Food webs, networks of feeding relationships in an ecosystem, provide fundamental insights into mechanisms that determine ecosystem stability and persistence. A standard approach in food-web analysis, and network analysis in general, has been to identify compartments, or modules, defined by many links within compartments and few links between them. This approach can identify large habitat boundaries in the network but may fail to identify other important structures. Empirical analyses of food webs have been further limited by low-resolution data for primary producers. In this paper, we present a Bayesian computational method for identifying group structure using a flexible definition that can describe both functional trophic roles and standard compartments. We apply this method to a newly compiled plant-mammal food web from the Serengeti ecosystem that includes high taxonomic resolution at the plant level, allowing a simultaneous examination of the signature of both habitat and trophic roles in network structure. We find that groups at the plant level reflect habitat structure, coupled at higher trophic levels by groups of herbivores, which are in turn coupled by carnivore groups. Thus the group structure of the Serengeti web represents a mixture of trophic guild structure and spatial pattern, in contrast to the standard compartments typically identified. The network topology supports recent ideas on spatial coupling and energy channels in ecosystems that have been proposed as important for persistence. Furthermore, our Bayesian approach provides a powerful, flexible framework for the study of network structure, and we believe it will prove instrumental in a variety of biological contexts.
The relationships among organisms in an ecosystem can be described by a food web, a network representing who eats whom. Food web organization has important consequences for how populations change over time, how one species extinction can cause others, and how robustly ecosystems respond to disturbances. We present a computational method to analyze how species are organized into groups based on their interactions. We apply this method to the plant and mammal food web from the Serengeti savanna ecosystem in Tanzania, a pristine ecosystem increasingly threatened by human impacts. This web is unusually detailed, with plants identified down to individual species and corresponding habitats. Our analysis, which differs from the compartmental studies typically done in food webs, reveals that functionally distinct groups of carnivores, herbivores, and plants make up the Serengeti web, and that plant groups reflect distinct habitat types. Furthermore, since herbivore groups feed across multiple plant groups, and carnivore groups feed across multiple herbivore groups, energy represents a wider range of habitats as it flows up the web. This pattern may partly explain how the ecosystem remains in balance. Additionally, our method can be easily applied to other kinds of networks and modified to find other patterns.
Citation: Baskerville EB, Dobson AP, Bedford T, Allesina S, Anderson TM, Pascual M (2011) Spatial Guilds in the Serengeti Food Web Revealed by a Bayesian Group Model. PLoS Comput Biol 7(12): e1002321. doi:10.1371/journal.pcbi.1002321
Editor: Lauren Ancel Meyers, University of Texas at Austin, United States of America
Received: January 11, 2011; Accepted: November 7, 2011; Published: December 29, 2011
Copyright: © 2011 Baskerville et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: We acknowledge the support of NSF grant EF-0827493 (Program on Theory in Biology) to S.A. and M.P., and of the DOE Computational Science Graduate Fellowship (grant DE-FG02-97ER25308) to E.B.B. T.B. was supported by the Howard Hughes Medical Institute, and M.P. is a Howard Hughes Medical Institute Investigator. A.P.D. acknowledges the McDonnell Foundation for a grant to support studies on food webs. T.M.A. was supported by an Early Career Project Grant from the British Ecological Society and a VENI Fellowship from NWO, The Netherlands. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Food webs, networks of feeding relationships in ecosystems, connect the biotic interactions among organisms with energy flows, thus linking together population dynamics, ecosystem function, and network topology. Ecologists have been using this powerful conceptual tool for more than a century –. One particularly relevant aspect of food webs is the subdivision of species into compartments or modules, a feature that has been proposed to contribute to food web stability by constraining the propagation of disturbances through a network . In this definition, compartments are alternately referred to as modules, clusters, or “communities” , and are defined by high link density within groups and low link density between them. A large literature has considered the presence of compartments of food webs, with early work concluding that compartmentalization results primarily from habitat boundaries, not from dynamical effects , although continuing theoretical work has shown that compartmentalization can affect stability , . One recent study shows that niche structure can result in compartmentalization , but the relationship between compartments and spatial habitat structure remains the strongest empirical pattern identified , .
Although compartmental structure may be significant at one scale of analysis, compartments alone do not account for much of the topological structure in food webs. Recent work with a probabilistic model considers a more flexible notion of groups, allowing link density to be high or low within any group or between any pair of groups . Groups can thus represent compartments in the previous sense, but can also represent trophic guilds or roles , , sets of species that feed on, and are fed on, by similar sets of species. By fitting models of this type to data, the dominant topological pattern in the network can be found, which may include compartments, trophic guilds, or some combination of the two. The initial application of this model to empirical food webs from different ecosystems has revealed a predominance of trophic guilds rather than compartments .
Two major challenges limit the application of this model in resolving the group structure of food webs and interpreting its biological basis. First, most food webs have poor resolution of primary producers; plants in terrestrial systems and phytoplankton in aquatic ones are typically represented by a few nodes that are highly aggregated taxonomically. Some are aggregated at multiple trophic levels, e.g., the Coachella Valley web ; others aggregate only the primary producers, e.g., the El Verde rainforest , which identifies basal taxa as categories of plant parts. Another recently published Serengeti food web includes highly aggregated primary producers and varying levels of aggregation at other trophic levels . Some webs that do include high resolution of plants include plant-herbivore bipartite networks, notably one lowland food-web from Papua New Guinea , and plant-insect-parasitoid “source webs” , . Because primary producers form the base of the food web, high resolution in those groups can facilitate a much better understanding of how spatial organization and habitat type percolate up the web, and how higher trophic levels cut across the habitat structure at lower levels.
Second, some technical problems have hindered the use of probabilistic models in analyzing group structure. Early food web models served as null models for food web structure and were tested by generating model webs and comparing summary statistics against data from real webs , . More recently, a more rigorous approach for measuring the goodness of fit of a model has been provided by maximum likelihood and model selection , . Two problems still remain within this framework. One is technical: standard model-selection criteria are not applicable to “discrete parameters” such as group membership. The second problem is more fundamental: there are many almost equally good arrangements, and it is desirable to extract information not just from a single best arrangement, but also from the rest of the ensemble.
The Bayesian approach is gaining popularity in ecological modeling due to the philosophical and conceptual appeal of explicitly considering uncertainty in parameter estimation as well as its methodological flexibility . This approach is especially well-suited for handling uncertainty in complex food web models, and allows us to overcome the limitations of the previous implementation of the group model. In network inference, there are only a few examples of complete Bayesian models ,  and a few examples of MCMC for maximum-likelihood inference , , but Bayesian inference in phylogenetics has been long established , , and provides a clear methodological analogue.
In this paper, we address the group structure of a newly assembled food web for the large mammals and plants of the Serengeti grassland ecosystem of Tanzania by applying a computational approach to the identification of groups based on Bayesian inference. We specifically ask whether the structure that emerges reflects the underlying spatial dimension, as delineated by the different plant communities that characterize different sub-habitats within the ecosystem, or whether it is determined by trophic dimensions in the form of species guilds that share functional roles.
The Serengeti has been studied as an integrated ecosystem for almost five decades –, and because of widespread popular familiarity with the consumer-resource dynamics of lions, hyenas, wildebeest, zebra and grasses, it provides a strong intuitive test for probabilistic food web models. Furthermore, all the primary producers in this Serengeti web are identified to the genus or species level. The plant diversity encompasses a number of distinct grass, herb, and woody plant communities on different soils and across a rainfall gradient . This well-documented structure allows us to examine the extent to which habitat structure defines network topology at multiple trophic levels. Although not yet a comprehensive community web, with the addition of more taxa, such as those in another recently published Serengeti web , this data set can become the most highly-resolved terrestrial web available.
The Serengeti Food Web Data Set
We compiled the Serengeti food web from published accounts of feeding links in the literature – along with some links known from personal observation. With a few exceptions, the taxa included are large mammalian carnivores and herbivores and the plant diets of the herbivores. In its current form it is not a comprehensive community web, nor does such a terrestrial web yet exist. Another recently published Serengeti food web is largely complementary, containing many bird, mammal, and invertebrate species not included here, but without high resolution of plants . We have not included invertebrates (insects and parasitic helminths) or birds, but are adding data for these groups for future studies.
The compiled food web (Tables S1 and S2) consists of 592 feeding links among 161 species (129 plants, 23 herbivores, and 9 carnivores). 507 of the links are herbivorous, and 85 are predatory. The fraction of all possible links (connectance, ), ignoring all biological constraints, is equal to 0.023. We attribute the low connectance, as compared to other existing food-web data sets, to the high taxonomic resolution of the plant community.
Performance of Model Variants
We compared marginal likelihood estimates of different model variants to determine which one best describes the Serengeti food web (see Methods). First, we find unequivocal support for the use of group-based models in describing the Serengeti food web, as compared with simple null models that ignore group structure, either by treating each species as its own group or by combining all species into a single group (Table 1). We also find that a flexible group model that allows for high or low connectance between and within groups vastly outperforms a compartmental model that restricts between-group connectance to be lower than within-group connectance, with a posterior odds ratio (Bayes factor) of against the compartmental model.
Additionally, the use of flexible priors vastly improves the fit of the basic model, for both link probability parameters and network partitions. The model variant with beta prior for link probabilities and Dirichlet process prior for partitions performed best. Next, in order, were (1) the model with beta link probability prior and uniform partition prior, (2) the model with uniform link probability prior and Dirichlet process partition prior, and (3) the model with both uniform priors. The strongest variant surpassed its closest competitior by 133 units of (natural) log-likelihood, corresponding to a posterior odds ratio of against the worse one, and surpassed the model with both uniform priors by 439 units of log-likelihood, a posterior odds ratio of . In all cases, 95% confidence intervals on the marginal likelihood estimates were less than one unit of log-likelihood, far less than the differences between models. Given this unequivocal support, we consider results only from the best model variant.
Identification of Model Parameters
We used samples from the posterior distribution to summarize model hyperparameters controlling link probabilities and partitions. The posterior mean number of groups is (95% credible interval ), and the mean value of the Dirichlet process parameter is () (Figure 1). The prior expectation of was 1.0 and the prior expectation of was . The finding of posterior values substantially greater than prior values strongly supports the presence of detailed group structure in the Serengeti food web.
The posterior output includes 30,000 partitions of the Serengeti food web into groups, nearly all distinct from each other. One partition appears 6 times; two partitions appear 3 times; 14 partitions appear 2 times, and the rest appear only once. For the sake of interpretation, we formed a consensus partition (Table S3) of 14 groups from the affinity matrix (Figure 2), which represents the fraction of partitions in all posterior samples in which pairs of species appear in the same group. On average, the consensus partition differs from sampled partitions by 5.6%, calculated as the fraction of species pairs that are assigned to the same group in one partition but to different groups in the other. By comparison, on average, individual sampled partitions differ from other sampled partitions by 7.9%. In addition, every sampled partition differs on average from the others by more than the consensus partition does, indicating the value of the consensus approach.
Species are identically ordered top to bottom and left to right according to the consensus partition as listed in Table 2. Hue indicates group identity; color saturation indicates the fraction of partitions in which species occupy the same group. Note that this image conveys information about group membership, not network connectivity.
Groups Identified in the Serengeti Food Web
The groups identified in the Serengeti food web in the consensus partition contain trophically similar species, with all groups restricted to a single trophic level (plants, herbivores, or carnivores). The consensus partition, with 14 groups, is shown in Table 2. The partition includes 2 groups of carnivores (groups 1–2), 4 groups of herbivores (groups 3–6), and 8 groups of plants (groups 7–14). On average, plant groups contain more species than herbivore and carnivore groups (16.1, 5.8, and 4.5, respectively). As evident in the affinity matrix, the carnivore and herbivore groups are well-defined, including several individual species or pairs of species with distinct diets. Plant groups demonstrate mild overlap, indicating a partially hierarchical relationship between smaller groups and larger groups. Figures 3, 4, and S1 show three alternate views of the food web, organized by the 14 -group consensus partition. Except for carnivore group 1, there are no connections within groups, and partitions are defined by targeted, directed connections between specific pairs of groups. For actual link densities between groups in the consensus partition, see Table S4.
The network is shown organized and colored by group according to the consensus partition listed in Table 2, and arranged by trophic level from left (plants) to right (carnivores). Plants are identified by the first letter of identified habitat type, if available: (G)rassland, (W)oodland, (R)iparian, (K)opje, (S)hrubland, (T)hicket, and (D)isturbed. Plant groups are labeled by significantly overrepresented habitat types, and species assigned to the overrepresented type are labeled with black borders. An interactive version of this figure will be made available at http://edbaskerville.com/research/serengeti-food-web/.
Nodes in the network are aggregated and colored by group according to the consensus partition listed in Table 2, and arranged by trophic level from left (plants) to right (carnivores). Line thickness indicates the link density between groups. Node area increases with the number of species in a group.
Habitat Signature and Food-Web Structure
Overall, plants of the same habitat type are significantly more clustered in groups than random according to weighted Shannon entropy. (Lower values of weighted entropy indicate higher levels of clustering; see Methods.) Mean weighted entropy across all posterior partitions is 1.25 , compared to a randomized mean value of 1.39 ().
Furthermore, the four largest plant groups reflect significant overrepresentation of four different habitat types, and either significant underrepresentation or no significant signal for other habitat types. In group 13, kopje plants are significantly overrepresented, comprising 36.7% of the group, compared to a random expectation of 18.1% (). Group 9 contains 60.4% grassland plants compared to a random expectation of 41.5% (), and includes 40.4% of individual species records in the plot data. All of the identified riparian species occur in group 11, comprising 31.8% of the group, compared with a 6.3% random expectation (). Finally, woodland plants comprise 66.7% of group 8, compared with a random expectation of 25.6% (). This result holds across all individual sampled partitions in the posterior output; each one includes four different groups with significant overrepresentation of kopje, grassland, riparian, and woodland habitat.
Plant groups are coupled by groups of herbivores, which are in turn coupled by groups of carnivores. Large migratory grazers (group 4, wildebeest, zebra, and gazelles) feed plant groups that include the dominant grass species in the ecosystem (group 9), predominantly riparian species (group 11), and a mixture of woodland species (Combretum molle, Digitaria diagonalis, Duosperma kilimandscharica, and others) and less common species (group 8). Group 7 represents a specific case where very high trophic similarity brings two spatially separate plants into the same group. Hyparrhenia rufa is found mainly in the north, and is a significant component of zebra and wildebeest diets during the dry season; in contrast, Digitaria scalarum dominates much of the plains and is eaten in large amounts by migrants during the rainy season when their nutritional needs are at a maximum due to calving and lactation. However, they are grouped together because of their mutual inclusion in the diets of the migratory species. Herbivores feeding in the longer grasslands, woodlands and in riparian habitats (group 3) couple groups 9 and 11. The hyraxes (group 5) and group 6 (giraffe, elephant, buffalo, and others) couple group 13, which bears a strong kopje signature, to groups biased toward other habitats. At the highest trophic level, the large carnivores (group 1) integrate across all the herbivore groups; smaller carnivores (group 2) show more specialized diets, reflecting the more distinct habitats in which they are usually found.
Spatial Guilds in the Serengeti Food Web
In order to analyze the group structure of the Serengeti food web, we used a flexible Bayesian model of network structure that includes no biological information aside from a set of nodes representing species and links representing their interactions. The groups that emerge from an otherwise blind classification of species make remarkable biological sense, and moreover reveal detailed patterns between habitat structure and network topology that expert intuition alone cannot. Species are divided into trophic guilds that reveal a strong relationship between the habitat structure of plant, herbivore, and carnivore groups and the structure of the network. At the coarsest scale, the groups in the Serengeti food web correspond to carnivores, herbivores, and plants. The further subdivisions that emerge within the trophic levels reveal connections between habitat types and feeding structure. This deeper analysis is made possible by high resolution at the plant level along with information about the habitat occupancy of different plants. Since different habitat types occupy distinct spatial locations in the Serengeti, the group structure thus reflects in part the flow of energy up the food web from different spatial locations, with herbivores integrating spatially separated groups of plants, and carnivores integrating spatially widespread herbivores. A priori, it was not clear precisely what kind of group structure would emerge in the Serengeti web from the use of the group model. In general, the more complex the web, the more useful these methods will be in helping to disentangle the complexity.
The food web presented here included only plants and mammals, but we hypothesize that the general conclusions will be largely robust to the addition of more species. Although the addition of birds, reptiles, invertebrates, and pathogens will likely add a significant number of new groups, they should not significantly modify the derived structure for mammals, since the insect-bird links reflect an almost parallel food web. To the extent that insect herbivores further differentiate plants, plant groupings may be affected, but we expect that the larger tendency for groups to reflect habitat structure will remain.
Recently, interesting theoretical and empirical work has highlighted the relationship between observed patterns of food-web structure and energy flow that seemingly relates to the trophic guild structure in the Serengeti. Rooney and colleagues  give evidence that real ecosystems may be dominated by nested sets of fast and slow “energy channels, ” each of which represents a food chain of trophic guilds. They suggest that this pattern may have a strong stabilizing effect, based on theoretical work by McCann on spatially coupled food webs . The group structure for the Serengeti web that emerges from our analysis supports a pattern of spatial coupling at multiple trophic levels: the grasslands have very high turnover rates compared to those of the kopjes and woodlands. This suggests a similar pattern of fast and slow energy channels to those described by Rooney and colleagues, with fast energy flow up through the highly seasonal but very productive grasses of the short-grass plains. These are almost completely consumed by wildebeest and zebra during their peak calving season, which are then in turn consumed by large predators (lions and hyenas). Although the migratory species of wildebeest and zebra form a crucial and major component of the diet of the predatory species, their high abundance and presence in open habitat places them at a lower per capita risk of predation. In contrast, the resident herbivore species living on kopjes and in the woodlands reproduce at slower rates and are consumed at higher per capita rates by large carnivores during the time when the carnivores are unable to feed on migratory wildebeest and zebra.
These patterns emerge directly from the topology of the food web without being explicitly labeled as different habitats upfront as was done in previous empirical work , showing that topological analysis can reveal structures that may be very significant for food-web dynamics. They are subtly different, however, from the proposed pure fast and slow chains, in that they incorporate the migration of the keystone species in the ecosystem, so the fastest energy chain is seasonally ephemeral and may only operate for three to four months in any year. We suspect that even within the sub-habitats of kopjes and woodlands there are similarly nested faster and slower chains that involve species for which we are still collating data (e.g., birds, small mammals, and insects). More generally, we see the identification of important structures in empirical food webs via probabilistic models as important for grounding future investigations into the relationship between structure and dynamics in empirical pattern.
Bayesian Analysis of Food-Web Structure
In this paper, we used a probabilistic model to analyze the structure of a single food web, an approach we have seen in only one other study based on a probabilistic version of the niche model  (see supporting text S1 for more discussion of probabilistic modeling of food webs). This approach has proved fruitful in Bayesian phylogenetics, where the combinatorial challenges are similar. Moreover, we view the group model as only a starting point for richer modeling efforts to help identify relevant processes that influence the structure of ecological communities.
In fact, the Bayesian approach described here provides a powerful general framework for encoding hypotheses about the structure of food webs and comparing models against each other, and we see it as a natural next step in the current trend of representing food-web models in a common way. Simple abstract models such as the niche model and the group model used here act as proxies for the high-dimensional trait space that determines feeding relationships in an ecosystem. The identification of actual traits that correspond to groups (or niche dimensions) is another valuable direction, so far followed primarily by finding correlations between compartments/groups  or niche values  and traits such as body size or phylogenetic relatedness. A more sophisticated, rigorous approach is to directly incorporate such traits into the probabilistic models themselves, either as predictors or as informed Bayesian model priors. Although the current work does not employ that approach, the results from the habitat analysis suggest that including additional information directly in the model would be a valuable approach.
The use of flexible, hierarchical priors for model parameters is another useful innovation of the Bayesian framework. The number of groups identified by the model increases dramatically with the use of a flexible beta prior distribution for link probability parameters. In that model variant, we effectively introduce two degrees of freedom to the model (the beta distribution parameters) but dramatically reduce the effective degrees of freedom of the link probability parameters. Note that we penalize parameters by using the marginal likelihood for model selection, so that the model selection represents a balance between goodness of fit and model complexity. Moreover, this structure makes intuitive sense: since most link probability parameters are simply zero, they should not be penalized. An alternate approach is to remove and add parameters to the model, but this hierarchical technique is much easier to implement in practice.
Advanced Markov-chain Monte Carlo methods make it possible to accurately estimate marginal likelihoods for probabilistic network models. Unlike information criteria such as AIC or BIC, an accurate estimate of the marginal likelihood provides a direct measurement of goodness of fit that takes into account the degrees of freedom in a model without making any asymptotic assumptions about parameter distributions , and can handle discrete parameters such as partitioning into groups that are not properly handled by AIC and BIC.
Additionally, the Bayesian approach also serves as a means to avoid fundamental issues inherent in network models with a large parameter space. One recent study has shown that, even in relatively small networks, a large number of good solutions exist for the standard modularity criterion , . A maximization algorithm is thus guaranteed to find a single local maximum of many—possibly even the best one, but certainly not one that captures the full range of good solutions. This problem arises whether the quantity to be maximized is a heuristic such as modularity or a likelihood value. The group model and other parameter-rich models presumably suffer from similar degeneracy problems. In the present case, we find that nearly every partition sampled from the posterior distribution is unique. Although MCMC sampling cannot reproduce the full posterior distribution, it is an important step in the right direction. Philosophical arguments aside, one of the main reasons for maximizing likelihood or modularity is simply that a single solution is far more tractable than a distribution. The consensus partitioning heuristic used here is an attempt to find a single partition that represents the posterior distribution reasonably well for the sake of interpretation and presentation (see Methods). More sophisticated approaches to collapsing partitions will be welcomed. However, since the Bayesian approach provides direct access to uncertainty in the form of the posterior distribution, quantitative analyses should be done across the whole distribution, and we follow that approach here.
The group model, based on the simple notion that groups of species may have similar feeding relationships to other groups, reveals that trophic guilds are the topologically dominant type of group in the Serengeti food web. The model also reveals an interesting relationship between habitat structure and network structure that corroborates recent ideas on spatial coupling in food webs. A theoretical study with a dynamical model suggests that this type of structure may contribute to ‘stability’ in the sense of the persistence of species . Now, by using group structures directly inferred from empirical webs, we can better guide investigations into the relationship between structure and various aspects of stability, for example robustness to secondary extinctions , . Although the Bayesian modeling approach is not new to network analysis in general , , it remains relatively rare. The Bayesian group model, and, more importantly, the general framework for modeling and model selection, naturally extend to other kinds of biological networks, such as metabolic and regulatory networks  and networks describing other ecological interactions such as pollination . We advocate this framework as a way to build stronger ties between hypothesis formulation, model building, and data analysis.
The Bayesian Group Model
In this work, we use Bayesian probabilistic models to analyze food webs; for a general introduction to the Bayesian modeling approach and details on the specific models used here, please see supporting text S1. We employ a generative model based on groups that treats the food-web network, represented as the presence or absence of each possible feeding link, as data. The group model , known as a stochastic block model in the statistical literature , was previously treated in a maximum-likelihood framework. In a Bayesian framework, both data and model parameters are treated probabilistically, making the object of inference a posterior distribution over model parameters rather than a point estimate. For a general overview of Bayesian inference, see section 3 of supporting text S1.
The group model (supporting text S1, section 2) divides species into some number of groups , thus determining a partition. All possible links between any pair of groups are assigned the same probability of existing, , for consumer group and resource group . If a between-group link probability is close to one, then there are likely to be many links with a species from group feeding on a species from group . A highly compartmental network can be generated by having lower between-group link probabilities (for ) than within-group link probabilities .
Priors and Model Variants
In general, priors may incorporate informed knowledge about the system, but in this case we simply use them to encode different variants of the same basic model. We use two distributions for partitions and two distributions for link probabilities, which are combined to form four different model variants. We also consider several null models for comparison.
For partitions, we employ two prior distributions: (1) a uniform distribution and (2) a distribution generated by the Dirichlet process, sometimes referred to as the “Chinese restaurant process” . Alternative (2) is controlled by an aggregation parameter that is in turn drawn from an exponential distribution with mean 1. The uniform distribution assigns equal prior probability to each possible partition, irrespective of the number of groups. Because there are far more ways to partition the network at an intermediate, but relatively high, number of groups, the uniform prior implicitly biases the model toward that number. For example, for a network of 100 nodes, there is an a priori expectation of groups. In contrast, the hierarchically structured Dirichlet process prior provides flexibility via the aggregation parameter . When is large, partitions tend to have many small groups; when is small, partitions tend to have fewer groups, with a skewed group-size distribution. See section 3.1 of supporting text S1 for mathematical details and a fuller discussion.
Link probability prior.
The two alternative prior distributions used for link probabilities are (1) a uniform distribution between 0 and 1, and (2) a beta distribution with shape parameters and , which are in turn governed by exponential distributions with mean 1. With and fixed at their means, alternative (2) reduces to a uniform distribution; at other values, the distribution may take a uniform, convex, concave, or skewed shape. The second alternative is thus structured hierarchically, with exponential hyperpriors for and governing the beta prior for link probabilities . For more details, see section 2.1 of supporting text S1.
We also consider two simple models without groups as null comparisons: (1) a directed random graph model (i.e., one group) with a uniform prior on a single link probability parameter , and (2) a fully parameterized model, with each species in its own group, and a link probability parameter matrix , also with a uniform link probability prior.
Finally, in order to explicitly restrict the model to detecting compartmental structure, we also consider a modification that requires all between-group link probabilities to be less than corresponding within-group link probabilities and . This is accomplished by adding a parameter for each between-group probability, and setting equal to .
Markov-chain Monte Carlo Sampling
We sample from the posterior distribution of model parameters using a Markov-chain Monte Carlo technique known as Metropolis-coupled MCMC, or , which improves mixing between multiple modes of the posterior distribution, and also allows improved estimation of the marginal likelihood . Software for performing MCMC sampling was implemented in Java, and is available from the corresponding author on request. A full treatment of MCMC is given in supporting text S1, section 4, including details on applying the method to the group model.
Bayesian Model Selection
In order to select a good model variant, we employ the marginal likelihood, the probability of data given a model integrated over all model parameters (partitions and link probability parameters). This approach extends the use of Bayes' rule to model selection as well as inference of parameter values. The ratio of the marginal likelihoods for two models is often called the Bayes factor –, and determines the posterior odds ratio of two models given equal prior odds. For details on marginal likelihood-based model selection, see text S1, section 5.
The output of an MCMC simulation includes a large number of network partitions representing draws from the posterior distribution. As these partitions are potentially all distinct from each other, but represent similar tendencies of species to be grouped together, it is useful to try to summarize the information contained in all the samples in a more compact form. To do this, we construct an affinity matrix with entries equal to the posterior probability that two species are grouped together. We use the affinity matrix to then form a consensus partition, using an average-linkage clustering algorithm (see supporting text S1, section 6). The affinity matrix is akin to the co-classification matrix previously used to identify uncertainty in end-points in a simulated annealing algorithm .
In order to test the overall presence of habitat signature in plant groups, we assigned plants to habitat types via one of three methods based on data availability. For plants present in 133 plots sampled from around the Serengeti , we assigned them to the habitat type of the plot in which they were most abundant; plot habitat types were assigned via a separately compiled map of habitat boundaries . Some plants were available from a study of kopje forbs . Finally, some were assigned from personal knowledge of the system.
We used a randomization test to measure the overall clustering of habitat in groups across sampled partitions. The habitat signature of an individual group was measured as the Shannon entropy—low entropy indicates an uneven distribution—of the assignment of species to habitats, , where is the habitat, is the group size, and there are species assigned to habitat within the group. The overal clustering signature for a partition was the average of the individual group entropies, weighted by the size of the groups, , for total species count . The p-value for the statistic is the probability that a partition drawn from the posterior distribution has overall clustering greater than or equal to a randomized partition with groups of identical size.
To test clustering significance of a specific habitat type in a specific grouping of species, we calculated the p-value as the probability that a randomized group of the same size would have as many or more species assigned to the chosen habitat type.
Adjacency matrix ordered by groups. Species are identically ordered top to bottom and left to right according to the consensus partition as listed in Table 2. White matrix entries indicate that the species in the column feeds on the species in the row. Columns that would indicate prey of plant groups are omitted. Note that in a modular network according to the standard definition, links would be concentrated on the diagonal of the adjacency matrix, since they occur within groups. By contrast, here links are concentrated in off-diagonal blocks.
Posterior distributions of link density parameters and . Color brightness indicates posterior density, estimated using the ks multivariate kernel density estimation package for R . Contours indicate cumulative density. The parameter is significantly lower than 1, indicating departure from a uniform distribution.
Distribution of link probability parameters. The prior distribution for link probability parameters, integrated over the priors for beta distribution parameters and , is indicated with a dotted line. The heat map shows beta distributions corresponding to the posterior distribution for and , with lightness indicating the posterior density of the parameter values.
Species in the Serengeti food web.
Feeding links in the Serengeti food web.
Link densities between groups in the consensus partition.
In this supplement, we describe the mathematical details of the modeling approach, including the Bayesian formulation of the group model, the Markov-chain Monte Carlo algorithm, and marginal likelihood estimation.
A.D. acknowledges the Frankfurt Zoological Society for logistical support in the Serengeti for his work on food webs, and the members of Serengeti Biocomplexity Project for many interesting discussions about the Serengeti food 419 web. M.P. is an investigator of the Howard Hughes Medical Institute.
Conceived and designed the experiments: EBB APD TB SA MP. Performed the experiments: EBB. Analyzed the data: EBB APD TMA. Contributed reagents/materials/analysis tools: EBB APD TB SA. Wrote the paper: EBB APD TB SA MP. Developed the software used in analysis: EBB. Compiled food-web data from published literature: APD. Contributed plant distribution data: TMA. Developed an interactive network visualization tool: TB.
- 1. Cohen JE (1994) Lorenzo camerano's contribution to early food web theory. Frontiers in Mathematical Biology. Berlin: Springer. volume 100 of Lecture Notes in Biomathematics. pp. 351–359.
- 2. Camerano L (1880) Dell'equilibrio dei viventi merce la reciproca distruzione. Accademia delle Scienze di Torino 15: 393–414.
- 3. Elton CS (1927) Animal Ecology. Text-Books of Animal Biology. London: Sidgwick & Jackson, Ltd.
- 4. May RM (1973) Stability and Complexity in Model Ecosystems. Princeton University Press.
- 5. Girvan M, Newman M (2002) Community structure in social and biological networks. Proc Natl Acad Sci U S A 99: 7821.
- 6. Pimm S, Lawton J (1980) Are food webs divided into compartments? J Anim Ecol 49: 879–898.
- 7. Teng J, McCann K (2004) Dynamics of compartmented and reticulate food webs in relation to energetic ows. American Naturalist 164: 85–100.
- 8. Thébault E, Fontaine C (2010) Stability of ecological communities and the architecture of mutualistic and trophic networks. Science 329: 853.
- 9. Guimera R, Stouffer D, Sales-Pardo M, Leicht E, Newman M, et al. (2010) Origin of compartmenttalization in food webs. Ecology 91: 2941–2951.
- 10. Krause A, Frank K, Mason D, Ulanowicz R, Taylor W (2003) Compartments revealed in food-web structure. Nature 426: 282–285.
- 11. Rezende E, Albert E, Fortuna M, Bascompte J (2009) Compartments in a marine food web associated with phylogeny, body mass, and habitat structure. Ecol Lett 12: 779–788.
- 12. Allesina S, Pascual M (2009) Food web models: a plea for groups. Ecol Lett 12: 652–62.
- 13. Burns T (1989) Lindeman's contradiction and the trophic structure of ecosystems. Ecology 70: 1355–1362.
- 14. Luczkovich JJ, Borgatti SP, Johnson JC, Everett MG (2003) Defining and measuring trophic role similarity in food webs using regular equivalence. J Theor Biol 220: 303–321.
- 15. Polis G (1991) Complex trophic interactions in deserts: an empirical critique of food-web theory. Am Nat 138: 123–155.
- 16. Reagan D, Waide R (1996) The food web of a tropical rain forest. University of Chicago Press.
- 17. de Visser SN, Freymann BP, Olff H (2011) The serengeti food web: empirical quantification and analysis of topological changes under increasing human impact. J Anim Ecol 80: 484–494.
- 18. Novotny V, Miller SE, Baje L, Balagawi S, Basset Y, et al. (2010) Guild-specific patterns of species richness and host specialization in plant–herbivore food webs from a tropical forest. J Anim Ecol 79: 1193–1203.
- 19. Martinez N, Hawkins B, Dawah H, Feifarek B (1999) Effects of sampling effort on characterization of food-web structure. Ecology 80: 1044–1055.
- 20. Memmott J, Martinez N, Cohen J (2000) Predators, parasitoids and pathogens: species richness, trophic generality and body sizes in a natural food web. J Anim Ecol 69: 1–15.
- 21. Cohen JE, Briand F, Newman CM (1990) Community Food Webs: Data and Theory. Biomathe matics. Springer.
- 22. Williams R, Martinez N (2000) Simple rules yield complex food webs. Nature 404: 180–183.
- 23. Allesina S, Alonso D, Pascual M (2008) A general model for food web structure. Science 320: 658–61.
- 24. McCarthy MA (2007) Bayesian Methods for Ecology. Cambridge University Press.
- 25. Hoff P, Raftery A, Handcock M (2002) Latent space approaches to social network analysis. J Am Stat Assoc 97: 1090–1098.
- 26. Park Y, Moore C, Bader JS (2010) Dynamic networks from hierarchical Bayesian graph clustering. PLoS ONE 5: e8118.
- 27. Clauset A, Moore C, Newman MEJ (2008) Hierarchical structure and the prediction of missing links in networks. Nature 453: 98–101.
- 28. Williams R, Anandanadesan A, Purves D (2010) The probabilistic niche model reveals the niche structure and role of body size in a complex food web. PLoS ONE 5: e12092.
- 29. Yang Z, Rannala B (1997) Bayesian phylogenetic inference using DNA sequences: a Markov chain Monte Carlo method. Mol Biol Evol 14: 717.
- 30. Mau B, Newton M, Larget B (1999) Bayesian phylogenetic inference via Markov chain Monte Carlo methods. Biometrics 55: 1–12.
- 31. Sinclair ARE, Norton-Griffiths M, editors. (1979) Serengeti, Dynamics of an Ecosystem. University Of Chicago Press.
- 32. Sinclair ARE, Arcese P, editors. (1995) Serengeti II: Dynamics, Management, and Conservation of an Ecosystem. University Of Chicago Press.
- 33. Sinclair ARE, Packer C, Mduma SA, Fryxell JM, editors. (2008) Serengeti III: Human Impacts on Ecosystem Dynamics. University Of Chicago Press.
- 34. McNaughton S (1983) Serengeti grassland ecology: the role of composite environmental factors and contingency in community organization. Ecol Monograph 53: 291–320.
- 35. Sinclair A, Mduma S, Brashares J (2003) Patterns of predation in a diverse predator–prey system. Nature 425: 288–290.
- 36. Casebeer R, Koss G (1970) Food habits of wildebeest, zebra, hartebeest and cattle in Kenya Masailand. Afr J Ecol 8: 25–36.
- 37. Cooper S, Holekamp K, Smale L (1999) A seasonal feast: long-term analysis of feeding behaviour in the spotted hyaena (Crocuta crocuta). Afr J Ecol 37: 149–160.
- 38. Hansen R, Mugambi M, Bauni S (1985) Diets and trophic ranking of ungulates of the northern Serengeti. J Wildl Manage 49: 823–829.
- 39. Murray M (1993) Comparative nutrition of wildebeest, hartebeest and topi in the Serengeti. Afr J Ecol 31: 172–177.
- 40. Talbot L, Talbot 495 M (1962) Food preferences of some East African wild ungulates. East Afr Agric For J 27: 131–138.
- 41. Talbot LM, Talbot MH (1963) The Wildebeest in Western Masailand, East Africa. Wildlife Monogr 12: 3–88.
- 42. Schaller G (1972) The Serengeti Lion. University of Chicago Press.
- 43. Caro T (1994) Cheetahs of the Serengeti Plains: Group Living in an Asocial Species. University of Chicago Press.
- 44. Kruuk H (1972) The Spotted Hyaena. University of Chicago Press.
- 45. McNaughton S (1985) Ecology of a grazing ecosystem: the Serengeti. Ecol Monograph 55: 259–294.
- 46. Vesey-FitzGerald D (1960) Grazing succession among East African game animals. J Mammal 41: 161–172.
- 47. Lamprecht J (1978) On diet, foraging behaviour and interspecific food competition of jackals in the Serengeti National Park, East Africa. Z Säugetierkd 43: 210–223.
- 48. Rooney N, McCann K, Moore J (2008) A landscape theory for food web architecture. Ecol Lett 11: 867–881.
- 49. McCann K, Rasmussen J, Umbanhowar J (2005) The dynamics of spatially coupled food webs. Ecol Lett 8: 513–523.
- 50. Bolker BM (2008) Ecological Models and Data in R. Princeton University Press.
- 51. Newman M (2006) Modularity and community structure in networks. Proc Natl Acad Sci USA 103: 8577.
- 52. Good B, De Montjoye Y, Clauset A (2010) Performance of modularity maximization in practical contexts. Phys Rev E 81: 46106.
- 53. Dunne J, Williams R (2009) Cascading extinctions and community collapse in model food webs. Phil Trans R Soc B 364: 1711.
- 54. Bodini A, Bellingeri M, Allesina S, Bondavalli C (2009) Using food web dominator trees to catch secondary extinctions in action. Phil Trans R Soc B 364: 1725.
- 55. Jeong H, Tombor B, Albert R, Oltvai Z, Barabási A (2000) The large-scale organization of metabolic networks. Nature 407: 651–654.
- 56. Bascompte J, Jordano P, Melián C, Olesen J (2003) The nested assembly of plant–animal mutualistic networks. Proc Natl Acad Sci U S A 100: 9383.
- 57. Wang Y, Wong G (1987) Stochastic blockmodels for directed graphs. J Am Stat Assoc 82: 8–19.
- 58. Ferguson T (1973) A Bayesian analysis of some nonparametric problems. Ann Stat 1: 209–230.
- 59. Geyer C (1991) Markov chain monte carlo maximum likelihood. In: Keramidas E, editor. Proceedings of the 23rd Symposium on the Interface. Computing Science and Statistics. pp. 156–163.
- 60. Lartillot N, Philippe H (2006) Computing Bayes factors using thermodynamic integration. Syst Biol 55: 195–207.
- 61. Jeffreys H (1935) Some tests of significance, treated by the theory of probability. Proc Cambridge Philos Soc 31: 203–222.
- 62. Jeffreys H (1961) Theory of Probability. The International Series of Monographs on Physics. 3rd edition. Oxford: Clarendon Press.
- 63. Kass R, Raftery A (1995) Bayes factors. J Am Stat Assoc 90: 773–795.
- 64. Sales-Pardo M, Guimera R, Moreira A, Amaral L (2007) Extracting the hierarchical organization of complex systems. Proc Natl Acad Sci U S A 104: 15224.
- 65. Anderson TM, Shaw J, Olff H (2011) Ecology's cruel dilemma, phylogenetic trait evolution and the assembly of serengeti plant communities. J Ecol 99: 797–806.
- 66. Reed DN, Anderson TM, Dempewolf J, Metzger K, Serneels S (2009) The spatial distribution of vegetation types in the serengeti ecosystem: the inuence of rainfall and topographic relief on vegetation patch characteristics. J Biogeogr 36: 770–782.
- 67. Poelchau M, Mistry S (2006) Forb diversity and community similarity of kopjes in the Serengeti national park, tanzania. Afr J Ecol 44: 38–46.
- 68. Duong T (2007) ks: Kernel density estimation and kernel discriminant analysis for multivariate data in R. J Stat Softw 21: 1–16.