1 Department of Biology, Philipps-University Marburg, Marburg, Germany

2 Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena, Germany

3 Department of Environment and Biodiversity, University of Salzburg, Salzburg, Austria


chemodiv is an R package for analysing phytochemical data. It includes a number of functions that makes it straightforward to quantify and visualize phytochemical diversity and dissimilarity for any type of phytochemical samples, such as herbivore defence compounds, volatiles or similar. Importantly, calculations of diversity and dissimilarity can incorporate biosynthetic and/or structural properties of the phytochemical compounds, resulting in more comprehensive quantifications of diversity and dissimilarity.

This introduction serves as a tutorial explaining the main intended use of all the functions in the package. A complete description of the package will be available in Petrén et al. 2022.


The current version of the package can be installed from CRAN. Alternatively, the developmental version of the package can be installed from GitHub using the install_github() function from the devtools package.

# Install current version

# Install developmental version
install.packages("devtools") # Install devtools if not already installed
# Load chemodiv

Using chemodiv

Data formatting

We illustrate the use of the chemodiv package by using data, included in the package, on floral scent of the plant Arabis alpina (Petrén et al. 2021). We use a subset of the data consisting of 87 individuals from three populations.

Two separate datasets are needed to use the full set of analyses in the chemodiv package.

The first dataset, which we call the sample dataset, should be a data frame containing data on the relative concentrations (proportions) of different compounds (columns) in different samples (rows):


#>   ZBetaOcimene EBetaOcimene Benzaldehyde MethylBenzoate Phenylacetaldehyde
#> 1   0.01584642  0.007014541    0.8540981    0.001959341                  0
#> 2   0.00000000  0.000000000    0.9116668    0.013874965                  0
#> 3   0.00000000  0.000000000    0.9305998    0.002476401                  0
#> 4   0.00000000  0.000000000    0.7920615    0.018483767                  0
#> 5   0.00000000  0.000000000    0.9251283    0.013249618                  0
#> 6   0.02653006  0.014940792    0.8090447    0.003321790                  0

The dataset contains the relative concentration of 15 phytochemical compounds in different samples.

The second dataset, which we call the compound dataset, should be a data frame containing, in each of three columns, the common name, SMILES and InChIKey IDs of all the compounds that are present in the sample dataset:


#>             compound                smiles                    inchikey
#> 3       Benzaldehyde      C1=CC=C(C=C1)C=O HUMNYLRZRPPJDN-UHFFFAOYSA-N
#> 5 Phenylacetaldehyde     C1=CC=C(C=C1)CC=O DTUQWGWMVIHBKE-UHFFFAOYSA-N
#> 6       Acetophenone     CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N

SMILES and InChIKey are chemical identifiers that are easily obtained for each compound by searching for compounds in PubChem. Searching for compounds by their common name, or a number of other chemical identifiers, will bring up the matching molecule, along with the SMILES and InChIKey. Additionally, various automated tools such as the PubChem Identifier Exchange Service or The Chemical Translation Service can be used to automatically obtain IDs for lists of compounds. The user has to compile the SMILES and InChIKey manually to ensure correctness, as lists of compounds very often contain compounds wrongly named, wrongly formatted, under various synonyms etc. which prevents efficient automatic translation of compound names to SMILES and InChIKey.

As the compound dataset consists of a list of known compounds, analyses in the chemodiv package will work best for sets of data, commonly generated by chemical ecologists using GC-MS, LC-MS or similar, where all or most compounds in the samples have been confidently identified.

When both datasets are prepared, we can use the function chemoDivCheck() to make sure that the sample dataset and the compound dataset are formatted correctly, so that they can be used by the other functions in the package:

chemoDivCheck(compoundData = alpinaCompData, sampleData = alpinaSampData)
#> The two datasets appear to be correctly formatted.

In addition to the sample and compound datasets, a third dataset indicating what groups different samples belong to can be used in the plotting functions below.


#> Population
#>  G1 It8  S1 
#>  17  37  33

In this case, our samples belong to three different populations: G1 (Greece), It8 (Italy) and S1 (Sweden).

Now we have all necessary datasets, which are correctly formatted, and we can begin with analyses.

Compound classification and dissimilarities

Two functions are used to classify and compare phytochemical compounds, and are applied to the compound dataset.

The function NPCTable() classifies compounds with NPClassifier (Kim et al. 2021). NPClassifier is a deep-learning tool that classifies phytochemical compounds into a hierarchical classification of three groups, pathway, superclass and class, largely corresponding to biosynthetic pathways:

alpinaNPC <- NPCTable(compoundData = alpinaCompData)

alpinaNPC[1,] # Classification of the first compound in dataset
#>       compound                smiles                    inchikey    pathway
#> 1 ZBetaOcimene CC(=CC/C=C(/C)\\C=C)C IHPKGUQCSIINRJ-NTMALXAHSA-N Terpenoids
#>       superclass                  class
#> 1 Monoterpenoids Acyclic monoterpenoids

Here, the first compound in the list, (Z)-beta-Ocimene, is classified as Terpenoids > Monoterpenoids > Acyclic monoterpenoids. The classification of the compounds is put into a data frame and can subsequently be used by other functions.

The function compDis() compares phytochemical compounds by calculating pairwise Jaccard dissimilarities between them. The dissimilarity calculations can be based on the biosynthesis and/or structure of the compounds. type = "NPClassifier" calculates dissimilarities based on the classification made by NPClassifier, which largely corresponds to biosynthetic pathways. type = "PubChemFingerprint" and type = "fMCS" are two similar methods that calculate dissimilarities based on the structure of the compounds. In this case, molecules that have similar substructures/features will have a low dissimilarity, while molecules not having similar substructures/features will have a high dissimilarity.

We calculate compound dissimilarities with type = "PubChemFingerprint".

alpinaCompDis <- compDis(compoundData = alpinaCompData,
                         type = "PubChemFingerprint")

alpinaCompDis$fingerDisMat[1:4, 1:4] # Part of compound dissimilarity matrix
#>                ZBetaOcimene EBetaOcimene Benzaldehyde MethylBenzoate
#> ZBetaOcimene      0.0000000    0.0000000    0.7027027      0.7191011
#> EBetaOcimene      0.0000000    0.0000000    0.7027027      0.7191011
#> Benzaldehyde      0.7027027    0.7027027    0.0000000      0.2637363
#> MethylBenzoate    0.7191011    0.7191011    0.2637363      0.0000000

The output from the function is a list with one or several compound dissimilarity matrices, depending on which type was used as input. If multiple type are used as input, a matrix with mean values of the other matrices will also calculated. Importantly, the resulting matrix of compound dissimilarities is used by other functions in the package that quantify phytochemical diversity and dissimilarity, and can be used to visualize how similar sets of compounds are to each other.

Diversity calculations

Calculations of phytochemical diversity is the core of the chemodiv package. Phytochemical diversity can be calculated for the sample dataset with functions calcDiv(), calcBetaDiv() and calcDivProf().

calcDiv() calculates alpha diversity for each sample (row) in the sample dataset. The function can calculate a number of different diversity and evenness indices, depending on what type is used as input. The default and recommended way of calculating diversity is as Hill numbers (Chao et al. 2014), which provides a number of advantages, including the use of the parameter q which controls the sensitivity of the measure to the relative concentrations of compounds. This can be done as “normal” Hill diversity, which depends on compound richness and evenness, and as functional Hill diversity, which additionally considers compound dissimilarity (Chiu & Chao 2014), utilizing the compound dissimilarity matrix from compDis(). This means that, for calculations of functional Hill diversity, a set of compounds that are biosynthetically/structurally different from each other is more diverse than a similar set of compounds that are biosynthetically/structurally more similar to each other.

We calculate functional Hill diversity for q = 1.

alpinaDiv <- calcDiv(sampleData = alpinaSampData, 
                     compDisMat = alpinaCompDis$fingerDisMat,
                     type = "FuncHillDiv",
                     q = 1)

#>   FuncHillDiv
#> 1    4.698821
#> 2    2.479441
#> 3    1.925043
#> 4    3.497343
#> 5    2.946872
#> 6    5.703370

The function outputs a data frame with samples as rows and the selected type of measures as columns.

calcDivProf() can be used to calculate Hill diversity for a range of q-values simultaneously, generating a so called diversity profile. This allows for a more nuanced exploration of the diversity.

We calculate a diversity profile for functional Hill diversity, using the default range of q = 0 to q = 3.

alpinaDivProf <- calcDivProf(sampleData = alpinaSampData,
                             compDisMat = alpinaCompDis$fingerDisMat,
                             type = "FuncHillDiv")

head(alpinaDivProf$divProf)[,1:5] # Part of the diversity profile data frame
#>          q0      q0.1      q0.2      q0.3      q0.4
#> 1 19.453742 15.693727 12.805088 10.609162  8.950470
#> 2  5.629633  4.918416  4.340654  3.879160  3.514778
#> 3  5.629633  4.566221  3.792641  3.237913  2.841879
#> 4 11.517752  9.660744  8.169274  6.987923  6.061618
#> 5 11.517752  8.982790  7.142494  5.836170  4.920329
#> 6 19.453742 16.340454 13.829040 11.825500 10.239775

The function outputs a list with input parameters and the diversity profile as a data frame, with samples as rows and diversity values at different values of q as columns.

calcBetaDiv() calculates beta diversity for a set of samples, in the Hill numbers framework. The function calculates a single beta-diversity value for the supplied sample data. This is calculated as beta = gamma / alpha, where gamma is the diversity of the pooled data set and alpha represents the mean diversity of individual samples.

alpinaBetaDiv <- calcBetaDiv(sampleData = alpinaSampData,
                             compDisMat = alpinaCompDis$fingerDisMat,
                             type = "FuncHillDiv")

#>          Type q    gamma    alpha     beta
#> 1 FuncHillDiv 1 9.998989 2.594547 3.853847

The function outputs a data frame with type of beta diversity calculated, q, and values for gamma diversity, mean alpha diversity and beta diversity.

Sample dissimilarities

Calculations of pairwise phytochemical dissimilarities between samples can be made with the function sampDis(). This calculates Bray-Curtis dissimilarities and/or Generalized UniFrac dissimilarities (Chen et al 2012, Junker 2018) between samples in the sample dataset. Generalized UniFrac dissimilarities utilize the compound dissimilarity matrix from compDis(), such that two samples containing more biosynthetically/structurally different compounds have a higher pairwise dissimilarity than two samples containing more biosynthetically/structurally similar compounds.

We calculate phytochemical dissimilarity as Generalized UniFrac dissimilarities:

alpinaSampDis <- sampDis(sampleData = alpinaSampData,
                         compDisMat = alpinaCompDis$fingerDisMat,
                         type = "GenUniFrac")

alpinaSampDis$GenUniFrac[1:4, 1:4] # Part of sample dissimilarity matrix
#>            1          2          3          4
#> 1 0.00000000 0.05244257 0.04518892 0.04880070
#> 2 0.05244257 0.00000000 0.01254811 0.06126169
#> 3 0.04518892 0.01254811 0.00000000 0.05839175
#> 4 0.04880070 0.06126169 0.05839175 0.00000000

The output from the function is a list with one or several sample dissimilarity matrices, depending on which type was used as input.

Molecular network

Function molNet() uses a matrix generated by the compDis() function to create a molecular network of the phytochemical compounds, and calculates some properties of the network. Such networks are useful to visualize relationships between compound similarities and abundances.

We create a molecular network based on the compound dissimilarity matrix. We can also include the the NPClassifier classification, where the “pathway” group will control node colour. We manually set cutOff = 0.75 in this case. This limits the number of edges between nodes, as edges are only plotted between nodes if their similarity (where similarity = 1 - dissimilarity) is larger than the cut-off value.

alpinaNetwork <- molNet(compDisMat = alpinaCompDis$fingerDisMat,
                        npcTable = alpinaNPC,
                        cutOff = 0.75)

#>               Length Class     Mode   
#> networkObject 15     tbl_graph list   
#> nCompounds     1     -none-    numeric
#> nNpcPathways   1     -none-    numeric
#> modularity     1     -none-    numeric

The output is a list including the network object, and some basic network parameters.

Chemodiversity and network plots

Once we have calculated different measures of phytochemical diversity and dissimilarity using the above functions, two plotting functions can be used to conveniently create different types of plots and molecular networks.

molNetPlot() creates a basic plot of the molecular network generated by the molNet() function. We create a single molecular network for the whole dataset, including compound names and the classification by NPClassifier.

molNetPlot(sampleData = alpinaSampData,
           networkObject = alpinaNetwork$networkObject,
           npcTable = alpinaNPC,
           plotNames = TRUE)

Nodes represent individual compounds. They are coloured by their “pathway” classification by NPClassifier. Node size corresponds to the mean proportional concentration of the compounds in the samples. Edge widths represent compound similarity, and are only plotted for similarities higher than the cutoff value. We see that the floral scent bouquet consists mostly of compounds belonging to the “Shikimates and Phenylpropanoids” pathway. These compounds are connected to each other in a network, but separated from the three “Terpenoids” compounds, indicating that the two groups of compounds belonging to different pathways are also structurally different to each other.

chemoDivPlot() can be used to conveniently create basic plots of the different types of diversity and dissimilarity measurements calculated by the functions above. Four types of plots can be created, in any combination. With argument compDisMat a dendrogram visualizing compound dissimilarities is created. With argument divData, diversity/evenness values are visualized with boxplots. With argument divProfData a diversity profile will be created. With argument sampDisMat sample dissimilarities will be visualized as an NMDS plot. Grouping data can be supplied with argument groupData.

chemoDivPlot(compDisMat = alpinaCompDis$fingerDisMat,
             divData = alpinaDiv,
             divProfData = alpinaDivProf,
             sampDisMat = alpinaSampDis$GenUniFrac,
             groupData = alpinaPopData)

The output consists of the selected plots. The dendrogram visualizes similarities between compounds in a way complementary to the molecular network above, with the three terpenoids having a high dissimilarity to the other compounds. The boxplot indicates that the functional Hill diversity of the floral scent compounds is highest in the G1 population. Further analyses can examine more exactly what components of diversity are higher in this population. The diversity profile demonstrates how at q = 1 (shown also in boxplot) diversity is highest for population G1, but at q = 0, where compound proportions are not taken into account, diversity is highest for population It8. Finally, the NMDS indicates that all three populations are compositionally/structurally different to each other, and that in population It8, dissimilarities between samples in the same population is lower than for the other two populations.

In this example, we end at the plots visualizing phytochemical diversity and dissimilarity. Such plots may inform about patterns of variation within and between groups of samples that represent different populations, species etc. Importantly, testing for associations between measures of diversity/dissimilarity and variables such as herbivore performance, pollinator visitation rates and plant fitness may provide insights on the effects of phytochemical variation on plants for various ecological interactions and evolutionary processes.

Shortcut function

The function quickChemoDiv() uses many of the above functions to in one simple step calculate and visualize chemodiversity for users wanting to quickly explore their data using standard parameters. This can be used to generate the same four types of plots as above.

quickChemoDiv(compoundData = alpinaCompData,
              sampleData = alpinaSampData,
              groupData = alpinaPopData,
              outputType = "plots") # Not run

Solutions to common questions and issues


Chao, A., C.-H. Chiu, and L. Jost. 2014. Unifying Species Diversity, Phylogenetic Diversity, Functional Diversity, and Related Similarity and Differentiation Measures Through Hill Numbers. Annu. Rev. Ecol. Evol. Syst. 45:297–324.

Chen, J., K. Bittinger, E. S. Charlson, C. Hoffmann, J. Lewis, G. D. Wu, R. G. Collman, F. D. Bushman, and H. Li. 2012. Associating microbiome composition with environmental covariates using generalized UniFrac distances. Bioinformatics 28:2106–2113.

Chiu, C.-H., and A. Chao. 2014. Distance-Based Functional Diversity Measures and Their Decomposition: A Framework Based on Hill Numbers. PLoS ONE 9:e100014.

Junker, R. R. 2018. A biosynthetically informed distance measure to compare secondary metabolite profiles. Chemoecology 28:29–37.

Kim, H. W., M. Wang, C. A. Leber, L.-F. Nothias, R. Reher, K. B. Kang, J. J. J. van der Hooft, P. C. Dorrestein, W. H. Gerwick, and G. W. Cottrell. 2021. NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products. J. Nat. Prod. 84:2795–2807.

Petrén, H., P. Toräng, J. Ågren, and M. Friberg. 2021. Evolution of floral scent in relation to self-incompatibility and capacity for autonomous self-pollination in the perennial herb Arabis alpina. Annals of Botany 127:737–747.

Petrén H., T.G. Köllner and R.R Junker. 2022. Quantifying chemodiversity considering biochemical and structural properties of compounds with the R package chemodiv. bioRxiv doi: 10.1101/2022.06.08.495236.