Respiration of Lampreys

1980 ◽  
Vol 37 (11) ◽  
pp. 1711-1722 ◽  
Author(s):  
S. V. Lewis

In lampreys, though the gross morphology of the branchial chamber and the method of ventilating the gills are radically different from that found in gnathostomes, the total gill area of larval (1462–2717 mm2∙g−1) and adult (1402–2337 mm2∙g−1) lampreys, the ultrastructure of the gills, and the thickness of the water–blood barrier are similar to active teleosts. The standard rates of oxygen consumption of ammocoetes are low, values for medium-sized Ichthyomyzon hubbsi ranging from 18.1 μL∙g−1∙h−1 at 3.5 °C to 90.1 μL∙g−1∙h−1 at 22.5 °C. The consumption rates increase during metamorphosis rising in Lampetra fluviatilis held at 10 °C from 29.3 to 60.4 μL∙g−1∙h−1, and at the same time a circadian rhythm of consumption develops; maximum rates occur in the dark. Adult lampreys have consumption rates ranging from 66.1 μL∙g−1∙h−1 in L. fluviatilis to 36.9 μL∙g−1∙h−1 in Petromyzon marinus, and Q10's in the temperature range 5–15 °C are from 1.6 to 4.83. Sexually mature males of L. planeri and L. fluviatilis have higher metabolic rates than the females. The active oxygen consumption of P. marinus at 332.5 μL∙g−1∙h−1 is within the range reported for teleosts. Resting ventilation rates are higher in adults than ammocoetes and reach maximum values in sexually mature spawning males. Hypoxia results in an increase in the ventilation and heart rates.Key words: lampreys, respiration; gills, morphology; oxygen consumption, sexual maturity, ventilation rates

2011 ◽  
Vol 214 (15) ◽  
pp. 2512-2521 ◽  
Author(s):  
S. J. M. Hughes ◽  
H. A. Ruhl ◽  
L. E. Hawkins ◽  
C. Hauton ◽  
B. Boorman ◽  
...  

1982 ◽  
Vol 39 (7) ◽  
pp. 1012-1020 ◽  
Author(s):  
Kathleen M. Sullivan ◽  
Kenneth L. Smith Jr.

We measured respiration, growth, ingestion, and excretion rates for sablefish, Anoplopoma fimbria, collected off southern California at a depth of 500 m and maintained in the laboratory. We also measured the water, protein, and lipid content of white skeletal muscle in both laboratory-held and field fish. Sablefish fed a large ration (14% of wet body weight) every 7–10 d showed growth rates two to three times higher than known growth rates for field fish. On a reduced ration (4% of wet body weight) sablefish grew at rates similar to field fish, but white muscle composition varied significantly from field fish. Oxygen consumption rates under constant temperature conditions showed a decrease in the weight-specific oxygen consumption rates with increase in body weight, ranging from routine metabolic rates of 195.8 mg O2∙kg−1∙h−1 for a 0.25-kg fish to 60.8 mg O2∙kg−1∙h−1 for a 2.78-kg fish. Based on measurements of respiration and excretion, sablefish were estimated to have 162 d of energy stored in the body lipids and did not show signs of starvation stress with food deprivation up to 6 mo in the laboratory. Energy allocation shows very slow growth rates, low conversion efficiencies, and low metabolic rates as adjustments made to large, infrequent meals.Key words: physiological responses, benthopelagic fish, growth, metabolic rate, respiration, excretion


Author(s):  
John R. B. Lighton

Measuring oxygen consumption rates in aquatic media is the only practical method for determining the metabolic rates of cell cultures and aquatic organisms. This chapter describes the three principal variations of aquatic respirometry—closed and open system (or flow-through) respirometry, and headspace respirometry—together with procedures for calibrating aquatic respirometry systems, acquiring data from them, and analyzing the resulting data. Appendix 2 describes the operation of the widely used Clark dissolved oxygen electrode, the characteristics of common electrode membrane materials, and necessary routine maintenance. Common problems are discussed and trouble-shooting guides are included.


1973 ◽  
Vol 30 (9) ◽  
pp. 1367-1370 ◽  
Author(s):  
F. W. H. Beamish

The logarithm of standard oxygen consumption of adult Petromyzon marinus increased linearly with the logarithm of weight at each of 5, 10, and 15 C. The proportionate change in standard oxygen consumption for a given change in temperature was independent of size, the mean regression coefficient being 0.949. Standard oxygen consumption for a sea lamprey of fixed weight increased from 52.7 to 124.0 mg/kg per hr over the range 5–20 C with the greatest changes occurring between 10–15 C, 64.5–114.3 mg/kg per hr. Active oxygen consumption was estimated for a few individuals at 10 C and found to be 475.5 mg/kg per hr, within the range reported for teleosts.


2013 ◽  
Vol 4 (1) ◽  
Author(s):  
Beth N. Orcutt ◽  
C. Geoffrey Wheat ◽  
Olivier Rouxel ◽  
Samuel Hulme ◽  
Katrina J. Edwards ◽  
...  

1958 ◽  
Vol 35 (2) ◽  
pp. 383-395
Author(s):  
R. W. EDWARDS

1. The oxygen consumption rates of 3rd- and 4th-instar larvae of Chironomus riparius have been measured at 10 and 20° C. using a constant-volume respirometer. 2. The oxygen consumption is approximately proportional to the 0.7 power of the dry weight: it is not proportional to the estimated surface area. 3. This relationship between oxygen consumption and dry weight is the same at 10 and at 20° C.. 4. The rate of oxygen consumption at 20° C. is greater than at 10° C. by a factor of 2.6. 5. During growth the percentage of dry matter of 4th-instar larvae increases from 10 to 16 and the specific gravity from 1.030 to 1.043. 6. The change in the dry weight/wet weight ratio during the 4 larval instar supports the theory of heterauxesis. 7. At 20° C., ‘summer’ larvae respire faster than ‘winter’ larvae.


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