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K. Mather (1935)
Meiosis in LiliumCytologia, 6
The nature of tetraploidy in Primula kaoensis
H. Warmke (1937)
CYTOLOGY OF THE PACIFIC COAST TRILLIUMSAmerican Journal of Botany, 24
Levan Levan (1936)
“Die Zytologie von Allium Cepa xfistulosum”Hereditas, Lund, 21
(1935)
Meiosis in Crepis. I and 11
(1936)
Chiasma localisation in Mecostetlrus grossus I,. and Metrioptera brarhyptera L. (Orthoptera)
威成 前田 (1937)
ネギ, タマネギ, 雜種F1, F2, 戻雜種に於けるキアズマ觀察The Japanese Journal of Genetics, 13
(1932)
Pairing behaviour and chiasrna formation in plants with a structurally STONE, I
Darlington Darlington (1935a)
“The time, place and action of crossing‐over”J. Genet., 31
(1937)
T h e pairing coefficient
(1940)
The causal sequence of meiosis. I. Chiasma formation and the order of HALDANE
Stone Stone, Mather Mather (1932)
“The origin and behaviour of chiasmata. IV. Diploid and triploid Hyacinths”Cytologia, Tokyo, 4
Maeda Maeda (1937)
“Chiasma studies in Allium fistulosum, Allium Cepa, and their F 1 , F 2 , and back‐cross hybrids”Jap. J. Genet., 13
Mather Mather (1939)
“The determination of position in crossing‐over. III. The evidence of rnetaphase chiasmata”J. Genet., 39
(1940)
The causal sequence of meiosis . I . Chiasma formation and the order of
(1939)
1939. cross hybrids.
Darlington Darlington (1931)
“Meiosis”Biol. Rev., 6
(1936)
Chiasma localisation in Mecostetlrus grossus I
Richardson Richardson (1936)
“Structural hybridity in Lilium Martagon album x LHansonii”. J. Genet., 32
Lamm Lamm (1936)
“Cytological studies on inbred rye”Hereditas, Lund, 22
C. Darlington (2017)
The Internal Mechanics of the Chromosomes I—The Nuclear Cycle in
Sansome Sansome (1939)
“Pairing behaviour and chiasrna formation in plants with a structurally heterozygous pair in Pisum”Genetics, 21
“ The consequences of structural hybridity in I X u m x testaceurn
(1937)
Genet . 35 , 1 - 24 . heterozygous pair in Pisum . ” Genetics , 21 , 42 - 33 . triploid Hyacinths . Cytologia , Tokyo , 4 , 16 - 25 . 37 , 303 - 32 ; The nature of tetraploidy in Primula kaoensis . ”
Darlington Darlington (1936)
“The external mechanics of the chromosomes”Proc. roy. Soc. B, 121
P. Koller (1936)
The Origin and Behaviour of ChiasmataCytologia, 7
H. Barber (1940)
The suppression of meiosis and the origin of diplochromosomesProceedings of the Royal Society of London. Series B - Biological Sciences, 128
(1937)
On some tetraploid spermatocytes in Chrysochraon dispar (Orth.).
(1939)
T h e genetic structure of Tulipa
C. Darlington (1936)
The External Mechanics of the Chromosomes. I--The Scope of EnquiryProceedings of The Royal Society B: Biological Sciences, 121
Mather Mather (1934)
“The behaviour of meiotic chromosomes after X‐irradiation”Hereditas, Lund, 19
hybridity on male and female cells of Lilium
(1939)
T h e genetic structure of Tulipa. 111. Meiosis in Polyploids
(1935)
Genomanalyse bei Trificitm und Aegilops
Weitere Untersuchungen an Aegilops x Triticum und Aegilops x Aegilops-Bastarden
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“The genetic structure of Tulipa. IV. Balance, selection and fertility”J. Genet., 38
H. Kihara, F. Lilienfeld (1935)
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(1931)
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1-24. heterozygous pair in Pisum
(1935)
“ Genomanalyse bei Trificitm und Aegilops . VI . KIHARA , H . & IALIENFELD , F . KIJNGSTEDT , H . ( 1937 ) . “ On some tetraploid spermatocytes in Chrysochraon dispar
J. Haldane (1931)
The Cytological Basis of Genetical InterferenceCytologia, 3
G. Beadle (1933)
Further Studies of Asynaptic MaizeCytologia, 4
(1939)
T h e determination of position in crossing-over. 111. The evidence of rnetaphase
(1935)
Meiosis in Crepis
C. Darlington (1936)
The External Mechanics of the Chromosomes. IV--Abnormal Mitosis and MeiosisProceedings of The Royal Society B: Biological Sciences, 121
(1939)
T h e genetic structure of Tulipa. IV. Balance, selection and chiasmata
L. Stone, K. Mather (1932)
The Origin and Behaviour of Chiasmata, IVCytologia, 4
(1936)
Structural hybridity in Lilium Martagon album x L . Hansonii
(1937)
Chiasma studies in Allium fistulosum, Allium Cepa, and their F l
(1936)
T h e occurrence in nature of asynapsis in Allium amplectens
Summary 1. The uniform series of chromosome movements we know as meiosis (pairing, torsion, reproduction, crossing‐over, co‐orientation, segregation) can now be placed in a causal sequence. This serves two purposes: to be tested as a working hypothesis and to be applied to the understanding of the characteristic variations of which meiosis is susceptible. 2. Comparison of mutants, hybrids and other genetically controlled variants shows that these variations arise from three main sources: (i) the point at which the pairing chromosomes make contact; (ii) the time available for pairing; (iii) the amount of torsion capable of being developed in the parts of the chromosomes which are paired. 3. All species are, as such, characteristically co‐ordinated with regard to these variables. They may be classified as procentric (Mecostethus) or proterminal (Chry‐sochruon) in the initiation of pairing. This difference affects the relative frequency of crossing‐over in chromosomes of two main types, with the centromere near an end and away from it (Fritillariu, Lilium). 4. Exceptional cells, and individuals arising by segregation from hybrids, show that co‐ordination within the cell and the individual is not physiologically inherent in meiosis. Unco‐ordinated behaviour can take place in regard to all three prime variables (Allium, Lilium and Trillium). 5. The time limit to pairing may be imposed artificially by heat treatment or X‐raying. We then have artificial localization of crossing‐over (Uvularia, Vicia). 6. The amount of torsion depends on the speed of pairing and this in turn on the size of the nucleus. Doubling the chromosome number therefore reduces the crossing‐over frequency (Primula, Allium, Solanum, etc.). 7. The preservation of torsion depends on the early contact of a chromosome at two points. The more numerous contact points of triploids therefore increase their frequency of crossing‐over per unit length paired, at the same time changing its distribution (Fritillaria, Tulipa, Drosophila). 8. All species hybrids are structural hybrids. Their pairing is therefore slower and is cut short by the time limit. Hence their crossing‐over is reduced and relatively localized, unless the extreme of localization has already been reached in the parents (Triticum, Lilium). 9. The study of the three prime variables is therefore necessary for the understanding of the causal sequence of meiosis and of the conditions of stability and coherence in species.
Biological Reviews – Wiley
Published: Jul 1, 1940
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