Modelling growth and reproduction of Antarctic krill, Euphausia superba, based on temperature, food and resource allocation amongst life history functions

2017 ◽  
Vol 75 (2) ◽  
pp. 738-750 ◽  
Author(s):  
Andrew John Constable ◽  
So Kawaguchi

Abstract Estimates of productivity of Antarctic krill, Euphausia superba, are dependent on accurate models of growth and reproduction. Incorrect growth models, specifically those giving unrealistically high production, could lead to over-exploitation of the krill population if those models are used in setting catch limits. Here we review available approaches to modelling productivity and note that existing models do not account for the interactions between growth and reproduction and variable environmental conditions. We develop a new energetics moult-cycle (EMC) model which combines energetics and the constraints on growth of the moult-cycle. This model flexibly accounts for regional, inter- and intra-annual variation in temperature, food supply, and day length. The EMC model provides results consistent with the general expectations for krill growth in length and mass, including having thin krill, as well as providing insights into the effects that increasing temperature may have on growth and reproduction. We recommend that this new model be incorporated into assessments of catch limits for Antarctic krill.

BMC Genomics ◽  
2010 ◽  
Vol 11 (1) ◽  
Author(s):  
Paul J Seear ◽  
Geraint A Tarling ◽  
Gavin Burns ◽  
William P Goodall-Copestake ◽  
Edward Gaten ◽  
...  

2012 ◽  
Vol 36 (2) ◽  
pp. 300
Author(s):  
Peng-xiang XU ◽  
Ying-chun LI ◽  
Guo-ping ZHU ◽  
Hui XIA ◽  
Liu-xiong XU

1982 ◽  
Vol 33 (1) ◽  
pp. 71 ◽  
Author(s):  
T Ikeda ◽  
P Dixon

Live E. superba were transported from Antarctic waters to a tropical laboratory where observations at the temperature of -0.5�C (0 to - 1.0�C), were made of intermoult period of specimens fed a mixture of microalgae (Dunaliella tertiolecta and Phaeodactylum tricornutum) or artificial pet fish food or starved. Mean intermoult period was 26.4-27.1 days for fed specimens and 29.6 days for starved specimens, with no relation to the size of specimens. The moult accounted for a loss of 2.63-4.35% of animal dry weight, which is equivalent to 1.1-1.8% of animal nitrogen or 1.4-2.3% of animal carbon. The contribution of moults to detritus in the Antarctic Ocean was estimated as 0.11 g C m-2 per year.


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