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Evaluating multiple criteria for species delimitation: an empirical example using Hawaiian palms (Arecaceae: Pritchardia)
© Bacon et al; licensee BioMed Central Ltd. 2012
- Received: 3 November 2011
- Accepted: 22 February 2012
- Published: 22 February 2012
Robust species delimitations are fundamental for conservation, evolutionary, and systematic studies, but they can be difficult to estimate, particularly in rapid and recent radiations. The consensus that species concepts aim to identify evolutionarily distinct lineages is clear, but the criteria used to distinguish evolutionary lineages differ based on the perceived importance of the various characteristics of evolving populations. We examined three different species-delimitation criteria (monophyly, absence of genetic intermediates, and diagnosability) to determine whether currently recognized species of Hawaiian Pritchardia are distinct lineages.
Data from plastid and nuclear genes, microsatellite loci, and morphological characters resulted in various levels of lineage subdivision that were likely caused by differing evolutionary rates between data sources. Additionally, taxonomic entities may be confounded because of the effects of incomplete lineage sorting and/or gene flow. A coalescent species tree was largely congruent with the simultaneous analysis, consistent with the idea that incomplete lineage sorting did not mislead our results. Furthermore, gene flow among populations of sympatric lineages likely explains the admixture and lack of resolution between those groups.
Delimiting Hawaiian Pritchardia species remains difficult but the ability to understand the influence of the evolutionary processes of incomplete lineage sorting and hybridization allow for mechanisms driving species diversity to be inferred. These processes likely extend to speciation in other Hawaiian angiosperm groups and the biota in general and must be explicitly accounted for in species delimitation.
- Lineage sorting
Species are a fundamental unit in biological studies and their robust delimitation is essential to many fields of evolutionary biology, particularly systematics, biogeography, and conservation biology. Lineage separation and divergence form a temporal process that may render populations monophyletic, reproductively isolated, ecologically divergent, and/or morphologically distinctive. These properties serve as operational criteria for systematists to delimit species and they can occur at different times or orders during speciation. De Queiroz [1, 2] proposed that at the root of all modern species concepts is the general agreement on the fundamental nature of species: species are separately evolving metapopulation lineages. The perspective that species are lineages, and that multiple criteria should be used to identify them, has been termed the general lineage species concept . Applying this lineage-based framework to species delimitation shifts the focus from a single operational criterion and increases the importance of sampling multiple lines of evidence. Species delimitation is notoriously difficult when alternative criteria delimit incongruent species boundaries, but this is to be expected in recent radiations (e.g. [3–5]). Evaluating multiple criteria not only increases our ability to detect recently separated lineages, but also can provide stronger support for lineage separation when they are in agreement [2, 6, 7].
The difficulty in recognizing species and their limits (the "species problem" ) is particularly compounded on islands. Because most islands are considerably younger terrestrial systems than continental areas , there has generally been less time for the completion of speciation processes. Time is an important factor for incomplete lineage sorting because the existence of ancestral polymorphism and differential extinction thereof can cause bias in phylogenetic inference (e.g. ) and the identification of distinct lineages (e.g. ). Furthermore, the tendency for island colonizers to quickly fill available habitat often leads to species that are ecologically isolated but not considerably diverged genetically, potentially leading to hybridization if mating barriers are broken down due to secondary contact (e.g. [12, 13]). The evolutionary processes of incomplete lineage sorting and hybridization cause the "species problem" to be compounded on young, volcanic islands. Hawai'i is the longest archipelago on earth and has developed linearly in a sequential fashion from a volcanic hotspot . Recent study of the extant high islands has shown that the terrestrial biota evolved over the last 29-23 Ma  and that they harbor the highest degree of endemism of any known flora [16, 17]. The species richness of the Hawaiian Islands also contributes to the Polynesian/Micronesia biodiversity hotspot . Difficulties in delimiting species is not restricted to angiosperms on the Hawaiian Islands (e.g. [19–24]), but has also been highlighted in Hylaeus bee  and spoon tarsus Drosophila  studies.
Species concepts can address both the evolutionary patterns consistent with evolution along lineages and the evolutionary processes that are fundamental in maintaining distinct lineages (e.g. ). Under the phylogenetic species concept I (PSCI ), species are defined as "the smallest aggregation of populations (sexual) or lineages (asexual) diagnosable by a unique combination of character states in comparable individuals" (p. 211 ). To apply PSCI, fixed (or mutually exclusive) character-state differences are used as evidence to infer that gene flow has ceased between the sampled populations in population aggregation analysis (PAA ). An alternate version of the phylogenetic species concept (PSCII) requires exclusivity to recognize a species and differs from PSCI by basing species recognition strictly on monophyletic groups (; properly exclusive lineages ). A third alternative is the genotypic cluster species concept (GSC ), which defines species as genetic groups with few or no intermediates between them. The GSC can be implemented using a variety of clustering algorithms or assignment tests. Looking across species delimitation criteria allows for the implementation of the general-lineage species concept where the greater the number of criteria satisfied by a putative lineage, the more likely it is to represent an independent evolutionary trajectory .
Adaptive radiations are difficult evolutionary scenarios to evaluate because phylogenetic lineages may be so recently separated that each species' alleles have not coalesced since the time of speciation . Among recently diverged species, genealogies inferred from independent genomic regions are likely to disagree due to the differential sorting of ancestral polymorphism into daughter lineages such that each inferred gene tree might differ from the species tree (e.g. ). Because estimation of a coalescent species tree explicitly models incomplete lineage sorting, its comparison with the simultaneous-analysis [42, 43] allows for the inference of hybridization from any incongruence between the two topologies when only orthologous alleles are sampled.
In this study we aim to provide a comprehensive assessment of species diversity in Pritchardia using a multifaceted approach and independent sources of plastid, nuclear, and morphological data to assess three species-delimitation criteria - monophyly, the absence of genotypic intermediates, and diagnosability using mutually exclusive character states. We test whether currently recognized Pritchardia species merit taxonomic recognition as distinct evolutionary lineages, particularly with respect to the accumulation of evidence in favor of their delimitation. We also take advantage of the power of the coalescent to infer the species tree to understand potential conflicts in our results that can be introduced by incomplete lineage sorting and/or hybridization.
Conformance of currently recognized Hawaiian Pritchardia with three distinct criteria for species delimitation
elliptica Lanai City
Four distinct lineages were identified within Pritchardia microsatellite data using PAA, 33 in the sequence data and 12 in morphology, although individuals with missing data for diagnostic characters were left out of aggregations to avoid collapsing otherwise distinct groups (Additional file 2). For example, in the sequence data seven terminals had missing data for diagnostic characters and were arbitrarily assigned to a single group rather than collapsing the otherwise diagnosable groups. Due to differential sampling only the individuals sampled for the sequence dataset were used to perform PAA across the microsatellite and morphological data. In the three datasets we generated for this study, 43 lineages were indentified that are diagnosable and satisfy the PSCI. Of the 43 PSCI species, unique combinations of character states support 18 currently recognized Pritchardia species (Table 1).
The Hawaiian Islands have an unparalleled number of well-studied examples of adaptive evolution because of their high ecological heterogeneity, volcanic origin, and isolation from the nearest continental land mass . Despite the limited time available for diversification in comparison to ancient landmasses [15, 47], the Hawaiian Islands have the highest degree of endemism of any known flora [16, 32]. Within the Hawaiian Islands, many angiosperms show evidence for recent and rapid radiations, which frequently make species delimitation difficult (e.g. [21–26]). We applied three species-delimitation criteria to identify evolutionary lineages in Hawaiian Pritchardia. Robust species delimitations are important for Pritchardia because many of the currently recognized species are of conservation concern and threats continue to increase due habitat degradation and invasive herbivores and competitors .
We applied the criterion of monophyly to test whether currently recognized Pritchardia species are distinct evolutionary lineages using PSCII. Maximum parsimony (MP) analysis of the A1 matrix revealed support for P. affinis, P. glabrata, P. kaalae, P. perlmanii and P. remota as clades (Figure 2). Although these are weakly supported lineages, they satisfy the monophyly requirement of PSCII . Despite its popularity, monophyly as inferred from a phylogenetic tree may be a poor indicator of whether evolutionary lineages are distinct in the presence of gene flow [49, 50] or due to the error associated with randomly sampling few individuals from a complex underlying genealogy . Furthermore, decoupling hybridization from incomplete lineage sorting on a phylogeny is difficult in recently diverged species because both produce the same pattern of few to no polymorphisms between morphologically identifiable species [52–54].
The genotypic cluster criterion defines species as "distinguishable groups of individuals that have few or no intermediates when in contact" (p. 296 ). A Bayesian assignment test was used to quantify the degree of admixture (essentially the absence of intermediates) between species. Although issues can arise with imperfect geographical sampling, especially in cases of isolation by distance or environmental gradients (e.g. ), strong signal for the delimitation of P. affinis, P. aylmer-robinsonii, P. hardyi, P. munroi, and P. schattaueri was detected with high probability of assignment to unique populations. A lack of intermediates satisfies this species criterion and these five groups are distinct evolutionary lineages according to the GSC. On the other end of the speciation spectrum, sympatric species appear to have ongoing gene flow among lineages where the probabilities of membership among some heterogeneous individuals and populations were shared (Figure 5), particularly in the mountains of Kaua'i and O'ahu.
Under the criterion of diagnosability, species are identified as the smallest aggregation of populations diagnosable by a unique combination of character states . Using PAA, 43 lineages were identified as diagnosable and although they conform to PSCI as independent lineages, we do not advocate their formal recognition as species. Rather, our goal was to implement the general lineage species concept using multiple species-delimitation criteria to reach a more stable taxonomic solution for the Hawaiian Pritchardia. Furthermore, PAA can be highly sensitive where incomplete sampling of characters, individuals within populations, or populations can each lead to incorrect assessment of species . In our Hawaiian Pritchardia data, the nucleotide sequence matrix had 24% percent missing or ambiguous data, which was mostly due to a lack of sampling in the Malate synthase (MS) gene (Additional file 1). The microsatellite and morphological matrices had only 0.05% missing data. Between one and six individuals were sampled per population with an average of 1.5 individuals and 1.7 populations per species in the nucleotide sequences of the A1 matrix. Between one and 34 individuals were sampled per population with an average of seven individuals and two populations per species for the microsatellite matrix. The morphological matrix comprised character states that were fixed within currently recognized species and were not typically scored from the actual specimens used in the sequence-based and microsatellite analyses. Additionally, ten of the morphological characters were derived from species descriptions [29, 30] rather than herbarium material. Certainly no study is immune to these types of weakness, but we recognize that undersampling of individuals within populations and populations within species have affected the PAA results in this study by over-splitting and thus increasing the number of apparent species.
Distinct evolutionary lineages of Pritchardia
As currently defined, Pritchardia species are primarily recognized by their geographic distributions and a suite of morphological characters [29, 30]. Yet when considering distinct evolutionary lineages identified in this study, none of the Pritchardia species satisfy all the species-delimitation criteria that we applied. Some species-delimitation criteria recognize more lineages than others in part because criteria are met at different times during cladogenesis . Furthermore, when considering the amount of data used in the application of each criterion to infer species delimitations in Hawaiian Pritchardia we found the method that uses the most data, PAA, was the most powerful because it recognized the greatest number of splits.
Seven Pritchardia lineages satisfy two species-delimitation criteria (P. affinis, P. glabrata, P. hardyi, P. kaalae, P. munroi, P. remota, and P. schattaueri). The taxonomic status of P. affinis and P. remota are discussed in the interpretation of the A2 and coalescent species trees (see below). Pritchardia lanaiensis and P. elliptica were recently synonymized into P. glabrata , yet our results are inconsistent with this designation because of the diagnostic grouping of all P. glabrata sensu stricto individuals in PAA (Additional file 2).
Pritchardia hardyi, P. munroi, and P. schattaueri are all distinct lineages based on the species-delimitation criteria of a lack of intermediates and the presence of diagnostic character states. These results are consistent with Hodel's  description of morphological autapomorphies that define each of these three independent lineages. Pritchardia kaalae is identified as an independent lineage based on the formation of a monophyletic group and the presence of diagnostic character states. Despite its distinction as an independent lineage, P. kaalae appears to have significant levels of admixture based on the Structure results, particularly with Waianae and central Ko'olau (Waiava) populations of P. martii (Figure 5). Admixture may be indicative of the Pritchardia-dominated ancestral forest of the extensive O'ahu plain that spanned the Waianae and Ko'olau mountains and facilitated gene flow between ranges [46, 56]. The once-contiguous palm forest likely formed an isolation-by-distance-based cline of gene flow, and extinction of the intervening lowland populations may have subsequently formed reproductively isolated lineages.
Eleven Pritchardia lineages satisfy only one species-delimitation criterion (P. arecina, P. forbesiana, P. gordonii, P. hillebrandii, P. lowreyana, P. maideniana, P. perlmanii, P. viscosa, P. waialealeana, and P woodii). Some of these Pritchardia lineages may be recognized as independent due to the sampling artifacts described above. This is particularly a concern with P. gordonii and P. woodii, which were only sampled for morphology, and P. hillebrandii, which was not sampled for the sequence data. Future efforts to tease apart distinct evolutionary lineages in Pritchardia should focus on these particular groups, as well as areas of sympatry, with increased sampling of both individuals within populations and of populations within species.
Sister-group and inter-specific relationships of Pritchardia
In previous studies the sister group of Pritchardia has been inferred to be either Copernicia (53% bootstrap, BS, in maximum representation with parsimony analysis ; < 50% JK/BS and 0.89 PP ) or Washingtonia (52% BS ). Our study is consistent with previous work showing the close relationships among the three genera (Copernicia, Pritchardia, and Washingtonia). In the A1 and A2 matrices, Copernicia and Washingtonia together are inferred to be the sister group to Pritchardia with strong support (100% JK; Figures 2 and 3).
We formed composite terminals  from the A1 matrix where taxa were combined at a level for which monophyly is assumed a prior thereby reducing missing data. Sequence data was augmented with allozyme and morphological data to construct the A2 matrix for simultaneous analysis of inter-specific relationships (Figure 3). The A2 matrix did not incorporate potential hybrid lineages because of the terminal omission iterations and was compared to the coalescent species tree to assess effects of incomplete lineage sorting. In the A2 tree, P. thurstonii is sister to the Hawaiian clade, which is well supported as monophyletic (97% JK) and consistent with Bacon et al. (64% BS/65% JK ). Zielger  proposed the sister relationship between Fijian and Hawaiian Pritchardia based on his hypothesis of an adaptive shift in fruit size upon colonization of the Hawaiian Islands. The sister relationship between Fijian and Hawaiian angiosperms has also been noted in Cyrtandra  and Pittosporum [21, 26], but not in taxa that ultimately descended from American ancestors , such as Pritchardia.
The strongly supported sister relationship P. aylmer-robinsonii and P. remota (98% JK, Figure 3) is consistent with their synonymy . Excluding P. remota from Nihoa and Ni'ihau, the backbone of the Hawaiian clade is a trichotomy. Weak support was provided for a sister relationship between P. hardyi and P. viscosa (53% JK), which had been previously suggested based on their flat leaf blades, the density of lepidia on the abaxial surface of the leaf, and their stiff leaf tips . Hodel  also identified a close relationship between P. maideniana (including P. affinis) and P. hillebrandii based on morphological aspects of the lepidia and inflorescences, for which we inferred a well-supported P. maideniana sensu lato (89% JK) that was weakly supported as sister to P. hillebrandii (54% JK).
The coalescent-species-tree approach has been suggested to be a more accurate estimation of lineage splitting than concatenation because it can model the stochastic forces that drive population divergence [40, 62–64]. Yet missing data and other issues with species-tree estimation such as mutational and coalescent variance can have detrimental effects on modeling incomplete lineage sorting (e.g. ). Another important consideration with species-tree estimation is that species are defined a priori and the coalescent model assumes species are monophyletic. This can be highly unlikely in recent radiations where ancestral species are still extant. Despite these issues, the advantage of directly modeling intraspecies polymorphism and incomplete lineage sorting makes species-tree estimation an important approach to data exploration in the identification of evolutionary lineages, especially in rapid species radiations .
The coalescent-species-tree topology provided moderate branch support for three clades that are consistent with recent synonymy [P. aylmer-robinsonii (0.75 PP), P. maideniana (0.76 PP), and P. napaliensis (0.71 PP); Figure 4]. The species tree identified P. flynnii and P. waialealeana as sister taxa, which together are sister to P. minor (Figure 4). Lastly, individuals planted by early Hawaiian naturalist George Munro in Lana'i City, Lana'i had been hypothesized to represent the extinct P. elliptica lineage (R.W. Hobdy, pers. comm. 2008), but are here shown to be consistent with a P. marti source from O'ahu (0.76 PP; see also Additional file 3) and separated from P. elliptica individuals collected from natural populations in Kunoa Valley by eight branches, one of which is highly supported (1.0 PP; Figure 4). Secondly, the species tree was used to test for congruence with the simultaneous-analysis A2 topology. Because the two distinct methods generally resolved the same well-supported clades, we can infer that the extrapolation from the gene trees to the phylogenetic tree is likely accurate in the simultaneous analysis. This is not to say that the process of lineage sorting has not occurred, but rather we have no evidence that it has confounded the species-level relationships inferred from the simultaneous-analysis tree.
Incomplete lineage sorting, the tempo of radiation, and hybridization in Pritchardia
The identification of distinct evolutionary lineages is a necessary precursor to the delimitation of species . Satisfaction of multiple species criteria can ensure accurate, stable, and uncontroversial species delimitations (e.g., [4, 7]). For taxa of conservation concern, accurate identification of lineages may facilitate management efforts by focusing on distinct species, rather than ambiguous groups. Our results, which are based on data from both the plastid and nuclear genomes, show little sequence differentiation among most Pritchardia species. The lack of differentiation may be due to incomplete lineage sorting, the tempo of the Pritchardia radiation, and/or hybridization between sympatric species, and distinguishing between these factors can be difficult.
Incomplete lineage sorting is one hypothesis for gene-tree incongruence and a lack of resolution within island radiations. Differential lineage sorting can bias species inference and may be further compounded by the estimated long generation time for other tropical understory palms that have undergone island colonization (e.g., 68-year mean in the Fijian endemic Balaka microcarpa ). Large ancestral effective population sizes have been hypothesized from fossil evidence and Pritchardia has been shown to be the dominant component of pre-human Quaternary forests on the Hawaiian Islands (2.6 Ma-822 year before present [67, 68]). Despite this, coalescence times for Hawaiian Pritchardia species are likely to be shorter than their continental tribal counterparts. Congruence between the simultaneous and species-tree analyses together with information on coalescence times suggests that differential lineage sorting did not drive current diversity patterns within Pritchardia.
A general trend emerging from this and other phylogenetic studies on the Hawaiian flora is the difficulty in estimating relationships among woody and long-lived groups [e.g., Cyrtandra , lobeliads (e.g. ), Melicope ; Metrosideros [21, 70]; Pittosporum [22, 23]; Pyschotria ; Santalum , Schiedea , and the silversword alliance (e.g. )]. Another example is Hawaiian Pritchardia. Aside from the sympatric species, the lack of resolution may be caused by the insufficient time for divergence between lineages. Because of the age of the oldest extant Hawaiian Island (Nihoa; 7.3 Ma [14, 15, 47]) and because the Pritchardia colonization of the Hawaiian Islands was estimated to occur between 3.5-8 Ma (mean stem to crown-stem ages ), an average of three new species would have had to form every million years to account for the 24 currently recognized species in the radiation. Clearly this rapid rate of cladogenesis has not allowed for much divergence within the Hawaiian Pritchardia radiation.
We also suggest that hybridization has played a key role in the diversification of Hawaiian Pritchardia lineages from geographic regions of sympatry of Kaua'i (P. flynnii, P. limahuliensis, P. minor, P. napaliensis, P. waialealeana, and P. viscosa) and O'ahu (P. bakeri, P. kahukuensis, and P. martii). Removing wildcard terminals through the use of Adams consensus trees may be biased towards deletion of hybrids given that they are expected to be resolved as basal lineages  and our iterative exclusion process is consistent with the exclusion of hybrids because 66% (22 of the 33) of the excluded terminals were from areas of high sympatry such as in the Makaleha and Namolokamain ranges in Kaua'i and in the Ko'olau Mountains of O'ahu. Examination of the character conflict present was hampered by a general lack of resolution in the gene trees (each nDNA versus the single cpDNA tree; Additional files 4 and 5). Despite this, review of the parsimony-informative sequence characters revealed six polymorphisms found on both forward and reverse sequence reads that suggest introgression in two genes given how different the alleles are (nuclear MS amongst P. perlmanii individuals and plastid trnD-trnT amongst P. hardyi individuals). Although widespread hybridization has been observed in cultivation [74, 75], it has been difficult to detect in the field due to the high phenotypic plasticity that characterizes Pritchardia [29, 32].
The ability to hybridize is common among island species (e.g. ) and has likely been a major force in shaping other Hawaiian angiosperm lineages such as Metrosideros [21, 70], Pittosporum [22, 23], and silverswords (e.g. ). Outside of the lack of reproductive barriers or incompatibility mechanisms, anthropogenic change on the archipelago may have caused a breakdown of species boundaries. For example, native Hawaiians cultivated Pritchardia species in coastal settlements and although they had a variety of ethnobotanical uses (reviewed in ), the leaves and fibers were primarily used for thatching. The movement of plants by humans could have introduced new genotypes into existing coastal native species and admixed with other cultivated species. Also, the likely extinction of natural pollinators and dispersers and the introduction of invasive species that generally have higher mobility and efficiency  may also facilitate gene flow between populations and species.
Research at the interface of population genetics and phylogenetics is greatly expanding, as seen in the increasing numbers of publications on coalescent methods to infer species trees (e.g. [40, 62–64]). A limitation to the current implementations of species-tree methods is the assumption of lack of gene flow among lineages, yet in empirical studies this assumption is often violated, especially at the taxonomic level these methods are designed for. Although there are methods that model gene flow as well as the coalescent (i.e., the isolation-with-migration model of Hey & Nielsen  or the hierarchical approximate Bayesian computation approach of Huang et al. ), these approaches do not provide an estimate of a species tree under a model of divergence with gene flow and may be less powerful than species-tree estimates because they require such strong priors (e.g., on migration rates ). To best address species delimitation in rapid radiations, especially in island groups like Pritchardia palms, methods that allow for simultaneously capturing vertical and horizontal inheritance of genetic information are needed, but are not yet available ( but see ).
Total genomic DNA was extracted from silica-gel dried leaves following Alexander et al. . Sequences for three plastid (matK, ndhF, and trnD-trnT) and four nuclear loci (CISPs 4 and 5, MS, and RPB2) were generated ([84–88] respectively). Amplified products were purified using Qiagen PCR purification kits and sequenced by the Cancer Research Center DNA Sequencing Facility at the University of Chicago or at Macrogen. All 502 new sequences generated in this study have been deposited in GenBank under accession numbers JF904936 to JF905438 (Appendix A).
Two phylogenetic analyses were conducted within Pritchardia. A1 included sequence data generated from seven loci and microsatellite data coded as multistate characters with heterozygous individuals coded as subset polymorphisms. Sampling for A1 included all previously recognized Pritchardia species except for P. gordonii and P. woodii, which are both recently described species with highly restricted distributions and are considered endangered . Based on a recent tribal-level analysis  two species of each of the most closely related genera (Copernicia and Washingtonia) and three other Coryphoideae (Cryosophila, Phoenix, and Sabal) were sampled as outgroups. The initial simultaneous analysis included 105 terminals.
Preliminary nucleotide alignments were obtained independently for each of the seven loci using default parameters in MUSCLE v3.6  and manual adjustments were performed in MacClade v4.03  following Simmons . Each parsimony-informative character was confirmed by rechecking chromatograms in Aligner (CodonCode Corp., MA). MP tree searches were conducted using 1,000 random addition tree-bisection-reconnection (TBR) searches in PAUP* v4.0b10  with a maximum of ten trees held per replicate. MP JK analyses  were conducted using PAUP* and 1,000 replicates were performed with 100 random addition TBR searches per replicate. Maximum likelihood (ML ) analyses of nucleotide and microsatellite characters from each of the molecular data matrices were performed. jModeltest v0.1.1  was used to select the best-fit likelihood model for each data matrix using the Akaike Information Criterion  without considering invariant-site models following Yang . Searches for optimal ML trees and 1,000 BS replicates  in the CIPRES Portal v2.2 used the RAxML-HPC2 algorithm [99, 100]. Adams consensus trees  from parsimony analyses were examined using the A1 dataset to identify wildcard terminals  of uncertain phylogenetic position that were then omitted. Iterations were conducted until a trade-off was reached between sacrificing taxonomically important terminals and gaining resolution in the strict consensus tree. A total of 72 of the original 105 terminals were included in the final A1 matrix.
List of the Pritchardia morphological characters that were included in analysis 2
1. Hastula shape
0 = rounded
1 = triangular, apiculate
2. Degree of panicle branching
0 = two orders
1 = three orders
3. Inflorescence length
0 = shorter than petioles
1 = equal
2 = longer than petioles
4. Petiole fiber density
0 = scare to moderate
1 = abundant
5. Abaxial leaf blade folds
0 = glaucous
1 = cottony, mealy indumentum
6. Abaxial leaf blade cover
0 = green
1 = silvery-gray
7. Leaf blade shape
0 = nearly circular
1 = diamond
8. Leaf blade with waxy, glaucous bloom
0 = absent
1 = present
9. Leaf blade surface
0 = flat
1 = nearly flat, undulate
10. Leaf tips
0 = drooping
1 = stiff
11. Lepidia density
0 = absent
1 = incompletely covered
2 = completely covered
12. Rachillae tomentum
0 = glabrous
1 = velutinous
2 = floccose, lanate
13. Rachillae viscosity
0 = absent
1 = present
14. Style - ovary ratio
0 = equal
1 = style longer
2 = style shorter
15. Outer calyx venation
0 = absent
1 = conspicuous
2 = present near opening with finer lines
16. Calyx indumentum
0 = glabrous
1 = tomentose
2 = viscous
17. Fruit ridges
0 = absent
1 = present
18. Fruit shape
0 = globose
1 = ellipsoid
2 = ovoid
3 = obovoid
4 = oblate
19. Fruit length
0 = < 3 cm
1 = > 3 cm
The coalescent species tree was inferred using *BEAST in BEAST v1.6.1 [62, 103]. *BEAST infers coalescent species trees from multilocus data and has been shown to have advantages in computational speed and accuracy over similar methods when applied to rapid radiations  Coalescent-species-tree methods estimate each gene genealogy independently and assume that conflict between gene trees is due exclusively to incomplete lineage sorting. The sequence data from the A1 matrix was analyzed to avoid the inclusion of any potential hybrids. Each of the seven sequenced loci was unlinked to allow for variation in substitution models and the clock models for the chloroplast loci were linked to account for its presumed single hierarchical history. The analysis was run using a Yule species tree prior and the GTR+Γ model of nucleotide substitution with four rate categories. The Markov chains were run for 50 million generations and repeated 10 times to test for Markov chain Monte Carlo chain convergence and to ensure effective sample sizes (ESS) exceeded 200. Burn-in was determined in Tracer v1.5 based on ESS and parameter trajectories and was then removed in LogCombiner v1.6.1. Tree files were summarized in biopy v0.1.2 , the posterior was resampled, and the variance among 100 random resampled species trees was visualized in DensiTree . We also estimated a single coalescent species tree in FigTree v1.3.1 by combining all tree files in LogCombiner v.1.6.1 . We compared the coalescent species tree with the simultaneous analysis to determine whether accounting for incomplete lineage sorting resulted in a different topology. The coalescent species tree and the A1 and A2 topologies also allowed for testing of recent synonymy of species (; Pritchardia affinis into P. maideniana, P. aylmer-robinsonii into P. remota, P. elliptica and P. lanaiensis into P. glabrata, and P. limahuliensis into P. napaliensis).
Population structure analyses
To test for the presence of intermediates between Hawaiian Pritchardia species, five microsatellite markers  were amplified in 197 individuals representing all 28 of the previously recognized species. PeakScanner software was used for allele calling and FlexiBin v2 was used to bin alleles . GenoDive v20b19  was used to test for Hardy-Weinberg equilibrium within populations with the default settings. Using the default settings, Microchecker v.2.2.3  was used to check for stutter, large-allele dropout, or evidence for null alleles based on a 99% confidence interval. A Bayesian procedure (Structure v2.3.2 ) was used that minimizes the deviation from Hardy-Weinberg and linkage equilibrium within each putative cluster by the fractional assignment of individual genomes to K populations. The admixture model was implemented with correlated allele frequencies and without the use of a priori information from populations of origin. Simulations included 10 iterations for each K value from K = 1 to 30, with a 100,000-generation burn-in and 100,000 chain length. The most probable number of genetically homogeneous groups (K) was determined by the ΔK statistical procedure  as implemented in Structure Harvester v0.6 . Multimodality across the 10 replicate iterations of the Structure analysis was addressed by permuting 1,000 times using the greedy algorithm and averaging across membership coefficients in CLUMPP ; the results were graphically displayed using Distruct v1.1 .
Population aggregation analysis
Mutually exclusive character states were used to test if gene flow had ceased between the sampled populations . To examine whether previously recognized species were diagnosable and satisfy the PSCI, character-state differences were identified using PAA. As more populations are incorporated into PAA, each is compared to all species previously delimited. Each time a species profile is aggregated due to the inclusion of another population, the new profile is compared to all other species profiles to check if further aggregation is needed. We used PAA for the microsatellite, morphological, and sequence data independently of each other (because of differences in which terminals were sampled), and then performed PAA across all three data types to detect diagnosable groups. Missing and ambiguous data were treated as polymorphic for all states present, but these entries were not used to collapse otherwise diagnosable groups in PAA (J. I. Davis, pers. comm. 2011).
List of taxa sampled with taxonomic authorities, voucher information, and GenBank accession numbers for new sequences generated for this study. Fairchild Tropical Botanical Garden and National Tropical Botanic Garden are abbreviated as FTBG and NTBG respectively.
Pritchardia affinisBecc.- C. Gemmil 83 (PTBG), FTBG DNA Bank 1850, Hawai'i; CISP4 JF904936, CISP5 JF905062, matK JF905351, ndhF JF905121, RPB2 JF905197, trnDT JF905269. P . affinisBecc.- S. Perlman 13745 (PTBG), FTBG DNA Bank 1851, Hawai'i; CISP4 JF904937, CISP5 JF905023, matK JF905352, ndhF JF905122, RPB2 JF905198, trnDT JF905270. P. arecinaBecc.- K. Wood 7991 (PTBG), FTBG DNA Bank 1853, Maui; CISP4 JF904938, matK JF905353, ndhF JF905123, RPB2 JF905199, trnDT JF905271. P. arecinaBecc.-Baker 1183 (K), Royal Botanic Gardens, Kew DNA Bank 15960, Maui; CISP4 JF904939, CISP5 JF905024, matK JF905354, ndhF JF905124, RPB2 JF905200, trnDT JF905272. P. aylmer-robinsoniiH.St.John- FTBG Live Collection 85184C, FTBG DNA Bank 14, Ni'ihau; CISP4 JF904940, CISP5 JF905025, matK JF905355, ndhF JF905125, RPB2 JF905201, trnDT JF905273. P. aylmer-robinsoniiH.St.John-NTBG Live Collection, Ni'ihau; CISP4 JF904941, CISP5 JF905026, matK JF905356, ndhF JF905126, RPB2 JF905202, trnDT JF905274. P. bakeriHodel-Bacon Pupukea1 SN, O'ahu; CISP4 JF904942, RPB2 JF905203. P. bakeriHodel-Bacon Pupukea2 SN, O'ahu; CISP4 JF904943, CISP5 JF905027, RPB2 JF905204. P. bakeriHodel-Bacon Pupukea3 SN, O'ahu; CISP4 JF904944. P. bakeriHodel-Bacon Pupukea4 SN, O'ahu; CISP4 JF904945. P. bakeriHodel-Bacon Kuliouou3 SN, O'ahu; CISP4 JF904989, matK JF905402, MS JF905094, ndhF JF905164, trnDT JF905316. P. bakeriHodel-Bacon Kuliouou5 SN, O'ahu; CISP4 JF904990, matK JF905403, MS JF905095, ndhF JF905165, trnDT JF905317. P. bakeriHodel-Bacon Kuliouou8 SN, O'ahu; CISP4 JF904991, matK JF905404, MS JF905096, ndhF JF905166, RPB2 JF905244, trnDT JF905318. P. beccarianaRock- J. Horn 4953 (PTBG), FTBG DNA Bank 1863, Hawai'i; CISP4 JF904946, CISP5 JF905063, matK JF905357, ndhF JF905127, RPB2 JF905205, trnDT JF905275. P. beccarianaRock-Wood 8911 (PTBG), Hawai'i; CISP4 JF904947, CISP5 JF905028, matK JF905358, RPB2 JF905206, trnDT JF905276. P. ellipticaRock & Caum-cultivated 320 Mahana St. Lana'i City, Lana'i; CISP4 JF904948, matK JF905361. P. ellipticaRock & Caum-cultivated 452 Lana'i St. Lana'i City, Lana'i; CISP4 JF904949, CISP5 JF905029, matK JF905362, ndhF JF905128, RPB2 JF905207, trnDT JF905277. P. ellipticaRock & Caum-cultivated 712 Puulani St. Lana'i City, Lana'i; CISP4 JF904950. P. ellipticaRock & Caum-Oppenheimer SN1, Kunoa Valley, Lana'i; CISP4 JF904951, CISP5 JF905030, matK JF905363, ndhF JF905129, RPB2 JF905208, trnDT JF905278. P. ellipticaRock & Caum-Oppenheimer SN6, Kunoa Valley, Lana'i; CISP5 JF905031, matK JF905359, ndhF JF905130, trnDT JF905279. P. ellipticaRock & Caum-Oppenheimer SN7, Kunoa Valley, Lana'i; CISP4 JF904952, CISP5 JF905032, matK JF905364, ndhF JF905131, trnDT JF905280. P. ellipticaRock & Caum-Oppenheimer SN8, Kunoa Valley, Lana'i; CISP4 JF904953, CISP5 JF905033, matK JF905360, RPB2 JF905209. P. flynniiLorence & Gemmill-Wood 12718B (PTBG), Kaua'i; CISP4 JF904954, matK JF905366, MS JF905087, RPB2 JF905210. P. flynniiLorence & Gemmill-Wood 12718C (PTBG), Kaua'i; CISP4 JF904955, matK JF905365. P. flynniiLorence & Gemmill-NTBG Live Collection, Kaua'i; CISP4 JF904956, CISP5 JF905034, matK JF905367, ndhF JF905132, RPB2 JF905211, trnDT JF905281. P. flynniiLorence & Gemmill-Tangalin 1476 (PTBG), Kaua'i; CISP4 JF904957, matK JF905368, MS JF905097, RPB2 JF905212, trnDT JF905282. P. flynniiLorence & Gemmill-Tangalin 1478 (PTBG), Kaua'i; CISP4 JF904958, CISP5 JF905035, matK JF905369, ndhF JF905133, RPB2 JF905213, trnDT JF905283. P. flynniiLorence & Gemmill-Tangalin 1480 (PTBG), Kaua'i; trnDT JF905284. P. forbesianaRock- J. Horn 4948 (FTBG), FTBG DNA Bank 1798, Maui; matK JF905370, ndhF JF905134, RPB2 JF905214, trnDT JF905285. P. forbesianaRock-NTBG Live Collection, Maui; CISP4 JF904959, CISP5 JF905036, matK JF905371, ndhF JF905135, RPB2 JF905215, trnDT JF905286. P. glabrataBecc. & Rock-FTBG DNA Bank 824, Maui; CISP4 JF904960, CISP5 JF905037, matK JF905372, ndhF JF905136, RPB2 JF905216. P. glabrataBecc. & Rock-Oppenheimer SN1, Maui; CISP4 JF904961, CISP5 JF905038, matK JF905373, RPB2 JF905217, trnDT JF905287. P. glabrataBecc. & Rock-Oppenheimer SN4, Maui; CISP4 JF904962, CISP5 JF905039, matK JF905374, MS JF905098, ndhF JF905137, RPB2 JF905218, trnDT JF905288. P. glabrataBecc. & Rock-Oppenheimer SN5, Maui; CISP4 JF904963, CISP5 JF905040, matK JF905375, MS JF905099, ndhF JF905138, RPB2 JF905219, trnDT JF905289. P glabrataBecc. & Rock-Oppenheimer SN6, Maui; CISP4 JF904964, matK JF905376, ndhF JF905139, RPB2 JF905220, trnDT JF905290. P. hardyiRock-Trauernicht 428 (PTBG), Kaua'i; CISP4 JF904965, matK JF905377, RPB2 JF905221, trnDT JF905291. P. hardyiRock-Trauernicht 429 (PTBG), Kaua'i; matK JF905378, ndhF JF905140. P. hardyiRock-Trauernicht 430 (PTBG), Kaua'i; CISP4 JF904966, matK JF905379, ndhF JF905141. P. hardyiRock- J. Horn 4938 (PTBG), Kaua'i, FTBG DNA Bank 1848; CISP4 JF904967, CISP5 JF905064, matK JF905380, MS JF905088, ndhF JF905142, RPB2 JF905222, trnDT JF905292. P. hardyiRock-J. Horn 4951 (PTBG), FTBG DNA Bank 1858, Kaua'i; CISP4 JF904968, CISP5 JF905065, matK JF905381, MS JF905089, ndhF JF905143, RPB2 JF905223, trnDT JF905293. P. hardyiRock-Tangalin 1705 (PTBG), Kaua'i; trnDT JF905294. P. hillebrandiiBecc.-FTBG Live Collection 2000301A, FTBG DNA Bank 646, Moloka'i; CISP4 JF904969, CISP5 JF905041, matK JF905382, ndhF JF905144, RPB2 JF905224, trnDT JF905295. P. hillebrandiiBecc.-S. Zona 1006 (FTG), FTBG DNA Bank 834, Moloka'i; CISP4 JF904970, CISP5 JF905042, matK JF905383, ndhF JF905145, RPB2 JF905225, trnDT JF905296. P. kaalaeRock-S. Zona 1008 (FTG), FTBG DNA Bank 835, O'ahu; CISP4 JF904973, CISP5 JF905043, matK JF905386, ndhF JF905148, RPB2 JF905228, trnDT JF905299. P. kaalaeRock-K. Wood 300 (PTBG), FTBG DNA Bank 1833, O'ahu; CISP4 JF904971, CISP5 JF905066, matK JF905384, ndhF JF905146, RPB2 JF905226, trnDT JF905297. P. kaalaeRock-S. Perlman 16710 (PTBG), FTBG DNA Bank 1847, O'ahu; CISP4 JF904972, CISP5 JF905067, matK JF905385, ndhF JF905147, RPB2 JF905227, trnDT JF905298. P. kahukuensisCaum-Kawelo SN (BISH), O'ahu; CISP4 JF904974, CISP5 JF905044, matK JF905387, ndhF JF905149, RPB2 JF905229, trnDT JF905300. P. lanaiensisBecc. & Rock-Bacon 88, Lana'i; CISP4 JF904975, CISP5 JF905045, matK JF905388, ndhF JF905150, RPB2 JF905230, trnDT JF905301. P. lanaiensisBecc. & Rock-Bacon 126, Lana'i; CISP4 JF904976, CISP5 JF905068, matK JF905389, ndhF JF905151, RPB2 JF905231, trnDT JF905302. P. lanaiensisBecc. & Rock-S. Perlman 16385 (PTBG), FTBG DNA Bank 1845, Lana'i; CISP4 JF904977, CISP5 JF905069, matK JF905390, MS JF905100, ndhF JF905152, RPB2 JF905232, trnDT JF905303. P. lanaiensisBecc. & Rock-Perlman 19968 (PTBG), Lana'i; CISP4 JF904978, CISP5 JF905046, matK JF905391, ndhF JF905153, RPB2 JF905233, trnDT JF905304. P. lanigeraBecc.-K. Wood 7611 (PTBG), FTBG DNA Bank 1846, Hawai'i; CISP4 JF904979, CISP5 JF905070, matK JF905392, MS JF905101, ndhF JF905154, RPB2 JF905234, trnDT JF905305. P. limahuliensisH.St.John- J. Horn 4947 (PTBG), FTBG DNA Bank 1831, Kaua'i; CISP4 JF904980, matK JF905393, MS JF905102, ndhF JF905155, RPB2 JF905236, trnDT JF905307. P. limahuliensisH.St.John-NTBG Live Collection, Kaua'i; CISP4 JF904981, CISP5 JF905071, matK JF905394, MS JF905103, ndhF JF905156, RPB2 JF905235, trnDT JF905308. P. lowreyanaRock ex Becc.- J. Horn 4943 (PTBG), FTBG DNA Bank 1794, Moloka'i; CISP4 JF904982, CISP5 JF905072, matK JF905395, ndhF JF905157, RPB2 JF905237, trnDT JF905309. P. lowreyanaRock ex Becc.-Wood 9236 (PTBG), Moloka'i; CISP4 JF904983, CISP5 JF905047, matK JF905396, ndhF JF905158, RPB2 JF905238, trnDT JF905310. P. martii(Gaudich.) H.Wendl.- Bakutis Waianae SN1, O'ahu; CISP4 JF904984, CISP5 JF905048, matK JF905397, ndhF JF905159, RPB2 JF905239, trnDT JF905311. P. martii(Gaudich.) H.Wendl.- Bakutis Waianae SN2, O'ahu; CISP4 JF904985, CISP5 JF905049, matK JF905398, MS JF905090, ndhF JF905160, RPB2 JF905240, trnDT JF905312. P. martii(Gaudich.) H.Wendl.- Bacon Waiava1, O'ahu; CISP4 JF904988, CISP5 JF905052, matK JF905401, ndhF JF905163, RPB2 JF905243, trnDT JF905315. P. martii(Gaudich.) H.Wendl.- Bacon Waiava7, O'ahu; CISP4 JF904986, CISP5 JF905050, matK JF905399, MS JF905104, ndhF JF905161, RPB2 JF905241, trnDT JF905313. P. martii(Gaudich.) H.Wendl.- Bacon Waiava15, O'ahu; CISP4 JF904987, CISP5 JF905051, matK JF905400, ndhF JF905162, RPB2 JF905242, trnDT JF905314. P. martii(Gaudich.) H.Wendl.- J. Horn 4937 (PTBG), FTBG DNA Bank 1855, O'ahu; CISP4 JF904992, CISP5 JF905073, matK JF905405, ndhF JF905167, RPB2 JF905245, trnDT JF905319. P. martii(Gaudich.) H.Wendl.- J. Horn 4954 (PTBG), FTBG DNA Bank 1859, O'ahu; CISP4 JF904993, CISP5 JF905074, matK JF905406, ndhF JF905168, RPB2 JF905246, trnDT JF905320. P. martii(Gaudich.) H.Wendl.-NTBG live collection, O'ahu; CISP4 JF904994, CISP5 JF905053, matK JF905406, ndhF JF905169. P. minorBecc.-Trauernicht 432 (PTBG), Kaua'i; matK JF905408. P. minorBecc.-Trauernicht 434 (PTBG), Kaua'i; CISP4 JF904995, matK JF905409, ndhF JF905170. P. minorBecc.-Trauernicht 435 (PTBG), Kaua'i; CISP4 JF904996, matK JF905410, MS JF905105, ndhF JF905171, trnDT JF905321. P. minorBecc.-J. Horn 4946 (PTBG), FTBG DNA Bank 1797, Kaua'i; CISP4 JF904997, CISP5 JF905075, matK JF905411, ndhF JF905172, RPB2 JF905247, trnDT JF905322. P. minorBecc.- S. Zona 1033 (FTG), FTBG DNA Bank 845, Kaua'i; CISP4 JF904998, CISP5 JF905054, matK JF905412, ndhF JF905173, RPB2 JF905248, trnDT JF905323. P. minorBecc.- -Tangalin 1708 (PTBG), Kaua'i; trnDT JF905324. P. mitiaroanaJ.Drans. & Y.Ehrh.- S. Perlman 19346 (PTBG), FTBG DNA Bank 1857, Cook Islands; CISP4 JF904999, CISP5 JF905076, matK JF905413, MS JF905091, ndhF JF905174, RPB2 JF905249, trnDT JF905325. P. mitiaroanaJ.Drans. & Y.Ehrh.-Perlman 19346 (PTBG), Cook Islands; CISP4 JF905000. P. cf. mitiaroanaJ.Drans. & Y.Ehrh.-Meyer SN 'pericularum', French Polynesia; CISP4 JF905006, CISP5 JF905057, matK JF905419, MS JF905108, ndhF JF905181, RPB2 JF905254, trnDT JF905332. P. cf. mitiaroanaJ.Drans. & Y.Ehrh.-Meyer SN 'vuylstekeana', French Polynesia; CISP4 JF905019, CISP5 JF905085, matK JF905434, MS JF905118, ndhF JF905193, RPB2 JF905265, trnDT JF905346. P. munroiRock- J. Horn 4942 (PTBG), FTBG DNA Bank 1832, Moloka'i; CISP4 JF905001, CISP5 JF905077, matK JF905414, ndhF JF905175, RPB2 JF905250, trnDT JF905326. P. munroiRock- S. Zona 1036 (FTG), FTBG DNA Bank 841, Moloka'i; CISP4 JF905002, CISP5 JF905055, matK JF905415, ndhF JF905176, RPB2 JF905251, trnDT JF905327. P. napaliensisH.St.John- S. Perlman 11297 (PTBG), FTBG DNA Bank 1860, Kaua'i; CISP4 JF905003, CISP5 JF905078, matK JF905416, MS JF905106, ndhF JF905177, RPB2 JF905268, trnDT JF905328. P. napaliensisH.St.John-Wood 9087 (PTBG), Kaua'i; CISP4 JF905004, CISP5 JF905056, matK JF905417, MS JF905092, ndhF JF905178, trnDT JF905329. P. pacificaSeem. & H.Wendl.- FTBG Live Collection 93691D, FTBG DNA Bank 18, Fiji; CISP4 JF905005, CISP5 JF905079, ndhF JF905179, RPB2 JF905252, trnDT JF905330. P. pacificaSeem. & H.Wendl.-J. Horn 4952 (PTBG), FTBG DNA Bank 1861, Fiji; CISP5 JF905080, matK JF905418, MS JF905107, ndhF JF905180, RPB2 JF905253, trnDT JF905331. P. perlmaniiGemmill-Wood 7331 (PTBG), Kaua'i; CISP4 JF905007, matK JF905421, MS JF905109, ndhF JF905183, trnDT JF905333. P. perlmaniiGemmill-Wood 8091 (PTBG), Kaua'i; CISP4 JF905008, CISP5 JF905058, matK JF905422, MS JF905110, ndhF JF905184, RPB2 JF905255, trnDT JF905334. P. perlmaniiGemmill-NTBG Live Collection, Kaua'i; matK JF905420, MS JF905111, ndhF JF905182, trnDT JF905335. P. remota(Kuntze) Becc.- J. Horn 4955 (PTBG), FTBG DNA Bank 1844, Nihoa; CISP4 JF905009, CISP5 JF905081, matK JF905423, ndhF JF905185, RPB2 JF905256, trnDT JF905336. P. remota(Kuntze) Becc.-J. Horn 4936 (PTBG), FTBG DNA Bank 1865, Nihoa; CISP4 JF905010, CISP5 JF905082, matK JF905424, ndhF JF905186, RPB2 JF905257, trnDT JF905337. P. remota(Kuntze) Becc.-Montgomery Botanical Center Live Collection 29, Nihoa; CISP4 JF905011, matK JF905425, MS JF905112, RPB2 JF905258, trnDT JF905338. P. schattaueriHodel-J. Horn 4939 (PTBG), FTBG DNA Bank 1843, Hawai'i; CISP4 JF905012, CISP5 JF905083, matK JF905426, MS JF905113, ndhF JF905187, RPB2 JF905259, trnDT JF905339. P. schattaueriHodel- S. Zona 1001 (FTG), FTBG DNA Bank 839, Hawai'i; CISP4 JF905013, CISP5 JF905059, matK JF905427, MS JF905114, ndhF JF905188, RPB2 JF905260, trnDT JF905340. P. thurstoniiF.Muell. & Drude-NTBG Live Collection, Fiji; CISP4 JF905014, CISP5 JF905060, matK JF905428, MS JF905115, ndhF JF905189, RPB2 JF905261, trnDT JF905341. P. viscosaRock- J. Horn 4943 (PTBG), FTBG DNA Bank 1795, Kaua'i; CISP4 JF905015, CISP5 JF905084, matK JF905429, ndhF JF905190, RPB2 JF905262, trnDT JF905342. matK JF905430, ndhF JF905191. P. viscosaRock-Tangalin 1693 (PTBG), Kaua'i; CISP4 JF905016, matK JF905431, MS JF905116, RPB2 JF905263, trnDT JF905343. P. viscosaRock-Tangalin 1694 (PTBG), Kaua'i; CISP4 JF905017, matK JF905432, MS JF905117, RPB2 JF905264, trnDT JF905344. P. viscosaRock-Perlman 16679A (PTBG), Kaua'i; CISP4 JF905018, matK JF905433, MS JF905093, ndhF JF905192, trnDT JF905345. P. waialealeanaRead-Trauernicht 423 (PTBG), Kaua'i; matK JF905436, trnDT JF905347. P. waialealeanaRead-Lorence 8446 (PTBG), Kaua'i; CISP4 JF905021, matK JF905435, ndhF JF905194, trnDT JF905348. P. waialealeanaRead- J. Horn 4950 (PTBG), FTBG DNA Bank 1863, Kaua'i; CISP4 JF905020, CISP5 JF905086, matK JF905437, MS JF905119, ndhF JF905195, RPB2 JF905266, trnDT JF905349. P. waialealeanaRead-NTBG Live Collection, Kaua'i; CISP4 JF905022, CISP5 JF905061, matK JF905438, MS JF905120, ndhF JF905196, RPB2 JF905267, trnDT JF905350.
The authors thank Ane Bakutis, Susan Ching, Don Hodel, Leland Miyano, Hank Oppenheimer, Steve Perlman, Geovanni Romero, Natalia Tangalin, Clay Trauernicht, Dick Watling, and Ken Wood for assistance with fieldwork; Jean-Yves Meyer and Lauren Weisenberger for DNA samples; Don Hodel and David Lorence for insightful feedback and discussions; Don Hodel for the use of the Pritchardia hillebrandii image; and Gabriel Johnson (Smithsonian) and Arwen Milroy (Colorado State University) for lab assistance. This research was supported by a National Tropical Botanical Garden McBryde Graduate Student Fellowship, an NSF-DDIG (DEB-1010731) award, a Smithsonian Pre-Doctoral Fellowship, a Montgomery Botanical Center Research Associateship, the Hunt Institute Lawrence Memorial Award, and the Bruno Klinger Memorial Scholarship to C.D.B.
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