교육데이터 활용•지원 서비스

This dataset consists of one data file presenting data from 4 experiments conducted under aquarium controlled conditions manipulating levels of suspended sediments, temperature and nutrient enrichment. The experiments measured the conditions effect on early life history stages like gamete fertilisation success, embryo development, larval survivorship and larval settlement of the coral Acropora tenuis. The aim of this study was to assess the impacts of different levels of suspended sediments together with temperature or nutrient enrichment and estimate their size effect on different early life history stages of the coral Acropora tenuis and determine the stages that are more vulnerable to the combination of these stressors. Methods: Experiment 1: 5 levels of suspended sediments (0, 5, 10, 30 or 100 mg l-1) were combined with either 3 levels of nutrients (+0, +0.3, or +0.6 mg organic carbon (OC) l-1 filtered sea water (FSW)), or 3 levels of temperature (27, 30, or 32 °C) to produce 30 experimental treatments. For each treatment combination, twelve replicate 50 ml clear polypropylene chambers were prepared, each containing 25 ml of the modified seawater. Eggs were added to half of the chambers (~200 eggs per chamber), and sperm aliquots to the other half. Chambers were transferred into temperature incubators at the designated temperature. After 30 min, sperm and egg chambers were combined to initiate fertilisation, resulting in a total of 180 chambers across the 30 treatments (6 per treatment). The final sperm concentration was 5 × 104 ml-1. Chambers were returned into incubators, and gently shaken every 30 minutes to maintain sediments suspended. When the second cleavage was observed (1.5 h after fertilisation), 2 ml of zinc formalin fixative were added to terminate embryo development. Fertilisation success (proportion of eggs fertilised) was assessed under a stereomicroscope. Where NA, sample loss occurred due to spill out from the 50 ml clear polypropylene chambers during incubation. Experiment 2: Embryos fertilised under control conditions were exposed to the 30 treatment combinations from the early gastrula stage (8-h old) until they were ciliated larvae (~36-h old). Six water baths (400 l) were used to maintain seawater temperatures. For each treatment, four replicate experimental systems were set up and -250 embryos added to each experimental tank. Suspended sediment concentrations were derived from turbidity readings taken every 6 h in each experimental tank. After 28 h larvae were transferred to six-well polystyrene tissue culture plates maintained at 27 °C in a temperature-controlled room. Each well contained 10 ml FSW at 27 °C and ~10 larvae (n = 24 wells for each suspended sediment and nutrient enrichment combination, and n = 12 wells for each suspended sediment and temperature combination). When larvae where 5-d old, 2-mm2 chips of live crustose coralline algae (CCA) Porolithon onkodes were added to induce larval settlement. After 24 h, the number of settled larvae in each well was recorded. Where NA, sample loss occurred due to spill out from the 50 ml clear polypropylene chambers prior to estimating settlement success. Experiment 3: For each of the 30 treatment combinations, six replicate 100 ml clear polystyrene chambers were prepared containing 80 ml of the appropriately modified seawater and 3-d old larvae (n = 20 larvae per replicate). Chambers were placed in mechanical rollers to keep sediments suspended. Rollers were kept in temperature incubators to maintain target temperatures. Larvae were exposed to treatment conditions for 48 h, with one water change after 24 h. After exposure, larvae from each replicate were counted and transferred to six-well polystyrene tissue culture plates For experiment 3a, 7 replicates with 20 larvae each were used while experiment 3b had 14 replicates with 10 larvae each. CCA chips were added to each well and settlement success was assessed after 24 h. Where NA, sample loss