資源描述:
《云南龍膽種子萌發(fā)特性研究》由會員上傳分享,免費在線閱讀,更多相關內(nèi)容在工程資料-天天文庫。
1、云南龍膽種子萌發(fā)特性研究摘要:?文以云南龍膽(Gentianayunnanensis)種子為試驗材料,經(jīng)赤霉素、氯化鈣、硝酸鉀的不同濃度處理,用不同溫度浸種,置不同光照下培養(yǎng),研宄其萌發(fā)特性。結果表明:云南龍膽種子經(jīng)室溫培養(yǎng)10d即可萌發(fā);在不同浸種溫度下萌發(fā)率相差不顯著。蒸餾水室溫浸種,24h/d光照培養(yǎng)萌發(fā)率為50%,自然光照培養(yǎng)萌發(fā)率為60%,黑暗條件培養(yǎng)萌發(fā)率為14.00%,光照與黑暗培養(yǎng)萌發(fā)指標差異顯著(P〈0.05)。3種試劑浸種,萌發(fā)率最高的為300mg/L赤霉素處理,萌發(fā)率為82%,其次為0.2%氯化鈣處理,萌發(fā)率為72%,1.5%硝酸鉀浸種萌發(fā)率為70%,對照萌
2、發(fā)率為60%o試劑處理,自然光照室溫培養(yǎng)20d至種子不再萌發(fā)為止測其根長,根長最長為硝酸鉀浸種,為7.38±0.62mm,其次為氯化餌浸種,為6.83±0.96mm,最短為赤霉素浸種,為5.94±0.90腿,對照為5.34±2.02腿。試劑處理與對照差異不顯著(P〉0.05)。光能促進云南龍膽種子萌發(fā),試劑處理不僅能提高云南龍膽種子萌發(fā)率,而且能促進胚根與胚軸的伸長。本文采集自網(wǎng)絡,本站發(fā)布的論文均是優(yōu)質論文,供學和研宄使用,文中立場與本網(wǎng)站無關,版權和著作權歸原作者所有,如有不愿意被轉載的情況,請通知我們刪除匕轉載的信息,如果需要分享,請保留本段說明。關鍵詞:云南龍膽;種子萌發(fā)
3、;氯化鈣;赤霉素;硝酸鉀中圖分類號S567.239文獻標識碼A文章編號1007-7731(2017)10-0029-05Abstract:Inthisstudy,seedsofGentianayunnanensiswereusedasexperimentalmaterial,differentconcentrationsofgibberellin,calciumchlorideandpotassiumnitrate,differenttemperaturelevelsforsoakingseedsanddifferentlightconditionswereselectedtot
4、reattheseeds.Theresultsshowedthat10dayscultivationatroomtemperaturewasenoughfortheseedofGentianayunnanensistogerminatewhiletherewasnosignificantdifferenceforseedgerminationrateunderdifferentlevelsofsoakingtemperature.Thegerminationrateofseedsoakedindistilledwateratroomtemperatureand24h/dlight
5、conditionwas50%while60%inthenaturallightconditionsand14%inthedarklightconditions.Therewasasignificantdifferenceforseedgerminationratebetweendarkandlightconditions(P<0.05).Thehighestseedgerminationrateamongdifferentconcentrationsofreagentswas82%whichtreatedin300mg/Lgibberellinsolution,followin
6、gwas72%whichtreatedin0.2%calciumsolutionandthelastwas60%whichtreatedin1.5%potassiumsolutionwhile60%fortheCK.Aftertreatedwithdifferenttypesofreagents,rootlengthweremeasureduntiltheseedswerenolongertocontinuegerminateafter20dayscultivationatroomtemperatureandnaturallightcondition.Theresultsshow
7、edthatthelengthoflongestrootwas7.38+0.62mmwhichseedsweretreatedinpotassiumsolution,followingwas6.83+0.96mmwhichseedsweretreatedincalciumandthelastwas5.94±0.90minwhichseedsweretreatedingibberellinsolutionwhile5.34±2.02mmfortheCK.Therewasnosign