Exploring Carnivorous Plant Habitats Based on Images from Social Media
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"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
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. -
Colchicine Induction of Tetraploid and Octaploid Drosera Strains from D. Rotundifolia and D. Anglica
© 2021 The Japan Mendel Society Cytologia 86(1): 21–28 Colchicine Induction of Tetraploid and Octaploid Drosera Strains from D. rotundifolia and D. anglica Yoshikazu Hoshi1*, Yuki Homan1 and Takahiro Katogi2 1 Department of Plant Science, School of Agriculture, Tokai University, 9–1–1 Toroku, Higashi-ku, Kumamoto 862–8652, Japan 2 Graduate School of Agriculture, Tokai University, 9–1–1 Toroku, Higashi-ku, Kumamoto 862–8652, Japan Received September 21, 2020; accepted October 15, 2020 Summary Artificial tetraploid and octaploid strains were induced from the wild species of Drosera rotundifolia (2n=2x=20) and D. anglica (2n=4x=40), respectively. The optimal condition of colchicine-treatments for poly- ploid inductions was determined first. A flow cytometry (FCM) analysis showed that the highest mixoploid score of D. rotundifolia was 20% in the treatment of 0.3% for 2 days (d), or 0.5% for 3 d, while the highest mixoploid score of D. anglica was 20% in the treatment of 0.5% for 2 d. Next, to remove chimeric cells, adventitious bud inductions were carried out using the FCM-selected individuals in both species. One strain from a total of 360 colchicine-treated leaf explants in each species had pure chromosome-double numbers of 2n=40 (tetraploid) in D. rotundifolia and 2n=80 (octaploid) in D. anglica. In both species, the guard cell sizes of the chromosome- doubled strains were larger than those of the wild types. The leaves of the chromosome-doubled strains of D. ro- tundifolia were larger than those of the wild diploid D. rotundifolia, while the leaves of the chromosome-doubled strains of D. -
Carnivorous Plant Responses to Resource Availability
Carnivorous plant responses to resource availability: environmental interactions, morphology and biochemistry Christopher R. Hatcher A doctoral thesis submitted in partial fulfilment of requirements for the award of Doctor of Philosophy of Loughborough University November 2019 © by Christopher R. Hatcher (2019) Abstract Understanding how organisms respond to resources available in the environment is a fundamental goal of ecology. Resource availability controls ecological processes at all levels of organisation, from molecular characteristics of individuals to community and biosphere. Climate change and other anthropogenically driven factors are altering environmental resource availability, and likely affects ecology at all levels of organisation. It is critical, therefore, to understand the ecological impact of environmental variation at a range of spatial and temporal scales. Consequently, I bring physiological, ecological, biochemical and evolutionary research together to determine how plants respond to resource availability. In this thesis I have measured the effects of resource availability on phenotypic plasticity, intraspecific trait variation and metabolic responses of carnivorous sundew plants. Carnivorous plants are interesting model systems for a range of evolutionary and ecological questions because of their specific adaptations to attaining nutrients. They can, therefore, provide interesting perspectives on existing questions, in this case trait-environment interactions, plant strategies and plant responses to predicted future environmental scenarios. In a manipulative experiment, I measured the phenotypic plasticity of naturally shaded Drosera rotundifolia in response to disturbance mediated changes in light availability over successive growing seasons. Following selective disturbance, D. rotundifolia became more carnivorous by increasing the number of trichomes and trichome density. These plants derived more N from prey and flowered earlier. -
Drosera Intermedia in a Northern Michigan Bog
Assessment of microhabitat differences between Drosera rotundifolia and Drosera intermedia in a northern Michigan bog Andrew David University of Michigan Biological Station EEB 381, General Ecology August 19, 2010 Professor Cathy Bach Abstract The purpose of this study was to investigate microhabitat differences between two species of sundews, Drosera rotundifolia and Drosera intermedia. I tested several hypotheses: D. rotundifolia density increases with increasing height above a fixed low point, while D. intermedia density decreases with height; D. rotundifolia grows primarily on red Sphagnum moss, while D. intermedia grows primarily on green Sphagnum; the densities of both Drosera species increase with decreasing pH; the density of neither Drosera species is affected by water conductivity or dissolved oxygen content. At Mud Lake Bog in Cheboygan County, Michigan, I recorded the species of Drosera plants, as well as the height of the plants above a fixed low point and the color of Sphagnum moss on which they were growing. I also measured the pH, conductivity, and dissolved oxygen content of the water in which the plants were growing. Densities of both Drosera species decreased with increasing height, though the trend was stronger for D. intermedia. D. rotundifolia grew significantly more on red Sphagnum than did D. intermedia, while D. intermedia grew significantly more on green Sphagnum than did D. rotundifolia. D. rotundifolia density varied significantly with neither pH, conductivity, nor dissolved oxygen. D. intermedia density increased significantly with decreasing pH and increasing conductivity, but not with dissolved oxygen. My results were consistent with past research, and conclusively illustrated the differences in microhabitat preferences between the two Drosera species. -
National List of Vascular Plant Species That Occur in Wetlands 1996
National List of Vascular Plant Species that Occur in Wetlands: 1996 National Summary Indicator by Region and Subregion Scientific Name/ North North Central South Inter- National Subregion Northeast Southeast Central Plains Plains Plains Southwest mountain Northwest California Alaska Caribbean Hawaii Indicator Range Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes FACU FACU UPL UPL,FACU Abies balsamea (L.) P. Mill. FAC FACW FAC,FACW Abies concolor (Gord. & Glend.) Lindl. ex Hildebr. NI NI NI NI NI UPL UPL Abies fraseri (Pursh) Poir. FACU FACU FACU Abies grandis (Dougl. ex D. Don) Lindl. FACU-* NI FACU-* Abies lasiocarpa (Hook.) Nutt. NI NI FACU+ FACU- FACU FAC UPL UPL,FAC Abies magnifica A. Murr. NI UPL NI FACU UPL,FACU Abildgaardia ovata (Burm. f.) Kral FACW+ FAC+ FAC+,FACW+ Abutilon theophrasti Medik. UPL FACU- FACU- UPL UPL UPL UPL UPL NI NI UPL,FACU- Acacia choriophylla Benth. FAC* FAC* Acacia farnesiana (L.) Willd. FACU NI NI* NI NI FACU Acacia greggii Gray UPL UPL FACU FACU UPL,FACU Acacia macracantha Humb. & Bonpl. ex Willd. NI FAC FAC Acacia minuta ssp. minuta (M.E. Jones) Beauchamp FACU FACU Acaena exigua Gray OBL OBL Acalypha bisetosa Bertol. ex Spreng. FACW FACW Acalypha virginica L. FACU- FACU- FAC- FACU- FACU- FACU* FACU-,FAC- Acalypha virginica var. rhomboidea (Raf.) Cooperrider FACU- FAC- FACU FACU- FACU- FACU* FACU-,FAC- Acanthocereus tetragonus (L.) Humm. FAC* NI NI FAC* Acanthomintha ilicifolia (Gray) Gray FAC* FAC* Acanthus ebracteatus Vahl OBL OBL Acer circinatum Pursh FAC- FAC NI FAC-,FAC Acer glabrum Torr. FAC FAC FAC FACU FACU* FAC FACU FACU*,FAC Acer grandidentatum Nutt. -
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. -
Species Accounts
Species accounts The list of species that follows is a synthesis of all the botanical knowledge currently available on the Nyika Plateau flora. It does not claim to be the final word in taxonomic opinion for every plant group, but will provide a sound basis for future work by botanists, phytogeographers, and reserve managers. It should also serve as a comprehensive plant guide for interested visitors to the two Nyika National Parks. By far the largest body of information was obtained from the following nine publications: • Flora zambesiaca (current ed. G. Pope, 1960 to present) • Flora of Tropical East Africa (current ed. H. Beentje, 1952 to present) • Plants collected by the Vernay Nyasaland Expedition of 1946 (Brenan & collaborators 1953, 1954) • Wye College 1972 Malawi Project Final Report (Brummitt 1973) • Resource inventory and management plan for the Nyika National Park (Mill 1979) • The forest vegetation of the Nyika Plateau: ecological and phenological studies (Dowsett-Lemaire 1985) • Biosearch Nyika Expedition 1997 report (Patel 1999) • Biosearch Nyika Expedition 2001 report (Patel & Overton 2002) • Evergreen forest flora of Malawi (White, Dowsett-Lemaire & Chapman 2001) We also consulted numerous papers dealing with specific families or genera and, finally, included the collections made during the SABONET Nyika Expedition. In addition, botanists from K and PRE provided valuable input in particular plant groups. Much of the descriptive material is taken directly from one or more of the works listed above, including information regarding habitat and distribution. A single illustration accompanies each genus; two illustrations are sometimes included in large genera with a wide morphological variance (for example, Lobelia). -
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] -
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. -
Southern Gulf, Queensland
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
Delete Darlingtonia Californica from Appendix II
Prop. 11.11 CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II Proposals resulting from reviews by the Plants Committees A. Proposal Delete Darlingtonia californica from Appendix II. B. Proponent Swiss Confederation. C. Supporting Statement 1. Taxonomy 1.1 Class: Dicotyledonae 1.2 Order: Nepenthales 1.3 Family: Sarraceniaceae 1.4 Genus: Darlingtonia 1.4.1: Species: Darlingtonia californica Torrey 1.5 Scientific synonyms: 1.6 Common names: English: California pitcherplant, cobra lily French: Spanish: 1.7 Code numbers: 2. Biological Parameters 2.1 Distribution USA, West Coast, from Oregon to North California on a 160 km long strip between Roseburg (Oregon) and Santa Rosa (California). Along the coast, it appears in northern Curry County and extends north sporadically to Sandlake in Tillamook County. 2.2 Habitat availability From sea level to 2800 m. 2.3 Population status In the center of its range from Del Norte-Trinity-Shasta-Siskiyou County (California) to Curry & Josephine County (Oregon) this species is rather abundant. It is not uncommon throughout this area to find several colonies numbering between 1000-3000 specimens with abundant habitat for expansion and few threats to their survival because many locations are very difficult to access (Rondeau, pers.comm. to von Arx, 1999). At the southern limit of its range in Nevada County it is quite abundant and grows on remote sites; while in 3 nearby Counties (Butte, Plumas and Sierra) it has never been abundant, and it is now scattered and diminishing due to the combined effects of logging and succession into other vegetation types. Prop. 11.11 – p.