Agarolytic culturable bacteria associated with three antarctic subtidal macroalgae

Bacterial communities of Antarctic marine macroalgae remain largely underexplored in terms of diversity and biotechnological applications. In this study, three Antarctic subtidal macroalgae (Himantothallus grandifolius, Pantoneura plocamioides and Plocamium cartilagineum), two of them endemic of Antarctica, were investigated as a source for isolation of agar-degrading bacteria. A total of 21 epiphytic isolates showed agarolytic activity at low temperature on agar plates containing agar as the sole carbon source. 16S rRNA identification showed that the agar-degrading bacteria belonged to the genera Cellulophaga, Colwellia, Lacinutrix, Olleya, Paraglaciecola, Pseudoalteromonas and Winogradskyella. The agarase enzyme from a potential new species of the genus Olleya was selected for further purification. The enzyme was purified from the culture supernatant of Olleya sp. HG G5.3 by ammonium sulfate precipitation and ion-exchange chromatography. Molecular weight of the agarase was estimated to be 38 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The purified enzyme exhibited activity at 4 °C, retaining >?50% of its maximum activity at this temperature. This is the first study reporting the phylogeny of agar-degrading bacteria isolated from Antarctic subtidal macroalgae and the results suggest the huge potential of Antarctic algae-associated bacteria as a source of cold-active hydrolytic enzymes of biotechnological interest.     

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.     

Studies toward the comprehension of fungal-macroalgae interaction in cold marine regions from a biotechnological perspective

In marine ecosystems, macroalgae are the habitat for several microorganisms, fungi being among them. In the Antarctic benthic coastal ecosystem, macroalgae play a key role in organic matter cycling. In this study, 13 different macroalgae from Potter Cove and surrounding areas were sampled and 48 fungal isolates were obtained from six species, four Rhodophyta Ballia callitricha, Gigartina skottsbergii, Neuroglossum delesseriae and Palmaria decipiens, and two Phaeophyceae: Adenocystis utricularis and Ascoseira mirabilis. Fungal isolates mostly belonged to the Ascomycota phylum (Antarctomyces, Cadophora, Cladosporium, Penicillium, Phialocephala, and Pseudogymnoascus) and only one to the phylum Mucoromycota. Two of the isolates could not be identified to genus level, implying that Antarctica is a source of probable novel fungal taxa with enormous bioprospecting and biotechnological potential. 73% of the fungal isolates were moderate eurypsychrophilic (they grew at 5–25 °C), 12.5% were eurypsychrophilic and grew in the whole range, 12.5% of the isolates were narrow eurypsychrophilic (growth at 15–25 °C), and Mucoromycota AUe4 was classified as stenopsychrophilic as it grew at 5–15 °C. Organic extracts of seven macroalgae from which no fungal growth was obtained (three red algae Georgiella confluens, Gymnogongrus turquetii, Plocamium cartlagineum, and four brown algae Desmarestia anceps, D. Antarctica, Desmarestia menziesii, Himantothallus grandifolius) were tested against representative fungi of the genera isolated in this work. All extracts presented fungal inhibition, those from Plocamium cartilagineum and G. turquetii showed the best results, and for most of these macroalgae, this represents the first report of antifungal activity and constitute a promising source of compounds for future evaluation.     

Adaptation and acclimation of growth and photosynthesis of five Antarctic red algae to low temperatures

Temperature requirements for growth, photosynthesis and dark respiration were determined for five Antarctic red algal species. After acclimation, the stenothermal species Gigartina skottsbergii and Ballia callitricha grew at 0 or up to 5 °C, respectively; the eurythermal species Kallymenia antarctica, Gymnogongrus antarcticus and Phyllophora ahnfeltioides grew up to 10 °C. The temperature optima of photosynthesis were between 10 and 15 °C in the stenothermal species and between 15 and 25 °C in the eurythermal species, irrespective of the growth temperature. This shows that the temperature optima for photosynthesis are located well below the optima from species of other biogeographical regions, even from the Arctic. Respiratory rates rose with increasing temperatures. In contrast to photosynthesis, no temperature optimum was evident between 0 and 25 °C. Partial acclimation of photosynthetic capacity to growth temperature was found in two species. B. callitricha and Gymnogongrus antarcticus acclimate to 0 °C, and 5 and 0 °C, respectively. But acclimation did in no case lead to an overall shift in the temperature optimum of photosynthesis. B. callitricha and Gymnogongrus antarcticus showed acclimation of respiration to 5 °C, and P. ahnfeltioides to 5 and 10 °C, resulting in a temperature independence of respiration when measured at growth temperature. With respect to the acclimation potential of the species, no distinction can be made between the stenothermal versus the eurythermal group. (Net)photosynthetic capacity:respiration (P:R) ratios showed in all species highest values at 0 °C and decreased continuously to values lower than 1.0 at 25 °C. In turn, the low P:R ratios at higher temperatures are assumed to determine the upper temperature growth limit of the studied species. Estimated daily carbon balance reached values between 4.1 and 30.7 mg C g⁻¹ FW day⁻¹ at 0 °C, 16:8 h light/dark cycle, 12–40 μmol m⁻² s⁻¹. Received: 4 November 1999 / Accepted: 7 March 2000     

Animal associations with the dominant species of shallow water macrophytes along the coastline of the Vestfold Hills,Antarctica

Benthic grab samples, taken through core holes in sea-ice 1983, returned eight species of marine macrophytes which had associated fauna on at least one sample. A total of 24 animal taxa were found on these eight macrophytes. Phyllophora antarctica had a significantly greater biomass of attached fauna per unit of macrophyte biomass than any of the other seven species. It also had the greatest variety of epiphytic fauna (21 taxa). Phyllophora antarctica was the only macrophyte collected from comparatively protected Ellis Fjord, apart from filamentous algae, including Cladophora subsimplex and Geminocarpus austrogeorgiae, which were found in the most landward basin. It therefore played an important role in the ecology of the fjord. Palmaria decipiens was commonly collected at more exposed coastal sites and was dominant in Long Fjord, characterized here as intermediate in terms of water movement. Sixteen animal taxa were collected from this macrophyte with the greatest numbers being found in July and August. Only four animal taxa were collected from Iridaea cordata. The other five macrophyte species from which epiphytic animals were collected (Porphyra endiviifolium, Plocamium cartilagineum, Desmarestia menziesii, Himantothallus grandifolius and Cladophora subsimplex had animals associated with them on less than half the occasions when they were found.     

Halogenating activities detected in Antarctic macroalgae

 Halogenating activities were determined in samples of 18 cultivated species of brown, red and green macroalgae from the Antarctic. Activities for the halogenating organic compounds with bromide, iodide and chloride were found. Investigated red algae (rhodophytes) showed higher brominating and iodinating activities compared to brown (phaeophytes) and green (chlorophytes) algae. The highest brominating and iodinating activities were measured in the red algae Plocamium cartilagineum (1.11±0.01 U g^-1 wet algal weight and 0.18 U g^-1 wet algal weight, respectively) and Myriogramme mangini (3.62±0.17 U g^-1 wet algal weight and 4.5 U g^-1 wet algal weight, respectively). Chlorinating activities were detected in the red alga Plocamium cartilagineum only (0.086 U g^-1 wet algal weight). Received: 12 February 1996/Accepted: 20 June 1996     

Contribution of the UV component of natural sunlight to photoinhibition of photosynthesis in six species of subtidal brown and red seaweeds

Field‐collected specimens of three species of Laminaria and three species of subtidal red algae (Delesseria sanguinea, Plocamium cartilagineum and Phyllophora pseudoceranoides) were exposed to natural summer sunlight on Helgoland (southern North Sea) for up to 4 h at 15 °C. Dark‐adapted variable fluorescence (F_v : F_m) was measured immediately after these treatments, and following 6, 24 and 48 h of recovery in moderate irradiances of white light. The response of plants to the full spectrum of natural sunlight was compared with that to PAR alone, UV‐A + visible, UV‐A + UV‐B, or UV‐A alone. The F_v : F_m values of all species were reduced to minimal values after 4 h in all of these treatments, but those of the more resistant species (Laminaria spp. and P. pseudoceranoides) were higher after shorter exposures to UV radiation alone than to PAR with or without UV. The recovery of F_v : F_m in all species was also more rapid in the two treatments that contained UV radiation alone than in those that included PAR. These results suggest that it is the high irradiances of PAR in natural sunlight which are responsible for the photoinhibition of photosynthesis of subtidal seaweeds and that the current ambient irradiances of UV radiation (either UV‐B or UV‐A) in northern temperate latitudes would not contribute significantly to this photoinhibition.     

COMPARATIVE STUDY ON THE PHOTOSYNTHETIC PROPERTIES OF PRASIOLA (CHLOROPHYCEAE) AND NOSTOC (CYANOPHYCEAE) FROM ANTARCTIC AND NON‐ANTARCTIC SITES1

The terrestrial cyanobacterium Nostoc commune Vaucher ex Bornet et Flahault occurs worldwide, including in Japan and on the Antarctic continent. The terrestrial green alga Prasiola crispa (Lightf.) Kütz. is also distributed in Antarctica. These two species need to acclimate to the severe Antarctic climate including low ambient temperature and desiccation under strong light conditions. To clarify this acclimation process, the physiological characteristics of the photosynthetic systems of these two Antarctic terrestrial organisms were assessed. The relative rate of photosynthetic electron flow in N. commune collected in Japan and in Antarctica reached maxima at 900 and 1,100 μmol photons · m^?2 · s^?1, respectively. The difference seemed to reflect the presence of high amounts of UV‐absorbing substances within the Antarctic cyanobacterium. On the other hand, the optimal temperatures for photosynthesis at the two locations were 30°C–35°C and 20°C–25°C, respectively. This finding suggested a decreased photosynthetic thermotolerance in the Antarctic strain. P. crispa exhibited desiccation tolerance and dehydration‐induced quenching of PSII fluorescence. Re‐reduction of the photooxidized PSI reaction center, P700, was also inhibited at fully dry states. Photosynthetic electron flow in P. crispa reached a maximum at 20°C–25°C and at a light intensity of 700 μmol photons ? m^?2 ? s^?1. Interestingly, the osmolarity of P. crispa cells suggested that photosynthesis is performed using water absorbed in a liquid form rather than water absorbed from the air. Overall, these data suggest that these two species have acclimated to optimally photosynthesize under conditions of the highest light intensity and the highest temperature for their habitat in Antarctica.     

Variations in the halogenated monoterpene metabolites of Plocamium cartilagineum and P. violaceum

Observed variations in the halogenated monoterpene content of Aplysia californica were due to digestion of Plocamium cartilagineum and Plocamium violaceum. Whereas Plocamium violaceum was chemically homogeneous, some variation in the composition of halogenated monoterpene composition of individual plants of P. cartilagineum was observed.     

Temperature responses of growth, photosynthesis, fatty acid and nitrate reductase in Antarctic and temperate Stichococcus

Stichococcus, a genus of green algae, distributes in ice-free areas throughout Antarctica. To understand adaptive strategies of Stichococcus to permanently cold environments, the physiological responses to temperature of two psychrotolerants, S. bacillaris NJ-10 and S. minutus NJ-17, isolated from rock surfaces in Antarctica were compared with that of one temperate S. bacillaris FACHB753. Two Antarctic Stichococcus strains grew at temperature from 4 to 25°C, while the temperate strain could grow above 30°C but could not survive at 4°C. The photosynthetic activity of FACHB753 at lower than 10°C was less than that of Antarctic algae. Nitrate reductase in NJ-10 and NJ-17 had its optimal temperature at 20°C, in comparison, the maximal activity of nitrate reductase in FACHB753 was found at 25°C. When cultured at 4–15°C a large portion of unsaturated fatty acids in the two Antarctic species was detected and the regulation of the degree of unsaturation of fatty acids by temperature was observed only above 15°C, though the content of the major unsaturated fatty acid αC18:3 in FACHB753 decreased with the temperatures elevated from 10 to 25°C. Elevated nitrate reductase activity and photosynthetic rates at low temperatures together with the high proportion of unsaturated fatty acids contribute to the ability of the Antarctic Stichococcus to thrive.     

Temperature requirements for growth and survival of macroalgae from Disko Island (Greenland)

The temperature requirements for growth and upper temperature tolerance were determined in 16 macroalgal species collected on Disko Island (Greenland). The upper survival temperatures were examined in 1°C steps, and growth measured at 5°C intervals between 0 and 20°C using a refined method, where the fresh weight was determined weekly or fortnightly over a period of 5 or 6 weeks. To express temperature-growth responses, growth rates of temperature-acclimated plants were taken. Two groups with different temperature requirements were identified: (1) A stenothermal group includingAcrosiphonia arcta, Acrosiphonia sonderi, Urospora penicilliformis, Devaleraea ramentacea, Desmarestia aculeata, Pilayella littoralis, growing between 0 and (10 to) 15 (or 20)°C with optima between 0 and 10°C. The upper survival temperatures in these species and inChromastrum secundatum, Chromastrum virgatulum, Chordaria flagelliformis were between 17 and 23°C (duration of experiment: 2 weeks). (2) A eurythermal group includingEnteromorpha clathrata, Enteromorpha intestinalis andPolysiphonia urceolata growing between 0 and 20°C with growth optima at 10 or 15°C. The upper survival temperatures in these species and inChaetomorpha tortuosa, Bangia atropurpurea andEudesme virescens were between 24 and 31°C. These algal species showed little adaptation to the Arctic temperatures. In contrast, algae from the first group exhibited a relatively high adaptation to low temperatures — approaching the low temperature requirements of Antarctic algae. The results are discussed in relation to the geographic distribution of individual species.     

Temperature adaptation of soil bacterial communities along an Antarctic climate gradient: predicting responses to climate warming

Soil microorganisms, the central drivers of terrestrial Antarctic ecosystems, are being confronted with increasing temperatures as parts of the continent experience considerable warming. Here we determined short‐term temperature dependencies of Antarctic soil bacterial community growth rates, using the leucine incorporation technique, in order to predict future changes in temperature sensitivity of resident soil bacterial communities. Soil samples were collected along a climate gradient consisting of locations on the Antarctic Peninsula (Anchorage Island, 67 °34′S, 68 °08′W), Signy Island (60 °43′S, 45 °38′W) and the Falkland Islands (51 °76′S 59 °03′W). At each location, experimental plots were subjected to warming by open top chambers (OTCs) and paired with control plots on vegetated and fell‐field habitats. The bacterial communities were adapted to the mean annual temperature of their environment, as shown by a significant correlation between the mean annual soil temperature and the minimum temperature for bacterial growth (T_min). Every 1 °C rise in soil temperature was estimated to increase T_min by 0.24–0.38 °C. The optimum temperature for bacterial growth varied less and did not have as clear a relationship with soil temperature. Temperature sensitivity, indicated by Q₁₀ values, increased with mean annual soil temperature, suggesting that bacterial communities from colder regions were less temperature sensitive than those from the warmer regions. The OTC warming (generally <1 °C temperature increases) over 3 years had no effects on temperature relationship of the soil bacterial community. We estimate that the predicted temperature increase of 2.6 °C for the Antarctic Peninsula would increase T_min by 0.6–1 °C and Q₁₀ (0–10 °C) by 0.5 units.     

Feinbau und Teilung bei Plastiden einiger Florideen-Arten

Zusammenfassung Die Plastiden von 6Florideen-Arten sind elektronenmikroskopisch auf ihren Feinbau untersucht worden. Sie zeigen, ohne Ausnahme, die auch für andere Algen bekannte Lamellen-Struktur. Im Gebiet des Pyrenoids vonRhodochorton floridulum sind nur sp?rliche Lamellen zu erkennen. BeiGigartina Teedii sind überdies verschiedene Plastiden-Teilungsmodi und verschiedene Stadien des Teilungsprozesses abgebildet worden.

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Commercial farming of <Emphasis Type="BoldItalic">Asparagopsis armata</Emphasis> (Bonnemaisoniceae,Rhodophyta) in Ireland,maintenance of an introduced species?

The distribution of the gametophytes of Asparagopsis armata in Ireland currently encompasses a 75 km radius from a seaweed farm that commercially cultivates this species. This is a smaller range than the historic distribution shows since its arrival in Ireland in 1939. Fragmentation of this alga to seed ropes at a commercial seaweed farm seems to maintain the populations of this introduced species. Without this commercial seaweed farm A. armata would probably not flourish on the Irish west coast and this farm appears to act as a source pool for the populations. The sea surface temperatures (SSTs) of Irish waters are suitable for growth, survival and asexual reproduction of the tetrasporophyte and gametophyte; however, they may not be warm enough for sexual reproduction. The effect of temperature on the life cycle and distribution are discussed. Three species, i.e., Ulva lactuca, Plocamium cartilagineum and Cryptopleura ramosa, were hosts for epiphytic A. armata in summer in over 60% of the collected samples.     

Healing and regeneration responses in Gigartina skottsbergii (Rhodophyta, Gigartinales): optimization of vegetative propagation for cultivation

The red alga Gigartina skottsbergii is becoming increasingly valuable as a resource to providing the raw material for the carrageenan industry established in Chile and elsewhere. As a result, wild stocks of the species are subject to intense harvesting by local fishermen. With the current levels of harvesting, it seems likely that natural stands of G. skottsbergii will soon collapse. Although cultivation seems an alternative, knowledge regarding the biology of the species is exceedingly limited. This study reports the first attempt to determine the optimal conditions for vegetative propagation of this species in the laboratory. For this purpose, the processes of wound healing and regeneration of frond fragments and haptera were studied under controlled conditions of temperature, light, and media strength. Our results demonstrated that excised tissues of G. skottsbergii were able to seal the exposed areas in approximately 20 days, by a wound healing process characterized by a re-differentiation of medullary cells into a normal cortex. Our data also demonstrated that frond fragments are better than haptera for propagation purposes. The development of new cortical tissue at the cut surface is followed, within 60 days, by localized blade-like outgrowths along the repaired area. Furthermore, the healing and regenerative responses in both frond fragments and haptera differed in efficiency according to the various combinations of factors, with optimum of 10–15 °C, 5 ?mol m^?2 s^?1 and plain seawater or standard SFC medium for the fronds. The two types of responses were negatively affected by seawater enriched with a double concentration of nutrients.     

Temperature response of CO<Subscript>2</Subscript> exchange and dissolved organic carbon release in a maritime Antarctic tundra ecosystem

We examined the temperature response of CO₂ exchange and soil biogeochemical processes in an Antarctic tundra ecosystem using laboratory incubations of intact tundra cores. The cores were collected from tundra near Anvers Island along the west coast of the Antarctic Peninsula that was dominated by the vascular plants Colobanthus quitensis and Deschampsia antarctica. After the initial 8-week incubation at moderate growth temperatures (12/7°C, day/night), the tundra cores were incubated for another 8 weeks at either a higher (17/12°C) or lower (7/4°C) temperature regime. Temperature responses of CO₂ exchange were measured at five temperatures (4, 7, 12, 17, and 27°C) following each incubation and soil leachates were collected biweekly over the second incubation. Daytime net ecosystem CO₂ exchange (NEE) per unit core surface area was higher across the five measurement temperatures after the warmer incubation (17/12°C > 7/4°C). Responses of ecosystem respiration (ER) were similar at each measurement temperature irrespective of incubation temperature regimes. ER, expressed on a leaf-area basis, however, was significantly lower following the warmer incubation, suggesting a downregulation of ER. Warmer incubation resulted in a greater specific leaf area and N concentration, and a lower δ¹³C in live aboveground C. quitensis, but a higher δ¹³C in D. antarctica, implying species-specific responses to warming. Concentrations of dissolved organic C and N and inorganic N in soil leachates showed that short-term temperature changes had no noticeable effect on soil biogeochemical processes. The results suggest that downregulation of ER, together with plant species differences in leaf-area production and N use, can play a crucial role in constraining the C-cycle response of Antarctic tundra ecosystems to warming.     

Interactions between carbon dioxide and oxygen in the photosynthesis of three species of marine red macroalgae

Summary

Red algae have the highest known selectivity factor (S_rel) for CO₂ over O₂ of ribulose bisphosphate carboxylase-oxygenase (RUBISCO). This allows the prediction that a red alga relying on diffusive supply of CO₂ to RUBISCO from air-equilibrated solution should have less O₂ inhibition of photosynthesis than would an otherwise similar non-red alga with a lower S_rel of RUBISCO. Furthermore, RUBISCO shows an increased S_rel values at low temperatures. The prediction that O ₂inhibition of photosynthesis should be small for marine red algae relying on diffusive CO₂ entry growing in the North Sea with an annual temperature range of 4–16°C was tested in O₂ electrode experiments at 12°C. Phycodrys rubens and Plocamium cartilagineum, which rely on diffusive CO₂ entry showed, as predicted, only a small inhibition at lower inorganic C concentrations. Palmaria palmata, which has a CO₂ concentrating mechanism, had the expected negligible O ₂ inhibition of photosynthesis at any inorganic C concentration except (non-significantly) for saturating inorganic C.     

Diversity in the influence of temperature on the growth rates of freshwater algae, and its ecological relevance

1. Growth rates of seven species of planktonic algae were determined in culture over a range of temperature from 2 to 35 °C. Additional observations on growth and viability were made for 13 species in the temperature range 20–35 °C. 2. There was a wide range of growth rates between species at their optimal temperatures, from 1.7 divisions day^?1 (Asterionella formosa) to 0.3 divisions day^?1 (Ceratium furcoides). 3. There were considerable differences between species for growth at low and high temperature. Certain algae, including the diatom A. formosa and the flagellates Cryptomonas marssonii, Dinobryon divergens and Eudorina unicocca var. unicocca, had growth rates of 0.4 divisions day^?1 or more at 5 °C. The cyanophyte Tychonema (formerly Oscillatoria) bourrellyi, the xanthophyte Tribonema sp., the desmid Staurastrum cingulum and the large dinoflagellate C. furcoides grew poorly or not at all at this temperature. All 21 species tested could grow at 25 °C, but many – including most of the diatoms, some cyanophytes, and all the flagellates – failed to grow persistently at 30 °C. Only Aphanizomenon flos‐aquae survived with moderate increase at 35 °C, a lethal temperature for the other species. 4. The applicability was considered of proposed quantitative formulations of the rate‐temperature relationship. Simple exponential relationships applied only to very limited lower ranges of temperature. The relationship proposed by B?lehrádek was a better fit over a wider temperature range, but still excluded rate‐decline at high temperature. 5. The interspecific differences found are of potential significance for restrictions in natural distributions associated with season, altitude (especially above 500 m) and latitude.     

New records of temperate and sub-Antarctic marine benthic macroalgae from Antarctica

 During visits to several localities on the South Shetland Islands and the Antarctic Peninsula in summer 1994 we made collections of marine benthic algae. Among the algae we collected were three new records for Antarctica [Petalonia fascia (OF Müller) Kuntze; Enteromorpha intestinalis (L.) Nees; Rhodymenia subantarctica Ricker] and seven other species [Scytosiphon simplicissimus (Clemente) Cremades; Chordaria linearis (Hooker et Harvey) Cotton; Halopteris obovata (Hooker et Harvey) Sauvageau; Acrosiphonia arcta (Dillwyn) J. Agardh; Enteromorpha compressa (L.) Nees; Bangia atropurpurea (Roth) C. Agardh; Porphyra plocamiestris Ricker] that had been reported on only one or two previous occasions (or, in one case, three). The ten species detailed in this paper fall into two groups: four species previously known from sub-Antarctic islands and/or locations in southern South America, and six species having a wider distribution in temperate regions. We discuss the possibility that the less accessible subtidal habitats of some species may have prevented earlier discovery. Other species may be comparatively recent adventives, most likely introduced with shipping. In view of possible global climate changes, species of this latter group are regarded as suitable organisms for monitoring changes of water temperature. Received: 12 December 1995/Accepted: 14 April 1996     

Temperature requirements for the growth of young sporophytes of Undaria pinnatifida and Undaria undarioides (Laminariales, Phaeophyceae)

The relative growth rate of young sporophytes of Undaria pinnatifida (Harvey) Suringar and Undaria undarioides (Yendo) Okamura was examined in order to understand the difference in distribution of these two species around the coast of Japan. The optimal temperature for growth of both species was similar at 20°C and the upper critical temperature for growth was also similar, at 27°C for U. pinnatifida and 26°C for U. undarioides. Therefore, the optimal and upper critical temperatures for growth of the young sporophytes are not the main factors determining the distribution of each species. Next, the lower critical temperatures for growth were examined. For the young sporophytes of U. pinnatifida, the lower limit was less than 5°C while for those of U. undarioides it was 15°C. Thus, the difference in the lower critical temperature for growth between the two species was approximately 10°C. During the period of young sporophyte growth in the field, the temperature at the mouth of Ise Bay, Japan, where U. pinnatifida occurs, ranges from 12.7°C in December to 13.1°C in April, with a minimum of 7.9°C in February. Our experiments indicate that young sporophytes are able to grow throughout this period. The temperature off Hamajima, Japan, where U. undarioides occurs, ranges from 19.1°C to 14.8°C during the same time period. Again, young sporophytes are able to growth throughout this period, although minimum winter temperatures are only just high enough for growth. These natural temperature ranges during the growth season of the sporophytes agree well with the experimentally determined temperature requirements for growth of each species. Therefore, the difference between the two species in the critical temperature required for growth of the young sporophytes, especially in the low temperature range, is one of the major factors determining the distribution pattern of each species.