Literature DB >> 3860070

A natural toxic defense system: cardenolides in butterflies versus birds.

L P Brower, L S Fink.   

Abstract

We have verified that wild birds can become conditioned to reject naturally toxic insects either visually (experiment 1) or by taste (experiment 2). We have also verified, however, that unconditioned taste rejection of noxious chemicals by wild birds also occurs (experiment 3). Such unconditioned responses to the aposematic visual and taste cues of many insects, in fact, often appear to be as important as, or more important than, conditioned responses. In a large number of laboratory feeding experiments with wild birds as predators of aposematic insects, initial and/or long-term rejection occurs without prior laboratory conditioning experience. Although in some experiments the birds may have previously been exposed to (and therefore perhaps conditioned by) the aposematic prey in the wild, other experiments have used naive birds or insects whose ranges do not overlap those of the birds. Wiklund and Jarvi, for example, tested the response of 47 naive hand-raised birds of four species to five aposematic insect species, and found that 69/136 (51%) insects were rejected visually without even tasting, while 63 were tasted and then rejected. Only four of the insects were actually ingested. Similarly, in Bowers' study of the response of Massachusetts blue jays to aposematic western U.S. Euphydryas butterflies, several blue jays consistently rejected the butterflies visually or by taste without having eaten any. While these studies were not designed to separate neophobic effects from innate visual and/or taste aversions, they do differentiate between conditioned and unconditioned responses. Since both conditioned and unconditioned rejections can be demonstrated in the lab by insectivorous birds, and our available field evidence does not yet let us distinguish the mechanisms behind the observed patterns, our initial question, of the relative importance of conditioned versus unconditioned rejection mechanisms in different natural situations, is not yet answerable. The most important requirement of a food-rejection strategy is that it prevents both poisoning and starvation. We have shown, however, that rejection of a noxious insect by a bird can take place at four distinct levels (visual, non-destructive taste sampling, destructive taste sampling, or post-ingestional physiological rejection), the first three of which may be either unconditioned or conditioned by a physiological reaction to ingestion.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 3860070     DOI: 10.1111/j.1749-6632.1985.tb27072.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  10 in total

1.  What toxicity may result from ingestion of the plant pictured below? Answer: cardioactive steroid toxicity from common milkweed.

Authors:  Nicholas S Simpson; Jon B Cole; Heather Ellsworth
Journal:  J Med Toxicol       Date:  2013-09

2.  Uptake and sequestration of ouabain and other cardiac glycosides inDanaus plexippus (Lepidoptera: Danaidae): Evidence for a carrier-mediated process.

Authors:  C Frick; M Wink
Journal:  J Chem Ecol       Date:  1995-05       Impact factor: 2.626

3.  Disentangling taste and toxicity in aposematic prey.

Authors:  Øistein Haugsten Holen
Journal:  Proc Biol Sci       Date:  2012-12-19       Impact factor: 5.349

4.  Sequestration of host plant glucosinolates in the defensive hemolymph of the sawfly Athalia rosae.

Authors:  C Müller; N Agerbirk; C E Olsen; J L Boevé; U Schaffner; P M Brakefield
Journal:  J Chem Ecol       Date:  2001-12       Impact factor: 2.626

5.  Effectiveness of cardenolides as feeding deterrents toPeromyscus mice.

Authors:  J I Glendinning
Journal:  J Chem Ecol       Date:  1992-09       Impact factor: 2.626

6.  Comparative unpalatability of mimetic viceroy butterflies (Limenitis archippus) from four south-eastern United States populations.

Authors:  David B Ritland
Journal:  Oecologia       Date:  1995-08       Impact factor: 3.225

7.  Cardenolide connection between overwintering monarch butterflies from Mexico and their larval food plant,Asclepias syriaca.

Authors:  J N Seiber; L P Brower; S M Lee; M M McChesney; H T Cheung; C J Nelson; T R Watson
Journal:  J Chem Ecol       Date:  1986-05       Impact factor: 2.626

8.  Mediation of cardiac glycoside insensitivity in the monarch butterfly (Danaus plexippus): Role of an amino acid substitution in the ouabain binding site of Na(+),K (+)-ATPase.

Authors:  F Holzinger; M Wink
Journal:  J Chem Ecol       Date:  1996-10       Impact factor: 2.626

Review 9.  Defence mitigation by predators of chemically defended prey integrated over the predation sequence and across biological levels with a focus on cardiotonic steroids.

Authors:  Shabnam Mohammadi; Lu Yang; Matthew Bulbert; Hannah M Rowland
Journal:  R Soc Open Sci       Date:  2022-09-07       Impact factor: 3.653

10.  Predators of monarch butterfly eggs and neonate larvae are more diverse than previously recognised.

Authors:  Sara L Hermann; Carissa Blackledge; Nathan L Haan; Andrew T Myers; Douglas A Landis
Journal:  Sci Rep       Date:  2019-10-04       Impact factor: 4.379

  10 in total

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