Botany Plant Interactions with Insects, Nematodes, Symbionts and Other
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Composition of Extrafloral Nectar Influences Interactions Between the Myrmecophyte Humboldtia Brunonis and Its Ant Associates
J Chem Ecol (2012) 38:88–99 DOI 10.1007/s10886-011-0052-z Composition of Extrafloral Nectar Influences Interactions between the Myrmecophyte Humboldtia brunonis and its Ant Associates Megha Shenoy & Venkatesan Radhika & Suma Satish & Renee M. Borges Received: 30 August 2010 /Revised: 23 November 2011 /Accepted: 11 December 2011 /Published online: 11 January 2012 # Springer Science+Business Media, LLC 2012 Abstract Ant–plant interactions often are mediated by higher sucrose concentrations and certain essential/non-essential extrafloral nectar (EFN) composition that may influence plant amino acid mixtures. The mutualistic Technomyrmex visitation by ants. Over a 300 km range in the Indian Western albipes (southern study site) preferred sucrose over glucose Ghats, we investigated the correlation between the EFN com- or fructose solutions and consumed the leaf EFN mimic to a position of the myrmecophytic ant-plant Humboldtia brunonis greater extent than the floral bud EFN mimic. This young leaf (Fabaceae) and the number and species of ants visiting EFN. EFN mimic had low sugar concentrations, the lowest viscosity EFN composition varied among H. brunonis populations and and sugar:amino acid ratio, was rich in essential amino acids, between plant organs (floral bud vs. young leaf EFN). In and appeared ideally suited to the digestive physiology of T. general, EFN was rich in sugars with small quantities albipes. This preference for young leaf EFN may explain the of amino acids, especially essential amino acids, and had greater protection afforded to young leaves than to floral buds moderate invertase activity. In experiments at the study sites by T. albipes, and may also help to resolve ant–pollinator with sugar and amino acid solutions and with leaf or conflicts. -
Predation Success by a Plant-Ant Indirectly
Predation success by a plant-ant indirectly favours the growth and fitness of its host myrmecophyte Alain Dejean, Jérôme Orivel, Vivien Rossi, Olivier Roux, Jérémie Lauth, Pierre-Jean G. Malé, Régis Céréghino, Céline Leroy To cite this version: Alain Dejean, Jérôme Orivel, Vivien Rossi, Olivier Roux, Jérémie Lauth, et al.. Predation success by a plant-ant indirectly favours the growth and fitness of its host myrmecophyte. PLoS ONE, Public Library of Science, 2013, vol. 8 (3), pp. 1-6. 10.1371/journal.pone.0059405. hal-00913754 HAL Id: hal-00913754 https://hal.archives-ouvertes.fr/hal-00913754 Submitted on 4 Dec 2013 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License Open Archive TOULOUSE Archive Ouverte (OATAO) OATAO is an open access repository that collects the work of Toulouse researchers and makes it freely available over the web where possible. This is an author-deposited version published in : http://oatao.univ-toulouse.fr/ Eprints ID : 10202 To link to this article : DOI:10.1371/journal.pone.0059405 URL : http://dx.doi.org/10.1371/journal.pone.0059405 To cite this version : Dejean, Alain and Orivel, Jérôme and Rossi, Vivien and Roux, Olivier and Lauth, Jérémie and Malé, Pierre-Jean G. -
Macaranga-Ant Plants Optimize Investment in Biotic Defence
Journal of Experimental Botany, Vol. 52, No. 363, Plants under Stress Special Issue, pp. 2057–2065, October 2001 Adaptations to biotic and abiotic stress: Macaranga-ant plants optimize investment in biotic defence K. Eduard Linsenmair1,5, Martin Heil1,4, Werner M. Kaiser2, Brigitte Fiala1, Thomas Koch3 and Wilhelm Boland3 1 Lehrstuhl fu¨ r Tiero¨ kologie und Tropenbiologie (Zoologie III), Theodor-Boveri-Institut, Biozentrum, Am Hubland, D-97074 Wu¨ rzburg, Germany 2 Lehrstuhl fu¨ r Molekulare Pflanzenphysiologie und Biophysik (Botanik I), Julius-von-Sachs-Institut, Julius-von-Sachs-Platz 2, D-97082 Wu¨ rzburg, Germany 3 Max-Planck-Institut fu¨ r chemische O¨ kologie, Carl Zeiss-Promenade 10, D-07745 Jena, Germany Received 12 February 2001; Accepted 21 June 2001 Abstract incurred when counterbalanced by defensive effects of mutualistic insects. Obligate ant plants (myrmecophytes) in the genus Macaranga produce energy- and nutrient-rich food Key words: Ant plant, anti-herbivore defence, mutualism, bodies (FBs) to nourish mutualistic ants which live myrmecophyte, tropics. inside the plants. These defend their host against biotic stress caused by herbivores and pathogens. Facultative, ‘myrmecophilic’ interactions are based on the provision of FBs anduor extrafloral nectar Introduction (EFN) to defending insects that are attracted from the vicinity. FB production by the myrmecophyte, Many tropical plants of different taxonomic groups M. triloba, was limited by soil nutrient content under have evolved mutualisms with ants (Beattie, 1985; field conditions and was regulated according to the Buckley, 1982; Ho¨lldobler and Wilson, 1990; McKey presence or absence of an ant colony. However, and Davidson, 1993). In most cases, ants are used as an increased FB production promoted growth of the indirect (Price et al., 1980), ‘biotic’ defence mechanism. -
Diversity of Ant-Plant Interactions: Protective Efficacy in Macaranga Species with Different De,Grees of Ant Association
Oecologia (1994) 97: 186-192 ("' Springer-Verlag 1994 Brigitte Fiala " Harald Grunsky . Ulrich Maschwitz K. Eduard Linsenmair Diversity of ant-plant interactions: protective efficacy in Macaranga species with different de,grees of ant association Received: 9 June 1993/ Accepted: 20 November 1993 Abstract The pioneer tree Macaranga in SE Asia has dence for any specific relationships. The results of this developed manyfold associations with ants. The genus study strongly support the hypothesis that non-specific, comprises all stages of interaction with ants, from facul facultative associations with ants can be advantageous tative relationships to obligate myrmecophytes. Only for Macaranga plants. Food bodies appear to have low myrmecophytic Macaranga offer nesting space for ants er attractive value for opportunistic ants than EFN and and are associated with a specific ant partner. The non may require a specific dietary adaptation. This is also myrmecophytic species are visited by a variety of differ indicated by the fact that food body production in the ent ant species which are attracted by extrafloral nec transitional M. hosei does not start before stem struc taries (EFN) and food bodies. Transitional Macaranga ture allows a colonization by the obligate Cremato species like M. hosei are colonized later in their develop gaster species. M. hosei thus benefits from facultative ment due to their stem structure. Before the coloniza association with a variety of ants until it produces its tion by their specific Crematogaster partner the young first domatia and can be colonized by its obligate mutu plants are visited by different ant species attracted by alist. EFN. These nectaries are reduced and food body pro duction starts as soon as colonization becomes possible. -
Does Biological Intimacy Shape Ecological Network Structure? a Test Using a Brood Pollination Mutualism on Continental and Oceanic Islands
Received: 29 December 2016 | Accepted: 14 March 2018 DOI: 10.1111/1365-2656.12841 RESEARCH ARTICLE Does biological intimacy shape ecological network structure? A test using a brood pollination mutualism on continental and oceanic islands David H. Hembry1 | Rafael L. G. Raimundo2 | Erica A. Newman3 | Lesje Atkinson1 | Chang Guo4 | Paulo R. Guimarães Jr.2 | Rosemary G. Gillespie1 1Department of Environmental Science, Policy, and Management, University of California, Berkeley, California 2Departamento de Ecologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, SP, Brazil 3School of Natural Resources and the Environment, University of Arizona, Tucson, Arizona 4Department of Integrative Biology, University of California, Berkeley, California Correspondence David H. Hembry, Department of Ecology & Abstract Evolutionary Biology, University of Arizona, 1. Biological intimacy—the degree of physical proximity or integration of partner Tucson, AZ. Email: [email protected] taxa during their life cycles—is thought to promote the evolution of reciprocal specialization and modularity in the networks formed by co-occurring mutualistic Present addresses species, but this hypothesis has rarely been tested. David H. Hembry, Department of Ecology and Evolutionary Biology, University of 2. Here, we test this “biological intimacy hypothesis” by comparing the network ar- Arizona, Tucson, Arizona chitecture of brood pollination mutualisms, in which specialized insects are simul- Rafael L. G. Raimundo, Laboratório taneously parasites (as larvae) and pollinators (as adults) of their host plants to de Ecologia Animal, Departamento de Engenharia e Meio Ambiente and that of other mutualisms which vary in their biological intimacy (including ant- Programa de Pós-Graduação em Ecologia myrmecophyte, ant-extrafloral nectary, plant-pollinator and plant-seed disperser e Monitoramento Ambiental, Centro de Ciências Aplicadas e Educação, Universidade assemblages). -
Seed Dispersal Mutualisms Are Essential for the Survival of Diverse Plant Species and Communities Worldwide
ABSTRACT YOUNGSTEADT, ELSA KRISTEN. Neotropical Ant-Gardens: Behavioral and Chemical Ecology of an Obligate Ant-Plant Mutualism. (Under the direction of Coby Schal.) Seed dispersal mutualisms are essential for the survival of diverse plant species and communities worldwide. An outstanding but poorly understood ant-seed mutualism occurs in the Amazonian rainforest, where arboreal ants collect seeds of several taxonomically diverse plant species and cultivate them in nutrient-rich nests, forming abundant hanging gardens known as ant-gardens (AGs). AG ants and plants are dominant members of lowland Amazonian ecosystems, and their interaction is obligate and apparently species-specific. Though established AGs are limited to specific participants, it is unknown at what stage specificity arises. Seed fate pathways in AG epiphytes are undocumented, and the recognition cues that mediate the mutualism are unknown. Here the species specificity of the AG ant-seed interaction is assessed, and chemical cues are characterized that elicit seed- finding and seed-carrying in AG ants. To examine the specificity of the ant-seed interaction, general food baits and seeds of the AG plant Peperomia macrostachya were offered on alternate days at 108 bait stations. Seventy ant species were detected at food baits and could have interacted with AG seeds, but only three species collected P. macrostachya seeds, and 84% of observed seed removal by ants was attributed to C. femoratus. In a separate experiment, arthropod exclusion significantly reduced AG seed removal rates, but vertebrate exclusion did not. Thus species specific seed dispersal, rather than post-dispersal processes, appears to be the primary determinant of the distribution of AG plants. -
A Temporary Social Parasite of Tropical Plant-Ants Improves the Fitness of a Myrmecophyte
A temporary social parasite of tropical plant-ants improves the fitness of a myrmecophyte Alain Dejean & Céline Leroy & Bruno Corbara & Régis Céréghino & Olivier Roux & Bruno Hérault & Vivien Rossi & Roberto J. Guerrero & Jacques H. C. Delabie & Jérôme Orivel & Raphaël Boulay Abstract Myrmecophytes offer plant-ants a nesting place that Azteca andreae, whose colonies build carton nests on in exchange for protection from their enemies, particularly myrmecophytic Cecropia, is not a parasite of Azteca– defoliators. These obligate ant–plant mutualisms are com- Cecropia mutualisms nor is it a temporary social parasite of mon model systems for studying factors that allow A. alfari; it is, however, a temporary social parasite of A. horizontally transmitted mutualisms to persist since para- ovaticeps. Contrarily to the two mutualistic Azteca species sites of ant–myrmecophyte mutualisms exploit the rewards that are only occasional predators feeding mostly on provided by host plants whilst providing no protection in hemipteran honeydew and food bodies provided by the return. In pioneer formations in French Guiana, Azteca host trees, A. andreae workers, which also attend hemi- alfari and Azteca ovaticeps are known to be mutualists of pterans, do not exploit the food bodies. Rather, they employ myrmecophytic Cecropia (Cecropia ants). Here, we show an effective hunting technique where the leaf margins are A. Dejean (*) : C. Leroy : O. Roux : J. Orivel V. Rossi CNRS; Écologie des Forêts de Guyane (UMR-CNRS 8172), CIRAD; Écologie des Forêts de Guyane (UMR-CIRAD 93), Campus Agronomique, Campus Agronomique, 97379 Kourou Cedex, France 97379 KOUROU Cedex, France e-mail: [email protected] B. Corbara R. J. -
The Diversity of Ant–Plant Interactions in the Rainforest Understorey Tree, Ryparosa (Achariaceae): Food Bodies, Domatia, Prostomata, and Hemipteran Trophobionts
Blackwell Publishing LtdOxford, UKBOJBotanical Journal of the Linnean Society0024-4074© 2007 The Linnean Society of London? 2007 1543 353371 Original Article ANT–PLANT INTERACTIONS IN RYPAROSAB. L. WEBBER ET AL . Botanical Journal of the Linnean Society, 2007, 154, 353–371. With 5 figures The diversity of ant–plant interactions in the rainforest understorey tree, Ryparosa (Achariaceae): food bodies, domatia, prostomata, and hemipteran trophobionts BRUCE L. WEBBER1*, JOACHIM MOOG2, ALAN S. O. CURTIS3 and IAN E. WOODROW1 1School of Botany, The University of Melbourne, Vic. 3010, Australia 2Department of Zoology, J.W. Goethe University, Siesmayerstr. 70, D-60054 Frankfurt am Main, Germany 3Daintree Discovery Centre, Cow Bay, Qld 4873, Australia Received February 2006; accepted for publication January 2007 Ant–plant relationships, with variability in both intimacy and the trophic structure of associations, are described for the Austro-Malesian rainforest tree genus Ryparosa (Achariaceae). The range of associations involves opportunistic interactions between plants and foraging ants, mediated by food bodies, and tighter associations in which ant col- onies, tending hemipteran trophobionts, reside permanently in plant structures with different degrees of adaptation to house ants. Our study provides strong baseline data to suggest that Ryparosa could become a new model system for examining the evolutionary radiation of ant-related traits. To define the diversity of ant–plant associations in Ryparosa, we first present a review of ant-plant terminology and an outline of its use in this study. Field studies of ant interactions with food bodies in myrmecotrophic R. kurrangii from Australia and the association between myrmecoxenic R. fasciculata and two Cladomyrma plant-ant species on the Malay Peninsula provide detailed exam- ples of ant–plant interactions. -
Common Epiphytes and Lithophytes of BELIZE 1 Bruce K
Common Epiphytes and Lithophytes of BELIZE 1 Bruce K. Holst, Sally Chambers, Elizabeth Gandy & Marilynn Shelley1 David Amaya, Ella Baron, Marvin Paredes, Pascual Garcia & Sayuri Tzul2 1Marie Selby Botanical Gardens, 2 Ian Anderson’s Caves Branch Botanical Garden © Marie Selby Bot. Gard. ([email protected]), Ian Anderson’s Caves Branch Bot. Gard. ([email protected]). Photos by David Amaya (DA), Ella Baron (EB), Sally Chambers (SC), Wade Coller (WC), Pascual Garcia (PG), Elizabeth Gandy (EG), Bruce Holst (BH), Elma Kay (EK), Elizabeth Mallory (EM), Jan Meerman (JM), Marvin Paredes (MP), Dan Perales (DP), Phil Nelson (PN), David Troxell (DT) Support from the Marie Selby Botanical Gardens, Ian Anderson’s Caves Branch Jungle Lodge, and many more listed in the Acknowledgments [fieldguides.fieldmuseum.org] [1179] version 1 11/2019 TABLE OF CONTENTS long the eastern slopes of the Andes and in Brazil’s Atlantic P. 1 ............. Epiphyte Overview Forest biome. In these places where conditions are favorable, epiphytes account for up to half of the total vascular plant P. 2 .............. Epiphyte Adaptive Strategies species. Worldwide, epiphytes account for nearly 10 percent P. 3 ............. Overview of major epiphytic plant families of all vascular plant species. Epiphytism (the ability to grow P. 6 .............. Lesser known epiphytic plant families as an epiphyte) has arisen many times in the plant kingdom P. 7 ............. Common epiphytic plant families and species around the world. (Pteridophytes, p. 7; Araceae, p. 9; Bromeliaceae, p. In Belize, epiphytes are represented by 34 vascular plant 11; Cactaceae, p. 15; p. Gesneriaceae, p. 17; Orchida- families which grow abundantly in many shrublands and for- ceae, p. -
Geographical Variation of Mutualistic Relationships Between Macaranga Myrmecophytes and Their Ant Partners: Research Plans in Sarawak
<S2-2> Geographical variation of mutualistic relationships Title between Macaranga myrmecophytes and their ant partners: research plans in Sarawak Shimizu-kaya, Usun; Inui, Yoko; Ueda, Shouhei; Itino, Takao; Author(s) Itioka, Takao Proceedings of the symposium "Frontier in tropical forest research: progress in joint projects between the Forest Citation Department Sarawak and the Japan Research Consortium for Tropical Forests in Sarawak" (2016), 2016: 146-153 Issue Date 2016-06 URL http://hdl.handle.net/2433/227119 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University S2-2 Geographical variation of mutualistic relationships between Macaranga myrmecophytes and their ant partners: research plans in Sarawak Usun Shimizu-kaya 1,2,6, Yoko Inui 3, Shouhei Ueda 4,5, Takao Itino 4 and Takao Itioka 1 1 Graduate School of Human and Environmental Studies, Kyoto University, Kyoto, Japan 2 Center for Ecological Research, Kyoto University, Otsu, Japan 3 Osaka Kyoiku University, Kashiwara, Osaka, Japan 4 Sinshu University, Matsumoto, Japan 5 Osaka Prefecture University, Sakai, Japan 6 Author for correspondence (e-mail: [email protected]) Abstract Myrmecophytes have mutualistic associations with plant-inhabiting ants (so-called plant-ants). They provide plant-ants with nest space and sometimes foods, and in return, the plant-ants protect their host-plants against herbivores, pathogens and climbing plants. In the tree genus Macaranga (Euphorbiaceae), 26 species are myrmecophytic, among which 18 species are distributed in Sarawak. The relationships between Macaranga myrmecophytes and plant-ants are remarkable for their high species-specificity and strong interdependency. For 20 years, we have studied the myrmecophyte-plant-ant relationships and their effects on the herbivorous insect assemblage associated with Macaranga plants at Lambir Hills National Park (LHNP), where 17 Macaranga species, including 12 myrmecophytic species, are distributed. -
Ecological Dynamics of Mutualist/Antagonist Communities
vol. 162, supplement the american naturalist october 2003 Ecological Dynamics of Mutualist/Antagonist Communities Judith L. Bronstein,1,* William G. Wilson,2 and William F. Morris2 1. Department of Ecology and Evolutionary Biology, University of Understanding how interspecific interactions drive Arizona, Tucson, Arizona 85745; changes in the abundance and genetic composition of spe- 2. Department of Biology, Duke University, Durham, North cies has been a major goal of ecology and evolutionary Carolina 27708 biology for well over a century. To make empirical studies more feasible and theoretical studies analytically tractable, much of this work has focused on interactions between pairs of species, in isolation from the broader ecological abstract: One approach to understanding how mutualisms func- community. Yet, extracting pairwise interactions from their tion in community settings is to model well-studied pairwise inter- community context is unrealistic at best and misleading actions in the presence of the few species with which they interact at worst (Bronstein and Barbosa 2002; Stanton 2003). most strongly. In nature, such species are often specialized antagonists Most interactions are likely to be relatively weak and dif- of one or both mutualists. Hence, these models can also shed light fuse, such that removing any one partner species will have on the problem of when and how mutualisms are able to persist in minimal effects on the species with which they associate the face of exploitation. We used spatial stochastic simulations to -
Spiders, Ants and an Amazonian Myrmecophyte: a Tale of Trophic Cascades by Cassiano S
403 Spiders, Ants and an Amazonian Myrmecophyte: a Tale of Trophic Cascades by Cassiano S. Rosa1,2 & Og DeSouza1 ABSTracT Plants providing structures in which ants can shelter are often used in studies of trophic cascades. In such systems, predation on ants by specialist top predators may reduce the impact of ants on herbivores, to the plants’ detriment. These cascading top predator effects on herbivores and plants may be as follows: (1) numerical, through a reduction in the number of ants upon which the top predator can feed; or (2) functional, through a top predator’s effect on the behavioral, morphological, or physiological traits of its ant prey. Detecting the existence of cascading effects in such systems and disentangling these two potential components can be difficult. In this paper, we aim to quantify these components in an Amazonian myrmecophytic system, emphasizing the experimental and analytical procedures that can be used to separate the two components. We describe a trophic cascade from spiders through ants to herbivores using a full factorial experimental design combined with an analysis of the statistical interactions in a two-way analy- sis of deviance. In addition, we disentangle the density- and trait-mediated interactions using a one-way analysis of deviance on the presence of spiders in relation to (1) the number of ants in domatia and (2) the efficiency of ants in detecting intruders. The experimental and analytical procedures described support the conclusion that the trophic cascades in this system are primarily due to trait- rather than density-mediated indirect interactions. Keywords: Mutualism, antipredator prey behavior, statistical interactions, food web, cascading effect INTrodUCTioN Interactions between plants and predators are commonly reported in tropi- cal biomes, such as when plants provide sheltering structures (‘domatia’) for 1Dept.