Fernando Finger

Prof. Dr. Fernando Finger

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 1997 in Plant Physiology
Verified
Journal Article
Closed access
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LLL. M. Lagrimini
L. M. Lagrimini
VGV. Gingas
V. Gingas
Fernando FingerFernando Finger
Fernando Finger
SRS. Rothstein
S. Rothstein
TLTty. Liu
Tty. Liu
On the basis of the biological compounds that they metabolize, plant peroxidases have long been implicated in plant growth, cell wall biogenesis, lignification, and host defenses. Transgenic tobacco (Nicotiana tabacum L.) plants that underexpress anionic peroxidase were generated using antisense RNA. The antisense RNA was found to be specific for the anionic isoenzyme and highly effective, reducing endogenous transcript levels and total peroxidase activity by as much as 1600-fold. Antisense-transformed plants appeared normal at initial observation; however, growth studies showed that plants with reduced peroxidase activity grow taller and flower sooner than control plants. In contrast, previously transformed plants overproducing anionic peroxidase were shorter and flowered later than controls. Axillary buds were more developed in antisense-transformed plants and less developed in plants overproducing this enzyme. It was found that the lignin content in leaf, stem, and root was unchanged in antisense-transformed plants, which does not support a role for anionic peroxidase in the lignification of secondary xylem vessels. However, studies of wounded tissue show some reduction in wound-induced deposition of lignin-like polymers. The data support a possible role for tobacco anionic peroxidase in host defenses but not without a reduction in growth potential.

1 December 2004 in Agroforestry Systems
Verified
Journal Article
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MCMônica Matoso Campanha
Mônica Matoso Campanha
RSRicardo Henrique Silva Santos
Ricardo Henrique Silva Santos
GFGilberto Bernardo de Freitas
Gilberto Bernardo de Freitas
HMHermínia Emília Prieto Martinez
Hermínia Emília Prieto Martinez
SGSilvana Lages Ribeiro Garcia
Silvana Lages Ribeiro Garcia
Fernando FingerFernando Finger
Fernando Finger

5 May 2009 in Euphytica
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Journal Article
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Elizanilda Ramalho do RêgoElizanilda Ramalho do Rêgo
Elizanilda Ramalho do Rêgo
MRMailson Monteiro Do Rêgo
Mailson Monteiro Do Rêgo
Fernando FingerFernando Finger
Fernando Finger
CCCosme Damião Cruz
Cosme Damião Cruz
VCVicente Wagner Dias Casali
Vicente Wagner Dias Casali

1 April 2007 in Scientia Horticulturae
Verified
Journal Article
Closed access
SLSérgio D. Lannes
Sérgio D. Lannes
Fernando FingerFernando Finger
Fernando Finger
ASAdilson R. Schuelter
Adilson R. Schuelter
VCVicente W.D. Casali
Vicente W.D. Casali

1 September 2021 in Ornamental Horticulture
Verified
Journal Article
Open access
LCLucas Cavalcante da Costa
Lucas Cavalcante da Costa
FAFernanda Ferreira de Araujo
Fernanda Ferreira de Araujo
WRWellington Souto Ribeiro
Wellington Souto Ribeiro
MSMirelle Nayana de Sousa Santos
Mirelle Nayana de Sousa Santos
Fernando FingerFernando Finger
Fernando Finger
The longevity of cut flowers is limited by their ephemeral nature and by multiple stresses. Impairment in water uptake, depletion of stored carbohydrates, increases in both respiratory activity and ethylene production are signatures of flower senescence. A wide range of techniques is available to extend flower preservation, including the use of flower preservative solutions, ethylene action inhibitors, growth regulators, and control of temperature and flower dehydration. The use of sucrose in pulsing solution, or as a component of vase solution, extends the vase life of flowers by either improving water balance and energy or delaying the senescence via reductions in ethylene biosynthesis. Inhibitors of ethylene production and action affect the longevity by extending the vase life of some ethylene-sensitive flowers. Flowers have intense respiratory activity, which may deplete the limited reserves of carbohydrates in the tissues. Lower temperatures markedly reduce both carbon dioxide concentration and ethylene production as well as its action. However, chilling-sensitive flowers, such as bird-of-paradise, heliconia, orchid, and ginger, cannot be stored below 10 to 13°C due to the intense development of tissue discoloration.

1 October 2004 in Postharvest Biology and Technology
Verified
Journal Article
Closed access
KKKaren L. Klotz
Karen L. Klotz
Fernando FingerFernando Finger
Fernando Finger