青蟹幼期投喂天然食物Phronima sp.和Artemia salina的RNA/DNA比值性能研究

Sri Mulyani, Erni Indrawati, Syamsul Bahri
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摘要

鱼苗的可得性和质量是蓝蟹养殖的主要问题,其幼虫期死亡率高。RNA/DNA比值是评价蟹苗质量的参数之一,包括健康、营养和生长条件。本研究旨在分析phonima sp.作为盐渍蒿(Artemia salina)的替代饲料,在养殖池养殖前对青蟹(crablet 5)幼期RNA/DNA比值性能的影响。该研究于2023年2月在Takalar咸淡水养殖渔业中心(BPBAP)的螃蟹孵化场进行。本研究采用定量实验完全随机设计(CRD), 5个处理,3个重复。蒿属植物与蒿属植物的比例为:处理A 100%蒿属植物;B组100%蒿属;C组75%青蒿素和25%青蒿素;D处理:25%青蒿素和75%青蒿素;E:青蒿75%+青蒿25%。结果表明,与单独饲料(100%的Phronima sp或100%的Artemia salina)相比,盐蒿与Phronima sp的混合饲料提高了蟹的RNA/DNA比率。RNA/DNA比值最高的饲料组合为处理E (Phronima sp. 25% + Artemia salina 75%), RNA/DNA比值为2.02 +0.032 ng/µL。
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RNA/DNA Ratio Performance of Blue Swimming Crab (Portunus pelagicus) Fed with Natural Food Phronima sp. and Artemia salina in Juvenile Phase
The availability and quality of fry is a major problem in blue swimming crab aquaculture, with the high mortality at the larval stage. RNA/DNA ratio is one of the parameters that can be used to evaluate the quality of crab fry, including health, nutrition, and growth conditions. This study aims to analyze the effect of Phronima sp. as a substitute feed for Artemia salina on the RNA/DNA ratio performance of blue swimming crab in juvenile phase (crablet 5) during rearing before cultivation in aquaculture ponds. This research was conducted at the Crab Hatchery Unit of the Brackish Water Aquaculture Fisheries Center (BPBAP) Takalar in February 2023. The study used a quantitative experimental completely randomized design (CRD) with five treatments and three repetitions. The ratio of Phronima sp. and Artemia sp. used were: Treatment A 100% Phronima sp; Treatment B 100% Artemia sp; Treatment C 75% Phronima sp and 25% Artemia sp; Treatment D 25% Phronima sp and 75% Artemia sp.; and E: Phronima 75%+Artemia salina 25%. The results showed that Artemia salina combined with Phronima sp. increased the RNA/DNA ratio of the crab compared to a single feed (100% Phronima sp. or Artemia salina 100%). The feed combination with the highest RNA/DNA ratio was shown in treatment E (Phronima sp. 25% + Artemia salina 75%) with an RNA/DNA ratio of 2.02 +0.032 ng/µL.
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