How
do plants decide when it's time to make
flowers?
Finally
scientist have some answers.
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Cancer, heart disease, smoky
bars, and hotel rooms stale with
the stench of old
ashtrays--there's nothing very
good to be said about tobacco.
But delve into the plant's murky
past and you will find something
precious: the miraculous
Maryland Mammoth, a plant that
amazed turn-of-the-century
farmers because it kept growing
and growing and growing, long
after other types of tobacco had
stopped churning out leaves and
had begun producing pretty,
trumpet-shaped flowers instead. |
Maryland
Mammoth was good for growers. Every
ten-foot-high giant produced twice as
many dryable, sellable, smokable leaves
as the average plant could yield. It was
to prove even better, though, for
scientists who wanted to know how plants
make flowers--more specifically, how
they decide when to make them.
It's important for a plant, this
flowering decision, since popping up
one's delicate budlets in the midst of a
bleak, dark winter could be seriously
detrimental to reproductive success.
It's important for people, too,
since
every grain, fruit, vegetable, and
ornamental plant has its own
prerequisites for flowering, and only by
understanding these prerequisites can
farmers and breeders work with them,
maybe alter them, so that humankind can
grow crops when and where it wants. As
for those of us who garden at
home--well, flowering science lies
behind everything from knowing why
lettuce bolts after a cold snap to why,
if you planted the right flowers in an
ideally situated garden, you could count
off the weeks like a clock simply by
noting what is blooming when.
A cursory survey of the plant kingdom
might discourage one from seeking clear,
generalizable principles governing the
whys and whens of flowering. All over
the world, plants are doing different
things for their own special reasons:
flowering in springtime before their
leaves unfurl so that their blossoms are
showy for pollinating insects or are
exposed to the wind that carries the
pollen; flowering just in time to beat
the frost; flowering when it's wet
enough or dry enough or when other
plants aren't hogging the birds or
insects needed for pollination. Some of
the strategies are extreme. The
Brazilian jaboticaba tree waits for a
drenching monsoon and then blooms like
there's no tomorrow. The North American
pink lady's slipper orchid flowers
during the springtime flight of the
queen bumblebee. Then there's bamboo,
which grows without flowering for years
(120 years in one remarkable species),
and then suddenly whole acres decide
it's time to flower. They then die en
masse, leaving vast swaths of land bare
and brown, and the giant panda wondering
where its next meal is coming from.
Clearly, if there is a grand unifying
theory behind flowering, it can be
summed up in one short phrase: find a
strategy that works.
Despite all this variability, broad
patterns behind flowering do
exist--patterns that scientists can
study in their own favorite,
easy-to-breed-and-grow plant, with
confidence that what they find out will
be relevant to many other species.
Maryland Mammoth, a mutant variety that
appeared unexpectedly in a field of
standard Narrowleaf tobacco back in
1906, was a perfect case in point.
The difference between Maryland Mammoth
and other varieties of tobacco was that
the former flowered so late in the year
that frost often cut it down before seed
had even set. This frustrated farmers,
since it meant that the only way to get
seed was to grow the plant in
greenhouses. But it fascinated Harry
Ardell Allard and Wightman Wells Garner,
two scientists working in 1918 at a U.S.
Department of Agriculture research farm
in Arlington, Virginia (right where the
Pentagon sits today). The duo set out to
tackle the mystery.
They learned that while most commercial
varieties of tobacco grow until they
reach a certain size and age, Maryland
Mammoth stops growing only if the days
shorten to a certain critical length.
Picture Garner and Allard hefting pots
of Maryland Mammoth into light-tight
little houses every afternoon at four,
then hefting them back outdoors again at
nine the following morning, to
artificially give the plants long nights
of seventeen hours and short days of
just seven hours. The result was
flowers. And seeds. In July. Meanwhile,
out in the field, Maryland Mammoth was
basking in fourteen-hour summer days and
was a long way from flowering. Garner
and Allard concluded that the plants
were measuring day length and that
sensing either light or dark was the way
they were doing it.
With this knowledge, it was now easy
enough to get Maryland Mammoth seed by
growing the plant in winter in southern
Florida, where the weather was mild and
the days short. More important, it soon
became clear that many, many plants,
both wild and commercially bred, exhibit
a similar photoperiod response--that is,
they have daylength requirements for
flowering, although the length varies
with latitude and lifestyle. Take plants
like chrysanthemums or asters or summer
wheat. All flower when the days start
getting shorter, giving them time to
enjoy the long sunny summer but still
get their blooms out before the frost.
Or think of the lilies that bloom in
time for Easter, when the days are
getting longer and winter has finally
passed.
Decades of research are beginning to
reveal how plants perform this trick. To
sense the light, plants use molecules
called photoreceptors. Some, known as
phytochromes, were discovered four
decades ago; they are most sensitive to
wavelengths in the red portion of the
electromagnetic spectrum. Other, very
recently discovered photoreceptors
called cryptochromes sense blue light.
Yet other molecules, which sense
ultraviolet light, are still lurking out
there, waiting to be found.
Having sensed the light, plants need to
be able to "count" and to leap into
flower-making action when day (or night)
length is just right. Here's where the
science of circadian rhythms enters the
picture. Circadian rhythms are regular
rhythms of growth and activity,
occurring roughly every twenty-four
hours. They control everything from when
animals sleep, wake, and are most alert,
to when an insect emerges from its pupal
case or a flower produces nectar.
All these organisms have biochemical
clocks that enable them to perform a
host of activities and cellular
processes in a neat, timely fashion.
With its clock, a plant can crank up
production of its light-harvesting
enzymes before dawn and make the most of
every iota of daylight. It can time the
opening and shutting
of the pores in its
leaves so that gases enter when they're
needed and precious water is retained
when they're not. Some plants shut their
flowers at night to protect them from
the cold and the pollen-damaging dew and
open them up in the day so that insects
and birds can visit and pollinate them.
Others open theirs at night to greet
bats and moths. So precise is this
flower-opening stunt that a gardener
could conceivably tell not only what
week it is by when different species
bloom but also what hour it is by noting
when certain blooms open up.
Researchers have pinpointed many of the
genes involved in circadian rhythms and
have come up with an elegant model for
just how proteins tick and tock and thus
orchestrate an organism's daily
functions. Circadian clocks, which have
proved remarkably similar in nearly all
the organisms studied (the one exception
so far appears to be blue-green algae),
are complicated and not yet fully
understood. In fruit flies, the focus of
most of the research, the story goes
something like this: Two proteins,
called period and timeless, build up
slowly in a cell. When these become
plentiful enough, they prevent the
production of two other proteins--clock
and cycle--without which, however, they
themselves can no longer be made. So now
period and timeless disappear from the
cell. This allows clock and cycle to be
produced again, which eventually brings
period and timeless back into the
picture. And on and on, in an
approximately twenty-four-hour rhythm.
A circadian clock is essential for
responding to daylight: destroy it and
you're left with a befuddled plant that
doesn't know when to flower. But even
with a clock in good working order, a
"Time to Flower!" signal must travel up
from the leaves to the apex of the
plant, which will continue churning out
leaf after leaf until it gets
instructions to do otherwise. Scientists
know the signal must come from the
leaves, because if you provide plant A
with the appropriate flower-triggering
day length, then cut off a leaf and
graft it onto plant B--which has never
experienced that day length--plant B
will dutifully flower. Something in the
foreign, transplanted leaf travels up
the plant and trips some developmental
switch.
The identity of that something is still
a mystery, sixty years after it was
given the name florigen. Which isn't to
say that scientists haven't sleuthed
away like crazy trying to find out.
Yeast extract, acids, vitamins--you name
it--they've all been spritzed onto
plants at one time or another in the
hope that a blossom would ensue.
Frustratingly, no clear and simple
picture has emerged from all these
efforts. But some scientists today are
leaning toward an idea known as the
theory of multifactorial control. This
means that a medley of
substances--perhaps sundry plant
hormones such as gibberellins and
cytokinins, along with a burst of
sucrose and calcium ions--travel up to
the bud, triggering flowering only when
all the substances are present and
accounted for in just the right ratios.
The complexity of flower induction is
also reflected in the number of genes
involved in the process. In Arabidopsis
thaliana (most of the genetic work on
flowering has been done on this little
mustard weed), there are now in excess
of forty known flowering-time genes.
When inactivated, some of these genes,
such as those named hasty and speedy,
result in mutants that flower too soon;
others, such as gigantea, sca, and
constans, produce mutants that flower
too late. Many of these genes are
involved in controlling the plant's
response to day length. But many others
aren't. When it comes to flowering,
photoperiodism is by no means the only
game in town.
Most plants, for instance, go through a
juvenile phase, just as humans do.
Reproduction during that phase is
strictly verboten, and genes like hasty
appear to be part of the brake. And many
plants, such as sunflowers and most
tobacco varieties, pay no attention to
the length of day or night; they grow
until they reach a certain size, and
then kaboom! they bloom. The timing of
that decision depends on the balance of
a whole slew of genes, some of them
pushing the plant toward reproduction,
others cold-showering the inclination.
Different balances of these pluses and
minuses translate into different
flowering times.
Then there's temperature. With some
plants, such as lettuce, a quick cold
snap tells them winter is coming, and
they'll flower posthaste. But many
others need a more protracted period of
cold before they deign to put out
blooms, which is why inhabitants of warm
climes have to shove their tulip and
daffodil bulbs into the fridge if
they're ever to get more than one
springtime's worth of color from them.
It's also why farmers who plant wheat
and barley in the fall choose varieties
that require this same chilly treatment,
known as vernalization. This way they'll
be sure their crops will grow
vegetatively through the winter and
yield an abundant harvest in the spring.
The more scientists know about
flowering, the more they can play with
the process in the plant of their choice
and this makes for great agricultural
potential. Treating lily bulbs with
cytokinin hormones can mean early
flowers and more of them. As for
vernalization, growers would like to
save money by chilling bulbs for the
shortest time possible, yet they have to
be sure they've successfully flipped the
molecular flowering switch, or their
bulbs will be no good. Diagnostic tests
for successful vernalization, based on
genes that turn on when this switch gets
flipped, are under development.
Genetic engineering, too, can do
remarkable things to flowering. Not
everyone agrees it's desirable to fool
Mother Nature this way, but there's no
denying the potential significance of
the results. Getting a plant to flower
even slightly earlier or later than
normal can extend the geographical range
of a particularly favored variety, and
fast flowering also means faster
breeding. Experimenting with
Arabidopsis, for example, molecular
biologists have created early bloomers
by inserting extra copies of various
flowering genes into the plant. They've
even engineered plants that will flower
on command, in response to a gene that
turns on when exposed to the right
chemical trigger. Efforts are afoot to
do similar things with economically
valuable plants such as sunflowers,
lettuce, and cereals.
One flowering gene, called leafy, has
already been inserted into aspen trees,
with spectacular results. Normally
aspens wait ten to twenty years before
they flower, which makes them less than
popular for breeding. In the leafy
aspen, flowers spring forth from
inch-high seedlings after a mere three
months. Tree breeding at last becomes a
viable, do-it-in-your-own-lifetime
proposition.
With all this going on, who knows what
the plants of the future will be like?
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After earning a Ph.D. in
genetics from the University of
California, Davis, Rosie Mestel
("Rhythm and Blooms") repaired
to the laboratory to study,
among other things, fruit flies.
A couple of years later--and
without a backward glance at the
flies--she segued from handson
science to science journalism.
Mestel, left (with her daughter,
Renee), has been a reporter for
Discover, the U.S. correspondent
for New Scientist, and a
contributing editor for Health
and Earth magazines; she is
currently on the staff of the
Los Angeles Times, where, as
well as writing about health and
medicine, she contributes a
weekly column. |
Her last
Natural History article was "The Genetic
Battle of the Sexes" (2/98). Rodica
Prato, born in Bucharest, Romania,
studied architecture before becoming a
freelance illustrator. Her work has
appeared in dozens of books and
magazines. She illustrated "Searching
for the Wild Bactrian Camel" in last
month's Natural History.
COPYRIGHT American Museum of
Natural History & Gale Group
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