Carnivorous Plants with Hybrid Trapping Strategies
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Carnivorous Plant Newsletter Vol 47 No 1 March 2018
What’s new in the world of carnivorous plants – Summary of two symposia held in July 2017 Simon Poppinga • Albert-Ludwigs-Universität Freiburg • Germany • simon.poppinga@ biologie.uni-freiburg.de Firman Alamsyah • Ctech Labs and Indonesian Carnivorous Plant Community • Indonesia Ulrike Bauer • University of Bristol • UK Andreas Fleischmann • Botanische Staatssammlung München • Germany Martin Horstmann • University of Bochum • Germany Saskia Klink • University of Bayreuth • Germany Sebastian Kruppert • University of Bochum • Germany Qianshi Lin • University of British Columbia • Canada Ulrike Müller • California State University Fresno • USA Amanda Northrop • University of Vermont • USA Bartosz J. Płachno • Jagiellonian University in Kraków • Poland Anneke Prins • Middlesex University • UK Mathias Scharmann • ETH Zürich • Switzerland Dagmara Sirová • University of South Bohemia • Czech Republic Laura Skates • University of Western Australia • Australia Anna Westermeier • Albert-Ludwigs-Universität Freiburg • Germany Aaron M. Ellison • Harvard Forest • USA • [email protected] Dozens of scientific papers about carnivorous plant research are published each year on diverse topics ranging from new species descriptions, through phylogenetic approaches in taxonomy and systematics, to ecology and evolution of botanical carnivory, biomechanics and physiology of traps, among many others. By the time a paper is published, however, it is already “old news” because the salient results often are presented months or even years earlier at scientific conferences. Such meetings are the perfect venues to discuss ongoing research and “hot” topics and present them to colleagues from around the world. The first and last authors of this report were in the lucky situation to organize symposia about carnivorous plant biology during two major conferences: Simon Poppinga chaired a one-day ses- sion—“Carnivorous plants - Physiology, ecology, and evolution”—on July 6, 2017, as part of the Annual Main Meeting of the Society for Experimental Biology (SEB) in Gothenburg, Sweden. -
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. -
FLORA from FĂRĂGĂU AREA (MUREŞ COUNTY) AS POTENTIAL SOURCE of MEDICINAL PLANTS Silvia OROIAN1*, Mihaela SĂMĂRGHIŢAN2
ISSN: 2601 – 6141, ISSN-L: 2601 – 6141 Acta Biologica Marisiensis 2018, 1(1): 60-70 ORIGINAL PAPER FLORA FROM FĂRĂGĂU AREA (MUREŞ COUNTY) AS POTENTIAL SOURCE OF MEDICINAL PLANTS Silvia OROIAN1*, Mihaela SĂMĂRGHIŢAN2 1Department of Pharmaceutical Botany, University of Medicine and Pharmacy of Tîrgu Mureş, Romania 2Mureş County Museum, Department of Natural Sciences, Tîrgu Mureş, Romania *Correspondence: Silvia OROIAN [email protected] Received: 2 July 2018; Accepted: 9 July 2018; Published: 15 July 2018 Abstract The aim of this study was to identify a potential source of medicinal plant from Transylvanian Plain. Also, the paper provides information about the hayfields floral richness, a great scientific value for Romania and Europe. The study of the flora was carried out in several stages: 2005-2008, 2013, 2017-2018. In the studied area, 397 taxa were identified, distributed in 82 families with therapeutic potential, represented by 164 medical taxa, 37 of them being in the European Pharmacopoeia 8.5. The study reveals that most plants contain: volatile oils (13.41%), tannins (12.19%), flavonoids (9.75%), mucilages (8.53%) etc. This plants can be used in the treatment of various human disorders: disorders of the digestive system, respiratory system, skin disorders, muscular and skeletal systems, genitourinary system, in gynaecological disorders, cardiovascular, and central nervous sistem disorders. In the study plants protected by law at European and national level were identified: Echium maculatum, Cephalaria radiata, Crambe tataria, Narcissus poeticus ssp. radiiflorus, Salvia nutans, Iris aphylla, Orchis morio, Orchis tridentata, Adonis vernalis, Dictamnus albus, Hammarbya paludosa etc. Keywords: Fărăgău, medicinal plants, human disease, Mureş County 1. -
Evaluating the Adaptive Evolutionary Convergence of Carnivorous Plant Taxa Through Functional Genomics
Evaluating the adaptive evolutionary convergence of carnivorous plant taxa through functional genomics Gregory L. Wheeler and Bryan C. Carstens Department of Evolution, Ecology, & Organismal Biology, The Ohio State University, Columbus, OH, United States of America ABSTRACT Carnivorous plants are striking examples of evolutionary convergence, displaying complex and often highly similar adaptations despite lack of shared ancestry. Using available carnivorous plant genomes along with non-carnivorous reference taxa, this study examines the convergence of functional overrepresentation of genes previously implicated in plant carnivory. Gene Ontology (GO) coding was used to quantitatively score functional representation in these taxa, in terms of proportion of carnivory- associated functions relative to all functional sequence. Statistical analysis revealed that, in carnivorous plants as a group, only two of the 24 functions tested showed a signal of substantial overrepresentation. However, when the four carnivorous taxa were analyzed individually, 11 functions were found to be significant in at least one taxon. Though carnivorous plants collectively may show overrepresentation in functions from the predicted set, the specific functions that are overrepresented vary substantially from taxon to taxon. While it is possible that some functions serve a similar practical purpose such that one taxon does not need to utilize both to achieve the same result, it appears that there are multiple approaches for the evolution of carnivorous function in plant genomes. Our approach could be applied to tests of functional convergence in other systems provided on the availability of genomes and annotation data for a group. Submitted 27 October 2017 Accepted 13 January 2018 Subjects Bioinformatics, Evolutionary Studies, Genomics, Plant Science Published 31 January 2018 Keywords Carnivorous plants, Gene Ontology, Functional genomics, Convergent evolution Corresponding author Gregory L. -
Deletion of Cephalotus Follicularis from Appendix II
Prop. 11.6 CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA A. PROPOSAL Deletion of Cephalotus follicularis from Appendix II. B. PROPONENT Commonwealth of Australia (Environment Australia) C. SUPPORTING STATEMENT The monotypic genus Cephalotus is an insectivorous plant endemic to south western Australia. It occurs on wetland margins throughout the southwest corner of Western Australia. This portion of Western Australia has a high rainfall and as a result there are extensive areas of suitable habitat, especially on the south coastal plain. Within its range are large areas of government owned forests, National Parks and other reserves where the species is common and is likely to occur in vast numbers. The species is easily propagated from small segments of rhizomes and, as a result, it is commonly traded and is widely cultivated. Morphological variation in wild populations is not evident. As the species is easily propagated, it is unlikely that cultivated stocks are derived from wild collections. Cephalotus follicularis has been identified by the CITES Plants Committee under the Ten Year Review as a candidate for deletion from Appendix II as there has been no recorded trade in wild taken specimens since the species was listed. The proposal received full endorsement of the 5th meeting of the CITES Plants Committee in Mexico, May 1994. 1. Taxonomy 1.1. Class Magnoliatae 1.2. Order Rosales 1.3. Family Cephalotaceae 1.4. Genus/species Cephalotus follicularis Labillardière 1806 1.5. Common name Western Australian pitcher plant; Albany pitcher plant 2. Biological data 2.1. Distribution The area of distribution ranges over 400 km from NW to SE and corresponds with the meso- mediterranean climate of the extreme south western part of Australia. -
The Miniature Genome of a Carnivorous Plant Genlisea Aurea
Leushkin et al. BMC Genomics 2013, 14:476 http://www.biomedcentral.com/1471-2164/14/476 RESEARCH ARTICLE Open Access The miniature genome of a carnivorous plant Genlisea aurea contains a low number of genes and short non-coding sequences Evgeny V Leushkin1,2, Roman A Sutormin1, Elena R Nabieva1, Aleksey A Penin1,2,3, Alexey S Kondrashov1,4 and Maria D Logacheva1,5* Abstract Background: Genlisea aurea (Lentibulariaceae) is a carnivorous plant with unusually small genome size - 63.6 Mb – one of the smallest known among higher plants. Data on the genome sizes and the phylogeny of Genlisea suggest that this is a derived state within the genus. Thus, G. aurea is an excellent model organism for studying evolutionary mechanisms of genome contraction. Results: Here we report sequencing and de novo draft assembly of G. aurea genome. The assembly consists of 10,687 contigs of the total length of 43.4 Mb and includes 17,755 complete and partial protein-coding genes. Its comparison with the genome of Mimulus guttatus, another representative of higher core Lamiales clade, reveals striking differences in gene content and length of non-coding regions. Conclusions: Genome contraction was a complex process, which involved gene loss and reduction of lengths of introns and intergenic regions, but not intron loss. The gene loss is more frequent for the genes that belong to multigenic families indicating that genetic redundancy is an important prerequisite for genome size reduction. Keywords: Genome reduction, Carnivorous plant, Intron, Intergenic region Background evolutionary and functional points of view. In a model In spite of the similarity of basic cellular processes in eu- plant species, Arabidopsis thaliana, number of protein- karyotes, their genome sizes are extraordinarily variable. -
Giant Cephalotus of Unknown Origins
Giant Cephalotus of unknown origins Dick Chan • P.O. Box 2252 • Pasadena • California 91102 • USA • [email protected] Introduction I have been growing Cephalotus follicularis for over 20 years. Initially, I was obsessed with grow- ing specimen-type Cephalotus of different clones and to prove once-and-for-all that this was not a difficult plant to grow. Countless plants have met their demise as I experimented with various meth- ods of cultivation. For those that have survived and flourished, I noticed one plant in particular that grew larger, more vigorous, and had a different pitcher/leaf morphology than Cephalotus ‘Hummer’s Giant’ and the typical Cephalotus. However, I do not believe this plant to be just a better-grown speci- men of ‘Hummer’s Giant’. Through the years, I have given and sold this plant to individuals calling it the “Bubble Giant”, however, I have not received nor heard any feedback as to the well-being of those plants. So, for those reading this article and have received this plant from me, I would appreciate seeing some photos. For the remainder of this article, this plant will be referred to as the “unknown”. Origins During my initial spark-of-entry into the hobby, I started collecting Cephalotus cuttings, plants, stems, and leaves from anyone who had the plant and was willing to give or sell a piece to me. Be- cause of that activity, this plant is of an unknown origin because of the feverish pace by which I went about amassing what I had hoped would become a genetically diverse collection of plants. -
Testing Darwin's Hypothesis About The
vol. 193, no. 2 the american naturalist february 2019 Natural History Note Testing Darwin’s Hypothesis about the Wonderful Venus Flytrap: Marginal Spikes Form a “Horrid q1 Prison” for Moderate-Sized Insect Prey Alexander L. Davis,1 Matthew H. Babb,1 Matthew C. Lowe,1 Adam T. Yeh,1 Brandon T. Lee,1 and Christopher H. Martin1,2,* 1. Department of Biology, University of North Carolina, Chapel Hill, North Carolina 27599; 2. Department of Integrative Biology and Museum of Vertebrate Zoology, University of California, Berkeley, California 94720 Submitted May 8, 2018; Accepted September 24, 2018; Electronically published Month XX, 2018 Dryad data: https://dx.doi.org/10.5061/dryad.h8401kn. abstract: Botanical carnivory is a novel feeding strategy associated providing new ecological opportunities (Wainwright et al. with numerous physiological and morphological adaptations. How- 2012; Maia et al. 2013; Martin and Wainwright 2013; Stroud ever, the benefits of these novel carnivorous traits are rarely tested. and Losos 2016). Despite the importance of these traits, our We used field observations, lab experiments, and a seminatural ex- understanding of the adaptive value of novel structures is of- periment to test prey capture function of the marginal spikes on snap ten assumed and rarely directly tested. Frequently, this is be- traps of the Venus flytrap (Dionaea muscipula). Our field and labora- cause it is difficult or impossible to manipulate the trait with- fi tory results suggested inef cient capture success: fewer than one in four out impairing organismal function in an unintended way; prey encounters led to prey capture. Removing the marginal spikes de- creased the rate of prey capture success for moderate-sized cricket prey however, many carnivorous plant traits do not present this by 90%, but this effect disappeared for larger prey. -
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. -
Assessing Genetic Diversity for the USA Endemic Carnivorous Plant Pinguicula Ionantha R.K. Godfrey (Lentibulariaceae)
Conserv Genet (2017) 18:171–180 DOI 10.1007/s10592-016-0891-9 RESEARCH ARTICLE Assessing genetic diversity for the USA endemic carnivorous plant Pinguicula ionantha R.K. Godfrey (Lentibulariaceae) 1 1 2 3 David N. Zaya • Brenda Molano-Flores • Mary Ann Feist • Jason A. Koontz • Janice Coons4 Received: 10 May 2016 / Accepted: 30 September 2016 / Published online: 18 October 2016 Ó Springer Science+Business Media Dordrecht 2016 Abstract Understanding patterns of genetic diversity and data; the dominant cluster at each site corresponded to the population structure for rare, narrowly endemic plant spe- results from PCoA and Nei’s genetic distance analyses. cies, such as Pinguicula ionantha (Godfrey’s butterwort; The observed patterns of genetic diversity suggest that Lentibulariaceae), informs conservation goals and can although P. ionantha populations are isolated spatially by directly affect management decisions. Pinguicula ionantha distance and both natural and anthropogenic barriers, some is a federally listed species endemic to the Florida Pan- gene flow occurs among them or isolation has been too handle in the southeastern USA. The main goal of our recent to leave a genetic signature. The relatively low level study was to assess patterns of genetic diversity and of genetic diversity associated with this species is a con- structure in 17 P. ionantha populations, and to determine if cern as it may impair fitness and evolutionary capability in diversity is associated with geographic location or popu- a changing environment. The results of this study provide lation characteristics. We scored 240 individuals at a total the foundation for the development of management prac- of 899 AFLP markers (893 polymorphic markers). -
Nepenthes Argentii Philippines, N. Aristo
BLUMEA 42 (1997) 1-106 A skeletal revision of Nepenthes (Nepenthaceae) Matthew Jebb & Martin Chee k Summary A skeletal world revision of the genus is presented to accompany a family account forFlora Malesi- ana. 82 species are recognised, of which 74 occur in the Malesiana region. Six species are described is raised from and five restored from as new, one species infraspecific status, species are synonymy. Many names are typified for the first time. Three widespread, or locally abundant hybrids are also included. Full descriptions are given for new (6) or recircumscribed (7) species, and emended descrip- Critical for all the Little tions of species are given where necessary (9). notes are given species. known and excluded species are discussed. An index to all published species names and an index of exsiccatae is given. Introduction Macfarlane A world revision of Nepenthes was last undertaken by (1908), and a re- Malesiana the gional revision forthe Flora area (excluding Philippines) was completed of this is to a skeletal revision, cover- by Danser (1928). The purpose paper provide issues which would be in the ing relating to Nepenthes taxonomy inappropriate text of Flora Malesiana.For the majority of species, only the original citation and that in Danser (1928) and laterpublications is given, since Danser's (1928) work provides a thorough and accurate reference to all earlier literature. 74 species are recognised in the region, and three naturally occurring hybrids are also covered for the Flora account. The hybrids N. x hookeriana Lindl. and N. x tri- chocarpa Miq. are found in Sumatra, Peninsular Malaysia and Borneo, although rare within populations, their widespread distribution necessitates their inclusion in the and other and with the of Flora. -
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]