scholarly journals In Vitro Responses of Tissues from Rhododendron Plants With and Without Tissue Proliferation

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 873D-873
Author(s):  
Yiqin Ruan ◽  
Mark H. Brand

Rhododendron `Montego' shoot cultures initiated from plants with and without tissue proliferation (TP and NTP) served as explant sources for all studies (Note: in vitro TP shoot cultures produce primarily dwarf shoots, some long shoots, and stem tumors). Calli induced from TP leaves and tumors and NTP leaves were cultured on woody plant (WP) medium containing NAA and 2-iP. During the first 4 weeks of culture, calli from NTP leaves had higher relative growth rates than calli from TP leaves or tumors. However, calli from TP leaves and tumors grew faster than calli from NTP leaves for all subculture periods that followed. Shoot tips (5 mm) were excised from TP dwarf shoots, TP long shoots, and NTP shoots and were cultured on WP medium with or without 15 μM 2-iP. Shoot tips from TP dwarf and long shoots multiplied on medium without 2-iP, averaging 18.4 and 1.7 shoots per shoot tip in 12 weeks, respectively. Shoot tips from NTP shoots only multiplied when maintained on 2-iP-containing medium. When placed on 2-iP-containing medium, both types of TP shoot tips produced clusters of callus-like nodules that gave rise to highly tumorized, short shoots or leafy meristems.

1984 ◽  
Vol 62 (3) ◽  
pp. 446-453 ◽  
Author(s):  
J. Cartey Caesar ◽  
Alastair D. Macdonald

Postflush observations on shoots of Betula papyrifera Marsh. indicated that long and short shoots differ in a range of morphological characteristics. Long shoots developed from distal axillary buds and short shoots developed from proximal axillary buds on the previous year's long shoots. Consequently, the potential of a bud to develop into a long shoot decreased basipetally. Potential long-shoot buds had higher bud-relative growth rates, stem-relative growth rates, leaf-relative growth rates, and stem dry weights during the course of postflush growth. Changes in leaf thickness, expressed in terms of specific leaf area and specific leaf weight, indicated that long shoots temporarily had thinner leaves than did short shoots a few weeks after flushing. Net assimilate requirements in long shoots for late leaf and internodal expansion may explain these observations. Nearing maturity, long-shoot early leaves became thicker, possibly owing to greater shoot vigour and (or) higher photosynthetic efficiency. Consequently, mature long-shoot early leaves possessed larger and thicker laminae, longer petioles, more side nerve pairs, and tended to grow more in length than width than short-shoot leaves on shoots of comparable age. Leaves of older short shoots, 2–10 years old, attained a greater size and had longer petioles than those of 1-year-old short shoots. Stem elongation and the development and expression of leaves in long shoots seemed to have a correlative influence on the overall vigour of long shoots.


HortScience ◽  
2000 ◽  
Vol 35 (1) ◽  
pp. 136-140 ◽  
Author(s):  
Mark H. Brand ◽  
Yiqin Ruan ◽  
Richard Kiyomoto

To characterize the in vitro behavior of Rhododendron `Montego' with tissue proliferation (TP) to cytokinin and auxin, comparisons were made of normal [TP(–)], dwarf TP [TP(+) dwarf], and long TP [TP(+) long] shoot cultures. On basal medium TP(–) and TP(+), long shoots failed to multiply and had a low relative growth rate (RGR) of 0.1, whereas TP(+) dwarf shoots produced 31.8 shoots per tip, with most shoots being <5 mm long, and RGR was 0.3. Addition of 15 μm 2iP to basal medium induced the production of more than six shoots per TP(–) tip and doubled their RGR; TP(+) long shoots produced 16.8 shoots, most <5 mm long, and had an RGR of 0.3; TP(+) dwarf shoots produced only 16% as many shoots as on basal medium, but still exhibited an increase in RGR. Leaves from TP(–) and TP(+) sources failed to produce shoots on basal medium, but 74% of TP(–) leaves formed shoots when cultured on 1 μm IBA and 30 μm 2iP. TP(+) leaves were able to form shoot meristems on media containing only 5 μm 2iP (26% of explants), but these meristems failed to elongate into shoots. Calli from TP(–) leaves, TP(+) leaves, and TP(+) tumors grown on medium containing 10 μm NAA and 15 μm 2iP had higher RGRs than the same calli on basal medium during the first 8 weeks of culture. Over time, RGR decreased in both TP(–) and TP(+) leaf calli, but increased in TP(+) tumor callus. The increased RGR resulted from differentiation of shoot meristems on 85% of the calli between week 4 and week 8. Our results suggest that TP(+) tissues have altered hormone metabolism or sensitivity that leads to dramatic differences in in vitro behavior and probably contributes to tissue proliferation observed in whole plants. Chemical names used: 6-(γ,γ-dimethylallylamino) purine (2iP); indole-3-butyric acid (IBA); α-naphthaleneacetic acid (NAA).


1996 ◽  
Vol 26 (9) ◽  
pp. 1556-1568 ◽  
Author(s):  
Thimmappa S. Anekonda ◽  
Richard S. Criddle ◽  
Lee D. Hansen ◽  
Mike Bacca

Seventeen Eucalyptus species and 30 rapid-growing Eucalyptuscamaldulensis trees (referred to as plus trees), growing in a plantation were studied to examine relationships among measured plant growth and respiratory parameters, geographical origins, and growth climate. The respiratory parameters measured at two different temperatures by isothermal calorimetry were metabolic heat rate, rate of CO2 production, and the ratio of heat rate to CO2 rate. Metabolic heat rate was also measured as a continuous function of temperature by differential scanning calorimetry in the range of 10 to 40 °C. Tree growth was measured as rates of height and stem volume growth. The values of respiratory and growth variables of Eucalyptus species are significantly correlated with latitude and altitude of origin of their seed sources. The maximum metabolic heat rate, the temperature of the maximum heat rate, the temperature coefficients of metabolic rate, and the temperatures at which the slopes of Arrhenius plots change are all genetically determined parameters that vary both within and among species. Measurement of growth rate–respiration rate–temperature relationships guide understanding of why relative growth rates of Eucalyptus species and individual genotypes differ with climate, making it possible to identify genotypes best suited for rapid growth in different climates. The temperature dependence of respiration rates is an important factor determining relative growth rates of eucalypts in different climates. To achieve optimum biomass production the temperature dependence of individual plants must be matched to growth climate.


1967 ◽  
Vol 69 (3) ◽  
pp. 305-315 ◽  
Author(s):  
J. E. Jackson

Growth analysis of cotton crops sown in the Sudan Gezira at monthly intervals between August and May revealed a marked seasonal pattern of growth. Irrespective of plant age and fruiting state growth of non-senescent plants was slowest during the cool winter months. Relative growth rates of young plants were highest in August, September and early October due to the high specific leaf areas and fairly high net assimilation rates found then. They were lowest when minimum temperatures were lowest. Net assimilation rates were also lowest in the coolest months, probably as a result of restricted growth. High temperatures in the spring reduced fruiting. It is concluded that low minimum temperatures and high evaporation rates are both associated with slow growth, and play a large part in determining the characteristic decline of growth rates of cotton sown at the usual date in August.I wish to thank the Chief of the Research Division, Ministry of Agriculture, Sudan, for permission to publish this paper and to record my gratitude to the team of field and laboratory assistants, especially Salih Saad and Hassan Osman, who helped in the work.


2013 ◽  
Vol 41 (2) ◽  
pp. 638 ◽  
Author(s):  
Aylin OZUDOGRU ◽  
Diogo Pedrosa Corrêa Da SILVA ◽  
Ergun KAYA ◽  
Giuliano DRADI ◽  
Renato PAIVA ◽  
...  

The study focused on an economically-important ornamental outdoor shrub, Nandina domestica, with the aims to (i) optimize an effective in vitro conservation method, and (ii) develop a cryopreservation protocol for shoot tips by the PVS2 vitrification and droplet-vitrification techniques. For in vitro conservation of shoot cultures, the tested parameters were sucrose content in the storage medium (30, 45, 60 g/L) and storage temperature (4 °C or 8 °C). Cryopreservation was performed by applying the PVS2 vitrification solution, in 2-ml cryovials or in drops over aluminum foil strips, for 15, 30, 60 or 90 min at 0 °C, followed by the direct immersion in liquid nitrogen of shoot tips. Results show that N. domestica shoots can be conserved successfully for 6 months at both the temperatures tested, especially when 60 g/L sucrose is used in the storage medium. However, conservation at 4 °C showed to be more appropriate, as hyperhydricity was observed in post-conservation of shoots coming from storage at 8 °C. As for cryopreservation, a daily gradual increase of sucrose concentration (from 0.25 to 1.0 M) produced better protection to the samples that were stored in liquid nitrogen. Indeed, with this sucrose treatment method, a 30-min PVS2 incubation time was enough to produce, 60 days after thawing, the best recovery (47% and 50%) of shoot tips, cryopreserved with PVS2 vitrification and droplet-vitrification, respectively.


1989 ◽  
Vol 40 (2) ◽  
pp. 293 ◽  
Author(s):  
DR Eagling ◽  
RJ Sward ◽  
GM Halloran

Measurements were made on the effect of barley yellow dwarf virus (BYDV) infection on the early growth of four commercial cultivars of ryegrass (Lolium spp.) under two different temperatures (24�C and 16�C). At 24'C, BYDV infection was associated with reduced root dry weight (30-40%) in all cultivars; the effect of infection on shoot dry weight and leaf area was variable. At 16�C, the effect of BYDV infection was variable, being associated with increases in root dry weight, shoot dry weight, and leaf area in one cultivar (Grasslands Ariki) and decreases in another (Victorian). In two other cultivars, root dry weight, shoot dry weight and leaf area were not significantly affected (P>0.05) by infection with BYDV.At 24�C, the reductions in root dry weight associated with BYDV infection were not concomitant with reductions in the root relative growth rates. Up to at least 28 days after inoculation (46-50 days after germination) reductions in root dry weight were associated with both aphid-feeding damage and virus infection. Experiments with the cultivar Victorian, showed that shoot dry weight was not significantly affected (P>0.05) by feeding with viruliferous (BYDV) or non-viruliferous aphids (Rhopalosiphum padi L.). At 16�C, changes in root and shoot dry weight were associated with changes in the root and shoot relative growth rates.


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