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Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging

BACKGROUND: Fluorochrome staining is among the most widely used techniques to study growth dynamics of echinoderms. However, it fails to detect fine-scale increments because produced marks are commonly diffusely distributed within the skeleton. In this paper we investigated the potential of trace el...

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Autores principales: Gorzelak, Przemysław, Dery, Aurélie, Dubois, Philippe, Stolarski, Jarosław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574115/
https://www.ncbi.nlm.nih.gov/pubmed/28855950
http://dx.doi.org/10.1186/s12983-017-0227-8
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author Gorzelak, Przemysław
Dery, Aurélie
Dubois, Philippe
Stolarski, Jarosław
author_facet Gorzelak, Przemysław
Dery, Aurélie
Dubois, Philippe
Stolarski, Jarosław
author_sort Gorzelak, Przemysław
collection PubMed
description BACKGROUND: Fluorochrome staining is among the most widely used techniques to study growth dynamics of echinoderms. However, it fails to detect fine-scale increments because produced marks are commonly diffusely distributed within the skeleton. In this paper we investigated the potential of trace element (manganese) labeling and subsequent cathodoluminescence (CL) imaging in fine-scale growth studies of echinoderms. RESULTS: Three species of sea urchins (Paracentrotus lividus, Echinometra sp. and Prionocidaris baculosa) were incubated for different periods of time in seawater enriched in different Mn(2+) concentrations (1 mg/L; 3 mg/L; 61.6 mg/L). Labeling with low Mn(2+) concentrations (at 1 mg/L and 3 mg/L) had no effect on behavior, growth and survival of sea urchins in contrast to the high Mn(2+) dosage (at 61.6 mg/L) that resulted in lack of skeleton growth. Under CL, manganese produced clearly visible luminescent growth fronts in these specimens (observed in sectioned skeletal parts), which allowed for a determination of the average extension rates and provided direct insights into the morphogenesis of different types of ossicles. The three species tend to follow the same patterns of growth. Spine growth starts with the formation of microspines which are simultaneously becoming reinforced by addition of thickening layers. Spine septa develop via deposition of porous stereom that is rapidly (within less than 2 days) filled by secondary calcite. Development of the inner cortex in cidaroids begins with the formation of microspines which grow at ~3.5 μm/day. Later on, deposition of the outer polycrystalline cortex with spinules and protuberances proceeds at ~12 μm/day. The growth of tooth can be rapid (up to ~1.8 mm/day) and starts with the formation of primary plates (pp) in plumula. Later on, during the further growth of pp in aboral and lateral directions, secondary extensions develop inside (in chronological order: lamellae, needles, secondary plate, prisms and carinar processes), which are increasingly being solidified towards the incisal end. Interradial growth in the ambital interambulacral test plates exceeds meridional growth and inner thickening. CONCLUSIONS: Mn(2+) labeling coupled with CL imaging is a promising, low-cost and easily applicable method to study growth dynamics of echinoderms at the micro-length scale. The method allowed us to evaluate and refine models of echinoid skeleton morphogenesis.
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spelling pubmed-55741152017-08-30 Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging Gorzelak, Przemysław Dery, Aurélie Dubois, Philippe Stolarski, Jarosław Front Zool Research BACKGROUND: Fluorochrome staining is among the most widely used techniques to study growth dynamics of echinoderms. However, it fails to detect fine-scale increments because produced marks are commonly diffusely distributed within the skeleton. In this paper we investigated the potential of trace element (manganese) labeling and subsequent cathodoluminescence (CL) imaging in fine-scale growth studies of echinoderms. RESULTS: Three species of sea urchins (Paracentrotus lividus, Echinometra sp. and Prionocidaris baculosa) were incubated for different periods of time in seawater enriched in different Mn(2+) concentrations (1 mg/L; 3 mg/L; 61.6 mg/L). Labeling with low Mn(2+) concentrations (at 1 mg/L and 3 mg/L) had no effect on behavior, growth and survival of sea urchins in contrast to the high Mn(2+) dosage (at 61.6 mg/L) that resulted in lack of skeleton growth. Under CL, manganese produced clearly visible luminescent growth fronts in these specimens (observed in sectioned skeletal parts), which allowed for a determination of the average extension rates and provided direct insights into the morphogenesis of different types of ossicles. The three species tend to follow the same patterns of growth. Spine growth starts with the formation of microspines which are simultaneously becoming reinforced by addition of thickening layers. Spine septa develop via deposition of porous stereom that is rapidly (within less than 2 days) filled by secondary calcite. Development of the inner cortex in cidaroids begins with the formation of microspines which grow at ~3.5 μm/day. Later on, deposition of the outer polycrystalline cortex with spinules and protuberances proceeds at ~12 μm/day. The growth of tooth can be rapid (up to ~1.8 mm/day) and starts with the formation of primary plates (pp) in plumula. Later on, during the further growth of pp in aboral and lateral directions, secondary extensions develop inside (in chronological order: lamellae, needles, secondary plate, prisms and carinar processes), which are increasingly being solidified towards the incisal end. Interradial growth in the ambital interambulacral test plates exceeds meridional growth and inner thickening. CONCLUSIONS: Mn(2+) labeling coupled with CL imaging is a promising, low-cost and easily applicable method to study growth dynamics of echinoderms at the micro-length scale. The method allowed us to evaluate and refine models of echinoid skeleton morphogenesis. BioMed Central 2017-08-25 /pmc/articles/PMC5574115/ /pubmed/28855950 http://dx.doi.org/10.1186/s12983-017-0227-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Gorzelak, Przemysław
Dery, Aurélie
Dubois, Philippe
Stolarski, Jarosław
Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging
title Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging
title_full Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging
title_fullStr Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging
title_full_unstemmed Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging
title_short Sea urchin growth dynamics at microstructural length scale revealed by Mn-labeling and cathodoluminescence imaging
title_sort sea urchin growth dynamics at microstructural length scale revealed by mn-labeling and cathodoluminescence imaging
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574115/
https://www.ncbi.nlm.nih.gov/pubmed/28855950
http://dx.doi.org/10.1186/s12983-017-0227-8
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