Autecological investigation on marine diatoms 3. Thalassiosira nordenskioeldii and Chaetoceros diadema

The temperature range for the best competitive position by growth of Thalassiosira nordenskioeldii Cleve has been determined by comparing generation times. It ranges from-1.5° to 6°C. At these temperatures, especially at lower light intensities, it was one of the fastest growing species, whereas above 6°C many other species grew faster. High light intensities at increasing temperatures became damaging. A flowering of the cold oligo-eurytherm diatom T. nordenskioeldii occurs not only in the upper layers, but can also occur at greater depth simultaneously, because decreasing daylengths at 6°C had the least influence on its growth. Continuous light at 6°C had a positive influence on its growth. The start of the T. nordenskioeldii spring flowering under the Arctic Sea Ice is discussed in connection with the occurrence of enclosed marine diatoms in Polar Sea Ice. The influence of the winter temperature on the spring flowering of the North Sea, the southern border for flowerings of T. nordenskioeldii, is discussed. For Chaetoceros diadema (Ehrenberg) Gran the best competitive position by growth is reached at-1.5° to about 6°C. It has the best opportunity of reaching high cell numbers at the lowest temperatures of the range. The occurrence of the cold oligo-eurytherm diatom Ch. diadema in plankton samples at temperatures above 10°C need not be incorret, for the species did grow in cultures at 12° and 16°C. The wrong interpretation of the experimentally determined optimum temperature of e.g. T. nordenskioeldii caused a discrepancy between experimental results and field data that does not exist. The question is discussed whether ecologically it is relevant to talk about a temperature optimum. On account of the results of T. nordenskioeldii the question of the adaptation of diatom cultures for the start of the real experiments is discussed.     

Optimal growth and maximal survival temperatures of Atlantic Laminaria species (Phaeophyta) in culture

The effects of temperature on growth rate of rapidly-growing cultured macrosporophytes of 9 isolates of Atlantic Laminaria comprising 4 species have been investigated. No significant population variation was observed within species despite wide variations in temperature between the original collecting sites. L. saccharina showed a broad temperature optimum in the 10°–15°C range, whereas L. longicruris had a sharp optimum at 10°C. L. digitata and L. hyperborea grew more slowly, with only slightly sub-optimal growth over a wide temperature range, but with peaks at 10°C (L. digitata) and 15°C (L. hyperborea). The maximum survival temperatures of individual male and female vegetatively-growing gametophytes were ascertained for these species plus the Arctic L. solidungula, and were as follows: L. saccharina and L. longicruris, 23°C; L. digitata (male), 23°C; L. digitata (female), 22°C; L. hyperborea, 21°C; L. solidungula, 18°C. The lack of within-species differences demonstrates that the success of the genus in areas with different temperature regimes is brought about by phenotypic plasticity of individuals rather than the selection of temperature races or ecotypes.     

Temperature tolerance and latitudinal range of brown algae from temperate Pacific South America

Lower and upper survival temperatures of microthalli of 25 species of South American Phaeophyceae isolated from central Peru (14°S) to the Canal Beagle (55°S) were determined using 2-wk exposure for the upper and 4-wk exposure for the lower limit. All species survive 4 wks at -2°C. With respect to the upper limit, species reported only from southernmost South America tolerate 19.9 to 24.5°C (n=8), and species occurring from Cape Horn to central Chile 24.6 to 27.4°C (n=7). Three species that occurred as far north as northern Chile and Peru before the 1982–1983 El Niño event, and whose northern limit was dramatically shifted southwards in 1983, tolerate 20.8 to 25.3°C, whereas five species that have survived in Peru tolerate 25.6 to 28.5°C. Tinocladia falklandica which tolerates 27.8 to 28.1°C but lives only in southernmost South America and Striaria attenuata, which tolerates 31.6 to 31.9°C but occurs at ca. 42°S, are exceptional. Their high temperature tolerance may have no adaptive value in South America. They are restricted to the cold-temperate region due to low temperature requirements for reproduction or for reasons yet unknown. In general, the northern distributional limits of the Phaeophyceae studied along the temperate Pacific coast of South America are reproduction boundaries, except in El Niño years when they are redefined according to the species' upper suvival limits. Temperature tolerance of isolates from northern Chile and Peru agrees well with maximum temperatures reached during the 1983 El Niño.     

Effects of various temperature cycles on the larval development of the gastropod molluscCrepidula fornicata

Veligers ofCrepidula fornicata (L.) were reared for 12 days at constant temperatures of 15°, 20°, 25°, 30° and 35°C, and at 5 C° daily cycles of equal periodicity (COEP) over the temperature ranges 15° to 20°C, 20° to 25°C, 25° to 30°C and 30° to 35°C. COEP consisted of equal periods (6 h) of maximum temperature, minimum temperature, and uniformly increasing and decreasing temperature each 24 h period. Survival was high and not influenced by cyclic or constant temperature from 15° to 30°C. At 35°C and COEP 30° to 35°C, all larvae died before Day 6. Shell growth rate increased markedly over the range 15° to 25°C, and growth rates at cyclic temperatures in this range were intermediate between growth rates at the corresponding constant temperatures. Larvae reared at COEP 15° to 20°C and COEP 30° to 35°C had discontinuities in their shells due to inhibition of shell secretion during the adverse part of each temperature cycle. Groups ofc. fornicata veligers were exposed for 2 days to daily temperature cycles of equal and unequal periodicity in the critical 30° to 35°C range. [Cycles of unequal periodicity (COUP) consisted of unequal periods (varying between 3 and 15 h) of maximum and minimum temperature and uniformly increasing and decreasing temperature each 24 h period.] These veligers showed shell growth although their body tissue declined, as indicated by decreasing carbon content per larva. Least shell growth and most body tissue loss occurred in those cycles with the longest exposure to higher temperature. Larvae exposed for arious days to the mildest 30° to 35°C COUP (15 h at 30°C, 3 h increasing temperature, 3 h at 35°C and 3 h decreasing temperature) recovered and resumed normal growth when transferred to constant 30°C, but their growth was retarded in proportion to the number of days in the temperature cycle. Rates of shell growth of veligers in temperature cycles show an immediate effect of environmental temperature, while changes in carbon content per larva better reflect the effects of temperature on general metabolism and survival.     

Physiological ecology of four Polysiphonia species (Rhodophyta,Ceramiales)

Photosynthesis and respiration of 4 species of the marine red algal genus Polysiphonia were evaluated under a variety of light, temperature and salinity conditions. The manometric results were compared with the local distribution and abundance of each species. The species can be separated into two distinct categories based on their overall distribution and temperature optima: (1) cold water plants [P. lanosa (L.) Tandy and P. elongata (Hudson) Sprengel], with peak photosynthesis at 21° to 24°C, but with active photosynthesis as low as 5°C; (2) plants with warm-water affinities [P. nigrescens (Hudson) Greville and P. subtilissima Montagne], having photosynthetic optima at 27° to 30°C, and exhibiting little or no photosynthesis below 10°C. The plants from the first group exhibit thermal injury at temperatures of 25°C and show a narrow tolerance to low salinities during periods of high temperatures. The plants from the second group show thermal injury at 30°C and have a wider tolerance to low salinities. The horizontal distribution of the 4 Polysiphonia species within the Great Bay Estuary System of New Hampshire, USA, is primarily governed by their tolerances to high temperatures and low salinities. The temperature optimum for each of the species corresponds to its particular estuarine distribution. Thus, P. subtilissima, having the highest temperature optimum, penetrated furthest into the Estuary, while P. lanosa, having the lowest temperature optimum, was restricted to the more coastal stations. There was a good correspondence between the natural distribution patterns and the manometric results.Published with the approval of the Director of the New Hampshire Agricultural Experiment Station as Scientific Contribution No. 731.Scientific Contribution No. 4 of the Jackson Estuarine Laboratory.     

Temperature tolerance of the estuarine prawn Upogebia africana (Anomura,Crustacea)

Continuous temperature measurements were made in a typical South East African estuary. Mean summer (November to March) temperatures were in the range 19° to 24°C, and in winter (June to August) from 13° to 16°C. Large daily temperature fluctuations of 6° to 10°C occurred in summer; these appear to result from tidal movement of cool sea water into the estuary. In winter, temperature fluctuations were much smaller (3° to 5°C). The burrowing prawn Upogebia africana (Obtmann) was found to have an upper lethal temperature of 29°C in both winter and summer. The resistance time of prawns to temperatures above 30°C was much greater in summer than in winter. It was possible to acclimate winter prawns and increase their resistance time to a level comparable to that of summer individuals. A latent period of 40 h occurred before acclimation effects were detectable. Long-term exposure of prawns to high temperatures did not increase their resistance above that of summer prawns. Water at a temperature above this upper lethal temperature is not pumped through the burrows. This avoidance behaviour considerably increases the ability of U. africana to withstand short-lived temperature extremes.     

Effect of high temperatures on the ultrastructure of Leydig cells in Mytilus galloprovincialis

Individuals of the mussel Mytilus galloprovincialis (L), collected from the Black Sea, were subjected to relatively high temperatures (25°, 28° and 30°C) for 60 h Ultrastructural studies on Leydig cells of the mantle indicated progressive modifications in their structure. Mainly, we established that a continuous decrease of glycogen quantity in the cells took place as the temperature raised, while the lipid content increased, up to 28°C. Between 28° and 30°C the lipid content decreased as a result of a pronounced degradation process. An increase of membrane permeability and the disturbance in the synthesis of mucoproteic secretory granules were observed. It is concluded that for Mytilus galloprovincialis the thermal adaptation zone ranges between 25° and 28°C. 28°C is the upper tolerable limit temperature, while 30°C acts as a lethal temperature.     

Larval viability and heterozygote deficiency in populations of marine bivalves: evidence from pair matings of mussels

Using a pressurized temperature gradient, which rapidly equilibrates bacteria to a wide range of temperature and pressures, temperature ranges for growth and survival of Vibrio harveyi (strain B 392) were found to narrow with increasing pressures. Both temperature and pressure ranges were greater in an enriched seawater medium than in unenriched seawater. Using a kinetics apparatus, V. harveyi was also exposed to gradual changes in temperature and pressure, simulating a particle sinking at approximately 200 m d^-1 from surface waters (17 °C; 1 bar pressure) to 3 400 m (4°C; 340 bars pressure). With gradual temperature changes, cells were able to grow and survive at lower temperatures than they had in rapid equilibration experiments. Gradual pressurization, however, did not increase pressure tolerance. Under all experimental conditions, the combined effects of low temperatures and high pressures were lethal for V. harveyi. It is hypothesized that temperature and pressure stratify the ocean into regions of growth, survival, and death for V. harveyi, and perhaps other bacteria.     

Yolk utilization and growth to yolk-sac absorption in summer flounder (Paralichthys dentatus) larvae at constant and cyclic temperatures

Rates of development, growth and yolk conversion efficiency were determined in larvae of the summer flounder Paralichtys dentatus at constant temperatures of 21°, 16°, 12° and 5°C and in temperature cycles of 21°–16°, 16°–11°, and 11°–5°C. In constant incubation temperatures, development rate increased with increasing temperature. Larvae reared in the cyclic temperature regimes exhibited development rates intermediate to those at the temperature extremes of the cycle. All larvae reared at 5°C and in the 11°–5°C cycle regime died prior to total yolk-sac absorption. Although development rates were temperature dependent, no significant differences in notochord length ash-free dry weight or yolk utilization efficiency were found at the time of total yolk-sac absorption. The similarity in growth and yolk utilization efficiency for larvae reared under these various temperature regimes suggests that the physiological mechanisms involved are able to compensate for temperature changes encountered in nature.Contribution No. 195 from EPA, Environmental Research Laboratory, Narragansett, Rhode Island 02882, USA     

Effect of temperature on the proliferation of Gymnodinium breve and Gomphosphaeria aponina

The effect of temperature on the growth and proliferation of two marine microorganisms, the toxigenic dinoflagellate Gymnodinium breve, and a potential bio-control organism, the blue-green alga Gomphosphaeria aponina, was determined by culturing the organisms in thermal gradients established by heating and cooling the opposite ends of an aluminum bar that had been adapted to hold culture tubes. Gradients were linear and stable for the duration of each trial. There was no relationship between variations in light and growth of the organisms. Gymnodinium breve showed optimum growth at 22°C, and proliferated over a range of temperatures (17° to 30°C). Below 17°C cultures of G. breve declined in growth, and at 4°C the organisms died within 5 h. Above 31°C there was rapid decline in viability of cells, and at 33.5°C the organism died within 24 h. Gomphosphaeria aponina showed optimum growth between 24° and 29°C, with a maximum at 27°C. Growth at temperatures greater than 31°C was minimal, but the organism survived. Limitation may be due to repression of the bio-synthesis of an iron-transport compound.     

Metabolic responses of the sympagic amphipodsGammarus wilkitzkii andOnisimus glacialis to acute temperature variations

Acutely elevated seawater temperatures had pronounced metabolic effect on the Arctic under-ice amphipodsGammarus wilkitzkii andOnisimus glacialis, collected in May 1986 and 1988 in the Barents Sea. An increased rate of oxygen consumption vs temperature was observed for both species. In the range from 0° to 10 °CG. wilkitzkii andO. glacialis exhibit Q₁₀ values of 3.4 and 3.6, respectively. The results also indicate increased ammonia excretion rates forG. wilkitzkii andO. glacialis by an elevation of temperature from 0° to 10°C, with an overall Q₁₀ of 1.9 and 2.3, respectively. The present study demonstrates an increased O:N ratio with ambient temperature elevation from 0° to 10°C forG. wilkitzkii andO. glacialis, with overall Q₁₀ values of 2.0 and 1.6, respectively. This indicates a temperature-induced change in the metabolic substrate towards lipids.     

Response of gametophytes of Ecklonia radiata (Laminariales) to temperature in saturating light

Gametophytes of Ecklonia radiata (C.Ag.)J.Ag. from two New Zealand locations with different field temperature ranges were exposed to temperatures of 5° to 26°C in saturating light. Plants from Goat Island Bay (Lat. 36° 16S, Long. 174°48E) grew in 9.3° to 25°C and reproduced in 9.3° to 24°C. There was no growth at 8°C and plants died at 26°C. Plants from the cooler location, Houghton Bay (Lat. 41°20S, Long. 174°40E), grew from 8° to 24°C and reproduced up to 15°C but not at 21.5°C. The plants did not grow at 6°C and died at 26°C. The timing of the first cell division and subsequent growth rate were retarded close to the upper and lower tolerance limits. Reproduction was a broad optimum of roughly 12° to 20°C. Within this range, fertile female gametophytes grown at lower temperatures had fewer, larger cells and thus fewer potential ova than those grown at higher temperatures.     

Temperature,salinity and ultraviolet irradiation effects on the growth of strains of Nitzschia ovalis

Three strains of Nitzschia ovalis Arnott grew at temperatures from 15°–36°C and at salinities from 5–40 S Optimum growth occurred at combinations of 25°, 27.5° and 30°C and 25, 30 and 35S. This estuarine benthic diatom tolerates wide salinity and temperature conditions while demonstrating resistance to ultraviolet irradiation at 350 nm.     

A response-surface approach to the combined effects of temperature and salinity on the larval development of Adula californiensis (Pelecypoda: Mytilidae). I. Survival and growth of three and fifteen-day old larvae

Laboratory experiments of a factorial design were used to examine the combined effects of temperature and salinity on the survival and growth of early and late-stage larvae of Adula californiensis (Phillippi, 1847). Response-surface curves were generated to predict optimal conditions for survival and growth in order to better understand the successful recruitment of this species within the Yaquina Bay estuary (Oregon, USA). Three-day old cultured larvae were more sensitive to reduced salinity than were 15-day old larvae. However, the 15-day old larvae showed a narrower temperature tolerance than the 3-day old larvae. A. californiensis larvae survived over a wider range of temperatures near optimum salinities than at salinities near their lower tolerance limit, and conversely. Temperature and salinity ranges for maximum survival (10° to 15°C, 31 to 33) were narrower than the ranges which occur within the estuary where the adult populations exist. Larval size did not increase markedly during the 15-day rearing period, and was not greatly affected by temperature or salinity. No statistically significant temperature-salinity interaction was found for either survival or growth.     

Temperature ecotypes near the southern boundary of the kelp Laminaria saccharina

Effects of temperature on survival, growth, and photosynthesis were compared for two USA populations of Laminaria saccharina Lamour. One population was located in New York State, near the southern latitudinal boundary of the species in the western North Atlantic. This southern boundary population was exposed to ambient temperatures 20°C for about 6 wk each summer. The second population was located in Maine, toward the center of the latitudinal range of the species, and was rarely exposed to temperatures>17°C. sporophytes from the New York (NY) population exhibited greater tolerance of high temperature than plants from the Maine (ME) site. Juvenile sporophytes from the two sites had similar rates of survivorship and growth at temperatures below 20°C, but showed different responses at 20°C in laboratory experiments. NY plants survived and grew for 6 wk at 20°C. ME plants showed negative growth during wk 2 and 100% mortality during wk 3. NY and ME plants held in situ at the NY site during June to September, 1985, also exhibited differential survivorship when ambient temperatures exceeded 20°C. Results of photosynthesis and dark respiration measurements on NY and ME plants grown at various temperatures suggested that the high-temperature tolerance of NY plants was attributable to their ability to maintain positive daily net C-fixation at 20°C. The high-temperature tolerance of the NY plants appeared to be due to genetic adaptation and is probably crucial to the persistence of the species near its southern boundary.     

Effect of temperature on the molting,growth and maturation of the antarctic krill Euphausia superba (Crustacea: Euphausiacea) under laboratory conditions

The effect of temperature on molting, growth, and maturation rates was studied on laboratory-maintained Euphausia superba. The length of intermolt periods (IMP's) was inversely proportional to temperature (20.10 d, SD=1.60, at 0.12°C; 16.87 d, SD=1.68, at 0.97°C; and 12.48 d, SD=0.90, at 4.48°C), and directly proportional to krill size at 0.12°C and 0.97°C. For individually maintained krill the maximum growth rate at 4.48°C (0.068 mm d^-1) was nearly twice that at 0.68°C (0.037 mm d^-1). There was no observable temperature effect on maturation rates. The maturation changes of juveniles at all temperatures indicated that more than two years are probably required to reach maturity. Mature males and females regressed to immature forms, suggesting that E. superba may reproduce in successive years. These results and previously reported field and laboratory data for E. superba and other euphausiid species suggest a 4+ year life span for this species.This work was supported by NSF grant DPP 76-23437     

Effects of temperature on the mortality and growth of Hawaiian reef corals

Three common species of Hawaiian reef corals, Pocillopora damicornis (L.), Montipora verrucosa (Lamarck) and Fungia scutaria Lamarck, were grown in a temperature-regulated, continuous-flow sea water system. The skeletal growth optimum occurred near 26°C, coinciding with the natural summer ambient temperature in Hawaii, and was lowest at 21° to 22°C, representing Hawaiian winter ambient. Levels of approximately 32°C produced mortality within days. Prolonged exposure to temperatures of approximately 30°C eventually caused loss of photosynthetic pigment, increased mortality, and reduced calcification. Corals lived only 1 to 2 weeks at 18°C. The corals showed greater initial resistance at the lower lethal limit, but ultimately low temperature was more deleterious than high temperature. Results suggest that a decrease in the natural water temperature of Hawaiian reefs would be more harmful to corals than a temperature increase of the same magnitude.Contribution No. 504 of the Hawaii Institute of Marine Biology.     

A dispersal model for larvae of the deep sea red crab Geryon quinquedens based upon behavioral regulation of vertical migration in the hatching stage

Behavioral responses to gravity, hydrostatic pressure, and thermoclines are described for Stage I zoeae of the deep sea red crab Geryon quinquedens Smith. Survival and rate of development as a function of temperature is presented for all larval stages. Although temperatures between 10° and 25°C have no direct effect upon survival, development time is five times longer at 10°C than at 25°C. Stage I larvae show strong negative response to gravity. Swimming rate increases with an increase in pressure up to 20 atm above ambient at 11°C, but not at 15°C. Swimming rates at 15°C are higher than those measured at 11°C at each pressure tested. Stage I larvae readily penetrate sharp thermoclines. Potential dispersal ranges of G. quinquedens larvae in the Mid-Atlantic Bight are suggested based on larval behavior, development time, and coastal hydrography. A testable recruitment model is proposed for G. quinquedens.Contribution no. 1365 of the Center for Environmental and Estuarine Studies     

Suitability of estuarine nursery zones for juvenile weakfish (Cynoscion regalis): effects of temperature and salinity on feeding,growth and survival

Juvenile weakfish, Cynoscion regalis (Bloch and Schneider, 1801), exhibit significant spatial diffrences in growth rate and condition factor among estuarine nursery zones in Delaware Bay. The potential influence of temperature and salinity on the suitability of estuarine nursery areas for juvenile weakfish was investigated in laboratory experiments by measuring ad libitum feeding rate, growth rate and gross growth efficiency of juveniles collected in Delaware Bay in 1990 (40 to 50 mm standard length; 1.4 to 2.1 g) in 12 temperature/salinity treatments (temperatures: 20, 24, 28°C; salinities: 5, 12, 19, 26 ppt) representing conditions encountered in different estuarine zones during spring/summer. Feeding rates (FR) increased significantly with temperature at all salinities, ranging from 10 to 15% body wt d^-1 at 20°C to 33–39% body wt d^-1 at 28°C. Specific growth rates (SGR) ranged from 1.4 to 9.4% body wt d^-1 (0.3 to 1.5 mm d^-1) and gross growth efficiencies (K ₁) varied from 13.6 to 26.4% across temperature/salinity combinations. Based on nonlinear multiple regression models, predicted optimal temperatures for SGR and K ₁ were 29 and 27°C, respectively. Salinity effects on SGR and K ₁ were significant at 24 and 28°C where predicted optimal salinity was 20 ppt. At these warmer temperatures, SGR and K ₁ were significantly lower at 5 than at 19 ppt despite higher FR at 5 ppt. Therefore, maximum growth rate and growth efficiency occurred under conditions characteristic of mesohaline nurseries. This finding is consistent with spatial patterns of growth in Delaware Bay, implying that physicochemical gradients influence the value of particular estuarine zones as nurseries for juvenile weakfish by affecting the energetics of feeding and growth. Laboratory results indicate a seasonal shift in the location of physiologically optimal nurseries within estuaries. During late spring/early summer, warmer temperatures in oligohaline areas permit higher feeding rate and faster growth compared to mesohaline areas. By mid-late summer, spatial temperature gradients diminish and mesohaline areas provide more suitable physicochemical conditions for growth rate and growth efficiency whereas oligohaline areas become energetically stressful. Substantial mortality occurred at 5 ppt and 28°C, providing additional evidence that oligohaline conditions are stressful during late summer. Furthermore, juveniles provided a choice among salinities in laboratory trials preferred those salinities which promoted higher growth rates. The extensive use of oligohaline nurseries by juvenile weakfish despite the potential for reduced growth rate and growth efficiency suggests this estuarine zone may provide a substantial refuge from predation.     

High-temperature tolerance of photosynthesis in the red alga Chondrus crispus

Chondrus crispus (Stackhouse) is a perennial red seaweed, common in intertidal and shallow sublittoral communities throughout the North Atlantic Ocean. In the intertidal zone, C. crispus may experience rapid temperature changes of 10 to 20C° during a single immerison-emerision cycle, and may be exposed to temperatures that exceed the thermal limits for long-term survival. C. crispus collected year-round at Long Cove Point, Chamberlain, Maine, USA, during 1989 and 1990, underwent phenotypic acclimation to growth temperature in the laboratory. This phenotypic acclimation enhanced its ability to withstand brief exposure to extreme temperature. Plants grown at summer seawater temperature (20°C) were able to maintain constant rates of lightsaturated photosynthesis at 30°C for 9 h. In contrast, light-saturated photosynthetic rates of plants grown at winter seawater temperature (5°C) declined rapidly following exposure to 30°C, reached 20 to 25% of initial values within 10 min, and then remained constant at this level for 9 h. The degree of inhibition of photosynthesis at 30°C was also dependent upon light intensity. Inhibition was greatest in plants exposed to 30°C in darkness or high light (600 mol photons m^-2s^-1) than in plants maintained under moderate light levels (70 to 100 mol photons m^-2s^-1). Photosynthesis of 20°C-acclimated plants was inhibited by exposure to 30°C in darkness or high light, but the degree of inhibition was less than that exhibited by 5°C-grown plants. Not only was light-saturated photosynthesis of 20°C plants less severely inhibited by exposure to 30°C than that of 5°C plants, but the former also recovered faster when they were returned to growth conditions. The mechanistic basis of this acclimation to growth temperature is not clear. Our results indicate that there were no differences between 5 and 20°C-grown plants in the thermal stability of respiration, electron transport associated with Photosystems I or II, Rubisco or energy transfer between the phycobilisomes and Photosystem II. Overall, our results suggest that phenotypic acclimation to seawater temperature allows plants to tolerate higher temperatures, and may play an important role in the success of C. crispus in the intertidal environment.