• Title/Summary/Keyword: distributional range

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A Feature Selection Technique based on Distributional Differences

  • Kim, Sung-Dong
    • Journal of Information Processing Systems
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    • v.2 no.1
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    • pp.23-27
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    • 2006
  • This paper presents a feature selection technique based on distributional differences for efficient machine learning. Initial training data consists of data including many features and a target value. We classified them into positive and negative data based on the target value. We then divided the range of the feature values into 10 intervals and calculated the distribution of the intervals in each positive and negative data. Then, we selected the features and the intervals of the features for which the distributional differences are over a certain threshold. Using the selected intervals and features, we could obtain the reduced training data. In the experiments, we will show that the reduced training data can reduce the training time of the neural network by about 40%, and we can obtain more profit on simulated stock trading using the trained functions as well.

Occurrence of sea lice, Caligus undulatus Shen and Li, 1959 (Copepoda: Siphonostomatoida: Caligidae) in plankton samples collected from Korea

  • Moon, Seong Yong;Park, Jong Sick
    • Journal of Species Research
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    • v.8 no.4
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    • pp.365-372
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    • 2019
  • We have conducted faunistic study of sea lice collected from marine plankton samples of western and southern coasts of Korea. These specimens were identified as Caligus undulatus Shen and Li, 1959, belonging to family Caligidae and order Siphonostomatoida with worldwide distribution. The range extension of C. undulatus is reported in addition to the previously known distributional range from the Northwest Pacific (China, Japan, and Korea), India, Brazil, and Mexico. This species can be distinguished from all previous reports with characteristics such as overall body proportions of both sexes, structure details of mouth appendages, armature of legs, and some variation in body size. The distributional range of C. undulatus is now given with its northern and south hemisphere limit being 40 to $10^{\circ}N$ in the Indo-Pacific and $30^{\circ}S$ in the Southwest Atlantic. This is the first record of its female occurring in Korea.

Derivation of uncertainty importance measure and its application

  • Park, Chang-K.
    • Proceedings of the Korean Operations and Management Science Society Conference
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    • 1990.04a
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    • pp.272-288
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    • 1990
  • The uncertainty quantification process in probabilistic Risk Assessment usually involves a specification of the uncertainty in the input data and the propagation of this uncertainty to the final risk results. The distributional sensitivity analysis is to study the impact of the various assumptions made during the quantification of input parameter uncertainties on the final output uncertainty. The uncertainty importance of input parameters, in this case, should reflect the degree of changes in the whole output distribution and not just in a point estimate value. A measure of the uncertainty importance is proposed in the present paper. The measure is called the distributional sensitivity measure(DSM) and explicitly derived from the definition of the Kullback's discrimination information. The DSM is applied to three typical discrimination information. The DSM is applied to three typical cases of input distributional changes: 1) Uncertainty is completely eliminated, 2) Uncertainty range is increased by a factor of 10, and 3) Type of distribution is changed. For all three cases of application, the DSM-based importance ranking agrees very well with the observed changes of output distribution while other statistical parameters are shown to be insensitive.

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A New Distributional Record of an Acheilognathine fish, Rhodeus sericeus (Pallas) (Cyprinidae, Pisces) in South Korea (납줄개 Rhodeus sericeus(Palla$) (잉어과. 어강)의 신분포지)

  • 채병수;양홍준
    • The Korean Journal of Zoology
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    • v.36 no.2
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    • pp.175-180
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    • 1993
  • Eighty one specimens of nhodeus sericeus (Pallas, 1176) were collected at the upper stream of the Som River (37$^{\circ}$32' 38" N, 127$^{\circ}$58' 57" E: Maegok-ri, Konggun-myon, Hoengsong-gun, Kanguvon-do, Korea) which is a tributary of the Namhan River. This is the first report of the species in the southern part of the Korean Peninsula. This species is well discriminated from the other species in the genus nhodeus by the following respects. The number of scales of transverse series is more than 34 (range 34-37, mean 35.7 $\pm$0.7). Head is echo감or and snout is Bonder than those of the other species. The upper part of the eve is always black and the lateral body surfaces are reddish purple. It had been hem that the southern limit of the distribution of Rhodeus sericeus was the Yonghung River in Hamgvongnam-do, north-eastern part of the Korean Peninsula. But their distributional range is extended more southerly to the Han River system which tons westward through the central part of the Korean Peninsula.Peninsula.

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A Phytogeographical Study on the Distribution of Bamboos in the Korean Peninsula (韓半島의 대나무類 分布와 그 環境要因에 관한 植物地理學的 硏究)

  • Kong, Woo Seok
    • The Korean Journal of Ecology
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    • v.8 no.2
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    • pp.89-98
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    • 1985
  • Correlations between horizontal distributions of bamboos (Bambusaceae) in the Korean peninsula and environmental factors were studied using taxanomic and geographical literatures, both old and current. The vertical distributions of bamboos on Mt. Chiri were also studied, and environmental factors limiting horizontal and vertical distributions were compared. There are 18 species of bamboos (belonging to 5 genera) distributed in the Korean peninsula. The distributional range of each genus were distinct, although overlapped. Northern limit of bamboos of any species was marked by the line connecting Paikryung Island (124。40'E, 38。00'N), Mt. Changsoo, Mt. Myungji, Mt. Myohyung and Myungchum (129。40'E, 41。10'N). The optimum range of bamboos was concluded to be restricted to several southern province, with annual precipitation over 1,200 mm. The limiting factors on the distribution were inferred to be low temperature and duration of it. Mean daily minimum temperature of January and the number of days with daily mean temperatures below zero during January showed close associations with the distributional range, and an environmental factors favouring the distributrion of bamboos appeared to be vicinity of warm sea current, deep and extended snow acculation and southern exposure. The vertical distribution of bamboos on Mt. Chiri was limited by low temperature, unfavorable topographic and edaphic conditions caused by steep slope. Difference in the vertical limits between SE and NW slopes are caused by the differences in temperature and precipitation between the slopes. Bamboos were more abundant in valleys than on the ridge, apparently because the deeper snow in the valleys protected the plants from low temperature, heavy winter winds and desiccation.

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Estimating potential range shift of some wild bees in response to climate change scenarios in northwestern regions of Iran

  • Rahimi, Ehsan;Barghjelveh, Shahindokht;Dong, Pinliang
    • Journal of Ecology and Environment
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    • v.45 no.3
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    • pp.130-142
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    • 2021
  • Background: Climate change is occurring rapidly around the world, and is predicted to have a large impact on biodiversity. Various studies have shown that climate change can alter the geographical distribution of wild bees. As climate change affects the species distribution and causes range shift, the degree of range shift and the quality of the habitats are becoming more important for securing the species diversity. In addition, those pollinator insects are contributing not only to shaping the natural ecosystem but also to increased crop production. The distributional and habitat quality changes of wild bees are of utmost importance in the climate change era. This study aims to investigate the impact of climate change on distributional and habitat quality changes of five wild bees in northwestern regions of Iran under two representative concentration pathway scenarios (RCP 4.5 and RCP 8.5). We used species distribution models to predict the potential range shift of these species in the year 2070. Result: The effects of climate change on different species are different, and the increase in temperature mainly expands the distribution ranges of wild bees, except for one species that is estimated to have a reduced potential range. Therefore, the increase in temperature would force wild bees to shift to higher latitudes. There was also significant uncertainty in the use of different models and the number of environmental layers employed in the modeling of habitat suitability. Conclusion: The increase in temperature caused the expansion of species distribution and wider areas would be available to the studied species in the future. However, not all of this possible range may include high-quality habitats, and wild bees may limit their niche to suitable habitats. On the other hand, the movement of species to higher latitudes will cause a mismatch between farms and suitable areas for wild bees, and as a result, farmers will face a shortage of pollination from wild bees. We suggest that farmers in these areas be aware of the effects of climate change on agricultural production and consider the use of managed bees in the future.

Distribution of Stream Incision Rates in the Northern Part of the Taebaek Mountains (태백 산지 북부의 하천 하각률 분포)

  • Lee, Gwang-Ryul
    • Journal of The Geomorphological Association of Korea
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    • v.25 no.4
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    • pp.1-19
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    • 2018
  • This study tries to identify distributional characteristics of stream incision rates at 23 points in the northern part of the Taebaek Mountains. Soyang-gang, Naerin-cheon, Odae-cheon, Dong-gang and upper reaches of Okdong-cheon Rivers closed to the Range show higher incision rates and the rates clearly decrease with distance from the Range. Therefore, the incision process in the northern part of the Range has been greatly influenced by uplift around the Range, and the Sobaek Mountain Range seem to play a role in the incision process. Limestone areas show lower incision rates due to degradation of terrace surface by dissolution. This study suggests that local hydrological, geological and geomorphological conditions can be regarded as an important factor in stream incision rates, although stream incision rates are greatly influenced by regional uplift.

Distribution of Evergreen Broad-leaved Plants and Climatic Factors (한반도 상록활엽수의 지리적 분포와 기후요소)

  • 구경아;공우석;김종규
    • Journal of the Korean Geographical Society
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    • v.36 no.3
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    • pp.247-257
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    • 2001
  • The relationships between the distribution of 132 species, 61 genera evergreen broad-leaved trees and shrubs(EBTS) and climatic factors have discussed. The distributional patterns of EBTS were categorized into seven groups on the basis of the number of distributing sites, distributional attitudes and latitudes. Out of seven group. the cold-tolerant EBTS were common at groups I and II, along tilth Empetrum nigrum var. japonicum. Diapensia lapponics subsp. obovata of group III. However, the warmth-tolerant EBTS were rich at groups III. IV V, and VI The lower distributional limits of cold-tolerant EBTS in the groups I and UU decreased as one moves toward south. The upper distributional limit of warmth-tolerant EBTS in the groups III, IV and V decreased with increasing latitude. However. no clear distributional tendency is noticed in the groups VI and VII. The range of warmth-tolerant EBTS appear to show close relationship with the January mean temperature -4 $\^{C}$ and January mean minimum temperature -9$\^{C}$ than others. On the other hand, that of the cold-tolerant EBTS seem to respond well to the August mean temperature 19$\^{C}$ and August mean maximum temperature 26$\^{C}$ than others.

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On the Distribution of Beech(Fagus, Fagaceae) and Beech-Dominated Forests in the Northern Hemisphere (북반구의 너도밤나무와 너도밤나무림의 분포에 관하여)

  • Yim, Yang-Jai
    • The Korean Journal of Ecology
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    • v.6 no.3
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    • pp.153-166
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    • 1983
  • The distribution of beech species (Fagus) and beech-dominated forests along climatic gradients in the Northern Hemisphere was studied by use of taxonomic and ecological literature. The genus Fagus as a whole occurs over the range of 4.5 to 20.0。C mean annual temperature and 600 to 1000 mm in lower limit, mean annual precipitation. At the higher end of the temperature range, beech occurs in zones with relatively high growing-season precipitation. Edaphically, beech species and beech-dominated forests tend to occur on mesic, moderately fertile sites. Beech-dominated forests occur in a limited portion of the climatic range of the genus with sensitive responses to other environmental factors. The distributional range of beech-dominated forests on a global scale depends more on climatic factors and geological events than on soil conditions or other factors, summarizing the facts obtained by many researchers on beech dominated forests.

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The Biology of the Pelagic Amphipod, Primno macropa Guer., in the Western North Pacific: 2. Geographical Distribution and Vertical Distributional Pattern

  • Yoo, Kwang-Il
    • The Korean Journal of Zoology
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    • v.15 no.2
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    • pp.87-91
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    • 1972
  • For the geographical distribution of Primno macropa it was distributed over all stations investigated, except surface tow in East China Sea, through all seasons. It is believed that this species is most cosmopolitan species in the western North Pacific. Veritical distributional range of P. macropa indicates at depths from surface to more than 1,500m and most deeper recored for the vertical occurrence was obtained from depth of 1,650-2,220m in Station 229 $(34^\\circ 44.3'N, 140^\\circ 04.4'E)$, off Nojima-Zaki, Central Japan. For the vertical distributional and migrational pattern it is a typical diurnal migrant in the western North Pacific; at depths from 100m to 500m at night and 400m to 700m at day in Oyashio population, and from surface to 200m at night and from 100m to 300m at day in Kuroshio population. In Kuroshio area, the population of P. macropa was distributed in somewhat shallower layers than in Oyashio area and it is suggested that the populations is different in region and season according to their stages consisting the population.

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