1984
DOI: 10.1007/978-94-009-6110-4_4
|View full text |Cite
|
Sign up to set email alerts
|

Assuring Seed Quality for Seedling Production: Cone Collection and Seed Processing, Testing, Storage, and Stratification

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
16
0
4

Year Published

1996
1996
2013
2013

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 20 publications
(20 citation statements)
references
References 17 publications
0
16
0
4
Order By: Relevance
“…Presowing treatments to speed germination are discussed in detail by several authors (Bonner et al 1974, Tanaka 1984. Typically, prechilling is done after an 8 to 24 hour period of moisture imbibition.…”
Section: Seed Dormancy and Pretreatmentmentioning
confidence: 99%
“…Presowing treatments to speed germination are discussed in detail by several authors (Bonner et al 1974, Tanaka 1984. Typically, prechilling is done after an 8 to 24 hour period of moisture imbibition.…”
Section: Seed Dormancy and Pretreatmentmentioning
confidence: 99%
“…In large commercial bare-root nurseries, sowing operations are often delayed. Consequently there is a risk that the seeds will germinate before sowing, or they get damaged during sowing operations (Tanaka 1984, Jensen 1997a). However, chilling at a lower seed moisture content (MC) level than the FI state may be preferable because it greatly reduces the risk of premature germination, and in some cases increases germination after pretreatment (Gosling et al 2003).…”
Section: Introductionmentioning
confidence: 99%
“…The TTC used was ''TTC sterile solution 1%, Scharlau Microbiology''. In this method, living cells stain red as the tetrazolium is reduced by dehydrogenase enzymes to form a stable red triphenyl formazan, which is insoluble in water (Tanaka 1984). To avoid any physical dormancy caused by the seminal cover (Cantos et al 1998), the embryos were tested in a completely bare condition.…”
Section: Methodsmentioning
confidence: 99%
“…This process was followed to avoid false results in the viability test, because juniper embryos exhibit physiological dormancy, as they are unable to develop a radicle due to an inhibition mechanism (Baskin and Baskin 1998). Next, embryos were cut and immersed in 2,3,5-triphenyl-tetrazolium chloride solution (hereafter TTC) diluted to 0.1% for 24 h in the dark, and at room temperature (Scharpf 1970;Tanaka 1984). The TTC used was ''TTC sterile solution 1%, Scharlau Microbiology''.…”
Section: Methodsmentioning
confidence: 99%