1 Phylogenetic dataset
Analysis was performed on a new matrix of 48 lophotrochozoan taxa, coded for 354 morphological characters (220 neomorphic, 134 transformational). The matrix can be viewed interactively at Morphobank project 3262; a static version can be downloaded directly in Nexus or TNT format.
Taxa include sipunculans and molluscs, which have previously been interpreted as having affinities with hyoliths. Other lophotrochozoan groups help to constrain the outgroup topology, and a diversity of brachiozoans helps to resolve the position of hyoliths within this group.
Characters are coded following the recommendations of Brazeau et al. (2019):
We have employed reductive coding (Wilkinson, 1995), using a distinct state to mark character inapplicability. Character specifications follow the structural syntax of Sereno (2007) in order to highlight ontological dependence between characters and emphasize the structure of the dataset.
We have distinguished between neomorphic and transformational characters (sensu Sereno, 2007) by reserving the token
0
to refer to the absence of a neomorphic (i.e. presence/absence) character. The states of transformational characters (i.e. characters that describe a property of a feature) are represented by the tokens1
,2
,3
, …We code the absence of neomorphic ontologically dependent characters (sensu Vogt, 2018) as absence, rather than inapplicability.
The complete dataset comprises 6774 character codings, plus 2240 inapplicable codings. (The amount and quality of data that is coded is more instructive than the number of cells that are ambiguous (Wiens, 1998, 2003), which, for completeness, is 7978). Of the 354 characters, the number that were coded with an applicable token for each taxon is:
Acaenoplax hayae | 106 | Heliomedusa orienta | 82 | Paterimitra | 88 |
Calvapilosa kroegeri | 94 | Kulindroplax perissokomos | 107 | Pedunculotheca diania | 72 |
Canadia spinosa | 111 | Leptochiton | 228 | Pelagiella | 87 |
Capitella | 223 | Lingula | 263 | Pelagodiscus atlanticus | 210 |
Chaetoderma | 219 | Loxosomella | 217 | Phoronis | 250 |
Conocardium elongatum | 85 | Mickwitzia muralensis | 78 | Phthipodochiton thraivensis | 79 |
Cotyledion tylodes | 79 | Micrina | 76 | Pojetaia runnegari | 88 |
Dailyatia | 71 | Micromitra | 86 | Polysacos vickersianum | 76 |
Dentalium | 234 | Mopalia | 226 | Serpula | 227 |
Eccentrotheca | 61 | Mytilus | 210 | Siphogonuchites multa | 46 |
Flustra | 217 | Namacalathus | 76 | Sipunculus | 259 |
Gasconsia | 76 | Neopilina | 192 | Terebratulina | 238 |
Glaphurochiton carbonarius | 77 | Novocrania | 247 | Tonicella | 265 |
Haliotis | 256 | Odontogriphus omalus | 95 | Wirenia | 193 |
Halkieria evangelista | 80 | Orthis | 76 | Wiwaxia corrugata | 109 |
Haplophrentis carinatus | 102 | Orthrozanclus | 81 | Yilingia spiciformis | 56 |
References
Brazeau, M. D., Guillerme, T., & Smith, M. R. (2019). An algorithm for morphological phylogenetic analysis with inapplicable data. Systematic Biology, online ahead of print. doi: 10.1093/sysbio/syy083
Sereno, P. C. (2007). Logical basis for morphological characters in phylogenetics. Cladistics, 23(6), 565–587. doi: 10.1111/j.1096-0031.2007.00161.x
Vogt, L. (2018). The logical basis for coding ontologically dependent characters. Cladistics, 34(4), 438–458. doi: 10.1111/cla.12209
Wiens, J. J. (1998). Does adding characters with missing data increase or decrease phylogenetic accuracy? Systematic Biology, 47(4), 625–640. doi: 10.1080/106351598260635
Wiens, J. J. (2003). Missing data, incomplete taxa, and phylogenetic accuracy. Systematic Biology, 52(4), 528–538. doi: 10.1080/10635150390218330
Wilkinson, M. (1995). Coping with abundant missing entries in phylogenetic inference using parsimony. Systematic Biology, 44(4), 501–514. doi: 10.1093/sysbio/44.4.501