Data from: Multiple morphological clocks and total-evidence tip-dating in mammals

Morphological integration predicts that correlated characters will coevolve; thus, each distinct suite of correlated characters might be expected to evolve according to a separate clock or 'pacemaker'. Characters in a large morphological dataset for mammals were found to be evolving according to seven separate clocks, each distinct from the molecular clock. Total-evidence tip-dating using these multiple clocks inflated divergence time estimates, but potentially improved topological inference. In particular, single-clock analyses placed several meridiungulates and condylarths in a heterodox position as stem placentals, but multi-clock analyses retrieved a more plausible and orthodox position within crown placentals. Several shortcomings (including uneven character sampling) currently impact upon the accuracy of total-evidence dating, but this study suggests that when sufficiently large and appropriately constructed phenotypic datasets become more commonplace, multi-clock approaches are feasible and can affect both divergence dates and phylogenetic relationships.Description of All Data Files on DryadDescription of All Data Files on Dryad (docx); this is also available on on the Biology Letters website. All numbered refs, such as [6], in the descriptions below refer to citations in the main Biology Letters paper or in this document.Description.docxA1_CharacterPartitionsFile_A1 (Excel). Table describing the 28 partitions (25 morphological, 3 molecular) and listing the included characters. Character numbering is based on the matrix from [6], available as MorphoBank Project 773 (http://dx.doi.org/10.7934/P773).B1_TreeRef6_MrBayesFile_Morph1-25File_B1 (plain text). The MrBayes [10] executable file to infer branch lengths for the 25 candidate morphological partitions, using the total-evidence Maximum Likelihood topology from [6]. The matrix consists of only the 46 extant taxa from [6], since molecular branch lengths (to which these morphological branch lengths have to be compared) cannot be ascertained for extinct taxa.B2_TreeRef6_MrBayesFile_Codons1-3File_B2 (plain text). The MrBayes executable file to infer branch lengths for the 3 candidate molecular partitions (and overall morphological branch lengths), using the total-evidence Maximum Likelihood topology from [6]. The matrix consists of the 46 extant taxa from [6].B3_TreeRef6_Parts1-28branchlengths_newickFile_B3 (newick format). The ClockstaR [3] treefile containing the trees with the branch lengths for the 28 candidate partitions obtained from the MrBayes analysis in files B1, B2. Note: ClockstaR treats all trees as unrooted, so different rootings of trees are of no consequence.B4_TreeRef9_MrBayesFile_Morph1-25File_B4 (plain text). The MrBayes [10] executable file to infer branch lengths for the 25 candidate morphological partitions, using the topology from [9]. The matrix consists of only the 46 extant taxa from [6], since molecular branch lengths (to which these morphological branch lengths have to be compared) cannot be ascertained for extinct taxa.B5_TreeRef9_MrBayesFile_Codons1-3File_B5 (plain text). The MrBayes executable file to infer branch lengths for the 3 candidate molecular partitions (and overall morphological branch lengths), using the topology from [9]. The matrix consists of the 46 extant taxa from [6].B6_TreeRef9_Parts1-28branchlengths_newickFile_B6 (newick format). The ClockstaR treefile containing the trees with the branch lengths for the 28 candidate partitions obtained from the MrBayes analysis in files B4, B5. Note: ClockstaR treats all trees as unrooted, so different rootings of trees are of no consequence.B7_ClockstarResultsFile_B7 (pdf). ClockstaR partition matrices and gap statistics for analyses using the guide tree from ref [6] (upper panels) and ref [9] (lower panels). From the 28 candidate partitions, both analyses identified an optimal number of 8 clock-partitions (pacemakers) of similar composition. Note that the order of partitions in these tables (molecular partitions uppermost) is different to that in Fig. 1, but the same as in Fig. B10.B8_Randomised_TOLMorph25p_TOL_GamFile_B8 (plain text). The MrBayes [10] executable file to infer branch lengths for the 25 randomised morphological partitions. The partitions were of the same size as the 25 original partitions (42-553 characters); morphological characters were randomly shuffled in Excel. The molecular data were not randomised. The matrix otherwise is identical to that in File B1.B9_Randomised_TreeRef6_Parts1-28branchlengths_newickFile_B9 (newick format). The ClockstaR [3] treefile containing the trees with the branch lengths for the 25 randomised morphological partitions, and the original (not randomised) 3 molecular partitions obtained from the MrBayes analysis as per file B2. Note: ClockstaR treats all trees as unrooted, so different rootings of trees are of no consequence.B10_Randomised_clockstar_ResultsFile_B10 (pdf). ClockstaR partition matrices and gap statistics for analysis using randomised morphological partitions, using the guide tree from ref [6]. From the 28 candidate partitions, the analysis preferred very many, or very few, morphological partitions, unlike the corresponding analysis of the original data (File B7, top) which preferred an intermediate number. Note that the order of partitions in these tables (molecular partitions uppermost) is different to that in Fig. 1, but the same as in Fig. B7.B11_ClockstaR_scriptFile_B11 (plain text). ClockstaR R script (and output) for the above analysis. Note filenames and paths need to be changed as appropriate.C1_PartitionFinderFile_C1 (zipped, plain text). Matrix with molecular data for 46 extant taxa (extracted from [6]), in Phylip format (mammals.phy); PartitionFinder [12] command file (cfg) with 71 candidate partitions (by genes and by codons, with noncoding genes treated as single candidate partitions); best scheme with 7 partitions requiring separate substitution models, found by PartitionFinder using the Bayesian Information Criterion with unlinked branch lengths.C2_1clock - MrBayes fileFile_C2 (plain text). MrBayes executable file for a total-evidence dating analysis of all 86 taxa in the matrix in [6], using a single relaxed (independent gamma rates) clock for all traits (morphological and molecular). The sampled ancestor birth-death tree prior [17], and the Markov model of morphological evolution [18,19], were used. Optimal substitution models and substitution-model-partitions were found with PartitionFinder for molecular data (see C1) and with stepping-stone analysis in MrBayes for morphological data as implemented in [10]. Numerous (>20) MCMC runs were initially performed for 5 million generations to investigate tuning, mixing and convergence. The final analysis was then performed with 4 runs of 20 million generations, with the first 30% of samples discarded as burnin.C2_1clock.mrbC3_1clock_PostburninTrees&Params_folderFile_C3 (zipped, plain text). The full MCMC tree and parameter output files from the MrBayes analysis in file C1. Only post-burnin samples are included to reduce file sizes. Run the MrBayes file in C2 (after disabling the MCMC command and setting burnin to 0) to generate consensus trees and statistics from these files.C4_1clock_con_figFile_C4 (approximate nexus format). The majority-rule consensus tree from the MrBayes analysis in files C1-2. Note: the wrong file was previously uploaded onto Dryad; I thank Joseph Brown for pointing this out.C5_1clock_topologyConvergenceFile_C5 (pdf). Convergence diagnostics for tree topologies sampled in C2. (A) AWTY [20] plots demonstrating similar posterior probabilities for all clades across 4 runs, and (B) at different stages in a single run. The topology convergence statistics from MrBayes and AWTY (standard deviation of split frequencies across runs) were also good ie low, being 20) MCMC runs were initially performed for 20 million generations to investigate tuning, mixing and convergence. The final analysis was then performed with 4 runs and the trees from 10 million post-burnin generations retained Note: The burnin for each run varies considerably due to variation in time to reach (apparent) stationarity, from 20 million to 50 million. For computational efficiency, the 4 runs were performed separately and in all cases, the last 10 million steps (after stationarity) were retained. However, the step numbers have been readjusted in file C8 below so they are all identical across runs (ie to a common burnin of 50 million), to facilitate downstream analyses e.g. generating summary statistics in MrBayes.C7_8clocks.mrbC8_8clocks_PostburninTrees&Params_folderFile_C8 (zipped, plain text). The full MCMC tree and parameter output files from the MrBayes analysis in file C7. Only post-burnin samples for each of the 4 runs (last 10 million, see below) are included to reduce file sizes. Run the MrBayes file in C7 (first disabling the MCMC command) and setting burnin to 0 to generate consensus trees and statistics. Run the relevant MrBayes file (disabling the MCMC command) and setting burnin to 0 to generate consensus statistics.C9_8clocks_con_figFile_C9 (approximate nexus format). The majority-rule consensus tree from the MrBayes analysis in files C6-7.C10_8clocks_topolConvergenceFile_C10 (pdf). Convergence diagnostics for tree topologies sampled in C8. (A) AWTY [20] plots demonstrating relatively good correlation (albeit with substantial variance) for all clades across 4 runs, and (A) high variation at different stages in a single run, but no obvious directional trends. The topology convergence statistics from MrBayes and AWTY (standard deviation of split frequencies across runs) were also relatively good ie being