On the etymology of the Japanese plural suffix and its possible connection to Korean

2021 ◽  
Vol 2 (1) ◽  
pp. 24-35
Author(s):  
Alexander Francis-Ratte

Abstract This paper presents an etymological analysis of the Japanese plural suffix tachi, Old Japanese tati. I propose that tati originates from a grammaticalization of an earlier Pre-Old Japanese phonological form *totwi, the non-bound reflex of which is the Old Japanese quasi-collective marker dwoti ‘fellow (person), everyone, together’. The reconstruction of a Pre-Old Japanese stem *totwi (Pre-Proto-Japanese /*tətəj/) with quasi-collective and plural function clarifies the possible connection of the Japanese plural suffix to the Korean plural suffix tul (Middle Korean tólh), which Whitman (1985, p. 217) proposed to be cognates but which has since been criticized on phonological and distributional grounds. I show that reconstructing the earliest form of the Japanese plural suffix as /*tətəj/ resolves each of the three phonological issues with the Japano-Koreanic comparison, creates a better morphosyntactic match between the two languages, and rules out a loanword relationship of the Japanese and Korean forms.

Author(s):  
Václav Blažek

This chapter presents all relevant forms of the cardinal numerals 1‒10, 20‒90, 100, and sometimes also teens and ordinals, in all described Transeurasian languages. Besides all modern languages, where maximum accuracy in transcription is preferred, the old literary and epigraphic languages (Orkhon Runic, Old Uyghur, Karakhanid, Old Oghuz, Chaghatai; Middle Mongol, Written Mongol; Jurchen, Manchu; Middle Korean; Old and Classic Japanese), are also analyzed, including some relic languages known only fragmentarily (Kuman, Old Bulgar; Kitan; Baekje, Silla; Koguryo). On the basis of regular phonetic correspondences the related forms are projected into the partial daughter protolanguages: Turkic, Mongolic, Tungusic, and Korean. Instead of Proto-Japonic, the Old Japanese forms serve for this purpose. Applying the comparative etymological method to the final comparison between these partial protolanguages should lead to identification of inherited cognates from borrowings in agreement with phonetic rules, semantic typology, and in the perspective of possible influences of hypothetical substrata, adstrata, and superstrata.


2020 ◽  
Vol 12 (5) ◽  
pp. 239
Author(s):  
Wenchao Li

This study tackles sequential voicing in Old Japanese with a focus on three matters: (a) the interaction of the eight vowels and aspirated consonants; (b) the association of the written system and sequential voicing; and (c) the interaction between the combinationality of each constituent and sequential voicing. Four hundred and seventy-two compound nouns of Old Japanese were collected from the corpus ‘The Japanese Lexicon: A Rendaku Encyclopedia’ by NINJAL. The findings reveal that (i) /k/ has the largest token number of sequential voicing and /p/ has the second largest token number, followed by /s/ and /t/; (ii) regarding the eight vowels /a/, /e1/, /e2/, /i1/, /i2/, /o1/, /o2/ and /u/, /a/ is most likely to form a [N1-N2] whose initial consonant is /k/, /p/ and /t/. It is not likely for the vowel /a/ to invite a voiced ‘/s/-initial’ N1’; /o1/ and /o2/ are both likely to combine with a voiced consonant /k/; /t/ and are less likely to yield a voiced /s/; /e1/ is more likely to invite a voiced consonant than /e2/, but /e1/ does not invite a voiced /p/; /e2/ does not yield a voiced /s/; and /i1/ is likely to take a voiced consonant than /i2/. /k/ and /t/ are the two consonants that are most likely to be voiced when forming a N-N with N1 ends with /i1/. /i2/ does not invite a voiced /p/, /s/ or /t/; /u/ never results in a voiced /s/; (iii) there is a split in the characters that renders a voiced phoneme or an unvoiced phoneme; and (iv) the semantic relationship of N1 and N2 in [N1-N2] that bears sequential voicing is of six types, of which the most frequent relationship of N1 and N2 is [Modifier - N2]. The [prefix-N2] construction is not subject to sequential voicing. 


2019 ◽  
pp. 77-82
Author(s):  
H. Yamamoto ◽  
S. Yamamoto ◽  
S. Funahashi ◽  
M. Ogawa ◽  
M. Miyashita ◽  
...  

2020 ◽  
Vol 2 (1) ◽  
pp. 94-107
Author(s):  
Alexander Vovin

Abstract This article argues for new internal evidence for the existence of the contrast between *r and *l in Old Korean and Proto-Korean on the basis of the Hyangchal data and Old Japanese transcriptional glosses as well as Korean loanwords in Manchu and Jurchen that were not analyzed in this way before. Namely, I will argue that combined Old Korean and Middle Korean data call for the reconstruction of two different types of liquids in the position before *i: both stay intact in Old Korean, but in Middle Korean the first type undergoes elision, whereas the second type stays intact. I then attempt to identify these two types on the basis of the internal evidence and parallel phenomena attested in the Greater Manchuria linguistic area and elsewhere.


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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