Is Swimming a Drag?
Erik Anderson says: Lights! Camera! Bluefish!
A dolphin
should not be able to swim. So said Cambridge University zoologist
James Gray in the 1930s. The friction caused by water moving over a
dolphin’s skin, he said, should be like swimming in cold molasses. But
dolphins obviously can swim, and Erik Anderson wants to find out why.
The paradox springs from a conflict between idealized models and a
reality that is difficult to observe and measure. In trying to
calculate drag-the force that slows the movement of an object through
air or water-Gray could only use formulas and observations based on the
flow of water over rigid, static bodies. The physical and mechanical
models fell short of the biological reality, and Gray and other
scientists were stuck with the implausible conclusion that the force a
dolphin or fish needed to overcome drag was greater than the force
their muscles could generate.
But the body of a swimming dolphin or fish is hardly rigid
or static. So instead of modeling the forces of drag, Erik Anderson has
combined 21st century lasers, robots, and cameras with old-fashioned
attention to microscopic detail to build an experiment that measures
the forces. “I want to know how a real fish swims,” says Anderson, a
student in the MIT/WHOI Joint Program. “I want to know their trade
secrets.”
The Accidental Tourist
In the summer of 1997, Anderson had an encounter that would change his
scientific life. As a master’s degree candidate from St. Francis Xavier
University (Nova Scotia), he visited WHOI for a study of the fluid
dynamics of squid motion. Anderson and colleagues had traveled to Woods
Hole because their subjects were abundant and accessible-the squid
Loligo pealei migrates through the waters off the WHOI pier every
spring-and because the Coastal Research Laboratory had a large flume
close to the delicate animal’s habitat.
One day while shooting high-speed, high-resolution images
of Loligo swimming in the flume, Anderson was approached by a man
who-without introducing himself-started asking questions about the
experiment. “I thought he was a tourist and I was very busy,” he
recalls, “so I brushed him off with simple answers.”
A week later, Anderson attended a scientific presentation
by WHOI Associate Scientist Mark Grosenbaugh of the Applied Ocean
Physics & Engineering Department. Anderson was curious to meet
Grosenbaugh, whose papers he had read. When Grosenbaugh stood up to
give his seminar, Anderson did a double take: Grosenbaugh had been his
“tourist.” “He was not a guy I should have been getting rid of,”
Anderson says.
Despite the awkward introduction, Anderson began talking
with Grosenbaugh and WHOI Associate Scientist Wade McGillis
(AOP&E). They are now his thesis advisors. “When they told me about
the fish-drag problem, it sounded like a logical step after the squid
work,” Anderson recalls. “I was especially drawn to the challenge of
engineering an experiment.”
Within a year, Anderson was admitted to the MIT/WHOI
Joint Program and began conducting experiments on a robotic tuna...and
hatching plans for one of the most sophisticated studies of fish
propulsion ever devised.
Swimming Against the Stream
Fish swim against two fluid forces: form drag and friction drag.
Anderson compares the physics to riding a bicycle. “When you cycle
through air-which is also a ’fluid’ medium-you feel pressure on your
chest and suction from a wake at your back,” Anderson notes. “The
pressure and suction are the source of form drag. Friction drag is
caused by the air sliding over your skin.”
In the 1970s, Japanese researchers who observed fluid
flowing over a waving rubber mat found that form drag may be almost
negligible on a swimming fish. They demonstrated that as a surface
undulates, fast-moving fluid is drawn closer to the surface, creating a
smaller wake and reducing suction. The streamlined shape of most fish
also results in reduced pressure in the front.
That leaves drag from friction, a force that has been
modeled and studied in idealized experiments, but not measured directly
on freely swimming fish. Anderson decided to use modern technology to
zoom in on the “boundary layer,” the critical zone around a fish where
the effects of friction have a measurable impact on the flow of water.
This layer is usually less than one centimeter thick.
The experiment seems simple enough: photograph the water
flowing through the boundary layer and across a fish’s skin. From such
pictures, Anderson can calculate the friction drag and visualize the
shape of the fluid flow, much as engineers study the flow of air over
airplane wings and cars. But as Anderson explains, “It was a
challenging engineering problem to build a data-taking apparatus that
could accurately measure friction drag.”
“No one’s been able to measure water’s speed in the
boundary layer of fish before,” says George Lauder, who studies the
flow around aquatic animals at Harvard University. “It’s extremely hard
to do, and Anderson’s system is the first to be able to accomplish
this.”
How does Anderson see water moving? He puts microscopic,
silver-coated beads into the flume as a tracer, then illuminates them
with a sheet of light from a laser. To capture an image of water within
12 millimeters (0.47 inches) of a fish’s skin, Anderson points a
high-resolution digital camera at the sheet of laser light from beneath
the flume. Another camera captures the same angle, but with a field of
view ten times larger, in order to get a general picture of the flow
inside and outside the boundary layer. A third camera snaps a side
view, recording the position where the laser impinges on the fish.
The three cameras and laser are synchronized in “dual pulses,” taking
pairs of freeze-frames two milliseconds apart. Lit by the laser, the
beads appear as tiny white dots against the photo’s black background.
The “image pairs” generated by any of the cameras are nearly identical
photos, but close inspection shows that the beads have moved slightly
from one exposure to the next. With the help of several sophisticated
computer programs that Anderson wrote himself, he can measure the
distance the beads travel, effectively measuring how fast the water in
the boundary layer traveled in millimeters per millisecond.
Anderson creates a map of water speed and direction along
the entire length of a fish. From measurements of how water velocity
changes with distance from the fish, he calculates friction drag at the
skin. With that data, Anderson can generate a complete picture of the
“shape” of the boundary layer and the friction drag along a wriggling
fish.
In the first year of his study, Anderson waited days,
sometimes weeks, for the fish to swim through his 1-centimeter-square
field of view. He surfaced, bleary-eyed, from his experiments with just
ten seconds of usable image data. With experience and increased funding
from the National Science Foundation, the Office of Naval Research, and
WHOI’s Ocean Ventures Fund, Anderson’s system has evolved from fixed
cameras on stands to cameras and the laser gliding on the motorized
rails of an 800-pound robot.
“Now, I just sit in front of the tank with the joystick,
training the laser on the fish,” Anderson says. These days, the heavy
lifting comes from sifting through the mountains of data. Each camera
captures hundreds of gigabytes of images per two-hour experiment.
Data isn’t the only thing Anderson catches with his
work. An avid angler who spent childhood weekends fishing with his dad,
he collects his own experimental “volunteers” (eel, mackerel, dogfish,
bluefish, and scup) in Vineyard Sound and Cape Cod Bay. “Having to fish
as part of my research is hilarious,” Anderson says. “All my fishing
buddies just laugh when they hear I get paid to go fishing.”
Something Fishy About Drag
Ever since Gray calculated that dolphins shouldn’t be able to swim,
there has been a controversy in the field of biomechanics: Is drag more
intense on a wriggling fish than on a rigid body like a submarine?
James Lighthill, another Cambridge scientist and the mathematical
genius who helped design the supersonic Concorde jet, predicted in the
1970s that the drag on a real fish would be up to five times greater
than on a stiff mock-up.
After observing real swimmers and crunching the data,
Anderson saw what Lighthill had predicted. “The friction drag on scup
and dogfish was higher than on a rigid body," Anderson says.
Essentially, the friction on a swimming fish is higher than that on a
coasting fish. “But we also calculated that a scup has two to twenty
times the strength needed to overcome this drag.” He reported his
findings in a 2001 paper in The Journal of Experimental Biology, a
publication that James Gray edited for 20 years.
Anderson suggests that his most important observation is that the
historical concept of “drag reduction" has been improperly defined when
it comes to swimming fish. “A true study of swimming fish should
compare the drag of one swimming motion compared to another, not a
swimming fish to a rigid model,” says Anderson. “A rigid eel goes
nowhere, so it doesn’t make any sense to compare its drag to a swimming
eel, unless you are studying swimming versus gliding...or trying to
decide whether vehicles should be rigid or fish-like.
“It’s possible that while a swimming fish has higher
friction drag than a rigid, fish-shaped model, a real fish might tune
its motion to have lower drag than another, similarly shaped fish,” he
adds. “This is the more interesting question: What slight differences
in swimming motion and body structure result in enhanced efficiency,
stability, or maneuverability?”
Much of the time, the key to minimizing friction drag is
to keep water flowing smoothly over the fish’s skin and to reduce
surface area. “For small and slow fish, the boundary layer is often
laminar or smooth,” Anderson notes. Some fish appear to have natural
drag-reducing strategies, such as slots where they can tuck their fins
for a sleeker profile.
But sometimes the opposite is true. “For some large and
fast fish, the boundary layer sometimes appears to be turbulent,”
Anderson says. The rough skin of sharks, for instance, may actually
stir up the boundary layer. Such turbulence, although it increases
friction drag, can decrease form drag by a greater amount. That’s
because an eddying boundary layer produces a smaller wake and decreased
suction at the tail end. (The same principle is at work in the dimples
on a golf ball.) Sharks have a method to counteract friction as well,
using tiny riblets along their surfaces to organize the turbulent flow
in a way that decreases friction.
Anderson’s research “has implications for the design of
more energy efficient underwater vehicles,” says Lauder. “His findings
might help show whether future vehicles should be flexible like a fish
or rigid like a submarine.” Along those lines, boat builders have
adopted some of nature’s ideas by using riblet technology on the hulls
of racing boats.
As Anderson finishes his Ph.D. dissertation on fish
motion, he is already daydreaming about how to put Gray’s dolphin
paradox to the test. He’d like to measure the drag on a live dolphin.
If he can find the resources and adapt the technology, he will put his
camera and laser system into a watertight backpack and snap shots of
the dolphin’s boundary layer as it swims. That’s assuming that a
dolphin actually can swim...
Originally published: March 1, 2003

