• Title/Summary/Keyword: epiphytism

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Ascophyllum and Its Symbionts. VII. Three-way Interactions Among Ascophyllum nodosum (Phaeophyceae), Mycophycias ascophylli (Ascomycetes) and Vertebrata lanosa (Rhodophyta)

  • Garbary, David J.;Deckert, Ron J.;Hubbard, Charlene B.
    • ALGAE
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    • v.20 no.4
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    • pp.353-361
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    • 2005
  • Ascophyllum nodosum (L.) Le Jolis has a systemic infection with the ascomycete Mycophycias ascophylli (Cotton) Kohlmeyer and Volkmann-Kohlmeyer with which it establishese a mutualistic symbiosis. In addition, A. nodosum is the host for the obligate red algal epiphyte, Vertebrata lanosa (L.) Christensen. Using light and electron microscopy we describe morphological and cytochemical changes occurring as a consequence of rhizoid penetration of V. lanosa into cortical host tissue. Rhizoids induce localized cell necrosis based on physical damage during rhizoid penetration. Host cells adjacent to the rhizoid selectively undergo a hypersensitive reaction in which they become darkly pigmented and become foci for hyphal development. Light and electron microscopy show that M. ascophylli forms dense hyphal aggregations on the surface of the V. lanosa rhizoid and extensive endophytic hyphal growths in the rhizoid wall. This is the first morphological evidence of an interaction between M. ascophylli and V. lanosa. We speculate that M. ascophylli may be interacting with V. lanosa to limit tissue damage to their shared host. In addition, the fungus provides a potential pathway for the transfer of materials (e.g., nutrients and photosynthate) between the two phototrophs.

Ascophyllum and Its Symbionts. VIII. Interactions Among Ascophyllum nodosum (Phaeophyceae), Mycophycias ascophylli (Ascomycetes) and Elachista fucicola (Phaeophyceae)

  • Deckert, Ronald J.;Garbary, David J.
    • ALGAE
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    • v.20 no.4
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    • pp.363-368
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    • 2005
  • The brown alga Ascophyllum nodosum and its mutualistic, ascomycete symbiont, Mycophycias ascophylli, form a complex ‘rganism’or symbiotum. Here we show the interaction of the symbiotum to the abundant brown algal epiphyte, Elachista fucicola. Microscopy of field-collected plants shows morphological responses of A. nodosum to the common epiphyte E. fucicola. When E. fucicola attaches to A. nodosum a bundle of several to dozens of rhizoids penetrates into the host. On the surface of the host, the cells proliferate to form a donut-shaped ring, 100-200 μm in height that surrounds the thallus of E. fucicola. A pit forms in advance of the rhizoids and the cells of A. nodosum break down. This leaves the network of fungal hyphae partially intact and intermingling with the epiphyte rhizoids and its lowermost cells. After the pit is formed, the cells of A. nodosum bordering the infection chamber redifferentiate an epidermal layer. Neither the host nor its mutualistic fungus, M. ascophylli appears to recognize E. fucicola as an invader and to prevent the attachment and growth of this epiphyte. Based on the physical damage to the host caused by invading rhizoids, we conclude that the relationship of E. fucicola to A. nodosum is that of a parasite and its host.

Ascophyllum nodosum and its symbionts: XI. The epiphyte Vertebrata lanosa performs better photosynthetically when attached to Ascophyllum than when alone

  • Garbary, David J.;Miller, Anthony G.;Scrosati, Ricardo A.
    • ALGAE
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    • v.29 no.4
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    • pp.321-331
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    • 2014
  • Vertebrata lanosa is an abundant and obligate red algal epiphyte of Ascophyllum nodosum that forms part of a complex and highly integrated symbiotic system that includes the ascomycete, Mycophycias ascophylli. As part of ongoing studies to resolve interactions among species in the symbiosis, we used pulse amplitude modulation fluorimetry of chlorophyll a fluorescence, from photosystem II (PSII), to measure the maximum quantum yield ($F_v/F_m$) of PSII [$QY(II)_{max}$] and relative photosynthetic electron transport rates (rETR), as a function of light intensity, in order to evaluate the photosynthetic capacity of the two algal symbionts in the field and in the laboratory under different treatments. Our primary question was 'Is the ecological integration of these species reflected in a corresponding physiological integration involving photosynthetic process?' In the laboratory we measured changes in $QY(II)_{max}$ in thalli of V. lanosa and A. nodosum over one week periods when maintained together in either attached or detached treatments or when maintained separated from each other. While the $QY(II)_{max}$ of PSII of A. nodosum remained high and showed no significant variation among treatments, V. lanosa showed decreasing performance in the following conditions: V. lanosa attached to A. nodosum, V. lanosa in the same culture, but not attached to A. nodosum, and V. lanosa alone. These results are consistent with observations in which rETR was reduced in V. lanosa maintained alone versus attached to A. nodosum. Values for $QY(II)_{max}$ in V. lanosa measured in the field in fully submerged thalli were similar to those measured in the laboratory when V. lanosa was attached to it obligate host A. nodosum. Our results provide evidence of a physiological association of the epiphyte and its host that reflects the known ecology.