First published online November 2, 2007
Journal of Experimental Biology 210, 3940-3945 (2007)
Published by The Company of Biologists 2007
doi: 10.1242/jeb.009555
Lung ventilation contributes to vertical lymph movement in anurans
Michael S. Hedrick1,*,
Robert C. Drewes2,
Stanley S. Hillman3 and
Philip C. Withers4
1 Department of Biological Sciences, California State University, East Bay,
Hayward, CA 94542, USA
2 Department of Herpetology, California Academy of Sciences, San Francisco,
CA 94103, USA
3 Department of Biology, Portland State University, Portland, OR 97207,
USA
4 Zoology, School of Animal Biology M092, University of Western Australia,
Crawley, Western Australia 6009, Australia

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Fig. 1. Influence of pulmonary pressure on lymph sac pressures. Changes in dorsal,
lateral and subvertebral lymph sac pressure as a function of pulmonary
pressure in anesthetized C. marinus (left column) and L.
catesbeiana (right column). All relationships were highly significant
(P<0.001, N=11; linear regression) with
r2 ranging from 0.19 to 0.72.
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Fig. 2. Subvertebral and brachial sac pressures measured for one C.
marinus during a single breath. Inspiration (solid horizontal line) and
expiration (broken horizontal line) are indicated above the subvertebral
pressure trace. Note that subvertebral sac pressure (top trace) increases
during inspiration with little or no change in brachial sac pressure (bottom
trace). During expiration there is a decrease in subvertebral sac pressure
that is rapidly transmitted to the brachial sac.
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Fig. 3. (A) Subvertebral sac pressure and brachial sac pressure during a breathing
sequence in one C. marinus. Arrows indicate expiration events
recorded in the subvertebral trace; note that rapid increases and decreases in
brachial lymph sac pressure occur, but are predominantly during expiration.
(B) Subvertebral sac pressure and pubic sac pressure during a breathing
sequence in one C. marinus. Arrows indicate expiration events
recorded in the subvertebral trace; note the rapid decreases in pubic sac
pressure that occur during expiration.
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Fig. 4. Frequency of occurrence (% of events) of combined brachial and pubic sac
pressure events with inspiration and expiration in C. marinus.
Brachial and pubic sac pressure events occurred much more frequently during
expiration than during inspiration (*P<0.001; unpaired
t-test). Values are means ± s.e.m. (N=10)
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Fig. 5. Pressure changes (Pa) that develop in the brachial lymphatic sac during
expiration in C. marinus and L. catesbeiana (means ±
s.e.m.) compared with the estimated range of 0.5–1.0 cm (50–100
Pa; shaded box) of gravitational pressure necessary to raise lymph to the
subvertebral lymph sac. Values were not different between the two species
(P>0.05).
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Fig. 6. Stylized models of C. marinus illustrating the hypothesis for the
effects of lung ventilation on vertical lymph movement. (A) Lung deflation
causes an increase in subvertebral lymph sac volume and a decrease in
pressure, resulting in movement of lymph from the brachial lymph sac.
Posterior skeletal muscles are also active during expiration, providing
movement of lymph vertically in the posterior portion of the animal. Red
arrows indicate the direction of lymph movement. (B) Lung inflation increases
the pressure within the subvertebral, dorsal and lateral lymph sacs and forces
lymph towards the anterior (Ant. LH) and posterior (Post. LH) lymph hearts.
Red arrows indicate the direction of lymph movement.
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© The Company of Biologists Ltd 2007