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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. -
Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae
OPEN ACCESS JCTS Article SERIES B Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae R.W. Sanders and T.C. Wood Core Academy of Science, Dayton, TN Abstract The morphological adaptations of carnivorous plants and taxonomic distributions of those adaptations are reviewed, as are the conflicting classifications of the plants based on the adaptations, reproductive morphology, and DNA sequences. To begin developing a creationist understanding of the origin of plant carnivory, we here focus specifically on pitcher plants of Nepenthaceae and Sarraceniaceae because their popularity as cultivated curiosities has generated a literature resource amenable to baraminological analysis. Hybridization records were augmented by total nucleotide differences to assess species similarities. Nonhybridizing species falling within the molecular range of hybridizing species were included in the monobaramin of the hybridizing species. The combined data support each of the three genera of the Sarraceniaceae as a monobaramin, but the three could not be combined into a larger monobaramin. With the Nepenthaceae, the data unequivocally place 73% of the species in a single monobaramin, strongly suggesting the whole genus (and, thus, family) is a monobaramin. The lack of variation in the carnivorous habit provides no evidence for the intrabaraminic origin of carnivory from non-carnivorous plants. An array of fascinating symbiotic relationships of pitchers in some species with unusual bacteria, insects, and vertebrates are known and suggest the origin of carnivory from benign functions of the adaptive structures. However, these symbioses still do not account for the apparent complex design for carnivory characteristic of all species in the two families. Editor: J.W. -
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. -
Effects of Poaching, Habitat Destruction, and Climate Change on Nepenthes
Effects of Poaching, Habitat Destruction, and Climate Change On Nepenthes Lucas Barron 4/27/19 Effects of Poaching, Habitat Destruction, and Climate Change On Nepenthes Lucas Barron; 4/27/2018 1 Effects of Poaching, Habitat Destruction, and Climate Change On Nepenthes When Dominick Gravine, and avid Nepenthes collector and seller, visited Borneo in March of 2013 to trek up the slopes of mount Trusmadi, he not only saw the endangered Nepenthes species that inhabit the misty slopes, but also the effects of the rapid urbanization of the local villages. He saw ‘palm oil plantations as far as the eye Dominick Gravine and his collection of Nepenthes can see.’ (-Gravine). “Palm oil plantations completely clear the land of its natural biodiversity.’ (-Gravine). “While in the local villages, I was offered many plants which were obviously taken from the wild. The locals see these plants as a source of money. The over collect and sell them to collectors.” (-Gravine) While climbing the mountains, he saw many seed stalks cut of many plants from people along the trails, which has a large impact on these plants’ ability to reproduce. Habitat destruction and excessive poaching is having a severe Nepenthes Veitchii 'Candy Dreams'; created by Dominick Gravine effect on plant species not only in places like Borneo, but also worldwide. Although many people deny human caused endangerment of plant species due to excessive poaching, reckless destruction of habitats globally, and climate change, Effects of Poaching, Habitat Destruction, and Climate Change On Nepenthes Lucas Barron; 4/27/2018 2 has a profound, and rather severe, effect on plant species globally, but especially in extremely delicate regions of the world, such as the Indonesian islands. -
Carnivorous Plant Newsletter of Australia
Volume 6 September, 1980. Registered as a Publication, Category B. Page 6 CPNA Page 1 EDITORS, : : : : KEN HATLEY. SUSAN HATLEY. CORRESPONDENCE ADDRESSED TO : C.P.N.A. Wandena Rd, B~allsbrook East. West Australia. 6084. Published Quarterly by C.P.N.A. Subscriptions $6-OO Annually. Back copies issued to late subscribers. ........................................................................... FROM THE EDITORS. We would like to start this issue with an apology for its late arrival to you. Unfortunately, we experienced an unexpected delay in the arrival of replacment parts for the copying equipment. The good news this issue is of course that spring is upon us again, and with it the regrowth of our dormant varieties ready to come forward and show off their beauty for yet another year. The response for articles for the newsletter is dissappointing to say the least. There is enough experienced c.p. growers in Australia capable of contributing write-ups to ensure the success of the CPNA for many years to come, but if the lack of interest continues the newsletter is doomed to failure. To put it bluntly, if you want your newsletter to continue then get behind it and give it your support. Good Growing, Editors. ........................................................................... ........................................................................... FRONT COVER - DROSERA GLANDULIGERA, HABITAT WEST AUSTRALIA. Vol 6 CPNA Page 2 C.P. LETTERBOX. Received a letter from Mrs I.D. Anderson of 23 Harrow St, Launceston, Tasmania 7250 asking of other members in Tasmania. As we don't now publish a list of subscribers we leave it to any member in her area to drop a line and swap C.P. -
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. -
Phylogeny and Biogeography of the Carnivorous Plant Family Droseraceae with Representative Drosera Species From
F1000Research 2017, 6:1454 Last updated: 10 AUG 2021 RESEARCH ARTICLE Phylogeny and biogeography of the carnivorous plant family Droseraceae with representative Drosera species from Northeast India [version 1; peer review: 1 approved, 1 not approved] Devendra Kumar Biswal 1, Sureni Yanthan2, Ruchishree Konhar 1, Manish Debnath 1, Suman Kumaria 2, Pramod Tandon2,3 1Bioinformatics Centre, North-Eastern Hill University, Shillong, Meghalaya, 793022, India 2Department of Botany, North-Eastern Hill University, Shillong, Meghalaya, 793022, India 3Biotech Park, Jankipuram, Uttar Pradesh, 226001, India v1 First published: 14 Aug 2017, 6:1454 Open Peer Review https://doi.org/10.12688/f1000research.12049.1 Latest published: 14 Aug 2017, 6:1454 https://doi.org/10.12688/f1000research.12049.1 Reviewer Status Invited Reviewers Abstract Background: Botanical carnivory is spread across four major 1 2 angiosperm lineages and five orders: Poales, Caryophyllales, Oxalidales, Ericales and Lamiales. The carnivorous plant family version 1 Droseraceae is well known for its wide range of representatives in the 14 Aug 2017 report report temperate zone. Taxonomically, it is regarded as one of the most problematic and unresolved carnivorous plant families. In the present 1. Andreas Fleischmann, Ludwig-Maximilians- study, the phylogenetic position and biogeographic analysis of the genus Drosera is revisited by taking two species from the genus Universität München, Munich, Germany Drosera (D. burmanii and D. Peltata) found in Meghalaya (Northeast 2. Lingaraj Sahoo, Indian Institute of India). Methods: The purposes of this study were to investigate the Technology Guwahati (IIT Guwahati) , monophyly, reconstruct phylogenetic relationships and ancestral area Guwahati, India of the genus Drosera, and to infer its origin and dispersal using molecular markers from the whole ITS (18S, 28S, ITS1, ITS2) region Any reports and responses or comments on the and ribulose bisphosphate carboxylase (rbcL) sequences. -
Carnivorous Plants with Hybrid Trapping Strategies
CARNIVOROUS PLANTS WITH HYBRID TRAPPING STRATEGIES BARRY RICE • P.O. Box 72741 • Davis, CA 95617 • USA • [email protected] Keywords: carnivory: Darlingtonia californica, Drosophyllum lusitanicum, Nepenthes ampullaria, N. inermis, Sarracenia psittacina. Recently I wrote a general book on carnivorous plants, and while creating that work I spent a great deal of time pondering some of the bigger issues within the phenomenon of carnivory in plants. One of the basic decisions I had to make was select what plants to include in my book. Even at the genus level, it is not at all trivial to produce a definitive list of all the carnivorous plants. Seventeen plant genera are commonly accused of being carnivorous, but not everyone agrees on their dietary classifications—arguments about the status of Roridula can result in fistfights!1 Recent discoveries within the indisputably carnivorous genera are adding to this quandary. Nepenthes lowii might function to capture excrement from birds (Clarke 1997), and Nepenthes ampullaria might be at least partly vegetarian in using its clusters of ground pitchers to capture the dead vegetable mate- rial that rains onto the forest floor (Moran et al. 2003). There is also research that suggests that the primary function of Utricularia purpurea bladders may be unrelated to carnivory (Richards 2001). Could it be that not all Drosera, Nepenthes, Sarracenia, or Utricularia are carnivorous? Meanwhile, should we take a closer look at Stylidium, Dipsacus, and others? What, really, are the carnivorous plants? Part of this problem comes from the very foundation of how we think of carnivorous plants. When drafting introductory papers or book chapters, we usually frequently oversimplify the strategies that carnivorous plants use to capture prey. -
TREE November 2001.Qxd
Review TRENDS in Ecology & Evolution Vol.16 No.11 November 2001 623 Evolutionary ecology of carnivorous plants Aaron M. Ellison and Nicholas J. Gotelli After more than a century of being regarded as botanical oddities, carnivorous populations, elucidating how changes in fitness affect plants have emerged as model systems that are appropriate for addressing a population dynamics. As with other groups of plants, wide array of ecological and evolutionary questions. Now that reliable such as mangroves7 and alpine plants8 that exhibit molecular phylogenies are available for many carnivorous plants, they can be broad evolutionary convergence because of strong used to study convergences and divergences in ecophysiology and life-history selection in stressful habitats, detailed investigations strategies. Cost–benefit models and demographic analysis can provide insight of carnivorous plants at multiple biological scales can into the selective forces promoting carnivory. Important areas for future illustrate clearly the importance of ecological research include the assessment of the interaction between nutrient processes in determining evolutionary patterns. availability and drought tolerance among carnivorous plants, as well as measurements of spatial and temporal variability in microhabitat Phylogenetic diversity among carnivorous plants characteristics that might constrain plant growth and fitness. In addition to Phylogenetic relationships among carnivorous plants addressing evolutionary convergence, such studies must take into account have been obscured by reliance on morphological the evolutionary diversity of carnivorous plants and their wide variety of life characters1 that show a high degree of similarity and forms and habitats. Finally, carnivorous plants have suffered from historical evolutionary convergence among carnivorous taxa9 overcollection, and their habitats are vanishing rapidly. -
Of the Pitcher Plants Nepenthes Mirabilis, Cephalotus Follicularis and Darlingtonia Californica
Oecologia (1997) 112:464±471 Ó Springer-Verlag 1997 W. Schulze á E.D. Schulze á J.S. Pate á A.N. Gillison The nitrogen supply from soils and insects during growth of the pitcher plants Nepenthes mirabilis, Cephalotus follicularis and Darlingtonia californica Received: 14 April 1997 / Accepted: 18 August 1997 Abstract This study investigated the nitrogen (N) ac- were assessed across a developmental sequence from quisition from soil and insect capture during the growth young plants lacking pitchers to large adults with up to of three species of pitcher plants, Nepenthes mirabilis, 38 pitchers. The data indicated dependence on soil Cephalotus follicularis and Darlingtonia californica. N until 4 pitchers had opened. Beyond that stage, 15N/14N natural abundance ratios (d15N) of plants and plant size increased with the number of catching pitchers pitchers of dierent age, non-carnivorous reference but the fraction of soil N remained high. Large plants, and insect prey were used to estimate propor- Cephalotus plants were estimated to derive 26 5.9% tional contributions of insects to the N content of leaves (mean SD of the three largest plants; range: 19±30%) and whole plants. Young Nepenthes leaves (phyllodes) of the N from insects. In Cephalotus we observed an carrying closed pitchers comprised major sinks for N increased d15N value in sink versus source pitchers of and developed mainly from insect N captured elsewhere about 1.2& on average. Source and sink pitchers of on the plant. Their d15N values of up to 7.2& were Darlingtonia had a similar d15N value, but plant N in higher than the average d15N value of captured insects this species showed d15N signals closer to that of insect (mean d15N value = 5.3&). -
Phylogeny and Biogeography of South American Marsh Pitcher Plant Genus Heliamphora (Sarraceniaceae) Endemic to the Guiana Highlands
bioRxiv preprint doi: https://doi.org/10.1101/2020.04.29.068395; this version posted April 30, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Phylogeny and Biogeography of South American Marsh Pitcher Plant Genus Heliamphora (Sarraceniaceae) Endemic to the Guiana Highlands Sukuan Liu and Stacey D. Smith Author for correspondence: Sukuan Liu, [email protected] Department of Ecology and Evolutionary Biology, University of Colorado Boulder, 1900 Pleasant Street, Boulder, Colorado 80309, U.S.A. Abstract: Heliamphora is a genus of carnivorous pitcher plants endemic to the Guiana Highlands with fragmented distributions. We presented a well resolved, time-calibrated, and nearly comprehensive Heliamphora phylogeny estimated using Bayesian inference and maximum likelihood based on nuclear genes (26S, ITS, and PHYC) and secondary calibration. We used stochastic mapping to infer ancestral states of morphological characters and ecological traits. Our ancestral state estimations revealed that the pitcher drainage structures characteristic of the genus transformed from a hole to a slit in single clade, while other features (scape pubescence and hammock-like growth) have been gained and lost multiple times. Habitat was similarly labile in Heliamphora, with multiple transitions from the ancestral highland habitats into the lowlands. Using Mantel test, we found closely related species tend to be geographically closely distributed. Placing our phylogeny in a historical context, major clades likely emerged through both vicariance and dispersal during Miocene with more recent diversification driven by vertical displacement during the Pleistocene glacial-interglacial thermal oscillations. -
The Plant-Ant Camponotus Schmitzi Helps Its Carnivorous Host-Plant Nepenthes Bicalcarata to Catch Its Prey
Journal of Tropical Ecology (2011) 27:15–24. Copyright © Cambridge University Press 2010 doi:10.1017/S0266467410000532 The plant-ant Camponotus schmitzi helps its carnivorous host-plant Nepenthes bicalcarata to catch its prey Vincent Bonhomme∗, Isabelle Gounand∗, Christine Alaux∗, Emmanuelle Jousselin†, Daniel Barthel´ emy´ ∗ and Laurence Gaume∗ ∗ Universite´ Montpellier II, CNRS, INRA, UMR AMAP: Botanique et Bioinformatique de l’Architecture des Plantes, CIRAD – TA A51/PS2 Boulevard de la Lironde, F-34398 Montpellier Cedex 5, France † INRA, UMR CBGP, Campus International de Baillarguet, CS 30016, 34988 Montferrier-sur-Lez, France (Accepted 24 August 2010) Abstract: The Bornean climber, Nepenthes bicalcarata, is unique among plants because it is both carnivorous and myrmecophytic, bearing pitcher-shaped leaves and the ant Camponotus schmitzi within tendrils. We explored, in the peat swamp forests of Brunei, the hypothesis that these ants contribute to plant nutrition by catching and digesting its prey.Wefirsttestedwhetherantsincreasedplant’scapturerate.Wefoundthatunlikemostplant-ants,C.schmitzidonot exhibit dissuasive leaf-patrolling behaviour (zero patrol on 67 pitchers of 10 plants) but lie concealed under pitcher rim (13 ± 6 ants per pitcher) allowing numerous insect visits. However, 47 out of 50 individuals of the largest visitor dropped into the pitchers of five plants were attacked by ants and the capture rate of the same pitchers deprived of their ambush hunting ants decreased three-fold. We then tested whether ants participated in plant’s digestion. We showed in a 15-d long experiment that ants fed on prey and returned it in pieces in seven out of eight pitchers. The 40 prey deposited in ant-deprived pitchers remained intact indicating a weak digestive power of the fluid confirmed to be only weakly acidic (pH ∼5, n = 67).