Life in the Open Ocean. Joseph J. Torres
Gnathophausia ingens, Science, 1968, Vol 160, Issue 3833, figure 1 (p. 1242). Reprinted with permission from AAAS.
Gnathophausia ingens has been the subject of several detailed studies by Childress and his students. Their studies paint a very complete picture of how the species copes with low oxygen. Rather than any exotic adaptations, such as unusual new respiratory structures, Gnathophausia has achieved its ability to thrive in the OMZ by very highly developed gas‐exchange and circulatory systems. Six major adaptations have been noted. First, G. ingens has a very high ventilation volume; that is, it can move a considerable amount of water over its gills per unit time: up to 81 kg min−1 (Figures 2.23 and 2.24). Second, it is very efficient at removing oxygen from the ventilatory stream, even when that stream is moving very rapidly over the gills. This property is known as the % utilization of oxygen and in Gnathophausia it can be as high as 90% (Figures 2.23 and 2.24). That high % utilization is achieved through its third, fourth, and fifth adaptations: a very high gill surface area to maximize the possibility for exchange (9–14 cm2 g−1 wet mass); a minimal diffusion distance in the gill filaments themselves (1.5–2.5 μm) to minimize the barrier for oxygen diffusion into the blood (very unusual for Crustacea); and a very effective blood pigment (hemocyanin) capable of taking up oxygen at very low concentrations (50% saturated at 0.19 kPa). A well‐developed circulatory system rounds out the suite of adaptations with the capability of delivering 225 ml kg−1 min−1.
Figure 2.23 Oxygen consumption rate, percent utilization of oxygen, and ventilation volume in Gnathophausia ingens as a function of oxygen partial pressure, mean of eight runs. Solid line represents oxygen consumption rate; dotted line represents % utilization; dashed line depicts measured ventilation volume; dot‐dash line is calculated ventilation volume.
Source: Figure 4 from Childress (1971), Biol. Bull. 141: 114. Reprinted with permission from the Marine Biological Laboratory, Woods Hole, MA.
Figure 2.24 Relationship between percent utilization and ventilation volume in Gnathophausia ingens utilizing the values given in Figure 2.23.
Source: Figure 5 from Childress (1971), Biol. Bull. 141: 115. Reprinted with permission from the Marine Biological Laboratory, Woods Hole, MA.
No other oxygen‐minimum‐layer species has been examined as well as G. ingens. Taken together, the several studies on the species’ respiratory physiology paint a complete picture of how it is possible to survive at vanishingly low oxygen concentrations. Nonetheless, a few pieces of the puzzle have been collected in other taxa to suggest that elements of the suite have been employed by other species to achieve the same end. The most important characteristic to look for is a Pc at or below the lowest PO2 encountered in nature. That characteristic has been observed in many of the Crustacea living in the oxygen minimum in the California borderland (8 mm Hg, Childress 1975; Childress and Seibel 1998). It has also been seen in at least one crustacean dwelling in the Eastern Tropical Pacific where the oxygen minimum layer is as low as 3 mm Hg O2: the galatheid red crab Pleuroncodes planipes with a Pc of 3 mm Hg (Quetin and Childress 1976).
Once an individual reaches its Pc, it responds behaviorally and metabolically. Since metabolism scales positively with activity level, activity is minimized, precipitously dropping metabolic demand for ATP. Any ATP deficit resulting from the inability to meet its needs aerobically must be made up by anaerobic glycolysis. The hypoxia‐induced drop in activity resulting in lowered ATP demand is termed metabolic suppression (Seibel 2011; Seibel et al. 2016) and is not confined to pelagic fauna. It is the first weapon any species can wield to reduce the demand for ATP and is exploited by intertidal species, such as bivalves, during low tide exposure (Hochachka and Somero 1984; Hochachka and Guppy 1987).
Pelagic cephalopods dwelling in the California oxygen minimum also exhibit low Pcs (3–7 mm Hg, Seibel et al. 1999). Data were collected from the vampire squid Vampyroteuthis infernalis, a fulltime resident of the California borderland’s oxygen minimum zone, on two characteristics of the “Gnathophausia suite”: gill diffusion capacity and blood pigment efficiency (Table 2.4). The diffusion capacity, DGO2, and oxygen affinity, P50, of Vampyroteuthis shown in Table 2.4 are indicative of a highly efficient gas‐exchange surface and a blood pigment capable of binding oxygen at extremely low concentrations. Both are quite close to those of Gnathophausia, suggesting that, with respect to these two important physiological characteristics, the species are employing a common strategy. Data from the other cephalopod species in Table 2.4 show substantially lower gill diffusion capacity and oxygen affinity in the species inhabiting more normoxic environments.
Vampyroteuthis has a much lower metabolic rate than Gnathophausia. On a mass‐specific basis, the vampire squid’s respiratory rate is a little less than 10% that of G. ingens. On one hand, Vampyroteuthis’ lower rate makes the job of the respiratory system a little easier because the absolute amount of oxygen required per unit time is less. On the other, because of the physics of diffusion it makes little difference, the oxygen gradient between environment and organism is still a tiny one. What might be expected, a priori, in Vampyroteuthis would be a lower capability for removing oxygen in quantity. Adaptations such as very high gill surface area and a highly developed circulatory system, important for delivering oxygen in quantity to satisfy tissue demands, would likely be less in evidence. For at least one of those characteristics, gill surface area, this appears to be the case; Vampyroteuthis has only a moderate gill surface area relative to other cephalopods (Madan and Wells 1996; Seibel et al. 1999).
Table 2.4 Metabolism (VO2 = ml O2 kg−1 min−1), gill diffusion capacity (DGO2 = ml O2 kg−1 kPa−1 min−1), blood‐water oxygen gradient (∆Pg = VO2/(DGO2; in kPa) and hemocyanin‐oxygen affinity (P50 = PO2 in kPa at 50% hemocyanin‐oxygen saturation) of Vampyroteuthis ingernalis in comparison to other cephalopods. Data for the lophogastrid crustacean, Gnathophausia ingens, are also shown.
Source: Reprinted by permission from Springer Nature Customer Service Centre GmbH: Springer Nature, Experimental Biology Online, Vampire Blood: respiratory physiology of the vampire squid (Cephalopoda: Vampyromorpha) in relation to the oxygen minimum layer, Seibel et al. (1999).
| Species | VO2 a | DGO2 | ∆Pg | P50 b |
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