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Foraging Modes of Carnivorous Plants Aaron M
Israel Journal of Ecology & Evolution, 2020 http://dx.doi.org/10.1163/22244662-20191066 Foraging modes of carnivorous plants Aaron M. Ellison* Harvard Forest, Harvard University, 324 North Main Street, Petersham, Massachusetts, 01366, USA Abstract Carnivorous plants are pure sit-and-wait predators: they remain rooted to a single location and depend on the abundance and movement of their prey to obtain nutrients required for growth and reproduction. Yet carnivorous plants exhibit phenotypically plastic responses to prey availability that parallel those of non-carnivorous plants to changes in light levels or soil-nutrient concentrations. The latter have been considered to be foraging behaviors, but the former have not. Here, I review aspects of foraging theory that can be profitably applied to carnivorous plants considered as sit-and-wait predators. A discussion of different strategies by which carnivorous plants attract, capture, kill, and digest prey, and subsequently acquire nutrients from them suggests that optimal foraging theory can be applied to carnivorous plants as easily as it has been applied to animals. Carnivorous plants can vary their production, placement, and types of traps; switch between capturing nutrients from leaf-derived traps and roots; temporarily activate traps in response to external cues; or cease trap production altogether. Future research on foraging strategies by carnivorous plants will yield new insights into the physiology and ecology of what Darwin called “the most wonderful plants in the world”. At the same time, inclusion of carnivorous plants into models of animal foraging behavior could lead to the development of a more general and taxonomically inclusive foraging theory. -
Status of Insectivorous Plants in Northeast India
Technical Refereed Contribution Status of insectivorous plants in northeast India Praveen Kumar Verma • Shifting Cultivation Division • Rain Forest Research Institute • Sotai Ali • Deovan • Post Box # 136 • Jorhat 785 001 (Assam) • India • [email protected] Jan Schlauer • Zwischenstr. 11 • 60594 Frankfurt/Main • Germany • [email protected] Krishna Kumar Rawat • CSIR-National Botanical Research Institute • Rana Pratap Marg • Lucknow -226 001 (U.P) • India Krishna Giri • Shifting Cultivation Division • Rain Forest Research Institute • Sotai Ali • Deovan • Post Box #136 • Jorhat 785 001 (Assam) • India Keywords: Biogeography, India, diversity, Red List data. Introduction There are approximately 700 identified species of carnivorous plants placed in 15 genera of nine families of dicotyledonous plants (Albert et al. 1992; Ellison & Gotellli 2001; Fleischmann 2012; Rice 2006) (Table 1). In India, a total of five genera of carnivorous plants are reported with 44 species; viz. Utricularia (38 species), Drosera (3), Nepenthes (1), Pinguicula (1), and Aldrovanda (1) (Santapau & Henry 1976; Anonymous 1988; Singh & Sanjappa 2011; Zaman et al. 2011; Kamble et al. 2012). Inter- estingly, northeastern India is the home of all five insectivorous genera, namely Nepenthes (com- monly known as tropical pitcher plant), Drosera (sundew), Utricularia (bladderwort), Aldrovanda (waterwheel plant), and Pinguicula (butterwort) with a total of 21 species. The area also hosts the “ancestral false carnivorous” plant Plumbago zelayanica, often known as murderous plant. Climate Lowland to mid-altitude areas are characterized by subtropical climate (Table 2) with maximum temperatures and maximum precipitation (monsoon) in summer, i.e., May to September (in some places the highest temperatures are reached already in April), and average temperatures usually not dropping below 0°C in winter. -
Descriptive Anatomy and Evolutionary Patterns of Anatomical Diversification in Adenia (Passifloraceae) David J
Aliso: A Journal of Systematic and Evolutionary Botany Volume 27 | Issue 1 Article 3 2009 Descriptive Anatomy and Evolutionary Patterns of Anatomical Diversification in Adenia (Passifloraceae) David J. Hearn University of Arizona, Tucson Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Hearn, David J. (2009) "Descriptive Anatomy and Evolutionary Patterns of Anatomical Diversification in Adenia (Passifloraceae)," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 27: Iss. 1, Article 3. Available at: http://scholarship.claremont.edu/aliso/vol27/iss1/3 Aliso, 27, pp. 13–38 ’ 2009, Rancho Santa Ana Botanic Garden DESCRIPTIVE ANATOMY AND EVOLUTIONARY PATTERNS OF ANATOMICAL DIVERSIFICATION IN ADENIA (PASSIFLORACEAE) DAVID J. HEARN Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, Arizona 85721, USA ([email protected]) ABSTRACT To understand evolutionary patterns and processes that account for anatomical diversity in relation to ecology and life form diversity, anatomy of storage roots and stems of the genus Adenia (Passifloraceae) were analyzed using an explicit phylogenetic context. Over 65,000 measurements are reported for 47 quantitative and qualitative traits from 58 species in the genus. Vestiges of lianous ancestry were apparent throughout the group, as treelets and lianous taxa alike share relatively short, often wide, vessel elements with simple, transverse perforation plates, and alternate lateral wall pitting; fibriform vessel elements, tracheids associated with vessels, and libriform fibers as additional tracheary elements; and well-developed axial parenchyma. Multiple cambial variants were observed, including anomalous parenchyma proliferation, anomalous vascular strands, successive cambia, and a novel type of intraxylary phloem. -
The Terrestrial Carnivorous Plant Utricularia Reniformis Sheds Light on Environmental and Life-Form Genome Plasticity
International Journal of Molecular Sciences Article The Terrestrial Carnivorous Plant Utricularia reniformis Sheds Light on Environmental and Life-Form Genome Plasticity Saura R. Silva 1 , Ana Paula Moraes 2 , Helen A. Penha 1, Maria H. M. Julião 1, Douglas S. Domingues 3, Todd P. Michael 4 , Vitor F. O. Miranda 5,* and Alessandro M. Varani 1,* 1 Departamento de Tecnologia, Faculdade de Ciências Agrárias e Veterinárias, UNESP—Universidade Estadual Paulista, Jaboticabal 14884-900, Brazil; [email protected] (S.R.S.); [email protected] (H.A.P.); [email protected] (M.H.M.J.) 2 Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, São Bernardo do Campo 09606-070, Brazil; [email protected] 3 Departamento de Botânica, Instituto de Biociências, UNESP—Universidade Estadual Paulista, Rio Claro 13506-900, Brazil; [email protected] 4 J. Craig Venter Institute, La Jolla, CA 92037, USA; [email protected] 5 Departamento de Biologia Aplicada à Agropecuária, Faculdade de Ciências Agrárias e Veterinárias, UNESP—Universidade Estadual Paulista, Jaboticabal 14884-900, Brazil * Correspondence: [email protected] (V.F.O.M.); [email protected] (A.M.V.) Received: 23 October 2019; Accepted: 15 December 2019; Published: 18 December 2019 Abstract: Utricularia belongs to Lentibulariaceae, a widespread family of carnivorous plants that possess ultra-small and highly dynamic nuclear genomes. It has been shown that the Lentibulariaceae genomes have been shaped by transposable elements expansion and loss, and multiple rounds of whole-genome duplications (WGD), making the family a platform for evolutionary and comparative genomics studies. To explore the evolution of Utricularia, we estimated the chromosome number and genome size, as well as sequenced the terrestrial bladderwort Utricularia reniformis (2n = 40, 1C = 317.1-Mpb). -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
'Placoderm' (Arthrodira)
Jobbins et al. Swiss J Palaeontol (2021) 140:2 https://doi.org/10.1186/s13358-020-00212-w Swiss Journal of Palaeontology RESEARCH ARTICLE Open Access A large Middle Devonian eubrachythoracid ‘placoderm’ (Arthrodira) jaw from northern Gondwana Melina Jobbins1* , Martin Rücklin2, Thodoris Argyriou3 and Christian Klug1 Abstract For the understanding of the evolution of jawed vertebrates and jaws and teeth, ‘placoderms’ are crucial as they exhibit an impressive morphological disparity associated with the early stages of this process. The Devonian of Morocco is famous for its rich occurrences of arthrodire ‘placoderms’. While Late Devonian strata are rich in arthrodire remains, they are less common in older strata. Here, we describe a large tooth-bearing jaw element of Leptodontich- thys ziregensis gen. et sp. nov., an eubrachythoracid arthrodire from the Middle Devonian of Morocco. This species is based on a large posterior superognathal with a strong dentition. The jawbone displays features considered syna- pomorphies of Late Devonian eubrachythoracid arthrodires, with one posterior and one lateral row of conical teeth oriented postero-lingually. μCT-images reveal internal structures including pulp cavities and dentinous tissues. The posterior orientation of the teeth and the traces of a putative occlusal contact on the lingual side of the bone imply that these teeth were hardly used for feeding. Similar to Compagopiscis and Plourdosteus, functional teeth were pos- sibly present during an earlier developmental stage and have been worn entirely. The morphological features of the jaw element suggest a close relationship with plourdosteids. Its size implies that the animal was rather large. Keywords: Arthrodira, Dentition, Food web, Givetian, Maïder basin, Palaeoecology Introduction important to reconstruct character evolution in early ‘Placoderms’ are considered as a paraphyletic grade vertebrates. -
Carnivorous Plant Newsletter Vol 48 No 3 September 2019
Growing Drosera murfetii Mark S. Anderson • Vancouver • Washington • USA • [email protected] In the few years since Drosera murfetii has become separated from Drosera arcturi as a new species it has become available to growers, though it is certainly not available everywhere. I feel it is sufficiently unusual and interesting to deserve a place in many carnivorous plant collections. I began growing this species several years ago when a generous group of friends gave me a plant, along with an implied “Good luck!” since little was known about its culture. Here are some of my experiences and thoughts about keeping this fascinating species alive and, maybe, thriving. Drosera murfetii is an odd-ball among sundews (Back Cover). With its strange simple-looking leaves with tentacled ends D. murfetii looks like nothing else, other than D. arcturi. It has been called D. arcturi “giant form” before it was given species status. The leaves are spear-shaped with a pro- nounced mid-rib and are sometimes completely without tentacles (Fig. 1). They have a ‘v’-shaped cross section, the two longitudinal sides separating as the leaf develops. Not very sundew- like. What is very much as you would expect is the tentacles. These grow along the upper surface of the leaf from 1/3 to 2/3 of the length farthest from the main plant and extending to the tip. Another strange thing about this species is the tentacles along the edges generally bend around the leaf to the back side of it. An adaptation al- Figure 1: Drosera murfetii. lowing the plant to catch insects crawl- ing up or landing on this side of the leaf? Drosera murfetii plants generally will have fewer leaves than are common with other Drosera and plants with only one leaf, or none, are not uncommon. -
Exploring the Role of Auxin in the Androgynophore Movement in Passiflora
Genetics and Molecular Biology, 38, 3, 301-307 (2015) Copyright © 2015, Sociedade Brasileira de Genética. Printed in Brazil DOI: http://dx.doi.org/10.1590/S1415-475738320140377 Research Article Exploring the role of auxin in the androgynophore movement in Passiflora Livia C.T. Scorza and Marcelo Carnier Dornelas Universidade Estadual de Campinas, Instituto de Biologia, Departamento de Biologia Vegetal, Campinas, SP, Brazil. Abstract The flowers of the species belonging to the genus Passiflora show a range of features that are thought to have arisen as adaptations to different pollinators. Some Passiflora species belonging to the subgenus Decaloba sect. Xerogona, show touch-sensitive motile androgynophores. We tested the role of auxin polar transport in the modula- tion of the androgynophore movement by applying auxin (IAA) or an inhibitor of auxin polar transport (NPA) in the flowers. We recorded the movement of the androgynophore during mechano-stimulation and analyzed the duration, speed, and the angle formed by the androgynophore before and after the movement, and found that both IAA and NPA increase the amplitude of the movement in P. sanguinolenta. We hypothesize that auxin might have a role in modulating the fitness of these Decaloba species to different pollination syndromes and demonstrate that an interspecific hybrid between insect- and hummingbird-pollinated Xerogona species present a heterosis effect on the speed of the androgynophore movement. Keywords: Passiflora, androgynophore, IAA, NPA, thigmotropism. Received: December 18, 2014; Accepted: April 15, 2015. Introduction Recently, we showed that in some Passiflora species, The genus Passiflora comprises about 500 species the androgynophore can also be a thigmotropic structure, which are mostly woody vines that present a huge diversity i.e., it has the capability to move in response to touch and in flower shape, colors and sizes. -
Insectivorous Plants”, He Showed That They Had Adaptations to Capture and Digest Animals
the Strange, the Ugly, and the Bizarre . carnivores, parasites, and mycotrophs . Plant Oddities - Carnivores, Parasites & Mycotrophs Of all the plants, the most bizarre, the least understood, but yet the most interesting are those plants that have unusual modes of nutrient uptake. Carnivore: Nepenthes Plant Oddities - Carnivores, Parasites & Mycotrophs Of all the plants, the most bizarre, the least understood, but yet the most interesting are those plants that have unusual modes of nutrient uptake. Parasite: Rafflesia Plant Oddities - Carnivores, Parasites & Mycotrophs Of all the plants, the most bizarre, the least understood, but yet the most interesting are those plants that have unusual modes of nutrient uptake. Things to focus on for this topic! 1. What are these three types of plants 2. How do they live - selection 3. Systematic distribution in general 4. Systematic challenges or issues 5. Evolutionary pathways - how did they get to what they are Mycotroph: Monotropa Plant Oddities - The Problems Three factors for systematic confusion and controversy 1. the specialized roles often involve reductions or elaborations in both vegetative and floral features — DNA also is reduced or has extremely high rates of change for example – the parasitic Rafflesia Plant Oddities - The Problems Three factors for systematic confusion and controversy 2. their connections to other plants or fungi, or trapping of animals, make these odd plants prone to horizontal gene transfer for example – the parasitic Mitrastema [work by former UW student Tom Kleist] -
New Placoderm Fishes from the Early Devonian B U C H a N G R O U P , E a S T E R N V I C T O R
PROC. R. SOC. VICT. vol. 96, no. 4, 173-186, Decemb er 1984 NEW PLACODERM FISHES FROM THE EARLY DEVONIAN BUCHAN GROUP, EASTERN VICTORIA By J ohn A. L ong Department of G eology, Australian National Universi ty, P.O . Box 4, Canberra, A.C .T. 2601 A bstract : Three new placoderms are described from the McLarty Member of the Murrindal Limestone (Early Devonian, Buchan Group). M urrindalaspis wallacei gen. el sp. nov. is a palae- acanthaspidoid characterized by having a high m edia n dorsal crest and lacking a m edian ventral keel. M. bairdi sp. nov. differs from the type species in having a low median dorsal crest and a median ventral groove. Taem asosteus m aclarliensis sp. nov. differs from the type species T. novaustrocam bricus W hite in the shape of the posterior region of the nuchal plate, the presence of canals between the infranuch al pits and the posterior face o f the nuchal plate, th e shape of the paranuchal plate, and the developm en t of the apronic lam ina of the anterior lateral plate. The placoderm s, A renipiscis westoUi Young, Errolosleus cf. E. goodradigbeensis Young, W ijdeaspis warrooensis Young, are recorded from the Buchan Group indicati ng close sim ilarity to the ichthyofauna of the contem poraneous M urrumbidgee Group, New Sout h W ales. Few fossil fishes have been studied from the Early been described from the Murrumbidgee and Mulga Devonian Buchan Group. M cCoy (1876) described some Downs Groups in New South Wales and the Cravens placoderm plates from this region as Asterolepis ornata Peak Beds in Queensland, with numerous sites yielding var. -
Carnivorous Plant Newsletter Vol 48, No 2, June 2019
Byblis in cultivation in the tropics and in temperate climates Gregory Allan • Birmingham • United Kingdom • [email protected] Cindy Chiang • Singapore • [email protected] This article has been written based mostly on the authors’ experiences in growing Byblis in the UK and in Singapore. It is hoped that growers in regions with different climates will be able to extrapo- late from the information provided here, adjusting the methods described below to suit their own growing conditions. Hopefully much of the information provided here is universal in its application. Introduction If any genus of carnivorous plants deserves to be better known, both by horticulturalists and botanists, it is Byblis. The common name (ironically rarely used by enthusiasts) for the genus is “rainbow plants”, on account of the prismatic effect that can be produced when the sun shines on their copiously-produced sticky glands. All species follow a basic morphological plan: they have a central stem from which radiate numerous filiform leaves and scapes with showy flowers that typi- cally have purple petals (although white forms of most species are known) and vivid yellow anthers. Virtually all parts of the plants are covered in mucilage-tipped stalked glands (colloquially referred to as “tentacles”), which efficiently capture small insects, as well as microscopic sessile digestive glands. Another interesting characteristic of the genus is the presence of pulvini in most, if not all, species. Pulvini are swellings at the base of pedicels which, usually after successful pollination, uti- lize hydraulics to bend the pedicel, and consequently the developing fruit, downwards towards the ground. This phenomenon was discovered by Brian Barnes in the early 21st century. -
Vascular Plant Families of the United States Grouped by Diagnostic Features
Humboldt State University Digital Commons @ Humboldt State University Botanical Studies Open Educational Resources and Data 12-6-2019 Vascular Plant Families of the United States Grouped by Diagnostic Features James P. Smith Jr Humboldt State University, [email protected] Follow this and additional works at: https://digitalcommons.humboldt.edu/botany_jps Part of the Botany Commons Recommended Citation Smith, James P. Jr, "Vascular Plant Families of the United States Grouped by Diagnostic Features" (2019). Botanical Studies. 96. https://digitalcommons.humboldt.edu/botany_jps/96 This Flora of the United States and North America is brought to you for free and open access by the Open Educational Resources and Data at Digital Commons @ Humboldt State University. It has been accepted for inclusion in Botanical Studies by an authorized administrator of Digital Commons @ Humboldt State University. For more information, please contact [email protected]. FLOWERING PLANT FAMILIES OF THE UNITED STATES GROUPED BY DIAGNOSTIC FEATURES James P. Smith, Jr. Professor Emeritus of Botany Department of Biological Sciences Humboldt State University Second edition — 6 December 2019 The focus is on families of plants found in the conterminous United States, including ornamentals. The listing of a family is not meant to imply that every species has that feature. I am using a fewfamily names, such as Liliaceae, Plantaginaceae, and Scrophulariaceae, in the traditional sense, because their limits remain unsettled. Parasitic on branches Dioscoreaceae