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RESEARCH ARTICLE
Contents Vol 56(8)

Extracellular fluid volume, urine filtration rate and haemolymph mixing time in the abalone, Haliotis iris Martyn: a comparison of 51Cr-EDTA and 14C-inulin as extracellular markers

H. H. Taylor A B and N. L. C. Ragg A
+ Author Affiliations
- Author Affiliations

A School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand.

B Corresponding author. Email: harry.taylor@canterbury.ac.nz

Marine and Freshwater Research 56(8) 1117-1126 https://doi.org/10.1071/MF05122
Submitted: 15 June 2005  Accepted: 6 October 2005   Published: 22 November 2005

Abstract

Measurement of extracellular fluid volume (ECFV, haemolymph or blood volume) of abalone is important for understanding respiratory and circulatory functions and for investigation of factors affecting meat recovery in the fishery. The compounds 14C-inulin and 51Cr-ethylenediaminetetraacetic acid (EDTA) were evaluated as markers for the determination of ECFV and primary urine formation (filtration) in New Zealand blackfoot abalone or paua, Haliotis iris. The volume of distribution of either marker reliably estimated ECFV after correction for clearance (56.6 ± 3.5 mL 100 g–1 soft tissue). 51Cr-EDTA was cleared from the haemolymph three to five times faster than 14C-inulin and was sequestered in the kidneys, digestive gland and mucous gland. 51Cr-EDTA was therefore unsuitable as a filtration marker. Urine filtration rate was best estimated from the appearance of inulin in the seawater (16.2 ± 2.1 mL 100 g–1 soft tissue day–1). The ECFV (inulin space) of isolated tissues ranged from 12–17 mL 100 g–1 tissue in the digestive gland, foot and adductor muscle to 60–70 mL 100 g–1 tissue in the kidneys, right ctenidium and epipodium. Equalisation of both markers between the efferent ctenidial vein and haemolymph lacunae of the shell adductor muscle occurred extremely slowly (t1/2 ~2 h, t0.95 ~8 h), confirming the poor perfusion of this anaerobic muscle.

Extra keywords: blood volume, circulatory system, EDTA, excretion, Gastropoda, inulin, Mollusca, ultrafiltration, urine.


Acknowledgments

This research was supported by the Marsden Fund of New Zealand (contract UOC 804). We thank Gavin Robinson for technical assistance throughout the project.


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