Investigating Adaptation and Competition in Carnivorous Plants
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Reports Ecological Analyses of Relationships Between Essen- and Frost 1991, Ellison and Gotelli 2002)
Ecology, 86(7), 2005, pp. 1737±1743 q 2005 by the Ecological Society of America PREY ADDITION ALTERS NUTRIENT STOICHIOMETRY OF THE CARNIVOROUS PLANT SARRACENIA PURPUREA AMY E. WAKEFIELD,1 NICHOLAS J. GOTELLI,1,3 SARAH E. WITTMAN,1 AND AARON M. ELLISON2 1University of Vermont, Burlington, Vermont 05405 USA 2Harvard University, Harvard Forest, P.O. Box 68, Petersham, Massachusetts 01366 USA Abstract. The carnivorous pitcher plant Sarracenia purpurea receives nutrients from both captured prey and atmospheric deposition, making it a good subject for the study of ecological stoichiometry and nutrient limitation. We added prey in a manipulative ®eld experiment and measured nutrient accumulation in pitcher-plant tissue and pitcher liquid, as well as changes in plant morphology, growth, and photosynthetic rate. Prey addition had no effect on traditional measures of nutrient limitation (leaf morphology, growth, or pho- tosynthetic rate). However, stoichiometric measures of nutrient limitation were affected, as the concentration of both N and P in the leaf tissue increased with the addition of prey. Pitcher ¯uid pH and nitrate concentration did not vary among treatments, although dissolved oxygen levels decreased and ammonia levels increased with prey addition. Ratios of N:P, N:K, and K:P in pitcher-plant tissues suggest that prey additions shifted these carnivorous plants from P limitation under ambient conditions to N limitation with the addition of prey. Key words: carnivorous plants; ®eld experiment; K:P ratio; N:K ratio; N:P ratio; nitrogen; nutrient limitation; phosphorus; Sarracenia purpurea; stoichiometry. INTRODUCTION many species alter production or morphology of car- nivorous organs in response to nutrient input (Knight Reports Ecological analyses of relationships between essen- and Frost 1991, Ellison and Gotelli 2002). -
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. -
A New Carnivorous Plant Lineage (Triantha) with a Unique Sticky-Inflorescence Trap
A new carnivorous plant lineage (Triantha) with a unique sticky-inflorescence trap Qianshi Lina,b,1, Cécile Anéc,d, Thomas J. Givnishc, and Sean W. Grahama,b aDepartment of Botany, University of British Columbia, Vancouver, BC V6T 1Z4, Canada; bUBC Botanical Garden, University of British Columbia, Vancouver, BC V6T 1Z4, Canada; cDepartment of Botany, University of Wisconsin–Madison, Madison, WI 53706; and dDepartment of Statistics, University of Wisconsin–Madison, Madison WI 53706 Edited by Elizabeth A. Kellogg, Donald Danforth Plant Science Center, St. Louis, MO, and approved June 5, 2021 (received for review October 30, 2020) Carnivorous plants consume animals for mineral nutrients that and in wetlands, including bogs, marly shorelines, and calcareous enhance growth and reproduction in nutrient-poor environments. spring-fed fens. In bogs, T. occidentalis is commonly found with Here, we report that Triantha occidentalis (Tofieldiaceae) represents recognized carnivorous plants such as Drosera rotundifolia a previously overlooked carnivorous lineage that captures insects on (Droseraceae) and Pinguicula vulgaris (Lentibulariaceae). During sticky inflorescences. Field experiments, isotopic data, and mixing the summer flowering season, T. occidentalis produces leafless models demonstrate significant N transfer from prey to Triantha, erect flowering stems up to 80 cm tall (12). These scapes have with an estimated 64% of leaf N obtained from prey capture in sticky glandular hairs, especially on their upper portions, a feature previous years, comparable to levels inferred for the cooccurring distinguishing Triantha from other genera of Tofieldiaceae round-leaved sundew, a recognized carnivore. N obtained via carnivory (Fig. 1). Small insects are often found trapped by these hairs; is exported from the inflorescence and developing fruits and may herbarium specimens are frequently covered in insects (Fig. -
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. -
The Microbial Phyllogeography of the Carnivorous Plant Sarracenia Alata
Microb Ecol (2011) 61:750–758 DOI 10.1007/s00248-011-9832-9 PLANT MICROBE INTERACTIONS The Microbial Phyllogeography of the Carnivorous Plant Sarracenia alata Margaret M. Koopman & Bryan C. Carstens Received: 6 November 2010 /Accepted: 15 February 2011 /Published online: 24 March 2011 # Springer Science+Business Media, LLC 2011 Abstract Carnivorous pitcher plants host diverse microbial Introduction communities. This plant–microbe association provides a unique opportunity to investigate the evolutionary process- The integration of ecosystem genetics, phylogenetics, and es that influence the spatial diversity of microbial commu- community ecology has provided important insights into nities. Using next-generation sequencing of environmental the diversity, assembly, evolution, and functionality of samples, we surveyed microbial communities from 29 communities [1–5]. By exploring ecosystems in an evolu- pitcher plants (Sarracenia alata) and compare community tionary framework, investigators can measure genetic composition with plant genetic diversity in order to interactions across variable temporal and spatial scales explore the influence of historical processes on the and gain insight into fundamental processes such as food population structure of each lineage. Analyses reveal web dynamics and nutrient cycling [1, 3, 4]. Studies that there is a core S. alata microbiome, and that it is integrating these fields initially focused on the genetics of similar in composition to animal gut microfaunas. The plant species that supply a variety of important resources spatial structure of community composition in S. alata and environmental structure to other organisms in the (phyllogeography) is congruent at the deepest level with ecosystem [6]. An intriguing extension of these studies, the dominant features of the landscape, including the and an important opportunity for community geneticists, is Mississippi river and the discrete habitat boundaries that to further investigate community level responses to host– the plants occupy. -
Spring 2014 for Web.Pub
Spring 2014 Page 1 Botanic Garden News The Botanic Garden Volume 17, No. 1 of Smith College Spring 2014 Orchidelirium at Smith Madelaine Zadik K aren Yu ’16 is a STRIDE scholar who has worked with me since 2012 on educational projects and exhibitions at the Botanic Garden. As a first year, Karen learned about the workings of the Botanic Garden, our plant collections, and our various educational activities, including exhibit production. The plan was that by the end of her two-year STRIDE placement, she would produce an exhibit of her own. She had to hit the ground running, as the exhibit Botanical Printing: Artful Collaborations on Paper and Cloth opened just a month and a half after her arrival. Karen wrote label copy and press releases, learned mounting techniques, helped design the gallery layout with our modular walls, and learned how to use our unique hanging system in the Church Exhibition Gallery. For our next exhibit, From Petals to Paper: Poetic Inspiration from Flowers, Karen was involved in the many months of planning leading up to the installation in March 2013. When given a choice of possible exhibit topics for her own project, Karen chose to use a collection of orchid prints by artist Florence Helen Woolward to create an exhibit that would help illuminate the world of orchids for the visiting public. The prints are from Thesaurus Woolwardiae, Orchids of the Marquis of Lothian, which contained reproductions of 60 of Woolward’s orchid paintings. Woolward produced an impressive body of work, especially considering that she was never formally trained in either art or botany. -
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. -
How the Venus Flytrap Kills and Digests Its Prey
How the Venus Flytrap Kills and Digests Its Prey The sensory hairs that detect the presence of an insect are visible within the red lobes of this trap, which belongs to a Venus flytrap, awaiting a meal. Venus flytraps are the speed demons of the plant world. In spite of belonging to a particularly sedate kingdom of organisms, these carnivorous plants snap shut their two-lobed traps in a tenth of a second to capture an insect meal, which they then digest. Just how they do this is not fully understood, but new research is exploring the mechanisms that allow a plant to become a predator. [Giant Plant Eats Rodents] The Venus flytrap turned to carnivory to survive in the nutrient-poor soil of its native habitat in North and South Carolina, in and around the Green Swamp. To get the nutrition it needs, the flytrap lures insects, including ants and flies, into the jaws of its trap. The trap's reddish interior and small nectar-secreting glands along its rim trick the insects into thinking they have found a flower, said Rainer Hedrich, a biophysicist at the University Wuerzburg in Germany. He and colleagues have revealed how hormones play a role in how the plant snaps up and digests its prey. How the flytrap kills Each side of the trap has three to four sensor hairs, each no longer than 0.2 inches (0.5 centimeters). An insect must trip a hair twice or two hairs within 20 seconds for the trap to respond; this allows it to avoid snapping shut on raindrops or other false alarms. -
Aldrovanda Vesiculosa: Friend Or Foe?
Waterwheel Aldrovanda vesiculosa: Friend or Foe? By Chris Doyle, CLM Restoring Balance. Enhancing Beauty. April 7, 2016 Waterwheel Aldrovanda vesiculosa • Perennial, Free-floating, Rootless Herbaceous Aquatic Plant • Although it looks like a bladderwort: − Family: Droseraceae (sundews) − Most common: The Venus Flytrap (Dionaea muscipula) • Carnivorous • Rare, worldwide • Documented in NJ • 2012 Description • Simple or sparsely-branched Stem – Stem is air-filled to aid in floatation – Stem length varies between four to 20 cm long • Whorls Consist of 4 to 9 Leaves – Up to 23 mm in diameter – Petioles tipped with a single trap (Lamina) Waterwheel Growth • Plant Growth is Strictly Directional • Continual senescence of older whorls at posterior end • Terminal apical bud at anterior end • Maintains near constant length during active growth • Growth Rate is Determined by Many Factors • Biotic, Abiotic, and Water Chemistry Growth and Habitat Factors for Waterwheel Biotic Factors Abiotic Factors • Associated Vegetation • Water Temp. – 30-70% cover is optimal • Water Depth – Bladderworts, Emergent – Minimal for turion overwintering Plants • Irradiance Prey Abundance • – 20% to 60% total sunlight optimal – Zooplankton abundance • pH – 6,000 to 20,000/L optimal – 5.0 to 6.8 seems optimal • Predation • Nutrient Loading • Filamentous algae abundance • Water Chemistry – High free CO2 needed Waterwheel Reproduction • Reduced Capacity to Sexually Reproduce – Typical of most aquatic plants – Sporadic/unpredictable flower production • Warmer climates = inc. -
Pinguicula Vulgaris L. Butterwortbutterwort, Page
Pinguicula vulgaris L. butterwortbutterwort, Page 1 State Distribution Photo by Susan R. Crispin Best Survey Period Jan Feb Mar Apr May Jun Jul Aug Sept Oct Nov Dec Status: State special concern Recognition: Pinguicula vulgaris is a small, herbaceous, insectivorous perennial with rosettes of 3-6 Global and state rank: G5/S3 distinctly yellowish-green leaves. The blunt, oblong- ovate to elliptic leaves, which narrow to the base, range Other common names: common butterwort, bog- to ca. 8 cm in length, curling slightly inward along violet, violet butterwort their upper margins. The upper leaf surface is covered with numerous enzyme-secreting glands that aid in Family: Lentibulariaceae (bladderwort family) the breakdown and digestion of small insects, and give the leaves a sticky-greasy feel when touched. This Range: Butterwort is a circumpolar species ranging slimy, watery surface also serves to attract and capture around the world in temperate and boreal regions. It is insect prey. The spurred purple flowers are solitary of widespread occurrence from Europe through Siberia. on 1.5-12 cm long, leafless peduncles (stalks) and Elsewhere this species occurs in the Arctic from Alaska have a white spot at the mouth. In addition to a well to Canada and East Greenland, extending southward developed basal spur, the flowers have a 3-lobed upper in North America to northeast Minnesota, northwest lip and 2-lobed lower lip, thus superficially resembling a Wisconsin, and through the Lake Superior region east violet. A single rosette may have produce up to three or to New York and New England. It is considered rare more flowering stalks. -
583–584 Angiosperms 583 *Eudicots and Ceratophyllales
583 583 > 583–584 Angiosperms These schedules are extensively revised, having been prepared with little reference to earlier editions. 583 *Eudicots and Ceratophyllales Subdivisions are added for eudicots and Ceratophyllales together, for eudicots alone Class here angiosperms (flowering plants), core eudicots For monocots, basal angiosperms, Chloranthales, magnoliids, see 584 See Manual at 583–585 vs. 600; also at 583–584; also at 583 vs. 582.13 .176 98 Mangrove swamp ecology Number built according to instructions under 583–588 Class here comprehensive works on mangroves For mangroves of a specific order or family, see the order or family, e.g., mangroves of family Combretaceae 583.73 .2 *Ceratophyllales Class here Ceratophyllaceae Class here hornworts > 583.3–583.9 Eudicots Class comprehensive works in 583 .3 *Ranunculales, Sabiaceae, Proteales, Trochodendrales, Buxales .34 *Ranunculales Including Berberidaceae, Eupteleaceae, Menispermaceae, Ranunculaceae Including aconites, anemones, barberries, buttercups, Christmas roses, clematises, columbines, delphiniums, hellebores, larkspurs, lesser celandine, mandrake, mayapple, mayflower, monkshoods, moonseeds, wolfsbanes For Fumariaceae, Papaveraceae, Pteridophyllaceae, see 583.35 See also 583.9593 for mandrakes of family Solanaceae .35 *Fumariaceae, Papaveraceae, Pteridophyllaceae Including bleeding hearts, bloodroot, celandines, Dutchman’s breeches, fumitories, poppies See also 583.34 for lesser celandine .37 *Sabiaceae * *Add as instructed under 583–588 1 583 Dewey Decimal Classification -
Snapping Mechanics of the Venus Flytrap (Dionaea Muscipula)
Snapping mechanics of the Venus flytrap (Dionaea muscipula) Renate Sachsea,1,2, Anna Westermeierb,c,1,2, Max Mylob,c, Joey Nadasdid, Manfred Bischoffa, Thomas Speckb,c,e, and Simon Poppingab,e aInstitute for Structural Mechanics, Department of Civil and Environmental Engineering, University of Stuttgart, 70569 Stuttgart, Germany; bPlant Biomechanics Group and Botanic Garden, University of Freiburg, 79104 Freiburg, Germany; cCluster of Excellence livMatS (Living, Adaptive and Energy-autonomous Materials Systems), Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, D-79110 Freiburg, Germany; dGrande Ecole MiM (Master in Management), ESSEC (École Supérieure des Sciences Économiques et Commerciales) Business School, 95021 Cergy-Pontoise, France; and eFreiburg Materials Research Center, University of Freiburg, 79104 Freiburg, Germany Edited by Julian I. Schroeder, Cell and Developmental Biology Section, Division of Biological Sciences, University of California San Diego, La Jolla, CA, and approved May 21, 2020 (received for review February 13, 2020) The mechanical principles for fast snapping in the iconic Venus distribution appears to be approximately linear, which is, as flytrap are not yet fully understood. In this study, we obtained explained below, too coarse to produce finite element (FE) time-resolved strain distributions via three-dimensional digital im- models behaving like the snap-through structures resembling a age correlation (DIC) for the outer and inner trap-lobe surfaces Venus flytrap. Such sudden change from one stable geometric throughout the closing motion. In combination with finite element configuration to another can be best understood by the analysis models, the various possible contributions of the trap tissue layers of equilibrium paths, which are essential for the analysis of the were investigated with respect to the trap’s movement behavior nonlinear deformation behavior of structures, as they allow the and the amount of strain required for snapping.