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“survival of encapsulated-dehydrated and cryopreserved (EDN)”

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Development, reproduction & morphology 2

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Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.

Taxon: OliveOlea europaeat0
Treatment: Thermal treatment of embryogenic callus for 1 d at 30 degree Ce0
Outcome: survival of encapsulated-dehydrated and cryopreserved (EDN)e0
Direction: increasee0
Value: 58%e0

Not reportedComparator

Verbatim

e0
“Thermal treatment of embryogenic callus for 1 d at 30 degree C was very effective to increase survival of encapsulated-dehydrated and cryopreserved (EDN) (58%) and EVN (68%) embryos.”
✓ located verbatim in the source · abstract, characters 626–808

t0
“olive”
✓ located verbatim in the source · title, characters 29–34

Title

Cryopreservation of 'Nabali' olive (Olea europea l.) somatic embryos by encapsulation-dehydration and encapsulation-vitrification.

R A Shibli; K H Al-Juboory PubMed

Other claims from this paper (7)

Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
Intervention effect Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.
Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.

Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.

Taxon: OliveOlea europaeat0
Treatment: Thermal treatment of embryogenic callus for 1 d at 30 degree Ce0
Outcome: survivale0
Direction: increasee0
Value: 68%e0

Not reportedComparator

Verbatim

e0
“Thermal treatment of embryogenic callus for 1 d at 30 degree C was very effective to increase survival of encapsulated-dehydrated and cryopreserved (EDN) (58%) and EVN (68%) embryos.”
✓ located verbatim in the source · abstract, characters 626–808

t0
“olive”
✓ located verbatim in the source · title, characters 29–34

Title

Cryopreservation of 'Nabali' olive (Olea europea l.) somatic embryos by encapsulation-dehydration and encapsulation-vitrification.

R A Shibli; K H Al-Juboory PubMed

Other claims from this paper (7)

Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
Intervention effect Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.
Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.

Breeding, agronomy & horticulture 2

Show all 2 →

Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.

Taxon: OliveOlea europaeat0
Treatment: Thermal treatment of embryogenic callus for 1 d at 30 degree Ce0
Outcome: survival of encapsulated-dehydrated and cryopreserved (EDN)e0
Direction: increasee0
Value: 58%e0

Not reportedComparator

Verbatim

e0
“Thermal treatment of embryogenic callus for 1 d at 30 degree C was very effective to increase survival of encapsulated-dehydrated and cryopreserved (EDN) (58%) and EVN (68%) embryos.”
✓ located verbatim in the source · abstract, characters 626–808

t0
“olive”
✓ located verbatim in the source · title, characters 29–34

Title

Cryopreservation of 'Nabali' olive (Olea europea l.) somatic embryos by encapsulation-dehydration and encapsulation-vitrification.

R A Shibli; K H Al-Juboory PubMed

Other claims from this paper (7)

Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
Intervention effect Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.
Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.

Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.

Taxon: OliveOlea europaeat0
Treatment: Thermal treatment of embryogenic callus for 1 d at 30 degree Ce0
Outcome: survivale0
Direction: increasee0
Value: 68%e0

Not reportedComparator

Verbatim

e0
“Thermal treatment of embryogenic callus for 1 d at 30 degree C was very effective to increase survival of encapsulated-dehydrated and cryopreserved (EDN) (58%) and EVN (68%) embryos.”
✓ located verbatim in the source · abstract, characters 626–808

t0
“olive”
✓ located verbatim in the source · title, characters 29–34

Title

Cryopreservation of 'Nabali' olive (Olea europea l.) somatic embryos by encapsulation-dehydration and encapsulation-vitrification.

R A Shibli; K H Al-Juboory PubMed

Other claims from this paper (7)

Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
Intervention effect Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.
Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.

Woody plants 2

Show all 2 →

Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.

Taxon: OliveOlea europaeat0
Treatment: Thermal treatment of embryogenic callus for 1 d at 30 degree Ce0
Outcome: survival of encapsulated-dehydrated and cryopreserved (EDN)e0
Direction: increasee0
Value: 58%e0

Not reportedComparator

Verbatim

e0
“Thermal treatment of embryogenic callus for 1 d at 30 degree C was very effective to increase survival of encapsulated-dehydrated and cryopreserved (EDN) (58%) and EVN (68%) embryos.”
✓ located verbatim in the source · abstract, characters 626–808

t0
“olive”
✓ located verbatim in the source · title, characters 29–34

Title

Cryopreservation of 'Nabali' olive (Olea europea l.) somatic embryos by encapsulation-dehydration and encapsulation-vitrification.

R A Shibli; K H Al-Juboory PubMed

Other claims from this paper (7)

Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
Intervention effect Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.
Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.

Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.

Taxon: OliveOlea europaeat0
Treatment: Thermal treatment of embryogenic callus for 1 d at 30 degree Ce0
Outcome: survivale0
Direction: increasee0
Value: 68%e0

Not reportedComparator

Verbatim

e0
“Thermal treatment of embryogenic callus for 1 d at 30 degree C was very effective to increase survival of encapsulated-dehydrated and cryopreserved (EDN) (58%) and EVN (68%) embryos.”
✓ located verbatim in the source · abstract, characters 626–808

t0
“olive”
✓ located verbatim in the source · title, characters 29–34

Title

Cryopreservation of 'Nabali' olive (Olea europea l.) somatic embryos by encapsulation-dehydration and encapsulation-vitrification.

R A Shibli; K H Al-Juboory PubMed

Other claims from this paper (7)

Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
Intervention effect Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.
Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.

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“survival of encapsulated-dehydrated and cryopreserved (EDN)”

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Development, reproduction & morphology 2

Breeding, agronomy & horticulture 2

Woody plants 2