Usually AABS has been fortunate to have at least one nationally or internationally acclaimed bonsai artist present a program to AABS each year. Scheduling these headliners has become increasingly difficult over the past few years since the artists' schedules are booked longer in advance than they used to be. Colin Lewis and Kathy Shaner, for example, are booked into 2006 and beyond.
David Kreutz of the St. Louis Bonsai Society, working with the program chairs of several Midwestern bonsai societies, has arranged for Marco Invernizzi from Milan , Italy to travel to the Midwest in April of this year. Marco has been scheduled to present programs in St. Louis, Cincinnati, Indianapolis, Kansas City, Ann Arbor, and Grand Rapids. Coordinating this many appearances is never possible without some clubs scheduling a visiting artist's program at a time outside their regular meeting schedule. We jumped at the chance to schedule Marco for Ann Arbor even though we had to scramble to find a place to have an extra meeting.
We were able to schedule Marco in Ann Arbor on Wednesday, April 13 and Thursday April 14th. The auditorium at Matthaei Botanical Gardens is not available on either evening so, on Wednesday, April 13 th , we have rented a section of the ballroom at the Holiday Inn that is at the intersection of US 23 and Plymouth Road . This is not our regularly scheduled time. Put this date on your calendars! This will be your best opportunity this year to participate in a program by this world renowned bonsai artist at our club .
On Thursday evening, April 14th room 139 at Matthaei Botanical Gardens has been reserved for a workshop with Marco.
Events with Marco during the day on Wednesday and Thursday will be announced as they are organized.
Marco Invernizzi is from Milan, Italy where he lived until age 21. He studied art and has a degree in design. His interest in bonsai began age 16 and he studied 5 years with Salvatore Liporace, and then went to Japan to study with Masahiko Kimura for almost 4 years.
More than 10 bonsai magazines have published Marco's articles; he is a full time bonsai professional and broker, and works for many nurseries, clubs and bonsai associations all over the world. Some of his best trees have won UBI awards and Ginkgo awards. In 2003, he published a book about his experience in Japan that will be soon translated into English.
return
to top
This discussion will emphasize proper light and touch on other environmental and horticultural principles as well. Four major plant functions are important determinants of plant growth and development:
Photosynthesis: Produces food using solar energy. Uses carbon dioxide and water as raw materials. Occurs only in cells containing chloroplasts. Releases oxygen. Occurs only in light.
Respiration: Oxidizes food, releasing energy within the plant. Occurs in all living cells. Uses Oxygen . Produces water and carbon dioxide. Occurs in the dark and in the light.
The term respiration as used here should not be confused with what we usually refer to as respiration with animals when we talk about breathing. We inhale oxygen that is transported to cells where the process of oxidation occurs. We exhale carbon dioxide, which is a by-product of oxidation.
Roots live in the dark, and they need to absorb and use oxygen . Oxygen transfuses through air 10,000 times faster than it does through water. A soil mix contains soil particles, water, and air. Too much water means too little air. Insufficient air in the soil retards plant growth. The only common agreement about bonsai soil is that it must be well drained (well aerated). Animals and plants will drown if sufficient oxygen is not available because of excess water.
Assimilation: Builds more complex compounds. Assimilation is costly in terms of energy consumption, so, if you see a bud or a branch starting to grow where you don't need or want it to grow, cut it off as soon as you notice it before it consumes more of the trees stored energy. This technique is referred to as energy management by some authors.
Transpiration: The process by which a plant loses water, primarily through pores (stomata) in the foliage. 90% of the water that enters the plant escapes in transpiration. The other 10% is used in chemical reactions and in plant tissues.
Since the primary topic of this discussion is light, our emphasis is on photosynthesis.
A leaf or a needle is, among other things, a solar panel. The active component in this solar panel is chlorophyll. Energy released from chlorophyll that is “excited” by sunlight is captured in the production of carbohydrate, and oxygen is released. This carbohydrate is analogous to a pile of wood that can burned (respiration) or used for construction (assimilation).
On earth almost all energy ultimately comes from or came from sunlight. Almost all life depends on photosynthesis that converts solar energy into food. Without chlorophyll we would all die. The plants don't need us. We need the plants, because we can't convert solar energy into food. We do respiration (oxidation), and assimilation but not photosynthesis.
Fossil fuel was once vegetation. It has been changed into its present form by millions of years of geologic process, and the carbon dioxide that was converted to carbohydrate millions of years ago by photosynthesis is now being released as we burn (oxidize) the fuel.
Roy G. Biv is a handy mnemonic to help remember the color of the visible spectrum or electromagnetic radiation.
(Infra red) Red Orange Yellow Green Blue Indigo Violet (ultra Violet)
Warm Low Energy -->Cool, High Energy
Longer Wave Length -->Shorter Wave Length|
650 nanometers (Red) --> 455 nanometers (Violet)
Light striking a particle or surface is either reflected or absorbed. Chlorophyll absorbs light from both ends of the visible spectrum but not from the middle (green). It reflects the green part of the spectrum. Seeing a green what the non-colorblind human brain perceives is reflected green light waves. It takes chlorophyll, a specific wavelength of light, and a visual center in the brain to “realize” green. So where does the “green” exist?
Chlorophyll cannot use green light. Plants do not need to be exposed to the warm side of the spectrum for vegetative growth (roots, shoots, and leaves). The warm side of the spectrum may be necessary for maximum fruiting and flowering, which is rarely a concern for the bonsai grower. Some fruit may be desirable, but too many flowers or too much fruit will weaken a miniaturized tree confined to a bonsai container. Thus, it is possible to grow very healthy green plants that will produce some flowers and fruit with just the cool end of the spectrum (cool white fluorescent light).
The basic unit of electric power is the watt
A kilowatt represents 1000 watts
A kilowatt-hour represents 1 kilowatt used for one hour. This is the standard unit for calculating electric power cost. DTE currently charges about $0.10 per kilowatt- hour.
Light intensity generated at its source is measured in lumens.
Light falling on a surface is measured in foot-candles.
How efficiently a light source (bulb) converts electric power to light be expressed as lumens per watt. The more lumens produced per watt the more efficiently a bulb coverts electric power to light.
100-watt tungsten standard 17.5
Tungsten halogen 22
40 watt fluorescent 22.3
1000 watt metal halide 100
1000 watt high pressure (HP) sodium 140
Lumens per watt information is usually clearly printed on the package of most commercially available light bulbs. Notice that the standard tungsten (incandescent) bulb is the most inefficient source of artificial light available.
The lumens emitted at a light source will be distributed over a progressively larger surface as the light source is moved further from the surface. The amount of light illuminating the entire surface will not change, but the intensity of light at a given area such as a square in will diminish. It will diminish in proportion to the square of the distance from the light source to the lighted surface. So if surface B is twice as far from the light source as surface A the illumination per unit of area of surface B (measured in foot candles) will be 1/4 th of the illumination of surface A…not 1/2. This phenomenon is often referred to as the inverse square rule.
An artificial lighting system places the light source within 1 inch to several feet from the top of the tree; so the foliage on the lower branches receives (reflects and absorbs) much less light than the foliage at the top of the tree. The further the light source is from the top of the tree the lower the impact of the inverse square rule, but the whole tree is exposed less overall light.
The sun is millions of miles away so the impact of the inverse square rule is infinitesimal. Metal halide lights are usually placed at least one foot above the top of the plant so the inverse square rule effect applies. Cool white fluorescent tubes are placed one or two inches from the top of the plants so the effect of the inverse square rule is considerable. Thus the height limit for small plants, including the pot, under cool white fluorescent lights is 8 inches assuming that only top lighting is used.
Jack Wikle positions fluorescent tubes about 9 inches above his bench surface and about 1 inch from the top of his tree. It follows that the tree-pot height limit with Jack's system is about 8 inches. Since cool white fluorescent lights emit mainly the blue end of the visible spectrum, the top of a plant will not burn if placed very close to the bulb.
Metal halide lights emit a full spectrum of light. The red end of the visible spectrum is warm, and the light emitted at a metal halide source creates so much heat that the plants must be placed at least 6 inches and usually a foot or more from the bulb. In fact, so much heat is generated that a ventilation system may be necessary depending on the total wattage of the metal halide lights and the size of the room.
Light, oxygen, water, temperature level, soil aeration, and nutrients need to be present within optimum ranges for maximum health to be realized. Why waste electricity on a waterlogged, under fertilized plant? Fortunately all living things are adaptable so a range rather than an exact number is sufficient.
The indoor gardener has some advantages over the outdoor gardener. If she is willing to incur the necessary expense, she can achieve a much higher level of control of critical factors such as heat, light, moisture, carbon dioxide level, air movement, and pest exposure (including human thieves) than the outdoor grower can hope to achieve.
However, the most effective HID lights produce only half the light intensity of the sun on a cloudless day, so the indoor grower must deal with limited light intensity. During S. E. Michigan winters days are short and usually cloudy, so the indoor gardener may achieve more light intensity with artificial lights than is available in a greenhouse.
The brightest source of indoor light is High Intensity Discharge (HID) lighting, either high pressure (HP) sodium or metal halide light bulbs. Metal halide lighting most closely simulates sunlight. HP sodium lighting has an unpleasant yellow color and is best for supplementing sunlight in a greenhouse.
How much light is enough? The total light to which a plant is exposed is a function of light intensity times light duration. There are several ways to measure light. Let us use foot-candles. The question then becomes how many foot-candles for how many hours?
The most efficient use of supplemental artificial light is to turn it on when the sun goes down and thereby increases the duration of light (Photoperiod) and to stop using the supplemental light when the sunlight reaches the intensity of the HID light.
Sunlight is free, and artificial light is expensive. How expensive is it? In 2004, electric power cost about $0.10 per kilowatt-hour. When it went from 9 cents to 10 cents per kilowatt-hour a spokesman from DTE claimed that the increase was only a penny per kilowatt-hour. He neglected to mention that a penny was a 10% increase!
OK, I'm excited! I want to get into indoor bonsai growing. How much is it going to cost me?
|
|
|
|
|
|
|
80 |
0.08 |
16 |
$0.01 |
$0.13 |
$3.84 |
400 |
0.4 |
16 |
$0.04 |
$0.64 |
$19.20 |
1000 |
1 |
16 |
$0.10 |
$1.60 |
$48.00 |
Two 40-watt fluorescent bulbs 9 inches above bench surface will effectively illuminate an area of 4 ft. by 1.75 feet or 7 square feet. So it costs $3.84 to light 7 square feet for one month or $0.55/sq.ft. /month.
A 1000-watt metal halide light will effectively light 100 square feet, which would cost $48/100 square feet or $0.48/square foot.
The above cost estimates will vary with hours of operation, the use of a light-moving device, and the optimum use of reflection. Remember, light intensity diminishes according to the inverse square rule. If its reflected back to the foliage significant increases in efficiency can be achieved.
Reflective Mylar 90-95
Flat White Paint 85-93
Semi-gloss 75-80
Flat yellow 70-80
Aluminum foil 70-75
Black (absorbs 90% of light) Less than 10
A 4 by 25 foot sheet of 1 mil Mylar costs about $25. A small amount of flat white paint is nearly as effective. The gloss on semi-gloss paint absorbs some light. A surface painted with flat white paint is rougher than a glossy surface, so there is more surface area to reflect the light.
Plants can adapt to different intensities of light within certain limits. The limits are different for each species. Many bonsai enthusiasts will put their trees in the shade for several days before a show. The trees adapt by producing more chlorophyll to compensate for the lower, so the amount of photosynthesis occurring will tend to stabilize. When the trees arrive at the show they look healthier because they are greener.
Some times when these trees go back into full sunlight without a gradual period of adjustment the leaves will “burn” do to the intense photochemical reaction of the direct sun with the elevated levels of chlorophyll.
The bonsai enthusiast is well advised to select plants that are well adapted to his indoor environment. He can manipulate the environment to suit his plants, or he can select plants to suit his environment. Little progress will be made struggling to keep unhealthy, mal-adapted plants alive in an unsuitable environment.
There are many lighting systems available that are not discussed in this article such a small metal halide systems and high intensity fluorescent systems. Once the reader understands the basic principles of indoor lighting he can design his own system and calculate the light intensity, set up costs, and operating costs of his system.
The successful system with appropriate plant materials will reward your efforts. If your plants are not healthy, change your system or try different plants.
Printed References
Meislik, Jerry FICUS The Exotic Bonsai: All you need to know about ficus is compiled in one source. Also discusses indoor growing and lighting.
Van Patten, George F., New Revised Gardening Indoors Easy, complete “how to” guide on high-tech indoor gardening.
Online Resources
www.bonsaihunk.8m.com Jerry Meislik's web site contains Jack Wikle's latest revision of his article explaining his technique for growing bonsai under cool white fluorescent light
www.bonsaiandsuiseki.com/unusual.htm
www.bonsai-bsf.com
www.fukubonsai.com
www.jimsmithbonsai.com
Wednesday,
January 26th
Lighting and other environmental factors for indoor bonsai
Pine styling and management: Doug Hawley
Wednesday,
Marc
Japanese Garden and General Design Principles: David Michener
Wednesday,
April 13th
Marco Invernizzi
Thursday,
April 14th
Marco Invernizzi
Wednesday,
April 27th
Bring your own tree
TBD
June 22nd
TBD
27th
TBD
A
TBD
A, A
Annual Show Yew styling and maintainence:
Bruce Baker
Auction
Club Members Family and Guest Potluck Dinner
December - No Membership Meeting
MERRY
CHRISTMAS!!
Call
Bill Heston at (734) 662-8699 if you have any questions
regarding programs.
return
to top
2005
AABS EXECUTIVE BOARD
President: Bill Heston (734) 662-8699
VicePresident: Hugh Danville (313) 455-7922
Program Chair: Bill Heston (734) 662-8699
Corresponding Secretary:
Recording Secretary:
Publicity Chair: Bill Cavers (734) 9964508
Treasurer: Joan Wheeler (734) 485-6306
Librarians: Robert Bishop,
Margaret Parker, Madelon Takken
Past President: Roger Gaede (517)-592-2249
Director for 2005: Arnold Wingblad (313) 255-1769
Director 2004: Cyril Grum (734) 995-9828
Show Chair: Hugh Danville (313) 4557922
Pete
Douglas (313) 8678644
AABS
AD HOC COMMITTEES
The AABS President, Bill Heston, is ex-officio member of all
committees except the Nomination Committee.
Auction Chair: TBD
Membership Chair: TBD
Paul
Kulesa
John
Parks
Ways
and Means Chair: John Parks
Web Master: Jarrett Knyal (webmaster@annarborbonsaisociety.org)
return to top |
|
by Jack Wikle
Notice particularly
the bolded terms in this
article, these are all mile markers that can be
useful in timing the work you do on your bonsai
and in keeping meaningful notes on your work.
Certainly, one of the appeals of growing bonsai
for many of us is the heightened sense of awareness
we experience – closeness to nature and its
cycles -- as we enjoy working with our trees. Even
needle-evergreens, seemingly unchanging to the casual
observer, exhibit a fascinating annual pattern in
their transitions through spring bud swelling, vigorous
shoot extension and eventual dormancy. As witnesses
to life’s ongoing rhythms, we are somehow
comforted by nature’s persistence.
Much of what I say here will be mostly familiar
to some readers. Hopefully, others will be helped
in feeling closer to nature and to their bonsai
and in being more alert to the needs of their trees
and the opportunities they offer.
It is, of course, energy from the sun captured by
photosynthesis -- taking place only in green plants
-- that drives almost all of life’s processes.
The notable exceptions to this are some obscure
bacteria that obtain their energy in other ways.
Simple carbohydrates, the product of photosynthesis,
are both fuel (ultimately oxidized to release energy)
and building materials (ultimately transformed into
a host of more complex compounds) that become the
substance of trees.
The transformation of simple carbohydrates into
plant tissue is just one of many unseen plant processes
having great energy “costs.” As a number
of authors have suggested, carbohydrate can be thought
of as “tree money.” When carbohydrate
expenditures -- this includes fueling routine cell
processes, new construction use, production of defensive
chemicals, and damage control when defenses are
breached – consistently exceed income from
photosynthesis, the tree eventually dies, typically
done in by decay organisms taking advantage of its
weakened condition. On the other hand, when carbohydrate
income exceeds expenditure, reserves are stored
– “banked” if you will –
in living tissues throughout the tree. The tree
consistently accumulating more carbohydrate than
it uses is a thriving tree that can tolerate considerable
adversity.
Even in very warm climates, the annual growth of
some trees is intermittent, but where seasonal climate
change prevails, winter dormancy with no growth
taking place is the common pattern. Be aware that
even in “deep dormancy,”
the living cells of trees are still consuming energy
– the cost of keeping the fire of life going
– although at a much reduced level. A tree
does not come out of dormancy with as much energy
reserve as it had going in.
Interestingly, the deep dormancy
tree is genetically programmed to require a certain
number of hours of cold exposure (as little as four
weeks to as much as three months or so depending
on species) before it can begin growth again. Temperatures
that satisfy this chilling requirement are cold
but not too cold. (Levels about 40 degrees F. are
known to be most effective.)
When a tree’s chilling requirement is met
and days lengthen, the tree enters a state of semi-dormancy
as root growth begins again and top growth is possible
with enough exposure (more than just a day or two)
to warm temperatures. The perceptible swelling of
buds which have been unchanging all winter will
be the first indication the tree is ready to push
out new shoot growth when warmed enough for long
enough. This is the “bud swell stage.”
When the largest buds (programmed to produce the
earliest and most vigorous growth) enlarge to the
point that green tips are evident, a strong “push”
of shoot growth is imminent. It is common for needle-evergreens
to also exhibit a discernable foliage-color change,
going from muted, somewhat rusty-green or yellowish
green to a brighter, more intense, green color about
this time in their cycle. At this “green
tip stage,” new root growth is already
well under way.
The exact timing will vary greatly with the kind
of tree and prevailing temperatures, but green-tip-buds
soon expand enough that the much compressed and
tightly folded tissues they contained have space
to unfurl sufficiently that a tiny leaf (or a pair
of leaves on opposite-leaved trees) can be seen
distinctly. This has been described as “first
leaf stage” in the tree cycle. On
some needle-evergreens, the growth erupting from
the green tipped bud will be seen as a tight cluster
of tiny needles. On the new pine shoot – often
referred to as a pine “candle” –
it will be some days before needles are discernable.
Some American authors have used the terms “pineapple
stage” for the apparently needleless candle
and “porcupine stage” for the candle
with small needles clearly visible.
On the deciduous tree, the new shoot is, at first,
just a leaf or a pair of leaves. This is followed
by another leaf or pair of leaves pushed beyond
the first. Then more and more leaves are produced
farther and farther along on the shoot that seems
to be telescoping outward as it lengthens. Typically,
the largest leaves will be toward the end of the
elongating shoot but not those at the tip which
are still very young. This outward “push”
of new shoot growth can be surprisingly rapid –
almost violent – on some kinds of trees with
several leaves appearing in a few hours on a warm
day and several times that many leaves appearing
in a few days when conditions are favorable.
This “soft shoot stage,”
with a number of leaves out and expanding while
more leaves keep appearing as the shoot lengthens
(shoots limp and needles still very short on needle-evergreens),
seems to be universally considered the most vulnerable
stage in the tree’s annual cycle. It is stored
carbohydrate reserves almost entirely that have
been used in this “new construction,”
and the new solar panels (fresh foliage) have yet
to produce enough carbohydrate to repay their “building
cost.”
Not surprisingly, the tree is genetically programmed
to keep something in the bank, to not use all its
resources in new growth, but reserve levels are
drawn down dramatically reaching an yearly low at
this time in the annual cycle. Interestingly, root
growth normally continues during the soft shoot
stage but at a much diminished rate. Peak top growth
and peak root growth are not simultaneous. In fact
it is typical for any treatment which stimulates
growth of one to limit growth of the other.
As weeks pass and new leaves accumulate -- and all
the while leaf blades keep expanding -- activity
of these new solar panels eventually results in
carbohydrate production that exceeds their construction
costs. New investment is paying off! And, the new
shoots begin thickening and stiffening. As this
maturation of shoots and foliage takes place, new
buds (structures with the potential of producing
future new shoot flushes) become increasingly evident,
at least one at the base of each leaf stem. Buds
along the shoot rather than at its tip are usually
referred to as “lateral buds.” Depending
on species, some of these new buds will eventually
be capable of producing shoots with leaves, some
shoots with flowers, and some shoots bearing both
leaves and flowers.
Some “determinate growth” kinds of trees
are genetically programmed to cease shoot elongation
for the year and form a prominent “terminal
bud” at the shoot tip in late spring or early
summer. Other species just keep adding foliage on
actively elongating shoots until growth is halted
by drought or cold late in the year. And, some kinds
produce intermittent shoot growth when lateral buds
formed earlier in the season, in turn, become active
producing shoots that are branches from the primary
shoot. Yes, branches on the branches in one growing
season. The hardened shoot, no longer elongating,
with leaves (or needles) fully expanded, and with
prominent buds now darkened in color rather than
green and tender, is said to be “mature.”
This “mature shoot stage” may
occur as early as late June on some kinds of trees
and well into September on others.
As shoot hardening progresses and more carbohydrate
is produced than is used in new construction, the
excess is increasingly diverted into trunk thickening
(widening the annual growth ring), into root growth,
and into storage which takes place in almost all
living parts of the tree. On the tree mature enough
to flower and produce seeds (encased in fruits or
nuts of any kind) significant amounts of energy
are consumed in this reproductive growth. Flowering
and fruiting activity typically limits other growth
and reduces buildup of stored carbohydrate reserves.
Incidentally, it has even been proven that retained
pine needles are storage sites for unused carbohydrate.
By the time, shoot elongation and leaf expansion
(or needle lengthening) are essentially complete
and new buds are easily discerned, stored reserves
have been building for some time. However, this
storage activity accelerates rapidly after shoot
growth slows and ceases, typically peaking sometime
in mid to late summer.
While genetic variation makes each species different,
this “matured shoot stage”
is thought to be second only to bud swell stage
in the spring as a good time for collecting, repotting,
heavy wiring, and other high stress work on the
tree. At this time, the healthy tree will have accumulated
enough stored reserves to tolerate the work you
want to do with it and still keep going. Work on
the sluggish tree, one that has been weak and struggling,
should be postponed until it shows definite signs
of recovery and increase in vigor.
In response to shortening day lengths and increasing
cold (and perhaps diminishing light intensity) trees
eventually begin to go dormant in preparation for
cold weather. The “first fall color”
on deciduous trees typically appears about the time
older needles on pines, usually needles produced
the previous season (“two year old”)
or the season before (“three year old”),
suddenly lose their green color and become noticeably
yellow then brown before being discarded. Yes, even
an evergreen sheds older foliage annually. Carbohydrates
and much of its nutrient element accumulation are
moved out of foliage to be discarded, before it
is shed, and moved back for storage in the tree’s
branches, trunk and root system.
From “peak fall color” until leaves
have dropped is a time of opportunity with some
trees and a time of caution with others. Even though
roots will continue to be active until the ground
is deeply frozen, carbohydrate production is greatly
diminished in evergreens and at a standstill in
deciduous trees. Making the tree dip into its stored
reserves to deal with avoidable stress at this time
adds greatly to the normal rigor of winter. As Stanley
Chinn, a very astute bonsai grower said to me years
ago, “The weak tree has barely enough money
to buy food and you are giving it a doctor bill
too.”
Be extra careful with non-native trees, especially
kinds of borderline hardiness, at this season. Often
they don’t read unfamiliar day length changes
and cold exposure signals clearly and may not go
dormant quickly enough to escape significant cold
damage. This is especially true if they are pushed
to continue earlier-season activity by ill-advised
late fertilization, pruning, wiring or unseasonally
high temperatures.
Some tree scientists, most notably Dr. Alex Shigo,
have suggested that the second most vulnerable stage
in a tree’s annual cycle is the first
fall color stage when nutrients are being
drained from leaves and returned to storage in the
rest of the tree. Shigo says we do not understand
completely why this is. We do know that root growth
continues through this period until stopped by cold,
and that work on the top of a tree almost always
inhibits root activity.
After leaf fall, dormancy deepens further, again
in reaction to shortening days and cold exposure.
Yes, exposure to cold, if not too extreme, makes
trees (tops and roots) more cold tolerant. When
dormancy becomes deep enough, the tree, in its minimum
maintenance phase, will not grow again until its
chilling requirement has been met. Then the annual
cycle begins again.
Jack Wikle
return
to top
|
Deadline for submissions to the newsletter is the 5th of the month.
return to top
For Sale or Wanted
10% of Sales go to AABS Club.
Member Ads are free.
Your Business Card Printed Here
$20 per year.
Contact:
return to top
|