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Ecol Evol
2021 Dec 01;1124:17734-17743. doi: 10.1002/ece3.8247.
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Mechanical defensive adaptations of three Mediterranean sea urchin species.
Voulgaris K
,
Varkoulis A
,
Zaoutsos S
,
Stratakis A
,
Vafidis D
.
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In the Mediterranean, Paracentrotus lividus and Sphaerechinus granularis are important drivers of benthic ecosystems, often coexisting in sublittoral communities. However, the introduction of the invasive diadematoid Diadema setosum, which utilizes venomous spines, may affect these communities. To describe the mechanical properties of the test and spines of these three species, specimens were collected in winter of 2019 from the sublittoral zone of the Dodecanese island complex, southeastern Aegean Sea. This region serves as a gateway for invasive species to the Mediterranean Sea. Crushing test was conducted on live individuals, while 3-point bending test was used to estimate spine stiffness. Porosity and mineralogy of the test and spine, thickness of the test, and breaking length of the spine were measured and compared, while the microstructural architecture was also determined. The test of S. granularis was the most robust (194.35 ± 59.59 N), while the spines of D. setosum (4.76 ± 2.13 GPa) exhibited highest flexibility. Increased porosity and thickness of the test were related to increased robustness, whereas increased flexibility of the spine was attributed to high porosity, indicating that porosity in the skeleton plays a key role in preventing fracture. The spines of S. granularis exhibited highest length after fracture % (71.54 ± 5.5%). D. setosum exhibited higher values of Mg concentration in the test (10%) compared with the spines (4%). For the first time, the mineralogy of an invasive species is compared with its native counterpart, while a comparison of the mechanical properties of different species of the same ecosystem also takes place. This study highlights different ways, in which sea urchins utilize their skeleton and showcases the ecological significance of these adaptations, one of which is the different ways of utilization of the skeleton for defensive purposes, while the other is the ability of D. setosum to decrease the Mg % of its skeleton degrading its mechanical properties, without compromising its defense, by depending on venomous bearing spines. This enables this species to occupy not only tropical habitats, where it is indigenous, but also temperate like the eastern Mediterranean, which it has recently invaded.
FIGURE 1. SEM micrographs of ambital interambulacral plates. (a). External surface of (i) Diadema setosum (scale barâmm, Ã15), (ii) Paracentrotus lividus, and (iii) Sphaerechinus granularis (scale barâ500 μm, Ã30). Notice that the plate of D. setosum possesses a bigger primary tubercle and less secondary ones. Images in circles present the porous stereom of each species (scale barâ50 μm, Ã500). (b). Cross section of the same plates. (i) D. setosum, (ii) P. lividus, and S. granularis (scale barâ50 μm, Ã400). (c). Inner surface of the plates. (i) D. setosum, (ii) P. lividus, and (iii) S. granularis (scale barâ50 μm, Ã400). Vectors indicate the mamelon in each species
FIGURE 2. SEM micrographs of the spines of the three species. (a, d, g) External view of Diadema setosum (scale barâ200 μm, Ã65), Paracentrotus lividus, and Sphaerechinus granularis (scale barâ100 μm, Ã140). (b, e, h) Longitudinal section of D. setosum (scale barâ100 μm, Ã100), P. lividus (scale barâ100 μm, Ã150), and S. granularis (scale barâ100 μm, Ã140). (c, f, i) Cross section of D. setosum (scale barâ200 μm, Ã85), P. lividus (scale barâ100 μm, Ã130), and S. granularis (scale barâ200 μm, Ã85). V, verticillation; L, lumen
FIGURE 3. Error plots of (a): load (N), thickness (mm), and porosity (%) for the tests and (b) of Young's modulus (GPa), breaking length (%), and porosity (%) for the spines of the three species. All data are means, ±2 SE; n = 10. * Indicates the groups with no statistical differences
FIGURE 4. Stressâstrain diagram of one representative spine per species after a threeâpoint bending test. The spines of Diadema setosum and most of the spines of Paracentrotus lividus exhibited linear stress increase and fracture after maximum input. On the contrary, most of the spines of Sphaerechinus granularis exhibited slopes indicating microfractures before the main fracture
FIGURE 5. XRD spectra of the test and spine of Diadema setosum. Notice the three different types of peaks corresponding to different types of Mgâ calcite, according to the Mg concentration in the crystal
Byrne,
Warming influences Mg2+ content, while warming and acidification influence calcification and test strength of a sea urchin.
2014, Pubmed,
Echinobase
Byrne,
Warming influences Mg2+ content, while warming and acidification influence calcification and test strength of a sea urchin.
2014,
Pubmed
,
Echinobase
Casewell,
Complex cocktails: the evolutionary novelty of venoms.
2013,
Pubmed
Di Giglio,
Are control of extracellular acid-base balance and regulation of skeleton genes linked to resistance to ocean acidification in adult sea urchins?
2020,
Pubmed
,
Echinobase
Doube,
BoneJ: Free and extensible bone image analysis in ImageJ.
2010,
Pubmed
Ellers,
Structural Strengthening of Urchin Skeletons by Collagenous Sutural Ligaments.
1998,
Pubmed
,
Echinobase
Lauer,
Strength, elasticity and the limits of energy dissipation in two related sea urchin spines with biomimetic potential.
2018,
Pubmed
,
Echinobase
Lessios,
Population structure and speciation in tropical seas: global phylogeography of the sea urchin Diadema.
2001,
Pubmed
,
Echinobase
Ma,
The grinding tip of the sea urchin tooth exhibits exquisite control over calcite crystal orientation and Mg distribution.
2009,
Pubmed
,
Echinobase
Mongiardino Koch,
A phylogenomic resolution of the sea urchin tree of life.
2018,
Pubmed
,
Echinobase
Motokawa,
Coordination between catch connective tissue and muscles through nerves in the spine joint of the sea urchin Diadema setosum.
2015,
Pubmed
,
Echinobase
Moureaux,
Structure, composition and mechanical relations to function in sea urchin spine.
2010,
Pubmed
,
Echinobase
Reilly,
The development of microcracking and failure in bone depends on the loading mode to which it is adapted.
1999,
Pubmed
Schneider,
NIH Image to ImageJ: 25 years of image analysis.
2012,
Pubmed
Shears,
Marine reserves demonstrate top-down control of community structure on temperate reefs.
2002,
Pubmed
,
Echinobase
Vafidis,
Population Density, Size Structure, and Reproductive Cycle of the Comestible Sea Urchin Sphaerechinus granularis (Echinodermata: Echinoidea) in the Pagasitikos Gulf (Aegean Sea).
2020,
Pubmed
,
Echinobase
Vafidis,
Abundance and population characteristics of the invasive sea urchin Diadema setosum (Leske, 1778) in the south Aegean Sea (eastern Mediterranean).
2021,
Pubmed
,
Echinobase
Varkoulis,
Chemical Composition and Microstructural Morphology of Spines and Tests of Three Common Sea Urchins Species of the Sublittoral Zone of the Mediterranean Sea.
2020,
Pubmed
,
Echinobase
Weber,
Unusual strength properties of echinoderm calcite related to structure.
1969,
Pubmed
,
Echinobase
Weiner,
Organic matrixlike macromolecules associated with the mineral phase of sea urchin skeletal plates and teeth.
1985,
Pubmed
,
Echinobase