gregkavarnos wrote:Any chance of you scanning and attaching the abovementioned page?
As befits their modular structure and the ability to grow from each of their modules,
unlike animals, plants have no use for a centralized brain and/or nervous
system. Instead of centralized brain tissue, a newly emerging field of plant science,
dubbed “plant neurobiology,” is suggesting that plants may actually have
thousands of brain-like entities that are involved in the emergence of intelligent
behavior. These entities are a type of tissue known as meristems. Current theories
suggest that the meristematic tissue, located at the tips of roots and shoots, combined
with the vascular strands capable of complex molecular and electrical signalling,
may well comprise the plant equivalent of the nervous/neuronal
system.54 In a groundbreaking text Communication in Plants, Baluška et al. echo
the pioneering work of Darwin:
Each root apex is proposed to harbour brain-like units of the nervous
system of plants. The number of root apices in the plant body is high,
and all “brain units” are interconnected via vascular strands (plant neurons)
with their polarly-transported auxin (plant neurotransmitter), to
form a serial (parallel) neuronal system of plants.55
Rather than following Darwin’s judgement that this plant nervous system is inferior
to that found in animals, plant neurobiology researchers regard this decentralized
assessment and response system to be the most effective for maximizing
plant fitness.56 Such a system is thought to enable decentralized behavior (i.e.,
growth), which allows plants to thrive in complex and everchanging rhizospheric
environments.
It has been proposed that in the plant the meristematic “brains” may exert
influence on the rest of the plant tissue by the transmission of signalling molecules
such as the hormone auxin. Auxins are manufactured at the root and shoot
apices, and it is thought that their movement is one method for allowing the
transfer of information throughout the individual. It has been proposed that the
end poles (cross walls of cells) are analogous to the synapse in animals.57 At so
called “plant synapses,” vesicular transport of auxin moves this signalling molecule
from cell to cell. Although the exact processes have yet to be uncovered, it
has been proposed that this extracellular transport of auxin “exerts rapid electrical
responses” across the plant synapse and “initiates the electrical responses of
plant cells.”58 Whatever the pathway within the plant, communication can occur
over long-distances, with information on the environmental and developmental
state of the roots being transferred to the shoots—as in the case of stomatal closure
during water stress. As well as auxin and electrical signals, plants produce
and use a variety of neurotransmitter molecules to communicate from cell to
cell. Dopamine, acetylcholine, glutamate, histamine, and glycine are all touted as
potential signalling chemicals between cells.59 Other complex communication
molecules include protein kinases, minerals, lipids, sugars, gases, and nucleic
acids. Trewavas has drawn attention to this complexity and notes that “from the
current rate of progess, it looks as though communication is likely to be as complex
as that within a [animal] brain.”60
In response to some of the assertions of plant neurobiologists, Alpi et al.
have suggested that the existence of plasmodesmata (microscopic channels, which
traverse plant cell walls and enable transport and communication between cells)
contradicts the idea of plant synapses and of auxin as a neurotransmitter, as their
existence facilitates extensive electrical coupling, precluding the need for any
cell-cell transmission of a neurotransmitter-like compound.61 However, this criticism
has been refuted by Brenner et al., who assert that although the exact pathways
are still to be discovered, auxin is known to be transported from cell-cell
and active, communicative plant behavior does take place.62 Along with the
exact mechanisms of electrical cell-cell coupling, they assert that investigating
these transfers represents an exciting field of study for understanding plant signalling
and behavior.
With thousands of meristems, a plant has potentially thousands of “brain
units.” It is proposed by advocates of plant neurobiology that plants integrate
sensory information and make decisions based upon communication between a
multitude of plant tissues such as the root meristems, interior meristems, and the
vascular tissues. Barlow has pointed toward the involvement of the vascular
tissue (xylem and phloem) in conveying APs from zones of special sensitivity to
other regions of the plant—an “informational channel” involved in organismal
organization.63 Trewavas has proposed that the meristematic tissue, which runs
throughout the plant, could be an integrative assessment and computational
tissue, acting with sensory input from local meristems.64 With active debate on
this topic, it is still to be uncovered whether this internal communication systems
are centralized, decentralized, or somewhere in between.65
The structural complexity of these communication networks within plants is
of great interest for an understanding of the intelligent behavior that plants display.
The eminent animal physiologist Denis Noble has recently argued that networkstyle
interactions (like those found in plants), actually organize and direct the
activity of all living beings. In The Music of Life, he disputes the view that a unitary,
external mind or self controls and directs the activity of living organisms.66
Against this Cartesian notion, Noble argues that it is decentralized communicative
networks that heterarchically self-organize and direct living activity.
In Noble’s view of systems biology, “there is no single controller.” no single
Cartesian mind substance, which is the director of living systems.67 Instead,
from a systems viewpoint, mental properties such as intelligence, reasoning, and
choice are thought to emerge from the interactions of physiological networks of
signalling and communication. As Evan Thompson puts it, the “emergent
process is one that results from collective self-organisation.”68 These principles of
heterarchical organization and the emergence of higher level properties are fundamental
principles of systems biology, which are elegantly summed up by
Fritjof Capra:
According to the systems view, the essential properties of an organism,
or living system, are properties of the whole, which none of the parts
have. They arise from the interactions and relationships between the
parts. These properties are destroyed when the system is dissected,
either physically or theoretically, into isolated elements.69
Although the exact pathways are still being investigated, we can state that from a
systems perspective, the interconnecting, heterarchical network of plant tissues
(including meristems) enables intelligent plant behavior, rather than the Cartesian
consciousness or free will alluded to by Struik et al.70