Combined effects of temperature and salinity on the complete development ofEurytemora velox (Crustacea: Calanoidea)

The calanoid copepodEurytemora velox was collected from rock pools at Castletown, Isle of Man, UK. Its optimum environmental requirements, particularly temperature and salinity, were determined, with a view to its possible future use as living food in intensive fish and shellfish farming. The species was cultured in 21 different temperature and salinity combinations. Investigations covered a period of two years from December 1983 to December 1985. Complete development from hatching to adult stage was followed in 21 temperature and salinity combinations. Nauplii suffered relatively high mortalities, indicating the sensitivity of this development stage to variations in temperature and salinity. Highest nauplii survival was observed in the combinations 15°C with 25 and 20 S and 20°C with 20 S, the highest copepodite survival at 10°C and 20 S. Lower salinities were tolerated better at higher temperatures and higher salinities at lower temperatures. Development time varied with the temperature and salinity combinations. Lower salinities at the lower temperatures of 10° and 15°C and both lower and higher salinities at 20°C prolonged development, particularly of the naupliar stage. Highest Q₅ values (i.e., rate of change of development with a 5 C° increase in temperature) were recorded for the naupliar stage. Statistical analysis indicated that salinity influences the survival of both nauplii and copepodites; however, this effect is not linear.     

Combined effects of temperature and salinity on fed and starved larvae of the mediterranean mussel Mytilus galloprovincialis and the Japanese oyster Crassostrea gigas

The combined effects of temperature, salinity and nutrition on survival and growth of larvae of the Mediterranean mussel Mytilus galloprovincialis and the Japanese oyster Crassostrea gigas were studied over a period of 7 d in the laboratory. Ripe adults, collected in spring and summer 1987 from natural populations in the Bay of Arcachon, France, were induced to spawn. Larvae of both species were cultured at four temperatures (15°, 20°, 25° and 30°C), four salinities (20, 25, 30 and 35S) per temperature, and two levels of nutrition (fed and unfed) per temperature/salinity combination. The fed larvae received a mixed algal diet of 50 cells each of Isochrysis galbana and Chaetoceros calcitrans forma pumilum per microlitre. In both bivalve species, larvae survived over a wide range of temperature and salinity, with the exception of mussel larvae, which died at 30°C. Statistical analysis indicated that nutrition had the greatest effect on larval development, explaining 64 to 75% of the variance in growth of M. galloprovincialis and 54 to 70% in growth of Crassostrea gigas. Unfed mussel larvae displayed little growth. Compared with temperature, the effect of salinity was very slight. M. galloprovincialis larvae exhibited best growth at 20°C and 35S and C. gigas at 30°C and 30S.     

The combined effects of salinity and temperature on larvae of the mussel Mytilus edulis

The combined effects of salinity and temperature on survival and growth of larvae of the mussel Mytilus edulis (L.) were studied. The effects of salinity and temperature are significantly related only as the limits of tolerance of either factor are approached. Survival of larvae at salinities from 15 to 40 is uniformly good (70% or better) at temperatures from 5° to 20°C, but is reduced drastically at 25 °C, particularly at high (40) and low (20) salinities. Larval growth is rapid at a temperature of 15 °C in salinities from 25 to 35, at 20 °C in salinities from 20 to 35. Optimum growth occurs at 20 °C in salinities from 25 to 30. Growth decreases both at 25° and 10 °C; the decline is most drastic at high (40) and low (20) salinities.Part of a study completed at the Bureau of Commercial Fisheries, Biological Laboratory, Milford, Connecticut, USA, while on a UNESCO Fellowship.     

The effect of salinity and cyclic temperature on larval development of the mud-crab Rhithropanopeus harrisii (Brachyura: Xanthidae) reared in the laboratory

Larvae of Rhithropanopeus harrisii (Gould) were reared from hatching to the first or second crab stages in 11 combinations of salinities and cyclic temperatures (5, 20, and 35 S at 20° to 25°C, 25° to 30°C, and 30° to 35°C; 25 S at 20° to 25°C and 30° to 35°C). The larvae survived to the megalops and first crab stages in all salinities and cycles of temperature other than 5 S at 30° to 35°C. The best survival to the megalops (94%) and first crab (90%) stages occurred in 20 S, 20° to 25°C. In all other combinations of salinities and temperatures there was a reduction in survival to the first crab stage. The duration of the larval stages was affected significantly by temperature, whereas the effect of salinity on the mean days from hatching to the first crab stage was not consistent at the different temperature cycles. Development to the first crab stage required the shortest time in 20 S, 30° to 35°C (mean 12.3 days), and the longest time in 5 and 35 S, 20° to 25°C (mean 22.6 days and 21.6 days, respectively). Megalops larvae reared in 35 S at all cycles of temperature, as well as larvae in 20 and 25 S, 30° to 35°C, showed a high percentage of abnormality, with the highest percentage occurring in 35 S, 30° to 35°C. It appears that larval development of R. harrisii is strongly influenced by environmental factors and not solely related to genetic differences.This research was supported by grants from the Nordic Council for Marine Biology and the U.S. Atomic Energy Commission [Grant No. At-(40-1)-4377].Contribution No. 116, Zoological Museum, University of Oslo, Norway.     

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.     

Effect of temperature and salinity on larval development of southern king crab (Lithodes antarcticus)

Larvae of Lithodes antarcticus Jacquinot were reared in October, 1981 from hatching to the glaucothoe stage at 16 temperature/salinity combinations (5.5°; 7.5°; 9.5° and 13.5°C; 26, 29, 32 and 35 S) to determine optimal environmental conditions for larval development. The highest survival percentage was obtained in the culture at 7.5°C and diminished according to temperature increase or decrease. High temperature cultures significantly shorten the larval life duration, but produce large mortalities. At 5.5°C mortality occurred almost exclusively during the moult to glaucothoe stage. Higher survival percentages were obtained as salinity was increased. In the lowest salinity culture (26 S) no zoea reached the post-larvae stage at culture temperatures. The best T/S combination was obtained at 7.5°C and 35 S, with a survival percentage of 29%. The shortest zoeal developments were obtained at 32 S in all culture temperatures. Salinity also affects larvae coloration: there is a pigment concentration on erythrophores, which causes a color decrease.     

Salinity tolerance,salinity preference and temperature tolerance in the high-shore harpacticoid copepod Tigriopus brevicornis

Tigriopus brevicornis (O. F. Müller) were collected in 1992 from rock pools close to U.M.B.S. Millport, Isle of Cumbrae, U.K. and acclimated to various combinations of salinity and temperature for at least 1 wk prior to laboratory experiments. Higher salinities of acclimation enhanced tolerance to high salinity stress, while tolerance of low salinities was hardly affected by acclimation salinity. Acclimation to low temperature (10°C) extended the survivable salinity range for T. brevicornis. High-salinity acclimation enhanced the survivable temperature range. Copepods acclimated to 60 survived significantly lower and higher temperatures than did 34-acclimated individuals. At high temperature, 75-acclimated female copepods had the highest median lethal temperature, 38.9°C. Females were significantly more resistant to high temperatures than males. The copepods were seen to have a very low median lethal temperature when frozen into solid ice for 2 h; 50% mortality occurred at-16.9°C in 10°C, 34-acclimated T. brevicornis. Salinity preference experiments demonstrated an ability to discriminate between salinities differing by as little as 3. Copepods acclimated to 34 chose salinities near their acclimation salinity; individuals acclimated to 5 favoured slightly higher salinities, while copepods acclimated to 60 chose rather lower salinities.     

Effects of temperature and salinity on larval development ofNecora puber (Brachyura: Portunidae)

Temperature and salinity affected both length of larval development and mortality inNecora puber collected in the Ría de A Coruña during December 1984 and January 1985. Development time decreased considerably with increased temperature. This decrease was sharper when temperature increased from 15° to 20°C than when it increased from 20° to 25°C. At 35S, average development took 48, 32 and 28 d at 15°, 20° and 25°C, respectively. At the three salinities tested (25, 30 and 35), larval development was completed only at 15°C, at 20°C/30 and 35S, and at 25°C/35S. Development times at 15° and 20°C were highly significantly different at both 35 and 30S (P 0.01). However, there were no significant differences between development times at 20° and 25°C (P > 0.05). Within any one specific temperature series, no significant difference was observed between the salinity values tested (P > 0.05). The duration of each of the five zoeal stages was similar within each and the same temperature/salinity combination, whereas the duration of the megalop was twice as long as any of the zoeal stages. The combination of the lowest temperature (15°C) and the highest salinity (35) tested resulted in the greatest larval survival of 28%. Highest mortality occurred at 25°C, at which temperature development was completed only at 35S. A sharp drop in larval survival was observed in the transition period Zoea V — megalop in all combinations of temperature and salinity tested. Within the limits of tolerance to temperature and salinity, the former effected more pronounced differences in the duration of larval development, while salinity appeared to constitute a limiting factor for survival.     

Laboratory study of effects of temperature and salinity on survival and larval development of a population of Rhithropanopeus harrisii from the Mondego River estuary,Portugal

Rhithropanopeus harrisii (Gould) is an introduced species in the estuary of the Mondego River (Portugal): it was first recorded from the Iberian Peninsula in 1989. The larval development of this population was studied under laboratory conditions at different temperatures and salinities, and showed a larval development pattern very similar to that reported for American estuarine populations of this species. Larval development was negatively correlated with temperature. Time to megalopa varied between 7 and 35 d; the first crab (C₁) was reached after a maximum of 11 to 43 d. Larval development was optimum at 25°C and 15S. Larval survival was maximum at 10, 15 and 20S at all three temperatures studied (20, 25 and 30°C). The percentage of abnormal megalopae increased with increasing salinity to a maximum (100%) at 30S; incidence of abnormality was not affected by temperature.     

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.     

The significance of temperature,salinity and zinc as lethal factors for the mussel Mytilus edulis in a polluted estuary

Mussels, Mytilus edulis L., were subjected to high temperatures, low salinities and dissolved zinc in order to investigate possible environmental hazards of a discharge of heated effluent near Newport on the Yarra River estuary, Victoria, Australia. Exposure to zinc at 0.8 mg l^-1 for 14 d in otherwise favourable conditions significantly increased mortality resulting from subsequent exposure to temperatures between 29° to 31°C for 24 h without added zinc. Mussels collected from water of temporarily lowered salinity (8–16 S) showed significantly lower thermal resistance than controls collected from marine salinities (35 S). Mussels taken from a marine environment and exposed to 10 S died at a rate which increased with temperature. Mussels acclimated for 14 d to combinations of 10°, 16° and 22°C and 22 and 35 S, and subsequently exposed to increased zinc concentrations accumulated zinc to levels which were independent of temperature and salinity. The zinc was lethal more quickly at 22°C and 35 S than at the lower temperatures and salinities. The modes of toxic action of the salinity, zinc and temperature factors are discussed and it is argued that zinc which has been found accumulated in mussels near Newport could be reducing their resistance to raised temperatures and perhaps other stresses, probably as a result of effects on lysosomal functioning. The evidence suggests that the heated effluent will accelerate any toxic effects of zinc or low salinities which occur near Newport and so poses a hazard in winter as well as in summer.     

Combined effects of temperature and salinity on embryos and larvae of the northern bay scallop Argopecten irradians irradians

The combined effects of temperature and salinity on embryonic development and on larval survival and growth to setting size of the northerm bay scallop Argopecten irradians irradians (Lamarck) were studied in the laboratory. A 6x6 complete factorial design was used; temperatures ranged from 10° to 35°C, at 5C° intervals, and salinities ranged from 10 to 35S, at 5S intervals. Response-surface contour diagrams were generated to provide estimates of conditions for optimal responses. Normal development of embryos occurred over a very narrow range of temperature and salinity. Survival of larvae occurred over a wider range of temperature and salinity than did embryonic development or growth of larvae. Satisfactory growth (>70% of the maximum observed value) occurred only at high temperature-high salinity conditions; optimal conditions for survival occurred at similar salinities, but at slightly lower temperatures. Temperatures of 35°C or greater and/or salinities of 10S or less were lethal for all life stages studied. Both salinity and temperature exerted significant effects on development and survival, but temperature was clearly the dominant factor influencing growth. It is suggested that northern bay scallop embryos and larvae be reared at their respective optimal temperature-salinity levels so as to increase efficiency of aquaculture operations.This paper is adapted from a thesis submitted to the College of Fisheries, University of Washington, in partial fulfillment of the requirements for the MS degree. This study was conducted at the NMFS Laboratory in Milford, Connecticut, USA     

Synergistic effects of cadmium and salinity combined with constant and cycling temperatures on the larval development of two estuarine crab species

The developmental stages from megalopa to third crab of the blue crab Callinectes sapidus Rathbun were tested in 12 combinations of cadmium (0, 50, and 150 ppb) and salinity (10, 20, 30, and 40) at 25°C. A reduction in survival and a significant delay in development from megalopa to third crab occurred within each salinity regime in 50 ppb compared with the control. Comparison of the delay in development within each salinity regime revealed that the sublethal effect of cadmium was most pronounced in the salinities normally preferred by C. sapidus. A similar comparison within each cadmium concentration, however, showed that the developmental time from megalopa to third crab was approximately the same irrespective of salinity. The developmental stages from hatch to first crab of the mud-crab Rhithropanopeus harrisii (Gould) were examined in 63 combinations of cadmium (0, 50, and 150 ppb), salinity (10, 20, and 30), constant temperature (20°, 25°, 30°, and 35°C) and cycling temperature (20° to 25°C, 25° to 30°C, and 30° to 35°C). The results indicated that cycling temperatures may have a stimulating effect on survival of the larvae compared to constant temperatures, both in the presence and in the absence of cadmium. Effects of cadmium and salinity and their interaction on the survival of the larvae from zoeae to megalopa were documented at most of the temperatures by analyses of variance. The zoeal larvae were more susceptible to cadmium than the megalopa. Effects of different combinations of cadmium and salinity on the duration of larval development were assessed by a t-test.     

Laboratory spawning and rearing of a marine fish,the silverside Menidia menidia menidia

Adult silversides, Menidia menidia menidia (Linnaeus), were collected in early March, 1974 and maintained in 3 recirculating seawater tanks in the laboratory. Respective groups were fed Moore-Clark Fry Fine at 3, 7 and 10% of their body weight per day. The photoperiod (light intensity approximately 2000 lux) was increased in increments of 10 min/day from 12 h light to 14 h light. The water temperature was increased by 1C°/day from the ambient collection temperature, 14°C, to 22°C. Twenty-four days after beginning laboratory conditioning, fish in each tank were stripped. There was a significant increase (², =0.05) in the number of ripe males at all three feeding levels, compared to an initial field-collected group that was checked at the beginning of the conditioning period. Females also showed significant increases in ripeness at the 7 and 10% but not at the 3% feeding level. The gonadal indices (gonad weight expressed as percentage of body weight) of both sexes were significantly greater than those measured for the initial field-collected group, but did not differ from those of adults collected from the field at the time laboratory conditioning was terminated. Techniques for maintaining eggs from field-ripened adults in the laboratory have been developed, and the effect of salinity on the percentage emergence of larvae determined. The highest emergence rate of larvae was 61% when eggs were maintained at 30 S. Emergence was 56% at 20 S and 47% at 10 S. The effect of delayed feeding on survival and growth of larvae was determined at 20 and 30 S and 25°C. Survival and growth was best for larvae fed Artemia sp. nauplii immediately after emergence at 30 S.Contribution No. 252, Gulf Breeze Environmental Research Laboratory.Associate Laboratory of the National Environmental Research Center, Corvallis, Oregon, USA.     

Respiration et excrétion azotée du zooplancton. I. Evaluation des niveaux métaboliques de quelques espèces de Méditerranée occidentale

The effects of sublethal concentrations of mercury in combination with stressful temperature-salinity regimes were considered for larval development of the fiddler crab Uca pugilator (Bosc.). Control organisms were compared to those treated with 1.8 ppb Hg for the following suboptimal regimes: 30°C, 30 S; 30°C, 20 S; 20°C, 30 S, and 20°C, 20 S. As physiological indicators of larval response, the survival rate, the O₂ consumption rate, and phototactic response were measured, following either acute 24 h doses of Hg, or chronic rearing in Hg. All response parameters were modified in larvae maintained under the suboptimal conditions; mercury compounded the effects.Supported by Grant No. 18080 FYI from the Environmental Protection Agency.     

Individual effects and interactions of salinity,temperature, and zinc on larval development of the grass shrimp Palaemonetes pugio. I. Survival and developmental duration through metamorphosis

Larvae of the estuarine grass shrimp Palaemonetes pugio (Holthuis) were reared from hatch through successful completion of metamorphosis in 80 combinations of salinity (3 to 31%), temperature (20° to 35°C), and zinc (0.00 to 1.00 ppm Zn⁺⁺). Response-surface methodology was employed to depict the individual effects and interactions of the three factors on survival and developmental duration through total larval development. Outside the optimal salinity-temperature conditions of 17 to 27 S and 20° to 27°C, viability of larvae was reduced by both the individual effects of salinity and temperature and interactions between the two factors. Survival capacity of larvae and resistance adaptations to salinity and temperature were progresively reduced by zinc concentrations from 0.25 to 1.00 ppm Zn⁺⁺. Response-surface analysis of the data suggested that the duration of total larval development of P. pugio was least at salinities from 18 to 23 and at temperatures from 30° to 32°C. At both higher and lower salinity-temperature conditions and in increasing zinc concentrations from 0.25 to 1.00 ppm Zn⁺⁺, developmental rates were retarded. A significant zinc-temperature interaction existed, whereby increasing zinc concentrations reduced both survival and developmental rates of larvae more at suboptimal temperatures. Larval resistance to zinc toxicity was least at supraoptimal salinities, indicative of a significant zinc-salinity interaction. The reduced viability, restricted euryplasticity, and retarded developmental rates of P. pugio larvae developing in media with low-level zinc contamination would limit the distributive properties of the pelagic phase in the life cycle of the species and reduce recruitment both into and out of the parent estuarine population.     

Effects of temperature and salinity acclimation of adults on larval survival,physiology, and early development of Lytechinus variegatus (Echinodermata: Echinoidea)

Larval survival and developmental rates of Lytechinus variegatus (Lamarck) were determined as a function of temperature and salinity in two experiments by: (1) directly transferring fertilized eggs to 35, 30, 27.5, 25, 20, 15, and 10S seawater at 18 and 23°C, and (2) acclimation of adult sea urchins to the conditions described above for 1 to 4 wk prior to spawning. Developmental rates and percent survival of larvae prior to metamorphosis decreased at salinities below 35 (Q₁₀ values for metamorphosis=0.380 to 0.384). Temperature and salinity significantly (P<0.05) affected metabolic rates of L. variegatus plutei. These results show that L. variegatus larvae are stenohaline when compared to larvae of other echinoderm species. LC₅₀ values (S), developmental rates, and survival to metamorphosis indicate that acclimation of adult sea urchins to lower salinity prior to spawing and fertilization does not enhance development or survival of embryos exposed to low salinity.     

Effects of salinity on respiration and nitrogen excretion in two species of echinoderms

The 30-d survival limit of Eupentacta quinquesemita and Strongylocentrotus droebachiensis is 12–13 S. The activity coefficient (1 000/righting time in seconds) of stepwise acclimated sea urchins declined from 16.3 at 30 S to 3.5 at 15 S. Oxygen consumption rates (QO₂) of both species held at 30 S and 13°C were highest in June and lowest in December. During the summer, when environmental salinity is most variable in southeastern Alaska, the QO₂ of both species held at 30, 20 and 15 S varied directly with salinity. Perivisceral fluid PO₂ varied directly with acclimation salinity in sea urchins, but not in sea cucumbers. Perivisceral fluid oxygen content of acclimated sea urchins was significantly lower at 15 and 20 S than at 30 S due to reduced PO₂ and extracellular fluid volume at the lower salinities. The QO₂ of both species varied directly with ambient salinity during a 30-10-30. semidiurnal pattern of fluctuating salinity. No change occurred in the average QO₂ of either species over a 15-30-15. semidiurnal pattern of fluctuating salinity. Sea urchin perivisceral fluid PO₂ declined as ambient salinity fluctuated away from the acclimation salinity in both cycles and increased as ambient salinity returned to the acclimation salinity. Total nitrogen excretion of stepwise acclimated sea cucumbers declined significantly from 30 to 15 S, but there was no salinity effect on total nitrogen excretion in sea urchins. Ammonia excretion varied directly with salinity in stepwise acclimated sea cucumbers (67–96% of total nitrogen excreted), but there was no salinity effect on ammonia excretion (89–95% of total nitrogen excreted) of sea urchins. Urea excretion did not vary with salinity in sea cucumbers (2–4% of total nitrogen excreted) or sea urchins (2–9% of total nitrogen excreted). Primary amines varied inversely with salinity in sea cucumbers (2–30% of total nitrogen excreted), but did not vary with salinity in sea urchins (2–4% of total nitrogen excreted). The oxygen: nitrogen ratio of both species indicated that carbohydrate and/or lipid form the primary catabolic substrate. The O:N ratio did not vary as a function of salinity. Both species are more tolerant to reduced salinity than previously reported, however, rates of oxygen consumption and/or nitrogen excretion are modified by salinity as well as season.     

Salinity tolerance of benthic estuarine diatoms as tested with a rapid polarographic measurement of photosynthesis

Measurements of net photosynthesis of benthic estuarine diatoms were made by polarographic registration of oxygen saturation. A measuring cell was constructed in which media with salinities of 2.0 to 100.7 were pumped over the algae between measurements. Diatoms from unialgal cultures and mixed populations from intertidal flats appeared to be highly tolerant of extreme salinities. During short-term exposures (20 min) the net photosynthesis of the algae did not drop below 70% of the initial values, within the salinity range 4.0 to 60.0. Prolonged exposure (up to 6 h) gave essentially the same results. Populations of benthic diatoms, sampled from field stations with mean salinities of about 30, 12, and below 5, showed only gradual differences in their tolerance of salinities between 2.0 and 33.7. Two species, Navicula arenaria and Nitzschia sigma, were cultured in media ranging in salinity from 8.0 to 45.0 and from 2.0 to 45, respectively. The tolerance to changing salinity was only slightly affected by the salinity of the medium in the preculture. The role of salinity in the production and distribution of intertidal diatoms is discussed.     

Effects of acute changes in temperature and salinity on the oxygen uptake of larvae of herring (Clupea harengus) and plaice (Pleuronectes platessa)

Routine oxygen uptake (QO₂) by yolk-sac and firstfeeding larvae of herring (Clupea harengus L.) and plaice (Pleuronectes platessa L.) was studied after acute change of temperature (8°, 13°, 18°C) and salinity (5, 12.7, 32, 40). In both species, QO₂ (l mg^-1 dry wt h^-1) of both larval stages increased with increasing temperature. Salinity effect on QO₂ varied: for yolk-sac larvae of both species a lower QO₂ was found at lower combined salinities (5 and 12.7); for feeding larvae a lower QO₂ was observed at 12.7 for both species, possibly due to the relatively smaller size of larvae used at this salinity. For both species, oxygen uptake increased as larvae grew and weight regression coefficients were between 0.74 and 1.33. At 32 S, no difference was found in oxygen consumption between species as a function of temperature.Based on a dissertation submitted in partial fulfillment of the requirements for the degree of Master of Science at the University of Stirling, Stirling, Scotland. The work was performed at the Dunstaffnage Marine Research Laboratory, Oban, Scotland