TOXICITY OF SUBTROPICAL MARINE ALGAE USING FISH MORTALITY AND RED BLOOD CELL HEMOLYSIS FOR BIOASSAYS1

Two bioassays (fish mortality and fish erythrocyte hemolysis) were used to survey for the presence of toxic principles in aqueous extracts of 19 species of marine macro-algae found in south Florida coastal waters. Extracts from six species (Chlorophyta—Anadyomene stellata (Wulfen) C. Ag., Caulerpa prolifera (Forsskål) Lamour., Penicillus capitatus Lamarck: Rhodophyta—Centroceras clavulatum (C. Ag.) Montague, Laurencia papillosa (Forsskål) Grev., L. poitel (Lamour.) Howe) showed lethal toxicity to the spotfin mojarra, Euconistomus argenteus Baird & Girard. Extracts from three species (Chlorophyta—A. stellata: Phaeophyta—Dictyota dichotoma (Hudson) Lamour.: Rhodophyta—Wrangelia penicillata C. Ag.) lysed erythrocytes of sea bream, Archosargus rhomboidalis (L.).     

BIOGEOGRAPHY AND ECOLOGY OF THE KELP/RED ALGAL SYMBIOSIS

A kelp/red algal symbiosis is described from nature based on extensive collections from the San Juan Islands, Washington. Kelp gametophytes were found as endophytes in the cell walls of seventeen species of red algae in three different kelp communities. Host red algae were mostly filamentous (e.g., Pleonosporium vancouverianum) or polysiphonous (e.g. Polysiphonia paniculata). The kelp gametophytes completed vegetative and reproductive development in the hosts with gametangia formed at the host surface and with sporophytes up to several mm in height being produced while still attached to the host. To date, none of the kelp gametophytes from nature have been identified to genus or species, although the gametophyte of Nereocystis luetkeana is a potential candidate for the symbiosis. Preliminary observations from Nova Scotia and the Isle of Man have not found the association in the Atlantic Ocean. Laboratory studies in Korea successfully reconstructed the symbiosis in the red alga Aglaothamnion oosumiense using zoospores of Undaria pinnatifida but not Laminaria religiosa. Here we outline the development of the symbiosis and discuss the potential adaptive significance of the kelp/red algal interaction.     

TRANSFER OF PRODUCTS BETWEEN EPIPHYTIC MARINE ALGAE AND HOST PLANTS1,2

The red alga Smithora naiadum is normally found only as an epiphyle on the sea grasses Phyllospadix scouleri and Zostera marina. I used ³²P and ¹⁴CO₂ to examine the chemical communication between host and alga. Both ³²P and the product of ¹⁴CO₂ light fixation moved from the host to the alga. Reverse movement between host and epiphyte was also demonstrated. Part of this transfer occurred through the plant and part occurred by leakage from the host into the medium and subsequent uptake by the alga. Although plants were initially labeled in the light, transfer of ¹⁴C was light independent. Transfer of ¹⁴C-labeled products between host and epiphyte was also shown for Punctaria orbiculata and Z. marina; for Microdadia coulteri on Grateloupia doryphora, and between Gonimophyllum skottsbergii and Botryoglossum ruprechtiana. Epiphyte-host associations do not require a penetrating rhizoid for an exchange of the isotopes tested. By their proximity alone, epiphytic flora are apparently capable l exchanging products before these are diluted by the sea.     

EFFECT OF LIGHT QUALITY ON POLYSACCHARIDE YIELD AND COMPOSITION OF TWO RED ALGAE

Porphyra perforata is a common seaweed inhabiting the upper intertidal zone, and as a consequence it experiences great fluctuations in tissue temperature and desiccation. The objective of this work was to evaluate the effect of ambient temperature and the tissue desiccation status on the photosynthetic performance of P. perforata. Photosynthetic performance was evaluated polarographically after the temperature or desiccation treatments. Maximum photosynthesis (P_max) occurred between 25 and 30° C and decreased at higher and lower temperatures, however, no significant differences were observed in the initial slope of photosynthesis (α) from 10 to 30° C. This suggests that the photosynthetic efficiency of this species does not decrease as a result of fluctuating temperatures during tidal emergence/submergence. P_max and α were relatively constant in tissue of P. perforata with 5 to 100% relative water content. This also suggests that natural desiccation rates during low tides do not decrease photosynthetic rates in this species. Variations in the synthesis of specific proteins as a result of fluctuations in temperature and relative water content in the tissue of P. perforata are being studied.     

EFFECT OF LYSOZYME (MURAMIDASE) ON MARINE AND FRESHWATER BLUE-GREEN ALGAE1

Marine blue-green algae, Lyngbya Lagerheimii, Microcoleus chthonoplastes, Plectonema terebrans, Agmenellum quadruplicatum, and freshwater blue-green algae, Anacystis nidulans, Anabaena variabilis, Nostoc muscorura, and Oscillatoria sp. treated with lysozyme (muramidase) formed spheroplasts but not protoplasts. The time needed for spheroplast induction varied with the species. Approximate internal osmotic pressures of the blue-green algae were determined. Marine algae generally had a higher osmotic pressure than freshwater algae.     

THE EVOLUTION OF PARASITISM IN THE RED ALGAE: MOLECULAR COMPARISONS OF ADELPHOPARASITES AND THEIR HOSTS1

In several groups of parasites including insect, flowering plant, fungal, and red algal parasites, morphological similarities of the parasites and their specific hosts have led to hypotheses that these parasites evolved from their hosts. But these conclusions have been criticized because the morphological features shared by parasite and host may be the result of convergent evolution. In this study, we examine the hypothesis, originally put forth by Setchell, that adelphoparasitic red algae, that is, parasitic red algae that are morphologically very similar to their hosts, evolved from their specific red algal hosts. Rather than comparing morphological features of parasites and hosts, small-subunit 18S nuclear ribosomal DNA and the internal transcribed spacer regions (ITSs) of the nuclear ribosomal repeat are compared for five parasites, their hosts, and related nonhosts from four red algal orders. These comparisons reveal that each of these adelphoparasites has evolved either directly from the host on which it is currently found, or it evolved from some other taxon that is closely related to the modern host. The parasites Gardneriella tuberifera, Rhodymeniocolax botryoides, and probably Gracilariophila oryzoides evolved from their respective hosts Sarcodiotheca gaudichaudii, Rhodymenia pacifica, and Gracilariopsis lemaneiformis, respectively. The parasite Faucheocolax attenuata evolved from either Fauchea laciniata or Fauchea fryeana and subsequently radiated onto the other host species. Presently this parasite is found on both hosts. Lastly, some parasitic genera such as Plocamiocolax are polyphyletic in their origins. A species of Plocamiocolax from an Antarctic Plocamium cartilagineum appears to have evolved from its host whereas the common Plocamiocolax pulvinata that occurs along the west coast of North America likely evolved from Plocamium violaceum and radiated secondarily onto its present day host, Plocamium cartilagineum.     

AN IN SITU STUDY OF RECRUITMENT,GROWTH AND SURVIVAL OF SUBTIDAL MARINE ALGAE: TECHNIQUES AND PRELIMINARY RESULTS12

Fouling plates (Plexiglas squares and concrete blocks) were bolted in a horizontal position to racks on the ocean floor at a depth of 12 m. Some of these were periodically taken from the sea, subjected to nondestructive microscopic survey in the laboratory, and then replaced. Others were: a) left undisturbed as controls; b) variously caged to exclude larger predatory animals; or, c) had sediment removed from them at intervals. Populations developing on the periodically surveyed plates were similar to those on undisturbed plates. Populations on undisturbed plates were significantly different from those on partially caged plates. The exclusion of large predators by complete caging resulted in highly significantly different communities from those on partially caged plates. Completely caged Communities were composed mainly of worms, barnacles and bryozoans. Summer-installed plates supported significantly different populations at the end of the experimental period (12 mo) from winter-installed plates. Plant growth rates were slow, not exceeding 2 cm/mo, and the mortality rates were often high. A few species had high rates of recruitment and survival each month. Most had high recruitment only in the most favorable growth periods and high loss rates. Physical conditions on the sea floor were measured. The methods developed during this study make it possible to quantitatively describe the growth and reproduction of populations of benthic marine algae in the sea.     

THE EVOLUTION OF RNA POLYMERASE II IN RED ALGAE

Cryptophytes are photosynthetic protists that have acquired their plastids through the secondary symbiotic uptake of a red alga. A remarkable feature of cryptophytes is that they maintain a reduced form of the red algal nucleus, the nucleomorph, between the second and third plastid membranes (periplastidial compartment, PC). The nucleomorph is thought to be a transition state in the evolution of secondary plastids with this genome ultimately being lost (e.g., as in heterokonts, haptophytes, euglenophytes) when photosynthesis comes under full control of the "host" nucleus. For this to happen, all genes for plastid function must be transferred from the nucleomorph to the nucleus. In this regard, it is generally assumed that nucleomorph genes with functions unrelated to plastid or PC maintenance are lost. Surprisingly, we show here the existence of a novel type of actin gene in the host nucleus of the cryptophyte, Pyrenomonas helgolandii , that has originated from the nucleomorph genome of the symbiont. Our results demonstrate for the first time that secondary symbionts can contribute genes to the host lineage that are unrelated to plastid function. These genes are akin to the products of gene duplication and provide a source of evolutionary novelty that could significantly increase the genetic diversity of the host lineage. We postulate that this may be a common phenomenon in algae containing secondary plastids that has yet to be fully appreciated due to a dearth of evolutionary studies of nuclear genes in these taxa.