American Journal of Plant Sciences, 2012, 3, 567-571
doi:10.4236/ajps.2012.35068 Published Online May 2012 (http://www.SciRP.org/journal/ajps)
567
Photoperiod Affects in Vitro Flowering in Wild Peanut
Arachis paraguariensis
Olubunmi Aina, Kenneth Quesenberry, Maria Gallo
Department of Agronomy, University of Florida, Gainesville, USA.
Email: ainab@ufl.edu
Received March 5
th
, 2012; revised March 22
nd
, 2012; accepted April 12
th
, 2012
ABSTRACT
Arachis paraguariensis, a wild peanut species, is a potential experimental system for studying the molecular mecha-
nisms of flowering in the genus Arachis. The present study was carried out to investigate the effect of photoperiod on in
vitro reproductive behavior of five genotypes of A. paraguariensis. Day-lengths of 12, 16 and 24 h were tested to
monitor in vitro flowering using growth chambers kept at 26˚C ± 1˚C and 60% ± 5% relative humidity under an illumi-
nation of 40 μmol·m
–2
·s
–1
. Flowering percentage of plantlets ranged from 35% to 93%, 20% to 75%, and 5% to 53% for
12, 16 and 24 h day-lengths, respectively. Genotype PI 262842 displayed the highest frequency of flowering under all
the day-length treatments but in vitro flower bud initiation was delayed. The highest mean flowering percentage of 65%
across all the genotypes for plantlets exposed to 12 h photoperiod is indicative that flowering induction actually oc-
curred. The results presented in this paper provide evidence for photoperiodic flowering response as well as the occur-
rence of short day-length-enhanced flowering in A. paraguariensis.
Keywords: Flower; Tissue Culture; Day-Length; Photoperiod; Peanut; Arachis; In Vitro
1. Introduction
Several wild Arachis species constitute important sources
of novel genes for improving cultivated peanut (Arachis
hypogaea L.). Of significant importance is Arachis para-
guariensis Chodat & Hassl., a perennial wild relative of
the peanut having novel traits including disease [1,2],
insect [3], and nematode [4] resistance. Low fruiting ef-
ficiency due to asynchronous flowering and pod forma-
tion is a persistent problem within the genus Arachis that
often results in considerable seed-yield losses and low
germination rates [5,6]. Although photoperiod sensitivity
within the genus Arachis is widely reported [7,8], the
specific role of environmental factors in the regulation of
its reproductive performance is poorly understood. For
example, results from field studies focusing on the ef-
fects of photoperiod on flowering in cultivated peanut
were inconsistent due to differential responses among
different cultivars [9,10].
Gaining a proper understanding of the molecular basis
for flowering mechanisms should enable the plant breeder
to efficiently manipulate reproduction processes for
achieving significant impacts on yield and other impor-
tant traits. In vitro flowering, a common phenomenon in
several plant species offers an ideal experimental system
for studying these mechanisms. Additionally, tissue cul-
ture techniques such as in vitro fertilization, peg culture
and embryo rescue can be explored as a means of over-
coming the long existing hybridization barriers between
cultivated peanut and several of its wild relatives.
In vitro tissue explants for plant regeneration are
grown on nutrient medium inside confined vessels; there-
fore, precise control of all environmental factors is ex-
pected. Nevertheless, seasonal effects of explant collec-
tion and culture initiation on plantlet regeneration have
been reported for many species [11-15]. Furthermore,
different cytokinins, sucrose concentrations, photoperiod,
and subculture time have been used to promote in vitro
flowering [4,11]. Flowering in vitro has been observed in
a few Arachis spp., however, the photoperiodic flowering
response in tissue culture is relatively rare and poorly
understood. Still et al. [16] and Li et al. [17] reported the
occurrence of flowering in tissue culture of A. para-
guariensis, but the environmental and genetic factors
involved were not investigated. In this study, a factorial
experiment in a completely randomized design with
sub-sampling was replicated two times to investigate the
influence of photoperiod on in vitro flowering of five
genotypes of A. paraguariensis.
2. Materials and Methods
2.1. Explant Source
Seeds of five genotypes of A. paraguariensis used for
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