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.
Ecol Evol
2020 Nov 03;1023:13544-13554. doi: 10.1002/ece3.6962.
Show Gene links
Show Anatomy links
Filter feeding, deviations from bilateral symmetry, developmental noise, and heterochrony of hemichordate and cephalochordate gills.
Larouche-Bilodeau C
,
Guilbeault-Mayers X
,
Cameron CB
.
Abstract
We measured gill slit fluctuating asymmetry (FA), a measure of developmental noise, in adults of three invertebrate deuterostomes with different feeding modes: the cephalochordate Branchiostoma floridae (an obligate filter feeder), the enteropneusts Protoglossus graveolens (a facultative filter feeder/deposit feeder) and Saccoglossus bromophenolosus (a deposit feeder). FA was substantially and significantly low in B. floridae and P. graveolens and high in S. bromophenolosus. Our results suggest that the gills of species that have experienced a relaxation of the filter feeding trait exhibit elevated FA. We found that the timing of development of the secondary collagenous gill bars, compared to the primary gill bars, was highly variable in P. graveolens but not the other two species, demonstrating an independence of gill FA from gill bar heterochrony. We also discovered the occasional ectopic expression of a second set of paired gills posterior to the first set of gills in the enteropneusts and that these were more common in S. bromophenolosus. Moreover, our finding that gill slits in enteropneusts exhibit bilateral symmetry suggests that the left-sidedness of larval cephalochordate gills, and the directional asymmetry of Cambrian stylophoran echinoderm fossil gills, evolved independently from a bilaterally symmetrical ancestor.
Figure 1. Photographs of (a) Saccoglossus bromophenolosus, (b) Protoglossus graveolens, and (c) Branchiostoma floridae. (a) and (b) were live specimens. (c) was stained and cleared. Scale bars equal 4 mm
Figure 2. Line drawing of the developmental stages of the gill slits and bars. Note that gill pores are ectodermal and drawn as solid lines, whereas gill slits and bars are endodermal and the slits are drawn as dotted lines. (a) Early gill slits are round in circumference and bordered by small lateral primary gill bars. (b) The primary gill bars develop around the gill slit elongating it to form the early stage secondary gill bars. (c) The secondary gill bars elongate ventrally, dividing the primary gill slit into two elongated secondary gill slits. (d) The secondary gill bars are fully developed. Gill slits are numbered in each drawing representing how we counted them gp, gill pore; pb, primary gill bar; ps, primary gill slit; sb, secondary gill bar; ss, secondary gill slit
Figure 3. Graphical representation of the distribution of the symmetry index (R‐L) for each species. Saccoglossus bromophenolosus (Hemichordata) is a deposit feeder, Protoglossus graveolens (Hemichordata) is a facultative filter feeder, and Branchiostoma floridae (Cephalochordata) is an obligate filter feeder. S. bromophenolosus, P. graveolens, and B. floridae have symmetry index distribution means of 0.15, 0.08, and −0.26 and symmetry index distribution standard deviations of 2.57, 1.12, and 0.80, respectively
Figure 4. Differences (a) in number of gill slits and (b) symmetry index (R‐L) squared residuals among species. Error bars represent the 95% confidence intervals; letters above each mean represent Tukey’s honest significant difference (HSD) groupings (p ≤ .05)
Figure 5. Representation of the two modes of the distribution of the symmetry index (R‐L) for each species (a) in the skewness, and (b) the kurtosis. S. bromophenolosus, P. graveolens, and B. floridae have a kurtosis of 7.25, 5.78, and 5.59, and a skewness of 0.23, 0.19, and −0.69, respectively. The distribution of the skewness and the kurtosis was calculated from 10,000 rounded normal distribution (µ = −0.01, σ = 1.50). In panel (a), the vertical lines beginning from the left represent the 5% quantile and the 95% quantile, respectively, and in panel (b), the vertical line represents the 95% quantile. The deposit feeder is S. bromophenolosus, the facultative filter feeder is P. graveolens, and the obligate filter feeder is the cephalochordate B. floridae
Figure 6. Photographs of the gill slit complexes of (a) Saccoglossus bromophenolosus, (b) Protoglossus graveolens, and (c) Branchiostoma floridae. (d) S. bromophenolosus gill slits complex in higher magnification, and (e) underdeveloped secondary gill slits following damage, and (f) a second ectopic gill complex posterior to the normal complex. Anterior is at the top with a section of cleared intestine in between. All scale bars equal 500 µm except for (b) were the scale bars equal 1,000 µm. In all photograph, the pharynx midline is dorsal except (c) where it is ventral. eg, ectopic gills; pb, primary gill bar; ps, primary gill slit; s, synapticula; sb, secondary gill bar; ss, secondary gill slit; ug, underdeveloped gill bar
Boorman,
The evolution of left-right asymmetry in chordates.
2002, Pubmed
Boorman,
The evolution of left-right asymmetry in chordates.
2002,
Pubmed
Cameron,
Particle retention and flow in the pharynx of the enteropneust worm Harrimania planktophilus: the filter-feeding pharynx may have evolved before the chordates.
2002,
Pubmed
Cameron,
Three new species of Glossobalanus (Hemichordata: Enteropneusta: Ptychoderidae) from western North America.
2013,
Pubmed
Caron,
Tubicolous enteropneusts from the Cambrian period.
2013,
Pubmed
,
Echinobase
De Coster,
Fluctuating asymmetry and environmental stress: understanding the role of trait history.
2013,
Pubmed
Dingerkus,
Enzyme clearing of alcian blue stained whole small vertebrates for demonstration of cartilage.
1977,
Pubmed
Dominguez,
Paired gill slits in a fossil with a calcite skeleton.
2002,
Pubmed
,
Echinobase
Dorken,
Evolutionary vestigialization of sex in a clonal plant: selection versus neutral mutation in geographically peripheral populations.
2004,
Pubmed
Duboc,
Left-right asymmetry in the sea urchin embryo is regulated by nodal signaling on the right side.
2005,
Pubmed
,
Echinobase
Fritzenwanker,
The Fox/Forkhead transcription factor family of the hemichordate Saccoglossus kowalevskii.
2014,
Pubmed
,
Echinobase
Gerhart,
Hemichordates and the origin of chordates.
2005,
Pubmed
Gillis,
A stem-deuterostome origin of the vertebrate pharyngeal transcriptional network.
2012,
Pubmed
Grande,
Evolution, divergence and loss of the Nodal signalling pathway: new data and a synthesis across the Bilateria.
2014,
Pubmed
Holland,
Early development of cephalochordates (amphioxus).
2012,
Pubmed
Holland,
Laboratory spawning and development of the Bahama lancelet, Asymmetron lucayanum (cephalochordata): fertilization through feeding larvae.
2010,
Pubmed
Humphreys,
Regeneration in the hemichordate Ptychodera flava.
2010,
Pubmed
Igawa,
Evolutionary history of the extant amphioxus lineage with shallow-branching diversification.
2017,
Pubmed
Kaji,
Amphioxus mouth after dorso-ventral inversion.
2016,
Pubmed
Kaul-Strehlow,
A detailed description of the development of the hemichordate Saccoglossus kowalevskii using SEM, TEM, Histology and 3D-reconstructions.
2013,
Pubmed
,
Echinobase
Lahti,
Relaxed selection in the wild.
2009,
Pubmed
Lowe,
Anteroposterior patterning in hemichordates and the origins of the chordate nervous system.
2003,
Pubmed
Luo,
Opposing nodal and BMP signals regulate left-right asymmetry in the sea urchin larva.
2012,
Pubmed
,
Echinobase
Miyamoto,
Morphological characterization of the asexual reproduction in the acorn worm Balanoglossus simodensis.
2010,
Pubmed
Nanglu,
Cambrian suspension-feeding tubicolous hemichordates.
2016,
Pubmed
Nishikawa,
A new deep-water lancelet (Cephalochordata) from off Cape Nomamisaki, SW Japan, with a proposal of the revised system recovering the genus Asymmetron.
2004,
Pubmed
Ogasawara,
Developmental expression of Pax1/9 genes in urochordate and hemichordate gills: insight into function and evolution of the pharyngeal epithelium.
1999,
Pubmed
Okai,
Characterization of gill-specific genes of the acorn worm Ptychodera flava.
2000,
Pubmed
Philippe,
Acoelomorph flatworms are deuterostomes related to Xenoturbella.
2011,
Pubmed
,
Echinobase
Rahman,
Cambrian cinctan echinoderms shed light on feeding in the ancestral deuterostome.
2015,
Pubmed
Rychel,
Evolution and development of the chordates: collagen and pharyngeal cartilage.
2006,
Pubmed
Rychel,
Development and evolution of chordate cartilage.
2007,
Pubmed
Rychel,
Anterior regeneration in the hemichordate Ptychodera flava.
2008,
Pubmed
Röttinger,
Nodal signaling is required for mesodermal and ventral but not for dorsal fates in the indirect developing hemichordate, Ptychodera flava.
2015,
Pubmed
Röttinger,
Evolutionary crossroads in developmental biology: hemichordates.
2012,
Pubmed
,
Echinobase
Sato,
Asymmetry in a pterobranch hemichordate and the evolution of left-right patterning.
2008,
Pubmed
Satoh,
An aboral-dorsalization hypothesis for chordate origin.
2008,
Pubmed
Simakov,
Hemichordate genomes and deuterostome origins.
2015,
Pubmed
,
Echinobase
Smith,
Deuterostomes in a twist: the origins of a radical new body plan.
2008,
Pubmed
,
Echinobase
Smith,
The oldest echinoderm faunas from Gondwana show that echinoderm body plan diversification was rapid.
2013,
Pubmed
,
Echinobase
Tague,
VARIABILITY OF A VESTIGIAL STRUCTURE: FIRST METACARPAL IN COLOBUS GUEREZA AND ATELES GEOFFROYI.
1997,
Pubmed
Westfall,
Kurtosis as Peakedness, 1905 - 2014. R.I.P.
2014,
Pubmed
Yu,
An amphioxus nodal gene (AmphiNodal) with early symmetrical expression in the organizer and mesoderm and later asymmetrical expression associated with left-right axis formation.
2002,
Pubmed
Zamora,
Plated Cambrian bilaterians reveal the earliest stages of echinoderm evolution.
2012,
Pubmed
,
Echinobase