Life in the Open Ocean. Joseph J. Torres
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Название: Life in the Open Ocean
Автор: Joseph J. Torres
Издательство: John Wiley & Sons Limited
Жанр: Биология
isbn: 9781119840312
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Figure 2.22 Oxygen consumption rate of the lophogastrid Gnathophausia ingens as a function of oxygen concentration (in milliliters of oxygen per liter). Open circles represent a single very active animal; closed circles represent the mean of 23 runs with 8 individuals; closed triangles represent a single non‐swimming animal. The vertical lines represent plus or minus one standard deviation.
Source: J. J. Childress, Oxygen minimum layer: vertical distribution and respiration of the mysid 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, СКАЧАТЬ