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First published online June 29, 2007
Journal of Experimental Biology 210, 2430-2435 (2007)
Published by The Company of Biologists 2007
doi: 10.1242/jeb.003541

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Intermittent hypoxia in eggs of Ambystoma maculatum: embryonic development and egg capsule conductance

J. Hunter Valls and Nathan E. Mills^*

Department of Biology, Harding University, Searcy, AR 72149, USA

^* Author for correspondence (e-mail: nmills{at}harding.edu)

Accepted 1 May 2007

	Summary

TOP Summary Introduction Materials and methods Results Discussion References

 
The spotted salamander Ambystoma maculatum breeds in shallow freshwater pools and imbeds its eggs within a common outer jelly matrix that can limit oxygen availability. The eggs are impregnated with the unicellular alga Oophilia amblystomatis, which produces oxygen during the day but consumes oxygen at night. This daily cycle of algal oxygen production drives a diurnal fluctuation of oxygen partial pressure (P_O2) within the eggs, the magnitude of which depends on the distance of an egg from the exterior of the jelly matrix and on the ambient P_O2 of the pond. We subjected A. maculatum eggs to fluctuating oxygen levels with a variable minimum P_O2 and an invariable maximum, to simulate natural conditions, and measured differences in developmental rate, day and stage at hatching, and egg capsule conductance (G_O2). Lower minimum P_O2 slowed development and resulted in delayed, yet developmentally premature hatching. G_O2 increased in all treatments throughout development, but P_O2 had no detectable effect on the increase. Intermittent hypoxia caused comparable but less pronounced developmental delays than chronic hypoxia and failed to elicit the measurable change in G_O2 seen in ambystomatid salamander eggs exposed to chronic hypoxia.

Key words: Ambystoma maculatum, hypoxia, amphibian, embryonic development, egg capsule conductance

	Introduction

TOP Summary Introduction Materials and methods Results Discussion References

 
Aquatic breeding amphibians lay eggs enclosed in jelly capsules of varying thickness and structure (Salthe, 1963). The egg capsule confers protection to the embryo (Ward and Sexton, 1981), but also presents a barrier to diffusive respiratory gas exchange (Seymour, 1994; Seymour and Bradford, 1987; Seymour and Bradford, 1995). Respiration is complicated for species with perforated egg masses in which adjacent eggs are tangentially connected through their outer egg jelly. Potentially poor ventilation and competition for dissolved oxygen among contiguous embryos can limit the partial pressure of oxygen (P_O2) surrounding an individual egg (Cohen and Strathmann, 1996; Seymour, 1995; Seymour and Bradford, 1995; Seymour and Roberts, 1991). For these species, oxygen delivery to the egg is facilitated through various methods including solar-driven convection of water through the interstices of an egg mass, suspending eggs in foam near the water surface, and spreading eggs in thin sheets or strands (Burggren, 1985; Pinder and Friet, 1994; Seymour, 1995; Seymour and Bradford, 1995; Seymour and Roberts, 1991).

Periodic hypoxia is unavoidable for eggs of the spotted salamander Ambystoma maculatum. It embeds its eggs within a common outer jelly matrix, forming an amorphous imperforated jelly mass (Gilbert, 1942; Pinder and Friet, 1994; Salthe, 1963). Convection is absent in these masses, and diffusion alone cannot deliver adequate oxygen to embryos near the center, especially in later development (Pinder and Friet, 1994). Additionally, a unicellular alga, Oophilia amblystomatis, shares a symbiotic relationship with A. maculatum embryos, likely utilizing CO₂ and nitrogenous waste inside the eggs while the embryos consume photosynthetic oxygen produced by the algae (Hutchison and Hammen, 1958; Gilbert, 1942; Gilbert, 1944). This symbiosis drives a diurnal P_O2 cycle: in the light, the egg mass may actually become hyperoxic due to oxygen production by O. amblystomatis, but in the dark, photosynthesis ceases and the algae consume oxygen needed for A. maculatum respiration. Consequently, eggs experience varying degrees of hypoxia at night, depending on their position relative to the surface of the egg mass and their developmental stage. During late development, P_O2 near the center of egg masses may fluctuate from <1 kPa in the dark to >30 kPa in the light (Bachmann et al., 1986; Pinder and Friet, 1994).

Chronic or extended hypoxia has been shown to delay or negatively alter development across vertebrate classes including Osteichthyes (Shang and Wu, 2004), Reptilia (Andrews, 2002; Warburton et al., 1995), Aves (Chan and Burggren, 2005; Dzialowski et al., 2002) and Mammalia (Khozhai et al., 2002; Rattner and Ramm, 1975). It has also been studied in anuran and caudate amphibians. In Pseudophryne bibroni, a frog with an incubation period comparable to that of A. maculatum, Bradford and Seymour (Bradford and Seymour, 1988) reported slowed development and developmentally premature hatching at chronic P_O2 of 12.2 kPa. In ambystomatid salamanders, chronic hypoxia is increasingly detrimental to embryonic survival and larval fitness as development progresses (Adolph, 1979). Chronic hypoxia can slow embryonic development, delay hatching, and increase the frequency of developmental abnormalities (Detwiler and Copenhaver, 1940; Mills and Barnhart, 1999). Additionally, embryos may hatch at an earlier developmental stage, presumably to eliminate the respiratory barrier of the egg capsule (Mills and Barnhart, 1999). While these chronic hypoxia studies provide a basis for our hypotheses, it is unknown whether the diurnally intermittent hypoxia naturally experienced by A. maculatum produces similar developmental alterations.

The oxygen conductance (G_O2) of an ambystomatid egg capsule can be described by the equation G_O2=K_O2(ESA/L), where K_O2 is Krogh's coefficient of oxygen diffusion in egg jelly (mm² min^–1 kPa^–1), ESA is the effective surface area of the egg capsule (mm²), and L is the capsule thickness (mm). Because amphibian eggs are spherical, ESA=4r_or_i and L=r_o–r_i, where r_o is the outer radius of the capsule, and r_i is the inner radius. Amphibian embryonic oxygen consumption (_O2) increases throughout development, and water is simultaneously absorbed into the capsular chamber, increasing capsule volume. The increasing volume causes ESA to increase and L to decrease, both of which result in an increase in G_O2 that compensates for the increasing _O2 of the embryo (Salthe, 1965; Seymour and Bradford, 1987; Seymour et al., 1991). Additionally, Mills et al. (Mills et al., 2001) found that ESA (and thus G_O2) of egg capsules of Ambystoma annulatum and A. talpoideum increased greater in response to chronic hypoxia than in normoxia.

To date, the ability of A. maculatum to compensate for hypoxia by increasing G_O2 has not been studied. Calculating G_O2 in A. maculatum is complicated by the common outer jelly matrix. Because the egg capsule and jelly matrix are both composed of mucopolysaccharides (Salthe, 1963), the matrix can be considered a shared part of the egg capsule, which has the functional effect of greatly increasing r_o, and thus L. Sensitivity analyses reveal that if r_o is large, G_O2 becomes relatively insensitive to r_o, and almost independent of L (Seymour, 1994). Therefore, r_i is likely the best indicator of G_O2 in A. maculatum eggs, and the inside of the capsule can be treated as the respiratory surface of the egg.

The effect of diurnally fluctuating oxygen levels on embryonic development and G_O2 of aquatic breeding amphibians is largely unknown, but it is important to consider in A. maculatum because hypoxia is a transient but regular occurrence. In this experiment, we exposed A. maculatum eggs to diurnally fluctuating P_O2 with a variable minimum and an invariable maximum P_O2. We predicted that embryos exposed to P_O2 fluctuations with lower minimums would decrease their developmental rate and delay hatching. We also predicted that eggs in P_O2 fluctuations with lower minimums would increase G_O2 proportionally more than those in fluctuations with higher minimums.

	Materials and methods

TOP Summary Introduction Materials and methods Results Discussion References

 
Eggs
An Ambystoma maculatum Shaw egg mass was collected from an ephemeral woodland pond approximately 3.4 km SSE of Center Hill, White County, AR, USA (35°13'57''N; 91°52'40''W) on 28 March 2006 and refrigerated at 5°C. On 30 March, all eggs were carefully removed from the outer jelly. We randomly assigned 12 eggs to each of five treatments, and the embryos were staged according to Harrison (Harrison, 1969) using a stereomicroscope (model SMT-1, Tritech Research, Los Angeles, CA, USA). Embryos were at Harrison stages 20–31 (median stage 27), and there was no initial difference in developmental stage between treatments (Kruskal–Wallis; H=0.184, P=0.996). Eggs were maintained in Plexiglas^TM trays with 14.3 mmx14.3 mm cylindrical wells. Both the top and bottom of the trays were covered with vinyl window screen to allow free flow of water through the wells.

Control of oxygen fluctuation and temperature
Dechlorinated tapwater was continuously pumped from a 60 l reservoir through a gas-stripping column (Barnhart, 1995) at a rate of 600 ml min^–1 to remove oxygen. As the water exited the column, P_O2 was approximately 1 kPa. The water was gradually reoxygenated in an aeration ladder in which the water flowed over a series of partitions from pool to pool. Aeration was enhanced by bubbling air in selected pools to obtain desired P_O2 levels. Water from five pools in the aeration ladder was siphoned into experimental chambers at 40 ml min^–1. Two randomly assigned replicate chambers received water from each pool, for a total of ten chambers. An egg tray containing six eggs was completely submerged in each chamber, yielding a sample size (N) of 12 eggs for each treatment. Each chamber continuously drained excess water back into the original reservoir, which was refilled with dechlorinated tapwater as evaporation occurred.

Oxygen was removed from the water in the gas-stripping column via a nitrogen gas counter-current. We connected the nitrogen to the column through a solenoid valve controlled by a clock-operated timer. The nitrogen was turned on to deoxygenate the water; to terminate oxygen removal, the nitrogen was turned off while simultaneously turning on an air compressor to replace the nitrogen in the column with air. The timers were set to create an 11:13 high:low P_O2 cycle. For 3 days immediately before and after the experiment, P_O2 measurements were taken hourly during the periods of increase and decrease to determine the P_O2 profiles for each treatment (Fig. 1). Mean minimum and maximum P_O2 levels for each treatment during the experiment are given in Table 1. From this point forward, treatments are identified by their mean minimum P_O2 (kPa) during the experimental period.

View larger version (10K): [in this window] [in a new window]   Fig. 1. Diurnal PO2 fluctuation profiles for each treatment immediately before and after the experimental period. Curves are based on hourly measurements taken during periods of PO2 fluctuation 3 days prior to and immediately following the experiment. Values are means ± s.d. (N=6).

To control P_O2 levels experienced by the eggs and maintain clarity of egg capsules for staging, the room was kept dark to prevent growth of O. amblystomatis. Water temperature in all treatments throughout the experiment was 15.6±0.2°C (mean ± s.d.). P_O2 (measured in percent of air saturation and converted to kPa) and temperatures were measured using a calibrated oxygen meter (model 550A, YSI Environmental, Yellow Springs, OH, USA). Water pH was measured using a calibrated pH meter (model 230A, Orion Research, Inc., Boston, MA, USA) during a 6-day period following the conclusion of the experiment. The pH did not differ among treatments (mean pH=6.77±0.06; ANOVA; F=0.056, P=0.994, N=180), and thus pH is not a covariate with P_O2 in this experimental system.

Staging and G_O2 measurements
Each egg tray was removed from its experimental chamber and submerged in oxygenated water from the aeration ladder for approximately 30 min daily for staging according to Harrison (Harrison, 1969). Developmental stage and day (counted from the day the experiment began) were recorded at hatching.

The inner radius (r_i) of eggs was measured to detect increases in G_O2, since r_i is the most influential parameter in determining G_O2 in A. maculatum (Seymour, 1994). To obtain r_i measurements, digital photographs were taken of all eggs initially (day 0), at a common time (day 8), and at a common developmental stage (Harrison stage 39). G_O2 increases in concert with developmental stage in some amphibians (Seymour et al., 1991); difference among treatments in r_i (thus G_O2) on day 8, when embryos were at Harrison stages 35–40, could be due to variation in developmental stage on that day. Therefore, photographs were also taken at a common stage (39) to isolate P_O2 as the cause for any difference in G_O2. Stage 39 was chosen because it was the most advanced stage reached before embryos began to hatch in the Mills and Barnhart study (Mills and Barnhart, 1999). A stage micrometer and egg were completely submerged in water, and photographs were taken through the stereomicroscope with a Nikon Coolpix 950 camera. Egg radii were determined from the photographs using UTHSCSA ImageTool 3.00 (University of Texas Health Science Center San Antonio 2002).

Analyses
Statistical analyses were performed using SAS 9.1 (SAS Institute, 2003) or SYSTAT 11.1 (Systat Software, Inc. 2003); for all tests P=0.05. Days to stage 39, days to hatching, and stage at hatching were used as indicators of development. Because developmental stages are ranked data, a Kruskal–Wallis test was used to determine the effect of minimum P_O2 on developmental stage at hatching. Day at hatching and days to stage 39 were transformed by natural logarithms to meet assumptions of normality and homogeneity of variances, and the General Linear Model (GLM) was used to perform a multivariate analysis of variance (MANOVA) evaluating the effect of minimum P_O2 on these variables. The GLM procedure was also used to perform a repeated-measures (RM) MANOVA of r_i of egg capsules in all P_O2 treatments on day 0, day 8, and at stage 39. Reported P values for MANOVAs are based on Pillai's Trace.

	Results

TOP Summary Introduction Materials and methods Results Discussion References

 
Two embryos (one each in the 11.5 and 6.7 kPa treatments) were inadvertently killed during the experiment and were excluded from all analyses. Survival rates of remaining embryos ranged from 82% (9 of 11) at 11.5 kPa to 100% (11 of 11) at 6.7 kPa, and there was no noticeable effect of treatment (Table 1).

Lower minimum P_O2 caused a significant delay in embryonic development compared to higher minimum P_O2 (MANOVA; F=2.93, d.f.=8, P=0.006); the developmental trajectories of all treatments generally diverged over time as embryos in lower P_O2 treatments experienced slowed development (Fig. 2). Post hoc univariate ANOVAs indicated that embryos in low P_O2 treatments took longer to reach stage 39 (F=3.04, d.f.=4, P=0.0265; Fig. 3A) and to hatch (F=6.02, d.f.=4, P=0.0006; Fig. 3B) than those in higher P_O2 treatments. Additionally, embryos in lower minimum P_O2 tended to hatch at an earlier stage of development (Kruskal–Wallis; H=18.789; P=0.001; Fig. 3C).

View larger version (12K): [in this window] [in a new window]   Fig. 2. Daily developmental differences among treatments. Lines terminate on the day the first embryo hatched in each treatment. Values are means ± s.e.m.; N=50. Reference lines at stages 32 and 38 facilitate recognition of the divergence of developmental trajectories among treatments. At stage 32, embryos in the 18.8 kPa treatment were approximately 1 day in development ahead of embryos in the 1.8 kPa treatment, whereas at stage 38 this difference had increased to 4 days.

View larger version (9K): [in this window] [in a new window]   Fig. 3. Effect of minimum PO2 on days to stage 39 (A), days to hatching (B), and stage at hatching (C). Values are means ± s.e.m., N=50. Lower nightly PO2 caused slowed development (A), delayed hatching (B), and developmentally premature hatching (C).

View larger version (4K): [in this window] [in a new window]   Fig. 4. Effect of minimum PO2 on increase in egg capsule inner radius (ri). Filled circles, mean proportional increase from the beginning of the experiment to day 8; open circles, mean increase from the beginning of the experiment to stage 39. Values are means ± s.e.m.; N=50. The degree of increase in ri was not significantly different among PO2 treatments.

	Discussion

TOP Summary Introduction Materials and methods Results Discussion References

Chronic hypoxia slowed development and caused embryos to hatch later and less developed at P_O23–4 kPa in A. maculatum and A. annulatum (Mills and Barnhart, 1999). We similarly observed a significant developmental deceleration resulting in delayed, yet developmentally premature hatching, particularly at minimum P_O2 levels 3.1 kPa (Fig. 3), albeit in our study the differences among treatments were less pronounced, likely due to intermittent normoxia. These results suggest that _O2 limitation by P_O2 in these treatments was substantial enough to cause detectable changes in development.

The P_O2 at which embryonic _O2 is limited and becomes P_O2 dependent is the critical P_O2 (P_c) (Burggren, 1998; Seymour and White, 2006). The _O2 of embryos exposed to P_O2>P_c is insensitive to P_O2 fluctuation. However, the _O2 of embryos exposed to P_O2<P_c decreases, and thus their developmental trajectories should be altered from those seen when P_O2>P_c. Because _O2 increases throughout development (Seymour and Bradford, 1987; Seymour and Roberts, 1991), it is logical that

P_c would increase in concert. Consequently, embryos in lower minimum P_O2 become _O2 limited earlier and for a larger portion of their development than embryos in higher minimum P_O2. Furthermore, the limitation will be more severe in that _O2 will be forced to decrease further with decreasing P_O2. As a result, the developmental trajectories of embryos in differing P_O2 fluctuations diverge through time (Fig. 2).

The finding that time and stage at hatching are significantly affected by slowed development at 3–4 kPa is ecologically relevant based on P_O2 measurements within A. maculatum egg masses (Pinder and Friet, 1994). In normoxic water, eggs 15–24 mm from the surface may experience nightly P_O24 kPa during middle development (Harrison stages 29–33). During late development (stages 38–43), this limiting P_O2 may be characteristic of eggs 8–15 mm from the surface. When in hypoxic water, typical of a eutrophic shallow pond at night, eggs even closer to the surface would experience limiting P_O2. Therefore, we would expect embryos near the center of an egg mass to exhibit delayed, yet developmentally premature hatching, which can reduce larval survival (Mills and Barnhart, 1999), reduce competitive ability (Smith, 1990), and increase the risk of predation (Petranka et al., 1987; Sih and Moore, 1993). This scenario resembles that of some marine invertebrates that also deposit their eggs in solid or near-solid gelatinous masses with sharply falling P_O2 gradients toward the center. In egg masses of the sea slug Melanochlamys diomedea and the polychaete worm Nereis vexillosa, delayed development of the innermost embryos results in hatching asynchrony (Chaffee and Strathmann, 1984; Cohen and Strathmann, 1996). Booth (Booth, 1995) observed aggrandized hatching asynchrony in the sand snail Polinices sordidus; peripheral embryos developed normally and hatched after 4 days, while those near the core of the mass delayed or even arrested development and hatched in 16–17 days.

Egg capsule conductance
We removed the common outer jelly matrix that surrounds A. maculatum eggs, which allowed us to precisely control ambient P_O2. The removal of this outer matrix alters both r_o and L, but r_i, the variable to which G_O2 is most sensitive when the egg capsule is relatively thick (Seymour, 1994), remains unchanged. The r_i (and thus G_O2) of egg capsules increased in our study, as was expected, but the amount of increase was not affected by hypoxia (Fig. 4). The lack of difference among treatments suggests that intermittent hypoxia does not elicit a compensatory change in G_O2 in A. maculatum. However, N. E. Mills did observe differences in r_i of egg capsules between chronic P_O2 treatments in the Mills and Barnhart study (Mills and Barnhart, 1999), but they were not quantified. This observation makes us hesitant to conclude that A. maculatum lacks the ability to manipulate G_O2.

The lack of a response is not consistent with the results seen in other ambystomatids exposed to chronic hypoxia. G_O2 of A. annulatum and A. talpoideum eggs increased greater in response to chronic low P_O2 than did that of eggs exposed to normoxia (Mills et al., 2001). However, consistent with the results of our study, Seymour et al. (Seymour et al., 1991) found that G_O2 in Pseudophryne bibroni eggs did not respond to hypoxia. They speculated that there should be little selective advantage in changing G_O2 for P. bibroni because their eggs are incubated in air. This same logic may also apply to A. maculatum in that the algae provide enough oxygen to minimize the selective advantage of changing G_O2.

The mechanism of increasing G_O2 has not been determined, but there is evidence that it is accomplished through manipulation of the osmotic gradient between the inner vitelline fluid and the surrounding water (Salthe, 1965; Seymour and Bradford, 1987). Ultimately, understanding the mechanism of G_O2 increase and its associated energetic cost, if any, would help elucidate the finding that intermittent hypoxia did not elicit an amplified G_O2 increase in A. maculatum. During this experiment, we assumed that changing G_O2 is an adaptive response to hypoxia on the part of the embryo. However, it is possible that it is not adaptive, but is rather an unrelated consequence of changes that take place in the embryo, such as alteration of metabolic pathways.

Finally, this study used r_i as a surrogate for G_O2, and ignored any changes in Krogh's coefficient of oxygen diffusion (K_O2) that could have occurred during incubation. K_O2 measures the permeability of the jelly capsule to oxygen, and is constant at a given temperature for a given medium (Seymour, 1994). However, there is no a priori reason to assume that the egg capsule material retains the same diffusive properties throughout incubation. In fact there is some evidence that it may change through time as the egg capsule slowly loses its integrity in A. talpoideum (Mills et al., 2001). If K_O2 does indeed change, we may be underestimating the change in G_O2 that takes place during development. Further studies are needed to fully understand the effects of hypoxia on G_O2.

In summary, naturally occurring intermittent hypoxia slows development of A. maculatum, causing delayed, yet developmentally premature hatching. In addition, intermittent hypoxia in our study did not elicit an amplified G_O2 increase, which was seen in other ambystomatids as a compensatory response to chronic hypoxia. These results can be applied to a natural setting; the treatments we provided are comparable to natural P_O2 fluctuations caused by the presence of O. amblystomatis within egg masses. Embryos near the center of egg masses experience the lowest nightly P_O2. Thus, they can be expected to experience slowed development, causing them to hatch later and be less developed than those embryos on the periphery. However, the guarantee of intermittent normoxia or even hyperoxia seems to eliminate the necessity to compensate for nightly hypoxia by amplifying G_O2. Further research is needed to understand the mechanisms used to modify G_O2. Also, the generality of these results needs to be determined for multiple A. maculatum populations as well as other aquatic anamniotic vertebrates.

List of abbreviations

AS

percent of air saturation

ESA

effective surface area of the egg capsule

G_O2

oxygen conductance

K_O2

Krogh's coefficient of oxygen diffusion

L

egg capsule thickness

P_c

critical P_O2

P_O2

partial pressure of oxygen

r_i

egg capsule inner radius

r_o

egg capsule outer radius

_O2

rate of oxygen consumption

	Acknowledgments

 
This undergraduate study was funded by the Ronald E. McNair Post-Baccalaureate Achievement Program and Harding University. M. Plummer provided laboratory space. E. Valls assisted with general laboratory duties and with data collection. C. Barnhart, M. Plummer, and two anonymous reviewers provided valuable input on the manuscript.

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