Fire-adapted Gondwanan Angiosperm floras evolved in the Cretaceous
© Lamont and He; licensee BioMed Central Ltd. 2012
Received: 29 June 2012
Accepted: 2 November 2012
Published: 22 November 2012
Fires have been widespread over the last 250 million years, peaking 60−125 million years ago (Ma), and might therefore have played a key role in the evolution of Angiosperms. Yet it is commonly believed that fireprone communities existed only after the global climate became more arid and seasonal 15 Ma. Recent molecular-based studies point to much earlier origins of fireprone Angiosperm floras in Australia and South Africa (to 60 Ma, Paleocene) but even these were constrained by the ages of the clades examined.
Using a molecular-dated phylogeny for the great Gondwanan family Proteaceae, with a 113-million-year evolutionary history, we show that the ancestors of many of its characteristic sclerophyll genera, such as Protea, Conospermum, Leucadendron, Petrophile, Adenanthos and Leucospermum (all subfamily Proteoideae), occurred in fireprone habitats from 88 Ma (83−94, 95% HPD, Mid-Upper Cretaceous). This coincided with the highest atmospheric oxygen (combustibility) levels experienced over the past 150 million years. Migration from non-fireprone (essentially rainforest-climate-type) environments was accompanied by the evolution of highly speciose clades with a range of seed storage traits and fire-cued seed release or germination mechanisms that was diagnostic for each clade by 71 Ma, though the ant-dispersed lineage (as a soil seed-storage subclade) was delayed until 45 Ma.
Focusing on the widespread 113-million-year-old family Proteaceae, fireproneness among Gondwanan Angiosperm floras can now be traced back almost 90 million years into the fiery Cretaceous. The associated evolution of on-plant (serotiny) and soil seed storage, and later ant dispersal, affirms them as ancient adaptations to fire among flowering plants.
Recent syntheses have highlighted geological evidence for the occurrence of fire since the Triassic, particularly over the last 65−125 million years (Cretaceous) , suggesting that fire may have had a major role in the evolution of Angiosperms [2–4]. However, fire as an important agent of natural selection has received little attention because fireprone floras are usually thought to have appeared only after the global climate became more arid and seasonal <15 million years ago (Ma) making their fire-related traits ‘exaptations’ at best [5, 6]. Recent trait-assignment studies have shown that fireprone floras likely existed in Australia [7, 8] and the Cape of South Africa [9, 10] earlier than that (up to 60 Ma) coinciding with the appearance of fire-adapted traits. However, estimates of the time of origin of ancestral fire-related traits and fireproneness of the habitat occupied by the root of the clade may still have been constrained by the a) insufficient age of the clade, or b) inability of the DNA in extant organisms to adequately reflect the fossil record because of lineage (ancestral DNA) loss. That is, the estimated time of origin of fire-related traits or fireprone habitats may be limited by the estimated age of the clade not necessarily by the inauguration of recurrent fires (though a cause-and-effect coincidence is possible).
Thus, inferring the time of origin of fireprone floras using individual genera within a family can be artificially constrained by extinction of certain lineages or age of the clade itself, ignoring the possibility that it was a change in the fire regime that stimulated the evolution of the clade in the first place. However, the family Proteaceae can be traced to 113 Ma (Lower Cretaceous)  and holds promise as a demonstration of unconstrained evolutionary responses to fire as it is considered to have rainforest-climate (non-fireprone) origins and its extant fire-adapted traits in fireprone floras are well known. Seeds stored on the plant (serotiny) and released via fire heat , or transferred to the soil via wind or ants  and cued to germinate by fire heat or smoke , Figure 1c−i, are critical functional traits in fireprone environments [3, 16, 17], as they enable seeds to germinate in response to fire when recruitment conditions are optimal (Figure 1j). Hence, we may view the various types of seed storage/release/germination as fire-adapted traits, in the sense of increasing fitness in the presence of fire . Seed storage/germination type is a conserved generic trait so that we were able to superimpose the three major syndromes of seed storage/germination (serotiny; soil – all dispersal types, ant-dispersed only) onto a recently produced Proteaceae chronogram (Figure 1a). Critically from an adaptation perspective (i.e. having evolved in response to the purported agent of selection, 16), we sought to test whether the three types of seed storage have evolved synchronously with the onset of fireprone habitats occupied by this family. If this were so it would be the first evidence of fire-adapted traits occurring among flowering plants as far back as the Cretaceous, a time of high flammability and escalating species diversification rates [1, 4].
We chose seed storage/release/germination traits as these are well documented for the entire family and are invariably diagnostic for each genus, and difficult to interpret as other than fire-adapted [8, 13]. Other putative fire-related traits that also have been examined in proteaceous genera, such as dead leaf retention, fire-stimulated flowering and resprouting [8, 10], have the disadvantages that they are poorly documented by comparison (e.g. rainforest species never burn to determine if they could resprout), are not clearly ancestral within the genus or definitely derived [8, 10], and/or not yet convincingly shown to have greatest fitness in the presence of recurrent fire. Much more research at the level of documenting occurrence of these traits and demonstrating superior fitness at the species level is required before their evolutionary history can be considered further.
Analysing the entire family Proteaceae confirmed that it was able to provide an unconstrained estimate of the time fire-related traits and fireprone floras originated (Figure 1a). Our ancestral state reconstructions, using both range expansion and fireprone trait allocation approaches (see Methods), were the same, showing that the origin of fireprone proteaceous floras can be traced to 88 (83−94, 95% HPD) Ma, at the root of the indehiscent clades (subfamilies Proteoideae and Symphionematoideae) and 25 million years (My) younger than the origin of the family clade . This time coincided with the migration of shrubby, fine-leaved ancestors from closed forest to fireprone habitats (D2 in Figure 1a). Thus, the first 25 My existence of the Proteaceae clade was confined to closed forest, but not until the indehiscent-fruited ancestors of the Proteoideae colonized fireprone sclerophyll woodland/forest (and later scrub- and mallee-heath) did its genera and species proliferate (Figure 1a). This difference in the pattern of speciation between fireprone and non-fireprone habitats was not the same for the dehiscent-fruited clade (Grevilleoideae) at the generic level but it was at the species diversification level within genera. For the entire family we identify five dispersal events from rainforest to fireprone environments that usually led to explosive speciation among their lineages, on average 4.4 times the rate in closed forest (Figure 1k). There appear to be six genera showing migration events in the reverse direction although four retained species or populations in fireprone habitats, two remained monotypic and Dilobeia has only three species (Figure 1a).
During the Coniacian−Campanian Stages of the Upper Cretaceous (geological boundaries according to the International Commission on Stratigraphy, see http://www.stratigraphy.org), fireprone clades appear with a wide array of seed storage/ release/germination responses to fire, especially in the Proteoideae. If seed storage as a trait is substituted for soil or canopy storage (as only binary traits may be analysed) then there is a minimum 0.40 probability of some form of storage at 88 Ma to certainty at 76 Ma (Additional File 3: Figure S3). The assignments indicate that the 70−90 Ma period was a time of much initiation, proliferation and extinction of traits among the early clades. By 74 (71−78) Ma, the stem of the Petrophile−Aulax clade suggests that serotiny may have arisen in the Australian region of Eastern Gondwana  while Banksia is the oldest extant serotinous genus there at 61 (56−67) Ma. Serotiny appeared last in the archetype sclerophyll genus, Hakea, arising independently from rainforest ancestors 16 Ma (Additional File 1: Figure S1). The stem of the Cape Proteeae (excluding Protea−Faurea) arose from Australian ancestors , so it is less clear for how long the Cape flora has been fireprone. The habitat type of the stem of Protea Faurea is fireprone because of the fireprone status of the surrounding lineages (plus Protea) but it is non-serotinous (unlike Protea) and lacks storage. At 49 (28−67) Ma, Aulax is the oldest extant genus in fireprone habitats of the Cape.
The Franklandia–Mimetes clade (SWA) originating 74 (71−78) Ma is the oldest with soil storage (Additional File 2: Figure S2). This is followed almost immediately, and independently, by the Stirlingia−Conospermum−Synaphea clade (SWA) originating 71 (60−80) Ma. Adenanthos−Leucadendron to Mimetes is the only clade in the Proteoideae with an aril (elaiosome) attached to the single-seeded fruit as an aid to dispersal and burial by ants (Figure 1e, S3). The stem of this elaborate dispersal/storage/germination response to fire is dated from 44.5 (32−58) Ma for Adenanthos in SWA and the Leucadendron to Mimetes subclade in the Cape (as the oldest member of this group in the Cape, Leucadendron actually has a wide array of storage mechanisms). These are among some of the earliest elaiosome-bearing lineages known and correspond to the advent of ants as reliable dispersal agents . In contrast, the highly speciose genus, Grevillea, was the only Grevilleoid to develop ant dispersal traits and this appeared very late (11 Ma). Overall, each of the three seed storage syndromes evolved closely and synchronously with fireprone habitats in this family (χ2 = 47.8 (serotiny), 55.4 (soil seedbank), 79.5 (ant-dispersed), P < 0.001, ).
Did these clades actually exist by then? The fossil record supports the existence of pollen with affinities to at least two extant genera in the Proteoideae, and 17 pollen types whose Proteaceae affinities are less prescribed, in eastern Gondwana (Zealandia, southern Australia – especially the Otway Basin,) during the Santonian-Campanian (86−71 Ma) [12, 19–24]. Dettmann and Jarzen  concluded that the southern Australian/Antarctic vegetation in this period must have been a mosaic of rainforest (though the angiosperm element would not have been dominant) and sclerophyll communities, with the Proteaceae prominent in the latter (Sauquet et al.  discredit most of their identifications at genus level but this does not invalidate their clear Proteaceae affinities that are not in dispute).
Did suitable habitats exist by then? By 90−85 Ma most of the current Australian portion of Eastern Gondwana had emerged due to sedimentation (high rainfall) and general elevation of the continent , including the Otway, Eromanga and Murray Basins. The sedimentary basins: Eucla, Officer and Surat, were already exposed by 100−90 Ma. In addition, various metasediments were uplifted/downwarped in the lower-mid-Cretaceous (Stirling−Barren Ranges in SW Australia, Great Dividing Range, Victorian Southern Uplands [6, 26]). Heavy leaching due to the high but seasonal rainfall during the Upper Cretaceous created oligotrophic sands and ferricretes [22, 27, 28]. There has even been the suggestion that the Proteaceae was a (mainly Cenozoic) driver in this process . Thus, well-drained, nutrient-poor substrates (sands, sandstones, quartzite, schists, laterites) of variable elevation and suitable for colonization by the evolving sclerophyll element were already widespread.
Is there direct evidence of fire at that time? Abundant charcoal is recorded in the Eromanga Basin, SW Queensland, at 100–94 Ma . Charcoal was noted among pollen samples in Zealandia at 94–85 Ma , together with other evidence “suggesting a generally broad occurrence of fire in the mid-Cretaceous across middle to high latitudes in the Southern Hemisphere” that the authors attributed in part to the high atmospheric oxygen. Charcoalified fragments (‘black wood’) made up 40% of the microsamples that contained pollen of > 7 Proteaceae species (including several with suggested Proteoideae affinities) in Zealandian sandstones at 88–71 Ma  indicating that “wildfires were part of the Late Cretaceous ecosystem”. Eklund et al.  studied 83-My-old charcoalified mesofossils of Angiosperms between Antarctica and Australia that they attributed to fires caused by volcanism near the collection site.
Was there selection against the fire-sensitive ancestors that might have biased the assignments? Figure 2 shows that net lineage proliferation at the generic level has continued steadily and in parallel for both fireprone and non-fireprone groups. This means that fire-sensitive clades did not become extinct at the expense of fire-tolerant clades that might have distorted the analysis – this is consistent with both being accommodated in different vegetation types through time preventing their extinction . If extinction was recent it would have to be on a massive scale to delete all trace of the non-fire-tolerant lineage. It seems that even during the last glacial maximum, rainforest species in eastern Australia, including Proteaceae, were able to survive in moister lowland refugia . Further, if (unrecorded) extinction of fire-sensitive taxa had occurred along basal stems of clades that our analysis currently assigns as in fireprone habitats, this would not alter the assignment as this (correctly) infers that the surviving lineage was fire-tolerant at that point in time. The only requirement then is to show that the lineage actually existed at that time via fossil evidence. In this regard it is noteworthy that 15 of the 26 pollen/leaf types assessed by Sauquet et al.  were allocated to the base of extant rainforest clades or sediments arising > 88 Ma, i.e. prior to the oldest time that our analysis identifies fireprone habitats for the Proteaceae. In addition, five are associated with younger rainforest clades, ten with fireprone habitats, and all 26 can be traced to extant genera (though few could be confidently assigned to any one), i.e. none necessarily implies an extinct lineage.
A related problem with the purported origin of the three extant fire-tolerant Proteaceae lineages in the Upper Cretaceous (Figure 1a) is the possible exterminatory effect of the subsequent early Eocene (40–56 Ma), one of the wettest periods known. Indeed, fire-derived inertinite in coal dropped markedly in Northern Hemisphere mires after 60 Ma . While the climate was especially wet and aseasonal throughout eastern Gondwana during the Eocene, it remained warm (except in the Tasmanian region) and much of the Central-West zones of the Australian portion of Gondwana had moderate and strongly seasonal rainfall . Atmospheric oxygen levels were up to 15% higher than currently and burn probability was the highest for the last 60 My (Figure 3). Further, deeply weathered sands or siliceous/lateritic rocks, often in open, well-drained parts of the landscape, were widespread and would have provided ideal refugia for the sclerophylls, especially Proteaceae, in their own communities [38, 40–42]. Indeed, the Proteaceae (Banksia-like wood, pollen akin to Petrophile, Adenanthos) at Lake Lefroy, SWA in the mid-Eocene accounted for 34% of all pollen (when Nothogfagus was omitted), with species richness values comparable with those in SWA scrub-heath today . Interestingly, where fire did occur around the eastern Otway Basin, it not only led to a severe reduction in Nothofagus but also in Proteaceae and Myrtaceae , implying that the species there were more vulnerable to fire than their western counterparts .
We therefore suggest that much of the fire-dependent, sclerophyll element contracted west during the Eocene. Some of these returned/expanded in a second wave of migration during the Oligocene-Miocene (e.g. Banksia ss, Eucalyptus) but usually remained poorly represented (e.g. Adenanthos, Petrophile), others did not return (e.g. Franklandia), while others only arose then but never reached eastern Australia (e.g. Dryandra). In support, Figure 3 shows no increase in proliferation rates of non-fireprone-habitat lineages at the expense of fireprone lineages in the 40–60 My period; if anything the reverse is true. In addition, we point to the exacerbated bias against increasingly isolated pockets of sclerophyll vegetation in the fossil record from lake sediments during particularly wet periods, and note that strongly fire-adapted Pinus in the NH (fossils) and Nuytsia in SWA (molecular dating) have also been recorded from the mid-Eocene [1, 10].
Finally, the two seed storage mechanisms that facilitate postfire germination and seedling recruitment were already appearing 88−81 Ma according to our analysis, though neither type prevailed in any clade, indicating that much diversification and extinction along the major stems must have been occurring. By 81 Ma, seed storage was firmly established in one basal clade. By 71 Ma, clades in fire-prone habitats were characterized by either soil or on-plant fruit storage (except for continuing variation in the Beauprea/Faurea/Protea clade). Note that the two rainforest genera in Proteoideae, Eidotheia and Delobeia, did not speciate to any extent (or suffered almost complete extinction), while two remained monotypic (Agastachys, Cenarrhenes) or had limited speciation (Beauprea, Faurea) in genera with populations or species respectively largely remaining in rainforest today. In particular, only Beauprea among the seven genera occupying mixed habitats has the capacity for seed storage, though it would be of interest to know why this once-widespread genus became extinct in Australia. The only genera lacking strong speciation once in fireprone habitats are Beaupreopsis, with a small soil-stored pyrene, that occurs in scrub-heath of New Caledonia and is monotypic (44), and Symphionema with two species in scrub-heath of NSW and possesses a thin-walled achene “expected to show some form of dormancy” . Comparing speciation rates overall between fireprone-habitat and non-fireprone sister clades (Figure 1k), the pivotal role of seed storage for successful occupation of fireprone habitats is supported (Figure 1a) and the two are highly correlated through time (P < 0.001) confirming their classification as true fire adaptations.
The mechanism of seed storage on the plant is different between the Grevilleoideae and Proteoideae: in the former, woody fruits protect and support the seeds and dehisce in response to heat and desiccation while, in the latter, bracts (assisted by branchlets in the case of Aulax) protect and support the fruits and spread to release the single-seeded fruits in response to heat and desiccation. This has arisen four times independently in the Grevilleoideae, and four times in the Proteoideae (Figure 1a). While they were treated as the one trait for purposes of the analysis this did not create origin artefacts as the two subfamilies remained independent with respect to the evolution of serotiny in the family.
All soil-stored seeds are actually one-seeded fruits in the Proteaceae (except Grevillea), comprising a thin pericarp (swollen at the base to form an elaiosome in the Adenanthos–Mimetes clade, Figure 1a), exotesta (of varying thickness and texture) and crystalliferous endotesta [46, 47]. The succulent-fruited Persoonieae (Persoonioideae) had an independent origin from the dry-fruited Proteoideae/Symphionematoideae that appeared independently five times (Figure 1a). Leucadendron has a possible sixth independent origin where our informal analysis of a cladogram for 62 of its 96 taxa  indicates that the ancestral state is serotiny with winged fruits followed by dormant nutlets and soil-stored achenes, followed much later by a few species with elaiosome-bearing achenes – this requires more detailed research, especially the need for smoke-stimulated germination throughout the genus. This is the only genus that had to be assigned mixed traits – in all others the assigned trait was part of the circumscription of the genus or shown to be the ancestral condition (Banksia; Protea, Lamont and He unpublished). The separate origins of soil-storage in the Stirlingia–Synaphea (71 Ma) and Franklandia–Mimetes (74 Ma) clades do not merge in the analysis (Figure 1a). Grevillea, with its exotesta modified into a brittle wing or aril attractive to ants, is unique among the dehiscent Proteaceae and had no effect on the outcomes for ancestral assignments of soil-storage.
Fireproneness among Gondwanan floras can now be traced back to the fiery Cretaceous and trait assignment affirms serotiny and soil seed storage, and later ant dispersal, as ancient adaptations to fire among flowering plants. Most species in over 90 extant flowering-plant families of the sclerophyll vegetation in Australia have some form of seed storage, and up to 25,000 seeds from many families are stored per m2 of soil in fireprone sclerophyll communities throughout the world . This means that other clades and floras should now be examined to see if they have a similarly ancient relationship with fire as a vital agent of natural selection favouring seed storage. Since Proteaceae is among the oldest of the eudicot families and only monocots (five orders have fire-tolerant members) migrated into fireprone habitats among older clades , it will be interesting to see if dates older than 88 Ma for fire-related traits can be identified among flowering plants. He et al.  have shown recently that fire-related traits appeared among pines (non-flowering) up to 126 Ma, but especially from 89 Ma when canopy seed storage originated in association with more intense, crown fires. The similarity of these two dates (c. 90 Ma), with one family confined to the Northern Hemisphere and the other to the Southern, is remarkable. However, other flowering plant orders/families well known for their fire-tolerant traits also arose around this time (see  for details) and this raises the prospect that we may have identified a time of great significance in the fire history of seed plants generally.
Sauquet et al. constructed a dated phylogeny for the 81 currently recognised genera in the Proteaceae. The age of each lineage was determined by Bayesian autocorrelation dating based on eight DNA regions and five fossil pollen age calibration points. We used the tree they obtained by the uncorrelated lognormal method (implemented in BEAST), as this was preferred by them since it produced similar age estimates to the other two methods they tried but had the advantage that it took phylogenetic uncertainty into account. The calibration points were determined after analysing 25 fossil palynomorph species, and a morphological matrix of 22 pollen characters and 113 taxa, to produce a highly accurate dated phylogeny for the family. The crown age of Proteaceae was dated at 113 Ma (108−118 Ma, 95% highest posterior density). The maximum clade credibility tree (with 86% of internal nodes at generic level having a posterior probability greater than 0.95) was used for downstream analysis.
The presence of fire-related seed storage/germination traits varies greatly in the Proteaceae. The key to maximum fitness is seed storage/release/germination cued to fire and establishment immediately after fire when the recruitment conditions are optimal. There is a wide array of seed storage/germination responses to fire, especially in Australia: ‘stones’ (pyrenes) that lie near the soil surface until stimulated to germinate by heat —Beauprea (may occur in fireprone maquis of New Caledonia  but was once widespread in Australia), Persoonieae (Figure 1); woody follicles and ‘cones’ that release their buoyant, nutrient-enriched diaspores following flame heat [13, 17]—Grevilleoideae, Proteoideae; plumed, hairy, leathery or chitinous diaspores that work their way into the soil, or are buried by ants, and germinate in response to smoke or desiccation caused by high soil temperatures during or after fire [15, 51]—Proteoideae.
Data on fire-related seed storage/germination for each genus were collated from the literature [13, 17, 52, 53] and our own fieldwork, and categorised as present or absent. If all known extant species within a genus shared a particular fire-related seed storage/germination syndrome then this trait was treated as diagnostic for the genus. Species current distribution in each genus (and outgroups) was compiled from the literature [12, 52], and categorised into fireprone and non-fireprone (essentially rainforest) environments that are the two major habitats of extant species in the Proteaceae. A fireprone environment was defined as subject to an average fire interval < 40 years (the mean lifespan of many fire-killed Proteaceae). The only uncertain genus was Bellendena that occurs in alpine scrub-heath of Tasmania, which appears subject to occasional fire but probably at > 40 year intervals, so it was assigned to the non-fireprone habitat type. If all known extant species share the same habitat type, this was treated as diagnostic for the genus. Where the habitat is variable within or between species the genus was assigned both traits. Seed and habitat traits for individual genera are provided in Figure 1a.
Ancestral habitat reconstruction and paleodispersal
Evolution of habitat and paleodispersal events was inferred on a phylogenetic tree of the Proteaceae by a maximum likelihood procedure. Maximum likelihood inference of ancient occupied habitat uses a dispersal-extinction-cladogenesis (DEC) model for habitat evolution that specifies instantaneous transition rates between discrete states (habitat type) along phylogenetic branches and applies it to estimating likelihoods of ancestral states (habitat inheritance scenarios) at the cladogenesis event . Ancestral habitat reconstruction and palaeodispersal was implemented in Lagrange. Genera in the Proteaceae were assigned to one of two habitats, non-fireprone (essentially rainforest) and fireprone environments, or both (where different species or populations occupied both habitat types). Dispersal between habitats was set as unconstrained. As an alternative approach, habitat was treated as a generic (heritable) trait as for the seed syndromes and analysed in the same way.
Ancestral state reconstruction for fire-related seed storage/germination
The tree file containing the maximum credibility clade tree with branch length (node age) generated by the molecular dating procedure, and trait files containing the discrete state for each genus were used for the analyses. Each of the three traits was analysed separately. Posterior distributions of log-likelihoods and the values of traits at the nodes of phylogenies were derived from a Bayesian MCMC method . The continuous-time Markov character model assumes trait states can evolve repeatedly between their possible states at any branch of the phylogenetic tree [55, 56] and constructs the ancestral trait at each internal node. This model allows the trait to change from the state it is in at any given moment to any other state over infinitesimally small intervals of time. The rate parameters of the model estimate these transition rates. As recommended, a reversible-jump (RJ-)MCMC was adopted . In RJ-MCMC, the Markov chain searches the posterior distribution of different models of evolution, and the posterior distributions of the parameters of these models.
In the MCMC mode, implemented in BayesMultiStates, a new set of rate parameters for the evolution model is proposed at each iteration of the Markov chain by changing the current values by an amount given by the ratedev parameter representing the deviation from the normal distribution . Three Markov chains were run for the trait and the acceptance rate was monitored for the newly proposed values of the rate parameters to determine a suitable value for the ratedev parameter. A value of ratedev was accepted if it generated an acceptance rate of 20−40%. A hyperprior seeding an exponential distribution from a uniform 0−30 distribution was also applied in Markov chain runs. The Markov chains were run for 107 iterations with a burn-in of 104, and the result was recorded every 2000th iteration. The ancestral state was defined unambiguously as the trait with the phylogenetic corrected posterior probability from  (posterior probability of trait value on the internal nodes × posterior probability of the existence of that node in phylogeny) greater than 0.95.
As this is an agglomerative nonexclusive technique (the opposite of synapomorphy assignment in traditional cladistics), the probability of a given trait assigned to a node is retained along its supporting stem until an assignment decision is made at the next node below it [18, 57, 58]. The new probability is affected by the length of the stem as well as the surrounding node probabilities, but, in the absence of any further data on the lineage, the trait probability is assumed to remain stable between nodes. This interpretation is consistent with that of other recent studies on clade, trait and paleodispersal assignment [12, 57–59] and has not led to any conflict with the fossil record [8, 57].
Evolutionary correlation of fire-related seed storage/germination and fireprone environments
We consider that extrapolating environmental traits into the past is valid only if it is tied to an associated limiting functional trait. We first test whether fire-related seed storage/germination in Proteaceae is positively correlated with fireprone environments over evolutionary time. Evolutionary correlation of fire-related seed storage/germination and fireprone environments was analyzed in BayesDiscrete. BayesDiscrete tests for correlated evolution between two binary traits by comparing the fit (log-likelihood) of two continuous-time Markov models. One is a model in which the two traits evolve independently on the tree (independent model). The other model allows the traits to evolve in a correlated fashion (dependent model). We adopted a RJ-MCMC following Pagel & Meade . A few test runs were executed to choose a ratedev value that produced an acceptance rate of 20−40% as recommended. Using the chosen ratedev value, a reversible jump dependent model was first tested. The analysis was repeated by confining the RJ chain to the independent model. In each model run, 5 × 106 iterations were implemented and the results were sampled every 2000 iterations. The harmonic mean was used to summarize the overall result. The log-Bayes factor, which is twice the difference between the two harmonic means derived from the dependent and independent models of evolution, was calculated. The log-Bayes factor is nominally distributed as a χ2 with degrees of freedom equal to the difference in the number of parameters between the two models . A difference between these two harmonic means greater than 9.49 indicates strong support (P < 0.05) for correlation between the two traits .
Net speciation rate
Differentiation in species diversification rate after each palaeo-dispersal was obtained by comparing the net speciation rate in two lineages after the divergence events. The number of species in each genus of Proteaceae was compiled from Sauquet et al.. Stem group net speciation rates were calculated as Rst = log(N)/t, where N is the number of extant species in the lineage, and t is the stem age .
We thank Hervé Sauquet for providing the dated phylogeny of the Proteaceae family , the Australian Research Council for financial support (project DP120103389), Claire Belcher for preparing the backbone of Figure 3, Katherine Downes for sharing ideas, and Juli Pausas and five anonymous referees for providing valuable comments on the manuscript.
- He T, Pausas JG, Belcher CM, Schwilk DW, Lamont BB: Fire-adapted traits of Pinus arose in the fiery Cretaceous. New Phytol. 2012, 194: 751-759. 10.1111/j.1469-8137.2012.04079.x.PubMedView ArticleGoogle Scholar
- Bowman DMJS, Balch JK, Artaxo P, Bond WJ, Carlson JM, Cochrane MA, D’Antonio CM, Defries RS, Doyle JC, Harrison SP, Johnston FH, Moritz MA, Prentice IC, Roos CI, Scott AC, Swetnam TW, van der Werf GR, Pyne SJ: Fire in the earth system. Science. 2009, 324: 481-484. 10.1126/science.1163886.PubMedView ArticleGoogle Scholar
- Bond WJ, Scott AC: Fire and the spread of flowering plants in the Cretaceous. New Phytol. 2010, 188: 1137-1150. 10.1111/j.1469-8137.2010.03418.x.PubMedView ArticleGoogle Scholar
- Brown SAE, Scott AC, Glasspool IJ, Collinsons ME: Cretaceous wildfires and their impact on the Earth system. Cretac Res. 2012, 36: 162-190.View ArticleGoogle Scholar
- Hopper SD, Gioia P: The Southwest Australian Floristic Region: evolution and conservation of a global biodiversity hotspot. Ann Rev Ecol Evol Syst. 2004, 35: 623-650. 10.1146/annurev.ecolsys.35.112202.130201.View ArticleGoogle Scholar
- Hopper SD: OCBIL theory: towards an integrated understanding of the evolution, ecology and conservation of biodiversity on old, climatically buffered, infertile landscapes. Plant Soil. 2009, 322: 49-86. 10.1007/s11104-009-0068-0.View ArticleGoogle Scholar
- Crisp MD, Burrows GE, Cook LG, Thornbill AH, Bowman DMJS: Flammable biomes dominated by eucalypts originated at the Cretaceous–Palaeogene boundary. Nature Commun. 2011, 2: 193-200.View ArticleGoogle Scholar
- He T, Lamont BB, Downes KS: Banksia born to burn. New Phytol. 2011, 191: 184-196. 10.1111/j.1469-8137.2011.03663.x.PubMedView ArticleGoogle Scholar
- Bytebier B, Antonelli A, Dirk U, Bellstedt DU, Linder HP: Estimating the age of fire in the Cape flora of South Africa from an orchid phylogeny. Proc R Soc B. 2011, 278: 188-195. 10.1098/rspb.2010.1035.PubMedPubMed CentralView ArticleGoogle Scholar
- Lamont BB, Downes KS: Fire-stimulated flowering among resprouters and geophytes in Australia and South Africa. Pl Ecol. 2011, 212: 2111-2125. 10.1007/s11258-011-9987-y.View ArticleGoogle Scholar
- Carpenter RJ, Jordan GJ, Lee DE, Hill RS: Leaf fossils of Banksia (Proteaceae) from New Zealand: an Australian abroad. Am J Bot. 2010, 97: 288-297. 10.3732/ajb.0900199.PubMedView ArticleGoogle Scholar
- Sauquet H, Weston PH, Anderson CL, Barker NP, Cantrill DJ, Mast AR, Savolainen V: Contrasted patterns of hyperdiversification in Mediterranean hotspots. Proc Natl Acad Sci USA. 2009, 106: 221-225. 10.1073/pnas.0805607106.PubMedPubMed CentralView ArticleGoogle Scholar
- Lamont BB, Le Maitre D, Cowling RM, Enright NJ: Canopy seed storage in woody plants. Bot Rev. 1991, 57: 277-317. 10.1007/BF02858770.View ArticleGoogle Scholar
- Dunn RR, Gove AD, Barraclough TG, Givnish TJ, Majer JD: Convergent evolution of an ant-plant mutualism across plant families, continents, and time. Evol Ecol Res. 2007, 9: 1349-1362.Google Scholar
- Flematti GR, Meritt DJ, Piggott MJ, Trengove RD, Smith SM, Dixon KW, Ghisalberti EL: Burning vegetation produces cyanohydrins that liberate cyanide and stimulate seed germination. Nature Commun. 2011, 10.1038/ncomms1356.Google Scholar
- Keeley JE, Pausas JG, Rundel PW, Bond WJ, Bradstock RA: Fire as an evolutionary pressure shaping plant traits. Trends Pl Sci. 2011, 16: 406-412. 10.1016/j.tplants.2011.04.002.View ArticleGoogle Scholar
- Groom PK, Lamont BB: Phosphorus accumulation in Proteaceae seeds: a synthesis. Plant Soil. 2010, 334: 61-72. 10.1007/s11104-009-0135-6.View ArticleGoogle Scholar
- Pagel M, Meade A: Manual: BayesTraits. 2007, http://www.evolution.rdg.ac.uk.Google Scholar
- Falcon-Lang HJ, Cantrill DJ, Nichols GJ: Biodiversity and terrestrial ecology of a mid-Cretaceous, high latitude floodplain, Alexander Island, Antarctica. J Geol Soc. 2001, 158: 709-724. 10.1144/jgs.158.4.709.View ArticleGoogle Scholar
- Askin RA: Late Cretaceous–early Tertiary Antarctic evidence for past vegetation and climates. The Antarctic Paleoenvironment: A Perspective on Global Change: Part One Antarctic Research Series, Volume 56. Edited by: Kennett JP, Warkne DA. 1992, Washington DC: AGU, 61-73.View ArticleGoogle Scholar
- Martin ARH: Paleogene proteaceous pollen and phylogeny. Alcheringa. 1995, 19: 27-40. 10.1080/03115519508619096.View ArticleGoogle Scholar
- Dettmann ME, Jarzen DM: Pollen evidence for Late Cretaceous differentiation of Proteaceae in southern polar forests. Can J Bot. 1991, 69: 901-906. 10.1139/b91-116.View ArticleGoogle Scholar
- Dettmann ME, Milnar RE, Douglas JG, Burger D, Fielding C, Clifford HT, Francis J, Jell P, Wade M, Rich T, Pledge N, Kemp A, Rozefelds A: Australian Cretaceous terrestrial faunas and floras: biostratigraphic and biogeographic implications. Cret Res. 1992, 13: 207-262. 10.1016/0195-6671(92)90001-7.View ArticleGoogle Scholar
- Vajda V, Raine JI: A palynological investigation of plesiosaur-bearing rocks from the Upper Cretaceous Tahora Formation, Mangahouanga, New Zealand. Alcheringa. 2010, 34: 359-374. 10.1080/03115518.2010.486642.View ArticleGoogle Scholar
- Gurnis M, Dietmar R, Müller LM: Cretaceous vertical motion of Australia and the Australian-Antarctic discordance. Science. 1998, 279: 1499-1504. 10.1126/science.279.5356.1499.PubMedView ArticleGoogle Scholar
- Monroe MH: Australia separates from Antarctica. 2011, http://austhrutime.com/separation.htm.Google Scholar
- Tardy Y, Kobilsek B, Paquet H: Mineralogical composition and geographical distribution of African and Brazilian periatlantic laterites. The influence of continental drift and tropical paleoclimates during the past 150 million years and implications for India and Australia. J Afr Earth Sci. 1991, 12: 283-295. 10.1016/0899-5362(91)90077-C.View ArticleGoogle Scholar
- Twidale CR, Bourne JA: The use of duricrusts and topographic relationships in geo-morphological correlation: conclusions based in Australian experience. Catena. 1998, 33: 105-122. 10.1016/S0341-8162(98)00065-4.View ArticleGoogle Scholar
- Pate JS, Verboom WH, Galloway PD: Co-occurrence of Proteaceae, laterite and related oligotrophic soils: coincidental associations or causative inter-relationships?. Aust J Bot. 2001, 49: 529-560. 10.1071/BT00086.View ArticleGoogle Scholar
- Bergman NM, Lenton TM, Watson AJ: COPSE: A new model of biogeochemical cycling over Phanerozoic time. Am J Sci. 2004, 304: 397-437. 10.2475/ajs.304.5.397.View ArticleGoogle Scholar
- Belcher CM, Yearsly JM, Hadden RM, McElwain JC, Rein G: Baseline intrinsic flammability of Earth’s ecosystems estimated from paleoatmospheric oxygen over the past 350 million years. Proc Natl Acad Sci USA. 2010, 107: 22448-22453. 10.1073/pnas.1011974107.PubMedPubMed CentralView ArticleGoogle Scholar
- Clarke JT, Warnock RCM, Donoghue PCJ: Establishing a time-scale for plant evolution. New Phytol. 2011, 192: 266-301. 10.1111/j.1469-8137.2011.03794.x.PubMedView ArticleGoogle Scholar
- Douglas AW: Flora of Australia,Eleagnaceae, Proteaceae.1. 1995, Melbourne: CSIROGoogle Scholar
- Lamont BB, Groom PK, Cowling RM: High leaf mass per area of related species assemblages may reflect low rainfall and carbon isotope discrimination rather than low phosphorus and nitrogen concentrations. Funct Ecol. 2002, 16: 403-412. 10.1046/j.1365-2435.2002.00631.x.View ArticleGoogle Scholar
- Pole MS, Douglas JG: Bennettitales, Cycadales and Ginkgoales from the mid Cretaceous of the Eromanga Basin, Queensland, Australia. Cret Res. 1999, 20: 523-538. 10.1006/cres.1999.0164.View ArticleGoogle Scholar
- Pole M, Philippe M: Cretaceous plant fossils of Pitt Island, the Chatham group, New Zealand. Alcheringa. 2010, 34: 231-263. 10.1080/03115511003659085.View ArticleGoogle Scholar
- Eklund H, Cantrill DJ, Francis JE: Late Cretaceous plant mesofossils from Table Nunatak, Antarctica. Cret Res. 2004, 25: 211-228. 10.1016/j.cretres.2003.11.004.View ArticleGoogle Scholar
- Longmore ME: Quaternary palynological record from perched lake sediments, Fraser Island, Queensland, Australia: rainforest, forest history and climatic control. Aust J Bot. 1997, 45: 507-526. 10.1071/BT96109.View ArticleGoogle Scholar
- Macphail M: Australian Palaeoclimates: Cretaceous to Tertiary – A review of palaeobotanical and related evidence to the year 2000. CRC LEME Open File Rep. 2007, 151:Google Scholar
- Macphail MK, Stone MS: Age and palaeoenvironmental constraints on the genesis of the Yandi channel iron deposits, Marillana Formation, Pilbara, northwestern Australia. Aust J Earth Sci. 2004, 51: 497-520. 10.1111/j.1400-0952.2004.01071.x.View ArticleGoogle Scholar
- Cowling RM, Proches S, Partridge TC: Explaining the uniqueness of the Cape flora: incorporating geomorphic evolution as a factor for explaining its diversification. Mol Phyl Evol. 2009, 51: 64-74. 10.1016/j.ympev.2008.05.034.View ArticleGoogle Scholar
- Itzstein-Davey F: Changes in the abundance and diversity of Proteaceae in south-western Australia: a review of an integrated palaeoenvironmental study. Geog Res. 2007, 45: 43-53. 10.1111/j.1745-5871.2007.00428.x.View ArticleGoogle Scholar
- Milne LA: Tertiary palynology: Beaupreaidites and new Conospermeae (Proteoideae) affiliates. Aust Syst Bot. 1998, 11: 553-603. 10.1071/SB97013.View ArticleGoogle Scholar
- Jaffré T, Rigault F, Dagostini G: Impact des feux de brousse sure les maquis lingo-herbacés des roches ultramafiques de Nouvelle-Calédonie. Adansonia. 1998, 20: 173-189.Google Scholar
- Myerscough PJ, Whelan RJ, Bradstock RA: Ecology of Proteaceae with special reference to the Sydney region. Cunninghamia. 2001, 6: 951-1015.Google Scholar
- Midgley JJ: The deviation, utility and implications of a divergence index for the fynbos genus Leucadendron (Proteaceae). Bot J Linn Soc. 1987, 95: 137-152. 10.1111/j.1095-8339.1987.tb01994.x.View ArticleGoogle Scholar
- Manning JC, Brits GJ: Seed coat development in Leucospermum cordifolium (Knight) Fourcade (Proteaceae) and a clarification of the seed covering structures in Proteaceae. Bot J Linn Soc. 1993, 112: 139-148. 10.1111/j.1095-8339.1993.tb00313.x.View ArticleGoogle Scholar
- Barker NP, Vanderpoorten A, Morton CM, Rourke JP: Phylogeny, biogeography, and the evolution of life-history traits in Leucadendron (Proteaceae). Mol Phylog Evol. 2004, 33: 845-860. 10.1016/j.ympev.2004.07.007.View ArticleGoogle Scholar
- Enright NJ, Mosner E, Miller BP, Johnson N, Lamont BB: Soil versus canopy seed storage and plant species coexistence in species-rich shrublands of southwestern Australia. Ecology. 2007, 88: 2292-2304. 10.1890/06-1343.1.PubMedView ArticleGoogle Scholar
- Auld TD, Denham AJ, Turner K: Dispersal and recruitment dynamics in the fleshy-fruited Persoonia lanceolata (Proteaceae). J Veg Sci. 2007, 18: 903-910.Google Scholar
- Brits GJ, Calitz FJ, Brown NAC, Manning JC: Desiccation as the active principle in heat stimulated seed germination of Leucospermum. R. Br. (Proteaceae) in fynbos. New Phytol. 1993, 25: 397-403.View ArticleGoogle Scholar
- Weston PH: Proteaceae. The Families and Genera of Vascular Plants. 2007, 9: 364-404. 10.1007/978-3-540-32219-1_42. SpringerView ArticleGoogle Scholar
- Rebelo T: Proteas: A Field Guide to the Proteas of Southern Africa. 2001, Vlaeberg: Fernwood Press, 2Google Scholar
- Ree RH, Smith SA: Maximum-likelihood inference of geographic range evolution by dispersal, local extinction, and cladogenesis. Syst Biol. 2008, 57: 4-14.PubMedView ArticleGoogle Scholar
- Pagel M, Meade A, Barker D: Bayesian estimation of ancestral states on phylogenies. Syst Biol. 2004, 53: 673-684. 10.1080/10635150490522232.PubMedView ArticleGoogle Scholar
- Pagel M: Detecting correlated evolution on phylogenies: a general method for the comparative analysis of discrete characters. Proc R Soc B. 1994, 255: 37-45. 10.1098/rspb.1994.0006.View ArticleGoogle Scholar
- Ward PS, Brady SG, Fisher BL, Schultz TR: Phylogeny and biogeography of Dolichoderine ants: effects of data partitioning and relict taxa on historical inference. Syst Biol. 2010, 59: 342-362. 10.1093/sysbio/syq012.PubMedView ArticleGoogle Scholar
- Schnitzler J, Barraclough TG, Boatwright JS, Goldblatt P, Manning JC, Powell MP, Rebelo T, Savolainen V: Causes of plant diversification in the Cape biodiversity hotspot of South Africa. Syst Biol. 2011, 60: 343-357. 10.1093/sysbio/syr006.PubMedView ArticleGoogle Scholar
- Couvreur TLP, Forest F, Baker WJ: Origin and global diversification patterns of tropical rain forests: inferences from a complete genus-level phylogeny of palms. BMC Biol. 2011, 9: 44-10.1186/1741-7007-9-44.PubMedPubMed CentralView ArticleGoogle Scholar
- Magallón S, Sanderson MJ: Absolute diversification rates in Angiosperm clades. Evolution. 2001, 55: 1762-1780.PubMedView ArticleGoogle Scholar
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