First published online January 31, 2007
Journal of Experimental Biology 210, 722-731 (2007)
Published by The Company of Biologists 2007
doi: 10.1242/jeb.02702
Oxygen in egg masses: interactive effects of temperature, age, and egg-mass morphology on oxygen supply to embryos
Amy L. Moran1,* and
H. Arthur Woods2
1 Department of Biological Sciences, Clemson University, Clemson, SC 29634
USA
2 Division of Biological Sciences, University of Montana, Missoula, MT 59812
USA

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Fig. 1. Egg masses of Tritonia diomedea. (A) Intact sections of egg masses
at two stages. Left, a 2-day-old mass; right, a 2-week-old mass. The width of
egg mass `rope' is approximately 3 mm. (B) Egg capsules within a 2-day-old egg
mass. Egg capsules are 800 µm across the longest dimension. (C)
2-day-old embryos removed from egg capsules. Embryos are approx. 90 µm
across the longest dimension.
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Fig. 2. Tritonia diomedea; respiration measurements of early embryos at
two temperatures. Each datum point shows the oxygen consumed in one single
respiration chamber, plotted against the number of capsules in the chamber.
Respiration of an individual capsule was estimated from the slope of the
regression line at each temperature (orange circles, 21°C;
b=863.1, r2=0.99; blue circles, 12°C;
b=495.1, r2=0.95). Error was calculated as the
s.e.m. of the slope (s.e.m. 21°C=201.6; s.e.m. 12°C=52.6). The
non-zero intercepts are an unexplained but very common phenomenon in
microrespiration measurements, and do not affect estimates of respiration rate
derived from the slope; see discussion elsewhere
(Marsh and Manahan, 1999 ).
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Fig. 3. Tritonia diomedea; metabolic rates of free embryos (filled
circles) compared to embryos in egg capsules (open circles) at three stages of
development. Each datum point ± s.e.m. was derived from a regression
equation as shown in Fig.
2.
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Fig. 4. Tritonia diomedea; effect of temperature on metabolic rates at
three developmental stages (blue circles=12°C; orange circles=21°C).
(A) Direct measurements on embryos in egg capsules. Each datum point ±
s.e.m. was derived from a regression equation as shown in
Fig. 2. (B) Estimated
per-embryo metabolic rates calculated by dividing the per-capsule rate by the
number of embryos per capsule (the latter number was either directly counted
or estimated from the mean number of embryos per capsule in other capsules
from the same mass; see text).
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Fig. 5. Tritonia diomedea; oxygen distributions in intact sections of egg
mass and in free embryo capsules at 12°C (blue circles) and 21°C
(orange circles). Effects of temperature and configuration for early-cleavage
stage embryos (left) and late-veliger stage embryos (right). Each point
represents the mean ± s.d. of three measurements.
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Fig. 6. Dendraster excentricus; artificial egg masses. (A) Representative
high- and low-embryo density artificial egg masses, constructed by casting
newly fertilized D. excentricus into low-melting point agarose. Both
masses are `medium diameter' masses, 4 mm in diameter. (B) Radial
profiles of oxygen through artificial masses of small, medium and large
diameter, obtained using a Clark-style microelectrode. Arrows indicate
position of midpoint.
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© The Company of Biologists Ltd 2007