Review Environ. Control in Biol., 36 (2), 59-75, 1998

Environmental Effects on the Growth of Plantlets in

Micropropagation

Qunyh Thi NGUYEN and Toyoki KozAI*

Laboratory of Plant Cell Technology, Institute of Tropical Biology, Ho Chi Minh City, Vietnam * Laboratory of Environmental Control Engineering , Faculty of Horticulture, Chiba University, Matsudo,

Chiba 271-8510; Japan

(Received January 13, 1998)

Research on environmental effects on the growth of plantlets in micropropagation is reviewed to give an overview on the subject conducted in the past decade, mainly to

environmental biologists and engineers. Effects of aerial environmental factors including light, carbon dioxide concentration, temperature, relative humidity, oxygen and ethylene on the growth and photosynthesis of plantlets in vitro are discussed. Then, effects of culture medium environmental factors including sugar concentration, concentrations of ion compo-

nents, osmotic potential and pH of the culture medium on the growth of plantlets in vitro are discussed. Lastly, effects of biological factors such as explant size and explant density

on the growth of plantlets in vitro are discussed. Effects of aerial, culture medium and biological factors on the photoautotrophic (totally photosynthesis dependent) growth of

plantlets are emphasized.

INTRODUCTION

Micropropagation is a plant tissue culture technique used for obtaining a large number of

genetically identical plantlets. Research on micropropagation has been focused mainly on the bio-chemical effects of medium composition (sugar, mineral salts, phytohormones, vita-

mins, amino acids, etc.) on the differentiation, rooting and growth of explants under aseptic conditions. As a result, research on the effects of physical environments on the growth of

plantlets in micropropagation is far behind that of plants in greenhouses and fields.Recent studies, however, have revealed that physical environmental factors considerably

affect the growth and development of plantlets in micropropagation. In the past decade, a significant number of original papers have been published on the environmental effects on the

growth of micropropagated plantlets. Those papers suggest that environmental control in micropropagation will become an essential technique to obtain good-quality plantlets on a desired date with low production costs. However, very few review papers on related issues have been published recently. This article gives an overview of research on the subject conducted in the past decade, mainly for environmental biologists and engineers who are not so familiar with the subject.

AERIAL ENVIRONMENT

1. Light 1.1 Light flux density. Photosynthetic photon flux density (PPFD), or, more simply,

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photosynthetic photon flux (PPF) at wavelengths between 400 and 700 nm, is one of the most important factors involving the photosynthesis of chlorophyllous cultures, especially shoots and plantlets (Fujiwara and Kozai, 1995). A high PPF has a beneficial effect on promoting

photosynthesis and growth, provided that CO2 concentration in the culture vessel is not as low as the CO2 compensation point of the cultures (Kozai et al., 1990).

High PPF accompanied with CO2 enrichment has been shown to promote photoautotro-

phic growth of Solanum tuberosum plantlets and simultaneously induce specific adaptations of photosynthetic response potential, while some other cultivars did not respond favorably

(Cournac et al., 1992). A higher PPF results in a greater dry weight of the plantlet associated with a greater difference between CO2 concentrations inside and outside the culture vessel, due to a higher net photosynthetic rate (a higher CO2 uptake rate) of plantlets (Kozai and Sekimoto, 1988).

The PPF and percent PPF transmission in culture vessels are affected by the type and light energy output of light sources, the material and shape of the vessel, the position of the vessel on the culture shelf, the position of the light sources with or without reflectors, the optical characteristics (reflectivity, etc.) of the culture shelf and the type of closures, etc. (Fujiwara et al., 1989). The PPF in culture vessels with a closure, even with a high light transmissivity, was significantly lower than that on the empty culture shelf (Fujiwara and Kozai, 1995). The remaining question is how to develop an appropriate lighting system that can provide a high

and relatively even distribution of PPF at a reduced electricity cost.1.2 Spectral distribution. The spectral distribution of light received by cultures is known

to be primarily determined by both the spectral characteristics of the light source and the culture vessel material (Fujiwara and Kozai, 1995). The spectral distribution of light from

different light sources significantly differ from each other. Fluorescent lamps, which produce much less far-red radiation than high-pressure sodium lamps, have been the primary light source used in micropropagation. The spectrum generally matches the requirements of cultures (Kozai, 1991 b). Line light sources such as fluorescent lamps generally give a relative-ly uniform horizontal distribution of PPF on the culture shelf when they are placed parallelly on the shelf at a height of 40-50 cm above the cultures. Photon flux ratios of red to far-red regions and of blue to red regions are considered as

important factors for photomorphogenesis of plants. Red and far-red light applied as part of

the culture regimen led to better rooting of azalea microcuttings than those cultured under conventional cool-white fluorescent lamps (Read and Economou, 1982). Fukuda and Kurata (1992) proved that red light had the effects of promoting shoot formation and growth, and inhibiting root induction of carrot embryos, though these adventitious shoots were ill

shaped.Dooley (1991) reported that the spectral light transmissivities of culture vessel materials

differed from each other. Thus, both the spectral distribution of the light source and the spectral light transmissivities of culture vessel materials should be considered when designing a lighting system for a culture room. More attention should be paid to the selection of light sources and culture vessels to provide light with the required wavelengths and photon flux for

photomorphogenesis and/or photosynthesis of cultures.Light-emitting diodes (LED), especially red LED and far-red LED, proved to have

advantages over fluorescent lamps in regulating photomorphogenesis, growth and the develop-ment of plantlets in micropropagation (Fujiwara and Kozai, 1995). Red and far-red were

proved to have a significant effect on potato shoot length when the ratio of red photon flux to PPF is greater than 0.5 and far-red photon flux to PPF is less than 0.02 (Miyashita et al.,

1995). Kirdmanee (1995) found that the internode length of Eucalyptus camaldulensis was about 1.5 times greater with supplemental far-red light than without. The increased internode

60(2) Environ. Control in Biol.

length was correlated with the increased cell length of stem epidermis.

1.3 Lighting direction. In conventional tissue cultures, the light source is placed 30-40

cm above the vessels, giving downward light to the plantlets in the vessels below. This downward lighting system does not always provide the best performance regarding the growth and quality of the cultures and electricity costs for lighting and cooling the culture room

(Fujiwara and Kozai, 1995).In a sideward lighting system, the vessels are arranged in line and the light source is placed

between the lines just beside the vessels, giving light to the plantlets mainly sideward through

vessel side walls. The sideward lighting system helps to promote the growth of plantlets in vitro and to control plantlet height at reduced costs. Light intensity in vessels of this system was about five times higher than that of the downward system, when the number of fluorescent tubes used in the sideward lighting system was the same as that used in the downward lighting system (Kozai et al., 1992b ; Hayashi et al., 1994). Leaves of in vitro plantlets received the light energy more evenly and uniformly in the sideward than in the downward lighting system. This results in relatively larger leaves at the bottom and smaller leaves at the top (Hayashi et

al., 1993). Plantlets in the sideward lighting system had relatively short internodes and slightly greater numbers of leaves than in the conventional system. Moreover, the required space can be minimized because the culture vessels can be stacked vertically (Kitaya et al., 1995).

The required culture space can be further reduced by using a sideward lighting system

with both diffusive optical fiber belts and a point light source paired with a shape-designed reflector in place of fluorescent lamps ( Kozai, 1991 a ; Kozai et al., 1992b ; Kozai and Smith, 1995). This system helps to reduce the cooling load of the culture room and to obtain an improved light spectral distribution without increasing air and leaf temperature when a thermal filter is installed between the point light source and the cross-section of diffusive

optical fibers in order to remove thermal radiation. With this system, the thermal radiation emitted from the point light source is eliminated by the thermal filter and only the photosyn-thetically active radiation (PAR) is passed through the transparent optical fibers into the culture room (the light source, reflector and thermal filter are all placed outside the culture room). The plantlets can receive an even light distribution, and the cooling cost can be reduced by about 75% because only the PAR is sent into the culture room.

Another modification of this system is a combination of diffusive optical fiber belts and a microwave-powered lamp, which is a small (30 mm in diameter) lamp with high light output

(450 klumen, 130 lumen W-1)(Dolan et al., 1992; Kozai and Kitaya, 1993; Kozai et al., 1995b).

2. Carbon dioxide concentration

Culture vessel closures have been traditionally designed mainly to prevent the entry of contaminants, but consequently restrict the gas exchange between inside and outside vessels

(Desjardins, 1995). Due to the limited gas exchange, C02 concentration in the culture vessel containing chlorophyllous tissues decreases sharply within 2 h after the beginning of the

photoperiod, then reaches a stable concentration, which is significantly lower than the stan-dard atmospheric C02 concentration (350 j mol mol-1), but higher than the C02 compensa-tion point (50-100 ,umol mol-1) until the end of photoperiod (Fujiwara et al., 1987; Kozai and Sekimoto, 1988; Hayashi et al., 1993). Kozai et al. (1986) proved that the stable C02 concentration during the most of photoperiod decreased with passage of days close to the C02 compensation point, as chlorophyllous tissues in an air-tight vessel grew to plantlets.

Under such low C02 concentrations in the vessel, the net photosynthetic rate of plantlets

in the vessel is close to zero, resulting in a negative daily C02 balance of plantlets in the vessel.

Vol.36, No.2 (1998) (3)61

This means that the integral of net photosynthetic rate over the photoperiod is smaller than

integral of dark respiration rate during the dark period.

The low CO2 concentration in the vessel, in turn, reveals the photosynthetic competence of plantlets in vitro, which results in a considerable interest of photoautotrophic micro-

propagation (Kozai, 1991a, c, d). In photoautotrophic micropropagation, sugar is not added to the medium, and the growth of plantlets depends solely on photosynthesis. Strictly

speaking, no organic substances including phytohormones, vitamins and amino acids, except for minerals, are added to the medium in this new method.

Photoautotrophic micropropagation is generally associated with higher light intensity and higher CO2 concentrations than in conventional micropropagation, in order to increase

photosynthesis of plantlets in vitro. The CO2 enrichment in photoautotrophic micropropaga-tion for chlorophyllous plantlets has clearly proved effective in promoting the photosynthetic ability and thus growth of in vitro shoots/plantlets (Kozai et al., 1987a, b ; Fujiwara et al., 1995; Kirdmanee et al., 1995a, b, c ; Heo et al., 1996; Seko and Kozai, 1996).

The CO2 concentration inside the vessel has been increased by increasing the vessel

ventilation rate or by actively controlling the C02 concentration inside the vessel. The use of microporous polypropylene filters with high gas permeability for increasing the vessel ventila-tion rate is gaining popularity for passively maintaining a relatively high CO2 concentration in the vessel (Kozai et al., 1988). Active control of CO2 concentration inside the vessel has also been achieved by directly injecting the gas into the vessel or by using a large vessel with a forced ventilation system for introducing CO2 enriched culture room air into the vessel

(Fujiwara et al., 1988; Kubota and Kozai, 1992).Photoautotrophic micropropagation can have a beneficial effect only for chlorophyllous

cultures which show a positive CO2 balance during the photoperiod at a CO2 concentration of 350 jcmol mol-1 or higher (Jeong et al., 1993). A relative constant CO2 concentration in a culture vessel can be observed only when the CO2 exchange rate between inside and outside of the vessel is balanced with the CO2 exchange rate of the cultures in the vessel (Fujiwara and Kozai, 1995).

Niu et al. (1996a, b), Niu and Kozai (1997) developed models for predicting the hourly and daily net photosynthetic rate (Pa) and CO2 concentration inside the vessels for Cymbidium and potato plantlets in vitro in order to determine optimal conditions to maximize the daily P, of in vitro plantlets by using computer simulations.

3. Temperature and DIF

The air temperature in culture vessels is considered to be almost the same as that outside

of the vessel or that of the culture room during almost all the dark period (Fujiwara and

Kozai, 1995). In the photoperiod, however, the air temperature difference will be close to or

more than 1•Ž when the irradiance or the net radiation flux density at the boundary of the

vessel was higher than 35 W m-2. Therefore, in order to maintain the temperature in the

vessels at a desired temperature, the air temperature in the culture room should be lowered by

about 1°C (Fujiwara and Kozai, 1995).

Kozai et al. (1992c) described the effect of the difference in air temperatures (DIF=Tp-Td) between the photoperiod (Tp) and the dark period (Td) on the stem or shoot elongation of

potato plantlets in vitro under enriched CO2 (1300-1500amol mol-1) and photoautotrophic conditions. The shoot length was shorter with decreasing DIF at both low and high PPF (74

and 147 pmol m-2 s-1), though shorter in high PPF than in low PPF in each of three DIF treatments (+ 10 DIF, 0 DIF, -10 DIF). However, the dry and fresh weights of plantlets were similar among the three treatments. A similar result was obtained with Mentha rotun-difolia plantlets in vitro (Jeong et al., 1996). The manipulation of DIF for controlling the

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shoot length and/or the plantlet height can be an important technique in micropropagation to

produce quality transplants for greenhouses or open fields.

4. Relative humidity

Relative humidity (RH) in the culture vessel is an important environmental factor that affects the water relations of plantlets or organs in vitro. RH is generally higher than 95% in an air-tight vessel containing plantlets (Fujiwara and Kozai, 1995).

The relation between (100-RH)% and water-vapor pressure deficit (WPD) is linear at high RHs (e.g., RH>90%) and room temperatures (ca., 20). The WPD is defined as the difference between the water vapor pressure of the air in question and the saturated water-vapor pressure of the air (100%RH) at the same temperature.

The transpiration rate of shoots/plantlets is nearly proportional to WPD (Fujiwara and

Kozai, 1995) and to their total leaf area or surface area. Then, WPD and thus the transpira-tion rate of plantlets for 98, 96 and 94%RH are, respectively, 2, 4 and 6 times greater than those for 99%RH at room temperatures. Absolute values of WPD and transpiration rate at high RHs are relatively small but their relative differences are significant. Moreover, the uptake rates of water and some kinds of minerals such as Ca increase with increasing the transpiration

rate. Thus, a small difference in RH at high RHs causes a significant difference in uptake rates of water and some kinds of ions.

Furthermore, high RH has been attributed to the poor development and disorders of the

physiological and morphological structures of plantlets resulting in the high mortality of plantlets after being transferred into ex vitro conditions (Kozai et al., 1993). A reduced RH (e.g., 95 to 90%) has been shown to improve plant growth, epicuticular wax deposition and stomatal function. Again, a small difference in RH at high RHs causes a significant difference in physiological and morphological characteristics of plantlets. By reducing RH in culture

vessels, vigorous potato plantlets with shorter shoot length and higher percentage of dry matter have been obtained without any significant decrease in plantlet dry weight (Kozai et al., 1993).

Tanaka et al. (1992) also showed that both RH in the vessel and transpiration rate of the

plantlets increased over time, when the in vitro cuttings grew into plantlets, due to the rapid increase in leaf area. The rate of leaf area increase was greater than the rate of WPD increase. It was then presumed that the abaxial leaf resistance to transpiration was greater as RH in the vessels was lower. Thus, the plantlets growing under a condition of low RH might be able to control excess water loss from their leaves and to withstand water stress when transplanted even directly from in vitro conditions to greenhouses or open fields (Tanaka et al., 1992). Therefore, a relative humidity of around 85-90% in the culture vessel at the rooting stage or the

last stage in vitro may help to produce qualified plantlets more able to withstand water stress after being transplanted from in vitro to ex vitro conditions (Tanaka et al., 1992).

Another concern is that RH in culture vessels varies in space and time in accordance with air temperature fluctuations, and is influenced by the gas exchange characteristics of the vessels

(Kozai et al., 1996b). Moreover, the lighting cycle affecting the air temperature inside the vessels might have an effect on the diurnal change in RH and the daily average RH in the vessels as well (Fujiwara and Kozai, 1995).

S. Oxygen

O2 concentration has an important effect on the photorespiration of photosynthetic C3

plants. At normal atmospheric (21%) 02 concentration, C3 plants grown ex vitro photo-autotrophically lose up to 50% of photosynthetically fixed carbon due to photorespiration. However, this release of CO2 due to photorespiration is prohibited by low 02 concentrations.

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The net photosynthetic rate (Ps) of Primula malacoides (C3 plant) plantlets in vitro at 1% O

2 (10 mmol mol-1) is about 3 times greater than 21% O2 and 1.5 times greater than 10% O2 when CO2 concentration was approximately 200 ,Lcmol mol-1 (Shimada et al., 1988). This suggested that the Pn of in vitro C3 plantlets increased with decreasing O2 concentration.

The effect of long-term exposure to low O2 concentrations on the growth of Chrysanth-enum morifolium (C3 plant), studied by Tanaka et al. (1991), demonstrated the fact that the increase of the plantlet dry weight for 30 d was significantly greater in 10% O2 than in 5,15 and 21% O2. It will become a practical application to control O2 concentration at about 10%, if one can find a simple way to keep O2 concentration in a small and airtight vessel at low levels for the entire culture period (Kozai et al., 1992a).

O2 concentration in a culture vessel decreases in accordance with increasing CO2 concen-tration in the vessels (Doi et al.,1989). In Caladium bicolor (C3 plant) plantlets, the decrease in O2 concentration in the vessels was equal to the increase in CO2 concentration ; whereas, in Dendrobium phalaenopsis (CAM plant) plantlets in vitro, the decrease in O2 concentration in the vessels was remarkably larger than the increase in CO2 concentration. These results

clearly showed that the change in O2 concentration in the vessels depends on the type of carbon fixation system (Fujiwara and Kozai, 1995).

It should be noted, however, that in conventional micropropagation the CO2 concentra-

tion in the vessel is generally in the range from 0.01 to 1-3% and thus the O2 concentration is

in the range between about 18 and 22%. That is, O2 concentration is never lowered to 10%

unless it is controlled artificially using O2 absorbants, for instance. On the other hand, the

change in O2 concentration from 21 to 18% does not affect the Pn of C3 plants.

6. C2H4 and gas diffusion coefficientThe gas C2H4 is known to cause numerous hormonal influences on plants. C2H4 concen-

tration in relatively air-tight culture vessels was reported to increase gradually with time up to more than 2 pmol mol-1 from 21 to 60 d after the start of a new culture. C2H4 has been implicated in the reduced growth of cultures of both Dahlia and Petunia (Gavinlertvanata et

al., 1979). The concentrations of C2H4 and toxic compounds (oxidation products of phenols) tend to be high in some cases in air-tight vessels (De Proft et al., 1985). In contrast to CO2 and O2, C2H4 is only released, not absorbed, by cultures and, therefore, it should be released to the outside of culture vessels once accumulated. A simple way to solve the problem is to increase the number of air exchanges of culture vessels by using a gas permeable filter over a hole on the cap or lid of the vessels, or by forced ventilation systems (Fujiwara and Kozai, 1995).

The diffusion of gas in culture vessels is also a considerably important process that helps to facilitate : (1) the exchange of gases (including water vapor) between cultures and the air in the headspace of the vessels, (2) the exchange of solutes (including dissolved gases) between cultures and medium, and (3) the uniformization of the spatial distribution of gases in the headspace and the solutes in the medium (Fujiwara and Kozai, 1995).

Under natural ventilation conditions, molecular diffusion might be dominant in the

headspace of culture vessels during most of the dark period. On the other hand, natural

convection is dominant during the photoperiod. Eddy diffusion becomes a dominant mode

of mass transfer in the headspace under forced ventilation conditions.

Kubota and Kozai (1992) suggested that forced ventilation increased the eddy diffusion coefficient of gases and the air flow speed and, thus, enhanced the CO2 uptake of cultures during the photoperiod to a greater level than when only CO2 concentration was increased.

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CULTURE MEDIUM ENVIRONMENT

1. Sugar concentration

Sugar, such as sucrose, fructose, glucose and sorbitol, is considered merely as a source of carbohydrate in the culture medium for the heterotrophic growth of cultures. The actual requirement for carbohydrate depends on the environmental conditions, particularly light intensity and CO2 concentrations in the vessel (Williams, 1995). Sugar supply to the culture medium has a negative effect on Pn which results in a feedback inhibition of rubisco, i.e., the low activity of rubisco explains the low rates of Pn in vitro plantlets (Hdider and Desjardins, 1994).

Kozai (1991d) suggested sugar be reduced or eliminated from the culture medium by

increasing CO2 concentration in the vessels and maintaining cultures under a high light intensity. The reduction or elimination of sugar will help to lower high production costs in conventional micropropagation. This is due to the loss of plantlets in vitro by biological contamination in the medium, the abnormal development of plantlets, the use of plant

growth-regulators, the difficult acclimatization of plantlets in vitro and the labor costs.This conclusion arose out from experiments on Cymbidium (Kozai et al., 1987b), and

carnation (Kozai and Iwanami, 1988) which demonstrated that the plantlet dry weight increase with time was greater in CO2-enriched than in CO2-nonenriched treatments regardless

of the sucrose concentrations. Nakayama et al. (1991) also proved in the potato culture that, 3 d after the start of culture, the Pn was 8-10 times greater in the sugar-free medium treatment than that in the sugar-containing medium (30 g L-1 sucrose) treatment when CO2 concentra-tion in the vessel was in the range of between 500 and 1 000 ,umol mol-1.

Moreover, in carnation cultures, the amount of sugar absorbed by the plantlets was only about 2-8% in weight of the initial sucrose content (Kozai and Iwanami, 1988). The total osmotic pressure caused by sugar should have increased with time as the hydrolysis of sucrose, a disaccharide, to monosaccharides (glucose and fructose) proceeded in the medium, though the total weight of sugar in the medium decreased by 10% (Kozai, 1991a). Fujiwara et al.

(1995) also demonstrated that the ratio of gross production by photosynthesis to dry weight increase of potato plantlets in vitro was estimated to be four times greater than that of

saccharides uptake at both inflow-air CO2 concentrations for the culture box, 350 and 1 000

1Lcmol mol-1.

2. Ion components

Plant tissue cultures respond differently to the overall mineral supply. Some species

grow better on media with lower ionic strength as compared to MS medium (Murashige and Skoog, 1962), whereas others grow better on MS medium (Williams, 1995). The optimum mineral requirements can also vary between explant types and stages of culture growth. The rate of uptake of an ion may exceed the rate of utilization creating a pool of available ions within a plant.

Furthermore, the environmental conditions are proved to have different effects on the ion

uptake of cultures in vitro. The ion uptake pathway involves a number of steps and processes beginning with the transport of ions. At each step of the pathway, the transport may be due to the diffusion along a concentration gradient, a mass flow driven by the transpiration stream or an active uptake selecting and depending on energy (Williams, 1992, 1995).

In vitro conditions may modify the relative activity of the normal transport mechanisms,

particularly where the mass flow is involved. It is likely that the mass flow would be limited by a high relative humidity within a closed culture vessel (Williams, 1992). Kozai et al.

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(1991) suggested that a reduction in relative humidity in the vessel enhances transpiration and thus mineral uptake, and that the growth under photoautotrophic conditions is enhanced under a low relative humidity (85-90%).

For the maximization of the culture growth, medium inorganic ion composition and

medium inorganic ion strength are critically important (Yang et al., 1995a) . Carnation

plantlets cultured in vitro grew better on a sugar-free medium with medium ionic composition widely used for hydroponic culture than on a sugar-free medium with half strength MS or on

medium containing sugar with either half strength MS or the hydropronic medium ionic

composition (Kozai et al., 1988).

The MS medium is, in fact, optimized for heterotrophic growth and/or differentiation of callus ; thus may not be optimal for photoautotrophic or photomixotrophic cultures . Kozai et al. (1991) examined the importance of mineral nutrition of strawberry plantlets in vitro under photoautotrophic and photomixotrophic conditions. A half strength of MS medium was used as basal nutrient ion composition. The experimental results showed that PO43- was absorbed rapidly (the percent residual of PO43- reached 3% on day 21) by the plantlets under the photoautotrophic conditions with high CO2 concentration . It was suggested that the Pn and, thus, photoautotrophic growth was further promoted if PO43- was available to the

plantlets at the later stage of growth. It was presumed that the initial amount of PO43- in the medium should be higher for photoautotrophic or photomixotrophic than for heterotrophic micropropagation. The percentage for all ions was the lowest under the photoautotrophic condition on day 14 and 21, except SO42- on day 14, as compared with those under the

photomixotrophic or heterotrophic conditions (Kozai et al., 1991).Nitrogen is in essential component for all plant growth. The absorption of NH4+ and

N03- is different according to species, and will influence the morphogenesis of plantlets in vitro (Williams, 1995). Potassium is abundant in plant tissues and reflects that supply exceeds demand by the plant in many cases. Therefore, it is not a problem in plant tissue culture , though some species (e.g., Manihot) are sensitive to high potassium concentrations (Williams , 1995).

Sulfur exists in agar at a significant concentration, even though in MS medium sulfur may be the second limiting mineral following phosphorus (Williams, 1991). Calcium plays an important role in the control of cell wall synthesis and maintenance of membrane integrity . An adequate supply of Ca is essential for the continued plant growth, while high Ca concen-trations may inhibit cell extension. Cytoplasmic Ca is also involved in the regulation of hormone responses to environmental factors such as light and temperature . Cultures may continue to grow for some time without an external supply of Ca until endogenous supplies are depleted. A typical symptom of Ca deficiency is shoot-tip necrosis due to poor distribu-tion of Ca at the shoot tip rather than absolute deficiency in the plantlets (Williams , 1995).

Magnesium is a component of chlorophyll and a cofactor for many enzyme reactions . Mg may substitute for Ca in some specific roles. Therefore, the relative supply of Mg may be

important where Ca uptake is limited. On the other hand , Na and Cl are not usually essential to normal plant growth and are mainly included in media to balance the ionic composition

when providing other elements (Williams, 1995).

Yang et al. (1995a, b) proved that with the increase of about 1/3 (or to 3 in case of Mgt, H2P04- and SO42-) of the ionic strength of Ca2+ , Mg2+ , H2P04- and SO42- supplied in full strength MS medium, dry weight, fresh weight, and leaf area of the strawberry plantlet in full strength of modified Hoagland and Arnon (1950) were significantly greater than those in 1/2 or full strength MS medium.

Micronutrients essentially exist in the culture media as catalysts for many biochemical

processes. Though required at low concentrations, sufficient quantities may be obtained to

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enable normal growth. It is difficult to see clearly the precise effect of micronutrients on the culture growth because of the potential for interaction between them. However, general symptoms of micronutrient deficiencies include shoot tip necrosis (B), leaf chlorosis (Fe, Zn, Mn), reduced lignification (Cu, Fe) and rosetting (Zn, Mn). The supply of Fe is usually more critical than other micronutrients because of the large levels required and the solubility

problems. Excess Mn can lead to Fe deficiency, while excess Fe or EDTA can reduce Zn uptake (Williams, 1995).

The concentration of inorganic ions in the culture medium decreases with time as they are

absorbed by shoots/plantlets in vitro. This decrease is affected not only by the initial concentration and uptake rate of each ion, but also by the volume of the medium per plantlet

(Kozai et al., 1991). The rate of decrease is greater when smaller amounts of medium are used, because it is determined by the amount of absorbed ions divided by the medium volume. In other words, the ion uptake rate, or amount of absorbed ion per unit time, is equal to the rate of decrease multiplied by the volume. However, the ion uptake rate depends on the medium concentration. On the contrary, the ion concentration increases with time when the

percent medium volume decrease per day due to evaporation from the medium and transpira-tion from the plantlets is greater than the percent ion concentration decrease due to the ion uptake per day. Some inorganic and organic substances are released from the explant and

plantlet to the medium in some cases.Thus, optimum nutrient composition should be dependent on the initial volume of the

medium and the rates of evaporation and transpiration when the medium is not renewed during a long-period culture (Kozai et al., 1992a). In plant tissue culture, the medium volume is usually relative small (4-10 mL per plantlet), so that the changes in ionic concentra-tions tend to be significant. Therefore, both initial medium volume and initial nutrient

concentration are important to determine the initial nutrient composition in the medium

(Kozai et al., 1995a).

3. Osmotic potential

Osmotic potential depends on the total molar (ions and molecules) concentration in the culture medium. Low medium osmotic potentials are associated with a high total molar

concentration of medium solutes. Sugar and mineral salts are main contributors. The increase of mineral and sucrose uptake, when plants grow, results in increasing osmotic

potential. However, the counteraction of the concurrent removal of water by transpiration and evaporation may decrease osmotic potential (Williams, 1995).

The osmotic potential of the medium influences many aspects of growth and development

of cultures. Osmotic potential of the culture medium involves osmotic potentials mainly caused by basic components, saccharide (sucrose, glucose and fructose) as a carbon source and osmoregulatory substance (manitol and sorbitol) (Fujiwara and Kozai, 1995).

In general, the osmotic potentials of widely used tissue culture media are lower as compared to those of hydroponic culture solutions. Thus, culture medium components are not only the nutrient substances, but also the causative substances of osmotic potentials affecting the water relations of plantlets in vitro (Fujiwara and Kozai, 1995).

Osmotic potentials caused by basic components and carbon source in the medium can be changed during the culture. The osmotic potential caused by saccharides decreased when sucrose was inverted into glucose and fructose by invertase located in the root surface ; whereas the osmotic potential caused by basic components increased as their solutes were absorbed by shoots. The sum of the two osmotic potentials was equal to the total osmotic potential of the MS liquid medium, which decreased gradually with time by approximately 90 kPa over 35 d

(Kinoshita et al., 1988). Hydrolysis of sucrose into glucose and fructose can bring about a

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relatively small change in osmotic potential in the medium ; whereas the incorporation of monosaccharides into culture media may cause a relative large change in osmotic potential

(Fujiwara and Kozai, 1995).

4. Supports

Gelling agents provide several advantages for plant tissue culture production and research as compared to liquid media. The use of gels provides the growing culture a beneficial

physical contact with a nutrient medium ; thus helps to prevent it from submersion in a liquid medium with relative low-oxygen concentration (Smith and Spomer , 1995). In other words, the use of a gelling agent will help to prevent hyperhydricity, and provides a good analogue of soil for root zone investigations. Gelled media, however , create some drawbacks, such as little adaptability to automation (gelled medium cannot be recirculated easily) , inactivation of some chemical components, and difficulty for cleaning vessels and removing the gel from

plantlet roots after the culture period. Moreover, gels, principally agar or gelrite, have also been cited as in vitro shoot or embryogenic cell growth inhibitors (Smith and Spomer , 1995), because they cannot be considered as inert components of the system, and both their chemical and physical properties can influence culture performance (Williams , 1992). Some experi-ments proved that an agar-gelled medium inhibited the plantlet growth in vitro as compared to that on liquid-based media (Debergh, 1983). On the other hand, shoots , which were generated in the more humid, less aerated, restricted in vitro environment with gelling agents, produced roots having underdeveloped vascular systems and proved to be less adaptable to acclimatization. Other supporting materials such as cellulose plugs , rockwool cubes, and vermiculite, which have a high air porosity, are proved to enhance the plantlet growth and , thus, survival percentage of plantlets ex vitro.

Takazawa and Kozai (1992) used Sorbarod, a fibrous cellulose plug , as supporting material in culture plastic vessels and cited that the greatest average fresh weight of plantlets , the largest percent dry matter, the smallest top/root fresh weight ratio and the shortest shoot were observed in Sorbarod treatment as compared with other treatments using agar as support-ing material.

Kirdmanee et al. (1995a) demonstrated that, under both CO2 enriched and CO2 non-enriched conditions, the palisade layer index, the Pn in vitro and the survival percentage ex vitro of Eucalyptus camaldulensis cultured in vitro photoautotrophically were the highest in the vermiculite followed by the plastic net, gelrite matrix and agar matrix (in descending order). Kozai et al. (1996a) also proved that both rockwool and vermiculite supports enhan-ced the root growth and chlorophyll concentrations of sweetpotato plantlets cultured

photoautotrophically in vitro as compared with the conventional agar gel. Nagae et al. (1995) showed that Gerbera plantlets developed vigorously and were much bigger under photoautotrophic conditions with CO2 enrichment and Rockwool Multiblock as a supporting material in the Culture Pack than those on sugar-contained agar medium in bottle .

Fujiwara et al. (1993) showed that the O2 diffusion coefficient decreased about 50% when agar in media increased from 0 to 8 g L-1, and about 25% more if adding 30 g L-1 sucrose into 8 g L-1 agar-gelled MS medium. Therefore, the poor rooting of shoots would partially result from low dissolved O2 concentration round the shoot base in the medium (Fujiwara and Kozai, 1995).

On the contrary, Kurata and Fukuda (1995) have indicated that the low dissolved oxygen

(DO) concentrations in liquid media in shake culture of carrot somatic embryos were prefer-able for regenerating plantlets from embryos.

68(10) Environ. Control in Biol.

S. pH

pH of medium is also one important factor affecting the growth, development and morphogenesis of in vitro plantlets. However, in many plant tissue cultures, the pH of the medium is largely taken for granted. A standard practice is to adjust the pH during prepara-tion of the medium and then to ignore it (Williams, 1992). It is well known that the pH of media does not usually remain constant (George, 1993), but changes both during media

preparation, particularly autoclaving, and in the presence of living plant material (Gamborg and Shyluk, 1981; Williams et al., 1990).

The change in pH when plant material is added seems to be due to an ion imbalance between the medium and the plant (Williams et al., 1990). This possibly results in a substantial efflux of minerals out of the plant into the medium. The equilibrium point depends on the species but is similar irrespective of the initial set pH (Williams, 1992). A major factor of this change is the balance between NO3- and NH4+ supply and uptake

(Congard et al., 1986). As this balance changes over the culture period, there may be an initial decrease in pH followed by an increase (Gamborg and Shyluk, 1981).

Congard et al. (1986) showed that the pH of plantlets depends on the developmental stage, beginning by a decrease in the primary root formation then an increase with the secondary roots. Kobayashi et al. (1995) also proved that pH slightly dropped within the first 2 weeks corresponding to the root formation of Torenia and, then, rose to 7.0 as compared to the initial pH of 5.6. The duration of rising pH corresponded to the time of formation and development of vegetative buds. After rising, pH rapidly dropped to 5.0 corresponding to the

period of formation and development of floral buds.Yoshihara and Hanyu (1992) demonstrated that in strawberry tissue culture using liquid

medium, pH dropped to about 4 from the initial 6 within the first 7 d, corresponding to the lag

phase of the callus growth. It also dropped to the same level in the growing stage of the intact plant after 20 to 30 d of culture. After the droppings, the pH rose to 6 or higher in both the cultures. However, little pH change and almost constant pH were observed in the multiple shoot culture. The results led to the conclusion that the preferential uptake of nitrogen sources affected the pH changes.

BIOLOGICAL EFFECTS

1. Plant size and physiological differences of explantsThe method of plant tissue culture applying the regeneration of plantlets from callus,

single cells and protoplasts has currently aroused the question of genetic stability of these

plantlets and the loss of the organ/embryo-forming capacity (Pierik, 1988). The use of somatic embryos or adventitious buds/shoots derived from the leaf, petiole, stem, stalk, corm, etc., in micropropagation is also restricted due to the fact that chances of obtaining mutated

plants are higher (Pierik, 1988).In commercial micropropagation, nodal sections, especially single-node stem cuttings,

and axillary buds are most commonly used as explants at the multiplication stage. Different leaf area and fresh weight of explants may cause the growth variation of regenerated plantlets. Pierik (1987) suggested that larger explants sometimes regenerated easier than smaller ones.

In photoautotrophic micropropagation, the leafy part of explants, instead of the stem part,

plays the most important role on the subsequent growth of regenerants because it helps to produce carbohydrates by photosynthesis (Miyashita et al., 1996). This means that under photoautotrophic conditions, the growth of a leafless explant is delayed, and the growth of leafy explants is promoted when their leaf area or mass of photosynthetic (chlorophyllous) organ is larger. Under photoautotrophic conditions, the leaf area of the explant had a greater

Vol.36, No.2 (1998) (11)69

effect than the nodal position in the mother plant or fresh weight of the explant on the

subsequent growth into plantlets, provided that the environment is favorable for photosynthe-sis (Miyashita et al., 1996).

In conventional micropropagation using sugar-containing medium , the increase of inter-node length of explants helps to improve the initial growth rate of explants due to its greater

mass of carbohydrates. Furthermore, when the internode is longer , manipulation for multi-plication is easier, especially in automation (Kozai et al., 1991). Marcelis-van Acker and Leutscher (1993) observed that two-node cuttings (longer piece of stem) with large leaf area

produced larger plantlets in cutting propagation ex vitro of rose and Schefflera. They also indicated that two-node cuttings with the upper leaf removed produced even larger plantlet

growth than single node cuttings did. Veierskov (1978) suggested that the effect of stem or internode length was related to carbohydrates accumulated at the basis cuttings in ex vitro

propagation of pea. The rate of propagation is also strongly dependent on the number of nodes (leaves) formed in vitro within a certain time period (Pierik , 1988). A larger explant produced a greater number of shoots in vitro than a small explant.

It was suggested that a reduction of light intensity associated with an increase in distance from top to base of nodal cutting position through a plant canopy and an increase of the stem length below the node affected the subsequent shoot growth , axillary bud break and root proliferation. In photoautotrophic micropropagation, the sideward lighting system seems to be a such desirable technique to enhance the subsequent growth and development of plantlets in vitro, as the system provides an even distribution of energy to the upper , middle and lower leaves of shoots/plantlets. This, thus, results in the relatively large leaves at the bottom and relatively small leaves at the top of shoots/plantlets (Kozai et al ., 1992b, 1995b).

The morphology of micropropagated plantlets , which derived from either axillary, adventitious or meristematic origin is equally as important as their physical characteristics when these plantlets are transferred as transplants to the greenhouse or the open field (Kozai et al., 1991). The generally required morphological characteristics of transplants are: (1) shortness and thickness of the main stem, (2) low shoot/root weight ratio , and (3) large leaf area with normal stomata and thick cuticular layers . The most important characteristic among them is the shortness and thickness of the main stem. However, in reality, the conventionally micropropagated transplants tend to be tall and thin due to factors of the in vitro environment (Kozai et al., 1991). With a proper control of physical and chemical environments in photoautotrophic tissue culture, the growth and development (fresh and dry weights, number of nodes, total leaf area, rooting and branching) of chlorophyllous explants/shoots will be enhanced, while morphological and physiological disorders such as hyperhy-

dricity (or glassiness), thin cuticular wax formation of leaves will be reduced . Thus, the uniformity of the plantlet growth increases , whereas the excess application of exogenous plant growth regulators is reduced (Kozai, 1991b).

2. Plant density

Kozai et al. (1989) proved that , under photoautotrophic conditions, the growth (fresh weight, dry weight, leaf area and number of unfolded leaves) of potato plantlets was substan-tially affected by the shoot/plantlet density inside the vessel . CO2 concentration, net photosynthetic rate and mineral component concentration decreased with increasing the plant density. With the same conditions of number of air exchanges and high/low PPF , the growth of potato plantlets in vitro was also proved to decrease with the increase of the plantlet density inside the vessel after 2 weeks of culture (Niu and Kozai , 1997).

70(12) Environ. Control in Biol.

3. Others

The chronological age of the potential explant and the season that the explant is obtained

are important only when they influence the extent of differentiation of the cells and their

physiological age. However, the age •geffect•h on the regeneration ability of explants is a

controversial issue in plant tissue culture (Read, 1992).

In vitro derived plantlets have recently been reported to be more regenerative than

explants taken from the field- or greenhouse-grown stock plants (Economou and Read, 1986; Liu and Sandford, 1988; Stamp et al., 1990). It can be generally accepted that these explants have undergone apparent physiological changes contributing to a better in vitro performance

(Read, 1992).It is obvious that disease-free stock plants are preferred for explants in vitro. The use of

meristem culture to produce virus-free plants may be helpful in some cases. The use of explants from virus-free stock plants in micropropagation will help to produce a large number of healthy plants in a limited time (Read, 1992).

CONCLUSION

The effects of physical and chemical environments on the growth and development of

plantlets in micropropagation have been significantly proved through several recent studies (Jeong et al., 1995). It is hoped that this article will contribute to the further understanding of the essential role of environmental control in micropropagation systems in order to optimize in vitro plantlet production at lower costs.

REFERENCES

Congard, B., Beaujard, F., Viemont, J. D. 1986. Les bruyeres in vitro. VI. Croissance de Calluna vulgaris sur milieu strictement nitrique ammoniacal et cinetique du pH en fonction du develop-ment des plantes. Can. J. Bot. 64: 959-964.

Cournac, L., Cirier, I., Chagvardieff, P. 1992. Improvement of photoautotrophic Solanum tuber-

osum plantlet culture by light and CO2: Differential development of photosynthetic characteris-

tics and varietal constraints. Acta Hortic. 319: 53-58.

Debergh, P. C. 1983. Effects of agar brand and concentration on the tissue culture medium.

Physiol. Plant. 59: 270-276.

De Proft, M. P., Maene, M. L., Debergh, P. 1985. Carbondioxide and ethylene evolution in the

culture atmosphere of Magnolia cultured in vitro. Physiol. Plant. 65: 375-379.

Desjardins, Y. 1995. Photosynthesis in vitro•\on the factors regulating CO2 assimilation in

micropropagation systems. Acta Hortic. 393: 45-61.

Doi, M., Oda, H., Asahira, T. 1989. In vitro atmosphere of cultured C3 and CAM plants in relation to day-lengths. Environ. Control in Biol. 27: 9-13. (JE)*

Dolan, J. T., Ury, M. G., Wood, C. H. 1992. A novel-high efficacy microwave powered light

source. Presented at 6 th Int. Symp. on the Science and Technology of Light Sources, Technical

University of Budapest, Budapest, pp 11.

Dooley, J. H. 1991. Influence of lighting spectra on plant tissue culture. Ann. Am. Soc. Agric.

Eng. Meeting, Chicago, Paper No. 917530, pp 8.

Economou, A. S., Read, P.E. 1986. Influence of light duration and irradiance on micropropaga-

tion of a hardy deciduous azalea. J. Am. Soc. Hortic. Sci. 112: 566-569.

Fujiwara, K., Kozai, T., Watanabe, I. 1987. Fundamental studies on environments in plant tissue culture vessels. (3) Measurements of carbon dioxide gas concentration in closed vessels contain-ing tissue cultured plantlets and estimates of net photosynthetic rates of the plantlets. J. Agric. Meteorol. 43: 21-30. (JE)

Vol.36, No.2 (1998) (13)71

Fujiwara, K., Kozai, T., Watanabe, I. 1988. Development of a photoautotrophic tissue culture sys-tem for shoot and/or plantlets at rooting and acclimatization stages. Acta Hortic. 230: 153-158.

Fujiwara, K., Kozai, T., Nakajo, Y., Watanabe, I. 1989. Effects of closures and vessels on light intensities in plant tissue culture vessels. J. Agric. Meteorol. 45: 143-149. (JE)

Fujiwara, K., Aitken-Christie, J., Kozai, T. 1993. Water potential of radiata pine shoots cultured in vitro under different relative humidities. Plant Tissue Cult. Lett. 10: 144-150.

Fujiwara, K., Kozai, T. 1995. Physical microenvironment and its effects. In•gAutomation and

Environmental Control in Plant Tissue Culture•h(ed. by Aitken-Christie, J., Kozai, T., Smith,

M. A. L.). Kluwer Academic Publishers, Dordrecht, The Netherlands, p. 319-369.

Fujiwara, K., Kira, S., Kozai, T. 1995. Contribution of photosynthesis to dry weight increase of in vitro potato cultures under different CO2 concentrations. Acta Hortic. 393: 119-126.

Fukuda, E., Kurata, K. 1992. Production of transplants of carrot (Daucus carota L.) through adventitious shoots by using red light. Acta Hortic. 319: 303-306.

Gamborg, O. L., Shyluk, J. L. 1981. Nutrition media and characteristics of plant cell and tissue

cultures. In•gPlant Tissue Culture Methods and Applications in Agriculture•h(ed. by Thorpe,

T. A.). Academic Press, New York, p 21-44.

Gavinlertvanata, P., Read, P. E., Heins, R. D., Wilkins, H. F. 1979. Influence of photoperiod and

daminozide stock plant treatments on ethylene and CO2 levels and callus formation from dahlia

leaf segment culture. J. Am. Soc. Hortic. Sci. 104: 849-852.

George, E. E. 1993. Plant Propagation by Tissue Culture. Part 1. The Technology, Ed. 2.

Exegetics Ltd., Edington, p 295-302.

Hayashi, M., Kozai, T., Tateno, M., Fujiwara, K., Kitaya, Y. 1993. Effects of the lighting cycle on the growth and morphology of potato plantlets in vitro under photomixotrophic culture conditions. Environ. Control in Biol. 31: 169-175.

Hayashi, M., Kozai, T., Ochiai, M. 1994. Effect of the sidewards lighting on the growth and morpholo-gy of potato plantlets in vitro. J of Society of High Technology in Agriculture, 5/6: 1-7.

Hdider, C., Desjardins, Y. 1994. Effects of sucrose on Pn and phosphoenolpyrovate carboxylase activity of in vitro culture strawberry plantlets. Plant Cell Tissue Organ Cult. 36: 27-33.

Heo, J. W., Kubota, C., Kozai, T. 1996. Effects of CO2 concentration, PPF and sucrose concentra-

tion on Cymbidium plantlet growth in vitro. Acta Hortic. 440: 560-565.

Hoagland, D. R. and Arnon, D. I. 1950. The water culture method for growing plants without

soil. Circ. 347. Berkeley. Calif. Agric. Exp. Station, Univ. of Calif., USA., pp 20.

Jeong, B. R., Fujiwara, K., Kozai, T. 1993. Carbon dioxide enrichment in autotrophic micro-

propagation: Methods and advantages. Hortic. Technol. 3: 332-334.Jeong, B. R., Fujiwara, K., Kozai, T. 1995. Environmental control and photoautotrophic

micropropagation. In•gHorticultural Review•h(ed. by Janick, J.), Vol. 17. John Wiley and Sons,

Inc., New York, p 125-172.

Jeong, B. R., Kozai, T., Watanabe, K. 1996. Stem elongation and growth of Mentha rotundifolia in vitro as influenced by photoperiod, photosynthetic photon flux and difference between day

and night temperatures. Acta Hortic. 440: 539-544.Kinoshita, T., Kozai, T., Fujiwara, K. 1988. Time course of osmotic potential of the MS liquid

medium at the multiplication stage in strawberry shoots. In Abstr. Japan Soc. Hort. Sci. Spring Meeting. Tokyo, p 234-235. (JE)

Kirdmanee, C. 1995. Environmental control and its effect in Eucalyptus micropropagation under

photoautotrophic conditions. Ph.D. Thesis. Chiba University, Matsudo, pp 173.Kirdmanee, C., Kitaya, Y., Kozai, T. 1995a. Effects of CO2 enrichment and supporting material

in vitro on photoautotrophic growth of Eucalyptus plantlets in vitro and ex vitro: Anatomical

comparisons. Acta Hortic. 393: 111-118.

Kirdmanee, C., Kitaya, Y., Kozai, T. 1995b. Effects of CO2 enrichment and supporting material

in vitro on photoautotrophic growth of Eucalyptus plantlets in vitro and ex vitro. In Vitro Cell . Dev. Biol.-Plant 31: 144-149.

Kirdmanee, C., Kitaya, Y., Kozai, T. 1995c. Rapid acclimatization of Eucalyptus plantlets by

controlling photosynthetic photon flux density and relative humidity . Environ. Control in Biol 33: 123-132.

Kitaya, Y., Fukuda, O., Kozai, T., Kirdmanee, C. 1995. Effects of light intensity and lighting

72(14) Environ. Control in Biol.

direction on the photoautotrophic growth and morphology of potato plantlets in vitro. Sci.

Hortic. 62: 15-24.

Kobayashi, S., Amaki, W., Higuchi, H. 1995. Effects of medium pH on shoot growth and

flowering of Torenia internodal stem segments in vitro. Acta Hortic. 393: 135-142.

Kozai, T., Fujiwara, K., Watanabe, I. 1986. Fundamental studies of environments in plant tissue culture vessels. (2) Effects of stoppers and vessels on gas exchange rates between inside and outside of vessels closed with stoppers. J. Agric. Meteorol. 42: 119-127. (JE)

Kozai, T., Iwanami, Y., Fujiwara, K. 1987a. Environment control for mass propagation of tissue cultured plantlets. (1) Effects of CO2 enrichment on the plantlet growth during the multiplica-tion stage. Plant Tissue Cult. Lett. 4: 22-26. (JE)

Kozai, T., Oki, H., Fujiwara, K. 1987b. Effects of CO2 enrichment and sucrose concentration under high photosynthetic photon fluxes on growth of tissue-cultured Cymbidium plantlets during the preparation stage. Symp. Florizel on Plant Micropropagation in Hort. Ind., Arlon, Belgium, p 135-141.

Kozai, T., Iwanami, Y. 1988. Effects of CO2 enrichment and sucrose concentration under high

photon flux on plantlet growth of carnation (Dianthus caryophyllus L.) in tissue culture during the preparation stage. J. Jpn. Soc. Hortic. Sci. 57: 279-288. (JE)

Kozai, T., Sekimoto, K. 1988. Effects of the number of air exchanges per hour of the closed vessel and the photosynthetic photon flux on the carbon dioxide concentration inside the vessel and the growth of strawberry plantlets in vitro. Environ. Control in Biol. 26: 21-29. (JE)

Kozai, T., Kubota, C., Watanabe, I. 1988. Effects of basal medium composition on the growth of

carnation plantlets in auto-and mixotrophic tissue culture. Acta Hortic. 230: 159-166.

Kozai, T., Nishiuchi, N., Fujiwara, K., Watanabe, I. 1989. Effects of planting density in the vessel on the growth and net photosynthetic rates of potato plantlets in photoautotrophic micro-

propagation. J. Jpn. Soc. Hortic. Sci. 58 (Suppl. 1): 244-245. (JE)Kozai, T., Oki, H., Fujiwara, K. 1990. Photosynthetic characteristics of Cymbidium plantlet in

vitro. Plant Cell Tissue Organ Cult. 22: 205-211.Kozai, T. 1991 a. Autotrophic micropropagation. In•gBiotechnology in Agriculture and Forestry

17: High-Tech and Micropropagation I•h(ed. by Bajaj, Y. P. S.). Springer-Verlag, New York,

NY, p 313-343.

Kozai, T. 1991b. Controlled environments in conventional and automated micropropagation. In

•g Cell Culture Somatic Cell Genetics of Plants•h(ed. by Vasil, I.), Vol. 8. Academic Press, New

York, NY, p 213-230.

Kozai, T. 1991c. Micropropagation under photoautotrophic conditions. In•gMicropropagation:

Technology and Application•h(ed. by Debergh, P. C., Zimmerman, R. H.). Kluwer Academic

Publishers, Dordrecht, The Netherlands, p 447-469.

Kozai, T. 1991d. Photoautotrophic micropropagation. In vitro Cell. Dev. Biol. 27P: 47-51.

Kozai, T., Iwabuchi, K., Watanabe, K., Watanabe, I. 1991. Photoautotrophic and photomixotro-

phic growth of strawberry plantlets in vitro and changes in nutrient composition of the medium. Plant Cell Tissue Organ Cult. 25: 107-115.

Kozai, T., Fujiwara, K., Hayashi, M., Aitken-Christie, J. 1992a. The in vitro environment and its

control in micropropagation. In•gTransplant Production Systems•h(ed. by Kurata, K., Kozai,

T.). Kluwer Academic Publishers, Dordrecht, The Netherlands, p 247-282.

Kozai, T., Kino, S., Jeong, B. R., Hayashi, M., Kinowaki, M., Ochiai, M., Mori, K. 1992b. A

sideward lighting system using diffusive optical fibers for production of vigorous micro-

propagated plantlets. Acta Hortic. 319: 237-242.Kozai, T., Kushihashi, S., Kubota, C., Fujiwara., K. 1992c. Effect of the difference between

photoperiod and dark period temperatures, and photosynthetic photon flux density on the shoot length and growth of potato plantlets in vitro. J. Jpn. Soc. Hortic. Sci. 61: 93-98. (JE)

Kozai, T., Kitaya, Y. 1993. Microwave lamps and their application as artificial light source for

plant growth. Nogyo Oyobi Engei 68: 988-996 (JE).Kozai, T., Tanaka, K., Jeong, B. R., Fujiwara, K. 1993. Effect of relative humidity in the culture

vessel on the growth and shoot elongation of potato (Solanum tuberosum L.) plantlets in vitro. J. Jpn. Soc. Hortic. Sci. 62 (2): 413-417.

Kozai, T., Smith, M. A. L. 1995. Environmental control in plant tissue culture. General introduc-

Vol.36, No.2 (1998) (15)73

tion and overview. In•gAutomation and Environmental Control in Plant Tissue Culture•h(ed.

by Aitken-Christie, J., Kozai, T., Smith, M. A. L.). Kluwer Academic Publishers, Dordrecht,

The Netherlands, p 301-318.

Kozai, T., Jeong, B. R., Kubota, C., Murai, Y. 1995a. Effects of volume and initial strength of medium on the growth, photosynthesis and ion uptake of potato (Solanum tuberosum L.)

plantlet in vitro. J. Jpn. Soc. Hortic. Sci. 64: 63-71.Kozai, T., Kitaya, Y., Fujiwara, K., Kino, S., Kinowaki, M. 1995b. Use of diffusive optical fibers

for plant lighting. Proc. International Lighting in Controlled Environments Workshop, Madison, p 325-333.

Kozai, T., Kitaya, Y., Kubota, C., Kobayashi, R., Watanabe, S. 1996a. Optimization of

photoautotrophic micropropagation conditions for sweetpotato (Ipomoea batatas (L.) Lam) plantlets. In Book of Abstracts. Int. Symp. on Plant Production in Closed Ecosystems-Automation, Culture and Environment. Aug., Narita, Japan, pp 133.

Kozai, T., Kubota, C., Sakami, K., Fujiwara, K., Kitaya, Y. 1996b. Growth suppression and

quality preservation of eggplant plug seedlings by low temperature storage under dim light. Environ. Control in Biol. 34: 117-121. (JE)

Kubota, C., Kozai, T. 1992. Growth and net photosynthetic rate of Solanum tuberosum L. in

vitro under forced and natural ventilation. HortScience 27: 1312-1314 .Kurata, K., Fukuda, E. 1995. Effect of dissolved oxygen concentration on carrot somatic embryo

production. Acta Hortic. 393: 91-96.Liu, Z. R., Sandford, J. C. 1988. Plant regeneration by organogenesis from strawberry leaf and

runner tissue. HortScience 23: 1057-1059.

Marcelis-van Acker, C. A. M., Leutscher, K. J. 1993. Effect of cutting on heterogeneity and growth of Rosa hybrida cv. Motrea and Schefflera arboricola cv. Compacta. Sci. Hortic. 54: 59-67.

Miyashita, Y., Kitaya, Y., Kozai, T., Kimura, T. 1995. Effects of red and far-red light on the

growth and morphology of potato plantlets in vitro: Using light emitting diode (LEDs) as a light source for micropropagation. Acta Hortic. 393: 189-194.

Miyashita, Y., Kitaya, Y., Kubota, C., Kozai, T. 1996. Photoautotrophic growth of potato

plantlets as affected by explant leaf area, fresh weight and stem length. Sci. Hortic. 65: 199-202.Murashige, T., Skoog, F. 1962. A revised medium for rapid growth and bioassays with tobacco

tissue cultures. Physiol. Plant. 15: 473-497.

Nagae, S., Takamura, T., Goi, M., Tanaka, M. 1995. Micropropagation of gerbera in the•gCul-

ture Pack•h-Rockwool system with sugar-free medium under non-sterile condition . Acta

Hortic. 393: 157-164.

Nakayama, M., Kozai, T., Watanabe, K. 1991. Effect of the presence/absence of sugar in the medium and natural/forced ventilation on the net photosynthetic rates of potato explants in vitro. Plant Tissue Cult. Lett. 8: 105-109. (JE)

Niu, G., Kozai, T., Kitaya, Y. 1996a. Simulation of the time courses of CO2 concentration in the

culture vessel and net photosynthetic rate of Cymbidium plantlets. Trans. ASAE 39: 1567-

1573.

Niu, G., Kozai, T., Mikami, H. 1996b. Simulation of the effects of vessel ventilation rate and light

intensity on the growth of potato plantlets cultured photoautotrophically in vitro. Acta Hortic.

440: 622-627.

Niu, G., Kozai, T. 1997. Simulation of the growth of potato plantlets cultured photoautotro-

phically in vitro. Trans. ASAE 40: 255-260.Pierik, R. L. M. 1987. In Vitro Culture of Higher Plants. Martinus Nijhoff Publishers, Dordrecht,

pp 344.Pierik, R. L. M. 1988. In vitro culture of higher plants as a tool in the propagation of horticul-

tural crops. Acta Hortic. 226: 25-40.

Read, P. E., Economou, A. 1982. Supplemental lighting in the propagation of deciduous azaleas . Proc. Int. Plant Prop. Soc. 32: 639-645.

Read, P. E. 1992. Environmental and hormonal effects in micropropagation . In•gTransplant

Production Systems•h(ed. by Kurata, K., Kozai, T.). Kluwer Academic Publishers, Dordrecht,

The Netherlands, p 231-246.

Seko, Y., Kozai, T. 1996. Effect of CO2 enrichment and sugar-free medium on survival and

74(16) Environ. Control in Biol.

growth of turfgrass regenerants grown in vitro. Acta Hortic. 440: 600-605.Shimada, N., Tanaka, F., Kozai, T. 1988. Effects of low O2 concentration on net photosynthesis

of C3 plantlets in vitro. Acta Hortic. 230: 171-175.

Smith, M. A. L., Spomer, L. A. 1995. Vessels, gels, liquid media and support systems . In

•g Automation and Environmental Control in Plant Tissue Culture•h(ed. by Aitken-Christie, J.,

Kozai, T., Smith, M. A. L.). Kluwer Academic Publishers, Dordrecht, The Netherlands, p

371-404.

Stamp, J. A., Colby, S. M., Meredith, C. P. 1990. Direct shoot organogenesis from leaves of grape

(Vitis spp.). Plant Cell Tissue Organ Cult. 22: 127-133.Takazawa, A., Kozai, T. 1992. Effect of types of culture vessels with supporting materials on the

growth of carnation plantlets in vitro. Environ. Control in Biol. 30: 65-70. (JE)Tanaka, K., Watanabe, Y., Shimada, N. 1991. Effect of O2 concentrations on growth of

Chrysanthenum morifolium plantlets in vitro cultured photoautotrophically and mixotrophical-ly. Environ. Control in Biol. 29: 107-116. (JE)

Tanaka, K., Fujiwara, K., Kozai, T. 1992. Effects of relative humidity in the culture vessel on the transpiration and net photosynthetic rates of potato plantlets in vitro. Acta Hortic . 319: 59-64.

Veierskov, B. 1978. A relationship between length of basis and adventitious root formation in pea

cuttings. Physiol. Plant. 42: 146-150.

Williams, R. R., Taji, A. M., Winney, K . 1990. The effect of Ptilotus plant tissue on pH of in vitro media. Plant Cell Tissue Organ Cult. 22: 153-158.

Williams, R. R. 1991. Factors determining mineral uptake in vitro. Acta Hortic . 289: 165-166.Williams, R. R. 1992. Towards a model of mineral nutrition in vitro . In•gTransplant Production

System•h(ed. by Kurata, K., Kozai, T.). Kluwer Academic Publishers, Dordrecht, The

Netherlands, p 213-229.

Williams, R. R. 1995. The chemical microenvironment . In•gAutomation and Environmental

Control in Plant Tissue Culture•h(ed. by Aitken-Christie, J., Kozai, T., Smith, M. A. L.).

Kluwer Academic Publishers, Dordrecht, The Netherlands, p 405-439.

Yang, C. S., Kozai, T., Fujiwara, K. 1995a. Effects of initial inorganic ion composition and initial total inorganic ion concentration of culture medium on the net photosynthetic rate and

growth of strawberry plantlets in vitro under photoautotrophic conditions. Environ. Control in Biol. 33: 71-77. (JE)

Yang, C. S., Kozai, T., Jeong, B. R. 1995b. Ionic composition and strength of culture medium

affect photoautotrophic growth, transpiration and net photosynthetic rates of strawberry

plantlets in vitro. Acta Hortic. 393: 219-226Yoshihara, T., Hanyu, H. 1992. pH changes in culture medium with progress of growing stages ,

callus, multiple shoots and intact plants of strawberry. Acta Hortic. 319: 291-294 .*JE: written in Japanese with English summary and capti

ons

<和文抄録>

マイクロプロパ ゲーシ ョンにおける小植物体の生長 におよぼ す環境要 因の影響

クイン ティ グエン・古 在 豊 樹*

熱帯生物研究所植物細胞工学研究室 ・*千葉大学園芸学部環境調節工学研究室

マイクロプロパゲーションにおける培養小植物体の生長におよぼす環境要因の影響に関する過

去約10年 間の研究を,環 境生物学および環境工学の研究者を対象に,総説的に解説した.最 初に,光,二 酸化炭素,温 度,相 対湿度,酸 素およびエチレンなどの気圏環境要因が培養小植物体の生長

および光合成におよぼす影響を考察した.つ いで,培 地糖濃度,各 種無機イオン濃度,浸 透ポテン

シャル,pHな どの培地環境要因が培養小植物体の生長におよぼす影響を議論した.最 後に,培 養小植物体の大きさおよび植え付け密度などの生物学的要因が培養小植物体の生長におよぼす影響

を議論した.

Vol.36, No.2 (1998) (17)75