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HIPPOCRATEA VOLUBILIS (CELASTRACEAE) IN COTUI COPAL FROM THE DOMINICAN REPUBLIC PDF

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COPAL COTUl (CELASTRACEAE) HIPPOCRATEA VOLUBILIS IN FROM THE DOMINICAN REPUBLIC L Chambers Kenton George O. Poinar, Jr. 376 Published estimates of the age of Cotui copal have ranged from Miocene young to as as 1000 ybp or less. Our conclusion that the Hippocratea flowers are assignable to the extant species H. volubilis strongly supports the latter, younger age, which was obtained from carbon-14 dating in 2 laboratories (“Beta Analytic” in the United States and “Harz aus dem Tennengebirge” Germany). in Hippocratea pollen is well represented in the fossil record (Muller hut our knowledge 1981), to these are the first fossil flowers of the genus to be discovered. MATERIALS AND METHODS The specimens were collected from the upper 8 inches Zambrana of Abajo near Los Ranchos soil at in the vicinity of Cotui, a village located in a valley between the Cordillera Central and Cordillera Septentrional, Dominican The Republic. material with Many is clear a yellow tinge. samples are collected by children who follow theplows during the planting of maize (personal correspondence from the late Jake Brodzinsky, 20 September 1987). The age of from fossilized resin Cotui is unclear. Because of its light color and fairly soft texture, has it been referred to as copal, a term used for semi-fossilized resin that possesses specific physical properties re- lated to color, hardness, melting and point, solubility (Poinar 1992). Age estimates range from under 1000 nee spectroscopy (Lambert et al. 2012). In support of the older age was the discovery, in the copal, of several 1999). Comparing the maturity of fossilized resins with that of their enclosing bedrock can provide information on the maturity, and relative age, biostratinomy of amber and copal. Such a study was conducted on amber and Cotut copal from mines & different in the Dominican Republic (Poinar Mastalerz 2000). Maturity of the bed- rock was determined by vitrinite and reflection that of the fossilized resin by FTIR (Fourier Transform Infrared The Analysis). study found that Cotui showed copal a lower degree of maturity than that of the matrix rock, indicating had that been washedinto it the older bedrock and fairly recently probably representsdeltaicdepos- us. Further analysis of Cotui copal revealed that the plant source was Hymenaea (Mas- of the resin courbaril & talerz Poinar, unpublished observations), a tree species that on still exists Hispaniola. ^ sepals 5, nTn shallowly cupulate (Fig. 2), ola^Tm ^ blunt-tipped, spreading, abaxially petals papillate, 5, mm mm llaanncceeoollaattee-elhptic, 2 ellint’ 2.1 long, 1.2 wide, «- 7-9-nerved, slightly overlapping the base (Fig. 5), tip at cu^ed,abaxialsurfacetomentulose with short, curved trichomes,adaxm^ T r L and dis- otherwise glabrous d d mctlyvemeddownwardtothebase(Figs.l,4,5),marginscilia^^^^^^^^^ mtn 1.7 high, 1 2) disc 1.3 "7 (Fig^ 1. above the mid-line the^uScTdr^r ’ 3) mm 0.5 O^mm recurved filaments (Figs. biiH d 1, 3, 4), mlrngplZ™" discussion For the purpose of comparison, we assumed that and Hippocratea Central which volubilis, widespread in is South America and the Caribbean re:gion, is likely to be the extant species most closely related to the fossil- 377 by Matthews elongated as illustrated style, The and Endress (2005, 49, 50). adaxial figs. pubescence of the petals consists of a con- spicuous band or arc of villous trichomes, pubes- which essentially similar to the is herbarium specimens of H. cence pattern in Such trichomes were, in fact, cited volubilis. by Smith 357) as a diagnostic (op. cit., p. genus. The petals of the flowers of the trait from photographs to be slightly con- appear shows microscopic study but careful nate, The disc them be basally imbricate. floral to upper and lower segments, divided into is from Smith’s illustration of H. thus differing However, similar 357). volubilis (op. cit., p. present in herbari- 2-parted discs are often um including specimens of that species, & many from the Caribbean region. In A. P. Rico (US2996523), Puerto 30929, Liogier and lower upper disc seg- example, the for with both ments are sharply differentiated, our In as in fossils. being papillate, parts Honduras Morton 7839, both C.V. & Howard and 9817, E.S. R.S. (US202361) on (US2228804), the Republic Dominican upper half of the disc is hand, the other The upper section of the disc is lower half. narrow papillate reduced a sometimes to D.K. Christo- anthers band below the (e.g., A NY pecu- Puerto Rico). pher 69, s.n., et al. mod- pubescence in both the petal of liarity zone of papil- em that a and flowers is fossil may may not be present or trichomes late band adaxial of villous tri- the proximal to in Fig. al- This illustrated 1, chomes. is though In the '’^S-'’0^)Se'UsH.v.««Us.HeUn.«ea.HU conservative tj Everglades of as the north as far extends ^ontothe and peduncle in the Cotui fos- androecium, & penar disc, Rorida pubescence ol (Long The Lakela 1971). specimens of H. herbarium available observed in ve that variauon ’ sils, as described within the above, within the falls are parts in the fossils of floral sizes the and width, volubilis. With length the exception of petal shorter (2.1 The petals are slightly 360). p. (op. cit., descnptio 1 ^nges species given Smith’s for H. in volubilis 379 850- M.A. AND R.D.E. MacPhee. 996. Age and paleogeographic origin of Dominican amber. Science 273:1 1 2005. Comparative floral structure and systematics in Celastrales (Celastraceae, Endress. 149:129-194. Lepidobotryaceae). Bot. Linn. Soc. Parnassiaceae, J. Muuer, 981 Fossil pollen records of extant angiosperms. Bot. Rev. 47:1-1 42. J. 1 . CA. Stanford, amber. Stanford University Press, PoiNAR, G.O., Jr. 1 992. Life in of amber. Acta determining the biostratinomy Taphonomy and M. Mastalerz. 2000. of fossilized resins: PoiNAR, G.O., Jr. GeoLHispanica 35:171-182. £ from Dominican copal, with the redescnptKjn of A new bug genus Empicoris Wolffe YA. 987. species of the Popov, 1 nudusMcAtee & Malloch. Stuttgarter Beitr. Naturk. Ser. B 134:1-9. 7:145-147. region. Molec. Phylogen. Evol. Baw B«j* Sous™, ano Y.-L Ou. 2000. De V. M.W. Ch«e, Hoor, CM. Mmton, D.E. Sans, C. M.F. F.r, A. S. S.B. gene sequences. Syst otpB and upon combined analysis of plastid rtnrt Phylogenetics of flowering plants based a 49:306-362. Biol. C 18:1-100. Naturk. Ser. ScHLEE, D. 1984. Bernstein-Neuigkeiten. Stuttgarter Beitr. C 28:1-10 Naturk. Ser. SoftEE, D. 1990. Das Bernstein-Kabinett. Stuttgarter Beitr. ’ The Simmons, M.P. 2004. Celastraceae. K.Kubitzki,ed. families ai In: 29-64. er-Verlag, Berlin. Vol. VI. Pp. A Simmons, M.P., C.C. Clevinger, V. Savoleinen, R.H. 88:313-325. ferred from phytochrome B and morphology. Amer. J. Bot. 19:353-366. Phylogen. Evol. Molec. nrDNA, phytochrome and morphology. atpB, rbcL, B, 3:341 -555. Hippocrateaceae.Brittonia Smith, A.C. 1940. The American species of [updat 201 2 sir July Version STtVENs, 2001 onwards. Angiosperm Phytogeny Website, 1 2, P.F. 2013. January org/MOBOT/research/APweb/>, accessed 21

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