• Title/Summary/Keyword: Bass numbers

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A NOTE ON BETTI NUMBERS AND RESOLUTIONS

  • Choi, Sang-Ki
    • Communications of the Korean Mathematical Society
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    • v.12 no.4
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    • pp.829-839
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    • 1997
  • We study the Betti numbers, the Bass numbers and the resolution of modules under the change of rings. For modules of finite homological dimension, we study the Euler characteristic of them.

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Prediction of movie audience numbers using hybrid model combining GLS and Bass models (GLS와 Bass 모형을 결합한 하이브리드 모형을 이용한 영화 관객 수 예측)

  • Kim, Bokyung;Lim, Changwon
    • The Korean Journal of Applied Statistics
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    • v.31 no.4
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    • pp.447-461
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    • 2018
  • Domestic film industry sales are increasing every year. Theaters are the primary sales channels for movies and the number of audiences using the theater affects additional selling rights. Therefore, the number of audiences using the theater is an important factor directly linked to movie industry sales. In this paper we consider a hybrid model that combines a multiple linear regression model and the Bass model to predict the audience numbers for a specific day. By combining the two models, the predictive value of the regression analysis was corrected to that of the Bass model. In the analysis, three films with different release dates were used. All subset regression method is used to generate all possible combinations and 5-fold cross validation to estimate the model 5 times. In this case, the predicted value is obtained from the model with the smallest root mean square error and then combined with the predicted value of the Bass model to obtain the final predicted value. With the existence of past data, it was confirmed that the weight of the Bass model increases and the compensation is added to the predicted value.

A UNIFORM STRONG LAW OF LARGE NUMBERS FOR PARTIAL SUM PROCESSES OF FUZZY RANDOM SETS

  • Kwon, Joong-Sung;Shim, Hong-Tae
    • Journal of applied mathematics & informatics
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    • v.30 no.3_4
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    • pp.647-653
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    • 2012
  • In this paper, we consider fuzzy random sets as (measurable) mappings from a probability space into the set of fuzzy sets and prove a uniform strong law of large numbers for sequences of independent and identically distributed fuzzy random sets. Our results generalize those of Bass and Pyke(1984)and Jang and Kwon(1998).

COMINIMAXNESS WITH RESPECT TO IDEALS OF DIMENSION ONE

  • Irani, Yavar
    • Bulletin of the Korean Mathematical Society
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    • v.54 no.1
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    • pp.289-298
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    • 2017
  • Let R denote a commutative Noetherian (not necessarily local) ring and let I be an ideal of R of dimension one. The main purpose of this note is to show that the category ${\mathfrak{M}}(R,\;I)_{com}$ of I-cominimax R-modules forms an Abelian subcategory of the category of all R-modules. This assertion is a generalization of the main result of Melkersson in [15]. As an immediate consequence of this result we get some conditions for cominimaxness of local cohomology modules for ideals of dimension one. Finally, it is shown that the category ${\mathcal{C}}^1_B(R)$ of all R-modules of dimension at most one with finite Bass numbers forms an Abelian subcategory of the category of all R-modules.

ON THE LOCAL COHOMOLOGY OF MINIMAX MODULES

  • Mafi, Amir
    • Bulletin of the Korean Mathematical Society
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    • v.48 no.6
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    • pp.1125-1128
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    • 2011
  • Let R be a commutative Noetherian ring, a an ideal of R, and M a minimax R-module. We prove that the local cohomology modules $H^j_a(M)$ are a-cominimax; that is, $Ext^i_R$(R/a, $H^j_a(M)$) is minimax for all i and j in the following cases: (a) dim R/a = 1; (b) cd(a) = 1, where cd is the cohomological dimension of a in R; (c) dim $R{\leq}2$. In these cases we also prove that the Bass numbers and the Betti numbers of $H^j_a(M)$ are finite.

COMINIMAXNESS OF LOCAL COHOMOLOGY MODULES WITH RESPECT TO IDEALS OF DIMENSION ONE

  • Roshan-Shekalgourabi, Hajar
    • Honam Mathematical Journal
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    • v.40 no.2
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    • pp.211-218
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    • 2018
  • Let R be a commutative Noetherian ring, a be an ideal of R and M be an R-module. It is shown that if $Ext^i_R(R/a,M)$ is minimax for all $i{\leq}{\dim}\;M$, then the R-module $Ext^i_R(N,M)$ is minimax for all $i{\geq}0$ and for any finitely generated R-module N with $Supp_R(N){\subseteq}V(a)$ and dim $N{\leq}1$. As a consequence of this result we obtain that for any a-torsion R-module M that $Ext^i_R(R/a,M)$ is minimax for all $i{\leq}dim$ M, all Bass numbers and all Betti numbers of M are finite. This generalizes [8, Corollary 2.7]. Also, some equivalent conditions for the cominimaxness of local cohomology modules with respect to ideals of dimension at most one are given.

Comparison of live shrimp bait catch efficiency in single line fishery

  • Koo, Myungsung;Munechika, Ishizaki;Cho, Samkwang;Bae, Bongseong;Cha, Bongjin
    • Fisheries and Aquatic Sciences
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    • v.24 no.11
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    • pp.383-389
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    • 2021
  • On the southern coast of South Korea, dark-banded rockfish, sea bass, and red seabream are caught by single-line fishing. In particular, red seabream and sea bass are caught in the Jeollanam-do region using gear with attached fishing hooks, such as longline and single-line gear, with live shrimp as bait. The objective of this study was to compare the catch efficiency of two types of live shrimp (naturally grown Shiba shrimp [Metapenaeus joyneri] and cultured whiteleg shrimp [Litopenaeus vannamei]) used as bait. The investigation included interviews, on-board surveys, and water tank experiments. Interviews were conducted with relevant parties to determine the preference for live shrimp as bait, and the results showed a greater preference for cultured whiteleg shrimp. Further, an on-board survey was conducted to compare catch efficiency between these two types of live shrimp bait for single-line fishing. The on-board investigations were conducted once or twice a month between June and October. In total, the amounts of fish caught using naturally grown Shiba shrimp and cultured whiteleg shrimp were 56 and 52, respectively. Of these, the numbers of sea bass, the primary target fish species, caught using naturally grown Shiba shrimp and cultured whiteleg shrimp were 43 and 40, respectively. Thus, the results showed that there was almost no difference in the number of fish caught based on the bait used. However, according to a water tank experiment, cultured whiteleg shrimp survived longer than naturally grown Shiba shrimp.

Infection Status of Estuarine Fish and Oysters with Intestinal Fluke Metacercariae in Muan-gun, Jeollanam-do, Korea

  • Cho, Shin-Hyeong;Kim, In-Sang;Hwang, Eun-Jung;Kim, Tong-Soo;Na, Byoung-Kuk;Sohn, Woon-Mok
    • Parasites, Hosts and Diseases
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    • v.50 no.3
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    • pp.215-220
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    • 2012
  • The source of human infection with intestinal flukes was surveyed in estuarine fishes, including the dotted gizzard shad, common sea bass, common blackish goby, redlip mullet, black sea bream, and oyster collected from Muan-gun, Jeollanam-do, Korea during August and September 2007. Collected fishes and oysters were artificially digested in pepsin-HCl solution and examined under a stereomicroscope. In 36 shads (Konosirus punctatus) and 20 basses (Lateolabrax japonicus) examined, Heterophyopsis continua metacercariae were found in 58.3% and 100%, and their average numbers were 12.0 and 6.3 per infected fish, respectively. In 34 gobies (Acanthogobius flavimanus) examined, metacercariae of H. continua were detected in 79.4%, Stictodora lari in 97.1%, and Acanthotrema felis in 92.1%, and their average numbers were 45.8, 189.3, and 235.3 per infected fish, respectively. In 37 redlip mullets (Chelon haematocheilus), Heterophyes nocens metacercariae were found in 56.8%, Pygidiopsis summa in 94.6%, and Stictodora fuscata in 45.9%, and the average metacercarial densities were 17.4, 31.3, and 35.1 per infected fish, respectively. In 30 black sea breams (Acanthopagrus schlegeli) and 45 oysters (Crassostrea gigas) examined, no metacercariae were detected. From the above results, it has been confirmed that the dotted gizzard shad, common sea bass, common blackish goby, and redlip mullet from Muan-gun, Jeollanam-do, Korea are infected with the metacercariae of heterophyid flukes.