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Rich Zingiberales
RESEARCH ARTICLE INVITED SPECIAL ARTICLE For the Special Issue: The Tree of Death: The Role of Fossils in Resolving the Overall Pattern of Plant Phylogeny Building the monocot tree of death: Progress and challenges emerging from the macrofossil- rich Zingiberales Selena Y. Smith1,2,4,6 , William J. D. Iles1,3 , John C. Benedict1,4, and Chelsea D. Specht5 Manuscript received 1 November 2017; revision accepted 2 May PREMISE OF THE STUDY: Inclusion of fossils in phylogenetic analyses is necessary in order 2018. to construct a comprehensive “tree of death” and elucidate evolutionary history of taxa; 1 Department of Earth & Environmental Sciences, University of however, such incorporation of fossils in phylogenetic reconstruction is dependent on the Michigan, Ann Arbor, MI 48109, USA availability and interpretation of extensive morphological data. Here, the Zingiberales, whose 2 Museum of Paleontology, University of Michigan, Ann Arbor, familial relationships have been difficult to resolve with high support, are used as a case study MI 48109, USA to illustrate the importance of including fossil taxa in systematic studies. 3 Department of Integrative Biology and the University and Jepson Herbaria, University of California, Berkeley, CA 94720, USA METHODS: Eight fossil taxa and 43 extant Zingiberales were coded for 39 morphological seed 4 Program in the Environment, University of Michigan, Ann characters, and these data were concatenated with previously published molecular sequence Arbor, MI 48109, USA data for analysis in the program MrBayes. 5 School of Integrative Plant Sciences, Section of Plant Biology and the Bailey Hortorium, Cornell University, Ithaca, NY 14853, USA KEY RESULTS: Ensete oregonense is confirmed to be part of Musaceae, and the other 6 Author for correspondence (e-mail: [email protected]) seven fossils group with Zingiberaceae. -
BANANAS in Compost Is Moisture and to Keep Excellent for the Bananas Heavily CENTRAL Improving the Mulched
Manure or plants good soil and BANANAS IN compost is moisture and to keep excellent for the bananas heavily CENTRAL improving the mulched. soil. They also Bananas are hardy FLORIDA prefer a moist plants in Central soil. Bananas are Florida but tempera- ananas are a commonly grown not very drought tures below 34˚F will plant in Central Florida. They are tolerant and need damage the foliage. usually grown for the edible fruit supplemental Following a freeze, B watering during bananas can look and tropical look, but some are grown for their colorful inflorescences or dry periods. They pathetic with the ornamental foliage. Bananas are members are also heavy brown, lifeless foliage of the Musaceae Family. This family feeders and hanging from the includes plants found in the genera should be fed stem, but don’t let this Ensete, Musa, and Musella. Members of several times a fool or discourage you. year for optimum Once the weather this family are native mainly to south- Musa mannii eastern Asia, but some are also found growth. A good warms, new growth wild in tropical Africa and northeastern balanced fertilizer, such as 6-6-6 or quickly begins and green leaves arise. Australia. They are cultivated throughout 10-10-10 with micronutrients is best. After a couple of months, the plants are the tropics and subtropics and are an Also an application of extra potassium lush and healthy. The stems will not be important staple in many diets. Bananas (potash) is beneficial to the plants. Most damaged unless temperatures drop are not true trees but rather are large, bananas are susceptible to nematodes, so below 24˚F. -
Building the Monocot Tree of Death
Received Date: Revised Date: Accepted Date: Article Type: Special Issue Article RESEARCH ARTICLE INVITED SPECIAL ARTICLE For the Special Issue: The Tree of Death: The Role of Fossils in Resolving the Overall Pattern of Plant Phylogeny Short Title: Building the monocot tree of death Building the monocot tree of death: progress and challenges emerging from the macrofossil-rich Zingiberales 1,2,4,6 1,3 1,4 5 Selena Y. Smith , William J. D. Iles , John C. Benedict , and Chelsea D. Specht Manuscript received 1 November 2017; revision accepted 2 May 2018. 1 Department of Earth & Environmental Sciences, University of Michigan, Ann Arbor, MI 48109 USA 2 Museum of Paleontology, University of Michigan, Ann Arbor, MI 48109 USA 3 Department of Integrative Biology and the University and Jepson Herbaria, University of California, Berkeley, CA 94720 USA 4 Program in the Environment, University of Michigan, Ann Arbor, MI 48109 USA 5 School of Integrative Plant Sciences, Section of Plant Biology and the Bailey Hortorium, Cornell University, Ithaca, NY 14853 USA 6 Author for correspondence (e-mail: [email protected]); ORCID id 0000-0002-5923-0404 Author Manuscript This is the author manuscript accepted for publication and has undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1002/ajb2.1123 This article is protected by copyright. All rights reserved Smith et al.–Building the monocot tree of death Citation: Smith, S. Y., W. J. D. -
The Evolutionary and Biogeographic Origin and Diversification of the Tropical Monocot Order Zingiberales
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 49 2006 The volutE ionary and Biogeographic Origin and Diversification of the Tropical Monocot Order Zingiberales W. John Kress Smithsonian Institution Chelsea D. Specht Smithsonian Institution; University of California, Berkeley Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Kress, W. John and Specht, Chelsea D. (2006) "The vE olutionary and Biogeographic Origin and Diversification of the Tropical Monocot Order Zingiberales," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 49. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/49 Zingiberales MONOCOTS Comparative Biology and Evolution Excluding Poales Aliso 22, pp. 621-632 © 2006, Rancho Santa Ana Botanic Garden THE EVOLUTIONARY AND BIOGEOGRAPHIC ORIGIN AND DIVERSIFICATION OF THE TROPICAL MONOCOT ORDER ZINGIBERALES W. JOHN KRESS 1 AND CHELSEA D. SPECHT2 Department of Botany, MRC-166, United States National Herbarium, National Museum of Natural History, Smithsonian Institution, PO Box 37012, Washington, D.C. 20013-7012, USA 1Corresponding author ([email protected]) ABSTRACT Zingiberales are a primarily tropical lineage of monocots. The current pantropical distribution of the order suggests an historical Gondwanan distribution, however the evolutionary history of the group has never been analyzed in a temporal context to test if the order is old enough to attribute its current distribution to vicariance mediated by the break-up of the supercontinent. Based on a phylogeny derived from morphological and molecular characters, we develop a hypothesis for the spatial and temporal evolution of Zingiberales using Dispersal-Vicariance Analysis (DIVA) combined with a local molecular clock technique that enables the simultaneous analysis of multiple gene loci with multiple calibration points. -
Banana Cultivation in South Asia and East Asia: a Review of the Evidence from Archaeology and Linguistics
Banana Cultivation in South Asia and East Asia: A review of the evidence from archaeology and linguistics Dorian Q. Fuller and Marco Madella Research Abstract South Asia provides evidence for introduced banana cul- the present and what can be suggested for the early and tivars that are surprisingly early in the Indus Valley but mid Holocene from palaeoecological reconstructions. Ar- late elsewhere in India. Although phytolith data are still chaeological evidence for bananas in these regions re- limited, systematic samples from fourteen sites in six re- mains very limited. Our purpose in this contribution is to gions suggest an absence of bananas from most of Neo- situate those few data points of prehistoric banana phyto- lithic/Chalcolithic South Asia, but presence in part of the liths and seeds within the history of appropriate sampling Indus valley. Evidence from textual sources and historical (e.g., for phytoliths) that might have provided evidence for linguistics from South Asia and from China suggest the bananas, thus highlighting the potential for more inten- major diffusion of banana cultivars was in the later Iron sive future efforts. We also review some evidence from Age or early historic period, c. 2000 years ago. Never- historical linguistics and textual historical sources on the theless Harappan period phytolith evidence from Kot Diji, early history of bananas in India and China. suggests some cultivation by the late third or early second millennium B.C., and the environmental context implies Cultivated and Wild hybridization with Musa balbisiana Colla had already oc- Bananas in South Asia curred. Evidence of wild banana seeds from an early Ho- locene site in Sri Lanka probably attests to traditions of There is hardly a cottage in India that has not its grove utilisation of M. -
Musa Species (Bananas and Plantains) Authors: Scot C
August 2006 Species Profiles for Pacific Island Agroforestry ver. 2.2 www.traditionaltree.org Musa species (banana and plantain) Musaceae (banana family) aga‘ (ripe banana) (Chamorro), banana, dessert banana, plantain, cooking banana (English); chotda (Chamorro, Guam, Northern Marianas); fa‘i (Samoa); hopa (Tonga); leka, jaina (Fiji); mai‘a (Hawai‘i); maika, panama (New Zealand: Maori); meika, mei‘a (French Polynesia); siaine (introduced cultivars), hopa (native) (Tonga); sou (Solomon Islands); te banana (Kiribati); uchu (Chuuk); uht (Pohnpei); usr (Kosrae) Scot C. Nelson, Randy C. Ploetz, and Angela Kay Kepler IN BRIEF h C vit Distribution Native to the Indo-Malesian, E El Asian, and Australian tropics, banana and C. plantain are now found throughout the tropics and subtropics. photo: Size 2–9 m (6.6–30 ft) tall at maturity. Habitat Widely adapted, growing at eleva- tions of 0–920 m (0–3000 ft) or more, de- pending on latitude; mean annual tempera- tures of 26–30°C (79–86°F); annual rainfall of 2000 mm (80 in) or higher for commercial production. Vegetation Associated with a wide range of tropical lowland forest plants, as well as nu- merous cultivated tropical plants. Soils Grows in a wide range of soils, prefer- ably well drained. Growth rate Each stalk grows rapidly until flowering. Main agroforestry uses Crop shade, mulch, living fence. Main products Staple food, fodder, fiber. Yields Up to 40,000 kg of fruit per hectare (35,000 lb/ac) annually in commercial or- Banana and plantain are chards. traditionally found in Pacific Intercropping Traditionally grown in mixed island gardens such as here in Apia, Samoa, although seri- cropping systems throughout the Pacific. -
Phylogenetic Relationships of Monocots Based on the Highly Informative Plastid Gene Ndhf Thomas J
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 4 2006 Phylogenetic Relationships of Monocots Based on the Highly Informative Plastid Gene ndhF Thomas J. Givnish University of Wisconsin-Madison J. Chris Pires University of Wisconsin-Madison; University of Missouri Sean W. Graham University of British Columbia Marc A. McPherson University of Alberta; Duke University Linda M. Prince Rancho Santa Ana Botanic Gardens See next page for additional authors Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Givnish, Thomas J.; Pires, J. Chris; Graham, Sean W.; McPherson, Marc A.; Prince, Linda M.; Patterson, Thomas B.; Rai, Hardeep S.; Roalson, Eric H.; Evans, Timothy M.; Hahn, William J.; Millam, Kendra C.; Meerow, Alan W.; Molvray, Mia; Kores, Paul J.; O'Brien, Heath W.; Hall, Jocelyn C.; Kress, W. John; and Sytsma, Kenneth J. (2006) "Phylogenetic Relationships of Monocots Based on the Highly Informative Plastid Gene ndhF," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 4. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/4 Phylogenetic Relationships of Monocots Based on the Highly Informative Plastid Gene ndhF Authors Thomas J. Givnish, J. Chris Pires, Sean W. Graham, Marc A. McPherson, Linda M. Prince, Thomas B. Patterson, Hardeep S. Rai, Eric H. Roalson, Timothy M. Evans, William J. Hahn, Kendra C. Millam, Alan W. Meerow, Mia Molvray, Paul J. Kores, Heath W. O'Brien, Jocelyn C. Hall, W. John Kress, and Kenneth J. Sytsma This article is available in Aliso: A Journal of Systematic and Evolutionary Botany: http://scholarship.claremont.edu/aliso/vol22/iss1/ 4 Aliso 22, pp. -
Musalogue: Diversity in the Genus Musa
A catalogue of Musa germplasm Diversity in the genus Musa Jeff Daniells, Christophe Jenny, Deborah Karamura and Kodjo Tomekpe CIRAD The mission of the International Network for the Improvement of Banana and Plantain is to sustainably increase the productivity of banana and plantain grown on smallholdings for domestic consumption and for local and export markets. The Programme has four specific objectives: . To organize and coordinate a global research effort on banana and plantain, aimed at the development, evaluation and dissemination of improved cultivars and at the conservation and use of Musa diversity . To promote and strengthen collaboration and partnerships in banana-related research activities at the national, regional and global levels . To strengthen the ability of NARS to conduct research and development activities on bananas and plantains . To coordinate, facilitate and support the production, collection and exchange of information and documentation related to banana and plantain. INIBAP is a programme of the International Plant Genetic Resources Institute (IPGRI), a Future Harvest Centre. The International Plant Genetic Resources Institute (IPGRI) is an autonomous international scientific organization, supported by the Consultative Group on International Agricultural Research (CGIAR). IPGRI's mandate is to advance the conservation and use of genetic diversity for the well-being of present and future generations. IPGRI's headquarters is based in Rome, Italy, with offices in another 19 countries worldwide. It operates through -
Musaceae), a Monotypic Genus from Yunnan, China
Ann. Bot. Fennici 42: 461–467 ISSN 0003-3847 Helsinki 19 December 2005 © Finnish Zoological and Botanical Publishing Board 2005 Microsporogenesis and male gametogenesis in Musella (Musaceae), a monotypic genus from Yunnan, China Chun-Ying Xue*, Hong Wang & De-Zhu Li Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650204, Yunnan, People’s Republic of China (*corresponding author’s e-mail: [email protected]) Received 27 Sep. 2004, revised version received 11 Mar. 2005, accepted 21 June 2005 Xue, C.-Y., Wang, H. & Li, D.-Z. 2005: Microsporogenesis and male gametogenesis in Musella (Musaceae), a monotypic genus from Yunnan, China. — Ann. Bot. Fennici 42: 461–467. Microsporogenesis and male gametogenesis of Musella (Musaceae), a monotypic genus endemic to Yunnan, China, are described for the first time. The anthers are tet- rasporangiate. The formation of the anther wall is of the basic type. The mature anther wall consists of an epidermis, an endothecium, many middle layers and a two-layered glandular tapetum with uninucleate cells. The old anther wall consists of an epidermis with annular and helical thickenings and reduced endothecium. Successive cytokinesis follows meiosis of the microspore mother cell thence forming a T-shaped or isobilat- eral tetrad of microspores. Pollen grains are 2-celled. The generative cell nucleus is clavate in shape. Some special features and relationships between anther structure and pollinator type are discussed. Key words: development, embryology, male gametogenesis, microsporogenesis, Musaceae, Musella Introduction of plants with three genera Musa, Ensete and Musella and some 45–48 species, is restricted The order Zingiberales has long been regarded to the Old World (Cronquist 1981, Andersson in the taxonomic literature as a natural mono- 1998). -
A Multi Gene Sequence-Based Phylogeny of the Musaceae (Banana) Family Pavla Christelová1, Miroslav Valárik1, Eva Hřibová1, Edmond De Langhe2 and Jaroslav Doležel1*
Christelová et al. BMC Evolutionary Biology 2011, 11:103 http://www.biomedcentral.com/1471-2148/11/103 RESEARCHARTICLE Open Access A multi gene sequence-based phylogeny of the Musaceae (banana) family Pavla Christelová1, Miroslav Valárik1, Eva Hřibová1, Edmond De Langhe2 and Jaroslav Doležel1* Abstract Background: The classification of the Musaceae (banana) family species and their phylogenetic inter-relationships remain controversial, in part due to limited nucleotide information to complement the morphological and physiological characters. In this work the evolutionary relationships within the Musaceae family were studied using 13 species and DNA sequences obtained from a set of 19 unlinked nuclear genes. Results: The 19 gene sequences represented a sample of ~16 kb of genome sequence (~73% intronic). The sequence data were also used to obtain estimates for the divergence times of the Musaceae genera and Musa sections. Nucleotide variation within the sample confirmed the close relationship of Australimusa and Callimusa sections and showed that Eumusa and Rhodochlamys sections are not reciprocally monophyletic, which supports the previous claims for the merger between the two latter sections. Divergence time analysis supported the previous dating of the Musaceae crown age to the Cretaceous/Tertiary boundary (~ 69 Mya), and the evolution of Musa to ~50 Mya. The first estimates for the divergence times of the four Musa sections were also obtained. Conclusions: The gene sequence-based phylogeny presented here provides a substantial insight into the course of speciation within the Musaceae. An understanding of the main phylogenetic relationships between banana species will help to fine-tune the taxonomy of Musaceae. Background breeding is hampered by the absence of sexual repro- The global annual production of bananas and plantains duction and narrow genetic basis. -
Enset in Ethiopia: a Poorly Characterized but Resilient Starch Staple Heada=Headb=Heada=Headb/Heada Headb=Headc=Headb=Headc/Headb James S
BList1=SubBList1=BList1=SubBList BList1=SubBList3=BList1=SubBList2 Annals of Botany XX: 1–20, 2019 SubBList1=SubSubBList3=SubBList1=SubSubBList2 doi: 10.1093/aob/mcy214, available online at www.academic.oup.com/aob SubSubBList3=SubBList=SubSubBList=SubBList SubSubBList2=SubBList=SubSubBList=SubBList SubBList2=BList=SubBList=BList REVIEW Downloaded from https://academic.oup.com/aob/advance-article-abstract/doi/10.1093/aob/mcy214/5303834 by University of Leicester user on 31 January 2019 Keywords=Keywords=Keywords_First=Keywords Keywords=HeadA=Keywords_Last=HeadA Enset in Ethiopia: a poorly characterized but resilient starch staple HeadA=HeadB=HeadA=HeadB/HeadA HeadB=HeadC=HeadB=HeadC/HeadB James S. Borrell1,*, Manosh K. Biswas2, Mark Goodwin2,†, Guy Blomme3, Trude Schwarzacher2, HeadC=HeadD=HeadC=HeadD/HeadC J. S. (Pat) Heslop-Harrison2, Abebe M. Wendawek4, Admas Berhanu5, Simon Kallow6,7, Steven Janssens8, Extract3=HeadA=Extract1=HeadA Ermias L. Molla9, Aaron P. Davis1, Feleke Woldeyes10, Kathy Willis1,11, Sebsebe Demissew1,9,12 and CORI_HeadA=CORI_HeadB=CORI_HeadA=CORI_HeadB/HeadA Paul Wilkin1 CORI_HeadB=CORI_HeadC=CORI_HeadB=CORI_HeadC/HeadB 1Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK, 2Department of Genetics and Genome Biology, University of CORI_HeadC=CORI_HeadD=CORI_HeadC=CORI_HeadD/HeadC Leicester, LE1 7RH, UK, 3Bioversity International, c/o ILRI, PO Box 5689, Addis Ababa, Ethiopia, 4Department of Biology, CORI_Extract3=CORI_HeadA=CORI_Extract1=CORI_HeadA Hawassa University, Hawassa, Ethiopia, 5Department of Biology -
Phlogeny and Biogeography of the Prayer Plant Family Linda M
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 51 2006 Phlogeny and Biogeography of the Prayer Plant Family Linda M. Prince Rancho Santa Ana Botanic Garden W. John Kress Smithsonian Institution Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Prince, Linda M. and Kress, W. John (2006) "Phlogeny and Biogeography of the Prayer Plant Family," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 51. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/51 Aliso 22, pp. 645-659 © 2006, Rancho Santa Ana Botanic Garden PHYLOGENY AND BIOGEOGRAPHY OF THE PRAYER PLANT FAMILY: GETTING TO THE ROOT PROBLEM IN MARANTACEAE 1 3 2 LINDA M. PRINCE • AND W. JOHN KRESS 1Rancho Santa Ana Botanic Garden, 1500 North College Avenue, Claremont, California 91711-3157, USA; 2National Museum of Natural History, Department of Botany, MRC-166, Smithsonian Institution, Washington, D.C. 20013-7012, USA 3Corresponding author ([email protected]) ABSTRACT Marantaceae are the second largest family in the order Zingiberales, with approximately 31 genera and 535 species. Earlier studies based on morphological and molecular characters could not confidently determine the relationships among major lineages of the family, nor could they identify the basal branch of the family tree. Phylogenetic analyses of DNA sequence data from all three genomic com partments (chloroplast: matK, ndhF, rbcL, rps16 intron, and trnL-trnF intergenic spacer; mitochon drion: cox!; nucleus: ITS region and the 5'-end of 26S) for a restricted set of taxa were conducted under parsimony criteria to define the root node and to assess geographical distribution patterns.