org/etd/the-open-u/oai:oro.open.ac.uk:54878","repository":{"repo_id":"the-open-u","name":"The Open University","base_url":"https://oro.open.ac.uk/cgi/oai2"},"display":{"title":"Environmental Factors Affecting Pre-Maturity <i>Alpha</i>-Amylase Activity in Winter Wheat (<i>Triticum aestivum</i>)","abstract":"Pre-maturity <i>alpha</i>-amylase activity (PMAA) in the absence of sprouting is one of four causes of low Hagberg falling number (HFN) in UK winter wheat (<i>Triticum aestivum</i>), reducing the quality and value of milled flour. Other causes include the retention of pericarp <i>alpha</i>-amylase activity (RPAA), pre-maturity sprouting (PrMS) and post-maturity sprouting (PoMS). This thesis investigated the effects of environmental factors on PMAA which currently occurs in a variable and unpredictable fashion under UK weather conditions.<br></br><br></br>A multi-site field experiment on four cultivars (Haven, Hornet, Pastiche and Riband), at four sites (Harper Adams University College, University of Nottingham, University of Aberdeen and ADAS-Bridgets) between 1994-1996 was undertaken to:- establish the frequency of the causes of low HFN; examine the relationship between grain drying-rate and PMAA; determine if it was possible to predict combine harvest HFN.<br></br><br></br>A range of techniques including a visual sprouting assessment, fluorescein dibutyrate staining, iso-electric focusing and a beta-limit dextrin gel and iodine staining test were used to allow the cause of low HFN to be established. Of the forty crops analysed, 22 cases (45%) had detectable amounts of <i>alpha</i>-amylase activity. PMAA was identified solely in 2 cases (5%), in combination with PoMS in 8 cases (20%), in combination with RPAA in one case (2%), with PoMS occurring solely in 11 cases (28%). The HFN fell below the breadmaking standard of 250 s in 18 of the 36 site x year x cultivar combinations analysed. This was attributed solely to PMAA in two cases (11%), a combination of PMAA and PoMS in a further eight cases (44%) and solely to PoMS in eight cases(44%). There were no cases where PrMS or RPAA reduced the HFN to below 250 s.<br></br><br></br>The hypothesis that PMAA is related to the grain drying-rate between 40-20 % moisture content was tested. Grain drying-rate was determined by linear regression analysis using moisture content measurements made at regular intervals during grain development. In site x year x cultivar combinations where PMAA was detected the grain drying-rate was significantly (P = 0.047) lower (mean = 1.90 <i>cf</i>. 2.30% moisture loss day<sup>-1</sup>), suggesting a slow grain drying-rate enhances PMAA. However, the low frequency of occurrence of PMAA in isolation prevented quantification of this relationship.<br></br><br></br>Initiation of PMAA in the grain, was shown to occur from a grain moisture content of 47.8%. A pre-harvest sample taken by hand at 850 °C-days (35 % moisture, Zadoks growth stage 85-87) was shown to enable a prediction of combine harvest HFN to be made in the absence of subsequent rainfall and PoMS. The 95 % confidence limits associated with this HFN prediction were however wide.<br></br><br></br>The hypothesis that transient changes in temperature early in grain development may affect PMAA, before the onset of any grain drying-rate effects, was tested in five controlled-environment cabinet experiments. Of 36 cultivar x time of transfer combinations undertaken from a 16/ 10°C to a 26 /20°C temperature regime, six led to a significant increase (P < 0.05) arid one led to a significant decrease in PMAA. Of the 18 cultivar x time of transfer combinations undertaken from a 25 / 20°C to a 16 / 10°C temperature regime, one led to a significant increase and one led to a significant decrease in PMAA. A comparison between the field and controlled-environment experiment results highlighted that after conditions putatively stimulating PMAA had been encountered, subsequent environmental factors, such as mean temperature and relative humidity may also affect PMAA.<br></br><br></br>It was concluded that PMAA can be enhanced by transient increases in temperature before the grain reaches 40% moisture content and by a slow grain drying-rate between 40-20% moisture content. The variability in the results, however, also suggested other environmental factors were influencing PMAA.","abstract_html":"Pre-maturity &lt;i&gt;alpha&lt;/i&gt;-amylase activity (PMAA) in the absence of sprouting is one of four causes of low Hagberg falling number (HFN) in UK winter wheat (&lt;i&gt;Triticum aestivum&lt;/i&gt;), reducing the quality and value of milled flour. Other causes include the retention of pericarp &lt;i&gt;alpha&lt;/i&gt;-amylase activity (RPAA), pre-maturity sprouting (PrMS) and post-maturity sprouting (PoMS). This thesis investigated the effects of environmental factors on PMAA which currently occurs in a variable and unpredictable fashion under UK weather conditions.&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;A multi-site field experiment on four cultivars (Haven, Hornet, Pastiche and Riband), at four sites (Harper Adams University College, University of Nottingham, University of Aberdeen and ADAS-Bridgets) between 1994-1996 was undertaken to:- establish the frequency of the causes of low HFN; examine the relationship between grain drying-rate and PMAA; determine if it was possible to predict combine harvest HFN.&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;A range of techniques including a visual sprouting assessment, fluorescein dibutyrate staining, iso-electric focusing and a beta-limit dextrin gel and iodine staining test were used to allow the cause of low HFN to be established. Of the forty crops analysed, 22 cases (45%) had detectable amounts of &lt;i&gt;alpha&lt;/i&gt;-amylase activity. PMAA was identified solely in 2 cases (5%), in combination with PoMS in 8 cases (20%), in combination with RPAA in one case (2%), with PoMS occurring solely in 11 cases (28%). The HFN fell below the breadmaking standard of 250 s in 18 of the 36 site x year x cultivar combinations analysed. This was attributed solely to PMAA in two cases (11%), a combination of PMAA and PoMS in a further eight cases (44%) and solely to PoMS in eight cases(44%). There were no cases where PrMS or RPAA reduced the HFN to below 250 s.&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;The hypothesis that PMAA is related to the grain drying-rate between 40-20 % moisture content was tested. Grain drying-rate was determined by linear regression analysis using moisture content measurements made at regular intervals during grain development. In site x year x cultivar combinations where PMAA was detected the grain drying-rate was significantly (P = 0.047) lower (mean = 1.90 &lt;i&gt;cf&lt;/i&gt;. 2.30% moisture loss day&lt;sup&gt;-1&lt;/sup&gt;), suggesting a slow grain drying-rate enhances PMAA. However, the low frequency of occurrence of PMAA in isolation prevented quantification of this relationship.&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;Initiation of PMAA in the grain, was shown to occur from a grain moisture content of 47.8%. A pre-harvest sample taken by hand at 850 °C-days (35 % moisture, Zadoks growth stage 85-87) was shown to enable a prediction of combine harvest HFN to be made in the absence of subsequent rainfall and PoMS. The 95 % confidence limits associated with this HFN prediction were however wide.&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;The hypothesis that transient changes in temperature early in grain development may affect PMAA, before the onset of any grain drying-rate effects, was tested in five controlled-environment cabinet experiments. Of 36 cultivar x time of transfer combinations undertaken from a 16/ 10°C to a 26 /20°C temperature regime, six led to a significant increase (P &lt; 0.05) arid one led to a significant decrease in PMAA. Of the 18 cultivar x time of transfer combinations undertaken from a 25 / 20°C to a 16 / 10°C temperature regime, one led to a significant increase and one led to a significant decrease in PMAA. A comparison between the field and controlled-environment experiment results highlighted that after conditions putatively stimulating PMAA had been encountered, subsequent environmental factors, such as mean temperature and relative humidity may also affect PMAA.&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;It was concluded that PMAA can be enhanced by transient increases in temperature before the grain reaches 40% moisture content and by a slow grain drying-rate between 40-20% moisture content. The variability in the results, however, also suggested other environmental factors were influencing PMAA.","abstract_has_math":false,"creators":["Major, Bernard James"],"institution":"The Open University","degree_name":"phd","degree_level":"doctoral","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1999,"date_issued":"1999-12","date_published":"1999-12","updated_at":"2026-07-24T05:02:49Z","subjects":[],"languages":["en"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":null,"outbound_label":null,"outbound_source":null},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Major, Bernard James"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["1999-12-17"]},{"key":"dc:date.issued","label":"Date","values":["1999-12"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["The Open University"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://oro.open.ac.uk/54878/"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["phd"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://oro.open.ac.uk/54878/1/300239.pdf"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Pre-maturity <i>alpha</i>-amylase activity (PMAA) in the absence of sprouting is one of four causes of low Hagberg falling number (HFN) in UK winter wheat (<i>Triticum aestivum</i>), reducing the quality and value of milled flour. Other causes include the retention of pericarp <i>alpha</i>-amylase activity (RPAA), pre-maturity sprouting (PrMS) and post-maturity sprouting (PoMS). This thesis investigated the effects of environmental factors on PMAA which currently occurs in a variable and unpredictable fashion under UK weather conditions.<br></br><br></br>A multi-site field experiment on four cultivars (Haven, Hornet, Pastiche and Riband), at four sites (Harper Adams University College, University of Nottingham, University of Aberdeen and ADAS-Bridgets) between 1994-1996 was undertaken to:- establish the frequency of the causes of low HFN; examine the relationship between grain drying-rate and PMAA; determine if it was possible to predict combine harvest HFN.<br></br><br></br>A range of techniques including a visual sprouting assessment, fluorescein dibutyrate staining, iso-electric focusing and a beta-limit dextrin gel and iodine staining test were used to allow the cause of low HFN to be established. Of the forty crops analysed, 22 cases (45%) had detectable amounts of <i>alpha</i>-amylase activity. PMAA was identified solely in 2 cases (5%), in combination with PoMS in 8 cases (20%), in combination with RPAA in one case (2%), with PoMS occurring solely in 11 cases (28%). The HFN fell below the breadmaking standard of 250 s in 18 of the 36 site x year x cultivar combinations analysed. This was attributed solely to PMAA in two cases (11%), a combination of PMAA and PoMS in a further eight cases (44%) and solely to PoMS in eight cases(44%). There were no cases where PrMS or RPAA reduced the HFN to below 250 s.<br></br><br></br>The hypothesis that PMAA is related to the grain drying-rate between 40-20 % moisture content was tested. Grain drying-rate was determined by linear regression analysis using moisture content measurements made at regular intervals during grain development. In site x year x cultivar combinations where PMAA was detected the grain drying-rate was significantly (P = 0.047) lower (mean = 1.90 <i>cf</i>. 2.30% moisture loss day<sup>-1</sup>), suggesting a slow grain drying-rate enhances PMAA. However, the low frequency of occurrence of PMAA in isolation prevented quantification of this relationship.<br></br><br></br>Initiation of PMAA in the grain, was shown to occur from a grain moisture content of 47.8%. A pre-harvest sample taken by hand at 850 °C-days (35 % moisture, Zadoks growth stage 85-87) was shown to enable a prediction of combine harvest HFN to be made in the absence of subsequent rainfall and PoMS. The 95 % confidence limits associated with this HFN prediction were however wide.<br></br><br></br>The hypothesis that transient changes in temperature early in grain development may affect PMAA, before the onset of any grain drying-rate effects, was tested in five controlled-environment cabinet experiments. Of 36 cultivar x time of transfer combinations undertaken from a 16/ 10°C to a 26 /20°C temperature regime, six led to a significant increase (P < 0.05) arid one led to a significant decrease in PMAA. Of the 18 cultivar x time of transfer combinations undertaken from a 25 / 20°C to a 16 / 10°C temperature regime, one led to a significant increase and one led to a significant decrease in PMAA. A comparison between the field and controlled-environment experiment results highlighted that after conditions putatively stimulating PMAA had been encountered, subsequent environmental factors, such as mean temperature and relative humidity may also affect PMAA.<br></br><br></br>It was concluded that PMAA can be enhanced by transient increases in temperature before the grain reaches 40% moisture content and by a slow grain drying-rate between 40-20% moisture content. The variability in the results, however, also suggested other environmental factors were influencing PMAA."]},{"key":"dc:format","label":"Dc Format","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Environmental Factors Affecting Pre-Maturity <i>Alpha</i>-Amylase Activity in Winter Wheat (<i>Triticum aestivum</i>)"]}]}],"canonical_facts":{"dc:creator":["Major, Bernard James"],"dc:date":["1999-12-17"],"dc:date.issued":["1999-12"],"dc:description.abstract":["Pre-maturity <i>alpha</i>-amylase activity (PMAA) in the absence of sprouting is one of four causes of low Hagberg falling number (HFN) in UK winter wheat (<i>Triticum aestivum</i>), reducing the quality and value of milled flour. Other causes include the retention of pericarp <i>alpha</i>-amylase activity (RPAA), pre-maturity sprouting (PrMS) and post-maturity sprouting (PoMS). This thesis investigated the effects of environmental factors on PMAA which currently occurs in a variable and unpredictable fashion under UK weather conditions.<br></br><br></br>A multi-site field experiment on four cultivars (Haven, Hornet, Pastiche and Riband), at four sites (Harper Adams University College, University of Nottingham, University of Aberdeen and ADAS-Bridgets) between 1994-1996 was undertaken to:- establish the frequency of the causes of low HFN; examine the relationship between grain drying-rate and PMAA; determine if it was possible to predict combine harvest HFN.<br></br><br></br>A range of techniques including a visual sprouting assessment, fluorescein dibutyrate staining, iso-electric focusing and a beta-limit dextrin gel and iodine staining test were used to allow the cause of low HFN to be established. Of the forty crops analysed, 22 cases (45%) had detectable amounts of <i>alpha</i>-amylase activity. PMAA was identified solely in 2 cases (5%), in combination with PoMS in 8 cases (20%), in combination with RPAA in one case (2%), with PoMS occurring solely in 11 cases (28%). The HFN fell below the breadmaking standard of 250 s in 18 of the 36 site x year x cultivar combinations analysed. This was attributed solely to PMAA in two cases (11%), a combination of PMAA and PoMS in a further eight cases (44%) and solely to PoMS in eight cases(44%). There were no cases where PrMS or RPAA reduced the HFN to below 250 s.<br></br><br></br>The hypothesis that PMAA is related to the grain drying-rate between 40-20 % moisture content was tested. Grain drying-rate was determined by linear regression analysis using moisture content measurements made at regular intervals during grain development. In site x year x cultivar combinations where PMAA was detected the grain drying-rate was significantly (P = 0.047) lower (mean = 1.90 <i>cf</i>. 2.30% moisture loss day<sup>-1</sup>), suggesting a slow grain drying-rate enhances PMAA. However, the low frequency of occurrence of PMAA in isolation prevented quantification of this relationship.<br></br><br></br>Initiation of PMAA in the grain, was shown to occur from a grain moisture content of 47.8%. A pre-harvest sample taken by hand at 850 °C-days (35 % moisture, Zadoks growth stage 85-87) was shown to enable a prediction of combine harvest HFN to be made in the absence of subsequent rainfall and PoMS. The 95 % confidence limits associated with this HFN prediction were however wide.<br></br><br></br>The hypothesis that transient changes in temperature early in grain development may affect PMAA, before the onset of any grain drying-rate effects, was tested in five controlled-environment cabinet experiments. Of 36 cultivar x time of transfer combinations undertaken from a 16/ 10°C to a 26 /20°C temperature regime, six led to a significant increase (P < 0.05) arid one led to a significant decrease in PMAA. Of the 18 cultivar x time of transfer combinations undertaken from a 25 / 20°C to a 16 / 10°C temperature regime, one led to a significant increase and one led to a significant decrease in PMAA. A comparison between the field and controlled-environment experiment results highlighted that after conditions putatively stimulating PMAA had been encountered, subsequent environmental factors, such as mean temperature and relative humidity may also affect PMAA.<br></br><br></br>It was concluded that PMAA can be enhanced by transient increases in temperature before the grain reaches 40% moisture content and by a slow grain drying-rate between 40-20% moisture content. The variability in the results, however, also suggested other environmental factors were influencing PMAA."],"dc:format":["application/pdf"],"dc:identifier.uri":["https://oro.open.ac.uk/54878/1/300239.pdf"],"dc:language":["en"],"dc:publisher.institution":["The Open University"],"dc:relation.isreferencedby":["https://oro.open.ac.uk/54878/"],"dc:title":["Environmental Factors Affecting Pre-Maturity <i>Alpha</i>-Amylase Activity in Winter Wheat (<i>Triticum aestivum</i>)"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["doctoral"],"dc:type.qualificationname":["phd"]},"updated_at":"2026-07-24T05:02:49Z"}