The fact that they "follow" the Sun i.e. have a photo-tropism is more to do with growth than active pursuit isn't it?
In the same way that a seed sends a root downwards (positive geotropism and negative phototropism) and a shoot upwards (positive phototropism and negative geotropism), the stems of green plants actively seek out light in order to maximise the solar return for the energy invested in growth. However, they have no muscles to make them move so the only way to do this is by adding cells asymmetrically to make the plant grow in the direction of light.
I think this is what happens with the sunflower - it grows more on the side OPPOSITE the light, pushing the stem towards the light source. As the sun crosses the sky this growth pattern alters in step.
Whether plants can respond to moonlight, however, I have no idea. Therefore, how the flower gets itself back to pointing the right way again for the next sunrise, or if it even does anticipate sunrise, I am not sure...
Chris
- chris - 31st May 09
http://findarticles.com/p/articles/mi_m1134/is_4_108/ai_54574603/?tag=content;col1
Morning light arrives early on the high slopes of the Colorado Rocky Mountains. At 5:00 A.M., a climber on a westward route to the summit of a fourteen-thousand-foot peak can count on a cheerful welcome from thousands of snow buttercups (Ranunculus adoneus), their dazzling yellow flowers facing east in the glow of the sun's early light. It's as if, overnight, a blast of wind blew down the slope, all the little yellow umbrellas in its path. Then, as the sun moves across the sky from east to west, the buttercups turn to follow it, and their bright faces greet the climber once again as she makes her descent.
Solar-tracking, or heliotropic, flowers are most common in arctic and alpine environments, where the air is often cool and the growing season is short. The satellite dish-shaped flowers of the snow buttercup, the arctic poppy, and other heliotropic flowers collect the sun's rays so efficiently that they heat up, becoming as much as fourteen degrees Fahrenheit warmer than the air around them. These miniature saunas are enticing to insects, which are by and large unable to generate their own heat and must wait for the sun to warm them up before starting the day's activities. Anyone who has observed bees on a flower early in the morning, when they are so still as to seem drugged or nearly dead, is familiar with insects' dependence on external heat sources. Solar-tracking flowers provide their insect visitors with a warm retreat for basking, foraging, even mating. In return, the visitors pollinate their hosts. The considerable heat absorbed by heliotropic flowers also jump-starts the development of newly fertilized ovules, helping the plants complete seed maturation in as few as eight weeks.
Harsh arctic and alpine conditions provide a "motive" for solar tracking, but what of the means? The mechanisms that leaves use to follow the sun are much better known than those flowers use. Movement in solar-tracking leaves, first written about by Charles Darwin in his 1880 book The Power of Movement in Plants, can occur rapidly and is reversible--two defining features of heliotropism. In nasturtiums, for example, a specialized organ at the base of the leaf--the pulvinus--continually orients the leaf surface at a right angle to the sun's rays, maximizing light interception for photosynthesis. The plant equivalent of a muscle, the pulvinus consists of specialized extensor and flexor cells that swell or shrink with changes in turgor pressure (determined by the amount of water in the cell). As extensor cells swell and flexor cells shrink, the leaf blade is reoriented to track the changing position of the sun.
Experiments with the snow buttercup have begun to reveal the sensory and developmental processes that lead to heliotropism in flowers. My colleague Maureen Stanton, of the University of California, Davis, and I started with a simple yet vital question: How do flowers sense the position of the sun? We knew that light provides plants with information as well as energy. Photomorphogenesis (plants' developmental responses to light) begins with photosensitive molecules in the cells of certain plant organs. Phototropism (one kind of photomorphogenesis) orients growing organs toward a light source. The sunflower, which is the plant kingdom's version of a morning person, shows phototropic stem growth, with the flower at the tip of the main stem always facing east. While phototropism does not exhibit the reversibility seen in heliotropism, we reasoned that similar sensory mechanisms might be involved in true solar tracking.
Anecdote has it that in the nineteenth century, a Frenchman noticed that some plants situated behind bottles of red wine failed to grow toward the sunlight. This early observation suggested that short-wavelength blue light, known to be blocked by red pigment, was necessary for phototropism. Blue light was later shown to play a crucial role in changing turgor in the pulvinus of heliotropic leaves. To determine whether blue light also cues solar-tracking in flowers, we performed our "buttercup in a Wine bottle" experiment. But we had no intention of carrying cases of cabernet up to twelve-thousand-foot elevations in the Rockies. Instead, we constructed lightweight cubes out of red acrylic filters. In the evening, we placed the cubes over snow buttercup plants. The next morning, we discovered that the filters had completely disabled the plants' ability to locate the sun. The confused flowers faced every which way, on average more than thirty degrees away from the sun's rays. Flowers in the two groups of control plants--those surrounded by blue-light-transmitting filters and those simply left in the open--tracked the sun much more successfully, facing, on average, within fifteen degrees of it.
Our experiment with acrylic cubes confirmed that blue light guides the movement of heliotropic flowers. But which organs actually perceive the light signal and translate it into the biochemical language of plant growth? Molecular biologists approach such questions by searching for gene products involved in photomorphogenesis. Rebecca Sherry, formerly a colleague at the University of Missouri-Columbia, and I took a less sophisticated tack, simply removing portions of the buttercup plant and discerning whether what remained could accomplish the task of solar tracking. Inspired by the Queen of Hearts in Alice's Adventures in Wonderland, we began with the edict "Off with its head!" and decapitated a number of innocent snow buttercups, removing the solitary flowers from their supporting stems. Neighboring buttercups were spared, as controls. Surprisingly, we found that the stems of decapitated buttercups continued to move over the course of the day, along with those of the control plants, aligning the ghosts of flowers past with the rays of the sun. Barring a paranormal phenomenon, this result means that the guidance system for flower heliotropism is housed in the stem rather than in the flower.
The flower stem of a snow buttercup is divided into three regions by two sets of bracts (modified leaves) that form sheaths around the stem. To study it, we again took our cue from Darwin, who performed an experiment since repeated by countless college botany students. When he illuminated young canary grass seedlings with light from one side, Darwin found that their shoots responded by bending toward the light source--unless he placed a foil hat over the tip of the shoot. Darwin concluded that the upper part of the shoot senses light and somehow reports the light's whereabouts to the lower region of the stem, which does the bending. We now know that this involves the growth-promoting hormone auxin. This hormone moves away from the light source and collects on the shaded side of the stem, where it causes cells to elongate more rapidly than on the sunlit side, thus producing a bend.
Realizing that foil caps were a technique better suited to the English garden than to the breezy alpine provinces of snow buttercups, we used Liquid Paper (opaque correction fluid) as a sunscreen to block different portions of the flower stem from sunlight. We found that if we blocked only the tops of the buttercups' stems, the stems lost their tracking ability. In contrast, when we painted middle or bottom portions of the stems with Liquid Paper, the plants continued to track accurately. These findings place the guidance system for heliotropism in the upper portion of the stem, just below the flower. Yet the bend needed for solar tracking occurs in the middle of the stem, well below the site of light reception. What messenger coordinates these activities?
The obvious suspect was auxin. We collected bent buttercup stems to inspect under the microscope back at the laboratory. In nearly every instance, the cells on the side of the stem that had been in the shade were longer than those on the sunlit side, as expected with auxin-induced growth. In fact, during solar tracking, the sunlit side of a flower stem grows only about half as fast as the shaded side.
Our results have revealed that, mechanistically, heliotropic flowers have more in common with seedlings reaching for the sun than with solar-tracking leaves. Leaves, for the most part, must be capable of orienting independently of the central stem of a plant. Ivy stems, for example, grow toward shade ("looking" for something to climb on), while ivy leaves seek the sun. In contrast, solar-tracking flowers, as extensions of the tip of the central stem, may utilize the same machinery that, earlier in a plant's life, served to orient the seedling shoot. Going further with our exploration of flower heliotropism may require that we trade our polar fleece for lab coats. Applying the tools of molecular genetics may determine whether the same genes control both seedling phototropism and flower heliotropism. But how glad I am to have begun the search in the crisp mountain air, inspired by the spectacular views that greet snow buttercups every day.
- dentstudent - 31st May 09