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1 October 2010 Phylogeny and Recircumscription of Artocarpeae (Moraceae) with a Focus on Artocarpus
Nyree J. C. Zerega, M. N. Nur Supardi, Timothy J. Motley
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Moraceae is a large (∼1,050 species) primarily tropical family with several economically and ecologically important species. While its monophyly has been well supported in recent studies, relationships within the family at the tribal level and below remain unresolved. Delimitation of the tribe Artocarpeae has been particularly difficult. Classifications based on morphology differ from those based on phylogenetic studies, and all treatments include highly heterogeneous assemblages of genera that seem to represent a cross section of the family. We evaluated chloroplast and nuclear DNA sequence data for 60 Moraceae taxa representing all genera that have been included in past treatments of Artocarpeae and also included species from several other Moraceae tribes and closely related families as outgroups. The data were analyzed using maximum parsimony and maximum likelihood methods and indicate that none of the past treatments of Artocarpeae represent a monophyletic lineage. We present the most complete phylogenetic hypothesis for Artocarpeae and the genus Artocarpus to date. Inflorescence evolution and pollination are briefly discussed and the phylogenetic reconstructions are used to inform a revised treatment of Artocarpeae and the Artocarpus subgenera. The following new combinations are proposed: the genus Prainea is reduced to Artocarpus subgenus Prainea, and the series Cauliflori is raised to Artocarpus subgenus Cauliflori.

The mulberry family (Moraceae) comprises approximately 37 genera and 1,050 species (Berg et al. 2006) including several economically and ecologically important species such as breadfruit (Artocarpus altilis (Parkinson) Fosberg), paper mulberry (Broussonetia papyrifera Vent.), and figs (Ficus L.). The family is distributed throughout tropical and temperate regions worldwide, but its diversity is centered in the tropics. Based on molecular (Datwyler and Weiblen 2004; Zerega et al. 2005a) and combined morphological and molecular evidence (Clement and Weiblen 2009), the family is strongly supported as monophyletic, but an amazing diversity of complex inflorescence structures, pollination syndromes, breeding systems, and growth forms in the family has complicated its taxonomy at the tribal level and below. Despite the fact that the tribal circumscription of the Moraceae has come under frequent scrutiny by several investigators (Berg 1977a, b; Rohwer 1993; Berg 2001; Datwyler and Weiblen 2004; Berg et al. 2006; Clement and Weiblen 2009), tribe Artocarpeae has remained particularly difficult (Table 1). It has long been recognized as a highly heterogeneous and unnatural assemblage of pantropical taxa with no clear morphological synapomorphies and the genera included in the tribe have changed frequently.

The most recent floristic treatment of the tribe recognizes an Artocarpeae including five paleotropical genera (Artocarpus J. R. Forst., and G. Forst., Hullettia King ex Hook, f., Parartocarpus Baill., Prainea King ex Hook, f., and Treculia Decne ex Trécul) characterized by “pistillate inflorescences mostly formed of connate perianths, many seeded infructescences, and free fruits” (Berg et al. 2006). The results of phylogenetic studies differ from the floristic treatment in that two neotropical genera (Clarisia Ruiz & Pavón and Batocarpus Karsten) are also included within Artocarpeae, and the tribe is characterized by the reduction of stamen number, peltate interfloral bracts, vitreous silica, and straight filaments (Datwyler and Weiblen 2004; Zerega et al. 2005a; Clement and Weiblen 2009). Unfortunately, the phylogenetic studies did not include Hullettia or Treculia in their analyses and the placement of Parartocarpus was inconsistent (either being placed in Artocarpeae or a polyphyletic Moreae). Earlier floristic treatments also placed Clarisia and Batocarpus within Artocarpeae as well as additional neotropical (Bagassa Aubl., Poulsenia Eggers, and Sorocea A. St.-Hil.) and paleotropical (Antiaropsis K. Schum. and Sparattoscye Bureau) genera (Rohwer 1993; Berg 2001). Artocarpus (∼45 species; Berg et al. 2006) is the largest genus in the tribe, and the third largest genus in the Moraceae family (after Ficus and Dorstenia L.). As the type genus, its inclusion in the tribe is not in question, but what remains unclear is the monophyly of the genus, and exactly what other genera should be included in the tribe.

Artocarpus is distributed from Southeast Asia east into Oceania (Fig. 1A). Additionally, several Artocarpus species have been introduced throughout the tropics and are harvested for food (e.g. A. altilis, breadfruit; A. camansi Blanco, breadnut; and A. heterophyllus Lam., jackfruit). Treculia Decne. ex Trécul (three species) occurs in Africa and Madagascar, and its seeds are a source of food for humans. The other genera that have most recently been included in Artocarpeae have relatively few species and are of little economic value. Hullettia (two species) is restricted to the Malay penninsula and Sumatra. Parartocarpus (two species) ranges from Thailand east to the Solomon Islands. Prainea (two to four species) ranges from the Malay Peninsula to New Guinea. Batocarpus (three species) and Clarisia (three species), both range from Central to South America (Fig. 1B).

Artocarpus and the six smaller genera (Batocarpus, Clarisia, Hullettia, Parartocarpus, Prainea, and Treculia) that have been most recently included in Artocarpeae (Datwyler and Weiblen 2004; Clement and Weiblen 2009) all bear unisexual flowers, as do all Moraceae, and typically have unisexual infloresences. They are either monoecious or dioecious latex-producing trees, or rarely shrubs. Pistillate inflorescences are condensed capitate heads (or rarely uniflorous as in some Clarisia), which develop into syncarps and may attain enormous sizes in some species, up to 100 cm × 50 cm in A. heterophyllus, jackfruit (Jarrett 1959c, 1975). Staminate inflorescences are typically spicate or less frequently globose. Both pistillate and staminate inflorescences are typically comprised of numerous small, tightly packed flowers, which either sit upon (Artocarpus, Prainea, Treculia, Batocarpus, Clarisia) or are embedded in (Hullettia, Parartocarpus) a fleshy receptacle, and either have (Artocarpus, Prainea, Batocarpus, Clarisia, Treculia) or lack (Hullettia, Parartocarpus) a perianth (Jarrett 1959a; Berg 1977b) (Fig. 2). In pistillate inflorescences of Artocarpus, the perianths of adjacent flowers are fused together at least apically and medially (leaving syncarps with an even surface) or are fused medially and are free at the apices (leaving syncarps with a spiky or tuberculate surface) (Fig. 3). This allows the entire inflorescence to develop into a highly specialized syncarp formed by the enlargement of the entire female head even if only a portion of the flowers develop seeds (Jarrett 1976). However, in Prainea (Fig. 2), Batocarpus, and Clarisia adjacent pistillate perianths remain free so that only fertilized ovules enlarge. In Treculia adjacent pistillate perianths are not fused, but rather the stalks of the abundant interfloral bracts are fused for about half their length. The flowers are enclosed in cavities between the fused bracts and the entire inflorescence enlarges into a syncarp (Jarrett 1959c).


Comparison of the classification of Artocarpeae according to the four most recent treatments and findings from the present study. Berg (2001) included 12 genera in Artocarpeae and the classification history of these 12 genera is listed below. When Artocarpeae is listed, it indicates the genus is included in Artocarpeae in that treatment. An asterisk means the genus was moved to the indicated tribe. “Maintained“ means that in the present study the authors maintain the most recent transfer of the genus to a tribe other than Artocarpeae (Clement and Weiblen 2009).


FIG. 1.

Distribution of Artocarpeae. This treatment of the tribe Artocarpeae includes: A. one paleotropical genus (Artocarpus including Prainea as a subgenus) and B. two neotropical genera (Clarisia and Batocarpus). Several Artocarpus species, including A. altilis, A. camansi, and A. heterophyllus, are cultivated throughout the tropics. Scale bar for each map is 500 km.


The smaller genera do not have any recognized infrageneric taxa, but Artocarpus, which has been monographed twice (Trécul 1847; Jarrett 1959a, c, 1960a), has been subdivided. Trécul (1847) placed the 15 species of Artocarpus recognized at the time into two subgenera. Species with alternate, spirally arranged leaves, amplexicaul stipules, and annulate stipule scars were placed in subgenus Jaca Trécul (from the Malayalam word chakka given to jackfruit, A. heterophyllus). Those species with alternate, distichous leaves, nonamplexicaul stipules, and lateral stipule scars were placed in subgenus Pseudojaca Trécul.

Beccari (1902) noted that the only difference between Artocarpus and Prainea was the degree of fusion among adjacent pistillate perianths (with those in Artocarpus being completely to partially fused to one another and those in Prainea being entirely free) (Fig. 2). Renner (1907) maintained Trécul's (1847) subgeneric sections (Jaca and Pseudojaca), but reduced the genus Prainea to a third section within Artocarpus. His treatement was based largely on leaf and stipule characters that Prainea shared with the other two subgenera of Artocarpus. More recently, Jarrett (1959a, 1959b) rejected Renner's (1907) treatment of Prainea, maintained the two subgenera originally created by Trécul (1847), and changed subgenus Jaca to subgenus Artocarpus (resulting in subgenera Artocarpus and Pseudojaca). Jarrett (1959c, 1960a) also subdivided both subgenera into several sections and series (Table 2), and proposed for the first time a close affinity between Hullettia and Parartocarpus based on the shared presence of an inflorescence involucre, absence of a perianth, and pistillate flowers embedded in the receptacle.

FIG. 2.

Inflorescence sections. Longitudinal sections through pistillate (A-F) and staminate (G-K) inflorescences of species of Artocarpus, Prainea, Parartocarpus, Hullettia, and Treculia. A. Artocarpus hispidus (subgenus Artocarpus) exhibits medial adjacent perianth fusion. B. Artocarpus dadah (subgenus Pseudojaca) exhibits complete fusion of perianth apices. C. Prainea papuana exhibits no fusion between adjancent perianth apices, but dense interfloral bracts are present. D and E. Parartocarpus venenosus and Hullettia dumosa, respectively, lack perianths, and flowers are embedded directly in the receptacle. F. Flowers of Trecidia obovoidea are enclosed in cavities formed by the fusion of the stalks of abundant interfloral bracts. G and H. In A. hispidus (G) and Prainea papuana (H), adjacent staminate perianths are free and interfloral bracts are present. I and J. Staminate flowers of Parartocarpus venenosus ssp. forbesii and H. griffithiana lack perianths and are embedded in the receptacular tissue. K. Adjacent staminate perianths are free and interfloral bracts are present in T. acuminata. The scale bar in A — F is 1cm, and for G — K is 1 mm. In A — E, and G — J, the diagonal lines indicate receptacular tissue, the black indicates either pistils (A — E) or stamens (G — J), and the white indicates either perianth tissue or interfloral bracts. A, B — E, and G — J have been modified from Jarrett 1959 with permission from the Arnold Arboretum. Copyright ©President and Fellows of Harvard College, Archives of the Arnold Arboretum. F and K have been modified from Berg (1977a) with permission from the Bulletin du Jardin botanique national de Belgique.


FIG. 3.

Surface characteristics of Artocarpus. A. Species containing pistillate inflorescences with adjacent perianth apices fused apically have a smooth surface as in A. nitidus ssp. lingnanennsis (NZ4); B. species with perianth apices fused medially but free apically have a spiky surface, like A. heterophyllus (NZ6). Scale bar is 1 cm.



Characters used to define infrageneric taxa in the genus Artocarpus (sensu Jarrett 1959c, 1960a). All species epithets listed under “members of group” heading belong to the genus Artocarpus.


Objectives—Historically, Artocarpeae has represented a highly heterogeneous assemblage of genera, and various authors (Rohwer 1993; Berg 2001; Datwyler and Weiblen 2004; Berg et al. 2006; Clement and Weiblen 2009) have at one time or another placed its putative members in at least five different tribes (Artocarpeae, Castilleae, Moreae, Soroceae, and Antiaropsidae) (Table 1). Of the competing hypotheses regarding the circumscription of Artocarpeae, only two have been based on phylogenetic analyses (Datwyler and Weiblen 2004; Clement and Weiblen 2009). Unfortunately, samples from only 3–4 species of Artocarpus and none from Hullettia or Treculia were included in these studies. Using sequence data from the plastid (trnL intron and trnL-F spacer, trnL-F) and nuclear (ITS 1 and 2 and 5.8S rDNA) genomes, this study was designed to create a well-resolved phylogenetic hypothesis with which to: 1) test the monophyly of Artocarpeae, Artocarpus, and infrageneric divisions within Artocarpus and 2) develop a phylogenetic classification and treatment based on the results and morphological considerations. We present the most complete phylogenetic estimate for Artocarpeae and the genus Artocarpus to date, and also consider inflorescence evolution and pollination in the tribe.


Taxon Sampling—The ingroup included all genera that have been placed in Artocarpeae in the most recent circumscriptions (Berg 2001; Datwyler and Weiblen 2004; Berg et al. 2006; Clement and Weiblen 2009). Thus, the ingroup included two species each of Prainea, Treculia, Parartocarpus, and Sorocea, one species each of Hullettia, Bagassa, Batocarpus, Clarisia, Sparattosyce, Antiaropsis, Poulsenia, and 34 species and four subspecies of Artocarpus representing all subgenera, sections (except the monotypic sect. Glandulifolium Jarrett), and series (Appendix 1). Outgroup taxa belong to five other tribes of Moraceae and one species each of Ficus (Ficeae), Dorstenia and Brosimum Sw., (Dorstenieae), Castilla Cerv. (Castilleae), Morus L. (Moreae), and Maclura (Maclureae (sensu Clement and Weiblen 2009), as well as one species each of Humulus L. and Cannabis L. (Cannabaceae).

Sequence data for the two gene regions (ITS and the trnL-F region) were generated by the authors for all taxa with the exception of seven previously published sequences; nine sequences for trnL-F are missing (Appendix 1).

DNA Extraction, Amplification, and Sequencing—Leaf samples were collected either in silica gel or from herbarium sheets (Appendix 1). Genomic DNA was extracted from approximately 1 cm2 of dried leaf tissue using a modified CTAB (cetyltrimethylammonium bromide) method (Zerega et al. 2002).

DNA amplification for the ITS and trnL-F regions were performed in a 25 µl volume (1 × Taq buffer with 1.5 mM MgCl2 (Qiagen, Valencia, California), 1mg/ml BSA (bovine serum albumin), 2.5 mM each dNTP, 20 µM of each primer, 1 M betaine, 1 unit Taq polymerase (Qiagen), and ∼50 ng of genomic DNA). Amplification and cycle sequencing reactions were run on a Gene Amp PCR system 9600 (Applied Biosystems, Foster City, California).

Amplification of the trnL-F region utilized external primers “c” and “f,” and the internal primers “d” and “e” were also employed for amplification from herbarium specimens (Taberlet et al. 1991). Thermal cycling conditions for amplification of the trnL-F region were: 94°C for 3 min followed by 32 cycles of 94°C for 45 sec, 52°C for 30 sec, 72°C for 1 min 30 sec, and a final extension of 74°C for 7 min. The ITS region was amplified using forward (5′-AACAAGGTTTCCGTAGGTGA-3′) and reverse (5′-TATGCTTAAAYTCAGCGGGT-3′) primers, and for some herbarium specimens, internal primers were also employed (5′-GCAT CGATGAAGAACGTAGC-3′ and 5′-GCTACGTTCTTCATCGATGC-3′) (modified from Baldwin 1992; Nickrent et al. 1994; Baldwin et al. 1995). The PCR conditions for amplificaton of the ITS region were: 97°C for 50 sec, 30 cycles of 97°C for 50 sec, 53°C for 50 sec, 72°C for 1 min 50 sec, and a final extension of 72°C for 7 min.

Amplified products were purified with spin columns from the QIAquick PCR purification kit (Qiagen) following protocols provided by the manufacturer. Purified products were cycle sequenced in 10 µl reactions using Big Dye sequencing reagents and protocols (Applied Biosystems). Primers for cycle sequencing were the same as those used in the PCR reactions, but the internal primers “d” and “e” were also employed for all samples for the trnL-F region. Cycle sequencing conditions were: 95°C for 1 min, 32 cycles of 96°C for 10 sec, 50°C for 5 sec, 60°C for 3 min. Cycle sequencing products were purified on a sephadex column and data were collected on an ABI Prism 377 DNA sequencer (Applied Biosystems) and edited in Sequencher version 3.1.2 (Gene Codes Corporation, Ann Arbor, Michigan).

Sequence Alignment and Phylogenetic Analysis—Sequences from the ITS region were aligned using Clustal W (Chenna et al. 2003) followed by manual optimization. Sequences from the trnL-F region were easily aligned manually. Manual alignment and optimization were performed in Se-Al v2.0a7b (Rambaut 2001). For the trnL-F region, indels were coded as additional, unordered characters if they were bordered by stretches of unambiguously aligned nucleotides and were not a single nucleotide repeat. Indels were treated as the same state if they were the same size and their nucleotide sequence did not vary.

Data from ITS and the trnL-F regions were analyzed separately. The trees obtained for each region were examined for hard (bootstrap of 70% or higher) or soft (bootstrap below 70%) incongruences based on bootstrap support for nodes in both of the separate analyses. In the case of soft incongruences, conflicts likely reflect insufficient information in one or both of the datasets leading to an unstable position and considerable character evolution and resolution in the other, rather than different branching histories (Seelanan et al. 1997). Combining the data in such a scenario may lead to better resolution and more accurate phylogeny reconstruction, allowing the phylogenetic signal to assert itself over the noise. We did not employ the incongruence length difference test (ILD), as there were no hard incongruences between the datasets, and the ILD test has been shown to be a poor test of the comparability of separate data partitions (Hipp et al. 2004). Separate and combined maximum parsimony (MP) searches were performed using the ratchet as employed in Winclada 1.00.08 (Nixon 1999–2002) and NONA (Goloboff 1999) and maximum likelihood (ML) searches were performed in PAUP* 4.01b10 (Swofford 2002).

Maximum parsimony searches using the ratchet method were performed with uninformative characters excluded. The ratchet is able to more efficiently estimate phylogeny by randomly varying taxon order, holding fewer trees per replicate, sampling many tree islands, and holding fewer trees per island (Nixon 1999). Five sequential ratchet runs were performed and iterated 1,000 times per replicate, with 10 trees held per replicate. Each ratchet performs two searches, one in which all characters are equally weighted, and one search in which a random percentage of characters (determined by the user, 30% in this case) are weighted, but weights are not assigned to the same characters in each iteration. Trees from the independent searches are used to extract the most parsimonious trees.

For ML analyses, Modeltest version 3.7 (Posada and Crandall 1998) was used to select substitution models that best fit the separate and combined datasets. Heuristic searches were performed under ML with a neighbor joining tree as a starting topology and model parameters obtained with Modeltest under the Akaike Information Criterion (AIC) for model selection (Posada and Buckley 2004).

Clade support for both MP and ML phylogenies were assessed with a bootstrap analysis using 1,000 replicates with 100 random addition sequence replicates, and tree bisection and reconnection (TBR) branch swapping as implemented in PAUPá 4.01b10 (Swofford 2002).


ITS Analyses —The ITS dataset provided a total of 779 aligned nucleotides of which 416 were parsimony informative. The data matrix had 2.6% missing data. Parsimony searches recovered 111 most parsimonious trees (MPTs) of 1,984 steps, consistency index (CI) of 0.43, and retention index (RI) of 0.66. In the strict consensus tree ten nodes collapsed. For ML analyses a total number of 779 characters were used. Modeltest (Posada and Crandall 1998) identified a general time reversible model with a gamma distribution and proportion of invariable sites (GTR + I + G) as the best fitting model of sequence evolution for ITS. The single most likely ITS tree resulting from heuristic searches had a score of —lnL = 10917.89138 with a rate matrix of AC = 0.766900, AG = 1.388800, AT = 1.022600, CG = 0.376200, and CT = 2.729000, gamma = 1.2999, I = 0.1674, and base frequencies of A = 0.22130, C = 0.30450, G = 0.26900, and T = 0.20520. The MP strict consensus tree (not shown) and the ML tree (Fig. 4) revealed Artocarpeae as defined by any past circumscriptions to be polyphyletic. There are only two deep and three tip level relationships that differ between the ML and MP analyses of ITS, and these relationships have no support in either reconstruction. In the MP analysis, Maclura pomifera is sister to the rest of the Moraceae family, while in the ML analysis, it is sister to a clade comprising only Artocarpus, Prainea, Batocarpus, Clarisia, Morus, Sorocea, and Bagassa. In the ML analysis, the following taxa form a grade of three clades: 1) Dorstenia, Brosimum, and Treculia, 2) Ficus, Castilla, Poulsenia, Antiaropsis, and Sparattosyce, and 3) Hullettia and Parartocarpus. In the MP analysis, these clades are part of an unresolved and unsupported monophyletic group. The remaining differences between the ML and MP analyses of ITS are near the tips and involve minor rearrangements of Artocarpus camansi and A. petelotii.

FIG. 4.

Maximum likelihood analyses based on separate datasets. A. Tree based on ITS data, B. Tree based on trnL-F data. Bootstrap support ranges are indicated by symbols on branches: Gray circles = 90–100%, black circles = 80–89%, gray squares = 70–79%, and black squares = 60–69%.


trnL-F Analyses—The trnL-F dataset provided 1,140 aligned nucleotides of which 123 were parsimony informative. The data matrix had 13.7% missing data. Additionally, the trnL-F region provided five unambiguous parsimony informative indels which were coded as separate characters. Parsimony searches recovered 552 MPTs of 202 steps, CI = 0.75, and RI = 0.89. In the strict consensus tree (not shown) 26 nodes collapsed. For ML analyses, a total number of 1,140 characters were used. Modeltest (Posada and Crandall, 1998) identified a K81uf + G as the best fitting model of sequence evolution for the trnL-F dataset. The two most likely trnL-F trees resulting from heuristic searches had a score of -lnL = 3,905.04799 with a rate matrix of AC = 1.010600, AG = 1.832000, AT = 0.396900, CG = 0.825400, and CT = 1.832000, gamma = 1.2094, and base frequencies of A = 0.35970, C = 0.16200, G = 0.15900, and T = 0.31930. The ML trnL-F topology was more resolved than the MP analysis. In the MP consensus tree the following taxa form a grade of three clades: 1) Dorstenia, Brosimum, and Treculia; 2) Ficus and Castilla; and 3) Hullettia and Parartocarpus. In the ML analysis, these taxa form an unsupported monophyletic group (Fig. 4).

Combined Analyses—Comparing the phylogenies based on the separate analyses of ITS and trnL-F revealed only minor rearrangements at unsupported tips, with the exception of four instances where one dataset provided strong support for an arrangement of taxa while the other dataset provided weak or no support for an alternate arrangement (Fig. 4). There was 98% support for placement of Prainea papuana in a clade with Prainea limpato in the ITS tree, while its position was unresolved within the Artocarpus + Prainea clade in the trnL-F tree. Ficus carica was strongly supported (95% bootstrap) as sister to Castilla elastica (Castilleae) in the trnL-F tree, and it was sister to a clade comprising Castilla elastica, Antiaropsis decipiens, Sparattosyce dioica, and Poulsenia armata (all members of Castilleae) and Dorstenia choconiana, Brosimum lactescens, Treculia obovoidea, and T. africana (all members of Dorstenieae as defined here) in the ITS tree. Artocarpus lowii was strongly supported (96%) as part of a clade including members of series Rugosi in the trnL-F tree and was placed as sister to the breadfruit clade (with no support) in the ITS tree. Batocarpus and Clarisia were supported (88%) as sister taxa in the trnL-F tree, but there was no bootstrap support for their sister relationship in the ITS tree. As no hard incongruencies in relationships were present, the two datasets were combined. Parsimony searches of the combined datasets recovered 16 MPTs of 1,992 steps, CI = 0.43, and RI = 0.65. In the strict consensus tree, seven nodes collapsed (MP tree not shown). Additionally, the number of supported nodes increased in the combined analysis compared to either separate analysis. In the combined analysis, 35 nodes had support of 70% or higher, compared with 25 and 16 nodes in the ITS and trnL-F analyses, respectively. For ML analyses of the combined dataset, a total of 1919 characters (779 from ITS and 1,140 from trnL-F) were used. Modeltest (Posada and Crandall 1998) identified a general time-reversible model with a gamma distribution and a proportion of invariable sites (GTR + I + G) as the best fitting model of sequence evolution for the combined ITS and trnL-F dataset. The single most likely tree resulting from heuristic searches had a score of -lnL = 15,459.66603 with a rate matrix of AC = 0.674700, AG = 1.243500, AT = 0.557300, CG = 0.558200, and CT = 2.416800, base frequencies of A = 0.29870, C = 0.23990, G = 0.21290, and T = 0.24850, gamma = 0.586, and proportion of invariable sites = 0.2477. The ML and MP trees based on combined datasets differed only in the exact placement of A. fulvicortex within subgenus Pseudojaca and in whether Morus is sister to Bagassa + Sorocea (MP, 61% bootstrap) or Bagassa is sister to Morus + Sorocea (ML, 100% bootstrap) (Fig. 5). Data matrices and trees for this study are deposited in TreeBASE (study number S2347).


This study represents the most complete phylogeny of Artocarpeae and Artocarpus to date. Artocarpeae as treated here comprises three genera, which include a small neotropical lineage (Batocarpus and Clarisia) and a larger Southeast Asian/ Malesian lineage (Artocarpus including Prainea). Previous divergence date estimates for Moraceae suggest that these lineages diverged from one another 65.1 mya (52.2–80.6 mya) and that their split was facilitated via land migration from the Old to the New World across an Eocene North Atlantic Landbridge (Zerega et al. 2005a). The more comprehensive Artocarpeae phylogenetic reconstruction presented here will aid in testing this hypothesis and further understanding the timing and mechanisms for the movement of this group.

Artocarpeae Phylogeny—The delimitation of Artocarpeae has historically been difficult and circumscriptions have been variable. This study tested the monophyly of the tribe by including all genera that have been placed in the tribe in recent treatments (Berg 2001; Datwyler and Weiblen 2004; Berg et al. 2006; Clement and Weiblen 2009). Because the two molecular datasets presented here had no significant conflict, and the phylogenies based on the combined datasets for MP and ML analyses varied only in two poorly supported tip relationships, the ML tree based on the combined datasets will be referred to in the following discussion (Fig. 5). The data presented here indicate that none of the previous Artocarpeae classifications represent a monophyletic group, but rather the taxa once placed within the tribe are spread throughout several tribes of the Moraceae (Table 1). Because our results largely agree with the most recent Moraceae treatment of Clement and Weiblen (2009), with only a few differences, their tribal level treatment will be used as the framework within which to discuss the results.

CastilleaeAntiaropsis, Sparattosyce, and Poulsenia have been placed in the tribe Artocarpeae in recent treatments of the Moraceae family (Rohwer 1993; Berg 2001) (Table 1). The present study resolved Antiaropsis, Sparratosyce, and Poulsenia as part of the Castilleae clade and all three genera share the synapomorhpies that characterize Castilleae, namely an inflorescence involucre of imbricate bracts that only partially encloses the flowers (as opposed to fully enclosing in Ficeae). As such, we maintain the treatment of Castilleae as proposed by Datwyler and Weiblen (2004) and Clement and Weiblen (2009) (Table 1).

FIG. 5.

Maximum likelihood tree based on combined datasets from ITS and trnL-F. The tree on the left traces the number of stamens in staminate flowers. The tree on the right traces the degree of fusion among perianths from adjacent flowers in pistillate inflorescences. All species were scored for these characters. Bootstrap support ranges are indicated by symbols on branches: Black circles = 90–100%, gray circles = 80–89%, open circles = 60–69%.


MoreaeBagassa and Sorocea have both been placed in the tribe Artocarpeae (Rohwer 1993; Berg 2001). The most recent treatments of Moraceae place these genera in Moreae (Datwyler and Weiblen 2004; Clement and Weiblen 2009) and the present study supports this.

DorstenieaeTreculia was established by Decaisne in Trécul's (1847) monographic treatment of Artocarpeae, and it has been primarily treated in Artocarpeae ever since (Jarrett 1959a; Corner 1962; Rohwer 1993; Berg 2001; Datwyler and Weiblen 2004; Berg et al. 2006). However, in his treatment of African Moraceae, Berg (1977b) placed Treculia in a Moreae tribe that combined the Artocarpeae and Moreae tribes. Previous phylogenetic studies based on molecular data (Datwyler and Weiblen 2004; Zerega et al. 2005a; Clement and Weiblen 2009) did not include any Treculia species. The present study indicates that Treculia, the only African taxon included in previous circumscriptions of Artocarpeae, is nested with strong support within the tribe Dorstenieae, a tribe with numerous African and Madagascan members. While Corner (1962) and Berg (1977b) both hypothesized a possible alliance between Treculia and Parartocarpus based on similarities in inflorescences, infructescences, fruits, and seeds, affinities with Dorstenieae have never before been considered, and this placement is surprising. It is possible that a misinterpretation of character homologies (i.e. confusing flowers embedded in recaptacular tissue (e.g. Hullettia and Parartocaarpus) or the fused adjacent pistillate perianths of Artocarpus with the fused interfloral bract stalks of Treculia) may have led to the placement of Treulia in Artocarpeae. The Dorstenieae are quite variable, being the only tribe that exhibits the full range of habits from herbs, to succulent shrubs, to trees (Berg 2001). However, most genera in the tribe have bisexual inflorescences, which are typically not found in other Moraceae tribes apart from Ficeae. Treculia is a small genus (three species) and includes both dioecious and monoecious shrub and tree species. However, the female inflorescences of Treculia may have numerous abortive male flowers, male inflorescences often have pistillodes, and in one species, T. africana, bisexual inflorescences frequently occur (Jarrett 1959a; Berg 1977b). This lineage may represent an incomplete loss of bisexual inflorescences within the tribe Dorstenieae. Further phylogenetic, morphological, and developmental studies should be conducted to help elucidate this intriguing affinity of Treculia with Dorstenieae. We recommend that Treculia be transferred to Dorstenieae.

UnplacedParartocarpus and Hullettia have been placed in Artocarpeae in recent floristic treatments (Jarrett 1960b; Berg 2001; Berg et al. 2006). Phylogenetic studies have recorded conflicting placements of Parartocarpus within either Moreae or Artocarpeae, while Hullettia samples have not been included in these studies (Datwyler and Weiblen 2004, Zerega et al. 2005a; Clement and Weiblen 2009). The position of Hullettia has been in question since King's (1888) erroneous placement of the genus in the Conocephaleae. Renner (1907) excluded the genus from his treatment of the Artocarpeae and Conocephaleae, and was uncertain about its relationship to the other genera. Jarrett (1959a) first proposed a close relationship between Hullettia and Parartocarpus (a relationship strongly supported (100% bootstrap) by this study) based in part on the shared absence of perianths and flowers embedded in receptacular tissue. The two genera also share an inflorescence involucre that is absent in Artocarpus. The results presented here suggest that Hullettia and Parartocarpus may be sister to Ficeae + Castilleae + Dorstenieae, but there is no support for this relationship. Based on our results, the strongly supported clade of Hullettia and Parartocarpus may deserve tribal status. However, given the clade's unstable position in relation to three closely related tribes in this and previous analyses, further studies are warranted.

ArtocarpeaeBatocarpus, Clarisia, Prainea, and Artocarpus have all been placed in Artocarpeae in one or more recent treatments of the family (Jarrett 1959a; Rohwer 1993; Berg 2001; Datwyler and Weiblen 2004; Clement and Weiblen 2009). This placement is strongly supported (100% bootstrap) in the current study and it is recommended that the limits of Artocarpeae be reduced to comprise the species represented in these four genera. Artocarpeae as defined here are supported by a reduction in stamen number within the family (Fig. 5). Artocarpus, Prainea, Clarisia, and Batocarpus all have one (or less frequently two in Batocarpus and A. annulatus, and one to three in Clarisia) stamen per flower as compared to the more typical two to five in other Moraceae. The typical number of stamens per flower in the Moraceae is four, but exceptions exist in all of the tribes.

Batocarpus and Clarisia form a well-supported (100% bootstrap) clade that is sister to the more weakly supported (65% bootstrap) clade of Artocarpus + Prainea. Fosberg (1942) suggested that Clarisia and Batocarpus have close affinities with one another and that as the species of these two genera become better known, they may prove difficult to maintain as separate genera. Further studies focusing on all species of Clarisia and Batocarpus will be necessary to determine generic limits.

Artocarpus and Prainea Phylogeny—The relationship between Artocarpus and Prainea has long been recognized as a close one (Beccari 1902; Renner 1907; Jarrett 1959a). Renner (1907) viewed Prainea as an intermediate between Artocarpus subgenera Jaca (= Artocarpus) and Pseudojaca and placed it at the subgeneric level within the genus Artocarpus, while Jarrett (1959a, 1959b) treated Prainea as a separate but closely allied genus. Jarrett (1959a) placed priority on reproductive (lack of fusion among adjacent pistillate perianths in Prainea compared to partial to complete fusion in genus Artocarpus) over vegetative characters. Renner placed priority on leaf phyllotaxy and stipule characters (which Prainea shares with subgenus Pseudojaca), and leaf anatomy (which Prainea shares with subgenus Artocarpus). Prainea and subgenus Artocarpus both have glandular epidermal hairs with multicellular heads and resin-containing cells in the leaf mesophyll (with the exception of A. heterophyllus and A. integer which lack the latter), whereas subgenus Pseudojaca has unicellular epidermal gland hair heads and no resin-containing cells in the mesophyll. The combined phylogenetic evidence presented here supports Renner's treatment, as Prainea (two of four species sampled) is supported as a monophyletic group nested within the genus Artocarpus. Given the position of Prainea in the combined phylogeny and its morphological intermediacy between other subgenera of Artocarpus, it is treated here as a subgenus of Artocarpus.

The treatment of Prainea as a separate genus (Jarret 1959a, b) was based primarily on the degree of fusion among adjacent pistillate perianths. Interestingly, Jarrett noted that in young pistillate inflorescences of A. rigidus (subgenus Artocarpus), adjacent pistillate perianths are entirely free from one another. The thick-walled medial portions of the perianths become fused only later in development. Moncur (1985) also reported fusion of the medial portion of adjacent pistillate perianths in A. heterophyllus only after anthesis. Sharma (1965) studied the anatomy and morphology of eight Artocarpus species (seven from subgenus Artocarpus and one from subgenus Pseudojaca), and reported that adjacent pistillate perianths are free from one another at early stages in all eight species studied. He found that even before anthesis the middle region of the perianth begins to thicken outward due to rapid divisions and subsequent enlargement of the ground tissue. It is possible that Prainea represents a lineage within Artocarpus that has secondarily lost the ability to undergo delayed fusion. Delayed fusion of neighboring parts is a relatively rare phenomenon among angiosperms (Okimoto 1948, Moncur 1985) and would be of interest for further investigation.

Sister to subgenus Prainea is the species A. sepicanus, which has been treated as anomalous within subgenus Artocarpus because it shares characters with both sections Artocarpus (long slender male inflorescences) and Duricarpus (presence of well-developed interfloral peltate bracts) (Table 2) (Jarrett 1959b). In the phylogeny based on ITS, A. sepicanus is sister to a clade containing subgenus Prainea plus subgenus Pseudojaca. In the phylogeny based on trnL-F, A. sepicanus collapses within a clade comprised of subgenus Prainea and the rest of the genus Artocarpus. In the combined phylogeny, A. sepicanus is sister to subgenus Prainea. None of these placements have any support and the position of A. sepicanus remains problematic. Its leaf arrangement, stipule characters, partial fusion of adjacent pistillate perianths (with apices free), and presence of resin in the spongy mesophyll cells clearly match subgenus Artocarpus, rather than subgenera Pseudojaca or Prainea. Artocarpus sepicanus has a wide separation of the subapical style and the ventral hilum, which is unusual in Artocarpus, but is consistent with subgenus Prainea (Jarrett 1959a). It is possible A. sepicanus is of hybrid origin with putative parents in subgenera Prainea and Artocarpus. Although hybridization is rarely reported in Artocarpus, members of the breadfruit clade are known to hybridize (Fosberg 1960; Zerega et al. 2004b, 2005b). Given its problematic position and the lack of support for its sister relationship to subgenus Prainea, it is treated here within subgenus Artocarpus, with which it shares the most morphological characters.

Artocarpus has been divided into subgenera, sections, and series (Table 2). The two subgenera, Artocarpus (= Jaca) and Pseudojaca, originally described by Trécul (1847) and maintained by Renner (1907) Jarrett (1959a, c, 1960a), and Berg et al. (2006), are not entirely supported by the combined phylogeny presented here. Additionally, at the sectional and series level there is varying support as discussed below.

Artocarpus Subgenus Pseudojaca—Jarrett (1960a) described two sections within subgenus Pseudojaca: the monotypic Glandulifolium (not included in this analysis) and Pseudojaca (Table 2). Section Pseudojaca has strong support as a monphyletic group (100% bootstrap). It is well defined within the genus Artocarpus by both vegetative and floral synapomorphies (Table 2; Figs. 2, 3). Series Peltati is monophyletic, though with no support, while the monphyly of series Clavati could not be tested since only one (A. petelotii) of three species was included in this analysis. A previous Artocarpus phylogenetic analysis based on restriction fragment length polymorphism analyses of 11 species found neither subgenus to be monophyletic (as the position of A. nitidus was unresolved and A. chaplasha was sister to subgenus Pseudojaca) (Kanzaki et al. 1997).

Jarrett (1960a) recognized 19 species (several with numerous subspecies) within subgenus Pseudojaca series Peltati. In the present study, nine species and four subspecies were included. Among these, several have been subsequently treated differently by Berg et al. (2006), and these differences are addressed in the taxonomic treatment below in light of the present study.

Artocarpus Subgenus Artocarpus—Subgenus Artocarpus has been defined within the genus by both vegetative and floral synapomorphies (Table 2; Figs. 2, 3). Species in subgenus Artocarpus exhibit much greater morphological diversity than those in subgenus Pseudojaca, and Jarrett (1959c) described six series within two sections (Duricarpus and Artocarpus) (Table 2). The data presented here indicate that subgenus Artocarpus represents a strongly supported (100% bootstrap) monophyletic group, if series Cauliflori and the anomalous A. sepicanus are excluded from it.

Section Duricarpus is monophyletic with weak support (60% bootstrap), and members of the section share the morphological synapomorphy of indurate, free, pistillate perianth apices (Figs. 3, 5). The series described within section Duricarpus (Jarrett 1959c) are monophyletic (Asperifolii with 82% bootstrap support and Laevifolii with 61% bootstrap support).

In section Artocarpus, the free, pistillate perianth apices are flexuous rather than indurate as in section Duricarpus. Section Artocarpus (with the removal of series Cauliflori and A. sepicanus) is strongly supported (100% bootstrap) as monophyletic (Figs. 4, 5). Series Cauliflori is sister to subgenus Pseudojaca + Prainea. However, there is no support for this sister relationship. Members of Cauliflori are monophyletic (100% bootstrap) and, as the name suggests, share the synapomorphy of cauliflorous inflorescences, though inflorescences may also be axillary. They share the leaf arrangement (spirally arranged with amplexicaul stipules) and perianth fusion characters (adjacent pistillate perianths medially fused but free apically) with subgenus Artocarpus. They are allied with subgenus Pseudojaca in having compact mesophyll and the absence of resin in the spongy mesophyll cells (absent in A. heterophyllus and A. integer, not examined in A. annulatus). Jarrett (1959c) included A. heterophyllus (jackfruit) and A. integer (chempedak) in series Cauliflori, but A. annulatus had not yet been described at the time. The present study indicates that A. annulatus is also closely allied with these species with a sister relationship to A. integer. Artocarpus annulatus is endemic to Sarawak and known only from a few localities. Berg et al. (2006) considered A. annulatus to be part of section Duricarpus. However, it has flexuous perianth apices, indicative of section Artocarpus, rather than the indurated perianth apices of section Duricarpus. The inflorescences of A. annulatus can be axillary or cauliflorous (Kochummen 2000). In the treatment below, Cauliflori is raised to the subgeneric rank and comprises the three species discussed above.

The remaining species that Jarrett (1959c) included in section Artocarpus were in series Rugosi, Incisifolii or classified as anomalous. Series Rugosi is weakly supported as monophyletic if A. lowii is included within it. Apart from A. lowii, all the species in this clade have the synapomorphies listed in Table 2. The position of A. lowii in the separate analyses varies, being nested within Rugosi based on trnL-F and sister to breadfruit and its relatives based on ITS. It is possible that A. lowii may be of hybrid origin, with a member of the breadfruit clade serving as the maternal parent and a member of the Rugosi clade serving as the paternal parent. However, additional data and samples should be examined to determine the affinities of A. lowii.

Series Incisifolii was circumscribed based on the presence of multicellular peltate heads on the glandular hairs of the leaf epidermis (as opposed to either globose or depressed globose heads as in the rest of the genus) and on the occasional to consistent presence of pinnatifid adult leaves (Jarrett 1959c). While Artocarpus species outside of this series all have adult leaves with entire margins, several species in both subgenera exhibit pinnately lobed juvenile leaves. One species (A. anisophyllus) even has compound leaves, demonstrating the labile nature of leaf shape in this group and throughout the Moraceae family. The present study does not include all members originally included in series Incisifolii, but nonetheless indicates it does not represent a natural lineage. Additionally Berg et al. (2006) made several changes to species circumscriptions in this series and they are not maintained here, as described in the taxonomic treatment below.

Within subgenus Artocarpus there are three anomalous species (A. hirsutus, A. sepicanus, and A. nobilis) that Jarrett (1959c) did not assign to a section, as each species possesses characters that appear to be intermediate between sections Artocarpus and Duricarpus. The position of A. sepicanus was discussed above. In the case of A. hirsutus, it has long, slender, male inflorescences typical of section Artocarpus, but has indurate, free, perianth apices typical of section Duricarpus. The combined phylogeny strongly supports its placement within section Duricarpus. Artocarpus nobilis also has long, slender male inflorescences typical of section Artocarpus, but well-developed peltate interfloral bracts typical of section Duricarpus. The placement of A. nobilis is not shown in the phylogenies here as only the trnL-F spacer region was successfully sequenced for this species. When A. nobilis was included in the analyses, it always occurred within subgenus Artocarpus, but caused the resolution of sections Artocarpus and Duricarpus to collapse, possibly due to missing data or hybrid origin with parents from each section. Examination of additional plant material will be necessary before more definitive conclusions can be reached about this species.

Inflorescence Evolution and Pollination Biology—When writing about Moraceae, Corner (1962) stated that “No family has such small standardized flowers, yet such an astonsishing array of infructescences” and that Moraceae “holds many fascinating problems of vestigal features, transference of function, and parallel evolution.” This diversity of inflorescences and infructescences has confounded classification throughout the family, but may be indicative of the diversity in reproductive strategies. In Ficus, for example, the syconium inflorescence shows clear adaptations to the specialized mode of wasp pollination, and there are numerous examples of convergent evolution within the genus that continue to confound the efforts toward a phylogenetic classification (Rønsted et al. 2005).

Although pollination in other genera of Moraceae, like Artocarpus, has received less attention (van der Pijl 1953; Momose et al. 1998; Sakai et al. 2000; Sakai 2001; Zerega et al. 2004a), the inflorescence structures may provide clues. Within Artocarpeae, only limited data exist on pollination for a few Artocarpus species, and the conclusions, even within a species, are mixed (Corner 1962; Singh et al. 1963; Brantjes 1981; Primack 1983; Momose et al. 1998; Sakai et al. 2000). However, pollination by phytophagous insects, breeding in staminate inflorescences, and visiting pistillate inflorescences through deceit, may be more common than previously realized in Artocarpus and other Moraceae (van der Pijl 1953; Sakai et al. 2000; Sakai 2001; Berg 2001; Zerega et al. 2004a; Berg et al. 2006). In Artocarpus, staminate inflorescences with numerous tightly packed flowers, and frequently with interfloral bracts, provide a potentially attractive breeding site for insects, with ample pollen for larvae and opportunities of protection from predators. Additionally, the pistillate inflorescences of Artocarpus are well protected against phytophagous insects due to the fusion of adjacent perianths (subgenera Artocarpus and Pseudojaca), or in some cases interfloral bracts (section Duricarpus and subgenera Pseudojaca and Prainea), denying easy access to the ovules. It is clear that pollination syndromes in Artocarpeae are still largely unknown, empirical studies will be necessary for further elucidation, and a phylogenetic classification will be a useful tool to understand and interpret pollination in an evolutionary context.

Taxonomic Treatment of Artocarpeae—Artocarpeae has long been a heterogeneous, ill-defined, and ever-changing tribe within Moraceae (Corner 1962; Jarrett 1959a; Rohwer 1993; Berg 2001; Datwyler and Weiblen 2004; Berg et al. 2006; Clement and Weiblen 2009). Based on evidence from phylogenetic analyses of molecular data, and considering morphological characters, this treatment circumscribes a monophyletic Artocarpeae comprising two neotropical (Clarisia and Batocarpus) and one paleotropical (Artocarpus including Prainea) genus. Three genera are removed from recent circumscriptions of Artocarpeae: Parartocarpus and Hullettia form a monophyletic group that may warrant tribal status, and Treculia is transferred to Dorstenieae. When taxon circumscriptions have changed within the Artocarpeae genera, brief descriptions that highlight the unique characters of the group are included. When circumscriptions have not changed, descriptions are not included as they have been described in detail elsewhere (Jarrett 1959c, 1960a; Berg 2001; Berg et al. 2006).

I. ARTOCARPEAE R. Br. in Tuckey, Narr. Exped. Zaire, App. 5: 454. 1818. Euartocarpeae Trécul, Ann. Sci. Nat., Bot. ser. 3(8): 108. 1847, nom. inval. —TYPE: Artocarpus altilis (Parkinson) Fosberg.

Members of Artocarpeae can be trees, shrubs, or rarely climbers, and are either monoecious or dioecious. The leaves are simple (rarely compound), spirally alternate or distichous, and have either amplexicaul or nonamplexicaul stipules. The inflorescences are unisexual, and are typically axillary, but are cauliflorous in a few species. Interfloral bracts may be present or absent. The staminate inflorescences have numerous flowers with 2–4 connate tepals, and typically one stamen (occasionally 2–3 may be present) that is straight in bud. The pistillate inflorescences have one to more typically numerous flowers with 2–4 connate tepals, and adjacent perianths may be free or partially to completely fused to one another. The synapomorphy for the tribe is a reduction in stamen number compared to the rest of the family (although several Ficus species have also independently evolved a single stamen). The typical number of stamens in Moraceae is 4 or 5, but species in Artocarpeae typically have only one stamen per staminate flower, with a few species occasionally having 1–3 stamens. Members of Artocarpeae also share straight embryos, hypogeal germination (semihypogeal in Clarisia and not examined in Batocarpus), a chalazal that is basal relative to the ovary (not examined in Batocarpus and Clarisia), little to no endosperm, and large seeds (> 4 × 4 mm) (Jarrett 1959a, b, c, 1960a; Berg 2001).

Distribution—Genera in this tribe are indigenous to the Paleotropics (Artocarpus: Asia eastward into Australasia and Oceania) or the Neotropics (Batocarpus and Clarisia: Central and South America) (Fig. 1). Three species (A. altilis, A. camansi, and A. heterophyllus) are cultivated throughout much of the tropics.

GeneraArtocarpus J. R. & G. Forst., Batocarpus Karsten, and Clarisia Ruiz & Pavón.


1. Staminate inflorescences spicate with a distinct abaxial sterile strip; staminate flowers crowded in longitudinal rows; leaves alternate and distichous with lateral stipules; neotropical in distribution 2

2. Inflorescences axillary; pistillate inflorescences multiflorous and globose-capitate; fruiting perianth green Batocarpus

2. Inflorescences often cauliflorous, or if axillary then the bark at the base of the trunk reddish; pistillate inflorescences uniflorous or multiflorous and discoid-capitate; fruiting perianth red, orange, pale yellow, or greenish yellow) Clarisia

1. Staminate inflorescences spicate to globose to obovoid or clavate, lacking a distinct abaxial sterile strip; staminate flowers crowded but not in longitudinal rows; leaves alternate and distichous with lateral stipules or spirally alternate with amplexicaul stipules; paleotropical in distribution (however, some species of Artocarpus have been introduced and are cultivated throughout the tropics) 3

3. Perianths of adjacent pistillate flowers entirely free from one another; only fertilized flowers enlarging at maturity Artocarpus subgenus Prainea

3. Perianths of adjacent pistillate flowers partially to completely fused to form a syncarp; entire pistillate head enlarging at maturity 4

4. Leaves distichous; stipules lateral and nonamplexicaul, less than 1 cm, stipule scar not annulate; pistillate inflorescences with adjacent perianths fused apically, giving the inflorescence and syncarp a smooth/uniform surface Artocarpus subgenus Pseudojaca

4. Leaves spirally alternate; stipules fully amplexicaul, 1 cm or longer, leaving an annulate stipule scar; pistillate inflorescences with adjacent perianths fused only medially, leaving perianth apices free and giving the inflorescence and syncarp a spiky or bumpy surface 5

5. Inflorescences always axillary Artocarpus subgenus Artocarpus

5. Inflorescences develop directly from the trunk or branches of previous year's growth (cauli- or ramiflorous). Axillary inflorescneces may also be present and male inflorescences may have ring-like constrictions (in A. annulatus) Artocarpus subgenus Cauliflori

A. ARTOCARPUS J. R. & G. Forst., Char. Gen. Pl: 101, t. 51, 1775, nom. cons.—TYPE: Artocarpus altilis (Parkinson) Fosberg.

Sitodium Banks & Sol. ex Parkinson, J. Voy. South Seas 45. 1773.—TYPE: Rademachia incisa Thunb (= Artocarpus altilis (Parkinson) Fosberg).

Radermachia Thunb., Kongl. Svenska Vetensk. Akad. Handl. 37: 251. 1776 (‘Rademachia’).—TYPE: Radermachia incisa Thunb. (= Artocarpus altilis (Parkinson) Fosberg).

Polyphema Lour. Fl. Cochinch. 546. 1790.—TYPE: Polyphema jaca Lour (= Artocarpus heterophyllus Lamarck).

Prainea King ex Hook, f., Fl. Brit. India 5: 546. 1888. Artocarpus section Prainea Renner, Bot. Jahrb. Syst. 39: 366. 1907.— TYPE: Prainea scandens King.

Trees (possible climber in subgenus Prainea), monoecious (dioecious in subgenus Prainea). Leaves: simple (rarely compound — A. anisophyllus), alternate and spiral (subg. Artocarpus and Cauliflori) or alternate and distichous (subg. Pseudojaca and Prainea), large fully amplexicaul stipules (subg. Artocarpus and Cauliflori) or small lateral stipules (subg. Pseudojaca and Prainea). Inflorescences: unisexual, axillary or cauliflorous (subg. Cauliflori), interfloral bracts present or absent. Staminate inflorescences: with numerous tightly packed flowers with 2 (-4) connate tepals, stamens 1(-3), straight in bud. Pistillate inflorescences: with numerous tightly packed tubular flowers, adjacent perianths may be free (subg. Prainea) or partially (subg. Artocarpus and Cauliflori) to completely fused to one another (subg. Pseudojaca).

Distribution—Asia (China in the north, India in the west, Malesia in the south) eastward into Australasia, and Oceania. Three species (A. altilis, A. camansi, and A. heterophyllus) are cultivated throughout much of the tropics.

1. ARTOCARPUS subg. ARTOCARPUS. Artocarpus subg. Jaca Trécul, Ann. Sei. Nat. Bot. III, 8: 110. 1847. Artocarpus sect. Jaca (Trécul) Renner, Bot. Jahrb. Syst. 39: 363.1907. Artocarpus ser. Incisifolii F. M. Jarrett, J. Arnold Arbor. 40: 298. 1959.—TYPE: Artocarpus altilis (Parkinson) Fosberg.

Artocarpus sect. Duricarpus F. M. Jarrett, J. Arnold Arbor. 40: 137. 1959. Artocarpus ser. Asperifolii F. M. Jarrett, J. Arnold Arbor. 40: 143. 1959.—TYPE: Artocarpus rigidus Blume.

Artocarpus ser. Laevefolii F. M. Jarrett, J. Arnold Arbor. 40: 138. 1959.—TYPE: Artocarpus anisophyllus Miq.

Artocarpus ser. Angusticarpi F. M. Jarrett, J. Arnold Arbor. 40: 338. 1959.—TYPE: Artocarpus teysmannii Miq.

Artocarpus ser. Rugosi F. M. Jarrett, J. Arnold Arbor. 40: 343. 1959.—TYPE: Artocarpus elasticus Blume.

Subgenus Artocarpus has been described in detail elsewhere (Jarrett 1959c), and this is an abbreviated and modified description to accommodate the recircumscription to exclude series Cauliflori. Leaves: simple (compound in A anisophyllus), alternate and spiral, juvenile and adult leaves may be entire or pinnatified, hypodermis present or absent, resin cells present, spongy mesophyll cells loose. Stipules: large, amplexicaul, scars annulate. Inflorescences: axillary, interfloral bracts sparse or absent. Staminate inflorescence: cylindrical or clavate, rarely ellipsoid. Syncarp: cylindrical or ellipsoid, rarely subglobose; free perianth apices either flexuous, indurated, or aerolate.

The circumscription of subgenus Artocarpus here includes 31 species and differs from that of Berg et al. (2006) and Jarrett (1959c) in the exclusion of series Cauliflori, which is elevated to the subgeneric rank. Berg et al. (2006) made reference to Jarrett's sections and series within subgenus Artocarpus but did not maintain them. Due to the lack of monophyly for several of the series, we do not recognize them either. Berg et al. (2006) and Jarrett (1959c) also differed in the treatment of several species level circumscriptions as described below.

Since Jarrett's (1959c, 1960a) treatment of Artocarpus, several new species have been described (Jarrett 1975; Kochummen 2000). Among those assigned to subgenus Artocarpus, A. corneri and A. jarrettiae were reduced by Berg et al. (2006) to A. elasticus. These new species are endemic to Borneo and known from only a few collections and were not included in the present study, therefore Berg et al.'s (2006) treatment is followed here.

Berg et al. (2006) elevated A. melinoxylus subsp. brevipedunculatus to A. brevipedunculatus. Although A. melinoxylus and its subspecies were not sampled here, it is recommended that the changes be maintained. Morphological (leaf and peduncle characters) and geographical distributions support maintaining A. brevipedunculatus. Artocarpus brevipedunculatus is endemic to Borneo, whereas the rest of the diversity represented in A. melinoxylus is endemic to Indochina.

Among the species assigned to Jarret's (1959c) series Rugosi, Berg et al.'s (2006) treatment differed as follows: A. scortechinii was included in A. elasticus; and A. maingayi and A. sumatranus were included in A. kemando. In the present study, Artocarpus elasticus and A. scortechinii are strongly supported as sister, but their status as separate species is maintained here due to consistent and easily recognized morphological differences that suggest they are not experiencing gene flow. Artocarpus scortechinii has generally smaller parts compared to A. elasticus, elongate processes are absent on the syncarp in A. scortechinii and present in A. elasticus, and the upper surface of the leaves is smooth in A. scortechinii and rough in A. elasticus. In the present study, Artocarpus kemando and A. maingayi are strongly supported as sister; A. sumatranus was not included. The three species have differently shaped processes (free apical portion of perianths): umbonate in A. kemando, truncate in A. maingayi, and conical in A. sumatranus, and the length of the male peduncles varies: ∼0.5 cm in A. maingayi, between 0.7 and 1.3 cm in A. kemando, and ∼3.5 cm in A. sumatranus. Additionally, the leaves of A. sumatranus are larger and the leaf apices of A. kemando are acuminate, whereas they are rounded in A. maingayi. Given these differences, they are treated as three separate species here.

Series Incisifolii, as circumscribed by Jarrett (1959c), consists of four species endemic to the Philippines (A. blancoi, A. multifidus, A. pinnatisectus, and A. treculianus), one species native to the Moluccas (A. horridus), and the breadfruit complex which Jarrett (1959c) treats as one highly variable pantropical species, A. communis, but has recently been revised to include three species (A. altilis — breadfruit, A. camansi, and A. mariannensis) and hybrids (Zerega et al. 2005b). Berg et al. (2006) has more recently included A. blancoi, A. horridus, A. camansi, A. mariannensis, A. multifidus, and A. pinnatisectus within A. altilis, considering them all to represent a range of variation from the wild to cultivated form of breadfruit. The present study does not include all members of the series, but nonetheless indicates that series Incisifolii does not represent a natural lineage and Berg et al.'s (2006) changes are not maintained. Artocarpus treculianus and A. blancoi form a well-supported clade (100% bootstrap) that is sister to a clade containing the breadfruit and Rugosi clades and A. excelsus. Artocarpus blancoi and A. treculianus may be most closely allied with the unsampled species (A. pinnatisectus, A. horridus, and A. multifidus) as they all share the following characteristics: adult leaves frequently pinnatified and presence of inflated hairs on syncarp. Artocarpus altilis, A. camansi, and A. mariannensis form a separate, well-supported clade also characterized by the presence of adult pinnatified leaves, but lack the inflated hairs on the syncarp.

Jarrett (1959c) noted three anomalous species within subgenus Artocarpus: A. hirsutus, A. nobilis, and A. sepicanus. The present study indicates that the former two species are part of the subgenus and that the latter remains of uncertain affinity. Given the problematic position and lack of strong evidence detailed in the discussion, A. sepicanus is presently maintained here to be part of subgenus Artocarpus.

Distribution—Subgenus Artocarpus is concentrated in the Malesian region and is distributed in the Philippines, Moluccas, New Guinea, Malaya, Indonesia, Myanmar, Thailand, and the Nicobar Islands, with some species extending westward to Sri Lanka (A. nobilis) and the western Ghats of India (A. hirsutus), eastward into the uplifted limestone islands of Micronesia (A. mariannensis), and into the Asian mainland. The widely cultivated species A. altilis was domesticated from A. camansi and spreads into Oceania and throughout the tropics (Zerega et al. 2005b), whereas A. camansi is cultivated in Indonesia, Malaysia, the Caribbean Islands, tropical Central and South America, and coastal West Africa. Artocarpus altilis has also undergone introgressive hybridization with A. mariannensis in Micronesia (Fosberg 1960; Zerega et al. 2005b).

Species—There are 31 species included in this subgenus: Artocarpus altilis (Parkinson) Fosberg, A. anisophyllus Miq., A. blancoi (Elmer) Merr., A. brevipedunculatus (F. M. Jarrett) C. C. Berg, A. camansi Blanco, A. chaplasha Roxb., A. elasticus Reinw. ex Blume, A. excelsus Jarrett, A. hirsutus Lamarck, A. hispidus Jarrett, A. horridus Jarrett, A. kemando Miq., A. lanceifolius Roxb., A. lowii King, A. maingayi King, A. mariannensis Trécul, A. melinoxylus Gagnep., A. multifidus Jarrett, A. odoratissimus Blanco, A. nobilis Thwaites, A. obtusus Jarrett, A. pinnatisectus Merr., A. rigidus Blume, A. sarawakensis Jarrett, A. scortechinii King, A. sepicanus Diels, A. sericicarpus Jarrett, A. sumatranus Jarrett, A. tamaran Becc., A. teysmannii Miq., and A. treculianus Elmer.

2. Artocarpus subgenus Cauliflori (F. M. Jarrett) Zerega, stat. nov. Artocarpus ser. Cauliflori F. M. Jarrett, J. Arnold Arbor. 40: 327. 1959.—TYPE: Artocarpus integer (Thunb.) Merr.

Series Cauliflori was described by Jarrett (1959c), and it is elevated here to the subgeneric rank, with an abbreviated description. Leaves: simple, alternate and spiral, adult leaves entire, juvenile leaves may be lobed, hypodermis and resin cells absent, spongy mesophyll cells compact. Stipules: large amplexicaul, scars annulate. Inflorescences: solitary in leaf axils, cauliflorous or ramiflorous, interfloral bracts present (A. annulatus) or absent. Staminate inflorescence: cylindric to clavate (surface wrinkled by ring-like constrictions in A. annulatus). Syncarp: cylindric to clavate or ellipsoid, reaching enormous sizes (up to 100 × 50 cm) in A. heterophyllus and A. integer, free perianth apices flexuous.

Subgenus Cauliflori appears to be intermediate between subgenera Artocarpus and Pseudojaca. It shares the leaf arrangement (spirally arranged with amplexicaul stipules) and perianth fusion characters (adjacent pistillate perianths medially fused but free apically) with subgenus Artocarpus. It is allied with subgenus Pseudojaca in having compact mesophyll and the absence of resin in the spongy mesophyll cells (absent in A. heterophyllus and A. integer, not examined in A. annulatus).

This subgenus includes three species and is defined primarily by the presence of cauliflorous inflorescences, which are not found in the rest of the genus. Although affinities of A. annulatus to A. heterophyllus and A. integer have not previously been suggested, molecular evidence, as well as the presence of cauliflorous inflorescences, strongly supports the placement of A. annulatus in subgenus Cauliflori.

DistributionArtocarpus heterophyllus (jackfruit) is thought to be indigenous to the Indian subcontinent and possibly more specifically to the western Ghats of India (Wight 1843). Today it is cultivated throughout much of the tropics and subtropics. Artocarpus integer (chempedak) is distributed and cultivated in Thailand, Malaysia, and parts of Indonesia and Myanmar, and is thought to be indigenous to Sumatra, Borneo, Sulawesi, the Moluccas, and western New Guinea. It has been treated as two varieties, A. integer var. integer, a cultivated form, and the wild form A. integer var. silvestris. Artocarpus annulatus is endemic to Sarawak.

Species—Three species are included in this subgenus: Artocarpus annulatus Jarrett, A. heterophyllus Lamarck, and A. integer (Thunb.) Merr.

3. Artocarpus subg. Prainea (King) Zerega, Supardi, and Motley, stat. nov. Prainea King, in Hook. f., Fl. Brit. Ind. 5: 546. 1888. Artocarpus sect. Prainea (King) Renner, Bot. Jahrb. Syst. 39: 366. 1907.—TYPE: Prainea scandens King (= Artocarpus scandens (King) Renner).

Prainea was originally described by King (1888). Renner (1907) reduced it to sectional status within Artocarpus and Jarrett (1959b) resurrected it to generic status. It is reduced to subgeneric rank here. Leaves: simple, alternate and distichous, juvenile and adult leaves entire, hypodermis absent, resin cells present, spongy mesophyll cells loose. Stipules: small, nonamplexicaul, scars lateral or intrapetiolar. Inflorescences: axillary, interfloral bracts present. Staminate inflorescence: globose to short obovoid. Syncarp: globose, adjacent perianths completely free from one another.

The phylogenetic analysis of molecular data presented here indicates that Prainea is nested within Artocarpus, although there is no bootstrap support for this relationship. However, this position and the intermediacy of characters, as described above, of Prainea compared to other subgenera of Artocarpus indicates that Prainea represents a monophyletic group within Artocarpus that has lost the ability for belated fusion of adjacent pistillate perianths. Previous phylogenetic studies based on chloroplast ndhF and 26S rDNA sequences also placed Prainea within Artocarpus (Zerega et al. 2005a). Analysis of additional characters and all taxa may help to support this relationship further.

Jarrett (1959b) and Berg et al. (2006) recognized four or two species of Prainea, respectively. Berg et al. (2006) reduced P. frutescens into P. scandens and P. papuana into P. limpato because only “small” differences separated them. Descriptions of P. frutescens and P. scandens are based on limited material, however, P. scandens is unique as a climber, and P. frutescens and P. scandens occupy different niches (P. scandens is found in lowland evergreen forests to 2,500 ft. in Malaya, while P. frutescens is restricted to lowland evergreen forests to 200 ft. in Borneo). Prainea limpato and P. papuana occupy different ranges and the inflorescences of P. limpato are generally larger than those of P. papuana. Prainea limpato is found in lowland evergreen forest in Malaya, Sumatra, and Borneo while P. papuana is restricted to lowland evergreen forests in the Moluccas and New Guinea. Jarrett's (1959b) species level circumscription is maintained here.

Distribution—Malay Peninsula, Sumatra, Borneo, and New Guinea.

Species—There are four species included in this subgenus: Artocarpus frutescens (Becc.) Renner, A. limpato Miq., A. papuana (Becc.) Renner, and A. scandens (King) Renner.

4. ARTOCARPUS subg. PSEUDOJACA Trécul, Ann. Sci. Nat. Bot. III, 8:117.1847. Artocarpus sect. Pseudojaca (Trécul) Renner, Bot. Jahrb. Syst. 39: 368. 1907. Artocarpus ser. Peltati F. M. Jarrett, J. Arnold Arbor. 41: 83. 1960.—TYPE: Artocarpus lacucha Buch.—Ham.

Artocarpus ser. Clavati F. M. Jarrett, J. Arnold Arbor. 41: 130. 1960.—TYPE: Artocarpus hypargyreus Hance.

Artocarpus sect. Glandulifolium F. M. Jarrett, J. Arnold Arbor. 41: 134. 1960.—TYPE: Artocarpus altissimus (Miq.) J. J. Smith.

Subgenus Pseudojaca contains 24 species and is defined morphologically within the genus Artocarpus by its distichous leaf arrangement and complete fusion of adjacent pistillate perianth apices. Jarrett's (1960a) circumscription of subgenus Pseudojaca is upheld with a brief description. Leaves: simple, alternate and distichous, adult and juvenile leaves entire, hypodermis and resin cells absent, spongy mesophyll cells compact. Stipules: small, nonamplexicaul, scars lateral or intrapetiolar. Inflorescences: axillary (or staminate ones may be on short shoots or older wood), interfloral bracts abundant. Staminate inflorescence: globose to obovoid, cylindric or clavate. Syncarp: globose or lobed, pistillate perianths fused at least apically and medially to adjacent perianth apices.

Since Jarrett's (1959c, 1960a) treatment, several new Artocarpus species assigned to subgenus Pseudojaca have been described from China (A. gongshanensis, A. nanchuanensis, A. nigrifolius, and A. pithecogallus (Wu and Chang 1989), Borneo (A. albobrunneus; Berg et al. 2006), and Thailand (A. thailandicus; Berg 2005). None of these species were included in the present study, however, they all share the typical characters of subgenus Pseudojaca and their circumscription in Pseudojaca remains untested and unchanged.

Within subgenus Pseudojaca Berg et al. (2006) recently combined several species, subspecies, and varieties (A. dadah, A. fretessii, A. ovatus, and A. vrieseanus var. papillosus, and A. v. var. refractus) into A. lacucha Buch.-Ham. However, based on morphological characters, biogeographical distributions, and the phylogenetic analysis of molecular data of some of these species, these changes are not maintained. Among these species, the present study included A. dadah, A. ovatus, and A. lacucha. Phylogenetic analyses indicate that these three entities represent three distinct lineages, and that they are not sister to one another. Artocarpus ovatus is restricted to the Philipppines and does not overlap ranges with the other species. It is also readily distinguished by its long peduncles, 15–40 mm in the staminate inflorescence and 40–80 mm in the pistillate inflorescence (Jarrett 1960a). Artocarpus dadah is a common and variable species that has been described under multiple names at different times by the same author (see Jarrett 1960a). The variation within the species occurs chiefly in the length of the peduncles and in the indumentum (Jarrett 1960a). Three individuals of A. dadah were included in this study (all from Malaysia) and they are strongly supported (100% bootstrap) as a monophyletic group. While the ranges of A. dadah and A. lacucha overlap in Thailand and possibly Myanmar, the range of the former extends southward from there into the Malay peninsula and Indonesia, while the range of the latter extends northward and westward into monsoon forests of India, China, Bangladesh, and Indochina. They can be distinguished from one another based on the surface of the syncarp being finely ribbed in A. dadah. It is recommended that A. ovatus, A. dadah, and A. lacucha be treated as separate species.

Within subgenus Pseudojaca several species are divided into subspecies. Of these, only the subspecies of A. nitidus were included in the present study. Variation present in A. nitidus has been variously treated as separate species (Trécul 1847; Beccari 1902), separated into several subspecies (Jarrett 1960a), or treated as “informal entities” within A. nitidus (Berg et al. 2006). Four of the five A. nitidus subspecies described by Jarrett (1960a) were included in this analysis and are polyphyletic. Artocarpus nitidus subsp. griffithii and A. n. subsp. borneensis form a well-supported (100% bootstrap) monophyletic group sister to A. dadah. These two subspecies are similar, differing only in the indumentum on the syncarp, nearly glabrous in the former and densely pubescent in the latter. Artocarpus n. subsp. borneensis is restricted to the island of Borneo, while A n. subsp. griffithii overlaps this range and extends northward up to Yunnan in southern China. Artocarpus n. subsp. lingnannensis (extending from Southern China to Thailand) and A. n. subsp. humilis (restricted to Borneo) appear to represent two separate lineages. Their morphological differences are slight and are primarily leaf venation characters. All subspecies of A. nitidus were at one time or another described at the specific rank and subsequently demoted by Jarrett (1960a). Berg et al. (2006) treated four “informal entities” of A. nitidus in the Malesian area. The combined phylogeny presented here suggests that A. n. subsp. humilis, and A. n. subsp. lingnanennensis may warrant resurrection to specific rank (A. humilis Becc. (Beccari 1902) and A. parva Gagnep. (Gagnepain 1926), respectively). Artocarpus n. subsp. griffithii, and A. n. subsp. borneensis could be treated as a single variable species. However, additional data from the fifth subspecies (A. nitidus subsp. nitidus) is desirable before any action is taken.

Distribution—India, Sri Lanka, Myanmar, Thailand, Indochina, southern China, Malaysia, Indonesia, Australasia, Solomon Islands, Philippines.

Species—There are 24 species included in this subgenus: A. albobrunneus Berg, A. altissimus (Miq.) J. J. Smith, A. dadah Miq., A. fulvicortex, A. glaucus Blume, A. gomezianus Wall ex. Trécul, A. gongshanensis S. K. Wu ex C. Y. Wu & S. S. Chang, A. hypargyreus Hance, A. lacucha Buch.-Ham., A. longifolius Becc., A. nanchuanensis S. S. Chang, C. Tan, and Z. Y. Liu, A. nigrifolius C. Y. Wu, A. nitidus Trécul, A. ovatus Blanco, A. petelotii Gagnep., A. pithecogallus C. Y. Wu, A. reticulatus Miq., A. rubrovenius Warb., A. subrotundifolius Elmer, A. thailandicus C. C. Berg, A. tomentosulus Jarrett, A. tonkinensis A. Chev. ex. Gagnep., A. vrieseanus Miq., and A. xanthocarpus Teysm. and Binnend.

B. BATOCARPUS Karsten, Fl. Columb. 2: 67. 1863.—TYPE: Batocarpus orinocensis Karsten.

Annocarpus Ducke, Arch. Jard. Bot. Rio de Janiero 3: 38. 1922.—TYPE: Annocarpus amazonicus Ducke (= B. amazoncuns (Ducke) Fosberg).

We maintain Berg's (2001) circumscription of Batocarpus with a brief description. Leaves: simple, alternate and distichous, adult and juvenile leaves entire. Stipules: small, nonamplexicaul, scars lateral or intra petiolar. Inflorescences: axillary, interfloral bracts present or absent. Staminate inflorescence: spicate with an abaxial sterile strip. Syncarp: globose, adjacent pistillate perianths free from one another.

Distribution—Costa Rica to Amazonian Boliva.

Species—There are three species included in this genus: Batocarpus costaricensis Standley & L. O. Williams, B. amazonicus (Ducke) Fosberg, and B. orinocensis Karsten.

C. CLARISIA Ruiz & Pavón, Fl. Peruv. Chil. 128. 1794, nom. cons., non Clarisia Abat, 1792, nom. rejic.;—TYPE: Clarisia racemosa Ruiz & Pavón, typ. cons.

Sahagunia Liebmann, Kongel, Danske Vidensk. Selsk. Naturvidensk. Math. Afh. 5 (2): 316. 1851.—TYPE: Sahagunia mexicana Liebmann (= Clarisia biflora Ruiz & Pavón).

Soaresia Allemão, Revista Brazil. 1: 210. 1857, nom. rejic., non C. H. Schultz-Bip., 1863, nom. conserv. (Asteraceae).— TYPE: Soaresia nitida Allemão (= Clarisia racemosa Ruiz & Pavón).

Acanthinophyllum Allemão, Revista Brazil. 1: 368. 1858.— TYPE: Acanthiniphyllum strepitans Allemão (= Clarisia ilicifolia (Sprengel) Lanjouw & Rossberg).

Aliteria Benoist, Bull. Mus. Hist. Nat. (Paris), 2 (1): 163.1929.— TYPE: Aliteria sagotii Benoist (= Clarisia ilicifolia (Sprengel) Lanjouw & Rossberg).

Berg's (2001) circumscription of Clarisia reflects our phylogenetic findings. Leaves: simple, alternate and distichous, adult and juvenile leaves entire. Stipules: small, nonamplexicaul, scars lateral or intrapetiolar. Inflorescences: axillary or on leafless short shoots, interfloral bracts present. Staminate inflorescence: spicate with an abaxial sterile strip. Syncarp: capitate with adjacent pistillate perianths free from one another or uniflorous.

Distribution—From southern Mexico through Central America into Venezuela, Colombia, Ecuador, Peru, Bolovia, the Guianas, the Brazilian Amazon Basin, and eastern Brazil.

Species—There are three species included in this genus: Clarisia biflora Ruiz & Pavón, C. racemosa Ruiz & Pavón, and C. ilicifolila (Sprengel) Lanjouw & Rossberg.


The authors are grateful for the field assistance of C.Y. Chong, L. Y. Fah, A. Hussin, R. Kiapranis, R. Kiew M. Kostka, S. Lum, V. Novotny, L. Raulerson, and A. Rinehart. We would like to thank W. Clement, N. Cordeiro, H. Ndangalasi, D. Ragone, and G. Weiblen for specimens and DNA samples and two reviewers for helpful comments on the manuscript. Finally, we would like to thank the following institutions and herbaria for access to specimens: BRIT, CHIC, F, FTG, GH, GUAM, KEP, LAE, MIN, NY, PTBG, SAN, SING, US. This research was funded by the Lewis B. and Dorothy Cullman Foundation, NSF grant DEB0073161, The Garden Club of America Award in Tropical Botany, and The Explorers Club.



B. G. Baldwin 1992. Phylogenetic utility of the internal transcribed spacers of nuclear ribosomal DNA in plants: an example from the Compositae. Molecular Phylogenetics and Evolution 1: 3–16. Google Scholar


B. G. Baldwin , M. J. Sanderson , J. M. Porter , M. F. Wojciechowski , C. S. Campbell , and M. J. Donoghue . 1995. The ITS region of nuclear ribosomal DNA: a valuable source of evidence on angiosperm phylogeny. Annals of the Missouri Botanical Garden 82: 247–277. Google Scholar


O. Beccari 1902. Nelle Foreste di Borneo. Firenze: Tip. di S. Landi. Google Scholar


C. C. Berg 1977a. The Castilleae, a tribe of the Moraceae, renamed and redefined due to the exclusion of the type genus Olmedia from the “Olmedieae”. Acta Botanica Neerlandica. 26: 73–82. Google Scholar


C. C. Berg 1977b. Revisions of African Moraceae (excluding Dorstenia, Ficus, Musanga and Myrianthus). Bulletin du Jardin Botanique National de Belgique 47: 267–407. Google Scholar


C. C. Berg 2001. Moreae, Artocarpeae, and Dorstenia (Moraceae) with introductions to the family and Ficus and with additions and corrections to Flora Neotropica Monograph 7. New York: New York Botanical Garden. Google Scholar


C. C. Berg 2005. A new species of Artocarpus (Moraceae) from Thailand. Blumea 50: 531–533. Google Scholar


C. C. Berg , E. J. H. Corner , and F. M. Jarrett . 2006. Moraceae - genera other than Ficus. Leiden: National Herbarium Nederland. Google Scholar


N. B. M. Brantjes 1981. Nectar and the pollination of breadfruit, Artocarpus altilis (Moraceae). Acta Botanica Neerlandica 30: 345–352. Google Scholar


R. Chenna , H. Sugawara , K. Tadashi , R. Lopez , T. J. Gibson , D. G. Higgins , and J. D. Thompson . 2003. Multiple sequence alignment with the Clustal series of programs. Nucleic Acids Research 31: 3497–3500. Google Scholar


W. L. Clement and G. D. Weiblen . 2009. Morphological evolution in the mulberry family (Moraceae). Systematic Botany 34: 530–552. Google Scholar


E. J. H. Corner 1962. The classification of Moraceae. The Garden's Bulletin Singapore 19: 187–252. Google Scholar


S. L. Datwyler and G. D. Weiblen . 2004. On the origin of the fig: phylogenetic relationships of Moraceae from ndhF sequences. American Journal of Botany 91: 767–777. Google Scholar


F. R. Fosberg 1942. The genus Batocarpus Karst. (Moraceae). Proceedings of the Biological Society of Washington 55: 99–101. Google Scholar


F. R. Fosberg 1960. Introgression in Artocarpus in Micronesia. Brittonia 12: 101–113. Google Scholar


F. Gagnepain 1926. Quelques Artocarpus nouveaux d'Indo-Chine. Bulletin de la Société Botanique de France 73: 86–91. Google Scholar


P. Goloboff 1999. NONA (No Name) ver. 2. Tucuman, Argentina. Google Scholar


A. L. Hipp , J. C. Hall , and K. J. Sytsma . 2004. Congruence versus phylogenetic accuracy: revisiting the incongruence length difference test. Systematic Biology 53: 81–89. Google Scholar


P. K. Holmgren , N. H. Holmgren , and L. C. Barnett . 1990. Index Herbariorum 1: the herbaria of the world. New York: New York Botanical Garden. Google Scholar


F. M. Jarrett 1959a. Studies in Artocarpus and allied genera, I. General considerations. Journal of the Arnold Arboretum 40: 1–29. Google Scholar


F. M. Jarrett 1959b. Studies in Artocarpus and allied genera, II. A revision of Prainea. Journal of the Arnold Arboretum 40: 30–37. Google Scholar


F. M. Jarrett 1959c. Studies in Artocarpus and allied genera, III. A revision of Artocarpus subgenus Artocarpus. Journal of the Arnold Arboretum 40: 113–155, 298–368. Google Scholar


F. M. Jarrett 1960a. Studies in Artocarpus and allied genera, IV. A revision of Artocarpus subgenus Pseudojaca. Journal of the Arnold Arboretum 41: 73–139. Google Scholar


F. M. Jarrett 1960b. Studies in Artocarpus and allied genera, V. A revision of Parartocarpus and Hullettia. Journal of the Arnold Arboretum 61: 320–340. Google Scholar


F. M. Jarrett 1975. Four new Artocarpus species from Indo-Malesia (Moraceae). Blumea 22: 409–410. Google Scholar


F. M. Jarrett 1976. The syncarp of Artocarpus - a unique biological phenomenon. Garden's Bulletin, Singapore 24: 35–39. Google Scholar


S. Kanzaki , K. Yonemori , A. Sugiura , and S. Subhadrabandhu . 1997. Phylogenetic relationships between jackfruit, the breadfruit and nine other Artocarpus spp. from RFLP analysis of an amplified region of cpDNA. Scientia Horticulturae 70: 57–66. Google Scholar


G. King 1888. Artocarpus. Pp. 546–547 in Flora of British India, ed. J. D. Hooker . London: L. Reeve. Google Scholar


K. M. Kochummen 2000. Artocarpus J. R. & G. Forster. nom. conserv. Pp. 187–212 in Tree flora of Sabah and Sarawak, Malaysia, ed. E Soepadmo and L. G. Saw . Kuala Lumpur: Sabah Forestry Department, Forest Research Institute Malaysia, and Sarawak Forestry Department. Google Scholar


W. J. Kress , K. J. Wurdack , E. A. Zimmer , L. A. Wiegt , and D. H. Janzen . 2005. Use of DNA barcodes to identify flowering plants. Proceedings of the National Academy of Sciences USA 102: 8369–8374. Google Scholar


K. Momose , A. Hatada , R. Yamaoka , and T. Inoue . 1998. Pollination biology of the genus Artocarpus, Moraceae. Tropics 7: 165–172. Google Scholar


M. W. Moncur 1985. Floral ontogeny of the jackfruit, Artocarpus heterophyllus Lam. (Moraceae). Australian Journal of Botany 33: 585–593. Google Scholar


D. L. Nickrent , K. P. Schuette , and E. M. Starr . 1994. A molecular phylogeny of Arceuthobium (Viscaceae) based on nuclear ribosomal DNA internal transcribed spacer sequences. American Journal of Botany 81: 1149–1160. Google Scholar


K. C. Nixon 1999. The parsimony ratchet, a new method for rapid parsimony analysis. Cladistics 15: 407–414. Google Scholar


K. C. Nixon 1999–2002. WinClada ver. 1.0000. Ithaca, New York: Published by the author. Google Scholar


M. C. Okimoto 1948. Anatomy and histology of pineapple inflorescence and fruit. Botanical Gazette (Chicago, III.) 110: 217–231. Google Scholar


D. Posada and K. A. Crandall . 1998. Modeltest: testing the model of DNA substitution. Bioinformatics 14: 817–818. Google Scholar


D. Posada and T. R. Buckley . 2004. Model selection and model averaging in phylogenetics: advantages of the AIC and Bayesian approaches over likelihood ration tests. Systematic Biology 53: 793–808. Google Scholar


R. B. Primack 1983. Forester's guide to the Moraceae of Sarawak. Sarawak: Forest Department, Sarawak, Malaysia. Google Scholar


A. Rambaut 2001. Se-Al. Sequence alignment editor, version 2.0a7b. Oxford, U. K.: Department of Zoology, Oxford University. Google Scholar


O. Renner 1907. Beiträge zur Anatomie und Systematik der Artocarpeen und Conocephaleen, insbesondere der Gattung Ficus. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie 39: 319–448. Google Scholar


J. G. Rohwer 1993. Moraceae. Pp. 438–453 in The families and genera of vascular plants, ed. K. Kubitzki , J. G. Rohwer , and V. Bittrich . Berlin: Springer-Verlag. Google Scholar


N. Rønsted , G. D. Weiblen , J. M. Cook , N. Salamin , C. A. Machado , and V. Savolainen . 2005. 60 million years of co-divergence in the fig-wasp symbiosis. Proceedings. Biological Sciences 272: 2593–2599. Google Scholar


S. Sakai 2001. Thrips pollination in androdioecious Castilla elastica (Moraceae) in a seasonal tropical forest. American Journal of Botany 88: 1527–1534. Google Scholar


S. Sakai , M. Kato , and H. Nagamasu . 2000. Artocarpus (Moraceae)-gall midge pollination mutualism mediated by a male-flower parastic fungus. American Journal of Botany 87: 440–445. Google Scholar


T. Seelanan , A. Schnabel , and J. F. Wendel . 1997. Congruence and consensus in the cotton tribe (Malvaceae). Systematic Botany 22: 259–290. Google Scholar


M. R. Sharma 1965. Morphological and anatomical investigations on Artocarpus Forst. III. The flower. Phytomorphology 15: 185–201. Google Scholar


S. Singh , S. Krishnamurthi , and S. L. Katyal . 1963. Fruit culture in India. New Delhi: Indian Council for Agricultural Research. Google Scholar


G. G. Siniscalco , P. Caputo , and S. Cozzolino . 1997. Ribosomal DNA analysis as a tool for the identification of Cannabis sativa L. specimens of foresnic interests. Science & Justice 37: 171–174. Google Scholar


D. L. Swofford 2002. PAUP*: phylogenetic analysis using parsimony (*and other methods), version 4. Sunderland: Sinauer Associates. Google Scholar


K. J. Systma , J. Morawetz , J. C. Pires , M. Nepokroeff , E. Conti , M. Sjhra , J. C. Hall , and M. W. Chase . 2002. Urticalean rosids: circumscription, rosid ancestry, and phylogenetics based on rbcL, trnL-F, and ndhF sequences. American Journal of Botany 89: 1531–1546. Google Scholar


P. Taberlet , L. Gielly , G. Pautou and J. Bouvet . 1991. Universal primers for amplification of three non-coding regions of chloroplast DNA. Plant Molecular Biology 17:1105–1109. Google Scholar


A. Trécul 1847. Mémoire sur la famille des Artocarpées. Annales des Sciences Naturelles 3: 38–157. Google Scholar


L. Van der Pijl 1953. On the flower biology of some plants from Javawith general remarks on fly-traps (species of Annona, Artocarpus, Typhonium, Gnetum, Arisaema and Abroma). Annales Bogorienses 1: 77–99. Google Scholar


R. Wight 1843. Icones Plantarum lndiae Orientalis. Madras: J. B. Pharoah. Google Scholar


C. Y. Wu and S. S. Chang . 1989. Taxa nova nonnulla Moracearum Sinensium. Acta Botanica Yunnanica 11: 24–34. Google Scholar


N. J. C. Zerega , S. Mori , C. Lindqvist , Q. Zheng , and T. J. Motley . 2002. Using amplified fragment length polymorphisms (AFLP) to identify black cohosh (Actaea racemosa). Economic Botany 56: 154–164. Google Scholar


N. J. C Zerega , L. A. Mound , and G. D. Weiblen . 2004a. Pollination in the New Guinea endemic Antiaropsis decipiens (Moraceae) is mediated by a new species of thrips, Thrips antiaropsidis sp. nov. (Thysanoptera: Thripidae). International Journal of Plant Sciences 165: 1017–1026. Google Scholar


N. J. C. Zerega , D. Ragone , and T. J. Motley . 2004b. Complex origins of breadfruit (Artocarpus altilis, Moraceae): Implications for human migrations in Oceania. American Journal of Botany 91: 760–766. Google Scholar


N. J. C. Zerega , W. L. Clement , S. L. Datwyler , and G. D. Weiblen . 2005a. Biogeography and divergence times in the mulberry family (Moraceae). Molecular Phylogenetics and Evolution 37: 402–416. Google Scholar


N. J. C. Zerega , D. Ragone , and T. J. Motley . 2005b. Systematics and species limits of breadfruit (Artocarpus, Moraceae). Systematic Botany 30: 603–615. Google Scholar



Specimens used in the phylogenetic analyses. Herbarium abbreviations follow Index Herbariorum (Holmgren et al. 1990). For each specimen, the following is listed: sampled taxa, voucher specimen information [collection locality, collection number (herbarium code)], and GenBank accession numbers (ITS, trnL-F); — = sequence not obtained. Previously published sequences downloaded for inclusion in our analyses are indicated by an asterisk. Material acquired from herbarium samples, rather than leaf material dried on silica, is indicated by two asterisks.

© Copyright 2010 by the American Society of Plant Taxonomists
Nyree J. C. Zerega, M. N. Nur Supardi, and Timothy J. Motley "Phylogeny and Recircumscription of Artocarpeae (Moraceae) with a Focus on Artocarpus," Systematic Botany 35(4), 766-782, (1 October 2010).
Published: 1 October 2010
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