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An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV

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Abstract

An update of the Angiosperm Phylogeny Group (APG) classification of the orders and families of angiosperms is presented. Several new orders are recognized: Boraginales, Dilleniales, Icacinales, Metteniusiales and Vahliales. This brings the total number of orders and families recognized in the APG system to 64 and 416, respectively. We propose two additional informal major clades, superrosids and superasterids, that each comprise the additional orders that are included in the larger clades dominated by the rosids and asterids. Families that made up potentially monofamilial orders, Dasypogonaceae and Sabiaceae, are instead referred to Arecales and Proteales, respectively. Two parasitic families formerly of uncertain positions are now placed: Cynomoriaceae in Saxifragales and Apodanthaceae in Cucurbitales. Although there is evidence that some families recognized in APG III are not monophyletic, we make no changes in Dioscoreales and Santalales relative to APG III and leave some genera in Lamiales unplaced (e.g. Peltanthera). These changes in familial circumscription and recognition have all resulted from new results published since APG III, except for some changes simply due to nomenclatural issues, which include substituting Asphodelaceae for Xanthorrhoeaceae (Asparagales) and Francoaceae for Melianthaceae (Geraniales); however, in Francoaceae we also include Bersamaceae, Ledocarpaceae, Rhynchothecaceae and Vivianiaceae. Other changes to family limits are not drastic or numerous and are mostly focused on some members of the lamiids, especially the former Icacinaceae that have long been problematic with several genera moved to the formerly monogeneric Metteniusaceae, but minor changes in circumscription include Aristolochiaceae (now including Lactoridaceae and Hydnoraceae; Aristolochiales), Maundiaceae (removed from Juncaginaceae; Alismatales), Restionaceae (now re-including Anarthriaceae and Centrolepidaceae; Poales), Buxaceae (now including Haptanthaceae; Buxales), Peraceae (split from Euphorbiaceae; Malpighiales), recognition of Petenaeaceae (Huerteales), Kewaceae, Limeaceae, Macarthuriaceae and Microteaceae (all Caryophyllales), Petiveriaceae split from Phytolaccaceae (Caryophyllales), changes to the generic composition of Ixonanthaceae and Irvingiaceae (with transfer of Allantospermum from the former to the latter; Malpighiales), transfer of Pakaraimaea (formerly Dipterocarpaceae) to Cistaceae (Malvales), transfer of Borthwickia, Forchhammeria, Stixis and Tirania (formerly all Capparaceae) to Resedaceae (Brassicales), Nyssaceae split from Cornaceae (Cornales), Pteleocarpa moved to Gelsemiaceae (Gentianales), changes to the generic composition of Gesneriaceae (Sanango moved from Loganiaceae) and Orobanchaceae (now including Lindenbergiaceae and Rehmanniaceae) and recognition of Mazaceae distinct from Phrymaceae (all Lamiales).

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... Initially, members of the Cordiaceae were included within the Boraginaceae family as subfamilies of the Cordioideae [3][4][5][6]. This taxonomic treatment is still recognized by the Angiosperm Phylogeny Group (APG) and some phylogenetic studies [7][8][9]. On the other hand, a number of phylogenetic studies have identified Cordiaceae as a distinct family in the order Boraginales [10][11][12][13]. Previous studies on the phylogenetic relationships of the Cordiaceae family have totally relied on a small number of nuclear DNA, chloroplast, and mitochondrial genes [14]. ...
... The second clade consists of Cordiaceae, Ehretiaceae, and Heliotropiaceae; Cordiaceae resolved as sister to Ehretiaceae, which is consistent with previous phylogenetic studies [56,87]. Our results support treating the order Boraginales to include several distinct families, consistent with a number of recent molecular studies [1,12,56,88] and contrary to what the APG IV system suggested, which treated the Boraginales to include only one family, Boraginaceae [9]. ...
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Cordiaceae is a family comprising more than 400 species in the order Boraginales. The classification of this family has undergone changes over time, transitioning between family and subfamily status. In the present study, the complete chloroplast (cp) genomes of Cordia monoica and Cordia sinensis were sequenced, and their cp genomes were then characterized, analyzed, and compared to those of closely related taxa. The lengths of the cp genomes of C. monoica and C. sinensis were 151,813 bp and 152,050 bp, respectively. Both genomes consisted of 114 genes, divided into 4 ribosomal RNA genes, 30 transfer RNA genes, and 80 protein-coding genes. We observed a unique gene inversion in the trnM-rbcL region of both Cordia species. The long repeats analysis revealed that both species’ chloroplast genomes contained forward and palindromic repeats. The simple sequence repeats (SSRs) analysis detected 155 microsatellites in each genome, with the majority being mononucleotide repeats (A/T). Phylogenetic analysis based on maximum likelihood and Bayesian analyses confirmed two major clades in the order Boraginales: clade I comprised Boraginaceae, while clade II included Cordiaceae, Ehretiaceae, and Heliotropiaceae. This study expands our knowledge of the evolutionary relationships across the order Boraginales and offers useful genetic resources.
... Ceratophyllum submersum L., commonly known as soft hornwort, is a subaquatic plant whose genus is the only extant member in the order of Ceratophyllales, placed as a sister clade to the eudicots [1,2]. It is native to Europe, Africa and Asia and grows in stagnant freshwater bodies [3]. ...
... The phylogenetic tree (Fig. 2, for full tree see Additional file 4) classifies C. submersum close to its reference C. demersum and our D. purpurea plastome assembly close to the RefSeq D. purpurea plastome sequence generated by Zhao et al. [17]. The angiosperm clade is represented in accordance with the current APG IV classification except for the exact separation/placement of the Magnoliids and the Chloranthales, which is still controversial [2]. This underlines the significance of plastome sequences for modern plant phylogenetics [18]. ...
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Objective Eutrophication poses a mounting concern in today’s world. Ceratophyllum submersum L. is one of many plants capable of living in eutrophic conditions, therefore it could play a critical role in addressing the problem of eutrophication. This study aimed to take a first genomic look at C. submersum . Results Sequencing of gDNA from C. submersum yielded enough reads to assemble a plastome. Subsequent annotation and phylogenetic analysis validated existing information regarding angiosperm relationships and the positioning of Ceratophylalles in a wider phylogenetic context.
... to ensure scientific integrity and updating to current corrected nomenclature. The plant family assignments align to the Angiosperm Phylogeny Group IV guidance (Group et al., 2016). ...
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Background Mastitis is a disease of economic importance in dairy production systems. The common management regime for mastitis is the use of synthetic antibiotics, giving a new problem of antibiotic resistance. There is, therefore, a need to prospect for alternatives to conventional antibiotics from herbal plants. Objectives This systematic review evaluates the use of plants as alternatives for the control of mastitis in dairy cattle, focussing on the effectiveness of studied plants and plant‐based products and possible implications on the use of these products in livestock health. Methodology The PRISMA model was implemented with searches done in five electronic databases: Scopus, ScienceDirect, PubMed, Ovid and Research4Life. Data were extracted from 45 studies with 112 plant species from plant species belonging to 42 different families. The specific keywords were 'mastitis', 'dairy cows' and 'medicinal plants'. Results The most cited plant species included Allium sativum L., Azadirachta indica and Eucalyptus globulus Labill with the latter further exploring its components. Microbial species causing mastitis mainly were Staphylococcus aureus and Escherichia coli . The extraction methods used included maceration approach using ethanol, methanol and water as solvents for phytochemicals and chromatographic techniques for essential oils. A few studies explored the mode of action, and toxicities of the herbal extracts as well as evaluating their efficacy in clinical trials using animal models. Conclusion Plants with defined levels of phytochemicals were essential sources of antibacterials. Standardisation of analytical methods is required.
... As in Mienna et al. (2020), we rooted the tree using Pteridophyta. The resulting tree was verified by comparing it to the plant family phylogeny by the Angiosperm Phylogeny Group IV (APG IV, Chase et al. 2016;Stevens 2001). In cases where an accession was misplaced according to the APG IV phylogeny or genus assignment or occurred on relatively long branches, the alignment was checked for obvious errors in homology inference. ...
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Protected areas are one of the main strategic means for conserving biodiversity. Yet, the design of protected areas usually neglects phylogenetic diversity, an important diversity measure. In this paper we assess the phylogenetic diversity and species richness of vascular plants in Fennoscandian protected areas. We evaluate how much species richness and phylogenetic diversity is found within and outside protected areas, and the differences in plant diversity between different categories of protected areas. We also assess the differences in the diversity-area relationship of the different protected area categories in terms of both species richness and phylogenetic diversity. We build a multi-locus phylogeny of 1,519 native vascular plants of Norway, Sweden, and Finland. We estimate the phylogenetic diversity and species richness by combining the phylogeny with publicly available occurrence data and the currently protected area system of Fennoscandia. Our results indicate that protected areas in Fennoscandia hold more plant diversity when larger, and that phylogenetic diversity increases faster with area than species richness. We found evidence for more plant diversity outside of protected areas of the different countries of Fennoscandia than inside of protected areas, but no evidence for plant diversity differences between areas with different protection status. Hence, our results indicate that the current protected area system in Fennoscandia is no more effective in conserving phylogenetic diversity and species richness of vascular plants than a random selection of localities. Our results also indicate that planning conservation strategies around phylogenetic diversity, rather than species richness, might be a first step to protect vascular plant diversity more effectively.
... These uncertainties are magnified in angiosperms due to their extreme richness, complex evolution, and unresolved backbone topology and the timings of early divergences [28,33]. Analysing a sample of plausible angiosperm-wide phylogenies is currently intractable, but the two mega-phylogenies we used capture wide variation in divergence estimates while comprehensively sampling extant diversity and covering the deeper nodes in the phylogeny, which is crucial for the hypotheses we tested: the SB tree samples greater than 10 000 of the known greater than 13 000 genera in 401 of 416 families [40], while QJ samples approximately 7900 genera in 401 families. Regardless of which crown group age estimate for angiosperms we considered, numerous major lineages survive the K-Pg [8,27], and no difference in dynamics were recovered between phylogenies (figure 1). ...
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The Cretaceous–Palaeogene mass extinction event (K-Pg) witnessed upwards of 75% of animal species going extinct, most notably among these are the non-avian dinosaurs. A major question in macroevolution is whether this extinction event influenced the rise of flowering plants (angiosperms). The fossil record suggests that the K-Pg event had a strong regional impact on angiosperms with up to 75% species extinctions, but only had a minor impact on the extinction rates of major lineages (families and orders). Phylogenetic evidence for angiosperm extinction dynamics through time remains unexplored. By analysing two angiosperm mega-phylogenies containing approximately 32 000–73 000 extant species, here we show relatively constant extinction rates throughout geological time and no evidence for a mass extinction at the K-Pg boundary. Despite high species-level extinction observed in the fossil record, our results support the macroevolutionary resilience of angiosperms to the K-Pg mass extinction event via survival of higher lineages.
... The genomic age has made it clear that reticulate evolution is pervasive in the tree of life, and a strictly bifurcating phylogeny is rarely the best representation of evolution (Morales-Briones et al., 2021;Cooper et al., 2022;Debray et al., 2022;Smith et al., 2022;Zhao et al., 2022). Many different taxonomic hierarchies have been rearranged in the past decades as we have gained access to more genomic data and inference methods, such as for the flowering plants (APG: Byng et al., 2016), pteridophytes (PPG: Schuettpelz et al., 2016), birds (Jarvis et al., 2014), and mammals (Upham et al., 2019). ...
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Phylogenetic studies in the phylogenomics era have demonstrated that reticulate evolution greatly impedes the accuracy of phylogenetic inference, and consequently can obscure taxonomic treatments. However, the systematics community lacks a broadly applicable strategy for taxonomic delimitation in groups characterized by pervasive reticulate evolution. The red-fruit genus, Stranvaesia, provides an ideal model to examine the influence of reticulation on generic circumscription, particularly where hybridization and allopolyploidy dominate the evolutionary history. In this study, we conducted phylogenomic analyses integrating data from hundreds of single-copy nuclear (SCN) genes and plastomes, and interrogated nuclear paralogs to clarify the inter/intra-generic relationship of Stranvaesia and its allies in the framework of Maleae. Analyses of phylogenomic discord and phylogenetic networks showed that allopolyploidization and introgression promoted the origin and diversification of the Stranvaesia clade, a conclusion further bolstered by cytonuclear and gene tree discordance. With a well-inferred phylogenetic backbone, we propose an updated generic delimitation of Stranvaesia and introduce a new genus, Weniomeles. This new genus is distinguished by its purple-black fruits, thorns trunk and/or branches, and a distinctive fruit core anatomy characterized by multilocular separated by a layer of sclereids and a cluster of sclereids at the top of the locules. Through this study, we highlight a broadly-applicable workflow that underscores the significance of reticulate evolution analyses in shaping taxonomic revisions from phylogenomic data.
... Salicornieae are one of four tribes currently classified in subfamily Salicornioideae (Morales-Briones et al. 2021) in Amaranthaceae s.l. (APG IV 2016; including the former Chenopodiaceae). Salicornieae comprise c. 100 species (Piirainen et al. 2017), some of which are referred to as samphires (notably species of Salicornia L. and Tecticornia Hook.f.). ...
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Low temperature constitutes one of the main barriers to plant distributions, confining many clades to their ancestrally tropical biome. However, recent evidence suggests that transitions from tropical to temperate biomes may be more frequent than previously thought. Here, we study the evolution of cold and frost tolerance in the globally distributed and highly stress-tolerant Salicornieae (Salicornioideae, Amaranthaceae s.l.). We first generate a phylogenetic tree comprising almost all known species (85-90%), using newly generated (n = 106) and published nuclear-ribosomal and plastid sequences. Next, we use geographical occurrence data to document in which clades and geographical regions cold-tolerant species occur and reconstruct how cold tolerance evolved. Finally, we test for correlated evolution between frost tolerance and the annual life form. We find that frost tolerance has evolved independently in up to four Northern Hemisphere lineages but that annuals are no more likely to evolve frost tolerance than perennials, indicating the presence of different strategies for adapting to cold environments. Our findings add to mounting evidence for multiple independent out-of-the-tropics transitions among close relatives of flowering plants and raise new questions about the ecological and physiological mechanism(s) of adaptation to low temperatures in Salicornieae.
... Excluding non-native species, the final matrix consisted of 5244 records belonging to 1131 genera and 170 families. The names of all species were standardized using the R [80] software package 'plantlist' [81], with the order of families based on the nomenclature of Angiosperm Phylogeny Group IV [82]. ...
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Floristic regions, conventionally established using species distribution patterns, have often overlooked the phylogenetic relationships among taxa. However, how phylogenetic relationships influence the historical interconnections within and among biogeographic regions remains inadequately understood. In this research, we compiled distribution data for seed plants in Gansu, a region of significant biogeographic diversity located in northwestern China.We proposed a novel framework for floristic regions within Gansu, integrating distribution data and phylogenetic relationships of genera-level native seed plants, aiming to explore the relationship between phylogenetic relatedness, taxonomic composition, and regional phylogenetic delineation. We found that (1) phylogenetic relatedness was strongly correlated with the taxonomic composition among floras in Gansu. (2) The southeastern Gansu region showed the lowest level of spatial turnover in both phylogenetic relationships and the taxonomic composition of floristic assemblages across the Gansu region. (3) Null model analyses indicated nonrandom phylogenetic structure across the region, where most areas showed higher phylogenetic turnover than expected given the underlying taxonomic composition between sites. (4) Our results demonstrated a consistent pattern across various regionalization schemes and highlighted the preference for employing the phylogenetic dissimilarity approach in biogeographical regionalization investigations. (5) Employing the phylogenetic dissimilarity approach, we identified nine distinct floristic regions in Gansu that are categorized into two broader geographical units, namely the northwest and southeast. (6) Based on the phylogenetic graphic regions of China across this area.
... Bitkilerden elde edilen geleneksel ilaçlar, bu bitkilerde var olan biyoaktif bileşiklerden dolayı hayati öneme sahiptir (Yuan et al., 2020). Taksonomik olarak Sambucus L. cinsi Viburnaceae familyasının bir üyesi olarak kabul edilmiş (Chase et al., 2016), yaklaşık 29 tür ve belirsiz 77 tür olarak dünya çapında dağılım göstermektedir (GBIF, n.d.; POWO, n.d.). Tükçede Mürver İngilzcede ise Elders veya Elderberries olarak adlandırılır. ...
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Günümüzde Kara Mürver meyve ve çiçeklerinin en sık kullanımı gıda endüstrisinde renklendiricileri, meyve suları ve tatlandırıcı olmasına rağmen, meyve, çiçekler veya bunların ekstrelerinin fitokimyasal bileşimleri nedeniyle, nutrasötik içerik olarak kullanılan gıda takviyelerinin üretimi için potansiyel kullanımlarının yanı sıra ilaç endüstrisinde yüksek bir potansiyele sahiptirler. Aslında S. nigra, halk tıpında farklı hastalıklar tedavisi için yüzyıllardır kullanılmaktadır. Bununla birlikte, kullanımının ve değerinin genişletilmesi için, bitki meyve ve çiçeği fitokimyasallarının biyoyararlanımı, biyolojik aktiviteleri ve bunların moleküler mekanizmalar ve fitokimyasal bileşimi ile korelasyonu ile ilgili daha fazla araştırmaya ihtiyaç vardır. Ülkemizde de gıda ve sağlık alanında kullanımının artması, üretim ve tüketiminin yaygınlaştırılması amaçlı çalışmalar önem kazanmaktadır.
... Although data-driven research is slowly becoming more theoretical and predictive (Hogeweg, 2011), the creation of universal plant models is hindered by their overwhelming diversity. Not only is the phylogenetic diversity among flowering plants immense (The Angiosperm Phylogeny Group et al., 2016), but plants are exceptionally responsive to their environments (Sultan, 2000) and have evolved symbiotic interactions with and defense mechanisms against innumerable microbes (Mitchell et al., 2006). Furthermore, technical variability in data acquisition makes it difficult to exploit the huge amount of expression data archived in databases. ...
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The selection of Arabidopsis as a model organism played a pivotal role in advancing genomic science, firmly establishing the cornerstone of modern plant molecular biology. Competing frameworks to select an agricultural- or ecological-based model species, or to decentralize plant science and study a multitude of diverse species, were selected against in favor of building core knowledge in a species that would facilitate genome-enabled research that could assumedly be transferred to other plants. Here, over twenty years after sequencing the Arabidopsis genome and during which time sequencing data from other plant species has accumulated and computation enabling machine learning has evolved, we critically examine the ability of models based on Arabidopsis gene expression data to predict tissue identity in other flowering plant species. Comparing different machine learning algorithms, models trained and tested on Arabidopsis data achieved precision and recall values of up to 0.99 using the K-Nearest Neighbor method, whereas when tissue identity is predicted across the flowering plants using models trained on Arabidopsis data, precision values range from 0.70 to 0.75 and recall from 0.55 to 0.64, depending on the algorithm used. Below-ground tissue is more predictable than other tissue types, and the ability to predict tissue identity is not correlated with phylogenetic distance from Arabidopsis. Our data-driven results suggest that, in hindsight, the assertion that knowledge from Arabidopsis is translatable to other plants is not as strong as originally assumed, and that in the current era where sequencing data and computation abound, we should decentralize the scientific focus on Arabidopsis and embrace plant diversity.
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Tiandong is a vital traditional Chinese herbal medicine. It is derived from the tuber root of the Asparagus cochinchinensis according to the Pharmacopoeia of the people’s republic of China (2020 Edition). On account of the similar morphology, Asparagus meioclados and Asparagus munitus were used as Tian-Dong in southwest China. Chloroplast (cp) genomes are highly active genetic components of plants and play an extremely important role in improving the efficiency of the identification of plant species. To differentiate the medicinal plants belonging to the genus Asparagus, we sequenced and analyzed the complete plastomes (plastid genomes) of A. meioclados and A. munitus and obtained two plastomes whose length changed to 156,515 bp and 156,381 bp, respectively. A total of 111 unique genes have been detected in plastome, which included 78 protein-coding genes, 29 tRNA genes and 4 rRNA genes. In plastomes of A. meioclados and A. munitus, 14,685 and 14,987 codons were detected, among which 9942 and 10,207 had the relative synonymous codon usage (RSCU) values higher than 1, respectively. A. meioclados and A. munitus have 26 SSRs patterns, among which A. meioclados was 25 and A. munitus 21. The average Ka/Ks value was 0.36, and positive selection was detected in genes of the photosynthetic system (ndhF and rbcL) in Asparagus species. To perform the comparative analysis of plastomes, the two newly sequenced plastomes of the A. meioclados and A. munitus species were compared with that of A. cochinchinensis, and 12 hotspots, including 5 coding regions and 7 inter-genomic regions, were identified. Based on the whole plastome of Asparagus, 2 divergent hotspots (accD and rpl32-trnL-UAG) and 1 international barcode fragment (rbcL) were screened, which may be used as particular molecular markers for the identification of Asparagus species. In addition, we determined the phylogenetic relationship between A. meioclados and A. munitus in the genus Asparagus. This study enriches our knowledge of the molecular evolutionary relationships of the Asparagus genus and provides treasured data records for species identification, molecular breeding, and evolutionary analysis of this genus.
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The Urticaceae family (Rosales) comprises six tribes containing 61 genera, with about 2000 species distributed throughout tropical and subtropical regions. Taxonomic controversies concerning Urticaceae remain unresolved. This study aimed to characterize the specialized metabolites in Urticaceae genera and tribes in order to define their chemical profiles, micromolecular markers and the group evolutionary trends. Chemosystematic indexes—occurrence number (ON), oxidation index (OI) and skeleton specialization (SS)—and their evolutionary advancement parameters were calculated based on chemical literature data on Urticaceae flavonoids and triterpenes. Principal component analysis and hierarchical clusters were also performed. Altogether, 356 flavonoids and 607 terpenoids were analyzed. Flavonols and flavones with low protection indexes of flavonoid hydroxyls by O-glycosylation were observed. Moreover, triterpenes were predominant in the Urticaceae. The chemometric analysis confirmed that the Cecropieae tribe belongs to the Urticaceae family indicating similarities and dissimilarities due to metabolic micromolecular variability. Chemometric analysis revealed chemical similarities among several tribes of Urticaceae, including Urticeae, Elatostemateae, Boehmerieae, Parietarieae, Forsskaoleeae, and Cecropieae. C-glycosylated flavones in Cecropieae suggest an evolutionary transition consistent with their phylogenetic position in Urticaceae. These results demonstrate the usefulness of chemosystematics as a reliable tool for describing specialized metabolites in Urticaceae and for supporting molecular phylogenetic studies.
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La couverture forestière de la Côte d’Ivoire estimée à environ 16 millions d’hectares dans les années 1900 a connu une importante régression et elle est passée de nos jours à moins de 3 millions d’hectares. Cette réduction résulte de l’effet conjugué de l’urbanisation galopante, de l’agriculture et de l’exploitation des massifs forestiers en bois d’œuvre. Cette diminution a conduit à la perte des essences forestières commercialisables. La présente étude, réalisée dans la forêt classée de la Besso s’inscrit dans une vision d’amélioration de la productivité des plantations forestières pour un meilleur approvisionnement des industries du bois. Elle vise à identifier le modèle de reboisement offrant une diversité floristique élevée avec une meilleure croissance et qualité du bois. Les espèces utilisées sont Cedrela odorata L. (Meliaceae) et Gmelina arborea Roxb (Verbenaceae). Les travaux ont été effectués sur deux types de reboisement (plantation pure et agroforêt à base de caféier ou de cacaoyer). Plusieurs paramètres (quantitatifs et qualitatifs) ont été évalués suivant les types de reboisement. Il en ressort que l’agroforêt de type Cedrela odorata en association avec le caféier est le système le plus hétérogène avec un indice de Shannon de 3,47 et une valeur d’équitabilité de Piélou de 0,93. Cependant, Gmelina arborea en agroforêt avec le cacaoyer présente une bonne croissance annuelle (0,04 m). L’agroforêt de type Gmelina arborea associée au cacaoyer a fourni les meilleures valeurs de cylindricité et de rectitude. Les résultats de cette étude devraient aider à la réhabilitation des écosystèmes forestiers dégradés. The forest cover of Côte d'Ivoire estimated at around 16 million hectares in the 1900s has undergone a significant reduction and it is estimated today at under three million hectares. This reduction is the combined effect of a high rate of urbanization, agriculture, and logging industry. This reduction has led to a depletion of the forests in marketable species. This study on the Besso classified forest is part of a vision to improve the productivity of forest plantations for a better supply of wood industries. It aims to identify a reforestation model with a high floristic diversity with better growth and wood quality. The species used are Cedrela odorata L. (Meliaceae) and Gmelina arborea Roxb (Verbenaceae). Two types of reforestation in the Besso classified forest were carried out namely, pure reforestation plantation and agroforest (coffee and cocoa based). Several parameters (quantitative and qualitative) were evaluated according to the types of reforestation. The results show that the reforestation of Cedrela odorata-coffee agroforest is the most system environment with a Shannon index of 3.47 and a Pielou equitability value of 0.93. However, the Gmelina arborea-cocoa agroforest has the best annual growth rate (0.04 m). The qualitative parameters (cylindricity and straightness) are better in the Gmelina arborea-cocoa agroforest. All these results should help in the rehabilitation of degraded ecosystems and forests.
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A new species of the little-known genus Demarchus Jacoby was discovered at Pilu, East Taiwan, and is here described as Demarchus hsui sp. nov. The larvae and adults utilise showy mistletoes as food plants. Their remarkable biology is described in detail, including egg deposition and leaf mining behaviour. Their biology is compared with that of other members of the genus.
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CromoCat is a plant chromosome database that evolved from previous versions, as a repository of karyological information on the vascular flora of the Catalan Countries. CromoCat is designed as an independent database, managed by a team based at the University of Barcelona directed by J. Simon, available from its own webpage ( http://www.cromo.cat/ ) and from the Flora section of the Catalan Biodiversity Database - BDBC ( http://biodiver.bio.ub.es ). CromoCat contains at present (mid 2022) more than 68,000 records of karyological data belonging to more than 5000 taxa. A synthesis of the development of CromoCat, its functional system, achievements, limitations, and adopted solutions, during 25 years (1996-2021) and updated 2022, as well as the application to biodiversity conservation and management are outlined.
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Genome size is a plant character with far-reaching implications, ranging from impacts on the financial and computing feasibility of sequencing and assembling genomes all the way to influencing the very ecology and evolution of species. The increasing recognition of the role of genome size in plant science has led to a rising demand for comprehensive and easily accessible sources of genome size data. The Plant DNA C-values database has established itself as a trusted and widely used central hub for users needing to access available plant genome size data, complemented with related cytogenetic (ploidy level) and karyological (chromosome number) information where available. Since its inception in 2001, the database has undergone six major updates to incorporate newly available genome size information, leading to the most recent release (Release 7.1), which comprises data for 12,273 species across all the major land plant and some algal lineages. Here we describe how to use the database efficiently, making use of its different query and filtering settings.
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White-sand ecosystems form scattered patches across the lowland rainforests of the Amazonia and have been recognized for their extremely poor substrates and highly specialized flora. We focused on the white-sand flora of the Amazonas state in southern Venezuela, including six areas with white-sand habitats in the Atabapo, Camani, Pasimoni, Sipapo, and Ventuari river basins and the lowlands of Yapacana National Park. We provide a checklist of vascular plants based on 79 field inventories conducted in 50 sites within the 6 study areas. We describe the main patterns of taxonomic richness, alpha diversity, distribution, endemism, and life forms. The flora is unexpectedly rich, harboring 710 species, 287 genera, and 90 families. Twelve percent of the species are only known from the Venezuelan white-sand areas and about half of the species are white-sand endemics in the broader sense, i.e., considering the white-sand areas of Brazil, Colombia, and Venezuela. Woody elements dominate the life form spectrum of this flora (68% of taxa), whereas herbaceous forms account for 32% of the taxa. Melastomataceae, Rubiaceae, Fabaceae, Xyridaceae, and Poaceae are the most species-rich families, while the herbaceous genera Xyris and Utricularia are the richest in species, followed by the woody genera Ouratea and Myrcia. We found low floristic similarity among the six surveyed areas, reflecting a strong uneven distribution of taxa and the effect of local endemics. This spatial pattern of diversity is relevant for future conservation measures aiming to preserve the biodiversity of these singular ecosystems.KeywordsGuayana shieldAzonal vegetationMeadowRio Negro caatinga
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The varied patterns of genetic differentiation of vulnerable orchids populations (eg. Cattleya genus) urgently need to be known. Here, we present contextualized examples of genetic studies and discuss conservation challenges for orchids in the neotropical region, as the genetic diversity is essential for conservation and management actions of threatened species. In most of the sampled populations of Cattleya granulosa, an endangered orchid inhabiting the Atlantic Forest remnants, for example, there is a body of evidence of the occurrence of genetic bottlenecks. Our study showed that conservation genetics should consider the spatial distribution of genetic diversity in order to develop appropriate conservation strategies. Thus, further advances in the protection of genetic diversity are needed, since conventional databases and public policies may be insufficient in land use planning aiming at biodiversity conservation. In addition to the need to maintain genetic diversity, it is necessary to understand the reproductive and demographic characteristics caused by the interaction of a number of evolutionary and ecological mechanisms to maintain the evolutionary potential of an orchid species or population.KeywordsPlant conservation geneticsCattleya geneticsOrchidaceaeNeotropical orchidsThreatened orchids
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Antecedentes y Objetivos: La Alberca de Tacámbaro es uno de los tres lagos cráter que existen en Michoacán, México. El conocimiento que se tiene sobre la flora y vegetación de esta área protegida es inexistente. Por lo tanto, los objetivos del presente trabajo son: 1) elaborar una lista florística, 2) conocer el grado de endemismo de la flora y las especies clasificadas bajo alguna categoría de riesgo y 3) describir los tipos de vegetación presentes en La Alberca.Métodos: Se llevaron a cabo 20 salidas a campo, entre 2018 y 2023, para recolectar plantas vasculares que presentaran estructuras reproductivas. La identificación se realizó mediante literatura taxonómica, el cotejo con ejemplares tipo y el apoyo de especialistas en ciertos grupos taxonómicos. El material se depositó en los herbarios IEB, MEXU y MO. La vegetación se describió fisonómicamente, considerando la estratificación vertical, composición florística, dominancia y fenología foliar de las especies arbóreas.Resultados clave: Se determinaron 450 especies, agrupadas en 287 géneros y 92 familias. Asteraceae (79 especies), Fabaceae (60), Poaceae (25), Malvaceae (16) y Solanaceae (15) fueron las más diversas. A nivel genérico destacaron Desmodium (12 especies), Ipomoea (9), Solanum (8), Bletia (7), Euphorbia, Salvia y Stevia (5 cada uno). Las hierbas fueron la forma de crecimiento predominante (70.4%). El área presenta 141 (31.3%) especies endémicas de México y 19 están incluidas bajo alguna categoría de riesgo, de acuerdo con la NOM-059-SEMARNAT-2010, la IUCN y la CITES. Se describieron cuatro tipos de vegetación: bosque de Pinus, bosque de Pinus-Quercus, bosque tropical caducifolio y bosque tropical subcaducifolio.Conclusiones: La Alberca de Tacámbaro cuenta con una riqueza florística relevante (118 especies por ha). Este estudio aporta 345 especies no registradas para la flora del municipio Tacámbaro. Se reconoce una nueva especie de Nolina y el primer registro de Holographis peloria, Pherotrichis villosa y Prionosciadium lilacinum para Michoacán.
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Seridó is one of the driest regions in the Caatinga biome, Northeastern Brazil, affected by a long history of anthropogenic impact, and today it is considered a desertification region. A phytosociological survey of woody species was carried out in an area at Morada das Jandairas Farm (MJF), in Santana do Seridó, Rio Grande do Norte, which still has a significant arboreal component despite maintaining an extensive cattle production, and compared it with data from other five inventories carried out in the region. Seventeen species from ten botanical families were found, with Fabaceae and Euphorbiaceae being the most diversified. Commiphora leptophloeos and Croton blanchetianus stood out as the most important species. The high floristic composition similarity among the six compared studies indicates that the different phytophysiognomies may be result of anthropogenic action and regeneration processes. The relatively high Basal Area in the MJF (26.8 m² ha⁻¹) stands out even considering inventories carried out throughout the Caatinga region, which is largely due to the presence of many large trees (C. leptophloeos). Considerations about the ecological importance of large and old trees are made, with recommendations for the methodology of phytosociological inventories. Keywords Dry forests; Seasonally dry tropical forests; Semiarid; Quartzarenic soils; Old trees
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We describe the newly-discovered species Illicium gansuense (Schisandraceae), discovered in the Yuhe area of Giant Panda National Park, Gansu, China. Morphologically, I. gansuense resembles I. ternstroemioides and I. arborescens . However, the new species can be distinguished by its smaller leaf size, the larger number of tepals, tepal margin ciliate, and distinct flowering and fruiting seasons.
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Creating a multi-gene alignment matrix for phylogenetic analysis using organelle genomes involves aligning single-gene datasets manually, a process that can be time-consuming and prone to errors. The HomBlocks pipeline has been created to eliminate the inaccuracies arising from manual operations. The processing of a large number of sequences, however, remains a time-consuming task. To conquer this challenge, we develop a speedy and efficient method called Organelle Genomes for Phylogenetic Analysis (ORPA). ORPA can quickly generate multiple sequence alignments for whole-genome comparisons by parsing the result files of NCBI BLAST, completing the task in just one minute. With increasing data volume, the efficiency of ORPA is even more pronounced, over 300 times faster than HomBlocks in aligning 60 high-plant chloroplast genomes. The phylogenetic tree outputs from ORPA are equivalent to HomBlocks, indicating its outstanding efficiency. Due to its speed and accuracy, ORPA can identify species-level evolutionary conflicts, providing valuable insights into evolutionary cognition.
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Antecedentes: El noreste de México, estados de Coahuila, Nuevo León y Tamaulipas, constituye una región heterogénea que incluye sierras, planicies continentales y llanuras costeras con una infinidad de ambientes, substratos geológicos y gradientes altitudinales que favorecen la presencia de una rica biodiversidad. No existe una síntesis que documente la diversidad florística de esta región. Preguntas: ¿Cuál es la magnitud de la diversidad de plantas vasculares en el noreste de México?, ¿Cuáles son las familias y géneros con mayor número de especies?, ¿Cómo se distribuye geográficamente esta riqueza florística en toda la región y cuáles son sus elementos más característicos? Especies de estudio: 7,088 especies de plantas vasculares. Sitio de muestreo: estados de Coahuila, Nuevo León y Tamaulipas. Métodos: Se consultó literatura florística-taxonómica sobre la flora de la región y bases de datos de ejemplares para hacer un análisis espacial de la biodiversidad usando celdas de 1° de longitud y latitud. Se calculó la riqueza y el endemismo en la región, los estados y las celdas. Resultados: Para el noreste de México se reportan 7,088 especies de plantas vasculares, de las cuales 1,767 son endémicas de México. Conclusiones: El noreste de México registra una diversidad florística particularmente interesante y compleja, debido a que su territorio se ubica primordialmente fuera del neotrópico y porque constituye el límite boreal para muchos elementos de la flora de México.
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Impatiens rosea Lindl., an Indian endemic species of family Balsaminaceae, collected from Mahendragiri hills of Odisha state (Eastern Ghats), is reported here for the first time from the state. A detailed description and photographs are provided for easy identification of the species.
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We present here a revised classification of Santalales, an angiosperm order that contains 18 families, 160 genera, and over 2200 species. Both nonparasitic and parasitic flowering plants occur in the traditionally circumscribed family Olacaceae whereas all other families are composed entirely of parasites. The five evolutionary radiations of aerial parasitism produced mistletoes that constitute most of the generic and specific diversity seen in the order. This classification, although based primarily upon results from molecular phylogenetic investigations, brings together all currently available information that contributes to our understanding of relationships among these plants. Monophyletic groups (clades) obtained from molecular analyses were named using a Linnaean ranked system. Four new families are named that formerly resided in Santalaceae s.l.: Amphorogynaceae, Cervantesiaceae, Comandraceae, and Nanodeaceae. A new tribal and subtribal classification for Loranthaceae is presented where nine new subtribe names are proposed.
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The Caryophyllales constitute a major lineage of flowering plants with approximately 12500 species in 39 families. A taxonomic backbone at the genus level is provided that reflects the current state of knowledge and accepts 749 genera for the order. A detailed review of the literature of the past two decades shows that enormous progress has been made in understanding overall phylogenetic relationships in Caryophyllales. The process of re-circumscribing families in order to be monophyletic appears to be largely complete and has led to the recognition of eight new families (Anacampserotaceae, Kewaceae, Limeaceae, Lophiocarpaceae, Macarthuriaceae, Microteaceae, Montiaceae and Talinaceae), while the phylogenetic evaluation of generic concepts is still well underway. As a result of this, the number of genera has increased by more than ten percent in comparison to the last complete treatments in the Families and genera of vascular plants” series. A checklist with all currently accepted genus names in Caryophyllales, as well as nomenclatural references, type names and synonymy is presented. Notes indicate how extensively the respective genera have been studied in a phylogenetic context. The most diverse families at the generic level are Cactaceae and Aizoaceae, but 28 families comprise only one to six genera. This synopsis represents a first step towards the aim of creating a global synthesis of the species diversity in the angiosperm order Caryophyllales integrating the work of numerous specialists around the world.
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To date molecular data have not revealed the exact phylogenetic position of Balanophoraceae in relation to hemiparasitic Santalales. To elucidate the phylogeny of Santalales and the position of Balanophoraceae, three plastid genes (matK, rbcL, accD), three nuclear genes (SSU and LSU rDNA and RPB2) and one mitochondrial gene (matR) from 197 Santalales samples (including 11 Balanophoraceae species) were analyzed with parsimony, maximum likelihood and Bayesian inference methods. Our results demonstrate that Balanophoraceae is composed of two well-supported clades: a relatively slow-evolving one including Dactylantus, Hachettea, and Mystropetalon (Mystropetalaceae) and an extremely fast-evolving one composed of the remaining Balanophoraceae s.str. Support for monophyly of the two clades was low, thus it appears holoparasitism has arisen twice independently in Santalales. These two clades appeared during a time of great change in the order (ca. 100 Ma) when several major evolutionary innovations emerged, e.g., the root hemiparasites of Santalaceae s.l., the first aerial parasites (Misodendraceae), herbaceous root parasites (Schoepfiaceae), root parasitic Loranthaceae (the ancestors of aerial parasitic mistletoes), as well as the holoparasites in Balanophoraceae and Mystropetalaceae.
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Acceptance of a name is the ultimate provision for valid publication of new names under the International Code of Nomenclature for algae, fungi, and plants (McNeill & al. in Regnum Veg. 154. 2012). This is stressed in Art. 33.1, which requires that, after fulfilling all the other conditions of valid publication (if fulfilled separately), a name must be explicitly accepted in the place of its valid publication. However, evidence of such acceptance is not always obvious. An apparently problematic situation is presented by certain types of indices, bibliographic dictionaries and reviews whose purpose is to record botanical names and to deliver these names to the public. It may be stated in introductions to such works that they include accepted names or also synonyms, and certain records may be indicated as such. Nevertheless, a question remains: who is the author who accepted (as required in Art. 33.1 and 36.1) a particular name in such publications? Most commonly, and explicitly, indices recorded names that were supposed to have been accepted by their original authors. If a name inadvertently happened to appear as new in an index, the recorded place of its stated (presumed) original publication may be considered a reference to its basionym or replaced synonym or to a designation that was not validly published. If a basionym or replaced synonym can be found in the original publication, under Art. 46.3 the citation of the original author is not considered ascription and under Art. 46.2 the author of the index is the author of the new combination or replacement name. If the name of a new taxon is validated by reference to a description or diagnosis associated with a designation that was not validly published (e.g., a provisional name), under Art. 46.2 and Note 2 the new name is attributed to the original authorship unless Art. 46.4 applies. But in both situations, acceptance of a name (Art. 36.1) or explicit acceptance (Art. 33.1) is required by the recorder in the index in order for the new name to be validly published. Such evidence of (explicit) acceptance is typically missing in indices except for those that do contain original taxonomic assessments, for instance, the main volumes and the three first supplements of the Index Kewensis. The title and preface of the first volume of the Index Kewensis states that it provides " an enumeration of the genera and species of flowering plants […] together with […] their synonyms " , thus being " an Index to the names and authorities of all known flowering plants ". From these statements and the typesetting of the plant name list it is completely clear that the Index Kewensis was intended to provide accepted names of plant genera and species with their synonyms, in order to serve as a taxonomic and nomenclatural checklist of all plants known to date (actually phanerogams, as follows from the Latin title). From its fourth supplement onwards, the Index Kewensis had changed its style and policy, as explained in the introduction with the following statement: " Iterum nomina antea usitata sub nomina nunc utenda recitata sunt; nominibus nudis inter synonyma enumeratis nomina accepta addita sunt " (in English translation: Besides, the names used previously are cited under the names now to be used; accepted names are added to the nomina nuda that appeared in the synonymy). Greuter (in Candollea 40: 211–213. 1985), who translated this sentence, interpreted it as a statement of acceptance on the part of the compilers; however, we can see nothing in these words that goes beyond the mere recording of names accepted by the original authors: a name " now to be used " is a name proposed by a certain author as to be used and is accepted by that author, not necessarily by the compilers. No explicit statement or other evidence can be found concerning the acceptance of names specifically by the compilers of the Index Kewensis, and we agree with Meikle (in Biol. J. Linn. Soc. 3: 295–299. 1971), who also argued that in the later supplements " the editors [of the Index Kewensis] only included validly published names without passing judgement on them ". Another controversial case, in which explicit acceptance of names by the publishing author is absent, is an early dictionary of botanical terminology by Martinov (Tekhno-Botanicheskiy Slovar, published in 1820). Reveal (in Taxon 47: 851–856. 1998) concluded that botanical names that first appeared in Martinov (l.c.) were validly published in this book by the means of indirect references to descriptions in earlier works. However, Sennikov (in Komarovia 4: 138–154. 2006) disagreed, arguing that, as explained in the preface to Martinov's book, its only nomenclatural service was to bring together names in Latin for all the taxa at the ranks of " order " and " family " , as well as for some taxa at other ranks, which were used in various, sometimes conflicting, botanical classifications. Plant names in that book were presented as part of botanical terminology, without giving an opinion about the corresponding taxa and thus without explicit acceptance of the listed names. Reviews of published material such as books and articles may communicate botanical names as part of the contents in the same way as indices and dictionaries do. Even if they do so, unless the authors of such reviews express their personal opinion about them, the names they use cannot be treated as explicitly accepted in the reviews. Since recorders and reviewers do not usually assess the taxonomy behind the names that are being recorded, such names, even if appearing to be inadvertently " new " because of one or another technical mistake or misunderstanding of the original source, cannot be validly published according to Art. 33.1 and 36.1. To articulate this conclusion
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One of the major goals of systematics is to provide a synthesis of knowledge on the diversity of a group of organisms, such as flowering plants. Biodiversity conservation and management call for rapid and accurate global assessments at the species level. At the same time the rapid development of evolutionary biology with a spectrum of approaches to test species relationships and species limits, has revolutionized and is still revolutionizing the science of plant systematics including taxonomy. We explore the relevant scientific and technological developments with the aim to suggest a conceptual framework for an integrated monographic synthesis which can reach global coverage. Our exemplar group are the Caryophyllales, which are a lineage of worldwide distribution, comprising approx. 5% of flowering plant species diversity. The current situation of classification is marked by a transition from pre-phylogenetic treatments to taxonomic treatments increasingly evaluated in an evolutionary context. Structured data (both molecular and morphological), linked to well-documented specimens will be important as fundamental entities of information that can be subjected to evolutionary analysis. As a result, taxon concepts are established as hypotheses which then can be used as basis for a classification system in a second step. Global syntheses need to provide information and use a classification system that reflects the current state of knowledge. In order to accommodate the constantly improved understanding of the organisms, eventually also resulting in the change of taxon concepts, the treatments need to be dynamic. The workflow for a global monographic synthesis as outlined here is supported by currently available biodiversity informatics tools such as the EDIT Platform for Cybertaxonomy. The availability of electronic sources (names, protologues, type images, literature) greatly facilitates the access to information, but as our case shows, considerable efforts for data curation and research are still needed. The implementation of a global monographic synthesis such as the Caryophyllales requires the involvement of the global scientific community.
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A revised and updated classification for the families of flowering plants is provided. Many recent studies have yielded increasingly detailed evidence for the positions of formerly unplaced families, resulting in a number of newly adopted orders, including Amborellales, Berberidopsidales, Bruniales, Buxales, Chloranthales, Escalloniales, Huerteales, Nymphaeales, Paracryphiales, Petrosaviales, Picramniales, Trochodendrales, Vitales and Zygophyllales. A number of previously unplaced genera and families are included here in orders, greatly reducing the number of unplaced taxa; these include Hydatellaceae (Nymphaeales), Haptanthaceae (Buxales), Peridiscaceae (Saxifragales), Huaceae (Oxalidales), Centroplacaceae and Rafflesiaceae (both Malpighiales), Aphloiaceae, Geissolomataceae and Strasburgeriaceae (all Crossosomatales), Picramniaceae (Picramniales), Dipentodontaceae and Gerrardinaceae (both Huerteales), Cytinaceae (Malvales), Balanophoraceae (Santalales), Mitrastemonaceae (Ericales) and Boraginaceae (now at least known to be a member of lamiid clade). Newly segregated families for genera previously understood to be in other APG-recognized families include Petermanniaceae (Liliales), Calophyllaceae (Malpighiales), Capparaceae and Cleomaceae (both Brassicales), Schoepfiaceae (Santalales), Anacampserotaceae, Limeaceae, Lophiocarpaceae, Montiaceae and Talinaceae (all Caryophyllales) and Linderniaceae and Thomandersiaceae (both Lamiales). Use of bracketed families is abandoned because of its unpopularity, and in most cases the broader circumscriptions are retained; these include Amaryllidaceae, Asparagaceace and Xanthorrheaceae (all Asparagales), Passifloraceae (Malpighiales), Primulaceae (Ericales) and several other smaller families. Separate papers in this same volume deal with a new linear order for APG, subfamilial names that can be used for more accurate communication in Amaryllidaceae s.l., Asparagaceace s.l. and Xanthorrheaceae s.l. (all Asparagales) and a formal supraordinal classification for the flowering plants.
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Three families, Anarthriaceae, Restionaceae and Centrolepidaceae, are generally recognised in the restiid clade of Poales. A new phylogeny is presented, with fuller sampling of Australian taxa, based on analyses of trnL-F, trnK and rbcL data from the chloroplast genome. The findings agree with the major groups shown in previous molecular studies but provide a more substantial basis for reviewing the classification at family and generic levels. Anarthriaceae is sister to Restionaceae, with Anarthria sister to Lyginia+Hopkinsia. Centrolepidaceae, on an extremely long branch, appears embedded in Restionaceae in Bayesian trees; although it appears as sister to Restionaceae in analyses that are more subject to long-branch attraction (in parsimony analyses and those of data from the less-conserved trnL-F cpDNA region). Accepting the embedded position, which would make this a subfamily of Restionaceae, the basal division in the Restionaceae separates the African subfamily Restionoideae from the Australasian clade (Sporadanthoideae, Centrolepidoideae, Leptocarpoideae). In subfamily Leptocarpoideae, Eurychorda forms the basal branch. At the next dichotomy the Leptocarpus clade, together with the Winifredia clade, is separated from a diverse assemblage including Loxocarya, Chordifex, Baloskion, Desmocladus, Lepidobolus and allied genera. The phylogeny indicates that several currently recognised genera are not monophyletic and that changes to the generic classification are required. A matrix of morphological characters was prepared and these were mapped onto the Bayesian consensus DNA tree to identify synapomorphies of the clades and genera. Observations on leaf laminae indicate that fully or partially unifacial leaf laminae are a synapomorphy of the restiid clade. The morphological characterisation of the following are considered: the restiid clade, Anarthriaceae, Restionaceae enlarged to include subfamily Centrolepidoideae, Leptocarpus s.l. (including as potential synonyms Meeboldina and Stenotalis) and Desmocladus s.l. (including potentially Harperia, Onychosepalum and Kulinia).
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The origin of Geraniales (approximately 900 species in three families: Geraniaceae, Melianthaceae, and Vivianiaceae) is traced back to the Cretaceous of Gondwana, yet their geotemporal history is largely unknown because of a limited fossil record and incomplete phylogenies. In the present study, we provide the first fossil record of Vivianiaceae and a highly resolved molecular phylogeny for all extant Geraniales genera. Our results support the hypothesis that five (instead of three) families should be recognized in the order Geraniales: Francoaceae A. Juss. (Francoa, Greyia, Tetilla), Geraniaceae Juss. (Erodium, Geranium, Monsonia, Pelargonium), Hypseocharitaceae Wedd. (monogeneric), Melianthaceae Horan. (Bersama, Melianthus), and Vivianiaceae Klotzsch (Balbisia, Rhynchotheca, Viviania). The four major lineages (i.e. Geraniaceae, Francoaceae+Melianthaceae, Hypseocharitaceae, Vivianiaceae) all originated within a narrow time frame during the Eocene (36.9-49.9Mya) based on the five fossil calibration points. The divergence of most of the extant genera occurred much later, from the Miocene onwards. The South American-South African disjunction in Francoaceae apparently goes back to long distance dispersal with an estimated divergence time of the lineages in the Middle Miocene [11.2 (5.9-17.7)Mya]. Diversification in Melianthus appears to be much more recent than previously assumed [starting approximately 3.4 (1.9-5.2)Mya rather than approximately 8-20Mya]. However, divergence of the Andean Hypseocharis lineage [36.9 (31.9-42.8)Mya] significantly predates the main Andean uplift: Current distributions likely go back to northward migrations and subsequent extinctions in Patagonia. Similarly, Rhynchotheca, Balbisia, and Viviania have a current southern distribution limit >10°N of the fossil finds, indicating a massive northward displacement. The present evidence suggests that niche conservatism likely played a major role in the historical biogeography of Geraniales.
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Cleomaceae is a small pantropical family that is emerging as a promising system to investigate C4 photosynthesis, floral evolution, and comparative genomics. However, our understanding of these phenomena is hindered by a lack of a strong phylogenetic hypothesis, despite a number of previous studies. We reconstructed the phylogeny of the family using data from all three genomes, including three cpDNA (ndhF, matK, ycf1), one mtDNA (rps3), and one nrDNA (ITS) regions. Analyses strongly supported 15 clades: (1) Clade 1, which includes two Old World species, Cleome khorassanica and C. turkmena; (2) Cleome s.str., which includes the type C. ornithopodioides and Old World species; (3) Droserifolia, corresponding to three Old World species, C. droserifolia, C. fimbriata, C. quinquenervia; (4) Polanisia, equivalent to this New World genus; (5) Angustifolia, which includes four Old World species; (6) North American cleomoids, which includes four genera, Cleomella, Peritoma, Oxystylis, and Wislizenia; (7) Australian, which includes Old world species and worldwide weed Arivela viscosa; (8) Gynandropsis, equivalent to this monotypic genus; (9) Clade 6, which includes Old World species of Cleome and Dipterygium; (10) Dactylaena, corresponding to this genus and Physostemon; (11) African, which includes species distributed in Old World; (12) Andean, which includes Podandrogyne and tropical New World species of Cleome; (13) Melidiscus, which includes New World tropical species; (14) Cleoserrata, which includes New World tropical species; and (15) Tarenaya, a large New World clade. Major relationships amongst the clades are strongly supported for the first time, including North American cleomoids sister to all remaining Cleomaceae. While five genera are confirmed or newly identified here to be non-monophyletic (Cleome, Cleomella, Hemiscola, Peritoma, Tarenaya), six are supported (Cleoserrata, Dactylaena, Melidiscus, Physostemon, Podandrogyne, Polanisia). Thus, there are many taxonomic and evolutionary implications to our revised phylogenetic hypothesis.
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Asparagales are a diverse monophyletic order that has numerous species (ca. 50% of monocots) including important crop plants such as Allium, Asparagus, and Vanilla, and a host of ornamentals such as irises, hyacinths, and orchids. Historically, Asparagales have been of interest partly because of their fascinating chromosomal evolution. We examine the evolutionary dynamics of Asparagales genomes in an updated phylogenetic framework that combines analyses of seven gene regions (atp1, atpB, matK, ndhF, rbcL, trnL intron, and trnL–F intergenic spacer) for 79 taxa of Asparagales and outgroups. Asparagales genomes are evolutionarily labile for many characters, including chromosome number and genome size. The history and causes of variation in chromosome number and genome size remain unclear, primarily because of the lack of data in small clades in the phylogenetic tree and the lack of comparative genetic maps, apart from Allium and Asparagus. Genomic tools such as bacterial artificial chromosome (BAC) libraries should be developed, as both molecular cytogenetic markers and a source of nuclear genes that can be widely used by evolutionary biologists and plant breeders alike to decipher mechanisms of chromosomal evolution.
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Gisekiaceae are a monogeneric family of the core Caryophyllales distributed in arid regions of Africa and Asia. The only widespread species of the genus, Gisekia pharnaceoides, performs C4 photosynthesis based on CO2 compensation point measurements. This study investigates the C4 syndrome and its evolution in Gisekia. The infrageneric relationships, distribution and bioclimatic preferences of Gisekia are also investigated. Leaf gas exchange characteristics, activity of Rubisco and major C4 cycle enzymes, and ultrastructural characteristics of mesophyll and bundle sheath cells are studied for Gisekia pharnaceoides. δ(13)C values and leaf anatomy are analyzed for all species. A dated molecular phylogeny of 39 accessions representing all species of Gisekiaceae and 14 representatives of closely related core Caryophyllales families is generated using four cp markers and ITS. The precise current distribution and bioclimatic niche of Gisekia is assessed on the basis of 520 georeferenced specimen localities. All traditionally recognized species of Gisekia are C4 plants with atriplicoid Kranz anatomy. Gisekia pharnaceoides uses the NAD-ME biochemical type. The molecular phylogeny demonstrated two East African clades nested within South African clades, demonstrating migration along the arid areas of eastern Africa during the Late Miocene/Pliocene Epochs. Most traditionally defined species are polyphyletic. Gisekia represents an isolated C4 lineage within core Caryophyllales dating back to the Miocene Epoch and probably spread along the African arid corridor from a South African center of origin. The seven currently recognized species should be treated as one polymorphic species or species complex, Gisekia pharnaceoides agg.
Book
This volume presents systematic treatments for the families and genera of the Malpighiales, which more recently have been recognised as a new major group of the eudicots. Apart from several herbaceous lineages (already treated in Vol. IX of this series), the order consists mainly of rainforest trees, particularly those of the understorey. Accompanied by other early eudicot lineages, this reflects the well-documented origin of the group as invaders into the conifer-, cycad- and seed fern-dominated forests of the Cretaceous which, at that time, were transformed into the tropical rainforest biome. In this volume, 24 families with 429 genera comprising over 12,000 species are treated. Many of these belong to the vast family of the Euphorbiaceae (here conceived in a broader sense), followed by the Violaceae, whereas some of the remaining families are very small and even relictual. The revised classification includes a complete inventory of the genera belonging to the families treated in this volume, along with their diagnostic features and keys for their identification. References to the latest taxonomic literature and links to many different disciplines important to modern plant systematics make the volume a valuable source of information on the manifold aspects of plant diversity.