scholarly journals A method for the identification and characterization of clusters of schools along the transect lines of fisheries-acoustic surveys

2003 ◽  
Vol 60 (4) ◽  
pp. 872-884 ◽  
Author(s):  
Pierre Petitgas

Abstract The school-aggregation pattern (schools and clusters of schools) is presumed to play a significant role in determining pelagic fish-stock catchability. However, its analysis has seldom been undertaken because it requires field-behavioural data that is seldom available. Such information can now be obtained by analysing school-based data of fisheries-acoustic surveys. This paper proposes a method for doing so. The method allows for the identification of clusters of schools and the estimation of their parameters along one-dimensional, acoustic-survey transect lines. It is based on a spatial point-process approach that considers schools as point events occurring along the track sailed by a ship. More precisely, it is based on defining a maximum distance between schools in a cluster. This distance is chosen to optimize various criteria and in particular that of homogeneity concerning school location inside the clusters and school number per km. The algorithm is described and applied to a series of acoustic surveys carried out in the Bay of Biscay. The pertinence of the clusters obtained by the algorithm is evaluated by analysing which component of the spatial distribution of the schools corresponds to those clusters. This involves considering all the distances between school events and performing simulations of cluster point processes. The school clusters obtained by the proposed algorithm represent a small-range structure of a few kilometres when a longer-range structure of tens of kilometres was also present in the data.

1987 ◽  
Vol 241 (2) ◽  
pp. 353-360 ◽  
Author(s):  
R Jones ◽  
C R Brown

Previous investigations [Jones, Brown, von Glos & Gaunt (1985) Exp. Cell Res. 156, 31-44] have demonstrated the appearance of a new antigenic determinant (recognized by monoclonal antibody 2D6) on the plasma membrane of rat spermatozoa during post-testicular maturation in the epididymis. Identification of the 2D6 antigen on Western blots from one-dimensional SDS/polyacrylamide gels revealed that it co-migrated with a membrane protein (designated Mr 23,000 antigen) present on testicular and immature germ cells, suggesting that one antigen might be a modified version of the other. In the present work, however, we demonstrate that, although they have similar Mr and are present in soluble and membrane-bound forms, the 2D6 and Mr 23,000 antigens are biochemically and immunologically distinct molecules. The properties of the antigens are described and compared. The Mr 23,000 antigen is present on both testicular and cauda epididymidal spermatozoa, has a pI of 6.1, contains no detectable carbohydrate, is not tissue-specific and is degraded by V8 protease. By contrast, the 2D6 antigen is glycosylated, has a broad pI from 4.5 to 6.1, is tissue- and species-specific and is resistant to digestion with V8 protease. Its role in sperm-egg recognition is discussed.


Author(s):  
Kazuyuki MIYAKITA ◽  
Keisuke NAKANO ◽  
Masakazu SENGOKU ◽  
Shoji SHINODA

Diabetes ◽  
1992 ◽  
Vol 41 (9) ◽  
pp. 1165-1171 ◽  
Author(s):  
R. Kikkawa ◽  
K. Umemura ◽  
M. Haneda ◽  
N. Kajiwara ◽  
S. Maeda ◽  
...  

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