Conservatoire et Jardin botaniques de la Ville de Genève
Chambésy, GE, CHE
Families Collected
154
Genera Collected
375
Species Collected
342
Occurrences Recorded
666
Countries
6
Photos Taken
0
Occurrence Locations
Occurrence Timeline
Affiliated People (2)
Publications (50)
(3116) Proposal to conserve the name Pandanus amaryllifolius Roxb. against P. amaryllidifolius F. Voigt and P. amaryllifolius Roxb. ex Lindl. (Pandanaceae)
Vol. 74, Issue 5
pp. 1273-1274
DOI:
10.1002/tax.70041
Pandanus plastomes decoded: When climate mirrors morphology and phylogenetic relationships
Vol. 112, Issue 2
Premise
Pandanus Parkinson (Pandanaceae) is a large genus of paleotropical tree‐like monocots. Previous studies using small DNA regions questioned the monophyly of the seven Pandanus subgenera, but low phylogenetic branch support hindered further investigations. We aimed to (1) test Pandanus subgeneric monophyly, (2) identify clade morphological synapomorphies, (3) investigate correlations between leaf anatomy of water storage tissue and climatic differentiation across clades, and (4) construct hypotheses on the genus' spatiotemporal history.
Methods
We sequenced 50 Pandanus species using genome skimming and reconstructed plastomes with MITObim. We inferred partitioned RAxML phylogenetic trees to test subgeneric monophyly using Shimodaira–Hasegawa tests. We inferred a partitioned dated BEAST phylogenetic tree used for ancestral state reconstructions of morphological traits. Phylogenetic clades were used to compare climatic (Bioclim) and soil (UNESCO Digital Soil Map) conditions using random forests. We correlated present morphology and climatic niche with past climate events.
Results
Our phylogenetic analyses revealed two clades and four subclades. Only subgenus Coronata was monophyletic. Staminate synapomorphies were identified for three subclades. Hypertrophied and hyperplasic water‐storage tissue was a synapomorphy for clade II, correlating with more seasonal temperature and precipitation regimes and more well‐draining soil. Clades differentiated during the advent of the Southeast Asian monsoon in the early Miocene, whereas subclades differentiated during the Miocene Thermal Maximum.
Conclusions
Pandanus subgeneric classification needs to be revised. Hypertrophied hyperplasic water‐storage tissue is a key trait in Pandanus evolution, possibly explaining climatic and biogeographic patterns because it is key to maintaining photosynthesis during periods of hydric stress.
DOI:
10.1002/ajb2.16461
Pandanus ramromensis (Pandanaceae), a new species from Peninsular Thailand
Vol. 76, Issue 2
pp. 269-275
Pandanus ramromensis Callm., Y.W.Low & Buerki (Pandanaceae) from the summit of Khao Ram Rome (Nakhon Si Thammarat Province) in Peninsular Thailand is described here. The new species resembles Pandanus kedahensis H.St.John in its ecology and habit but differs by the dimensions of its leaves, leaf shape, syncarps and styles. The new species is provided with line drawings and field photographs, and is assigned a preliminary conservation status of Vulnerable (VU) using the IUCN Red List criteria.
DOI:
10.26492/gbs76(2).2024-09
Phylogenomics and the rise of the angiosperms
Vol. 629, Issue 8013
pp. 843-850
Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins5–7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes8. This 15-fold increase in genus-level sampling relative to comparable nuclear studies9 provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade.
DOI:
10.1038/s41586-024-07324-0
Phylogenomic analyses of Sapindales support new family relationships, rapid Mid-Cretaceous Hothouse diversification, and heterogeneous histories of gene duplication
Vol. 14
Sapindales is an angiosperm order of high economic and ecological value comprising nine families, c. 479 genera, and c. 6570 species. However, family and subfamily relationships in Sapindales remain unclear, making reconstruction of the order’s spatio-temporal and morphological evolution difficult. In this study, we used Angiosperms353 target capture data to generate the most densely sampled phylogenetic trees of Sapindales to date, with 448 samples and c. 85% of genera represented. The percentage of paralogous loci and allele divergence was characterized across the phylogeny, which was time-calibrated using 29 rigorously assessed fossil calibrations. All families were supported as monophyletic. Two core family clades subdivide the order, the first comprising Kirkiaceae, Burseraceae, and Anacardiaceae, the second comprising Simaroubaceae, Meliaceae, and Rutaceae. Kirkiaceae is sister to Burseraceae and Anacardiaceae, and, contrary to current understanding, Simaroubaceae is sister to Meliaceae and Rutaceae. Sapindaceae is placed with Nitrariaceae and Biebersteiniaceae as sister to the core Sapindales families, but the relationships between these families remain unclear, likely due to their rapid and ancient diversification. Sapindales families emerged in rapid succession, coincident with the climatic change of the Mid-Cretaceous Hothouse event. Subfamily and tribal relationships within the major families need revision, particularly in Sapindaceae, Rutaceae and Meliaceae. Much of the difficulty in reconstructing relationships at this level may be caused by the prevalence of paralogous loci, particularly in Meliaceae and Rutaceae, that are likely indicative of ancient gene duplication events such as hybridization and polyploidization playing a role in the evolutionary history of these families. This study provides key insights into factors that may affect phylogenetic reconstructions in Sapindales across multiple scales, and provides a state-of-the-art phylogenetic framework for further research.
DOI:
10.3389/fpls.2023.1063174
Flora of Singapore: Checklist and bibliography
Vol. 74, Issue (suppl.1)
pp. 3-860
A checklist of all species of bryophytes, lycophytes, ferns, gymnosperms and angiosperms that are found in the wild (native, naturalised and casual) in Singapore is presented. We have attempted to account for all names of species and infraspecific taxa that have ever been recorded for Singapore, along with the pertinent publications that reported each of these names. For each currently accepted name, the synonyms of relevance for Singapore are included. The native or non-native status for all taxa is given, along with the most recent national conservation assessment applied to each native taxon. If we were aware that the most recent assessment required an update, the taxon is newly assessed here. The checklist includes 2654 native taxa, 479 naturalised/casual taxa and 101 cryptogenic taxa.
DOI:
10.26492/gbs74(suppl.1).2022-01
Otto Warburg and his contributions to the screw pine family (Pandanaceae)
Vol. 51, Issue 1
Abstract
Otto Warburg (1859–1938) had a great interest in tropical botany. He travelled in South-East Asia and the South Pacific between 1885 and 1889 and brought back a considerable collection of plant specimens from this expedition later donated to the Royal Botanical Museum in Berlin. Warburg published the first comprehensive monograph on the family Pandanaceae in 1900 in the third issue of Das Pflanzenreich established and edited by Adolf Engler (1844–1930). The aim of this article is to clarify the taxonomy, nomenclature and typification of Warburg's contributions to the Pandanaceae. Considerable parts of Warburg's original material was destroyed in Berlin during World War II but duplicates survived, shared by Engler and Warburg with Ugolino Martelli (1860–1934). Martelli was an expert on the family and he assembled a precious herbarium of Pandanaceae that was later donated to the Museo di Storia Naturale dell'Università degli Studi di Firenze. Warburg published 86 new names in Pandanaceae between 1898 and 1909 (five new sections, 69 new species, five new varieties, two new combinations and five replacement names). A complete review of the material extant in B and FI led to the conclusion that 38 names needed a nomenclatural act: 34 lectotypes, three neotypes and one epitype are designated here. Twenty new synonyms are also proposed. One Freycinetia name and six Pandanus names are considered as incertae sedis. A total of 21 names published by Warburg are accepted: 11 in Freycinetia and ten in Pandanus. In addition, four names published in Pandanus by Warburg serve as the basionyms of accepted names in the genus Benstonea.
DOI:
10.3372/wi.51.51101
Pandanus grayorum (Pandanaceae), a new species endemic to north-eastern Queensland (Australia)
Vol. 34, Issue 4
pp. 327-335
DOI:
10.1071/sb20033
An updated infra‐familial classification of Sapindaceae based on targeted enrichment data
Vol. 108, Issue 7
pp. 1234-1251
Premise
The economically important, cosmopolitan soapberry family (Sapindaceae) comprises ca. 1900 species in 144 genera. Since the seminal work of Radlkofer, several authors have attempted to overcome challenges presented by the family’s complex infra‐familial classification. With the advent of molecular systematics, revisions of the various proposed groupings have provided significant momentum, but we still lack a formal classification system rooted in an evolutionary framework.
Methods
Nuclear DNA sequence data were generated for 123 genera (86%) of Sapindaceae using target sequence capture with the Angiosperms353 universal probe set. HybPiper was used to produce aligned DNA matrices. Phylogenetic inferences were obtained using coalescence‐based and concatenated methods. The clades recovered are discussed in light of both benchmark studies to identify synapomorphies and distributional evidence to underpin an updated infra‐familial classification.
Key Results
Coalescence‐based and concatenated phylogenetic trees had identical topologies and node support, except for the placement of Melicoccus bijugatus Jacq. Twenty‐one clades were recovered, which serve as the basis for a revised infra‐familial classification.
Conclusions
Twenty tribes are recognized in four subfamilies: two tribes in Hippocastanoideae, two in Dodonaeoideae, and 16 in Sapindoideae (no tribes are recognized in the monotypic subfamily Xanthoceratoideae). Within Sapindoideae, six new tribes are described: Blomieae Buerki & Callm.; Guindilieae Buerki, Callm. & Acev.‐Rodr.; Haplocoeleae Buerki & Callm.; Stadmanieae Buerki & Callm.; Tristiropsideae Buerki & Callm.; and Ungnadieae Buerki & Callm. This updated classification provides a backbone for further research and conservation efforts on this family.
DOI:
10.1002/ajb2.1693
New Guinea has the world’s richest island flora
Vol. 584, Issue 7822
pp. 579-583
DOI:
10.1038/s41586-020-2549-5
(2772) Proposal to conserve the name Pandanus ornatus Kurz (Benstonea ornata) against P. ornatus W. Bull with a conserved type (Pandanaceae)
Vol. 69, Issue 5
pp. 1115-1116
DOI:
10.1002/tax.12337
New combinations for two species in the genus Synima (Sapindaceae, Cupanieae) from Queensland (Australia)
Vol. 75, Issue 2
Abstract
Synima Radlk. is a small genus of Sapindaceae distributed in Australia, Indonesia (Moluccas and Western New Guinea) and Papua New Guinea with three species currently accepted. The genus can be recognized by its crested scales on the petals, a pericarp that dries thin and wrinkled, and the seed which has a fleshy, yellow-orange sarcotesta that is either small and basal or ± enclosing the seed. Previous taxonomic studies expressed doubts regarding the generic placement of two species belonging to the genus Sarcotoechia Radlk.: Sarcotoechia serrata S.T. Reynolds and Sarcotoechia heterophylla S.T. Reynolds. A phylogenetic framework has shown that Sarcotoechia is paraphyletic and Sarcotoechia serrata is sister to Synima. Further morphological evidence (e.g., crested petals) support the transfer of the latter two species to Synima and the new combinations are proposed here: Synima heterophylla (S.T. Reynolds) Callm. & Buerki and Synima serrata (S.T. Reynolds) Callm. & Buerki. A key to all species of Synima is presented.
DOI:
10.15553/c2020v752a7
A new micro-endemic species of Alectryon (Sapindaceae) from Koghis forest, New Caledonia
Vol. 45, Issue 1
pp. 156-162
DOI:
10.1600/036364420x15801369352414
Neotypification ofPandanus odorifer, the correct name for P. odoratissimus (Pandanaceae)
Vol. 70, Issue 1
pp. 182-184
DOI:
10.1002/tax.12406
Novelties from the Northern mountains complex of Madagascar V: A new threatened Pandanus (Pandanaceae) from the Kalobinono massif
Vol. 75, Issue 1
pp. 99
DOI:
10.15553/c2020v751a10
Two new genera of Sapindaceae (Cupanieae) from the southern Pacific: Lepidocupania and Neoarytera
Vol. 75, Issue 2
Phylogenetic analyses of the family Sapindaceae inferred from nuclear and plastid sequence data have revealed a high level of para- and polyphyly at the subfamilial, tribal, and generic levels. A phylogenetic study focusing on taxa in the southern Pacific belonging to tribe Cupanieae has shown that the two most species-rich genera, Arytera Blume and Cupaniopsis Radlk., are polyphyletic. This study aims to clarify generic limits among the taxa currently placed in these two genera by identifying morphological features that support monophyletic groups suitable for recognition at the generic level. Specimens deposited in major herbaria holding material of these taxa were examined to complement extensive field observations. Careful consideration of morphological features in light of previous taxonomic treatments and the results of phylogenetic analyses enabled us to propose a re-aligned generic framework for Cupanieae in which two new genera are described to accommodate species previously placed in Arytera and Cupaniopsis: viz., Lepidocupania Buerki, Callm., Munzinger & Lowry (21 species) and Neoarytera Callm., Buerki, Munzinger & Lowry (4 species). A total of 25 new combinations are made, lectotypes are designated for nine names (two first step and seven second-step), and one new synonym is established. A key to the newly circumscribed genera Arytera and Cupaniopsis, along with allied genera, is provided, accompanied by information on the distribution and ecology of each species.
DOI:
10.15553/c2020v752a9
A new species and a new synonym in Pandanus subg. Rykia (Pandanaceae) in Thailand
Vol. 73, Issue 1
pp. 115
DOI:
10.15553/c2018v731a12
Alectryon vitiensis: A new species of Sapindaceae endemic to Fiji
Vol. 25, Issue 4
pp. 421-429
DOI:
10.3417/d-16-00006
Navigating the ‘broad freeway’: ocean currents and inland isolation drive diversification in the Pandanus tectorius complex (Pandanaceae)
Vol. 44, Issue 7
pp. 1598-1611
Aim
To test for and describe the genetic structure of the Pandanus tectorius complex, a group of closely related ocean‐dispersed plants and members of the Indo‐Pacific coastal strand community.
Location
Tropical Indo‐Pacific (coastal East Africa to Polynesia).
Methods
We sampled 535 individuals (46 localities) from throughout the range of the complex. Fifteen microsatellite loci were used to detect and characterize population structure and estimate migration rates between island groups and broad regions.
Results
Hierarchical population structure was detected. Samples group into an eastern cluster (Hawaii and coastal South‐Central Pacific localities) and a western cluster [Western Pacific (WP) through Indian Ocean]. Within these two clusters, at least six regional subclusters were detected including samples from the Indian Ocean + South China Sea (SCS), Ogasawara Islands, WP, inland South‐Central Pacific, coastal South‐Central Pacific and Hawaii. Migration rates between regions are low leading to isolation and genetic differentiation while within regions, rates are much higher. In most cases, inland populations are genetically differentiated from nearby coastal counterparts.
Main conclusions
Substantial population structure occurs across the range of the P. tectorius complex due to dispersal limitation across stretches of open ocean and patterns of ocean currents. Low levels of asymmetric westward migration, consistent with the direction of ocean currents in the Pacific, links Hawaii and the South‐Central Pacific with populations further to the west preventing complete isolation. SCS + Indian Ocean populations are distinct from those in the Pacific due to limited dispersal between these regions. The isolation of inland populations on several islands also contributes to genetic differentiation. While population clusters have a clear geographical basis they are not completely congruent with previously recognized taxa.
DOI:
10.1111/jbi.12933
Biogeography and evolution of the screw-pine genus Benstonea Callm. & Buerki (Pandanaceae)
Vol. 71, Issue 2
pp. 217-229
Abstract
This study investigates the biogeography, evolution and systematics of Benstonea Callm. & Buerki (Pandanaceae) based on six plastid DNA regions and 54 specimens representing 36 species (60% of species generic diversity). Our maximum likelihood and Bayesian phylogenetic inferences support the monophyly of Benstonea and its close relationship with the speciose Pandanus Parkinson. Benstonea is subdivided into three clades exhibiting contrasting species diversities. Clades I and II have seven species each, whereas most of the species diversity occurs in clade III with 21 species. None of the sections defined by Stone in Pandanus subgenus Acrostigma (Kurz) B.C. Stone (now Benstonea) are retrieved monophyletic by our analyses. Biogeographical inference supports the origin of Benstonea on the Sunda shelf during the Miocene and shows several subsequent exchanges between Peninsular Malaysia and Borneo. Species in Indochina and the Indian continent originated in Peninsular Malaysia and all belong to clade I. Wallacea was colonized at least twice from Borneo sometimes during the Miocene and no back-dispersals were inferred. The Sunda shelf was colonized once, most likely from Halmahera. Finally, our analyses suggest that the Fijian endemic Benstonea thurstonii (C.H. Wright) Callm. & Buerki dispersed from either Australia or New Guinea during the Pleistocene.
DOI:
10.15553/c2016v712a8
Generic delimitations, biogeography and evolution in the tribe Coleeae (Bignoniaceae), endemic to Madagascar and the smaller islands of the western Indian Ocean
Vol. 96
pp. 178-186
DOI:
10.1016/j.ympev.2015.11.016
Two new threatened species of Benstonea Callm. & Buerki (Pandanaceae) from Sabah (Borneo, Malaysia)
Vol. 71, Issue 2
pp. 257-263
DOI:
10.15553/c2016v712a10
A taxonomic revision of the endemic New Caledonian genus Storthocalyx (Sapindaceae)
Vol. 41, Issue 2
pp. 387-400
DOI:
10.1600/036364416x691902
Lifting the curtain on our knowledge on New Guinean Benstonea (Pandanaceae)
Vol. 275, Issue 2
pp. 168
New Guinea is one of the centres of diversity of Benstonea (Pandanaceae), a genus distributed from India to Fiji. Ten species were previously recognised on this island and further field observations, accompanied by the study of available herbarium material have brought new insights into species delimitations within a group of caespitose species with a solitary terminal infructescence. The taxonomical identity of Benstonea odoardoi is elucidated and is considered here as a synonym of Benstonea lauterbachii. Three new combinations and a new name—based on names of Pandanus species previously treated as synonyms of Benstonea odoardoi—are proposed for four distinct species belonging to this group of caespitose species and restricted to Indonesian New Guinea and Papua New Guinea. Finally, Pandanus bintuniensis is here considered as a synonym of Benstonea permicron.
DOI:
10.11646/phytotaxa.275.2.8
The genus Pandanus Parkinson (Pandanaceae) on Halmahera island (Moluccas, Indonesia) with descriptions of three new species and a key to the species on the island
Vol. 70, Issue 2
pp. 179
Halmahera is the largest (c. 18,000 km2) island of the Moluccan archipelago, but naturalists have only sporadically visited Halmahera and it has remained very poorly explored botanically. However, an intensive botanical inventory project was undertaken between 2012 and 2014 in part of the island to inform flora biodiversity management for certain proposed mining activities. This effort has contributed over 3600 plant collections and nearly doubled the number of Pandanus Parkinson (Pandanaceae) specimens (bringing the total to 55) available for Halmahera. After careful examination of all available material and comparison with other material from the region, we are able to present the first overview of the genus for the island. We have identified ten species from the island of which three are new to science and not known elsewhere, while the other seven are all representatives of species already described from other localities. The new species are formally described here as Pandanus beguinii Callm. & A. P. Keim, Pandanus benstoneoides Callm., Buerki & Phillipson and Pandanus halmaherensis Callm. & A. P. Keim. The new species are provided with notes on their respective morphology and known distributional and ecological ranges, line drawings. Those three new species are assigned a preliminary status of Endangered following IUCN Red List Categories and Criteria. All ten species are illustrated with colour photographs and a key to the species is provided.
DOI:
10.15553/c2015v702a2
A long distance dispersal hypothesis for the Pandanaceae and the origins of the Pandanus tectorius complex
Vol. 83
pp. 20-32
DOI:
10.1016/j.ympev.2014.11.002
Incorporating evolutionary history into conservation planning in biodiversity hotspots
Vol. 370, Issue 1662
pp. 20140014
There is increased evidence that incorporating evolutionary history directly in conservation actions is beneficial, particularly given the likelihood that extinction is not random and that phylogenetic diversity (PD) is lost at higher rates than species diversity. This evidence is even more compelling in biodiversity hotspots, such as Madagascar, where less than 10% of the original vegetation remains. Here, we use the Leguminosae, an ecologically and economically important plant family, and a combination of phylogenetics and species distribution modelling, to assess biodiversity patterns and identify regions, coevolutionary processes and ecological factors that are important in shaping this diversity, especially during the Quaternary. We show evidence that species distribution and community PD are predicted by watershed boundaries, which enable the identification of a network of refugia and dispersal corridors that were perhaps important for maintaining community integrity during past climate change. Phylogenetically clustered communities are found in the southwest of the island at low elevation and share a suite of morphological characters (especially fruit morphology) indicative of coevolution with their main dispersers, the extinct and extant lemurs. Phylogenetically over-dispersed communities are found along the eastern coast at sea level and may have resulted from many independent dispersal events from the drier and more seasonal regions of Madagascar.
DOI:
10.1098/rstb.2014.0014
Novitates Neocaledonicae. II. Acropogon moratianus Callm., Munzinger & Lowry, sp. nov. (Malvaceae, Sterculieae): a rare and threatened new species from New Caledonia
Vol. 37, Issue 1
pp. 131-137
Abstract
A new species of Acropogon Schltr. (Malvaceae, Sterculieae) is described from New Caledonia. Acropogon moratianus Callm., Munzinger & Lowry, sp. nov. is endemic to three ultramafic massifs, Boulinda, Kopéto and Paéoua, along the north-western coast of Grande Terre. This rare, endangered species differs from other members of the genus by its large 5-lobed leaves whose abaxial surface is covered by erect to divergent stellate trichomes and the subspherical shape of its follicles, which bear a pointed apex. Line drawings and color photos are provided, along with a discussion of its morphological affinities and a preliminary risk of extinction assessment.DOI:
10.5252/a2015n1a8
Notes on Benstonea (Pandanaceae) from the islands of Halmahera, New Guinea and Sulawesi
Vol. 175, Issue 3
pp. 161
Benstonea (Pandanaceae) was circumscribed to include 57 species formerly placed in the genus Pandanus. Field observations, accompanied by the study of available herbarium material have brought new insights for the delimitation of certain problematic species, especially in the difficult group of species characterized by an axillary infructescence on a short peduncle covered by prophylls and the abscission of the basal portion of the drupe at maturity. New combinations, based on names in Pandanus previously treated as synonyms of Benstonea stenocarpa, are proposed for three distinct species of this group from Halmahera (Indonesia) and Papua New Guinea. The identity of Benstonea celebica, endemic to Sulawesi (Indonesia), is also elucidated and an epitype is designated for this species.
DOI:
10.11646/phytotaxa.175.3.6
Rediscovery of the genus Tsingya Capuron (Sapindaceae) and its phylogenetic position
Vol. 69, Issue 2
pp. 195
DOI:
10.15553/c2014v692a12
A new endemic species of Trigonachras (Sapindaceae) from Sabah, Malaysia (Borneo)
Vol. 88, Issue 2
pp. 19
DOI:
10.11646/phytotaxa.88.2.1
Notes on New Caledonian Pandanaceae: Identity and typifications of Pandanus decumbens (Brongn.) Solms and Pandanus reticulatus Vieill., with the new species Pandanus letocartiorum Callm. & Buerki
Vol. 68, Issue 1
pp. 51
DOI:
10.15553/c2013v681a4
Spatio-temporal history of the endemic genera of Madagascar
Vol. 171, Issue 2
pp. 304-329
DOI:
10.1111/boj.12008
A taxonomic revision of the endemic New Caledonian genus Podonephelium Baill. (Sapindaceae)
Vol. 38, Issue 4
pp. 1105-1124
DOI:
10.1600/036364413x674814
Corrections to Phytotaxa 112: Update on the systematics of Benstonea (Pandanaceae)
Vol. 125, Issue 1
pp. 59
After the publication of our Update on the systematics of Benstonea (Pandanaceae): When a visionary taxonomist foresees phylogenetic relationships (Callmander, Booth, Beentje & Buerki 2013), an error was brought to our attention:
DOI:
10.11646/phytotaxa.125.1.9
Update on the systematics of Benstonea (Pandanaceae): When a visionary taxonomist foresees phylogenetic relationships
Vol. 112, Issue 2
pp. 57
The paleotropical monocot Pandanaceae family comprises c. 700 species distributed into five genera: Benstonea (c. 60 spp.), Freycinetia (c. 250 spp.), Martellidendron (6 spp.), Pandanus (c. 450 spp.) and Sararanga (2 spp.). Benstonea was circumscribed to include species previously placed in Pandanus section Acrostigma (one of the four sections of Pandanus subgenus Acrostigma). New phylogenetic data show that the six species of the remaining three sections of subgenus Acrostigma (sections Epiphytica, Fusiforma and Platystigma) and a seventh species doubtfully placed in section Acrostigma (Pandanus microglottis) also belonged to Benstonea. This genus is therefore characterized by a suite of morphological characters, viz. stigmatic groove on the adaxial side of the stigma and a staminate flower reduced to 1 to 3 free stamens (sometimes joined at base). We therefore make here the necessary seven new combinations accompanied by one lectotypification in Benstonea, a genus that now reflects the view of the visionary Benjamin Stone who had already grouped these species in Pandanus subgenus Acrostigma based solely on morphology.
DOI:
10.11646/phytotaxa.112.2.4
Benstonea Callm. & Buerki (Pandanaceae): Characterization, Circumscription, and Distribution of a New Genus of Screw-Pines, with a Synopsis of Accepted Species
Vol. 67, Issue 2
pp. 323
Abstract
Pandanaceae, a palaeotropical monocot family of c. 700 species, comprises four currently recognized genera: Freycinetia Gaudich., Martellidendron (Pic. Serm.) Callm. & Chassot, Pandanus Parkinson and Sararanga Helms. Within Pandanus (c. 500 spp.), species of sect. Acrostigma Kurz [one of four sections comprising subg. Acrostigma (Kurz) B. C. Stone] possess highly distinctive morphological features (viz. sharp spiniform, linear styles with the stigmatic groove on the abaxial side of the style and a staminate flower reduced to 1 to 3 stamens) shared with two other species (likewise belonging to subg. Acrostigma but originally placed in sect. Fusiforma B. C. Stone) that separate them from all other congeners. Based on morphology, biogeography, and recent inferences from plastid DNA sequence data, we place these distinctive species in a new genus, Benstonea Callm. & Buerki, making the necessary new combinations for the 50 recognized species, accompanied by six lectotypifications, one epitytification and two neotypifications, and placing seventeen names in synonymy. A generic key is provided to facilitate distinguishing Benstonea from the four other genera of Pandanaceae. Comments are provided on the distribution, ecology and typification of each accepted species.
DOI:
10.15553/c2012v672a12
Phylogenetic inference of New Caledonian lineages of Sapindaceae: Molecular evidence requires a reassessment of generic circumscriptions
Vol. 61, Issue 1
pp. 109-119
Sapindaceae (Sapindales) are a conspicuous and diversified element of the New Caledonian flora, with ca. 67 species (ca. 90 % endemic) in 13 genera (four endemic: Gongrodiscus, Loxodiscus, Podonephelium, Storthocalyx). The phylogeny of New Caledonian Sapindaceae is inferred by adding 97 new samples, encompassing the full distributional and morphological range of the archipelago's genera, to a broad plastid and nuclear DNA sequence dataset that is representative of the family worldwide. Results from phylogenetic analyses indicate that members of the family on New Caledonia belong to two major clades, the Dodonaea group (placed within subfamily Dodonaeoideae) and the Cupania group (subfamily Sapindoideae), which exhibit strikingly different species diversities (ca. 89% of the species on New Caledonia belong to the Cupania group). Results support the monophyly of all four endemic genera and most of those that also occur elsewhere, with the exception of the morphologically similar Austro‐Pacific genera Arytera and Cupaniopsis, both of which have representatives in each of two well‐supported subclades within the Cupania group, suggesting at least two dispersals to New Caledonia (most likely from Australia). The results provide a robust phylogenetic framework for ongoing taxonomic revisions of Sapindaceae genera on New Caledonia and for investigating the spatio‐temporal history of the family in this biogeographically intriguing archipelago, although expanded sampling (including from other areas) and further analyses will be required to resolve generic limits among the taxa currently placed in Arytera and Cupaniopsis.
DOI:
10.1002/tax.611008
Straightening out the screwpines: A first step in understanding phylogenetic relationships within Pandanaceae
Vol. 61, Issue 5
pp. 1010-1020
Abstract
The Paleotropical monocot family Pandanaceae includes ca. 700 species assigned to four genera: Pandanus (ca. 500 spp.), Freycinetia (ca. 200 spp.), Martellidendron (6 spp.) and Sararanga (2 spp.). The most speciose genus, Pandanus, was classically subdivided into eight subgenera. Previous cladistic analyses revealed that several key morphological characters might have evolved independently several times, thus highlighting the need for a robust molecular phylogenetic framework to elucidate phylogenetic relationships and infrafamilial and infrageneric classification within this group. In this study, three plastid DNA regions (matK, trnQrps16, trnLtrnF) and 200 individuals (representing 134 species and 609 newly produced sequences)—spanning the taxonomic and biogeographic diversity of the family—are analyzed to test the monophyly at the familial and generic levels, and to infer phylogenetic relationships within the family. Particular emphasis is devoted to Pandanus with the aim of recognizing key morphological characters that reflect the evolutionary history of the genus. Phylogenetic inferences support the monophyly of Pandanaceae and establish Sararanga as sister to the rest of the family, with Freycinetia as sister to the PandanusMartellidendron pair. Although relationships are not wellresolved within the latter clade, three supported lineages are retrieved: (1) the Acrostigma clade comprising taxa of P. subg. Acrostigma, (2) the Martellidendron clade including taxa assigned to the genus Martellidendron and (3) the core Pandanus clade including taxa of all other subgenera of Pandanus. Morphological and biogeographic evidence supporting clade definitions are discussed in detail. This study provides the first phylogenetic backbone for Pandanaceae, which is sufficiently robust to serve as a springboard for future research into the evolutionary history of this neglected family.
DOI:
10.1002/tax.615008
A taxonomic revision of Gouania (Rhamnaceae) in Madagascar and the other islands of the Western Indian Ocean (the Comoro and Mascarene Islands, and the Seychelles)
Vol. 98, Issue 2
pp. 157-195
DOI:
10.3417/2007075
Nomenclatural changes in the Malagasy endemic genus Tina Schult. (Sapindaceae)
Vol. 66, Issue 1
pp. 124
DOI:
10.15553/c2011v661a13
How to kill two genera with one tree: clarifying generic circumscriptions in an endemic Malagasy clade of Sapindaceae
Vol. 165, Issue 3
pp. 223-234
DOI:
10.1111/j.1095-8339.2010.01106.x
Gouania tiliifolia: The Correct name for Gouania scandens
Vol. 21, Issue 4
pp. 481-482
DOI:
10.3417/2011078
Phylogeny and circumscription of Sapindaceae revisited: molecular sequence data, morphology and biogeography support recognition of a new family, Xanthoceraceae
Vol. 143, Issue 2
pp. 148-159
DOI:
10.5091/plecevo.2010.437
Molecular phylogenetic and morphological evidence supports recognition of Gereaua, a new endemic genus of sapindaceae from Madagascar
Vol. 35, Issue 1
pp. 172-180
DOI:
10.1600/036364410790862669
The genus Brackenridgea A. Gray (Ochnaceae) in Madagascar
Vol. 65, Issue 2
pp. 374
DOI:
10.15553/c2010v652a16
A synoptic revision of the genus Lepisanthes Blume (Sapindaceae) in Madagascar
Vol. 31, Issue 2
pp. 301-309
DOI:
10.5252/a2009n2a6
Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae)
Vol. 51, Issue 2
pp. 238-258
DOI:
10.1016/j.ympev.2009.01.012
Malagasy Dracaena Vand. ex L. (Ruscaceae): an investigation of discrepancies between morphological features and spatial genetic structure at a small evolutionary scale
Vol. 280, Issue 1-2
pp. 15-28
DOI:
10.1007/s00606-009-0162-z
A new threatened species of Pandanaceae from Northwestern Madagascar, Pandanus sermolliana
Vol. 18, Issue 4
pp. 421-424
DOI:
10.3417/2007101