Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
Sci Rep
2018 Jan 12;81:642. doi: 10.1038/s41598-017-19132-w.
Show Gene links
Show Anatomy links
Effects of larvae density and food concentration on Crown-of-Thorns seastar (Acanthaster cf. solaris) development in an automated flow-through system.
Uthicke S
,
Liddy M
,
Patel F
,
Logan M
,
Johansson C
,
Lamare M
.
???displayArticle.abstract???
Coral-eating Crown-of-Thorns Sea stars (Acanthaster spp.) are major contributors to coral reef loss in the Indo-Pacific region. A release from food limitation of their planktotrophic larvae through enhanced pelagic productivity is one of the main hypothesis explaining population outbreaks (''nutrient limitation hypothesis''). To improve the understanding of these outbreaks we developed an automated flow- through larvae rearing system that maintained food (microalgae) at set levels over the course of four 15d experiments. This resulted in stable food concentrations in experimental tanks. Increased algae concentrations had a significant positive effect on larval development and size at 10 and 15 days post fertilization (dpf). Larvae densities had no effect at 10 dpf. At 15 dpf greater larvae densities were associated with declines in larvae size. Larval development was slowed under higher larvae densities. Thus, the effects of algae concentration and larvae density were additive at 15 dpf, with larvae under low densities at a given algae concentration being further developed than those under higher densities. The development of a flow-through system gives greater insight into the effect of algae and larvae concentrations on Acanthaster development, and the system can be applied to further test the nutrient-limitation hypothesis for present and future outbreaks.
Figure 1. The modelled (see Table 2) proportion of larvae developed to mid-brachiolaria stage at 10 days post fertilisation. Confidence intervals derived from bootstrap (Nâ=â1000) analysis, dots represent partial residuals at the tank level derived from the model.
Figure 2. The modelled (see Table 2) proportion of larvae developed to late-stage Brachiolaria at 15 days post fertilisation. Confidence intervals derived from bootstrap (Nâ=â1000) analysis, dots represent partial residuals at the tank level derived from the model.
Figure 3. Modelled larvae length (A,B), width (C,D) and ratio (E,F) against algae concentration and larvae density of Acanthaster cf. solaris larvae 10 days post fertilisation. Confidence intervals derived from bootstrap (Nâ=â1000) analyses, dots represent partial residuals at the tank level derived from the model.
Figure 4. Modelled larvae length (A,B), width (C,D) and ratio (E,F) against algae concentration and larvae density of Acanthaster cf. solaris larvae 15 days post fertilisation. Confidence intervals derived from bootstrap (Nâ=â1000) analyses, dots represent partial residuals at the tank level derived from the model.
Figure 5. The percentage of larvae settling in different treatment conditions at the end of experiment 3 in 2015 and 2016. Well plates were used for settlement (nâ=â12 wells, except for the high chlorophyll treatment in experiment 3 in 2015 where nâ=â11).
Bolker,
Generalized linear mixed models: a practical guide for ecology and evolution.
2009, Pubmed
Bolker,
Generalized linear mixed models: a practical guide for ecology and evolution.
2009,
Pubmed
Brodie,
Are increased nutrient inputs responsible for more outbreaks of crown-of-thorns starfish? An appraisal of the evidence.
2005,
Pubmed
,
Echinobase
De'ath,
The 27-year decline of coral cover on the Great Barrier Reef and its causes.
2012,
Pubmed
,
Echinobase
Hart,
Functional Consequences of Phenotypic Plasticity in Echinoid Larvae.
1994,
Pubmed
,
Echinobase
Lamare,
In situ developmental responses of tropical sea urchin larvae to ocean acidification conditions at naturally elevated pCO2 vent sites.
2016,
Pubmed
,
Echinobase
Osborne,
Disturbance and the dynamics of coral cover on the Great Barrier Reef (1995-2009).
2011,
Pubmed
,
Echinobase
Uthicke,
Climate change as an unexpected co-factor promoting coral eating seastar (Acanthaster planci) outbreaks.
2015,
Pubmed
,
Echinobase
Uthicke,
Outbreak of coral-eating Crown-of-Thorns creates continuous cloud of larvae over 320 km of the Great Barrier Reef.
2015,
Pubmed
,
Echinobase
Uthicke,
Impacts of ocean acidification on early life-history stages and settlement of the coral-eating sea star Acanthaster planci.
2013,
Pubmed
,
Echinobase
Vogler,
Phylogeography of the crown-of-thorns starfish in the Indian Ocean.
2012,
Pubmed
,
Echinobase
Vogler,
A threat to coral reefs multiplied? Four species of crown-of-thorns starfish.
2008,
Pubmed
,
Echinobase
Wolfe,
Larval starvation to satiation: influence of nutrient regime on the success of Acanthaster planci.
2015,
Pubmed
,
Echinobase
Wolfe,
Superstars: Assessing nutrient thresholds for enhanced larval success of Acanthaster planci, a review of the evidence.
2017,
Pubmed
,
Echinobase