为优化加纳红树林牡蛎种子生产,分离和评估当地微藻分离物,作为饲养图里巴氏原螯虾幼虫的饲料

IF 1.1 Q3 FISHERIES
Eric Appiah Krampah, Paul Kojo Mensah, Emmanuel Acheampong, Edward Adzesiwor Obodai
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引用次数: 0

摘要

本研究探索了三种本地微藻分离物在实验室饲养实验中作为牡蛎幼虫饲料的潜力,以优化图利荚蒾(Crassostrea tulipa)的种子生产,支持其在西非海岸的大规模养殖。采用系列稀释技术,从西非加纳沿海水域分离出三种当地微藻--罗单孢藻(Rhodomonas sp.)、拟南美藻(Nannochloropsis sp.)和假单孢藻(Pseudanabaena sp.)。在实验室中,通过每天估算细胞密度来评估分离物的生长性能,直到观察到静止期为止。通过估算微藻分离物的生物体积、碳含量和能量含量来确定其特征。微藻的生物体积是根据估算的等效球形直径,采用建议的几何形状和公式计算得出的。碳重量和碳能量含量随后使用推导出的换算公式计算得出。三种微藻分离物显示出了在实验室进行大规模培养的潜力,但细胞密度的日增长率存在明显差异。Nannochloropsis sp.和 Rhodomonas sp.的最高和最低峰值密度分别为 2.4 × 105 和 1.5 × 105 cells mL-1,初始接种细胞密度为 1.05 × 105 cells mL-1。据估计,Rhodomonas sp.、Nannochloropsis sp.和 Pseudanabaena sp.的平均生物体积分别为 238.9、8.182 和 42.42 µm3,相应的衍生碳能量含量分别为 1.7 × 10-6、7.13 × 10-8 和 1.05 × 10-7 J。实验室饲养实验结果表明,单个微藻分离物在不同尺度上支持牡蛎幼体的生长和存活,但三种微藻分离物的混合饲料可促进郁金香幼体的生长和存活。当地的三种微藻分离物--Rhodomonas sp.、Nannochloropsis sp.和 Pseudanabaena sp.--都能很好地适应实验室培养条件,而观察到的以这些藻类食物喂养的牡蛎幼体在生长和存活率上的差异可能是由于不同物种的食物特性和生化成分不同造成的。然而,三种藻类食物的组合为郁金香幼体的最佳生长和存活提供了补充营养。这项研究结果表明,当地的微藻分离物有潜力支持 C. tulipa 的孵化饲养,这对西非商业红树林牡蛎水产养殖的发展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Isolation and evaluation of local microalgal isolates as feed for larval rearing of Crassostrea tulipa towards optimisation of mangrove oyster seed production in Ghana

Isolation and evaluation of local microalgal isolates as feed for larval rearing of Crassostrea tulipa towards optimisation of mangrove oyster seed production in Ghana

This study explored the potential of three local microalgal isolates as feed for oyster larvae in laboratory-rearing experiments, towards the optimisation of seed production of Crassostrea tulipa to support its large-scale farming along the West African coast. Three species of local microalgae—Rhodomonas sp., Nannochloropsis sp. and Pseudanabaena sp.—were isolated from waters off the coast of Ghana, West Africa, following a serial dilution technique. The growth performance of the isolates was assessed in the laboratory through daily estimation of cell density until the stationary phase was observed. Characterisation of the microalgal isolates was carried out by estimation of their biovolume, carbon content and energy content. Biovolumes of the microalgae were calculated from the estimated equivalent spherical diameters using proposed geometric shapes and formulae. Carbon weight and carbon energy content were subsequently calculated using derived conversions. The three microalgal isolates showed potential for large-scale cultivation in the laboratory with marked differences in daily increases in cell densities. Nannochloropsis sp. and Rhodomonas sp. recorded the highest and the lowest peak densities of 2.4 × 105 and 1.5 × 105 cell mL−1, respectively, from an initial inoculating cell density of 1.05 × 105 cell mL−1. The estimated mean biovolumes of Rhodomonas sp., Nannochloropsis sp. and Pseudanabaena sp. were 238.9, 8.182 and 42.42 µm3, respectively, and the corresponding derived carbon energy contents were 1.7 × 10−6, 7.13 × 10−8 and 1.05 × 10−7 J, respectively. Results from a laboratory rearing experiment indicated that the individual microalgal isolates supported the growth and survival of oyster larvae at different scales, but a mixed diet of the three promoted superior growth and survival of C. tulipa larvae. The three local microalgal isolates- Rhodomonas sp., Nannochloropsis sp., and Pseudanabaena sp.- were well adapted to laboratory culture conditions, and the observed differences in growth and survival of the oyster larvae fed on these algal diets could be due to the differences in diet properties and biochemical compositions of the different species. A combination of the three algal diets, however, provided complementaery nutrients for the optimal growth and survival of C. tulipa larvae. The outcome of this study shows that local microalgal isolates have the potential to support hatchery rearing of C. tulipa, which is essential for the development of commercial mangrove oyster aquaculture in West Africa.

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