Many of us involved in teaching botany feel a sense of urgency in our profession. Botany departments, botany majors, and botany curricula have gradually shrunk or disappeared from most colleges and universities in the US, and I suspect in many other parts of the world as well. Too many students are graduating with little or no understanding of the unique ways in which plants meet the challenges of survival and reproduction in the Earth’s diverse ecosystems. Biology faculty who don’t have training or experience with plants are often ill-prepared to relate to or take advantage of the unique contributions plants might make to their own teaching and research.
So if we have only a semester, or worse only a week or two,
to teach the fundamentals of plant life, and to pass on the exhilaration we
feel in the face of their diverse adaptations, how do we do it? If our non-botanical colleagues or teaching assistants have been
assigned to teach a beginning level segment on plants, how do we help them understand the
basics and develop some enthusiasm for the subject matter?
Some teachers prefer an ecological approach, emphasizing the
pivotal and diverse roles of plants in the ecosystem. Others prefer an approach emphasizing
applications to human technology, agriculture, nutrition or medicine. All of these approaches are useful in
developing interest, but may end up being too superficial with respect to fundamental
structure and function. Traditional
botany texts tend to be dry and encyclopedic.
Non-majors texts may be more
appropriate for most of today’s audience, but they still tend to avoid a side
of biology that I call the “why” questions.
One must have the “what” before the “why,” but it is the
latter that gives some context or meaning to the former. The “what” is the factual material one finds
in a textbook. The “why” is the
explanation of the “what.” For example, textbooks typically contain a little
section on the differences between monocots and dicots (or now monocots and
eudicots, awkwardly ignoring magnolids, waterlilies and other basal angiosperms). We are told that dicots typically have
net-veined leaves, vascular bundles arranged in a ring in the stem, and
secondary (woody) growth, while monocots typically have parallel-veined leaves,
vascular bundles scattered within the stem, and no secondary growth. That is the “what,” at least in a simplistic
sense, but there is typically no “why” to follow it.
Monocots are the
newer invention in plant architecture, having developed their unique structures
and way of growth as they split from ancient dicots. Why do their leaves have parallel veins? Why do they not have secondary growth? How do they interact differently with the
world than dicots, and how did their
innovative structures come about? (Hint: it has to do with ancestral monocots going “underground.” ) See the caption to the right, and for a
more extended exploration of these questions see my blog post: How
the grass leaf got its stripes.
“Why,” in scientific terms, has to do with the
process of adaptation. It’s the story of origins, of plants facing
environmental challenges and evolving innovative ways to cope. This is what makes botany interesting. It is also a way to make sense of the fundamental
features of plants, some of which may be dismissed as obscure and unimportant, but
which are loaded with both meaning and utility.
For another example, let’s take everyone’s favorite: life
cycles. Students already
sophisticated enough to know that sperm and egg in animals are produced through
the special kind of nuclear division called meiosis are truly puzzled by why
that does not happen in plants. Others
are surprised that plants produce sperm and egg at all. Meiosis mixes chromosomes and reduces a double set (diploid) into a single one (haploid) in each of the resulting cells. In animals the haploid cells combine into a diploid zygote, which develops into a new diploid individual In algae and plants, however, it's more complicated. Bear with me, even the short version is convoluted!
In the evolutionary story of sexual reproduction in plants, we find that the algae similar to those that gave rise to land plants, and simpler land plants themselves, are haploid and do produce sperm and egg directly. In both cases, however, the joining of sperm and egg does not result in a new plant, but rather in a short-lived diploid zygote that produces spores through meiosis. Spores are adapted for long-distance dispersal, and germinate to form new haploid plants that will eventually produce gametes. So spores, not gametes, are produced through meiosis in plants.
In the evolutionary story of sexual reproduction in plants, we find that the algae similar to those that gave rise to land plants, and simpler land plants themselves, are haploid and do produce sperm and egg directly. In both cases, however, the joining of sperm and egg does not result in a new plant, but rather in a short-lived diploid zygote that produces spores through meiosis. Spores are adapted for long-distance dispersal, and germinate to form new haploid plants that will eventually produce gametes. So spores, not gametes, are produced through meiosis in plants.
That story has primarily to do with the fact that plants
cannot move around to find mates, and that if they simply released sperm cells
to go off and find an egg on their own, it would lead at best to severe
inbreeding. Such a strategy works well
enough in some marine invertebrates, like sea stars, where currents can help
disperse the sperm cells, but on land, these tiny, fragile cells just don’t get
very far. Spores do the traveling for plants, taking the place of mate selection in mobile animals. Genetic diversity in plants depends on spores
from different genetic backgrounds landing close to one another, so that when
they develop into gamete-producing plants, suitable mates will be next to one
another.
Why are there no moss trees?") but this suffices to get spores above the low-growing moss foliage. In the land plants we call vascular plants, however, sporophytes became larger and larger, and in fact the trees, herbs, and grasses we see today are
actually the sporophyte generation of the plant life cycle. The egg- and sperm-producing “plants”
(gametophytes) - the equivalent of the algal or moss colonies, are hidden
within the embryonic seeds and pollen grains of these more advanced plants.
Yes, it’s complicated, but if the story unfolds from the perspective of how and why it evolved, it does make sense. And it is an important story. Understanding how plants and algae reproduce impacts both agriculture and ecology.
Yes, it’s complicated, but if the story unfolds from the perspective of how and why it evolved, it does make sense. And it is an important story. Understanding how plants and algae reproduce impacts both agriculture and ecology.
“Plant Life – A Brief History,” provides the adaptive perspective of plant features for students, instructors, and others interested in the biology of plants.
A very informative post! I can always look forward to an interesting read on your blog.
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