Literature DB >> 21159782

Traps of carnivorous pitcher plants as a habitat: composition of the fluid, biodiversity and mutualistic activities.

Wolfram Adlassnig1, Marianne Peroutka, Thomas Lendl.   

Abstract

BACKGROUND: Carnivorous pitcher plants (CPPs) use cone-shaped leaves to trap animals for nutrient supply but are not able to kill all intruders of their traps. Numerous species, ranging from bacteria to vertrebrates, survive and propagate in the otherwise deadly traps. This paper reviews the literature on phytotelmata of CPPs. PITCHER: Fluid as a Habitat The volumes of pitchers range from 0·2 mL to 1·5 L. In Nepenthes and Cephalotus, the fluid is secreted by the trap; the other genera collect rain water. The fluid is usually acidic, rich in O(2) and contains digestive enzymes. In some taxa, toxins or detergents are found, or the fluid is extremely viscous. In Heliamphora or Sarracenia, the fluid differs little from pure water. INQUILINE: Diversity Pitcher inquilines comprise bacteria, protozoa, algae, fungi, rotifers, crustaceans, arachnids, insects and amphibia. The dominant groups are protists and Dipteran larvae. The various species of CPPs host different sets of inquilines. Sarracenia purpurea hosts up to 165 species of inquilines, followed by Nepenthes ampullaria with 59 species, compared with only three species from Brocchinia reducta. Reasons for these differences include size, the life span of the pitcher as well as its fluid. MUTUALISTIC: Activities Inquilines closely interact with their host. Some live as parasites, but the vast majority are mutualists. Beneficial activities include secretion of enzymes, feeding on the plant's prey and successive excretion of inorganic nutrients, mechanical break up of the prey, removal of excessive prey and assimilation of atmospheric N(2).
CONCLUSIONS: There is strong evidence that CPPs influence their phytotelm. Two strategies can be distinguished: (1) Nepenthes and Cephalotus produce acidic, toxic or digestive fluids and host a limited diversity of inquilines. (2) Genera without efficient enzymes such as Sarracenia or Heliamphora host diverse organisms and depend to a large extent on their symbionts for prey utilization.

Entities:  

Mesh:

Year:  2010        PMID: 21159782      PMCID: PMC3025736          DOI: 10.1093/aob/mcq238

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  36 in total

1.  Enzymes from carnivorous plants (nepenthes). Isolation of the protease nepenthacin.

Authors:  J Jentsch
Journal:  FEBS Lett       Date:  1972-04-01       Impact factor: 4.124

Review 2.  Nutrient limitation and stoichiometry of carnivorous plants.

Authors:  A M Ellison
Journal:  Plant Biol (Stuttg)       Date:  2006-11       Impact factor: 3.081

3.  Signal transduction in the carnivorous plant Sarracenia purpurea. Regulation of secretory hydrolase expression during development and in response to resources.

Authors:  D R Gallie; S C Chang
Journal:  Plant Physiol       Date:  1997-12       Impact factor: 8.340

4.  Aspartic proteinases are expressed in pitchers of the carnivorous plant Nepenthes alata Blanco.

Authors:  Chung-Il An; Ei-ichiro Fukusaki; Akio Kobayashi
Journal:  Planta       Date:  2001-10-16       Impact factor: 4.116

5.  Nepenthes insignis uses a C2-portion of the carbon skeleton of L-alanine acquired via its carnivorous organs, to build up the allelochemical plumbagin.

Authors:  Heiko Rischer; Andreas Hamm; Gerhard Bringmann
Journal:  Phytochemistry       Date:  2002-03       Impact factor: 4.072

6.  [Investigations on the physiology of the glands of carnivorous plants : IV. The kinetics of chloride secretion by the gland tissue of Nepenthes].

Authors:  U Lüttge
Journal:  Planta       Date:  1966-03       Impact factor: 4.116

7.  Oxygen concentrations inside the traps of the carnivorous plants Utricularia and Genlisea (Lentibulariaceae).

Authors:  Lubomír Adamec
Journal:  Ann Bot       Date:  2007-08-23       Impact factor: 4.357

8.  Harmless nectar source or deadly trap: Nepenthes pitchers are activated by rain, condensation and nectar.

Authors:  Ulrike Bauer; Holger F Bohn; Walter Federle
Journal:  Proc Biol Sci       Date:  2008-02-07       Impact factor: 5.349

9.  Trap geometry in three giant montane pitcher plant species from Borneo is a function of tree shrew body size.

Authors:  Lijin Chin; Jonathan A Moran; Charles Clarke
Journal:  New Phytol       Date:  2010-01-22       Impact factor: 10.151

10.  The pitcher plant Sarracenia purpurea can directly acquire organic nitrogen and short-circuit the inorganic nitrogen cycle.

Authors:  Jim D Karagatzides; Jessica L Butler; Aaron M Ellison
Journal:  PLoS One       Date:  2009-07-07       Impact factor: 3.240

View more
  38 in total

Review 1.  Quite a few reasons for calling carnivores 'the most wonderful plants in the world'.

Authors:  Elzbieta Król; Bartosz J Płachno; Lubomír Adamec; Maria Stolarz; Halina Dziubińska; Kazimierz Trebacz
Journal:  Ann Bot       Date:  2011-09-21       Impact factor: 4.357

Review 2.  A novel insight into the cost-benefit model for the evolution of botanical carnivory.

Authors:  Andrej Pavlovič; Michaela Saganová
Journal:  Ann Bot       Date:  2015-05-06       Impact factor: 4.357

3.  Digestive mutualism in a pitcher plant supports the monotonic rather than hump-shaped stress-gradient hypothesis model.

Authors:  Felicia Wei Shan Leong; Weng Ngai Lam; Hugh Tiang Wah Tan
Journal:  Oecologia       Date:  2019-05-06       Impact factor: 3.225

Review 4.  Profiling the metabolic signals involved in chemical communication between microbes using imaging mass spectrometry.

Authors:  Nikolas M Stasulli; Elizabeth A Shank
Journal:  FEMS Microbiol Rev       Date:  2016-11-01       Impact factor: 16.408

5.  Secreted pitfall-trap fluid of carnivorous Nepenthes plants is unsuitable for microbial growth.

Authors:  Franziska Buch; Matthias Rott; Sandy Rottloff; Christian Paetz; Ines Hilke; Michael Raessler; Axel Mithöfer
Journal:  Ann Bot       Date:  2012-12-21       Impact factor: 4.357

6.  Environmental proteomics reveals taxonomic and functional changes in an enriched aquatic ecosystem.

Authors:  Amanda C Northrop; Rachel Brooks; Aaron M Ellison; Nicholas J Gotelli; Bryan A Ballif
Journal:  Ecosphere       Date:  2017-10-06       Impact factor: 3.171

7.  Proteome analysis of digestive fluids in Nepenthes pitchers.

Authors:  Sandy Rottloff; Sissi Miguel; Flore Biteau; Estelle Nisse; Philippe Hammann; Lauriane Kuhn; Johana Chicher; Vincent Bazile; Laurence Gaume; Benoit Mignard; Alain Hehn; Frédéric Bourgaud
Journal:  Ann Bot       Date:  2016-03       Impact factor: 4.357

8.  Regulation of Hydrolytic Enzyme Activity in Aquatic Microbial Communities Hosted by Carnivorous Pitcher Plants.

Authors:  Erica B Young; Jessica Sielicki; Jacob J Grothjan
Journal:  Microb Ecol       Date:  2018-04-20       Impact factor: 4.552

9.  Dipteran larvae and microbes facilitate nutrient sequestration in the Nepenthes gracilis pitcher plant host.

Authors:  Weng Ngai Lam; Kwek Yan Chong; Ganesh S Anand; Hugh Tiang Wah Tan
Journal:  Biol Lett       Date:  2017-03       Impact factor: 3.703

10.  Structural and functional characteristics of S-like ribonucleases from carnivorous plants.

Authors:  Emi Nishimura; Shinya Jumyo; Naoki Arai; Kensuke Kanna; Marina Kume; Jun-ichi Nishikawa; Jun-ichi Tanase; Takashi Ohyama
Journal:  Planta       Date:  2014-04-26       Impact factor: 4.116

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.