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J Exp Biol
2016 May 01;219Pt 9:1303-10. doi: 10.1242/jeb.129502.
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Ontogenetic changes in larval swimming and orientation of pre-competent sea urchin Arbacia punctulata in turbulence.
Wheeler JD
,
Chan KY
,
Anderson EJ
,
Mullineaux LS
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Many marine organisms have complex life histories, having sessile adults and relying on the planktonic larvae for dispersal. Larvae swim and disperse in a complex fluid environment and the effect of ambient flow on larval behavior could in turn impact their survival and transport. However, to date, most studies on larvae-flow interactions have focused on competent larvae near settlement. We examined the importance of flow on early larval stages by studying how local flow and ontogeny influence swimming behavior in pre-competent larval sea urchins, Arbacia punctulata We exposed larval urchins to grid-stirred turbulence and recorded their behavior at two stages (4- and 6-armed plutei) in three turbulence regimes. Using particle image velocimetry to quantify and subtract local flow, we tested the hypothesis that larvae respond to turbulence by increasing swimming speed, and that the increase varies with ontogeny. Swimming speed increased with turbulence for both 4- and 6-armed larvae, but their responses differed in terms of vertical swimming velocity. 4-Armed larvae swam most strongly upward in the unforced flow regime, while 6-armed larvae swam most strongly upward in weakly forced flow. Increased turbulence intensity also decreased the relative time that larvae spent in their typical upright orientation. 6-Armed larvae were tilted more frequently in turbulence compared with 4-armed larvae. This observation suggests that as larvae increase in size and add pairs of arms, they are more likely to be passively re-oriented by moving water, rather than being stabilized (by mechanisms associated with increased mass), potentially leading to differential transport. The positive relationship between swimming speed and larval orientation angle suggests that there was also an active response to tilting in turbulence. Our results highlight the importance of turbulence to planktonic larvae, not just during settlement but also in earlier stages through morphology-flow interactions.
Fig. 1. A comparison of the relative size and morphology of the 4- and 6-armed larva. Scale bars (lower right), 100â μm. PO, postoral arm; AL, anterolateral arm. Reported length scales are stomach length, mid-line body length and total length (where total length is defined as the distance from the base of the body to the oral hood, neglecting arm length).
Fig. 2. Larval movement and orientation tracking. (A) Sample experimental image, where an in-focus larva (with arms clearly visible) is highlighted by the white dashed box. Smaller white specks are passive particles and larger diffuse spots are out of focus larvae. (B) Close-up of the highlighted larva, with overlaid particle image velocimetry (PIV) velocity field (white arrows) surrounding it. Passive particle intensity is dimmed for clarity. (C) Sample time series of an individual larva's vertical swimming velocity as it was tracked in the field of view. (D) Close-up of the highlighted larva, with overlaid Cartesian coordinate system and shaded range of angles (â25 to 25Â deg from vertical) at which the larva was considered upright. (E) Sample time series of an individual larva's orientation angle from vertical as it was tracked in the field of view. The shaded region denotes the range of orientation angles at which the larva was considered upright.
Fig. 3. Larval swimming speed and time spent in vertical orientation at different turbulence intensities. (A,B) Median larval swimming speed (Vs) with 95% confidence intervals, with respect to the turbulence regime, for 4-armed larvae (A) and 6-armed larvae (B). (C,D) Median larval vertical swimming velocity (ws) with 95% confidence intervals, with respect to the turbulence regime, for 4-armed larvae (C) and 6-armed larvae (D). (E,F) Mean proportion of time spent by larvae within ±25 deg of the vertical orientation with 95% confidence intervals, with respect to the turbulence regime for 4-armed larvae (E) and 6-armed larvae (F).
Fig. 4. Correlation between swimming speed and orientation angle. (A,B) Track-averaged orientation angle (0 deg is vertical) versus track-averaged swimming speed (Vs; A) and track-averaged vertical swimming velocity (ws; B). Each point represents an individual 6-armed larva, using larvae from all turbulence regimes. (CâF) Probability distribution of track-averaged swimming speed in upright larvae (within ±25 deg of vertical; C) and tilted larvae (outside ±25 deg of vertical; D), and probability distribution of track-averaged vertical swimming velocity in upright larvae (E) and tilted larvae (F). Asterisks denote median speed or velocity for each distribution. Note that the x-axes for the tilted larvae (D and F) are reversed, so that they are mirror images of C and E, respectively.
Chan,
Acidification reduced growth rate but not swimming speed of larval sea urchins.
2015, Pubmed,
Echinobase
Chan,
Acidification reduced growth rate but not swimming speed of larval sea urchins.
2015,
Pubmed
,
Echinobase
Chan,
Biomechanics of larval morphology affect swimming: insights from the sand dollars Dendraster excentricus.
2012,
Pubmed
,
Echinobase
Chan,
Effects of ocean-acidification-induced morphological changes on larval swimming and feeding.
2011,
Pubmed
,
Echinobase
Clay,
Morphology-flow interactions lead to stage-selective vertical transport of larval sand dollars in shear flow.
2010,
Pubmed
,
Echinobase
Cowen,
Larval dispersal and marine population connectivity.
2009,
Pubmed
De Lillo,
Turbulent fluid acceleration generates clusters of gyrotactic microorganisms.
2014,
Pubmed
Durham,
Turbulence drives microscale patches of motile phytoplankton.
2013,
Pubmed
Durham,
Thin phytoplankton layers: characteristics, mechanisms, and consequences.
2012,
Pubmed
Fuchs,
Hydrodynamic sensing and behavior by oyster larvae in turbulence and waves.
2015,
Pubmed
Fuchs,
Active downward propulsion by oyster larvae in turbulence.
2013,
Pubmed
Gaylord,
Turbulent shear spurs settlement in larval sea urchins.
2013,
Pubmed
,
Echinobase
Gustafson,
Serotonin and contractile activity in the echinopluteus. A study of the cellular basis of larval behaviour.
1972,
Pubmed
,
Echinobase
Hadfield,
Rapid behavioral responses of an invertebrate larva to dissolved settlement cue.
2004,
Pubmed
Heyward,
Turbulence, cleavage, and the naked embryo: a case for coral clones.
2012,
Pubmed
Hinegardner,
Growth and development of the laboratory cultured sea urchin.
1969,
Pubmed
,
Echinobase
Kiørboe,
Flow disturbances generated by feeding and swimming zooplankton.
2014,
Pubmed
Levin,
Recent progress in understanding larval dispersal: new directions and digressions.
2006,
Pubmed
McDonald,
Earliest ciliary swimming effects vertical transport of planktonic embryos in turbulence and shear flow.
2012,
Pubmed
,
Echinobase
Metaxas,
Quantifying the "bio-" components in biophysical models of larval transport in marine benthic invertebrates: advances and pitfalls.
2009,
Pubmed
Miller,
Using computational and mechanical models to study animal locomotion.
2012,
Pubmed
Mogami,
Theoretical and experimental dissection of gravity-dependent mechanical orientation in gravitactic microorganisms.
2001,
Pubmed
,
Echinobase
Pechenik,
Larval experience and latent effects--metamorphosis is not a new beginning.
2006,
Pubmed
,
Echinobase
Pennington,
Consequences of the Calcite Skeletons of Planktonic Echinoderm Larvae for Orientation, Swimming, and Shape.
1990,
Pubmed
Roberts,
Geotaxis in motile micro-organisms.
1970,
Pubmed
Schindelin,
Fiji: an open-source platform for biological-image analysis.
2012,
Pubmed
Sodergren,
The genome of the sea urchin Strongylocentrotus purpuratus.
2006,
Pubmed
,
Echinobase
Strathmann,
Good eaters, poor swimmers: compromises in larval form.
2006,
Pubmed
,
Echinobase
Wada,
Modification of ciliary beating in sea urchin larvae induced by neurotransmitters: beat-plane rotation and control of frequency fluctuation.
1997,
Pubmed
,
Echinobase
Zimmer,
Chemical signaling processes in the marine environment.
2000,
Pubmed