- Research article
- Open Access
Phenotypic plasticity and morphological integration in a marine modular invertebrate
© Sánchez et al; licensee BioMed Central Ltd. 2007
- Received: 21 November 2006
- Accepted: 24 July 2007
- Published: 24 July 2007
Colonial invertebrates such as corals exhibit nested levels of modularity, imposing a challenge to the depiction of their morphological evolution. Comparisons among diverse Caribbean gorgonian corals suggest decoupling of evolution at the polyp vs. branch/internode levels. Thus, evolutionary change in polyp form or size (the colonial module sensu stricto) does not imply a change in colony form (constructed of modular branches and other emergent features). This study examined the patterns of morphological integration at the intraspecific level. Pseudopterogorgia bipinnata (Verrill) (Octocorallia: Gorgoniidae) is a Caribbean shallow water gorgonian that can colonize most reef habitats (shallow/exposed vs. deep/protected; 1–45 m) and shows great morphological variation.
To characterize the genotype/environment relationship and phenotypic plasticity in P. bipinnata, two microsatellite loci, mitochondrial (MSH1) and nuclear (ITS) DNA sequences, and (ITS2) DGGE banding patterns were initially compared among the populations present in the coral reefs of Belize (Carrie Bow Cay), Panama (Bocas del Toro), Colombia (Cartagena) and the Bahamas (San Salvador). Despite the large and discrete differentiation of morphotypes, there was no concordant genetic variation (DGGE banding patterns) in the ITS2 genotypes from Belize, Panama and Colombia. ITS1–5.8S-ITS2 phylogenetic analysis afforded evidence for considering the species P. kallos (Bielschowsky) as the shallow-most morphotype of P. bipinnata from exposed environments. The population from Carrie Bow Cay, Belize (1–45 m) was examined to determine the phenotypic integration of modular features such as branch thickness, polyp aperture, inter-polyp distance, internode length and branch length. Third-order partial correlation coefficients suggested significant integration between polypar and colonial traits. Some features did not change at all despite 10-fold differences in other integrated features. More importantly, some colonial features showed dependence on modular features.
Consequently, module integration in gorgonian corals can be shifted, switched or canalized along lineages. Modular marine organisms such as corals are variations on a single theme: their modules can couple or decouple, allowing them to adapt to all marine benthic environments.
- Phenotypic Plasticity
- Branch Length
- Internode Length
- Intraspecific Level
- Modular Concept
Important questions in the study of evolution are whether the characteristics of organisms are mutually independent or behave and evolve as integrated systems or modules, and whether the integration of modules can be shifted, switched or canalized along lineages . In modular colonial organisms, which form by the reiteration of identical units, the emergent forms are usually complex networks [2, 3]. Colony form in these invertebrates is a consequence of modular (polyp) replication, and if there is tight integration (e.g. pleiotropy or linkage disequilibrium) among modular and supra-modular traits (e.g. polyp aperture, inter-polyp distance or spacing, branch thickness, internode and branch length), then changes at the module level may lead to changes in colony architecture. Alternatively, different groups of traits may change semi-independently (or conditionally independently) if pressures or developmental mechanisms differ. It has been found that all characters are mutually associated, integration being strongest among the colony level (network) characters, which suggests that branching characters within colonial organisms can be independent of module characters in interspecies comparisons . Nevertheless, the integration or decomposition of modular features at the intraspecific level is unknown in marine modular organisms.
A particular attribute of gorgonian coral colonies is the existence of different levels of nested modularity, such as various types of microscopic sclerites (length variation 0.1–1 mm), polyps that always have eight pinnate tentacles (1–20 mm), and modular branches placed at nearly fixed internodes (1–50 cm), which are all repetitive modules but morphologically fixed features throughout the colony (e.g., [5–7]). Comparative analyses among several Caribbean gorgonians suggest decoupling of evolution at the polyp vs. branch levels . Consequently, evolutionary change in polyp form or size does not imply a change in colony form, or vice versa. These characteristics of marine modular invertebrates are consistent with the modular concept of phenotypic plasticity widely demonstrated in plants . In addition, developmental controls of colony form in gorgonian corals seem different from the traditional axial patterning of most unitary metazoans but are related to allometric changes in growth rate and reproductive onset or heterochrony [2, 7]. These features of astogenetic growth also accord with the view of developmental reaction norms as whole-organism allometric functions (e.g. ), which reveals once again that phenotypic plasticity should be considered a feature of modular traits . Could the modular concept of phenotypic plasticity explain the morphological integration of modularity in marine invertebrates such as corals?
Genetic differences among Pseudopterogorgia bipinnata morphotypes
Plasticity and morphologic integration in Pseudopterogorgia bipinnata
Significance levels among Third-order Partial Correlation Coefficients (PCC) for the five supra-modular variables (below the diagonal) and Bivariate (zero-order) correlation coefficients (above the diagonal). Complete name of variables: Polyp Aperture, Inter Polyp Distance, Thickness, Internode length an Branch lenght (see Fig. 3 for variable distributions and colony location)
The Pseudopterogorgia bipinnata complex provided a good model for exploring phenotypic plasticity and morphological integration at the intraspecific level. P. bipinnata did not show the same pattern of morphological integration found among species, which suggests tight morphological integration of all traits and decoupling of evolution at the levels of polyp (the colonial module sensu stricto) vs. branch/internode (an emergent modular feature produced by colonial growth) . Some features did not change at all despite 10-fold differences in other integrated features; more importantly, some colonial features showed dependence on modular features. The gorgonian corals Pseudopterogorgia bipinnata and P. kallos apparently belonged to the same species (at least phylogenetically), exhibiting remarkable plasticity, particularly in branch and internode lengths. Molecular evidence from nuclear and mitochondrial DNA sequences, as well as two microsatellite loci and ITS2 DGGE banding patterns, corroborated the view that the morphological differences corresponded to phenotypic plasticity. This finding differs from those in other corals (e.g. fire coral, Millepora dichotoma), where the different morphotypes found in different environments are associated with different fixed molecular patterns rather than phenotypic plasticity .
Allometric change during growth is a characteristic of gorgonian coral colonies. It is known that gorgonian colonies tend to spread their branches against unidirectional flow, forming a 2-dimensional network even after transplantation [12, 13]. In essence, most species vary from 3-D bush-like colonies in multidirectional flows to fan-like 2-D networks in environments with unidirectional flow (e.g. ). Other colonial traits such as axial core composition and stiffness differ considerably within species owing to the preferred level of water movement . This is related to gorgonian community structure, where many species overlap totally or partially along an environmental continuum in wave exposure and depth . This change in growth forms and preferences of species may be interpreted as allometric changes that enable resources to be exploited optimally . The observed change in P. bipinnata, in contrast, did not seem to follow a simple continuum allometric pattern but seems to support the modular concept of phenotypic plasticity . An integrated allometric change that produced the nested modularity of gorgonian corals would have to include changes in most traits; but it was clear that some traits changed less than others and one trait, inter-polyp distance, did not change at all across environments.
Traits may differ in their evolutionary constraints, but the rate of change of any one trait may or may not depend on others. For gorgonians, the pattern of phenotypic integration at the intraspecific level showed the same interdependence of branches and internodes as found at the interspecific level, but also showed an integrated loop among branch length and minute "polypar" traits such as branch thickness and polyp aperture. This was not wholly inconsistent with the interspecific pattern of decoupled evolution between the "colonial" vs. "polypar" traits  because despite a more than tenfold change in branch and internode lengths across habitats, interpolyp distance did not correlate (e.g., zero-order PCC) with any other feature, suggesting a decoupled mechanism of change for this trait. The link between micro- and macro-evolutionary changes in the shape of modules and colonies in gorgonian corals may possibly depend on which traits are independent and which are integrated.
When a species trait is invariant in different environments while others show different phenotypic responses, there may be canalization of this particular phenotype. However, it is difficult to determine the level of canalization since different factors may interact from gene expression to morphology, and life history traits to behavior . If the species Pseudopterogorgia bipinnata is divided in two lineages by a geographic barrier, for instance, their descendants could include short and long branched colonies that all have the same inter-polyp distance. On the other hand, inter-polyp distance might undergo a process of decanalization in which plasticity starts to occur under new environmental challenges. It is suggested that canalized traits can attain variability depending on the degree and conditions driving this event . In addition, phenotypic plasticity for some traits can be an adaptive response to new selective pressures (e.g. [18, 19]). The interplay between canalization and morphological integration might be the link from phenotypic plasticity to what we perceive as macroevolution.
One indication of the link between micro- and macro-evolutionary changes could be the interplay among plasticity and integration with genetic variability and assimilation (e.g., , but see ). The link between micro- and macro-evolutionary changes in the branch and polypar features of P. bipinnata seems to be related to constraints on change in some already-fixed features, but implies integration of changes in branch length with other unconstrained traits: inter-polyp distance, which varies widely among species , was constant at the intraspecific level. Moreover, other modular traits, apparently not integrated at the macroevolutionary level, became correlated with branch length at the intraspecific level (Fig. 4).
The three main phenotypes did not exhibit clines and were found in overlapping zones. Although the change of phenotype was apparently independent of genotype, two phenotypes were seldom seen side-to-side sharing the same environment (Fig. 1). This could mean that although this species has characteristic phenotypes at certain depths, there were exceptions where the ancestral, derived or intermediate phenotype could co-exist with a phenotype that was not expected to occur in these conditions. Speculatively, there could be maternal-specific developmental "signals" determining phenotype in marginal environments; or, alternatively, it could be an incipient case of genetic assimilation. It is also important to mention that phenotypic plasticity can show variations in which the population mean and variance change . Therefore, the presence of two morphotypes at the same depth may just be some type of variation occurring in some locations. It would be interesting to have more estimates of these overlapping zones so that more precise conclusions could be drawn. It would be even more desirable to place experimental colonies at in-between depths to see whether there is plasticity, as seems to be the case, or whether a phenotype becomes fixed. Nonetheless, more refined molecular and experimental approaches are needed to evaluate genotypic vs. phenotypic variance.
Module integration within gorgonian coral species can be shifted, switched or canalized along lineages. Marine modular organisms such as corals are variations on a single theme: their modules can couple or decouple, allowing them to adapt to all marine benthic environments. Adaptation to a certain environment does not always mean that the trait is fixed . Ecotypes can make some traits exhibit phenotypic plasticity but are not so extreme as to fix these traits in the species genome (see discussion in ). Nonetheless, genetic assimilation [20, 23] can be a viable event for octocorals, where habitat seems to be a conditioning factor for niche separation. Species that are geographically widely distributed, such as P. bipinnata, also tend to be widely distributed across reef habitats . This trend has been found in many groups of terrestrial organisms (e.g. ). Even so, there is no clear evidence of such a pattern in marine organisms. Phenotypic plasticity costs have been studied and it has been shown that the type of response by the organism determines its viability (e.g. the response of enzymes to the environment has little energetic cost in Stellaria longipes plants: ; see  for plasticity cost models). It remains unclear whether is it better for P. bipinnata to fix a certain phenotype or express it depending on the environment; the costs and benefits of this plasticity have yet to be defined.
Genetic differences among Pseudopterogorgia bipinnata morphotypes and congeners were initially estimated using mitochondrial and nuclear DNA sequences as well as two microsatellite loci allelic variation. Collected specimens were prepared for sclerites observations with compound microscope and a few sclerites were observed with Scanning Electron Microscopy (see methods in ). Mitochondrial sequences comprised the 5' end of msh1 gene using primers by [28, 29] and the nuclear sequences comprised a portion of the tandem array of ribosomal genes including complete ITS1, 5.8S and ITS2 sequences using primers by . DNA extractions were made according to  protocol using CTAB from alcohol preserved material (Ethanol 95%). PCR conditions were followed  and sequencing as in  using the Edge Biosystems kit and sequencing using BigDye 3.1 (AB 3100, capillary electrophoresis automated sequencer). The matrix editing, translation, and alignment for the diverse genes were accomplished using Bioedit  and ClustalW . Phylogenetic analyses were carried out in PAUP*  coupled with Modeltest for maximum likelihood analyses [36, 37]. New sequences were deposited in GENBANK (accession nos. EU04312–EU043127). Predicted RNA secondary structures were modeled for the portion corresponding to the ITS2 following the methods from .
Two heterologous microsatellite loci, Pel74 and Pel1, developed for the sister species Pseudopterogorgia elisabethae Bayer by  were used to assess finer genetic differences among morphotypes. For that purpose, 4 colonies from the Bahamas, 8 from Bocas del Toro (Panama), and 30 from different habitats around Carrie Bow Cay, Belize were screened. DNA extractions we made as above and PCR conditions as suggested by . Microsatellite alleles were visualized using an AB3100, capillary electrophoresis automated sequencer, with fluorescently labeled primers.
In addition, a study of the ITS2 variation among morphotypes and locations was done for 32 colonies from Belize (14), Panama (12), and Colombia (6). The ITS2 region was amplified using primers and protocols from . PCR reactions were separated in a Denaturing Gradient Gel Electrophoresis-DGGE (ABS) containing 8% polyacrilamide, 1× TAE Buffer and linear denaturing gradient from 40% to 80% of Urea and Formamide. Before electrophoresis the gels were pre-run at 60°C and 150 V for 20 min, followed by the electrophoresis at 60°C and 150 V for 9 h. The gels were stained with Ethidium Bromide during 15 min and analyzed using a BIORAD chemidoc system. All the reactions were conducted without CG-clamp.
Plasticity and morphologic integration in Pseudopterogorgia bipinnata were studied using the same traits and methods as in  for 30 colonies collected in the vicinity of Carrie Bow Cay, Belize, between 0.2 and 45 m of water depth (same colonies used for microsatellite loci above). Measurements (10 per colony, 30 colonies, 5 variables), included branch thickness, polyp aperture, inter polyp distance, internode and branch length. Patterns of morphological integration were examined as proposed by  using third-order Partial Correlation Coefficients (PCCs) that were determined among the studied variables .
Special thanks to University of the Andes (Facultad de Ciencias, Department of Biological Sciences), Bogotá, Colombia, a postdoctoral fellowship from the Smithsonian Institution-NMNH (2002–2003), COLCIENCIAS (Grant 120409–16825), National Natural Parks authority in Colombia (UAESPNN, PNNCR-SB), Invertebrate Workshop (2003) at Bocas Research Station, Bocas del Toro, Panama (STRI), Rachel Collin, Gabriel Jácome, La Tortuga Dive Shop (Christian Martinez), Howard Lasker, Klaus Ruetlzer, Stephen Cairns and Carrie Bow Cay, Belize, Smithsonian Station (NMNH-CCRE contribution No. 805).
- Magwene PM: New tools for studying integration and modularity. Evolution. 2001, 55 (9): 1734-1745.View ArticlePubMedGoogle Scholar
- Lasker HR, Sánchez JA: Allometry and Astogeny of modular organisms. Reproductive Biology of Invertebrates. Progress in Asexual Reproduction. Edited by: Hughes RN. 2002, New York: John Wiley, XI: 207-253.Google Scholar
- Lasker HR, Boller ML, Castanaro J, Sánchez JA: Modularity and determinate growth in a gorgonian coral. The Biological Bulletin. 2003, 205: 319-330. 10.2307/1543295.View ArticlePubMedGoogle Scholar
- Sánchez JA, Lasker HR: Patterns of Morphologic Integration in Branching Colonies of Marine Modular Organisms: supra-module organization in Gorgonian Corals. Proceedings of the Royal Society of London B. 2003, 270: 2039-2044. 10.1098/rspb.2003.2471. doi: DOI: 10.1098/rspb.2003.2471View ArticleGoogle Scholar
- Sánchez JA: Evolution and dynamics of branching colonial form in marine modular Cnidarians: Gorgonian Octocorals. Hydrobiologia. 2004, 530 (1): 283-290. 10.1007/s10750-004-2684-2.Google Scholar
- Preston KA, Ackerly DD: Allometry and evolution inmodular organisms. Modularity and Phenotypic Complexity. Edited by: Pigliucci M, Preston KA. 2004, Oxford UniversityPress, 80-106. 5–987Google Scholar
- Sánchez JA, Lasker HR, Nepomuceno EG, Sánchez JD, Woldenberg MJ: Branching and Self-Organization in Marine Modular Colonial Organisms: a Model. The American Naturalist. 2004, 163 (3): E24-39. 10.1086/382139. doi: 0003-0147/2004/16303–20458View ArticlePubMedGoogle Scholar
- de Kroon H, Huber H, Stuefer JF, van Groenendael JM: A modular concept of phenotypic plasticity in plants. New Phytologist. 2005, 166: 73-82. 10.1111/j.1469-8137.2004.01310.x.View ArticlePubMedGoogle Scholar
- Preston KA, Ackerly DD: Allometry and evolution in modular organisms. Modularity and Phenotypic Complexity. Edited by: Pigliucci M, Preston KA. 2004, Oxford University Press, 80-106.Google Scholar
- Sánchez JA, Zea S, Diaz JM: Gorgonian communities of two contrasting environments from oceanic Caribbean atolls. Bulletin of Marine Science. 1997, 61 (2): 61-72.Google Scholar
- Bayer FM: The shallow water Octocorallia of the West Indian region. Stud Fauna Curaçao. 1961, 12: 1-373.Google Scholar
- Meroz-Fine E, Brickner I, Loya Y, Ilan M: The hydrozoancoral Millepora dichotoma: speciation or phenotypic plasticity?. Mar Biol. 2003, 143: 1175-1183. 10.1007/s00227-003-1135-3.View ArticleGoogle Scholar
- Wainwright SA, Dillon JR: On the orientation of sea fans (Genus Gorgonia). Biol Bull. 1969, 136: 130-9. 10.2307/1539674.View ArticleGoogle Scholar
- Weinbauer MG, Velimirov B: Morphological variations inthe Mediterranean Sea fan Eunicella cavolini (Coelenterata, Gorgonacea) in relation to exposure, colony size and colony region. Bull Mar Sci. 1995, 56: 283-295.Google Scholar
- Jordan E, Nugent RS: Evaluación poblacional de Plexaura homomalla en la costa noreste de la Península de Yucatán (Octocorallia). An Centro Cienc Mar Limnol Univ Nal Auton Mexico. 1978, 5: 189-200.Google Scholar
- Lewis JC, Barnowski TF, Telesnicki GJ: Characteristics of Carbonates of Gorgonian Axes (Coelenterata, Octocorallia). Biol Bull. 1992, 183: 278-296. 10.2307/1542215.View ArticleGoogle Scholar
- Kim K, Lasker HR: Small-scale heterogeneity offertilization success in a broadcast spawning octocoral. J Exp Mar Biol Ecol. 1997, 214 (1–2): 107-120.Google Scholar
- Flatt T: The evolutionary genetics of canalization. The quarterly review of biology. 2005, 80: 287-316. 10.1086/432265.View ArticlePubMedGoogle Scholar
- Nussey DH, Postma E, Gienapp P, Visser ME: Selection on heritable phenotypic plasticity in a wild bird population. Science. 2005, 310: 304-306. 10.1126/science.1117004.View ArticlePubMedGoogle Scholar
- Price T, Qvarntröm A, Irwin DE: The role of phenotypic plasticity in driving genetic evolution. Proc R Soc Lond B. 2003, 270: 1433-1440. 10.1098/rspb.2003.2372.View ArticleGoogle Scholar
- Pigliucci M, Murren CJ: Genetic assimilation and a possible evolutionary paradox: can macroevolution sometimes be so fast as to pass us by?. Evolution. 2003, 57: 1455-1464.View ArticlePubMedGoogle Scholar
- de Jong G: Evolution of phenotypic plasticity: patterns of plasticity and the emergence of ecotypes. New Phytologist. 2005, 166 (1): 101-117. 10.1111/j.1469-8137.2005.01322.x.View ArticlePubMedGoogle Scholar
- Fordyce JA: The evolution consequences of ecological interactions mediated through phenotypic plasticity. J Exp Biol. 2006, 209: 2377-2383. 10.1242/jeb.02271.View ArticlePubMedGoogle Scholar
- Pigliucci M, Murren CJ, Schlichting CD: Phenotypic plasticity and evolution by genetic assimilation. J Exp Biol. 2006, 299: 2362-2367. 10.1242/jeb.02070.View ArticleGoogle Scholar
- Brown JH: Macroecology. 1995, University of Chicago Press: ChicagoGoogle Scholar
- Emery RJN, Chinnappa CC, Chmielewski JG: Specialization, plant strategies, and phenotypic plasticity in populations of Stellaria longipes along an elevational gradient. Int J Plant Sci. 1994, 155: 203-219. 10.1086/297160.View ArticleGoogle Scholar
- Ernande B, Dieckmann U: The evolution of phenotypic plasticity in spatially structured environments: implications of intraspecific competition, plasticity costs and environmental characteristics. J Evol Biol. 2004, 17: 613-628. 10.1111/j.1420-9101.2004.00691.x.View ArticlePubMedGoogle Scholar
- Sánchez JA, Cairns SD: An unusual new gorgonian coral from the Aleutian Islands, North Pacific, Alaska. Zool Med. 2004, 78: 265-274.Google Scholar
- France SC, Hoover LL: DNA sequences of the mitochondrial COI gene have low levels of divergence among deep-sea octocorals (Cnidaria: Anthozoa). Hydrobiologia. 2002, 471: 149-155. 10.1023/A:1016517724749.View ArticleGoogle Scholar
- Gutiérrez-Rodríguez C: Reproductive biology of theCaribbean gorgonian Pseudopterogorgia elisabethae and its effects on genetic variation. PhD Thesis. 2003, State University of New York at BuffaloGoogle Scholar
- France SC, Hoover LL: Analysis of variation in mitochondrial DNA sequences (ND3, ND4L, MSH) among Octocorallia (= Alcyonaria) (Cnidaria: Anthozoa). Bull Biol Soc Wash. 2001, 10: 110-118.Google Scholar
- Coffroth MA, Lasker HR, Diamond ME, Bruenn JA, Bermingham E: DNA fingerprints of a gorgonian coral: a method for detecting clonal structure in a vegetative species. Mar Biol. 1992, 114: 317-325. 10.1007/BF00349534.View ArticleGoogle Scholar
- Aguilar C, Sánchez JA: Phylogenetic hypotheses of gorgoniid octocorals according to ITS2 and their predicted RNA secondary structures. Mol Phylogenet Evol. 2007, 43: 774-786. 10.1016/j.ympev.2006.11.005.View ArticlePubMedGoogle Scholar
- Hall TA: BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999, 41: 95-98.Google Scholar
- Higgins DG, Thompson JD, Gibson TJ: Using CLUSTAL for multiple sequence alignments. Methods Enzymol. 1996, 266: 383-402.View ArticlePubMedGoogle Scholar
- Swofford DL: PAUP*: Phylogenetic Analysis Using Parsimony (*and ther methods). Version 4.0b10. 2002, Sunderland, Massachusetts: Sinauer AssociatesGoogle Scholar
- Posada D, Buckley TR: Model selection and model averaging in phylogenetics: advantages of the AIC and Bayesian approaches over likelihood ratio tests. Syst Biol. 2004, 53: 793-808. 10.1080/10635150490522304.View ArticlePubMedGoogle Scholar
- Gutiérrez-Rodriguez C, Lasker HR: Isolation and characterization of microsatellite loci in the Caribbean gorgonian Pseudopterogorgia elisabethae. Molecular Ecology Notes. 2004, 4: 153-155. 10.1111/j.1471-8286.2004.00595.x.View ArticleGoogle Scholar
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