• Atmosphere
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• v.16 no.4
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• pp.333-342
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• 2006

The long-term trends of global solar irradiance, air temperature, specific humidity and cloudiness measured at King Sejong station, Antarctica, during the period of 1988-2004, have been investigated. A statistically insignificant decrease, -0.21 $Wm^{-2}yr^{-1}$ (-0.26 %$yr^{-1}$, P<0.5) in global solar irradiance was found in an analysis from the time series of the monthly mean values, except for the increasing trends only in two months of January and June. The trends in irradiance are directly and inversely associated with the cloudiness trends in annual and monthly means. The trends in surface air temperature show a slight warming, $0.03^{\circ}Cyr^{-1}$ (1.88 %$yr^{-1}$, P<0.5) on the annual average, with cooling trend in the summer months and the warming in the winter. The exact relationship, if any, between the irradiance and temperature trends is not known. No significant tendency was found in specific humidity for the same periods. Recent (1996-2004) erythermal ultraviolet irradiance shows decreasing trend in annual mean, -0.15 $mWm^{-2}yr^{-1}$ (-1.18 %$yr^{-1}$, P<0.1) which is about five times the trends of global solar irradiance. The ratio of erythermal ultraviolet to global solar irradiance shows remarkable seasonal variations with annual mean value of 0.01 % and a peak in October and November, showing the increase of ultraviolet irradiance resulting from the Antarctic ozone hole. The sensitivity of global solar irradiance to the change in cloudiness is roughly $13%oktas^{-1}$ which is about twice of the value at the South Pole due to the difference in the average surface reflectance between the two stations. Much more sensitive values of $59%oktas^{-1}$ was found for erythermal UV irradiance than for the global solar irradiance.

• Journal of Plant Biology
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• v.36 no.3
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• pp.219-224
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• 1993

The effects of environmental factors on the growth of Enteromorpha compressa germlings from Daeyulri (34$^{\circ}$36'N; 127$^{\circ}$47'E), the southern cost of Korea were examined in laboratory culture through combinations of irradiance and salinity and temperature and salinity. They showed a maximum growth rate at 125 $\mu$E.m-2.s-1 and 32$\textperthousand$ of irradiance and salinity combination, and at 15$^{\circ}C$ and 32% of temperature and salinity combination. Optimal parameters for the growth of germlings were 15$^{\circ}C$, 125 $\mu$E.m-2s-1 and 32$\textperthousand$. The germlings of E. compressa were survived in a wide range of irradiance, temperature and salinity levels, even though they had relatively low irradiance optimum. In the field E. compressa occurred commonly during autumn and spring seasons and disappeared in summer, except for particular habitats. This may be caused by the salinity and water temperature of this area rarely drop below 26$\textperthousand$ and 8$^{\circ}C$ during winter. A broad tolerance to environmental and rapid growth of germlings made them a wide geographical distribution over the world and a survival in both the upper and lower intertidal zones.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.48 no.1
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• pp.88-95
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• 2015

The three endophytes, Blastophysa rhizopus, Bolbocoleon piliferum, Ulvella leptochaete, were isolated in a laboratory culture from a Grateloupia lanceolata thallus collected in Jeju. Effects of temperature and irradiance on growth and infection of the three species, were examined. Based on the unialgal cultures, their growth was examined under six temperatures (9, 13, 17, 21, 25, $29^{\circ}C$) and two irradiance levels (60, $100{\mu}mol\;m^{-2}s^{-1}$). Also, infection experiments to the five hosts (Ulva intestinalis, Scytosiphon lomentaria, Gracilaria verimiculophylla, Chondrus ocellatus, and Grateloupia elliptica) with three endophytes were carried out under four temperatures (10, 15, 20, $25^{\circ}C$) and two irradiance levels (60, $100{\mu}mol\;m^{-2}s^{-1}$). In culture of the endophytes, optimum growth was found in $100{\mu}mol\;m^{-2}s^{-1}$ in combination with $21^{\circ}C$. At the end of infection experiment, endophytes were observed at all the hosts. Among three endophytes, U. leptochaete was the most common at the five hosts. However, we did not observe any endophytes at all hosts tested under $10^{\circ}C$ condition. Based on this result, it appears that temperature acts as a limiting factor to infection of the three species.

• ALGAE
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• v.34 no.2
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• pp.153-162
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• 2019

Anthropogenic disturbances, including coastal habitat modification and climate change are threatening the stability of kelp beds, one of the most diverse and productive marine ecosystems. To test the effect of temperature and irradiance on the microscopic gametophyte and juvenile sporophyte stages of the rare kelp, Saccharina angustissima, from Casco Bay, Maine, USA, we carried out two sets of experiments using a temperature gradient table. The first set of experiments combined temperatures between $7-18^{\circ}C$ with irradiance at 20, 40, and $80{\mu}mol\;photons\;m^{-2}\;s^{-1}$. The second set combined temperatures of $3-13^{\circ}C$ with irradiance of 10, 100, and $200{\mu}mol\;photons\;m^{-2}\;s^{-1}$. Over two separate 4-week trials, in 2014 and again in 2015, we monitored gametogenesis, the early growth stages of the gametophytes, and early sporophyte development of this kelp. Gametophytes grew best at temperatures of $8-13^{\circ}C$ at the lowest irradiance of $10-{\mu}mol\;photons\;m^{-2}\;s^{-1}$. Light had a significant effect on both male and female gametophyte growth only at the higher temperatures. Temperatures of $8-15^{\circ}C$ and irradiance levels of $10-100{\mu}mol\;photons\;m^{-2}\;s^{-1}$ were conditions for the highest sporophyte growth. Sporophyte and male gametophyte growth was reduced at both temperature extremes-the hottest and coldest temperatures tested. S. angustissima is a unique kelp species known only from a very narrow geographic region along the coast of Maine, USA. The coupling of global warming with high light intensity effects might pose stress on the early life-history stages of this kelp, although, as an intertidal species, it could also be better adapted to temperature and light extremes than its subtidal counterpart, Saccharina latissima.

• 한국태양에너지학회:학술대회논문집
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• 2008.04a
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• pp.252-256
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• 2008

Photovoltaic (PV) modules output changes noticeable with variations in temperature and irradiance. In general it is has been shown that a $1^{\circ}C$ increase in temperature results in a 0.5% drop in output. In this paper, seven PV module types are analyzed for variation in temperature and irradiance, and the resulting output characteristics examined. The 7 modules types utilized are as follows; 3 poly crystalline modules, 2 single crystalline modules, 1 back contact single crystalline module and 1 HIT module. 3 groups of experiments are then conducted on the modules; tests with varying irradiance values, tests with module temperature varying under $25^{\circ}C$ and tests with module temperature varying over $25^{\circ}C$. The experiments results show that as temperature rises the follow is observed; Pmax decreases by 0.6%, Voc decreases by about 0.4%, and Isc increasing by between 0.03%${\sim}$0.08%. In addition, an irradiance decrease of 100 w/m2 translates into a 10% drop in Pmax.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.30 no.5
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• pp.312-317
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• 2017

In this paper, the effects of environmental variables on the output of the floating photovoltaic water systems, which were installed at the Hapcheon dam in South Korea, were investigated, and the correlations between them were analyzed. The system output was linearly proportional to the solar radiation or irradiance. The output was large in spring and autumn because of high irradiance, but low in the summer when the solar module temperature was high. The influence of the module temperature on the system output was limited in the summer, during which the module temperature change affected the system output more than the change of the irradiance did. In addition, in winter and summer, the module temperature tended to decrease with increasing windspeed, but windspeed did not affect module temperature significantly in the spring and autumn. On the other hand, in winter and spring, the irradiance decreased as the windspeed increased because of movement (or circulation) of the photovoltaic modules.

• Journal of Environmental Science International
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• v.20 no.8
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• pp.1041-1048
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• 2011

The purpose of this study was to analyze the effects on meteorological variables in Seoul, Busan and Jeju during the partial solar eclipse event of 22 July 2009 in Korea. Solar irradiance decreased 16 and 19 minutes after eclipse in Seoul and Busan, and 6 minutes before eclipse in Jeju. Minimum solar irradiance occurred 7 and 3 minutes after maximum eclipse in Seoul and Busan, respectively, and 8 minutes before maximum eclipse in Jeju. Solar irradiance began to increase after maximum eclipse in Seoul and Busan, and recovered to the original state as eclipse ended. On the other hand, recovery of solar irradiance after maximum eclipse in Jeju was slower than those of two cities. Temperature drop due to partial solar eclipse were $0.7^{\circ}C$, $4.0^{\circ}C$, $1.5^{\circ}C$ in Seoul, Busan, and Jeju, respectively, and time needed to arrive minimum temperature from maximum eclipse were each 12, 32, 30 minutes, respectively. Change of relative humidity during partial solar eclipse were 2.6%, 17.4%, 12.3% in Seoul, Busan, and Jeju, respectively. Temperature drop turned out to be sharper as altitude increases. Wind speed decreased by each about 1.1 m/s, 3.4 ms/s, 1.4 ms/s due to partial solar eclipse in Seoul, Busan, and Jeju. Soil temperature of 5 cm equally decreased by $0.2^{\circ}C$ in Seoul and Busan, soil temperature of 10 cm maintained almost constant, and soil temperature of 20 cm was hardly affected by eclipse.

• Korean Journal of Agricultural and Forest Meteorology
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• v.15 no.4
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• pp.291-297
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• 2013

Automated weather stations were installed at 9 locations with, three different elevations, (i.e., 50m, 100m, and 300m a.s.l.) with different slope and aspect in a small watershed ($50km^2$ area). Air temperature at 1500 LST and solar radiation accumulated for 1100-1500 LST were collected from January to December 2012. Topography of the study area was defined by a $30{\times}30$ m digital elevation model (DEM) grid. Accumulated solar irradiance was calculated for each location with the spatially averaged slope and aspect of surrounding circles with 5, 10, 15, 20, 25, and 30 grid cell radii, respectively. The 1500 LST air temperature from clear sky conditions with zero cloud amount was regressed to the 1100-1500 LST solar irradiance at 9 locations. We found the highest coefficient of determination ($r^2$ = 0.544) at 25 grid cell radius and the temperature variation in this study was explained by Y = 0.8309X + 0.0438, where Y is 1500 LST temperature (in $^{\circ}C$) and X is 1100-1500 LST accumulated solar irradiance (in $MJ/m^2$).

• Korean Journal of Fisheries and Aquatic Sciences
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• v.43 no.6
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• pp.715-722
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• 2010

The effects of temperature, salinity and irradiance on the growth of the harmful red tide dinoflagellate Cochlodinium polykrikoides Margelef isolated from the South Sea of Korea were examined in the laboratory. Growth was examined under the following combinations of temperature and salinity: 15, 20, 25 and $30^{\circ}C$, and 15, 20, 25, 30 and 35 psu at a constant irradiance of $180\;{\mu}mol/m^2/s$. No growth was observed with a temperature of $15^{\circ}C$ and a salinitiy of 15 psu. Moderate growth rates of more than 0.30 /day were obtained at $25^{\circ}C$ with salinities of 25.35 psu. These values are similar to in situ observations for this species. The maximum growth rate, 0.35 /day, was obtained at $25^{\circ}C$ and 30 psu. In light experiments, cell growth of C. polykrikoides was conducted with constant temperature ($20^{\circ}C$) and salinity (30 psu) under light photon flux densities (PFD) of 10, 25, 50, 70, 100, 150, 250 and $350\;{\mu}mol/m^2/s$. C. polykrikoides did not grow at $10\;{\mu}mol/m^2/s$. Cell growth was observed at irradiance values of $25\;{\mu}mol/m^2/s$ and above. The irradiance-growth curve was described as ${\mu}=0.30{\cdot}(I-15.27)/(I+27.22)$, (r=0.99). This suggests a compensation PFD of $15.27\;{\mu}mol/m^2/s$ and a maximum growth rate of 0.30 /day. In conclusion, C. polykrikoides prefers high salinity, temperature and irradiance in summer in Korea. These results provide important information for understanding the mechanism of C. polykrikoides blooms and developing technology to predict blooms of this organism in the field.

• Proceedings of the KIEE Conference
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• 2011.07a
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• pp.1316-1317
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• 2011

This paper presents analysis of temperature and light intensity characteristics of PV modules with solar cell type. Taking the effect of sunlight irradiance on the cell temperature, the first experiment takes ambient temperature as reference input and uses the solar insolation as a unique varying parameter. Then taking the effect of the cell temperature on sunlight irradiance, the second experiment takes 1000W/$m^2$ as reference input and uses the cell temperature as a unique varying parameter. As a result, varying sunlight irradiance, the Cell-Type with the smallest change in output is HIT and the Cell-Type with the biggest change in output is a-Si. Varying the cell temperature, the Cell-Type with the smallest change in output is a-Si and the Cell-Type with the biggest change in output is Single-Si. And considering both temperature and light intensity characteristics, the Cell-Type with the smallest change in output is HIT.