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Chromosome Numbers in the Coryphoideae1

Chromosome Numbers in the Coryphoideae1

1965 38 5

Chromosome Numbers in the Coryphoideae1

Robert W. Read

The Fairchild Tropical Garden , Coral Gables, Florida 33156, U. S. A.

Received January 10, 1965

The comprise some 34 genera of induplicate palmate and c ostapalmatel eaved palms distributed in nearly all tropical and subtropical regi ons of the world. Of these about 20 genera are represented as mature specimens in cultivation at th e Fairchild T ropical Garden, the Coconut Grove Palmetum (the former Montgomery Estate) a nd the United States Department of Agriculture Introduction Station all near Miami , Florida, U .S.A. The remaining 14 genera are either represented as juvenile at the Fai rchild Tropical Garden, (i.e. , , , , Johannesteijsman nia, , , and Tessmaniodoxa) or not in cultivation in the United States at all, (, Liberbaileya , Haitiella, Maxburretia, Pritchardiopsis, and Wissmannia). Because the identification of some palm in cultivation has been in confusion , many species already studied by early workers are doubtfully identified . Therefore an attempt has been made to restudy chromosome numbers of species in all genera , wherever available, in order to verify previous findings and to prevent the possibility of using counts from misidentified taxa . Voucher specimens representing all material used for the chro mosome counts reported by the present author are deposited at both the Liberty Hyde Bailey Hortorium, Cornell University and at the Fairchild Tropical Garden .

Materials and methods

All materials used by the present author for pollen-tube mitotic studies came from the

gardens listed earlier. Pieces of inflorescences having flowers at anthesis or buds about to open , are brought into an air-conditioned laboratory and allowed to remain several hours or overnight in

order to dry somewhat before pollen is collected or sown. Most of the anthers which open during this time should be relatively free from fungal contamination and will have pollen

ready for culture.

Pollen is sown on a nutrient medium (100 ppm H3BO3 in water; 0.02% colchicine in distilled water; 5-12% lactose and 5% gelatin) for the study of pollen-tube mitosis. After

the medium is heated slightly it is applied to cover glasses by means of a small cotton

swab. The pollen is dusted lightly over the surface of the dry medium and the cover

glass is then overturned onto a Van Tieghem cell which is lined with moist absorbent

paper. The Van Tieghem cells are maintained in an incubation chamber 26•Ž for about 8 hours, or until examination of sample slides indicates that mitosis is taking place. The

cover glasses are then processed by placing a drop of acetocarmine on the preparation, a

clean slide is lowered over the cover glass until it adheres. Slides are made permanent by means of a vapor-transfer technique described elsewhere (Read 1964).

Chromosome numbers The following list (Table 1) brings together the chromosome numbers 1 From work related to a project supported by National ScienceFoundation Grant No. G-18770and extension No. G.B.-1354. 386 R. W. Read Cytologia 30

Table 1. Chromosome numbers in the Coryphoideae

* Indicates counts made by the author and reported here for the first time . Numbers in parenthesis refer to voucher specimens.

(to be contiuned) 1965 Chromosome Numbers in the Coryphoideae 387

(contiuned)

(to be continued) 388 R. W. Read Cytologia 30

(contiuned)

for the subfamily published to date with the addition of more recent work by the author (Figs. 1-3). The nomenclature has been brought up to date except where it is impos sible to determine which species was actually used by former workers. Where the botani cal name used by the original worker differs from that which is presently accepted or is in doubt it is en closed within brackets -[ ]-. It is significant that with the exception of a single , Fig. 1. Camera-lucida drawings of palm chromosomes, enlarged , (reported approximately 1,945 times. a, humilis. b, Cryoso to have both n=8 phila aculeata. c, antillarum. d, filifera. and n=14 as e, chinensis. f, repens. g, Copernica yarey haploid numbers), var. yarey h, ritchiana. i, palmetto. j, thurstonii. all species repre sented in the 1965 Chromosome Numbers in the Coryphoideae 389

present study of the subfamily Coryphoideae have a haploid number of n=18. This number occurs again in of the Borassoideae, another group of induplicate costapalmate-leaved palms. The same number also occurs throughout the induplicate, pinnate-leaved genus which has often been closely associated with coryphoid genera; and again in the anomalous arecoid genus Roystonea, which has reduplicate pinnate . The size of the chromosomes varies considerably within a single genus and even to some extent in a single species or preparation, often depending on the pretreatments or amount of squash ing and pressure applied to the cover glasses. However, there is such a significant differ ence in the size of chromosomes be tween certain groups within the subfamily that it is thought to be worthy of note. Coryphoid genera with a great amount of floral specialization and modification of the inflorescence gen Fig. 2. Photomicrographs of palm chromosomes, corresponding erally have the to the camera-ludica drawings in Fig. 1, except j. largest chromo somes. Chamaerops humilis, hystrix, fortunei and hunzilis, all dioecious or polygamodioecious, have chrom osomes measuring 1.8 to 3ƒÊ in length at pollen-tube mitosis when colchi cine is used. brasiliensis and sp. (aculeata?) are not dioecious but have very condensed and large-bracted inflorescences and

Cryosophila species have flowers which are specialized to the degree that 390 R. W. Read Cytologia 30 apparently the pistils are not receptive until after the pollen has been shed. Both taxa have large chromosomes measuring 1-2 p. , and Zcnibia have bisexual flowers and are morphologically closely allied, with greatly reduced perianth parts and form a third group, with medium sized chromosomes. And Sabal, Livistona, , Nannorrhops, Pritchardia, Washingtonia, , Erythea, and Serenoa, with the least modified inflorescences, all have very small chromosomes 0.5-1.5,u long with very few up to 2 p in length.

Fig. 3. Photomicrograph and camera-lucida drawing of the chromosomes of Coccothrinax

argentata, the Florida silver-palm. 2,700•~. This photomicrograph was made with the

aid of a Reichert Phase-contrast microscope, recently acquired for cytological work.

Literature cited Bosh, Erich. 1947. Blutenmorphologische and zytologische Untersuchen an Palmen. Ber. Schweiz. Bot. Ges. 57: 86-89. Bowden, W. M. 1945. A list of chromosome numbers in higher plants. Amer. Jour. Bot. 32: 193. Darlington, C. D. and Janaki-Ammal, E. K. 1945. Chromosome Atlas of Cultivated Plants. Allen and Unwin, Ltd., London. Eichorn, Andre. 1953. Etude caryologique des Palmiers. I. Revue Cytol. et Biol. Vegetales 14: 13-29. - 1957. Nouvelle contribution a l'etude caryologique des Palmiers. Revue Cytol. et Biol. Vegetales 18: 139-151. Olah, Leslie V. 1954. The cytology of L. Part I. Ann. Bogor 1: 201-237. - 1962. Cytology of Corypha elata Roxburgh: The behavior of the nucleus during meiotic prophase. Bull. Torrey Club 89: 28-42. Read, Robert W. 1963. Palm Chromosomes, Principes 7: 85-88. 1965 Chromosome Numbers in the Coryphoideae 391

- 1964. Palm chromosome studies facilitated by pollen culture on a colchicine-lactose medium. Stain Tech. 39: 99-106. Sato, D. 1946. Karyotype alteration and phylogeny VI. Karyotype analysis in Palmae. Cytologia 14: 174-186. Sharma, A. K. and Sarkar, S. K. 1956. Cytology of different species of palms and its bearing on the solution of the problems of phylogeny and speciation. Genetica 28: 361-488. Sinoto, Y. 1929. Chromosome studies in dioecious plants with special reference to the allosomes. Cytologia 1: 109-191. Venkatasubban, K. E. 1945. Cytological studies in Palmae, Part I. Chromosome numbers in a few species of Palms of British and Ceylon. Proc. Indian Acad. Sci. 22: 193-207.