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1.
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.  相似文献   

2.
Temperature and daylength responses were determined in culture for isolates of the red alga Cystoclonium purpureum (Hudson) Batters from Nova Scotia (NS, Canada), Helgoland (HE, Germany), and Roscoff (RO, France). Most isolates survived temperatures of –1.5°/–2° to 23°C, whereas 25°C was lethal. Only the RO-gametophytes died at 23°C. Optimal growth conditions were 10°–20°C in both long and short days for the NS isolates and 8°–15°C and 8°–18°C at daylengths of >12 h for the RO and HE isolates, respectively. Tetrasporophytes and gametophytes of the NS isolate reproduced at 10°–20°C in long and short days within 5 months. At lower temperatures reproduction was limited or slow. The European isolates formed tetrasporangia at 10°–20°C (HE) or 5°–l8°C(RO), spermatangia at 5°–15°C (HE) or 5°–20°C (RO), and carpospores at 5°–15°C(HE) or 10°–15°C (RO). Short days either blocked or delayed reproduction of the European isolates. The phenology of C. purpureum was studied at Helgoland and Roscoff, where similar seasonal patterns were observed. In early spring, growth was rapid and plants started to form reproductive structures. In summer, tetra-and carpospores were shed followed by degeneration of the upright axes while branched holdfasts persisted. New upright axes and juvenile plants were formed in autumn, but these remained small during the winter months. Published data indicate that the seasonal pattern at Nova Scotia is similar, although the onset of growth and reproduction is delayed until the end of spring. These observations correspond well with the results of the experiments. The life history of C. purpureum is regulated by temperature and daylength. In the eastern Atlantic, the limiting effect of short days confines growth and reproduction to spring and summer. In the western Atlantic, low winter temperatures alone bring about the same seasonal pattern. After plants have reproduced, uprights degenerate in spite of continuing favorable conditions.  相似文献   

3.
4.
Development of powdery mildew Erysiphe (sect. Microsphaera) pulchra in dogwood (Cornus florida) was assessed over a 5‐year period (1996–2000). Variations in the timing of initial infection, disease severity, ascocarp formation, and primary inoculum density were evaluated. Ascocarps formed late in the growing season (September‐November) when relatively low temperatures (< 27°C) persisted for at least 2 weeks, but ascocarp abundance was not influenced by disease severity. Studies conducted in a controlled environment showed that low temperatures triggered ascocarp formation and neither day length nor host plant age affected ascocarp formation. Ascocarps formed within 12–14 days at 18°C/ 10°C (day/night) and 23°C/15°C, but required 25 days at 26°C/18°C; no ascocarps formed at 28°C/ 20°C. Because ascocarps are an important source of primary inoculum for dogwood powdery mildew, ascocarp survival was evaluated in a 2‐year study (1998–2000). 60–80% of mature, dark‐coloured ascocarps survived at ‐10°C and ‐20°C and maintained viable spores for 4 months, but only 4–12% of partially developed, light brown ascocarps survived at ‐10°C and ‐20°C in the first experiment and only 30–40% survived in the second experiment. Immature ascocarp initials (cream‐yellow in colour) withered and disintegrated at all temperatures (24°C/20°C, 4°C, ‐10°C, and ‐20°C). Because ascocarps need time to mature, the timing of ascocarp initiation affects ascocarp maturity and thus winter survival and primary inoculum density. The evaluation of spring inoculum dispersal to spore traps and trap plants in 1999 and 2000 showed that rainfall patterns in early spring influenced primary inoculum and thus the timing of initial infection.  相似文献   

5.
Hydromedion sparsutum is a locally abundant herbivorous beetle on the sub-Antarctic island of South Georgia, often living in close association with the tussock grass Parodiochloa flabellata. Over a 4-day period in mid-summer when the air temperature varied from 0 to 20°C, the temperature in the leaf litter 5–10 cm deep at the base of tussock plants (the microhabitat of H. sparsutum) was consistently within the range of 5–7.5°C. Experiments were carried out to assess the ability of H. sparsutum larvae collected from this thermally stable environment to acclimate when maintained at lower (0°C) and higher (15°C) temperatures. The mean supercooling points (freezing temperature) of larvae collected in January and acclimated at 0°C for 3 and 6 weeks and 15°C for 3 weeks were all within the range of −2.6 to −4.6°C. Larvae in all treatment groups were freeze tolerant. Acclimation at 0°C significantly increased survival in a 15-min exposure at −8°C (from 27 to 96%) and −10°C (from 0 to 63%) compared with the field-fresh and 15°C-treated larvae. Similarly, survival of 0°C-acclimated larvae in a 72-h exposure at −6°C increased from 20 to 83%. Extending the acclimation period at 0°C to 6 weeks did not produce any further increase in cold tolerance. The concentrations of glucose and trehalose in larval body fluids increased significantly with low temperature acclimation. Larvae maintained at 15°C for 3 weeks (none survived for 6 weeks) were less able to survive 1-h exposures between 30 and 35°C than the 0°C-treated samples. Whilst vegetation and snow cover are an effective buffer against low winter temperatures in many polar insects, the inability of H. sparsutum larvae to acclimate or survive at 15°C suggests that protection against high summer temperatures is equally important for this species. Accepted: 2 August 1999  相似文献   

6.
The development, survivorship, longevity, reproduction, and life table parameters of the Asian citrus psyllid, Diaphorina citri Kuwayama were evaluated at 10°C, 15°C, 20°C, 25°C, 28°C, 30°C and 33°C. The populations reared at 10°C and 33°C failed to develop. Between 15°C and 30°C, mean developmental period from egg to adult varied from 49.3 days at 15°C to 14.1 days at 28°C. The low‐temperature developmental thresholds for 1st through 5th instars were estimated at 11.7°C, 10.7°C, 10.1°C, 10.5°C and 10.9°C, respectively. A modified Logan model was used to describe the relationship between developmental rate and temperature. The survival of the 3rd through 5th nymphal instars at 15–28°C was essentially the same. The mean longevity of females increased with decreasing temperature within 15–30°C. The maximal longevity of individual females was recorded 117, 60, 56, 52 and 51 days at 15°C, 20°C, 25°C, 28°C and 30°C, respectively. The average number of eggs produced per female significantly increased with increasing temperature and reached a maximum of 748.3 eggs at 28°C (P<0.001). The population reared at 28°C had the highest intrinsic rate of increased (0.199) and net reproductive rate (292.2); and the shortest population doubling time (3.5 days) and mean generation time (28.6 days) compared with populations reared at 15–25°C. The optimum range of temperatures for D. citri population growth was 25–28°C.  相似文献   

7.
We determined the kind of seed dormancy in Schisandra arisanensis, an ANA grade ([A]mborellales [N]ymphaeales [A]ustrobaileyales) angiosperm with medicinal value. Seeds have small underdeveloped embryos, and following seed maturity their length increased approximately 360% before radicle emergence. Germination was delayed 6–8 weeks, and the percentage and rate were much higher at 15/6, 20/10 and 25/15°C than at 30/20°C. For seeds incubated at 5/5°C (8 weeks) → 15/6°C (4 weeks) → 20/10°C (8 weeks) → 25/15°C (12 weeks) → 20/10°C (5 weeks), embryos grew at 15/6°C → 20/10°C, and almost all seeds that germinated (89%) did so at 20/10°C → 25/15°C. When seeds were incubated in a complementary temperature sequence, 25/15°C (12 weeks) → 20/10°C (8 weeks) → 15/6°C (4 weeks) → 5/5°C (9 weeks) → 15/6°C (4 weeks), embryos grew at 25/15°C → 20/10°C. Nearly all seeds that germinated (93%) did so at 25/15°C → 20/10°C and at 15/6°C following 9 weeks at 5/5°C. Based on the temperature requirements for embryo growth and seed germination, seeds of this species have non‐deep simple morphophysiological dormancy (C1bB).  相似文献   

8.
Temperature requirements for growth, reproduction and formation of macrothalli of a day-neutral strain ofScytosiphon lomentaria from the Gulf of Thessaloniki were experimentally determined and correlated with the geographic distribution in the North Atlantic Ocean. The microthallus grew in a wider temperature interval and better at higher temperatures than did the macrothallus. Germlings acclimated to 5 or 15°C grew sufficiently (>20% of maximum rate) and developed into macrothalli at 5–25°C and 5–27°C. Macrothalli acclimated to 10 or 15°C grew sufficiently at 5–20°C. Macrothalli acclimated to 15°C survived at −1°C and reproduced at 5 to 23°C. Regardless of the acclimation temperature, germlings and macrothalli grew optimally (>80% of maximum rate) at 15–25°C and at 10–15°C. The experimental data explain only the southern distribution boundary ofScytosiphon in the North Atlantic. This boundary is composite in nature: on the European coasts it is a growth boundary, whereas on the American coasts it is a lethal one.  相似文献   

9.
Motile unicells of Olisthodiscus lutheus Carter aggregated to form encapsulated masses of nonmotile cells in a benthic stage throughout a temerature range of 15–30°C at salinities o f 10–50%. Motile cells were released from beneathic masses at 10–30°C but at 5°C, cells were not motile and at 0°C cells lysed. Exposure of benthic masses of I day to 8 wk to temperatures of 0–30C in lighted growth chambers resulted in mortality to cells kept below 10°C and normal growth at higher temperatures. Benthic stage cells kept tn darkness at the same temperatures exhibited mortality in all but those at 5 and 10°C. Cells at these thmoeratures remained viable 15 wk in continual darkness. Comparison of cell morphology of matile and benthic stage O. luteus to other Olisthodiscus species and the ecological implications o fthe benthic stage are discussed.  相似文献   

10.
The development of Puccinia hordei on barley cv. Zephyr   总被引:2,自引:0,他引:2  
Germination of uredospores of Puccinia hordei was similar on cover-slips and on the first leaves of barley seedlings (cv. Zephyr) at 100 % r.h. over the range 5–25 °C, being greatest at 20 °C. At 15, 20 and 25 °C maximum germination was attained in 6 h. No uredospores germinated on coverslips in humidities below saturation. The numbers of pustules which subsequently developed on plants incubated at 5, 10, 15 or 18 °C and 100 % r.h. for varying periods up to 24 h, were directly related to rise in temperature and length of incubation. The time from inoculation to eruption of pustules (generation time) was 6 days at 25 °C, 8 days at 20 °C, 10 days at 15 °C, 15 days at 10 °C and 60 days at 5 °C. Pustule production on inoculated plants which had been kept at 5 °C was rapidly accelerated when they were transferred to 20 °C. Data obtained at constant temperatures were used to predict generation times of the fungus in the field. The productivity of pustules, determined as weight of uredospores, was examined at 10, 15 and 20 °C. Significantly more spores were produced at 15 than at 10 °C and most were produced at 20 °C. The results are discussed in relation to those obtained by other workers and to the development of brown rust in the field.  相似文献   

11.
Culex quinquefasciatus plays a major role in the transmission of important parasites and viruses throughout the world. Because temperature is an important limiting factor on growth and longevity of all mosquito species, estimating the reaction norms provides very important basic information for understanding both plasticity and individual variations of the population. In the present study, Cx. quinquefasciatus were maintained at five different constant temperatures (15°, 20°, 23°, 27°, and 30°C) for two subsequent generations. Reproductive population parameters in blood‐fed mated females and longevities of virgin and blood‐fed mated adults reared at different temperatures were compared for the two generations. Longevity increased as temperature decreased within a range of 15° to 30°C for the unmated adults, and 15° to 27°C for the mated and blood‐fed adults. Generation times were as long as 124.07 and 106.76 days for two subsequent generations reared at 15°C, and the highest intrinsic rate of increase (rm) values were estimated at 0.22 and 0.18, respectively, from the cohorts reared at 27°C. For survival rates, reproductive rates (R0), and rm values, 30°C was found to be a critical temperature for this species. These cohorts produced the smallest amount of eggs (R0= 5.06), rm values decreasing across generations (from 0.11 to 0.06), and the survival rates from egg to adult were found to be insufficient (16.1 and 10.8%). Additionally, the rate of exponential increase with age and age specific mortalities (b) were calculated for the virgin cohorts. Age specific mortality rates increased as temperature decreased. The increase in mortality rates started to accelerate at 27°C and was more pronounced at 30°C, for both females and males. We estimated the coefficients of variation for the b values in which females have smaller coefficients than those of the males at all temperatures.  相似文献   

12.
Abstract. Diapause adults of Plautia stali Scott maintained at 20°C under short day conditions (LD 12:12 h) were exposed to four temperatures of 5–20°C to examine the effect on diapause development which was assessed in terms of oviposition. Diapause adults kept at 20°C under short day conditions changed their body colour gradually from brown to green and started egg laying after a prolonged preoviposition period. Those transferred to either 10 or 15°C also showed colour change but did not lay eggs. Bugs exposed to 5°C underwent neither body colour change nor oviposition and died more rapidly than those kept at higher temperatures. When 30-day-old diapause adults were chilled at 5, 10 or 15°C for 30 or 60 days and returned to 20°C and long day conditions (LD 16:8 h), the preoviposition period varied primarily depending on the chilling, but not on the temperature. On the other hand, when 60day-old diapause adults chilled for 30 days were observed at 20°C and long day conditions, their preoviposition period tended to be longer as the chilling temperature was lower In this case, a temperature of 10°C appeared to intensify diapause. Therefore, the effect of chilling on diapause development varied depending on the age at which insects were chilled. When chilled bugs were transferred to short day conditions at 20°C, most females failed to lay any eggs and some turned green, then after a while, some green bugs changed to brown again. These results indicate that bugs remained sensitive to short day conditions even after a 60-day chilling at 10 or 15°C.  相似文献   

13.
Feeding behavior of Plutella xylostella under optional to non-optional conditions was studied at 10°C, 15°C, 20°C, and 25°C on Indian mustard, Brassica juncea. The study reveals that the variety Pusa Bahar was significantly less preferred by the larvae as compared with Pusa Bold and Varuna under optional to non-optional conditions. Larvae of P. xylostella consumed more food at 25°C than 20°C, 15°C and 10°C. Larval survival was found to be highest on cabbage (control) as compared with Indian mustard and was found to vary with host plants and temperature. The larval survival decreased to 11.29% on Pusa Bahar at 10°C. Increasing the temperature from 10°C to 20°C, larval mortality resulted more on Varuna than Pusa Bahar and Pusa Bold. Developmental period was prolonged on Pusa Bold at 10°C while it was shortest on cabbage at 25°C. A total of 536.47 degree days were required to complete the development by immature stages on Varuna at 25°C and 421.64 degree days on cabbage.  相似文献   

14.
A sustainable colony allowed investigations into attachment substrates, diet and temperature in the development of the immature stages of Cq. linealis and its local congener Cq. xanthogaster. As immatures, these mosquitoes attach to submerged plants for respiration, and various field‐collected and laboratory‐raised plants were compared with non‐living substrates. Hydroponically‐grown wheat plant seedlings provided the most suitable attachment substrate. Development and survival of immatures to eclosion were investigated with three types and three quantities of a standardized diet. Development and survival at rearing temperatures between 10° and 30° C were also investigated. Diet type appeared to have little influence on development. However, at the lowest diet quantity, development to pupation was significantly reduced while the highest diet quantity impacted on the eclosion of pupae. Mean duration of immature development for Cq. linealis increased as temperature decreased. Time from 1st instar to median eclosion did not differ significantly between 23° C (6.0 weeks) and 25° C (5.3 weeks), although it was 10 weeks at 20° C, and 30° C was lethal. For Cq. xanthogaster, similarly, mean duration of immature development increased as temperature decreased, with development time from 1st instar to median eclosion significantly longer at 20° C (7.5 weeks) compared to 23° C (5.0 weeks) and 30° C (4.0 weeks).  相似文献   

15.
The mitotic and labelling incidence of intestine, liver, spleen and pancreas cells of Triturus cristatus carnifex adults kept at 15°C, 20°C, 25°C and 30°C were examined. Intestine mitotic and labelling incidences were highest at 25°C and lowest at 30°C. There was no significant difference between 15°C and 20°C. No such relationship could be shown for liver, spleen or pancreas, which had very much lower mitotic and labelling incidences. In culture, intestine mitotic and labelling incidences fell significantly within the first four hours, and maintained these low levels for the next five days. In contrast, liver mitotic and labelling incidences rose for 9–11 days, and then began to fall, while pancreas mitotic and labelling incidences reached peak values at day 5, and were kept in good condition for up to 14 days.  相似文献   

16.
Peristenus spretus Chen et van Achterberg (Hymenoptera: Braconidae), a parasitoid of the plant bug Apolygus lucorum (Hemiptera: Miridae), has been studied for use in augmentative biological control in China. Under laboratory conditions, we explored the development, survival, age-specific and potential lifetime fecundity, oviposition period and progeny sex ratio of P. spretus reared at six constant temperatures (15°C, 19°C, 23°C, 27°C, 31°C, 35°C) on the second instar nymphs of A. lucorum. At 15°C, male and female P. spretus took 48.7 ± 0.3 and 52.5 ± 0.3 days to complete their immature development, while developmental time was reduced by more than half at 23°C and 27°C. The parasitoid can only develop to the larval stage at 31°C and neither larva nor pupa survived at 35°C. The estimated lower developmental threshold of the immature stage was 7.3°C. When parasitoid adults were exposed at 15°C, females laid 90% of their eggs at first 19 days of oviposition and had an extended reproductive life. In contrast, females held at 27°C laid most of their eggs (90%) in their first of 10 days of oviposition and had shorter longevity. The highest potential lifetime fecundity of P. spretus was 671.2 ± 34.7 SE eggs produced over 23.4 ± 1.4 SE days at 23°C. At 15°C, 19°C and 23°C, sex ratios of reared parasitoids were male-biased, but at 27°C there was no male bias.  相似文献   

17.
The effect of the acclimation temperature on the temperature tolerance ofPorphyra leucosticta, and on the temperature requirements for growth and survival ofEnteromorpha linza was determined under laboratory conditions. Thalli ofP. leucosticta (blade or Conchocelis phases), acclimated to twenty-five degrees, survived up to 30°C, i.e. 2°C more than those acclimated to 15°C which survived up to 28°C. Lower temperature tolerance of bothPorphyra phases that were acclimated to 15°C was −1°C after an 8-week exposure time at the experimental temperatures. The upper temperature tolerance ofE. linza also increased by 2°C, i.e. from 31 to 33°C, when it was acclimated to 30°C instead of 15°C. The lower temperature tolerance increased from 1 to −1°C, when it was acclimated to 5°C instead of 15°C.E. linza thalli acclimated for 4 weeks to 5 or 10°C reached their maximum growth at 15°C, i.e. at a 5°C lower temperature than those acclimated to 15 or 30°C. These thalli achieved higher growth rates in percent of maximal growth at low temperatures than those acclimated to 15 or 30°C. Thalli acclimated for 1 week to 5°C reached their maximum growth rate at 20°C and achieved growth rates at low temperatures similar to those recorded for thalli acclimated to 15°C. Thalli ofE. linza acclimated for 4 weeks to 5°C lost this acclimation after being post-cultivated for the same period at 15°C. That was not the case with thalli acclimated for 8 weeks to 5°C and post-acclimated for 4 weeks to 15°C. These thalli displayed similar growth patterns at 10–25°C, while a decline of growth rate was observed at 5 or 30°C. The significance of the acclimation potential ofE. linza with regard to its seasonality in the Gulf of Thessaloniki, and its distribution in the N Atlantic, is also discussed.  相似文献   

18.
H. Dautel  W. Knülle 《Oecologia》1997,113(1):46-52
The occurrence of diapause and quiescence was investigated in Argas reflexus engorged larvae, nymphs I and nymphs II. For diapause experiments, larvae were maintained at five different locations: at constant 20°C long day (LD; 17 h light:7 h dark) or short day (SD; 10 h light:14 h dark), at two locations with natural photoperiod and temperature and at one location with natural photoperiod but constant 15°C. At 20°C, diapause incidence was low in physiologically young larvae, increased with larval age, and then decreased to zero in specimens of increased physiological age. This pattern, observed both at constant LD and SD, suggests that the propensity to diapause changes with the physiological age of the unfed larva. The duration of diapause decreased with increasing larval physiological age at all locations, resulting in a seasonally synchronized moulting pattern. The results suggest that A. reflexus larvae are photoperiodically sensitive both before and after feeding and that decreasing daylengths may be particularly strong inductive stimuli. The developmental zero and thermal constant of the larvae were determined as 13.24°C and 220 degree-days, respectively. Degree-day measurements revealed that larval A. reflexus may enter a diapause of different length when fed between August and December and kept at natural daylength. Development of engorged nymphs I and nymphs II, but not of larvae, was ultimatively restricted at a temperature of 37.5°C, but immediately resumed at 25°C, demonstrating the occurrence of quiescence at high temperatures. Similarly, at a low temperature of 15°C, many nymphs I and II did not develop within 58 months, but did so successfully after transfer to 25°C, without additional food intake. Received: 20 May 1997 / Accepted: 4 August 1997  相似文献   

19.
To resolve “the supply problem” in sponge-derived drug development and other biotechnological applications, current research is exploring the possibility of obtaining an alternative sustainable supply of sponge biomass through intensive aquaculture of sponges utilizing artificial seed rearing. This study aimed to investigate the technology of early juvenile sponge cultivation under controlled conditions. The effects of food, temperature, water flow, and light on the growth and survival of early juveniles of the marine sponge Hymeniacidon perlevis were examined. The concentrations of four types of food elements [microalgae (Isochrysis galbana), photosynthetic bacteria (Rhodopseudomonas), Fe3+ (FeCl3), and Si (Na2SiO3)] were investigated for early H. perlevis juvenile growth. Interestingly, temperature changes have striking effects on juvenile growth. Juvenile sponges grow faster when they are shifted to higher temperatures (18°C to 23°C) than when they are shifted to lower temperatures (18°C to 4°C to 23°C) or kept at a constant temperature (18°C). Periodic water flow and light cycles favor early juvenile sponge growth. Light was found to be a key factor in the color loss of early H. perlevis juveniles. Overall, size (area) increased as much as 29 times for H. perlevis juveniles under the tested controlled conditions.  相似文献   

20.
1. Field observations indicate that the ability to feed at different light intensities may differ between brown trout and Arctic charr, and this is the first study to test this experimentally. To establish a background level of feeding in daylight at midday, trout and charr in two size groups were kept in tanks (one fish per tank) at three constant temperatures (5.0, 10.8 and 13.0 °C) and each fish was offered, one at a time, 50 freshly killed shrimps (Gammarus pulex), the number eaten being recorded. Shrimps could only be taken in the water column because a metal mesh prevented access to dead shrimps on the tank bottom. In a first series of experiments, individual fish were kept at one of 10 natural light intensities (range 0.001–50 lx). In a second series, conditions were similar except that the fish tank was covered in black polyethylene and had a light‐tight lid with a shutter so that light levels could be kept constant, using artificial illumination. In a third series, the fish were fed in total darkness, but the false bottom was removed, allowing access to dead shrimps on the tank bottom as well as in the water column. 2. The results of the first and second series differed interspecifically but were very similar intraspecifically, with no significant differences between the food intake for the two size groups or in the experiments at 10.8 and 13.0 °C. Food intake remained fairly constant at light intensities between 50 lx (dusk or dawn) and 0.03 lx and was similar to that of fish feeding at midday. At 10.8 and 13.0 °C, food intake between 0.03 and 50 lx was higher for trout than for charr, mean values for shrimps eaten per fish being 39.9 for trout (range 36–44, n = 100 fish) and 32.0 for charr (range 28–38, n = 100), but at 5.0 °C, the situation was reversed with mean values of 15.1 for trout (range 11–18, n = 50 fish) and 19.8 for charr (range 17–22, n = 50). 3. As light intensity decreased from 0.04 to 0.001 lx, feeding rate decreased exponentially but was always higher for charr than for trout, with a mean number of shrimps eaten at 0.001 lx of 9.3 for trout (range 5–13, n = 20 fish) and 13.6 for charr (range 9–20, n = 20) at 10.8 and 13.0 °C, and 2.0 for trout (range 1–4, n = 10 fish) and 5.5 for charr (range 2–8, n = 10) at 5.0 °C. In total darkness (false bottom fitted), none of the 50 shrimps was taken by either species. When the false bottom was removed in the third series, the mean number of shrimps consumed over 24 h was eight for trout (range 3–11, n = 20 fish) and 14.9 for charr (range 9–20, n = 20) at 10.8 and 13.0 °C, and two for trout (range 0–4, n = 10 fish) and five for charr (range 3–8, n = 10) at 5.0 °C. 4. Therefore, the feeding ability of trout was superior to that of charr when using photopic vision in daylight and mesotopic vision at dusk and dawn, but inferior to that of charr when using scotopic vision at low light intensity. Charr were also superior at low temperatures and when foraging for food in total darkness. Therefore, as light intensity decreases after dusk in their natural habitat, the advantage in feeding will shift from trout to charr, with the reverse occurring as light intensity increases after dawn.  相似文献   

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