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Externí autoři: Hervé Etienne

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AmaranthusanatomyantioxidantsappleapplesArabidopsis thalianaarracachaAutomationautophagyautophagy-related genesautophagy.related genesbeechbeechnutBioreactorscalcium oxalateCannabis sativacarotenoidsCell densityChenopodiumchitinasesCleavage polyembryonyClonal deploymentCommercial companiesCommercializationCryopreservationcytokinin derivativesdesiccationdevelopmentDisanthusdormancyDouglas-firDouglas firembryoembryogenesisembryogenic cultureFagus sylvaticaflavonoidsfloral iductionflow cytometryfloweringForest reproductive materialgene expressiongerminationglucanaseshemphistochemistryimage analysisimmunolabellinginductionIn vitro propagationin vitro regenerationlarchLarix eurolepismaritime pinemicropropagationmicroscopynon-embryogenic cellsNorway spruceorganogenesisoxidative stressphenolic acidsphenolicsphenolsphotoperiodphytohormonesPicea abiespolyaminespolyphenolic compoundsproliferationProtein patternproteomePseudotsuga menziesiiputrescineResearchrootScale-upsignallingsomaclonal variationsomatic embryogenesisspermidinesperminestarchstarch grainsstereologystorage compoundsstorage proteinsTechnology transferTissue culturetissue culturestobacco cell culturetranscriptometransformationUV-B irradiationUV-B radiationVegetative propagationWoody fruit cropsWoody plantsyaconzygotic embryoβ-1,3-glucanases

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Figure 3. Morphology of three-week-old emblings developed from embryos desiccated at different relative humidity levels (G100, G95, and G90). (A) – Overview of emblings; (B) – Length of whole shoots (dark gray columns), hypocotyls (light gray columns), and primary roots (white columns). The image of the embling inserted in graph B shows the measured parts – shoot (s), hypocotyl (h), and root (r).

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