The Lichen Photobiont Genus Rhizonema (cyanobacteria) Exhibits Diverse Modes of Branching, Both False and True.

The recently described genus Rhizonema is among the most important cyanobacterial partners in lichen symbioses, but its morphological characterization in the genus diagnosis-true branching of the T-type-appears at odds with several published figures showing false branching. We investigated cyanobiont branching and cell division with light microscopy in two basidiolichens from Florida and one from Japan, including aposymbiotically cultured material of the latter. Mycobiont species identities (Cyphellostereum jamesianum, Dictyonema darwinianum, and D. moorei) and photobiont genus identity (Rhizonema) were corroborated with ITS and rbcLX sequences, respectively. Single and paired false branching occurred commonly in all three strains examined. False branches developed adjacent to necridic cells or heterocytes, or by separation of vegetative cells at compression folds in the trichome. Non-transverse cell divisions, usually oblique, were observed in two of the three Rhizonema strains examined. T-type true branches sometimes arose from such divisions, although oblique growth from the branch cell often resulted in ambiguous branch junctions. Additionally, Y-type true branches appeared to grow from contorted filaments. In cultured material, a kind of pseudo-branch sometimes arose from single- or several-celled segments liberated from trichome apices. The segments attached secondarily to filaments and grew there as apparent branches. We conclude that Rhizonema is a genus of considerable morphological flexibility, with multiple modes of branching possible in a single strain. While true branching or non-transverse divisions, when observable, may help distinguish Rhizonema from the phenotypically similar Scytonema, false branching occurs commonly in both genera, and therefore cannot be used to distinguish them.

Airborne ascospore discharge with co-dispersal of attached epihymenial algae in some foliicolous lichens.

PREMISE: Lichen-forming fungi that colonize leaf surfaces must find a compatible algal symbiont, establish lichen symbiosis, and reproduce within the limited life span of their substratum. Many produce specialized asexual propagules that appear to be dispersed by rain and runoff currents, but less is known about dispersal of their meiotic ascospores. In some taxa, a layer of algal symbionts covers the hymenial surface of the apothecia, where asci discharge their ascospores. We examined the untested hypothesis that their ascospores are ejected into air currents and carry with them algal symbionts from the epihymenial layer for subsequent lichenization. METHODS: Leaves bearing the lichens Calopadia puiggarii, Sporopodium marginatum (Pilocarpaceae), and Gyalectidium viride (Gomphillaceae) were collected in southern Florida. The latter two species have epihymenial algal layers. Leaf fragments with apotheciate thalli were affixed in petri dishes, with glass cover slips attached inside the lid over the thalli. Subsequent discharge of ascospores and any co-dispersed algae was evaluated with light microscopy. RESULTS: All three species discharged ascospores aerially. Discharged ascospores were frequently surrounded by a halo-like sheath of transparent material. In the two species with an epihymenial algal layer, most dispersing ascospores (>90%) co-transported algal cells attached to the spore sheath or wall. CONCLUSIONS: While water may be the usual vector for their asexual propagules, foliicolous lichen-forming fungi make use of air currents to disperse their ascospores. The epihymenial algal layer represents an adaptation for efficient co-dispersal of the algal symbiont with the next genetic generation of the fungus.

The cellular cortex in Collemataceae (lichenized Ascomycota) participates in thallus growth and morphogenesis via parenchymatous cell divisions.

According to a widely held view, fungi do not produce parenchymatous tissues. Following up on recent transmission electron microscopy (TEM) evidence that challenged this paradigm in several lichens, we employed scanning electron microscopy (SEM) to investigate the orientation of new anticlinal walls in the single-layered fungal cortex of six species of Collemataceae, a family of gelatinous cyanolichens with diverse surface morphologies. Examination of thallus surfaces in four species of Leptogium (L. austromericanum, L. burnetiae, L. chloromelum, L. marginellum) and two species of Scytinium (S. gelatinosum, S. lichenoides) revealed that recently formed septa adjoin to preceding septa in parenchymatous division. These cortical divisions were evident in the formation and development of thallus wrinkles, folds, isidia, and lobules in the six morphologically distinct taxa. Tomentum, by contrast, arose as filamentous outgrowths of the cortical cells. We conclude that the monostromatic cellular cortex in Collemataceae participates in surface growth and morphogenesis by means of parenchymatous cell divisions, in a remarkable parallel to plant meristems. Cortical cell divisions do not appear to drive morphogenesis, however, as very similar morphologies are achieved in the closely related genus Collema, which lacks a cortex altogether. These results provide evidence that parenchymatous cell division can indeed play a role in morphogenesis of fungal structures and show that SEM is a useful tool for distinguishing the orientation of anticlinal divisions in the cortex of gelatinous lichens.

Parenchymatous cell division characterizes the fungal cortex of some common foliose lichens.

PREMISE OF THE STUDY: Lichen-forming fungi produce diverse vegetative tissues, some closely resembling those of plants. Yet it has been repeatedly affirmed that none is a true parenchyma, in which cellular compartments are subdivided from all adjacent neighbors by cross walls adjoining older cross walls. METHODS: Using transmission electron microscopy (TEM), we tested this assumption by examining patterns of septum formation in the parenchyma-like cortex of three lichens of different phylogenetic affinities: Sticta canariensis, Leptogium cyanescens, and Endocarpon pusillum. KEY RESULTS: In the cortex of all three lichens, new septa adjoined perpendicularly or obliquely to previous septa. Septal walls possessed an electron-transparent core (median) layer covered on both sides by layers of intermediate electron density. At septal junctures, the core layer of the newer septum was not continuous with that of the older septum. Amorphous, electron-dense material often became deposited in the core region of older septal walls, and the septum gradually delaminated along its median into what could then be recognized as the distinct walls of neighboring cells. However, cells maintained continuity at pores, where adjacent remnants of the electron-transparent core layer suggested septal partition rather than secondary establishment of a lateral wall connection via anastomosis. CONCLUSIONS: Although fungal tissues first arise by the coalescence of filaments early in lichen ontogeny, the mature cortical tissues of some lichens are comparable to true parenchyma in the unrestricted orientation of their septal cross walls and the resulting ontogenetic relationship among neighboring cell compartments.

Heveochlorella (Trebouxiophyceae): a little-known genus of unicellular green algae outside the Trebouxiales emerges unexpectedly as a major clade of lichen photobionts in foliicolous communities.

Foliicolous lichens are formed by diverse, highly specialized fungi that establish themselves and complete their life cycle within the brief duration of their leaf substratum. Over half of these lichen-forming fungi are members of either the Gomphillaceae or Pilocarpaceae, and associate with Trebouxia-like green algae whose identities have never been positively determined. We investigated the phylogenetic affinities of these photobionts to better understand their role in lichen establishment on an ephemeral surface. Thallus samples of Gomphillaceae and Pilocarpaceae were collected from foliicolous communities in southwest Florida and processed for sequencing of photobiont marker genes, algal cultivation and/or TEM. Additional specimens from these families and also from Aspidothelium (Thelenellaceae) were collected from a variety of substrates globally. Sequences from rbcL and nuSSU regions were obtained and subjected to Maximum Likelihood and Bayesian analyses. Analysis of 37 rbcL and 7 nuSSU algal sequences placed all photobionts studied within the provisional trebouxiophycean assemblage known as the Watanabea clade. All but three of the sequences showed affinities within Heveochlorella, a genus recently described from tree trunks in East Asia. The photobiont chloroplast showed multiple thylakoid stacks penetrating the pyrenoid centripetally as tubules lined with pyrenoglobuli, similar to the two described species of Heveochlorella. We conclude that Heveochlorella includes algae of potentially major importance as lichen photobionts, particularly within (but not limited to) foliicolous communities in tropical and subtropical regions worldwide. The ease with which they may be cultivated on minimal media suggests their potential to thrive free-living as well as in lichen symbiosis.

The orientation of foliicolous lichen campylidia with respect to water runoff and its significance for propagule dispersal.

PREMISE OF THE STUDY: Some common leaf-dwelling lichen fungi produce asexual spores (conidia) within curved, dorsiventral structures called campylidia. Their shape and tendency to face in the same direction have generated speculation about how dispersal is accomplished. Here we tested the hypothesis that campylidia orient their spore-producing surface against runoff currents and examined the effects of hydration to better understand the spore dispersal mechanism. METHODS: Palm leaves bearing lichens (Calopadia) were surveyed with a dissecting microscope for campylidia with fibrous debris entangled around the base. Where possible, the direction of runoff flow was inferred from the position of the entangled debris; the angle between this direction and that toward which the spore-producing side faced was calculated for 67 campylidia. Other fresh-collected campylidia were photographed in the air-dry state and again after hydration. KEY RESULTS: Orientation of campylidia was strongly correlated with direction of runoff flow, such that the spore-producing side faced against oncoming runoff. Hydration of campylidia quickly resulted in swelling of the conidial mass beneath a thin flap of tissue covering the conidiogenous surface. The flap then bulged outward, exposing the conidial mass from above within its pocket-like compartment. CONCLUSIONS: Our results support previous contentions that water impact against campylidia is important in spore dispersal. However, the morphology of hydrated campylidia and their strong tendency to face upstream suggest that water currents impact laterally upon the thin tissue covering the hydrated conidial mass, thereby extruding spores apically. We contrast these findings with previous suggestions that campylidia act as splash cups.

Structure and in situ development of the microlichen Gyalectidium paolae (Gomphillaceae, Ascomycota), an overlooked colonist on palm leaves in southwest Florida.

PREMISE OF THE STUDY: Nondeciduous leaves of warm, humid climates can host highly specialized communities of diminutive lichens. The rarely reported Gyalectidium paolae, locally abundant on palm leaves in southwest Florida, may reproduce when as small as 0.15 mm diameter. We examined structural and developmental features to better understand the lifestyle of this extreme ephemeral. METHODS: Blocks containing resin-embedded thalli were sectioned and examined with TEM and SEM-BSE. Propagule development was studied with light microscopy applied to inoculated and naturally colonized plastic coverslips placed in the field. KEY RESULTS: Thallus areolae showed a heterogeneous covering that varied from cellular cortex to a simpler structure derived from fungal wall materials and sparse fungal cells of reduced diameter. Plates of crystalline deposits seemed to interrupt thallus structure, elevating the surface layer. No organized algal layer was present. Symbiont interactions were limited to appositional wall contacts with no haustorial penetration observed. Symbiotic propagules germinated promptly, but relative growth of fungal vs. algal components varied considerably. Smaller photobiont cells released from sporangia were present at the periphery of the thallus, or escaped to some distance. Fully formed hyphophores with abundant propagules appeared within 5 months, although there was evidence that propagule formation in Gyalectidium might occur much sooner. CONCLUSIONS: Gyalectidium paolae builds relatively simple thalli with limited fungal structure, prioritizing rapid formation of asexual propagules. Codispersal of algal symbionts permitted propagules to develop directly into thalli, but microenvironmental conditions may strongly influence survival and developmental equilibrium between the two symbionts necessary for success as a lichen.

Complete life cycle of the lichen fungus Calopadia puiggarii (Pilocarpaceae, Ascomycetes) documented in situ: propagule dispersal, establishment of symbiosis, thallus development, and formation of sexual and asexual reproductive structures.

PREMISE OF THE STUDY: The life histories of lichen fungi are not well known and cannot be readily studied in laboratory culture. This work documents in situ the complete life cycle of the widespread crustose lichen Calopadia puiggarii, which reproduces sexually and asexually on the surfaces of leaves. METHODS: Plastic cover slips held in a mesh frame were placed over leaves in the field and successively removed for microphotography of colonizing lichens. KEY RESULTS: Macroconidia produced within campylidia encircled photobiont cells and codispersed with them, a feature not reported previously for C. puiggarii. Dispersed macroconidia readily germinated and lichenized the photobionts. Algal cells were often dislodged from the encircling macroconidia, providing a likely source for the free-living populations observed. Aposymbiotically dispersed ascospores germinated and lichenized nearby algal cells soon after dispersal. Thallus areolae merged readily in early development, although adjacent mature thalli were often separated by growth inhibition zones. Pycnidia are reported for the first time in Calopadia; their pyriform microconidia probably function as male gametes (spermatia). Pycnidia, apothecia, and campylidia began development similarly as darkly pigmented primordia on the fungal prothallus. CONCLUSIONS: Abundant dispersal of ascospores, conidia, and photobionts allows C. puiggarii to quickly colonize leaves with the dual advantages of sexual and asexual reproduction, and with the added convenience of having its algal partner on hand. Fusions and prothallic capture of additional algae provide many opportunities for multiple mycobiont and photobiont genotypes to be combined in a single thallus, but the outcomes of such events remain to be explored.

Development of thallus axes in Usnea longissima (Parmeliaceae, Ascomycota), a fruticose lichen showing diffuse growth.

PREMISE OF THE STUDY: While cell wall thickening in plants is generally associated with tissue maturation, fungal tissues in at least two lichens continue to grow extensively while accumulating massively thickened cell walls. We examined Usnea longissima to determine how diffuse growth shapes morphological and anatomical development of thallus axes and how the highly thickened cell walls of the central cord behave in diffuse growth. METHODS: Fresh material was examined with light and epifluorescence microscopy and conventional and low-temperature SEM. Fixed material was embedded in Spurr's resin, microtome-sectioned, and examined with TEM and light microscopy. KEY RESULTS: Main axes consisted essentially of bare medullary cord tissue; their characteristic morphology developed by destruction of the overlying cortex and consequent stimulation of lateral branch formation. Fungal cells of the cord tissue continually deposited wall layers of electron-transparent substances and layered, electron-dense materials that include UV-epifluorescent components. Discontinuities were evident in the outermost layers; new branch cells grew through wall materials accumulated by older neighboring cells. CONCLUSIONS: Sustained diffuse growth of cord tissue in U. longissima underlies the structural transformation of a corticated thallus branch into a long axis. In the cord tissue, diffuse growth may be responsible for the increasingly disrupted appearance of the older, electron-dense cell wall layers, while new wall materials are laid down adjacent to the protoplast. Cell and tissue development appeared comparable to that observed previously in Ramalina menziesii, although accumulation of wall material was somewhat less extensive and with a greater proportion of electron-dense/UV-epifluorescent components.

The intertidal marine lichen formed by the pyrenomycete fungus Verrucaria tavaresiae (Ascomycotina) and the brown alga Petroderma maculiforme (Phaeophyceae): thallus organization and symbiont interaction.

The thallus formed by the marine pyrenomycete fungus Verrucaria tavaresiae and the phaeophycean alga Petroderma maculiforme was studied to elucidate the organization of the symbionts, determine the type of cellular contacts between them, and evaluate the status of the symbiosis as a lichen. Hand-sectioned and resin-embedded samples were examined with light and transmission electron microscopy. Within the uppermost portion of the cellular fungal tissue, separate algal filaments were arranged anticlinally. Protrusions of the fungal cell wall penetrated into adjacent algal walls but did not enter the cell lumen. A striking feature of these penetrations was the frequent separation of algal cell wall layers and insertion of fungal wall material between them. Algal filaments grew downward intrusively between fungal cells, often penetrating deeply into the fungal cell wall. Despite the exceptional nature of the phycobiont involved, the Verrucaria tavaresiae-Petroderma maculiforme symbiosis unequivocally fits the prevailing concept of a lichen. The distinctive interpenetrations observed between symbionts may be related to the integration of their different growth forms within a coherent tissue regularly subject to mechanical stresses. Periclinal cell divisions within and just below the algal layer may serve to replenish surface tissues lost to abrasion and herbivory.

In situ development of the foliicolous lichen Phyllophiale (Trichotheliaceae) from propagule germination to propagule production.

The vegetative cycle of the foliicolous lichen Phyllophiale, from propagule germination to propagule production, was studied by light microscope observation of thalli colonizing plastic cover slips placed within a lowland tropical forest. Discoid propagules germinated by growth of radially arranged fungal cells and developed directly into lichen thalli. The young lichen comprised a single disc of closely branched, radiating filaments of the algal symbiont Phycopeltis, covered by a network of fungal hyphae extending onto the substrate as a prothallus. The prothallic hyphae incorporated additional Phycopeltis thalli encountered on the substrate. The phycobiont formed a single layer, with individual algal thalli clearly distinguishable within the lichen. Radial growth ceased at points of contact between adjacent phycobiont thalli. The visible shape of the crustose lichen thallus corresponded to the perimeter of the phycobiont thalli within. Propagules were initiated at points corresponding to the margins of the phycobiont thalli, by vertical reorientation of horizontal algal filaments surrounded by fungal hyphae. The lichenized alga produced intercalary gametangia. Degeneration of propagules unsuccessful in lichen establishment sometimes resulted in free growth of the phycobiont. The alga generally maintained its shape, growth pattern, and reproductive independence within the lichen, while also participating in the formation of unique symbiotic propagules.

Reproductive strategies, relichenization and thallus development observed in situ in leaf-dwelling lichen communities.

• Suppositions about lichen reproductive strategies were investigated and elusive early stages of lichen ontogeny documented in a foliicolous lichen community. • Plastic coverslips attached to supportive netting were placed among foliicolous lichen communities within a neotropical lowland forest. The germination and development of diverse lichen propagules colonizing the coverslips were studied with light microscopy. • Foliicolous lichens were observed to begin development from lichenized vegetative propagules, aposymbiotic fungal spores, fungal spores dispersed together with attached phycobionts, and diahyphae. Aposymbiotically dispersed spores and diahyphae were capable of associating with compatible phycobionts encountered upon the substratum, following germination. • Many developing thalli produced characteristic structures (discoid isidia, thalline setae, pycnidia, etc.) which permitted their recognition as typical members of the foliicolous lichen community. Thalline setae in Tricharia were produced upon the prothallus, and subsequently incorporated into the thallus proper by advance of the lichenized thallus margin. Tricharia and other members of the Gomphillaceae showed a distinctive organization of symbionts in thallus growth, whereby the unicellular green phycobiont cells were positioned at the tips of advancing fascicles of mycobiont hyphae. In Coenogonium sp., branching filaments of the phycobiont Trentepohlia grew along prothallic paths initiated by the mycobiont.