CAP6938 Neuroevolution and Artificial Embryogeny Leaky Integrator Neurons and CTRNNs
LITERATURE CITEO - Shodhgangashodhganga.inflibnet.ac.in/bitstream/10603/32930/11/10_chapter...
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* Original not seen
I L L U 5 T R A T I 0_N S
Figs. 1-5
Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5.
A male shrub maintained in the Botanic Garden Kashmir University.
A branch bearing mature female cones.
A branch bearing mature male cones.
A monoecious branch bearing main and female cones.
A branch bearing more than one main cone arising in the axils of sterile scales.
Figs. 6 - 1 1
(Abbreviations* male cone j fomale conej mg. microsporangium; ml. micro*sporophyll; bac. bract-scale complex.)
Fig. 6. Current years shoot bearing male cones, x 3
Fig. 7. Mature male cons, x 9
Fig. 8. Currant years branch bearing female cone, x 3
Figs. 9-11. 1st, 2nd and 3rd yearfemale cones, x 9
rigs. 12-14
( Abb£e\*ation: cotyledonary leaf.)
r i g .
fig.
fig.
12* Progressive stages in seed germination of single-seeded cone, XI,
13. Simultaneous germination of two seeds in tuo-seeded cone. XI.
14. Saddling throuqh 1st, 2nd, 3rd and 4?th year of grouth. XI.
* ♦ %
13
(Abbreviations! rij, resin duct; atonylayer; £gf female gametophyte.)
Figs* 15 - 104.
Figs* 15 & 15a* Seed from 1-seeded eone and its cross section* x 14
Figs* 16 & 16a# Send from 2-seeded eone and Its cross section# x 14
Figs* 1? & 17 a* Seed from 3-seeded eons and its eross section* x 14
Figs* 18 & 18a. Seed from 4-seeded eone and its eross section* x 14
Fig.
Fig.
Fig.
Fig.
Figs. 19—22
(Abbreviations: fbf fibro-vascular element;t,, transfusion tissue.)
19. Vertical section of a young leaf.x 115
20. A nortion of mature leaf, x 114.
21. Q portion of leaf from fig. 19 enlarged, to shou vascular bundle. Note fibro- vascular elements, x 410.
22. Vascular bundle of a mature leafc, enlarged to shou transfusion tissue, x 360.
Figs, 23 - 27
(Abbreviations! mt. meristemoid; stomata pb# cells having dark contents.)
Fig. 23. Abaxial surface of a leaf shouingextent of resin canal, x 14
Fig. 24. Whole mount of a resin gland leading into canal. x14
Figs. 25& 26. Paradermal sections of a leafshouing stomatal development and mature stomata, x 544 & x 409
Fig. 27. Vertical section of a lea<f shouing sunken stomata, x 544 **
«*
11 I
23
Figs. 2 8 - 3 1
(Abbreviation; oct oil cells. )
Fig. 28.
Fig. 29.
Fig. 30.
Fig. 31.
Adaxial leaf surface showing stomata (Scanning electron micrograph ) x 300.
Adaxial epidermal peel of leaf showing two bands of stomata.(Note the bands meroing occasionally.)
x 93.
Adaxial view of bract-scale comlex bearing a feu stomata, x 566. A
Cross section of bract-scale complex showing spongy tissue, x 517.
Figs. 32-34
Fig, 32* Transection of young stem shauing three separate vascular bundles, x 110.
Fig. 33. Transection of young stem at a nodeshouing triffrcation of each bundle, x 110,
Fig . 34 Transection of one year old stem shouing vascular cylinder, x 110.
rig .
Fig.
Figs
(Abbreviations* leaf trace; fb. fibro- vaseular elements.)
Figs. 35-37
35# Tranaectinn of stem showing entrance of vascular trace into leaf, x 116.
36. Portion of fig. 35 enlarged to showfibro-vascular elements in leaf trace.x 525,
37. Transfusion tissue of Mature leaf magnified to shout tuo type a of thickenings, x 525.
Fig.
Fig.
Fig,
Fig.
(Abbreviations: c p . cross-field pit; u p . uood parenchyma.)
38. T.5. uood. Note grouth ring and scatteredwood parenchyma, x 90,
39* An enlarged portion of fig. 38 x 670
40, R. L, S. uood. Note crosa-fiald pits, x 150,
41, Portion of fig. 40 enlarged-x 450.
Figs* 38-41.
Fig,
f i g .
fig.
Fig.
(Abbreviation: pf, phloem fibers)
42. T.L.S, uood. x 88,
43. Portion of fig. 42 enlarged. (Notepresence of biseriate rays.) x 408
44. T,S. young root, x 88
45. Cross section of phloem, x 444
Figs, 42-45.
Figs. 46 - 56
(abbreviations: p, phloem; px, protoxylera; inx. metaxylem; clb. cotylodonary bundle; plb, plumular bundle).
Fig* 46. fl young seedling. Figs. 47-57 represent transection bettmen levels marked A and 9 x .3
Fig. 47. T.S. in the region of cotyledons, x 25
Fig. 48. Cofcylndonary bundle onlarqod fromfig. 47 & 264.
Fig. 49. T.S. through plumular ragion. x 259
Fig. 50. C0tyladonary bundle from fig. 49enlarged. (Note that pftloem and metaxylem masses have started bifurcating), x 264
Fig. 51. T.S. cotyledonary node, x 25
Fig. 52. Fig* 51 magnified, x 264
Fig* 53. T.S. through hypocotyl region, x 25
Fig. 54. Fig. 53 magnified, x 264
Fig. 55. T.S. of hypocotyl at sliqhtly louor level, x 25
Fig. 56. Fig. 55 enlarged, showing typical exarch structure, x 264
Figs. 5? - 64
(Abbreviations! ai . apical initials} aai. sub- apical initials; p m , pith mother ceils;E* P*thi li* foliage leaf; baa, bud scale primordiaj flp. foliate leaf primordia).
Tig, 57* A schematic diagram of the zonation of the shoot apex* (lAf apical initials; IB, surface layer on flanks; 2, subapical initials; 3, flanking merlstem; 4. pith mother cells and pith.)
Fig. 58. Longisection of shoot apex showing zonation. x 38?
Fig. 59-64. Longisection of apical buds indifferent growth periods* Fig. 59 shows bud in period of buS elongation. Figs, 61 and 62 represent the beginning anrt the end of bud scale formation. Figs. 63 and 64 represent the beginning and and of foliaqe leaf formation, x 36
Fig, 65
Fig, 65% Graph showing variations in thediamensions of the shoot apex during a year*
Microrii
Figs* 66-68.
fig* 66* Longlaootion of apical bud in incipient resting period, x 396*
fig* 67* Longiaeotion of apical bud in bud elongation period, x 396*
Fig* 68. Longlsection of apical bud showingbeginning of bud scale formation,x3%.
Figs. 69 - 71
Fig. 69. Longisection of apical bud showing end of bud scale formation, x 396*
Figs. 70 & 71. Longisections of apical budsshowing beginning and end of foliage leaf formation x 396.
(Abbreviations* bt. bract trace; at. seals trace)
Figs. 72 - 79, Vasculature of female cone, x 15
Figs* 80 - 83* Vasculature of male cone, x 15
Figs* 72 “ 83*
Fig* 84
(Abbreviations: Af female bud initiation;J3, Archesporium differentiation; £, Arches— porium deep seated; 0 9 pollination drop appears; E f megaspore mother cell differentiation; £, raicropyle closing; megaspore tetrad formation; H, free nucleate gametophyte formation;
enlargement of ovule; cellular female gametophyte formation; K # archegonial initial;C. archegonial complex formation; M., fertilization; N.f proembryo formation; 0, cotyledon differentiation; P # mature ovule,
j., male bud initiation; Jb, archesporial differentiation, £ t formation of wall layers; d, microspore mother cell formation; £» meiosis;T, pollen formation; difiiacenceS ht pollination;
development of male gametophyte).**
Fig* 84. Graphic recjfenaentatinn of thelife - history of Junlperi^s communis ssp. nana Syme. inrelation to the mc£ibh$.* of a year.
AU
G
rig3 . 85 - 105
(Abbreviations* ml. microsporophyllj a s . micro- sporongium; tpt tappturn.)
Fins, 85-98* Abaxial view oF microsporophylls (in ascending ordor) of a mala cone showing variation, x 9
Fig. 99. Adaxial vieu of a microaporophyll, x9
Fig, 100* Longisection of male bud showingmicroaporophyll initiation, x 25
Figs, 101 & 102. Longisections of young aporophylls shouing extent of the hypoie>rmal archesporium. x 274
Fig* 1(33 . Lonqisection of a sporophyll ahouing sterilization of tissue in%etueen tuo archesporial masses, x 274
Fig, 104* Cross section of undifferentiated microsporangiurn.(Note periclinal divisions in epidermis), x 274
Fig* 105* Cross section of a fully differentiated «icroranglutR,(Note periclinal divisions in epidermis), x 274
Figs. 106 - 112
(Abbreviations* rd. resin duct; m l . microsporophyll; m s . microsporanqium; p b , cells uith dense contents).
Fig, 106. Cross section of a microsporangium shouinq differential staining property of soma of the microspore mother cells, x 280
Fig. 107. Cross section of a mature microsporangia, (Note unthickened epidermal cells at the region of dahiscance. x 59
Fig. 108. Cross section of a Microsporangiumshowing degenerated wall layers at the microspore shedding stage#
X 280
Fig. 109, Portion of microsporangial uallenlarged to shou radially thickened epidermal cells, x 372
Fig. 110 & 111. Vertical and longisection of a microsporophyll showing resin duct and its extent, x 26
Fig* 112* Longisection of a mature mala eone. x 26
Fig, 113, Microspore mother cells displayingthe tendency of togetherness, x 933.
Fig, 114. 'Ucrospore mother cell atmetaphase I* x 1482.
Fig. 115. Wicrospors mother cell at anaphase I*x 1386
Fig, 116. A laggard and a bridge at anaphase I- x 1599
Fig£ 117 & 118* Telophase IX shoeing various typesA of spindle orientation* x 933.
Figs. 119 & 120. Various types of tetrads, x 933.
Figs. 113-120.
fig*
Fig.
fig.
Fig.
121* Pollen architecture (Scanning electron micrograph), x 2800,
122. ftcetolysed pollen grain, x 933.
123. Tangential section of a microsporangium showing tapetal cells*
124. A magnified tapetal cell, x 933,
Figs. 121 - 124.
x 420.
Fioa. 125 - 132
(Abbreviations: al. antheredial cell; tn.tube nucleus! ot» pollen tube; he. body cell? sc. stalk cell; we. male colls).
Fig, 125. A poller* grain uith an antberedial cell and a tube nucleus, x 362
Fig. 126. Two-colled pollen tube.(Noto sinous qrowfchjt x 362
Fig* 127, Pollon tube uith tube nucleus at the tip of the tube, x 265
Fig* 128. A three-celled branched pollan tube, x 265
Fig. 129. Longisection of nucellus showing two docfrtding pollen tuba^ x 265
Fig. 130. One year old pollen tube.(Note increase in the size of body cell), x 362
Fig, 131. Longiaection of an ovule uithmore than tuo pollen tubes, x 55
Fig. 132. Tuo male cells, x 266
Figs. 133 - 137
(Abbreviations* o, ovulej ocl. outer cell;3Cl. surface cellj oat, primary archesporial cell; 3U. sporo^genous tissue.).
Fig, 133. Outline diagram of L.S. of female shoot showing initiation of two ovules, x 27
Figs. 134-136. Longisection of young ovulesshowing successive stages in the formation of nucellus and archesporial tissue, x 383
Fig. 137. Longisection of ovule showing sporogenous tissue, x 288
(Abbreviations s ocl. outer cell ; scl. surface cell; pal« primary archesporial cell•)
Figs. 138 -140. Longisection of young ovulesshowing successive stages in the development of nucellus and archesporial tissue, x 665
Fig. 141. Longisection of ovule shouing deep seated archesporium. x 1050.
Figs. 142 - 146
(Abbreviations! int. integument; nu. nucellus; su. sporogenous tissue).
Fig, 142, Longisection of upper portion of an ovule C*- 3hai£«ctivation of cells of inner integument lining the micropyle, x 82
Figs, 143 & 144, Outline diagram of longisection of an ovule showing closure of micropyle. Area marked in fig, 143 enlarged in fig, 144, x 24 & x 259.
Figs, 145 & 146, Outline diagram of upper portion of nucellus showing formation of "rudimentary pollen chamber".Portion marked in fig, t45 enlarged in fig, 146, *24 & x 259,
Figs. 147 - 155
Fig.
Fig,
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig, 147. Sporogenous tissue with megaspore mother cell, x 401
148. flegaspor® mother cell at metaphase I.x 401
149. A megaspore diad. x 401
150* Linear tetrad uith functional chalazal Hmgaspore . x 401
151* Linear tetrad showing functional micropylar mngaspore. x 401
152. Linear tetrad showing third functional megaspore, x 401
153, Isobilateral megaspore tetrad.x 401
154. A nsgaspore triad, (Note failure of II division in upper diad cell and two nucleate female gametophyte).
X 401
155. Two linear megaspore tetrads in an ovule, x 401,
Fig#
Fig.
Fig.
Fig.
Figs, 156-159.
156, A megaspore mother cell, x 765.
157. Ad isoMlateral n^gaapore tetrad, x 765.
158, Functional msgaspore just before first division, x 765.
159, Sector of a free nuclear female gametophyta, (Wot© simultaneous divisions of nuclei), x 765.
Figs* 160 • 168,
Pigs* 160-162, 0net tuo and four nucleate female gametophyte. x 351
Figs. 163 & 164* Eight and sixteen-nucleate female gametophyte. x 351
Fig* 165. Section of female gamstophyte showing simultaneous nuclear divisions* x 351
Fig* 166* nature free-nucleate female gamstophyte* x 25
Figs, 16?* Portion of fig* 166# magnified* x 351
Fig, 168* Longisection of female gametophyteshowing initiation of uall formation,
x 351
Figs. 169 - 174
(Abbreviations! tn. tube nucleus; al. antheredial cell; b£f body cell )•
Fig. 169. Longisection of a young ovule showing 2-nucleate male gametophyta. x 697
Fig. 170. Pollen tube showing body cell, tube nucleus and stalk nucleus, x 561
Fig. 171. An archegonium in which zygoticnucleus has undergone first division.
x 765
Fig. 172. Flultinucleate cells of mature female gametophytlc tissue, x 450
Fig. 173. L.S. of female cone showing inter- locking of bract-scale complex at maturity, x 61
Fig. 174. L.S. of an ovule showing closure of micropyle. x 99
Figs. 175 - 183.
(Abbreviations: ni. neck initial; nc« nock cells;
tf central cell; go. archegonium; ot« pollen tube;, body cell; nu, nucellus; fa, female gametophyte)
Fig, 175, Part of a young archegonium, x 531
Figs, 175-178, Different modes of division of neck initial, x 531
Fig, 179, Central cell showing its division into ventral canal and egg nuclei, x 531
Fig, 180. Outline diagram of longisection of f am ale gametophyte shot^Lateral archegonia x 54
Fig, 181, Lateral archegonium in fig, 180 enlarged; x 531
Fig, 182, Outline diagram of longisection of nucellus showing pollen tube and archegonial complex, 54
Fig, 183, Longisection of micropylar portion of female gametophyte showing archegonial complex with archegonial jacket, x 271
175 176
Figs. 184 - 191
(Abbreviations: suspensor; e,t embryonal celleS| embryonal suspensor)
Figs. 184. Fusing male and egg nuclei. x600
Figs. 185 & 186. Eight and twelve - nucleate proembryo x 390
Fig. 187. A young embryo shouing beginning of suspensor elongation, x 62
Fig. 188. A young embryo uith embryonal suspensors. x 62
Figs. 189 A 190. Embryonal suspensors shouing abnormal lobing. x 62
Fig. 191. Longisection of mature female gametophytic cells shouing formation of multinucleate cell, x 293
Figs. 192 - 199.
(Abbreviations: auapenaor; e a . embryonal aua-pensor; a, embryonal cell )
Fig. 192. A mass of auapenaora showing thair embryonal nature and lobing of embryonal auapenaora.
x 62
Figs. 193 -198. Varied lobing patterns of embryonal auapenaora. x 293
Fig. 199. Swollen embryonal auapenaor. x 293
Figs. 200 - 209
(Abbreviations* j|# suspensor} es|t embryonalsuspensor; at, embryonal tube.;
fig. 200, A young embryo showing embryonal suspensory up to 6th order,(Note embryonic nature of suspensor tier), x 58
Figs, 201-204, Various typos of "embryonal tetrads", x 275
Figs, 205 & 206, Embryonal masses showing segmentation, x 275
Fig, 207, Formation of "twin" embryos, x 275
Fig. 208 & 209, Embryonal masses shouing initial and later stage of embryonal tubas.
x 275 & 58.
rig.
Pig.
rig.
Fig.
Fig.
Fig.
210. Ten weeks old embryo, x 53
211. Terminal cell at metaphase to form embryonal mass, x 666
212. Abnormal anaphasic separation of terminal cell, x 666
213. "Twin embryo" formation, x 61
214. narked area of fig. 213 enlarged, x 400
215. Isobilateral embryonal tetrad.
Figa. 210 - 215
x 384
Figs. 216 - 221
Fig. 216, Linear embryonal tetrad, x 368
Fig, 217, Embryonal mass showing embryonal tubes, x 59
Fig, 218, Uhole mount of a complex showing polyembryony, x 25
Fig, 219, L, S, embryo showing differentiation of root tip* x 77
Fig, 220, L. S, embryo showing partly differentiated stem tip, x 67
Fig, 221, U, S, of embryo showing a provascular strand, x 74
m i m -
(Abbreviations* nu. nucellus; su. sporogenous tissue; integument; ol, outer layer;11. inner layerJ roe, middle layer; fo. female gamBtophyts; em. embryo; ao. archegonium; pt. pollen tube; rd. resin duct).
Figs. 222 - 230.
Figs. 222. Outline diagram of longisection of pre-pollination ovule, x 20
Fig. 223. Portion marked (a ) in fig. 222 enlarged, x 210
Fig, 224. Outline diagram of longisection ofan ovula at free nuclear gametophytic stage, x 20
Fig. 225, Portion marked(A) in fig. 224 enlarged, x 210
Fig. 226, Outline diagram of longisection ofan ovule with archegonial complex, x 20
Fig. 227. Portion marked(A) in fig, 226 enlargedX 210
Fig, 228. Outline diagram of longisection of an ovule when young embryos are observed, x 20
Fig, 229, Portion marked (A) in fig, 228 enlarged, x 210
Fig. 230. Outline diagram of longisection of a mature 3eod. x 20
Figs. 231 - 230
(Abbreviations : m, male cone; £, ovule; ms. microsporangium; m l . microsporophyll)
Fig. 231. A branch bearing more than ona mala cones in axils of sterile bracts, x 3
Fig. 232. A hermaphrodite cono. x 9
Fig. 233. Outline diagram of a lonqisection of h rmophrodite cone, x 25
Fig. 234. Outline diagram of a hermaphrodite cone with abaxial ovule, x 25
Figs. 235 & 236. flegaspore mother cell and a linear magaspore tetrad in an ovule of a hermaphrodite cone, x 351
Fig. 237 & 238. Maturation of microsporangium in a hermaphrodite cone, x 351
231
235
AJ L ? J U U > J L X < Reprint )
Cytology of Juniperus CLoinmunta ssp. nana Syaa.
Ths nucleus £&(lt2)j 46-48 (1981).
CY CLO H EX IM ID E ON CHROMOSOM E PA IR IN G 45
type of cell division. Following treatment with the drug a small percentage of cells in the testis fail to show the expected nieiotic sequence and continue to proceed along a mitotic pathway. The evidence is quite conclusive, for no such abnormal development is observed in the nontreated males or males treated with distilled water. Thus, the follicles of the untreated adult insects contained cells in interphase of meiosis. Similar observations were made in the course of an earlier study using the antibiotic actino- mycin D (Jain and Singh 1967, 1969). The study has shown that some of the modifications of the meiotic process reported earlier by Stern and his colleagues (1. c.) on the basis of study of cells in culture can be reproduced in vivo.Stern and Hotta (1969 b), Hotta et al. (1968) and Roth and Parchman (1969, 1971) have suggested an important role for protein synthesis during the course of meiotic prophase of lily plants in relation to the process of chromosome pairing and crossing over. One of their important findings has been that treatment of meiotic cells in culture with cycloheximide inhibits the meiotic process. Meiotic development is completely arrested at the concentrations exceeding 2 /J-g/ml, and the selective inhibition of protein synthesis at lower concentrations of the chemical at the end of zygotene, causes a failure of chiasma formation (see Roth and Parchman 1969, 1971). The effect of cycloheximide is observed at all meiotic stages up to metaphase. The authors conclude that protein synthesis during the prophase interval may be necessary for chromosome pairing as well as for chiasma formation. However, the effect may be a direct one or an indirect one. The proteins could exert their indirect effect by being associated with the synthesis of D N A since certain nuclear proteins are essential to the syntheses of D N A and combinations of these syntheses that occur during zygotene and pachytene are essential to chromosome pairing and chiasma formation.
S u m m a ryAn interesting observation in the present study is the complete failure o f meiotic development in a small percentage o f spermatocytes in the desert locust— Schistocerca gregaria, following treatment o f the male insects with cycloheximide, with the result that these cells now show a mitotic type o f cell division. Treatment o f male locusts with this chemical when their spermatogonial cells are showing the mitotic development can be expected to suppress a number o f gene loci whose activity probably is a prerequisite for the meiotic sequence to develop.
Acknowledgements: I would like to thank Dr H K Jain, Director, Indian Agricultural Research Institute, for his help and guidance during this work. Thanks are also due to Professor S Ramanujam, Head, Division o f Genetics, for providing me the facilities. I am grateful to Dr K N Mehrotra, Head, Entomology Division o f this Institute for supplying me the stocks o f desert locust.
R eferen cesB a r b e r HN (1942) The e x p e r i m e n t a l c o n t r o l o f
c h r o m o s o m e p a i r i n g i n Fritillaria. J . Genet. 43: 359.
D o w r ic k GJ (1957) The influence o f temperature on meiosis. Heredity 11: 37.
H e n d e r s o n SA (1962) Temperature and chiasma formation in Schistocerca gregaria. II. Cytological effects at 40°G and the mechanism o f heat- induced univalence. Chromosoma 13: 437.
H e n d e r s o n SA (1969) Chromosome pairing, chias- mata and crossing over. In : A . Lima-de-Faria (ed), Handbook o f Molecular Cytology: Amsterdam. North-Holland Pub. Co. 326.
H o t t a Y, P a r c h m a n LG a n d S t e r n H (1968) Protein synthesis during meiosis. Proc. N a tl. Acad. Sci. U SA 60 : 575.
J a in H K a n d S i n g h U (1967) Actinomycin D- induced chromosome breakage and suppression o f meiosis in the locust, Schistocerca gregaria. Chromosoma 2 1 : 463.
J a in H K a n d S i n g h U (1969) RN A synthesis and chromosome behaviour in Schistocerca. In: Chromosomes Today. CD Darlington and K R Lewis (ed), Edinburgh: Oliver and Boyd,2 : 70.
J o h n B a n d N a y l o r B (1961) Anomalous chrom osome behaviour in the germline o f Schistocerca gregaria. Heredity 16: 187.
R o t h TF a n d P a r c h m a n LG (1969) Achiasmatic meiocytes produced by cycloheximidc disruption o f the synaptonemal complex at late zygonema. J . Cell Biol. 43: 120a.
R o t h TF a n d P a r c h m a n LG (1971) Alteration o f meiotic chromosomal pairing and synaptonemal complexes by cycloheximide. Chromosoma 35: 9.
S is l e r H D a n d S i e g e l M R (1967) Cycloheximide and other glutarimide antibiotics. In : A n tibiotics. D. Gottlieb and PD Shaw (ed), Beilin, Heidelberg: Springer-Verlag, 1: 283.
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CY TO LO G Y OF JU N IPE R U S 47
Ross and Duncan (1949), Stiff (1952), Mehra and Khoshoo (1956), Love and Love (1956), Jorgenson et al (1958), Evans and Rasmussen (1971), Mehra (1976), and Hall et al (1979). The studies
indicate that, of the 60 Juniperus species, 52 taxa under 16 species have so far been studied cytologically.Ofthese,33 are diploid (2n = 22), three triploid (2n=33) and 16 tetraploid (2n =44).
The present investigation confirms the earlier count of 2 n = 2 2 by Sax and Sax (1933), Love and Love (1956) and six cultivars or varieties by Hall et al (1979).
The subspecies under report has either median or submedian chromosomes only. The karyotypic details have known only in J . procera (Mehra and Khoshoo 1956) where two chromosomes have subterminal and the rest median or submedian centromeres.
Meiosis in the material under report is normal. The presence of laggards and, bridges in some cells at anaphase I might be an indication of some structural aberrations. This needs to be confirmed from pachytene studies.
The presence of three triploids and 16 tetraploids in this genus and variation in
48 SANTOSH M U JOO AND GL C H A R
chromosome morphology together with the present observation of laggards at anaphase I in this taxon indicate that polyploidy and chromosomal alteration might have played vital roles in evolution within this genus.
S u m m aryDetailed cytological studies have been carried out in Juniperus communis ssp. nana Syme. 11 and 22 have been found to be the haploid and diploid chromosome numbers respectively. Meiosis is by and large normal. However, in 5% of cells scored laggards and chromatin bridges have been observed at meiotic anaphase I.
Acknowledgements: The authors are grateful to Dr R N Gohil and Dr Ranjana K oul for valuable suggestions, and to Professor P Kachroo for providing laboratory facilities.
R eferencesD a l l im o r e W a n d J a c k s o n AB (1966) A handbook
o f Coniferae and Ginkgoaceae. London.E v a n s E G a n d R asm u ssen PH (1 9 7 1 ) C h r o m o s o m e
counts in three cultivars o f Juniperus L. Hot. Gaz. 132: 259.
H a l l M T , M u k h e r j e e A a n d C r o w l e y W (1979) Chromosome numbers o f cultivated junipers. B ot. G az. 140: 364.
J o r g e n s o n C A , S o r e n s e n T H a n d W e s t e r g a a r d M(1958) The flowering plants o f Greenland. A taxo-
nomical and cytological survey. B iol. Skr. Dansk Vidensk Selsk. 9 : 1.
L o v e A a n d L o v e D (1956) Cytotaxonomical conspectus o f Icelandic flora. Acta Horti. Gotoburgensis 20: 65.
M e h r a PN (1976) Conifers o f Himalayas with particular reference to Abies and Juniperus complex. The Nucleus 19: 123.
M e h r a PN a n d K h o s h o o T N (1956) Cytology o f conifers— I. J . Genet. 54: 165.
Ross JG a n d D u n c a n R E (1949) Cytological evidences o f hybridization between Juniperus virginiana and J . horizontalis. B u ll. T oney Bot. Club 76: 414.
S a x K a n d S a x HJ (1933) Chromosome numbers and morphology in the conifers. J . Arnold Arboretum 14: 356.
St i f f M L (1951) A n a t u r a l l y o c c u r r in g t r ip lo id j u n i p e r . Va. J . Sci. 2 :3 1 7 v id e P L Breed. Abstr. (1952) 22: N o . 1474.
the nucleus v o l 2 4 (1 , 2 ) : 4 8 - 5 6 , 1981
DIFFERENTIAL X R A Y SENSITIV ITY OF SY R IA N H A M ST E R C H R O M O SO M E S
G. K . M a n n a 1 a n d S. K . D e y 2
Department of Zoology, University of Kalyani, Kalyani 741 235, India
Received on April 28, 1981
After the artificial induction of gene mutation in Drosophila (Muller 1927), chromosome aberration in maize (Stadler 1928) and variation in Nicotiana (Goodspeed and Olson 1928), by X-rays,
1 Grateful acknowledgment is made to the University Grants Commission for the award o f a National Fellowship to G K M .
2 Present Address: Department of Zoology,Darjeeling Government College, Darjeeling, West Bengal.
tremendous progress has been made on the study of effects of ionizing radiations on chromosomes of human and mammalian models deploying more of cultured cells than in vivo condition (Bender 1964 a, b, 1968; Bender and Gooch 1962 a, b, 1963; Bender et al 1962; Bell and Baker 1962; Bick and Brown 1975; Dey and Manna 1978; Dzhemilev and Macha- variani 1976; Dubinin et al 1960; Ford et al 1957; Hsu et al 1962; Lyon and
AUa;i k)■/.- T ih;ary i i <■■&«*■
A ce ho ..
?! U N