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18. Wernier,
A. M.
A recent claim (Webster & Caron, Bee Culture 123:403-406):
"The evidence for dance language is strong," ignored
13 salient points published 21 years earlier in the same publication
(Wells & Wenner, Gleanings in Bee Culture 102:110-111,127).
I update, expand upon, and add to those points here.
The dance maneuver information is not sufficiently accurate to
account for supportive experimental results obtained by language
proponents; rather, the experimental designs used apparently
funnel recruits into "intended" sites. Von Frisch recognized
in 1937 (Wenner, with von Frisch, Bee World 74:90-98)
- that one gets no recruits with no odor. However, von Frisch
(and others at the time) failed to perceive that his 1940s experiments
lacked necessary controls against odor influencing results; later,
his results did not survive tests in double-controlled and strong
inference experiments. Only by using odor in single controlled
experiments can one obtain supportive results; therefore, one
can no longer justifiably explain "positive" results
with an uncritical assumption of "language" use.
Recruit search behavior is remarkably inefficient. Most recruits
require several flights out from the hive before locating the
target food source, are in the air many times longer than necessary
for a direct flight, and succeed only rarely unless one provides
sufficient odor at the site. One can easily see (use binoculars)
that recruits always fly zigzag into a target site from far downwind.
If an array of stations is provided, recruits end up near the
center of all-although a slight wind blowing along a line of
stations can alter a predictable distribution. Despite dancing,
recruitment more than 400 m downwind from a hive is negligible
unless many foragers make round trips and thereby provide an
aerial pathway of odor.
Crop-attached bees require no dancing for re-recruitment; they
will immediately return to their foraging area on the basis of
an odor stimulus alone. New recruits, by contrast, do not begin
arriving in quantity until almost an hour after foragers begin
regular trips and increase in frequency per unit time even if
the number of dancing bees is held constant. Recruit success
is thus dependent more upon the cumulative number of forager
trips (with time and with odor accumulation in the hive) than
upon the number of foragers involved. Success rate depends upon
odor concentration but not upon Nasonov gland secretions at the
food source or upon dance frequency in the hive. Finally, recruits
attending disoriented dances (dances without direction information)
can still find the "correct" site in the field.
No one seems to dispute the above known facts, so clearly researchers
have grossly neglected the role of odor in honey bee recruitment.
Furthermore, no one seems willing to provide a concise scientific
statement of the language hypothesis, one that can accommodate
all known facts. For those who wish to understand foraging ecology,
an increased emphasis on the role of odor in honey bee recruitment
should be very rewarding.
One can find a quite complete 1990 summary of most of the above
points (Wenner & Wells, Anatomy of a Controversy: The
Question of a "Language" Among Bees. Columbia University
Press) and a more recent clarification elsewhere (Wenner et
al., Am. Zool. 31:768-782).
Adrian M. Wenner
Ecol., Evol., & Mar. Biology
Univ. of California, Santa Barbara
Santa Barbara, CA 93106
e-mail: wenner@lifesci.ucsb.edu
This research was supported in
part by University of California Faculty Research grants and
the National Science Foundation (#9301468 and #9319489). |
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