scholarly journals Relationship of Muna Language, Ciacia, Tukang Besi and Culambacu (Lexicostatistic and Glotochronology Study)

Author(s):  
La Ino ◽  
Nanda Saputra

This article is motivated by the results of the 2019 SIL research that the languages ​​in Southeast Sulawesi Province vary in category. Some are strong and some are threatened. Among the languages ​​that are categorized as threatened are the Muna language, the Ciacia language, while the Tukang Besi language is included in the strong language group. However, there are still several languages ​​that have not been listed in the SIl research, namely the Culamabacu language. This article discusses the kinship between the Muna language, Ciacia language, the Tukang Besi language and the Culambacu language. This paper uses the theory of comparative historical linguistics with lexicostatistical and glotochronological methods. The results of the analysis of the four languages ​​are that the percentage of Muna and Ciacia language kinship is 49%, Muna language kinship with Tukang Besi 43%, Muna language with Culambacu language 36%, Ciacia language with Tukang Besi 43%, Ciacia language with Culambacu language is 37%, the Tukang Besi language is with Culambacu language 33%. Based on the glottochronology, the Ciacia language and Muna language have a separate year of 1912-1532, the Ciacia language and the Tukang Besi language have a separate year of 2279-183, the Ciacia language and Culambacu language have the years 2587-2211, the Muna language and the Tukang Besi language have a 2371-2335 year, Muna language with Culambacu language has the years 2658-2272, the Tukang Besi language with Culambacu language has a separate year 2885-2465.

2010 ◽  
Vol 7 (2) ◽  
pp. 201-219 ◽  
Author(s):  
Christopher I. Beckwith

The ethnolinguistic history of early East Asia depends on the comparative-historical study of the different languages. Scholars have long studied the early interrelationships among the major languages of East Asia, but only rarely according to the theory and methodology of scientific comparative-historical linguistics and linguistic typology, in which theories are expected to conform to the data. Among the many highly contested genetic relationship proposals in the region is the “Korean-Japanese theory”. Despite nearly a century of work by some very prominent scholars, no one has given a convincing demonstration of such a relationship, partly due to the paucity of supporting data, despite the fact that the two languages in question are vibrant and well attested. Now two leading scholars of Japanese and Korean linguistics who are familiar with each other's work, J. M. Unger and A. Vovin, have almost simultaneously published new books on the topic, one in favor of the theory, one against it. The contributions and flaws of the two books, and their position relative to the development of a scientific tradition of comparative-historical linguistics, are discussed. Special attention is paid to Koguryo, the extinct Japanese-related language once spoken on the Korean Peninsula that is crucial to any discussion of the historical relationship of Japanese and Korean.


1997 ◽  
Vol 24 ◽  
pp. 381-391 ◽  
Author(s):  
P.E.H. Hair

The extent of secure knowledge of the past of the groups of people known in scholarly literature as Baga is inconsiderable. This is in part because of the limited European interest in past times in the Baga homeland (on the coast of the post-colonial state of Guinée), and also in part because of limited scholarly investigations in recent times (the post-colonial state did not help by for long exiling or barring from access non-Marxist scholars).Ethnographic and linguistic investigations have been undertaken only since the mid-nineteenth century and still amount to very little, with even less in print. Archeological investigations have yet to begin, apart from the brave attempt of Fred Lamp to date certain artefacts stylistically. As a result, in the 1990s the connotation and exact range of application of the term “Baga” remain unclear and the precise linguistic relationship of “the Baga language” with those neighboring languages that appear to form a language group is known only in outline. What this means that it is impossible to sum up the earlier history of the Baga briefly. The reader who continues and bravely tackles the listing and discussion of sources that follows will, however, be able to assess how much of the history can be securely reconstructed.It is understandable that the desire to construct a history for the Baga has latterly turned on the interpretation of oral traditions. Such traditions now preferred by the Baga—or at least by certain sections, strata, or individuals—are patently of great interest to the anthropologist inasmuch as they depict what the present-day Baga, or some of them, wish to see as their past history and thus throw light on contemporary ideology and popular mindsets.


Paleobiology ◽  
1980 ◽  
Vol 6 (02) ◽  
pp. 146-160 ◽  
Author(s):  
William A. Oliver

The Mesozoic-Cenozoic coral Order Scleractinia has been suggested to have originated or evolved (1) by direct descent from the Paleozoic Order Rugosa or (2) by the development of a skeleton in members of one of the anemone groups that probably have existed throughout Phanerozoic time. In spite of much work on the subject, advocates of the direct descent hypothesis have failed to find convincing evidence of this relationship. Critical points are:(1) Rugosan septal insertion is serial; Scleractinian insertion is cyclic; no intermediate stages have been demonstrated. Apparent intermediates are Scleractinia having bilateral cyclic insertion or teratological Rugosa.(2) There is convincing evidence that the skeletons of many Rugosa were calcitic and none are known to be or to have been aragonitic. In contrast, the skeletons of all living Scleractinia are aragonitic and there is evidence that fossil Scleractinia were aragonitic also. The mineralogic difference is almost certainly due to intrinsic biologic factors.(3) No early Triassic corals of either group are known. This fact is not compelling (by itself) but is important in connection with points 1 and 2, because, given direct descent, both changes took place during this only stage in the history of the two groups in which there are no known corals.


Author(s):  
D. F. Blake ◽  
L. F. Allard ◽  
D. R. Peacor

Echinodermata is a phylum of marine invertebrates which has been extant since Cambrian time (c.a. 500 m.y. before the present). Modern examples of echinoderms include sea urchins, sea stars, and sea lilies (crinoids). The endoskeletons of echinoderms are composed of plates or ossicles (Fig. 1) which are with few exceptions, porous, single crystals of high-magnesian calcite. Despite their single crystal nature, fracture surfaces do not exhibit the near-perfect {10.4} cleavage characteristic of inorganic calcite. This paradoxical mix of biogenic and inorganic features has prompted much recent work on echinoderm skeletal crystallography. Furthermore, fossil echinoderm hard parts comprise a volumetrically significant portion of some marine limestones sequences. The ultrastructural and microchemical characterization of modern skeletal material should lend insight into: 1). The nature of the biogenic processes involved, for example, the relationship of Mg heterogeneity to morphological and structural features in modern echinoderm material, and 2). The nature of the diagenetic changes undergone by their ancient, fossilized counterparts. In this study, high resolution TEM (HRTEM), high voltage TEM (HVTEM), and STEM microanalysis are used to characterize tha ultrastructural and microchemical composition of skeletal elements of the modern crinoid Neocrinus blakei.


Author(s):  
Leon Dmochowski

Electron microscopy has proved to be an invaluable discipline in studies on the relationship of viruses to the origin of leukemia, sarcoma, and other types of tumors in animals and man. The successful cell-free transmission of leukemia and sarcoma in mice, rats, hamsters, and cats, interpreted as due to a virus or viruses, was proved to be due to a virus on the basis of electron microscope studies. These studies demonstrated that all the types of neoplasia in animals of the species examined are produced by a virus of certain characteristic morphological properties similar, if not identical, in the mode of development in all types of neoplasia in animals, as shown in Fig. 1.


Author(s):  
J.R. Pfeiffer ◽  
J.C. Seagrave ◽  
C. Wofsy ◽  
J.M. Oliver

In RBL-2H3 rat leukemic mast cells, crosslinking IgE-receptor complexes with anti-IgE antibody leads to degranulation. Receptor crosslinking also stimulates the redistribution of receptors on the cell surface, a process that can be observed by labeling the anti-IgE with 15 nm protein A-gold particles as described in Stump et al. (1989), followed by back-scattered electron imaging (BEI) in the scanning electron microscope. We report that anti-IgE binding stimulates the redistribution of IgE-receptor complexes at 37“C from a dispersed topography (singlets and doublets; S/D) to distributions dominated sequentially by short chains, small clusters and large aggregates of crosslinked receptors. These patterns can be observed (Figure 1), quantified (Figure 2) and analyzed statistically. Cells incubated with 1 μg/ml anti-IgE, a concentration that stimulates maximum net secretion, redistribute receptors as far as chains and small clusters during a 15 min incubation period. At 3 and 10 μg/ml anti-IgE, net secretion is reduced and the majority of receptors redistribute rapidly into clusters and large aggregates.


Author(s):  
D.L. Spector ◽  
S. Huang ◽  
S. Kaurin

We have been interested in the organization of RNA polymerase II transcription and pre-mRNA splicing within the cell nucleus. Several models have been proposed for the functional organization of RNA within the eukaryotic nucleus and for the relationship of this organization to the distribution of pre-mRNA splicing factors. One model suggests that RNAs which must be spliced are capable of recruiting splicing factors to the sites of transcription from storage and/or reassembly sites. When one examines the organization of splicing factors in the nucleus in comparison to the sites of chromatin it is clear that splicing factors are not localized in coincidence with heterochromatin (Fig. 1). Instead, they are distributed in a speckled pattern which is composed of both perichromatin fibrils and interchromatin granule clusters. The perichromatin fibrils are distributed on the periphery of heterochromatin and on the periphery of interchromatin granule clusters as well as being diffusely distributed throughout the nucleoplasm. These nuclear regions have been previously shown to represent initial sites of incorporation of 3H-uridine.


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