Cage colour and post-harvest K+ concentration affect skin colour of Australian snapper Pagrus auratus (Bloch & Schneider, 1801)

In an attempt to improve post-harvest skin colour in cultured Australian snapper Pagrus auratus , a two-factor experiment was carried out to investigate the effects of a short-term change in cage colour before harvest, followed by immersion in K + -enriched solutions of different concentrations. Snapper supplemented with 39 mg unesterified astaxanthin kg −1 for 50 days were transferred to black (for 1 day) or white cages (for 1 or 7 days) before euthanasia by immersing fish in seawater ice slurries supplemented with 0, 150, 300, 450 or 600 mmol L −1 K + for 1 h. Each treatment was replicated with five snapper (mean weight=838 g) held individually within 0.2 m 3 cages. L* , a* and b* skin colour values of all fish were measured after removal from K + solutions at 0, 3, 6, 12, 24 and 48 h. After immersion in K + solutions, fish were stored on ice. Both cage colour and K + concentration significantly affected post-harvest skin colour ( P 0.05), and there was no interaction between these factors at any of the measurement times ( P> 0.05). Conditioning dark-coloured snapper in white surroundings for 1 day was sufficient to significantly improve skin lightness ( L* ) after death. Although there was no difference between skin lightness values for fish held for either 1 or 7 days in white cages at measurement times up to 12 h, fish held in white cages for 7 days had significantly higher L* values (i.e. they were lighter) after 24 and 48 h of storage on ice than those held only in white cages for 1 day. K + treatment also affected (improved) skin lightness post harvest although not until 24 and 48 h after removal of fish from solutions. Before this time, K + treatment had no effect on skin lightness. Snapper killed by seawater ice slurry darkened (lower L* ) markedly during the first 3 h of storage in contrast with all K + treatments that prevented darkening. After 24 and 48 h of storage on ice, fish exposed to 450 and 600 mmol L −1 K + were significantly lighter than fish from seawater ice slurries. In addition, skin redness ( a* ) and yellowness ( b* ) were strongly dependent on K + concentration. The initial decline in response to K + was overcome by a return of a* and b* values with time, most likely instigated by a redispersal of erythrosomes in skin erythrophores. Fish killed with 0 mmol L −1 K + maintained the highest a* and b* values after death, but were associated with darker (lower L* ) skin colouration. It is concluded that a combination of conditioning snapper in white surroundings for 1 day before harvest, followed by immersion in seawater ice slurries supplemented with 300–450 mmol L −1 K + improves skin pigmentation after >24 h of storage on ice.

[1]  Paul L. Jones,et al.  Effect of cage colour and light environment on the skin colour of Australian snapper Pagrus auratus (Bloch & Schneider, 1801) , 2007 .

[2]  S. Chatzifotis,et al.  The effect of different carotenoid sources on skin coloration of cultured red porgy (Pagrus pagrus) , 2005 .

[3]  M. Izquierdo,et al.  Effect of different carotenoid sources and their dietary levels on red porgy (Pagrus pagrus) growth and skin colour , 2005 .

[4]  G. Flik,et al.  Effects of husbandry conditions on the skin colour and stress response of red porgy, Pagrus pagrus , 2004 .

[5]  G. Allan,et al.  Effects of dietary astaxanthin source and light manipulation on the skin colour of Australian snapper Pagrus auratus (Bloch & Schneider, 1801) , 2004 .

[6]  M. Pavlidis,et al.  Background colour influence on the stress response in cultured red porgy Pagrus pagrus , 2003 .

[7]  T. Ohshima,et al.  Effects of Soaking Solutions and Chilling Treatment of Pigment Movements in the Erythrophore of the Red-colored Marine Fish Beryx splendens , 1998 .

[8]  T. Ohshima,et al.  Skin Color Control of the Red Sea Bream (Pagrus major) , 1998 .

[9]  T. Ohshima,et al.  Effect of low temperature treatments on K+-induced melanosome aggregation in melanophores of cultured red sea bream. , 1998 .

[10]  S. Masazumi Morphological color changes in the medaka, Oryzias latipes, after prolonged background adaptation. I: Changes in the population and morphology of melanophores , 1993 .

[11]  R. Fujii Cytophysiology of fish chromatophores , 1993 .

[12]  R. Hardy,et al.  Synthetic astaxanthin deposition in pan-size coho salmon (Oncorhynchus kisutch) , 1992 .

[13]  C. Kitajima,et al.  Studies on Clearance of Black Lines in the Muscle of Cultured Fish. I. Reduction of Black Lines in the Muscle of Cultured Red Sea Bream and Improvement of the Body Color. , 1992 .

[14]  Oshima Noriko,et al.  Pigment aggregation is triggered by an increase in free calcium ions within fish chromatophores , 1988 .

[15]  H. Elwing,et al.  Pigment migration in fish erythrophores is controlled by alpha 2-adrenoceptors. , 1988, Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology.

[16]  R. Fujii,et al.  Control of chromatophore movements in teleost fishes , 1986 .

[17]  T. Kumazawa,et al.  Concurrent releases of norepinephrine and purines by potassium from adrenergic melanosome-aggregating nerve in Tilapia. , 1984, Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology.

[18]  M. Hadley,et al.  Mechanisms controlling pigment movements within swordtail (Xiphophoprus helleri) erythrophores in primary cell culture , 1978 .