Palms · collection at Nong Nooch Tropical Garden, Thailand, the exciting destination for this...

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Palms Journal of the International Palm Society Vol. 56(1) Mar. 2012

Transcript of Palms · collection at Nong Nooch Tropical Garden, Thailand, the exciting destination for this...

Page 1: Palms · collection at Nong Nooch Tropical Garden, Thailand, the exciting destination for this year’s IPS Biennial. See article by L. Lai, p. 41. Photo by Paul Craft. PALMS Vol.

PalmsJournal of the International Palm Society Vol. 56(1) Mar. 2012

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Features

Palm News 4

Palm Literature 49

CONTENTS

FRONT COVER

Trachycarpus martianus is known in the wild from Sikkim.See article by B.S. Kholia, p. 5. Photo by B.S. Kholia.

BACK COVER

Chestnut-colored fruits of Calamus castaneus. See article by N.Ruppert et al., p. 36.

The entire-leaf form of Hydriastelebeguinii in the Hortus Botanicuscollection at Nong NoochTropical Garden, Thailand, theexciting destination for this year’sIPS Biennial. See article by L. Lai,p. 41. Photo by Paul Craft.

PALMS Vol. 56(1) 2012

5 Rediscovery of Trachycarpus martianusin the Sikkim HimalayaB.S. KHOLIA

11 In Search of Juania australis with a FewObservations of Jubaea chilensis along the Way D.R. HODEL

21 A Detection of ThiabendazolFungicide in Coconut Palms Using a Bioassay M.L. ELLIOTT & T.K. BROSCHAT

28 Dypsis robusta Found in the WildJ. DRANSFIELD, J. MARCUS & D. TURK

31 The Critically Endangered Ceroxylonsasaimae Rediscovered in the WildR. BERNAL & H.F. MANRIQUE

36 New Shoots from Inflorescences inCalamus castaneus in Peninsular Malaysia N. RUPPERT, A. MANSOR & S.A.M. SAH

41 Nong Nooch and the IPS Biennial 2012 L. LAI

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NEWSPALM

Late 2011 saw a flurry of taxonomic papers in which a new genus,many new species and some new names for existing species werepublished. Perhaps the biggest surprise is the new genus Lanonia,which was published by Christine Bacon and Andrew Henderson(Systematic Botany 36: 883–895. 2011). It comes as a surprise becausemany of its species were described in 2008 in PALMS (52: 141–154) asdioecious species of Licuala from Vietnam. Bacon’s molecular studiesrevealed that these Vietnamese species comprised a lineage distinct fromthat of Licuala (just as Saribus was found to be distinct from Livistona,as she reported in PALMS last year). Lanonia is very poorly representedin cultivation, but we hope that these attractive fan palms will soonfind their way into collections around the world.

Drymophloeus has been down-sized as a result of a new molecular study of the subtribePtychospermatinae. Zona et al. transferred three species of Drymophloeus palms to the genusVeitchia and one to Ponapea (American Journal of Botany 98: 1716–1726. 2011). The new namesfor the species now banished from Drymophloeus are Veitchia subdisticha, V. pachyclada,V. lepidota and Ponapea hentyi. This publication also examined the geographic distributionsof the species of Ptychospermatinae and found evidence of repeated radiations from NewGuinea into the western Pacific and Australia. The study also confirmed that a palm from BiakIsland represents a second, as yet unnamed species of Adonidia.

Three palm articles appeared recently in the new journal Phytotaxa. The Sabal from Brazoria,Texas, long suspected of being a hybrid, was examined by Doug Goldman et al. in an open-access article (www.mapress.com/phytotaxa/content/2011/f/pt00027p025.pdf). Using moleculartools, the authors found support for the hypothesis that the palm is of hybrid origin but – muchto everyone’s surprise – not involving S. mexicana. They formally named the palm Sabal ×brazoriensis. Charlie Heatubun described seven new species of Areca, five of them endemic toBorneo, one to Sumatra and one to Cambodia. Several of these new species would makeattractive horticultural subjects. See a preview of the article at www.mapress.com/phytotaxa/content/2011/f/p00028p026f.pdf. Most recently, M.J. Sanín and G. Galeano produced a much-needed revision of the genus Ceroxylon, the famous wax palms of the Andes. Download thearticle at www.mapress.com/phytotaxa/content/2011/f/pt00034p064.pdf.

Marc Jeanson and colleagues described a new species of Caryota from Sulawesi (SystematicBotany 36: 600–604. 2011). The species, christened Caryota angustifolia, is distinguished byhaving very narrow, strap-like leaflets at the bases of the secondary rachises. The new speciesis a large, solitary-stemmed species similar to C. rumphiana and is currently in cultivation inBogor Botanical Garden, thanks to an earlier introduction of seeds by John Dransfield. Thepublication also includes a key to the five species of Caryota that occur east of Wallace’s Line.

Finally, we note with pleasure that IPS member José Antonio del Cañizo has brought out thethird edition of Palmeras, his highly accessible Spanish-language guide to cultivated palms.The book was published by Ediciones Mundi-Prensa and is available through www.amazon.es.Instead of the almost 700 pages of the second edition, this new edition is a massive 1153 pageslong and is correspondingly weighty. The substantial increase in size reflects the wealth of newpalm information that the author has included. The book is beautifully produced and in fullcolor throughout.

A. Henderson

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Rediscovery ofTrachycarpusmartianus inthe SikkimHimalaya

B.S. KHOLIA

Botanical Survey of India,Sikkim HimalayanRegional CenterP.O. RajbhawanGangtok 737 103,Sikkim, India

The largely Himalayan genus of solitary fan palms, Trachycarpus, has always

attracted plant lovers and nurserymen throughout the world, due mostly to its

cold hardiness. During the time of the British Raj the genus was not fully

understood in India, and only one (Brandis 1874, 1906), two (Griffith 1850;

Gamble 1881; Beccari & Hooker 1894) or three (Blatter 1926) species were

recognized from the Indian region, first in the genus Chamaerops and later

separated off into the genus Trachycarpus. In his thorough study of Asiatic palms,

Beccari (1931) provided taxonomy and distribution details of the genus as it was

then known, and Martin Gibbons and Tobias Spanner (1998a) published an up-

to-date version in 1998.

PALMS 56(1): 5–10

1. Trachycarpus martianusgrowing in front of workers’quarter at Temi Tea Garden,South Sikkim.

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At present, the number of species in the IndianHimalaya is five, including the extensivelycultivated and now naturalized Chusan fanpalm, T. fortunei. All of these species have amore or less restricted distribution; for exampleT. takil and T. latisectus are endemic to smallareas of the Kumaon and Darjeeling Himalayasrespectively. Trachycarpus martianus is reportedfrom small areas of Nepal and the Khasia Hills(Gibbons 2003). The palm growing in tinyareas in Manipur and on the Naga Hills,introduced into cultivation variously asTrachycarpus sp. ‘Manipur’ or ‘Naga Hills’(Kembrey 2004) and more recently describedas T. ukhrulensis Lorek and Pradhan (Lorek2004; Lorek & Pradhan 2006), has now beenidentified as the Thai mountain palm, T.oreophilus (Gibbons & Spanner 2009).

The Sikkim and Darjeeling Himalayas are themost extensively explored areas in the IndianHimalayan region. The Trachycarpus palms ofthis area at least have been well documented(Gamble 1881, Cowan & Cowan 1929, Beccari& Hooker 1894, Beccari 1931). Recently T.latisectus, a very beautiful species with markedtaxonomic characteristics, was discovered here(Gibbons & Spanner 1998b; Spanner et al.1997), and the old records of T. martianus fromBritish Sikkim (i.e., present Sikkim State ofIndia and the Darjeeling district of WestBengal) relate to this same species. On theother hand, Lorek (2007) reduced all thespecies with oval seeds growing in this Indianregion to subspecies of T. martianus, and henamed them as Khasyi form (subsp. khasianus),

Nepal form (subsp. martianus) and Rissoomform (subsp. latisectus) according to the placeof occurrence. He stated that “The locality inSikkim [Rungbong] which was mentioned byBeccari (based on Indian classical taxonomicliterature) has not been rediscovered up tonow.” He added, “Currently, it is not clearwhether the ‘Rissoom form’ (= ssp. latisectus)has its origin at Rungbong or not. Mayberelocating the Rungbong locality could throwmore light on this question.” Perhaps Rissomand Rungbong are two different places. Theneed to establish this becomes essential tosorting out what is going on with thetaxonomy and distribution of the ovoid-fruitedspecies of Trachycarpus.

During the plant survey of the South Districtof Sikkim in 2008, the author came across fivecultivated plants of a Trachycarpus palm infront of workers’ quarters at Temi tea gardens(Fig. 1). They have denticulate petioles (Fig. 2)and bear white woolly hairs in the youngerstage. They were without fruits. At first sightthey looked quite different from either of theother palms growing in this part of theHimalaya, i.e., the commonly cultivated T.fortunei and the recently discovered T. latisectus.On the basis of the denticulate petiole and thegeneral appearance, I presumed them to be T.martianus, but they could also possibly bemembers of the other group of Trachycarpuswith reniform seeds, i.e., T. oreophilus orsomething closely related.

Intriguingly a local guide explained wherethese palms had come from and described a

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2. Trachycarpus martianus showing denticulate petioles.

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local population. I was determined to visit theplace without delay. The next morning he andI left the Tandong Biodiversity Park at firstlight. We crossed the road that runs betweenDamthang and the Temi Tea Garden and thatleads ultimately up to Gangtok, the capital cityof Sikkim State. We climbed up about one anda half kilometers inside the forest and foundourselves on a narrow, gravelly and calm roadbetween dense forest of large Cupressus torulosaother native broad leaved trees and densepatches of thicket fern, Gleichenia gigantea. Atone point we left the road and followed anarrow path up into the forest. After a walk of6 or 7 km, at 2000 m, we reached a clearingand enjoyed the beauty of a bright and sunnyday and then climbed up the final 50 m tothe summit. A beautiful landscape was waitingfor us: the rays of the morning sun lit up theTeesta river and its wide valley a few kilometersto the east. We could see Rungpo, the gatewayof Sikkim, at the confluence of the Teesta andReshi Rivers, and in the southeast, the ridgesof Kalimpong and other areas of Darjeelingformed the horizon. Just below us we could seeour destination, the village of Rungbing, thevery same Rungbong where C.B. Clarkecollected Trachycarpus specimens more than ahundred years ago (Beccari 1931).

Presently we were on one of the historicalroutes between the Teesta valley and the GreatRangit valley, which were well connected withDarjeeling during the British time, before thedevelopment of motor roads in modernSikkim. These days this route is almostabandoned and rarely used even by the

villagers. After a short walk we left the road andstarted descending on a slanting connectingpath, which was partly blocked with densebushes and occasional big trees. After an easy2 km walk down we entered the village. Thelocals there were very surprised to see us atthis early hour, and assuming me to be a forestofficer, half expected a raid. Fortunately wewere able to reassure them of our goodintentions. My colleague Krishna asked thepeople about Pankha or Purbang (vernacularnames for the fan palm in the local Nepalesedialect), but we received largely negativeanswers.

We next made our way to where Krishnaremembered having seen a large fan palmsome ten or fifteen years ago. This magnificentpalm, still there, is about 10 or 11 m tall,growing at the top of a steep, rocky bank andwas heavy with seeds. It was overgrown withbushes and subtropical and temperate treesincluding Castanopsis indica, Quercus lamellosa,Ficus cordifolia, F. neriifolia, F. hirta, Saurauianapaulensis, Erythrina arborescens, Engelhardtiaspicata, Exbucklandia populnea, Macarangadenticulata, Echinocarpus dasycarpus and Alnusnepalensis. Furthermore, the base of the trunkwas completely hidden by steep rocks. Inbetween bushes and under the large trees, 4 or5 more, smaller palms were growing nearby. Allhad dry inflorescences.

Seed collection was very difficult due to theheight of the big palm and the rocky terrain;a small slip could result in a fall of 60 meters.We considered carefully the easiest and safest

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3. Seeds badly infected by insect larva.

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way of collecting fruits. Krishna produced asickle from his bag, and fixed it to a longbamboo cane using rope he made from grass.In the meantime the lady from a nearby housegave us valuable information about a wildpopulation. She guided us along a suitablepath, and after some effort we were at the baseof a fruiting palm. Using the prepared sickle,we cut a small fruiting branch leaving the restthere because they were still not mature. Wealso cut a leaf from nearby smaller plant, andit, together with the round oval seeds, whichwere badly infected by insects (Fig. 3), allowedus to identify it as T. martianus, a palm that hasnot been seen in the wild in Sikkim for over100 years!

We left the area and climbed upwards along asmall footpath along the ridge in search ofmore plants. After ascending half a kilometeror so, we left the main footpath and starteddescending into the forest. After a descent ofa kilometer in deep, southeast-facing forest,we began to follow a water supply pipebetween shrubs and trees, continuing downbetween thorny bushes, prickly climbers andlarge trees, clearing a passage with the help ofthe sickle. Monkeys began jumping from onetree to another upon seeing these unexpectedvisitors. In a deep gully, between big trees, wefound two fully grown palms. With great effortwe reached them to try to take pictures, but nosuitable angle was found due to the densecanopy. Alas there was no sign of fruits,seedlings or juveniles in the vicinity.

We decided to cross the small stream to checkout the warmer and more exposed side of thegully. When we were about to cross it at27°11’57.9”N; 88°25’28.0”E at 1680 m, wenoticed three big trees of about 7 or 8 m tallgrowing some 30 m above us (Fig. 4), but theywere also without fruits. Now we wereconfident that we were in the right place wherethe local guide had originally found the palms.We again found a small descending footpathperhaps used to visit the water tank, and wefollowed it for about one kilometer or so.Along the path and nearby we found up to ahundred different sized palms (Fig. 5), takingmany pictures at 27°11’57.7” N; 88°25’31.4”E.Many palms had died due to age, but somestumps were still remaining (Fig. 6). Thereseems to be no human interference with thepalms, but even so we saw no seeds orseedlings. Monkeys are common in the forest,so we concluded that the fruits are taken bymonkeys before they are ripe.

Around 3 p.m., we left the area seeing manymore individuals of Trachycarpus martianusgrowing below us on the southeast-facingslopes. We left with great satisfaction,returning to base via the old classical routerunning parallel to the top of Rangbing village.Since our visit, more cultivated palms havebeen reported from Sadam and other nearbyvillages in South Sikkim. These have all beencollected from the nearby forests.

Gamble and Clarke found Trachycarpus palmsin this area (Beccari 1931), however Brandis(1874) clearly stated that “No Chamaerops[Trachycarpus] has yet been reported fromSikkim,” and in his later publication (Brandis1906) does not record any Trachycarpus fromSikkim. Recently, during my visit to the CentralNational Herbarium in Calcutta (CAL) inJune–July 2010, I was unable to find theTrachycarpus collections of Gamble and Clarkefrom British Sikkim. The Indian Liaison Officerat RBG Kew was unable to trace the missingcollections of Clarke and Gamble. Could it bethat all the sheets collected by these renownedbotanists from British Sikkim were sent toBeccari and are still lying in the Beccari’s palmherbarium in Florence, Italy?

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4. Trachycarpus martianus in its natural habitat at27°11’59.9”N; 88°25’28.0”E.

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After analyzing Gamble’s (1881) lines – “InSikkim, I have only once found it, on the hillseast of Teesta river” – I am convinced thatGamble’s locality (“Rissom mountain nearDumsong beyond Darjeeling”) is definitely theKalimpong area where T. latisectus wasdescribed. On the other hand a young plantcollected by Clarke from “Rungbong at about1,200 m” is definitely from the lowerelevations of present day Rungbing village nearDamthang in the south district of Sikkim,where T. martianus still grows. Thus Rissomand Rungbong are two different places; thefirst is on the east side of the Teesta River inKalimpong in Darjeeling District where T.latisectus occurs; the second is on the westernflank of the river in present day South Districtof Sikkim where T. martianus grows. Thesecond locality has remained hidden orforgotten for more than a century. In anyevent, the rediscovery of Trachycarpusmartianus in its historical location after a

period of more than 100 years is an excitingevent, and one that will be welcomed by allenthusiasts of the genus.

Acknowledgments

Grateful thanks are due to Martin Gibbons ofEngland and Tobias Spanner of Germany forproviding literature, constant guidance andsupport and for improving the manuscript. Iam most thankful to Dr. M. Sanjappa, Directorand Dr. D.K. Singh Add. Director, BotanicalSurvey of India for providing the necessaryfacilities. Mr. Krishna caretaker of TandongBiodiversity Park, Sikkim is also acknowledgedfor his assistance in the field.

LITERATURE CITED

BECCARI, O. 1931. Asiatic Palms – Corypheae.Ann. Roy. Bot. Gard. Calcutta 13: 1–356.

BECCARI, O. AND J.D. HOOKER. 1894. OrderCLXIII. Palmae. In J.D. HOOKER, Flora ofBritish India, vol. VI. L. Reeve & Co. London.

BLATTER, E. 1926. The Palms of British Indiaand Ceylon, Oxford University Press,London.

BRANDIS, D. 1874. The forest flora of north-westand central India. W.H. Allen and Co. Ltd.,London.

BRANDIS, D. 1906. Indian Trees, ArchibaldConstable and Co. Ltd, London,

COWAN, A.M. AND J.M. COWAN. 1929. The treesof Northern Bengal. Calcutta.

GAMBLE, J.S. 1881. A Manual of Indian Timbers:An Account of the Structure, Growth,Distribution, and Qualities of Indian Wood,Office of the Superintendent of GovernmentPrinting, Calcutta,

GIBBONS, M. 2003. A Pocket Guide to Palms,Chartwell Book Inc, New Jersey.

GIBBONS, M. AND T. SPANNER. 1998a. Palms forSouthern California. Part Thirty:Trachycarpus. The Palm Journal 138: 8–17.

GIBBONS, M. AND T. SPANNER. 1998b. Trachycarpuslatisectus: The Windamere palm. Principes42: 24–29.

GIBBONS, M. AND T. SPANNER. 2009. Trachycarpustakil – lost and found, for now. Palms 53:96–101.

GRIFFITH, W. 1850. Palms of British East India,Charles A. Serrao, Calcutta.

KEMBREY, N. 2004. Trachycarpus sp. Manipur orNaga Hills. Chamaerops 49, publishedonline, visited July 2010.

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5. Trachycarpus martianus at 27°11’57.7”N;88°25’31.4”E.

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LOREK, M. 2004. Trachycarpus ukhrulensis, thesurvivor palm. The Palmateer 24(2): 13, 22,23.

LOREK, M. 2007. A taxonomic review ofTrachycarpus martianus (Wall.) H. Wendl.Curr. Sci. 92: 1678–1679.

LOREK, M. AND K.C. PRADHAN. 2006. A newspecies of Trachycarpus (Arecaceae) with

remarks on its unusual habitat. Bot. Jahrb.Syst. 126: 419–426.

SPANNER T., H.J. NOLTIE AND M. GIBBONS. 1997.Trachycarpus latisectus. Edinburgh J. Bot. 54:257–259.

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6. Stump of a dead palm.

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PALMS Hodel: In Search of Juania Vol. 56(1) 2012

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In Search ofJuania australiswith a FewObservations ofJubaea chilensisalong the Way

DONALD R. HODEL

University of CaliforniaCooperative Extension4800 E. Cesar Chavez Ave.Los Angeles, CA 90022 [email protected]

One of the most mysterious, enigmatic and fascinating palms must be Juania

australis. Its isolated habitat alone, on Robinson Crusoe Island (Juan Fernández)

off the coast of Chile, is more than sufficient to conjure up images of a remote,

far away, mysterious land, while the name of the island itself and its past role in

literary lore add immeasurably to this mystique. I visited Chile in November, 2010

with Marianne Hodel and Steve Daugherty, my former college roommate, to

explore for the rare J. australis in its isolated, island habitat and to observe the

famous and well known Jubaea chilensis in the wild.

PALMS 56(1): 11–20

1. At theHacienda delas Palmas deCocalán southof Santiago,Chile, theextensivepopulation ofJubaea chilensisinhabits theflat valleybottom and issemi-managedfor thebountiful cropof edible seedscalled coquitos.

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After the all-night flight from Los Angeles toSantiago, Chile, we rented an auto and droveto our hotel where we checked in and relaxedfor awhile before meeting Steve’s friend, EvaOchoa, for lunch. Over a traditional Chileanseafood extravaganza, we planned ouractivities for the next two weeks. Our plan wasto spend about 10 days in and aroundSantiago, making day trips to several locales tosee the famous Chilean wine palm, Jubaeachilensis, in the wild and cultivated around thecity. We would then make a four-day trip toRobinson Crusoe Island to see Juania australisafter which Marianne and I would travel toEaster Island for a few days before returning toLos Angeles.

Jubaea chilensis

Like California, central Chile, includingSantiago, has a Mediterranean climatecharacterized by cool, moist winters and warm,dry summers. November is late spring inSantiago, and typically the weather is mostlypleasant with warm, sunny days and coolnights although we experienced severalunusually cool days with clouds and rain. Wewere amazed at the similarity of the terrainand vegetation around Santiago with that ofsouthern California. The rocky hillsides werevariously covered with xerophytic shrubs,small trees, cacti and, at this time of year,

seasonal wildflowers, just like our chaparral inCalifornia. It was all the more amazing,though, to see some of these hills and valleyscovered densely with vast stands of Jubaeachilensis.

We visited three areas with Jubaea chilensis,including Quebrada Siete Hermanas near theport and tourist destinations of Valparaiso andVina del Mar west of Santiago, the Haciendade las Palmas de Cocalán south of Santiago(Fig. 1), and Parque Nacional La Campananorth of Santiago. The last two sites have thelargest populations of J. chilensis, 35,000 and62,500 adults each, respectively. While thispalm is most abundant in valley bottoms,where soil is deep and moisture is moreplentiful and available, it frequently inhabitsor even thrives on dry, well drained, rockyhilltops and ridges (Fig. 2). I was surprised andhad a difficult time understanding how thispalm could grow in such a harsh environment.At the Hacienda de las Palmas de Cocalán,where the palms are semi-managed for thebountiful fruits containing the edible seeds,called coquitos (small coconuts), we observedseveral, still-living and healthy-appearingspecimens with burned-out trunks, evidence ofthe occasional fires that ravage the palms andsurrounding area. Some were burned soextensively that only a perimeter layer of

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2. While Jubaea chilensis is most abundant in valley bottoms, where soil is deep and moisture is more plentifuland available, it frequently inhabits or even thrives on dry, well drained, rocky hilltops and ridges, as here atParque Nacional La Campana north of Santiago, Chile.

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sound tissue about 10 cm (4 inches) thickremained and, in some cases, only partiallyenclose the trunk, easily enabling a person tostep inside. These burned-out trunks stillsupported a healthy, full canopy of leaves.

Juania australis and Robinson Crusoe Island

After spending a few days in Santiago visitingseveral of the well known tourist sites, manyof them with exemplary specimens of Jubaeachilensis, we were ready and excited to visitRobinson Crusoe Island (otherwise known asJuan Fernández) in our quest to see Juaniaaustralis. Unfortunately, our plans unraveledslightly when the day before our departure thetravel agent who had made our arrangementsfor Robinson Crusoe Island (air, lodging andlocal guide), e-mailed me to say that theregularly scheduled airline on which we werebooked had decided not to fly to RobinsonCrusoe Island that week! We were stunnedbecause we were locked-in to our departure toLos Angeles and Marianne and I still had our

short trip to Easter Island, precluding us fromadjusting our schedule. This discouraging newsreminded me painfully what others had toldme about travel to Robinson Crusoe Island: itis not an easy place to get to, the airline thatserves it is unreliable and flights are frequentlycancelled or rescheduled with little or nonotice.

Fortunately, our savvy and resourceful travelagent quickly, at no additional coast, chartereda small, two-engine aircraft to take us toRobinson Crusoe Island. On the morning ofNovember 9, when Steve, Eva, Marianne andI arrived at one of the charter hangers at theairport, an agent met and told us that oneadditional passenger would be accompanyingus to Robinson Crusoe Island. As it turned out,the additional passenger was none other thanMichelangelo Trezza, the owner of the hotelwhere we would be staying for three nightson the island. At the time of our visit there wasonly one hotel operating on Robinson Crusoe

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3. Cultivated specimens of Juaniaaustralis in San Juan Bautista onRobinson Crusoe Island typically arebetter looking than their wildcounterparts and have a fairly robust,smooth, lime-green, conspicuouslyand densely ringed trunk supporting acompact, nearly spherical canopy of25 to 35, stiffly ascending tospreading to drooping, dark green,pinnate leaves.

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Island because the tsunami spawned by thepowerful earthquake that struck Chile inFebruary 2010 devastated San Juan Bautista,the only village on the island. The tsunamikilled over 20 people and destroyed nearly halfthe small village, including all the hotelsexcept one. We were the first tourists to visitRobinson Crusoe Island since the tsunami.

The flight from Santiago to Robinson Crusoewas uneventful but as we neared the islandthe skies suddenly became cloudy and wewould not see the sun again until we returnedto Santiago in three days. Once our plane hadlanded and we had collected our gear, welearned that the pilot would be staying withus for our three nights rather than makinganother trip back to Santiago and then backto the island again. From the airport we tooka short truck ride down to a small bay thatwas home to several hundred noisy sea lionsfrolicking in the rough surf or lyingcontentedly on the mossy rocks. From thesmall bay we took a rough, wet, two-hour, 18-km (11-mile) ride in a small, open boat to SanJuan Bautista. If not for the rain coverings wewere given upon boarding the salt spray wouldhave thoroughly soaked us and our gear.

Prior to the tsunami about 500 people lived onRobinson Crusoe Island, nearly all in San Juan

Bautista on Cumberland Bay, and they wereengaged in fishing, primarily lobster, and abudding eco-tourism industry. Now about 350people live on the island and, while fishing isstill the primary source of income, there ishope that tourism can get back on its feet withreconstruction of hotels and other necessaryinfrastructure.

Formerly known as Juan Fernández Island orMás a Tierra, the Chilean government renamedthe island Robinson Crusoe Island in 1966 toreflect is purported literary past. Many peopletheorize that Daniel Defoe based his 1719novel, Robinson Crusoe, on the experiences ofa Scottish castaway, Alexander Selkirk, whovoluntarily asked to be left on the island in1704 because of doubts of the seaworthinessof the vessel on which he sailed. After fouryears on the island he was rescued in 1709and returned to Europe to tell his tale.However, several other real-life incidences mayvery well have served as Defoe’s inspiration.

About 675 km (415 miles) west of Chile,Robinson Crusoe Island is the largest of threethat make up the Juan Fernández Islandsarchipelago (Alexander Selkirk and Santa Claraare the other two islands in the archipelago).The island covers 93 km2 (36 miles2) and risesvery precipitously to 916 m (3005 feet) at the

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4. The congested leaf bases of Juania australis, deeply split opposite the petiole, are loosely overlapping, donot form a crownshaft, and, like the petioles, are densely covered with grayish to tan or even rusty brown,felt-like indumentum.

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top of El Yunque, the highest point. Theremains of an ancient volcano, RobinsonCrusoe Island is extremely mountainous andspectacularly eroded with steep valleys andnarrow, razor-like ridges and is reminiscent ofsome of the picturesque, older islands inHawaii or the South Pacific.

Like the Chilean mainland, Robinson CrusoeIsland has a Mediterranean climate but thecold Humboldt Current sweeping up fromAntarctica provides significant modifications.Thus, it has a more moderate climate, not aswarm or cold as Valparaiso at roughly similarlatitude on the Chilean coast, and with littleseasonal variation. However, because of thecold Humboldt Current, the weather isfrequently cool, cloudy, misty or drizzly, andwindy, and reminded me much of SanFrancisco on the central California coast.Daytime high and nighttime low temperaturesin January, the warmest month, average 22ºC(71ºF) and 16ºC (61ºF), respectively, while inAugust, the coolest month, they are 15ºC(60ºF) and 10ºC (50ºF). A low -2ºC (29ºF) hasbeen recorded in October. Rain averages 170mm (7 inches) in July, the wettest month, and26 mm (1 inch) in February, the driest month.

Humidity is always high and the rainiestmonths of June and July average about 15 daysper month of rain or drizzle while the driestmonths of December and January averageabout six days per month of rain or drizzle.These records are for San Juan Bautista at sealevel but certainly the higher parts of theisland, which are frequently hidden in clouds,experience cooler temperatures and higherrainfall and humidity.

Pasture land and disturbed forest with manyinvasive, weedy exotic species, like Eucalyptus,Cupressus and Pinus, occur from sea level toabout 200 meters elevation. Lower montaneforest ranges from 200 to 400 meters elevation.Upper montane forest occurs above 400 meterselevation. Juania australis is restricted tomontane forest and is most common in uppermontane forest. Upper montane forests onsome of the higher mountains, which arenearly always enveloped in clouds, support anintriguing cloud forest. Robinson Crusoe Islandis rich in endemics, with 101 of the 146 nativeplant species (nearly 70%) found nowhere else.Most of the plants have relatives in SouthAmerica, New Zealand and Australia. Severalmembers of the sunflower family, whoserelatives are typically herbs in other locations,are trees on Robinson Crusoe Island. The entireisland was designated a World BiosphereReserve in 1977 because of its unique andendangered flora and fauna.

As our small boat pulled up to the wharf at SanJuan Bautista, the destruction from thetsunami was stunning. The lower half of thevillage adjacent to Cumberland Bay was gone,as if a giant hand had simply wiped it from theearth’s surface. Only a few very large and oldtrees and house foundations remained. As wewaited for the ride to our hotel, I looked up tothe steep and narrow ridgelines towering overthe village and here and there I was just ableto pick out a few specimens of Juania australisclinging precariously to nearly vertical cliffsnot too far above San Juan Bautista. Seeing thepalms above and so near to San Juan Bautistawas encouraging but, being an eternalpessimist and somewhat experienced insearching for palms in difficult-to-access places,I checked my optimism because I knew thatwhat seemed like a rather easy walk up to thepalms could easily be just the opposite.

After checking into the hotel and eating lunch,we discussed our plans for the next two dayswith Michelangelo, who would also serve asour guide in our search for Juania australis. The

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5. Juania australis clings tenaciously to a cliff nearMirador de Selkirk above San Juan Bautista onRobinson Crusoe Island.

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next day we would take a walk up a trailbehind San Juan Bautista to Mirador de Selkirk,a viewpoint at the top of the ridge overlookingthe village and bay near to the J. australis Ihad seen upon our arrival. Our second day’sactivities would take us on a much longer walkover several ridges to the southeast of San JuanBautista. We spent the remainder of theafternoon exploring the steep hillsides aroundthe hotel, looking at ferns and admiring theviews of the ocean crashing into the base ofthe precipitous slopes.

Michelangelo was full of confidence the nextmorning as he, Eva, Steve, Marianne and I setout for Mirador de Selkirk. He was sure wewould find our quarry, Juania australis. As wewalked toward the village we passed throughgroves of the Australian native Eucalyptusglobulus, the blue gum, which reminded memuch of the central and northern Californiacoasts. Much to our surprise as we passedthrough San Juan Bautista, we found severalcultivated specimens of J. australis adorning afew dooryards. Known locally as chonta, it isan unusual palm, not likely to be confusedwith any other. The fairly robust, smooth,lime-green, conspicuously and densely ringedtrunk supports a compact, nearly spherical

canopy of 25–35, stiffly ascending to spreadingto drooping, dark green, pinnate leaves withrelatively short petioles (Fig. 3). Leaf scars onthe lower part of the trunk, which wereproduced when the palm was young andgrowing more vigorously and or perhapsshaded, are frequently uneven andasymmetrical, with one side higher than theother, reminding me of those of Howeaforsteriana. In contrast, leaf scars near the topof the trunk just below the leaves are severelyclose set and congested, reminding me of thoseof Rhopalostylis baueri or R. sapida. The stiffpinnae are glossy dark green above and grayishbelow. The congested leaf bases, deeply splitopposite the petiole, are loosely overlapping,do not form a crownshaft, and, like thepetioles, are densely covered with grayish totan or even rusty brown, felt-like indumentum(Fig. 4). Simply looking at the leaf bases easilyreminds one of its relatives Ceroxylon,Oraniopsis appendiculata and even Ravenea.Unfortunately, none of the plants had flowersor fruits although they looked sufficiently largeand old to be mature. Michelangelo wasdelighted, jauntily declaring that we hadattained our objective for the trip. His spiritswere not in the least bit dampened when Ireminded him that I had come to see these

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6. Above Mirador de Selkirk on Robinson Crusoe Island Juania australis is exposed and, with its wind-battered,torn and frayed leaves, is not nearly as handsome as its cultivated counterparts in San Juan Bautista.

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palms in the wild, and he assured me that wewould soon see them at Mirador de Selkirk.

The trail to Mirador de Selkirk, like all the othertrails on the island, was unusually steep butafforded spectacular views of San Juan Bautistaand adjacent Cumberland Bay. We zigzaggedup the steep slope, passing through moistforests with short trees heavily laden withepiphytic ferns and a dense groundcover ofshrubs and other ferns. As we neared the topof the ridge Juania australis seemed tantalizingclose as they clung tenaciously to the nearvertical slopes 25–50 meters above us (Fig. 5).Finally we arrived at the top of the ridge andMirador de Selkirk where we enjoyedpanoramic views of the village and bay on oneside and the western end of the island on theother. Unfortunately we realized that we wouldbe unable to access the palms from this sitebecause the razor-sharp ridges leading away tothe north and south to the palms were simplytoo steep to negotiate without being a goat orprofessional mountain climber, neither ofwhich applied to us. Thus, I had to be contentwith viewing the palms from a distance and

trying to take a few shots with a telephoto lens(Fig 6). Despite the distance it was easy to seethat these palms, with their wind-battered,torn and frayed leaves, were not nearly ashandsome as their cultivated counterparts wehad just admired in San Juan Bautista. Thesewild palms had a hemi-spherical canopy ofmany fewer leaves with necrotic, gray- tobrown-tipped pinnae. I am sure that mydisappointment at not being able to reach thepalms was clear because Michelangeloconfidently assured me that we would reachthem the next day.

Like everyday during our stay on the RobinsonCrusoe Island, the next day dawned cloudy,drizzly, cool and windy. Eva and Steve decidedto remain at the hotel, but the pilot and oneof the hotel’s gardeners would joinMichelangelo, Marianne and me for ourarduous trek to the southeast to see Juaniaaustralis. We zigzagged up a very steep ridgedirectly behind the hotel and then crossed twosmall valleys and ridges before finally arriving,several hours later, on a grassy, windsweptplateau and large ridge overlooking a deep

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7 (left). A thrifty, wind-battered staminate plant of Juania australis in lower montane forest is exposed abovethe surrounding vegetation at El Cordon Piedra Agujereada, Robinson Crusoe Island. 8 (right). Old staminateinflorescences of this Juania australis at El Cordon Piedra Agujereada on Robinson Crusoe Island are heldamong the leaves.

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valley, an area known as El Cordon PiedraAgujereada. Across this valley and higher upwe could see extensive lower and uppermontane forest with numerous J. australispoking their leaves above the canopy. Excitedlydown we went into the deep valley and upthe other side, passing through lower montaneforest and panting heavily from the exertionof the climb before finally gaining access toupper montane forest. This dense, mossy, high-elevation forest was a delightful place,supporting an extensive understory of thecycad-like fern Blechnum cycadifolium andseveral, handsome tree ferns. The moss andleaf litter on the forest floor formed a spongylayer 30–60 cm (1–2 feet) deep and gave us abouncy sensation as we maneuvered our waythrough the dense undergrowth. Scattered hereand there were several J. australis that we couldactually touch and look right up the trunk intotheir wind-battered canopies! However, thesepalms were difficult to photograph because ofthe densely encroaching forest and not muchbetter looking than the palms we had seenfrom a distance the day before. They had thesame wind-torn and shredded leaves with gray-

and brown-tipped pinnae. Because we couldexamine these palms closely, though, we couldsee that some type of insect predator was alsoseverely ravaging the leaves.

Juania australis is dioecious, meaning there areseparate staminate (male, pollen-bearing) andpistillate (female, seed-bearing) plants. We werefortunate to find one staminate plant with oldinflorescences emerging among the leaves buthanging below them in nearby lower montaneforest that was sufficiently clear to photograph(Figs. 7 & 8). In upper montane forest wefound a pistillate plant with torn, tattered andravaged leaves that was in young fruit.Unfortunately we found no plants with maturefruit. We also noticed that during thedevelopmental phases from seedling to adultplant the palms display saxophone-typeestablishment growth and produce a “heel,”like other palms including Chamaedorearadicalis, Ravenea xerophila, Rhopalostylis spp.and Sabal spp.

We were in a special place, one in which wewanted to linger and were in no hurry to leave.We simply wanted to “soak up” the ambiance

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9 (left). Infructescences of Juania australis are showy when heavily laden with bright, red-orange fruits.Cultivated, Los Canelos, Viña del Mar, Chile. 10 (right). The showy infructescences of Juania australis aremostly held below the leaves and typically retain several, large, thick-papery, tan bracts that persist over thecluster of fruits. Cultivated, Los Canelos, Viña del Mar, Chile.

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of the moment. But the day was getting lateand we had a strenuous, four-hour walk toreturn to the hotel. We were a happy group aswe descended and then ascended a seeminglynever-ending series of valleys and ridges.However, our happiness was temperedsomewhat when Michelangelo twisted hisankle descending into one of the valleys,necessitating a 45-minute hiatus to recoverbefore he was able to continue on. We wererelieved finally to stagger into the hotel, takea warm shower, enjoy a lobster dinner, andshare our day’s adventures with Eva and Steve.

The next day we said our goodbyes to theattentive hotel staff and, after braving the wet,two-hour boat ride back to the west end of theisland and the airport, we departed on ourcharter flight to Santiago. After saying fondfarewells to the pilot and Michelangelo inSantiago, we dropped Eva off at her house andSteve, Marianne and I returned to our hotel.

Easter Island

The next day Marianne and I departed forEaster Island. While we both wanted to seethe famous remnants of the ancient Polynesiancivilization that once thrived on the island, Iwas keen to see the Jubaea chilensis that hadbeen transported from the Chilean mainland

by boat a few years ago in an attempt to“reforest” Easter Island, which is a sensitivesubject in Chile. In 1984 John Dransfield andothers published the name Paschalococosdisperta for an extinct palm that once inhabitedEaster Island. The name was based upon somefruit endocarps (shells) found in a cave andthat indicated the extinct palm was related toJubaea chilensis. It is thought that thePolynesians deforested Easter Island and in theprocess drove P. disperta to extinction. Theymay have cut the palms for food or shelter, andor used the trunks as rollers to move the largeand heavy moais (giant statues) from thequarries to various sites around the island.

A small controversy is raging in Chile aboutPaschalococos disperta and Jubaea chilensis. Onegroup believes that these two species are oneand the same and, thus, has made an effort toreestablish J. chilensis on Easter Island. Theother group believes that the two are distinctand, thus, there should be no efforts to reforestEaster Island with J. chilensis. At least one initialplanting of J. chilensis has been made, though,and small, still trunkless plants to 2 meters (6feet) overall height can be seen at theagriculture department arboretum and theairport. It seems unlikely that the two speciesare the same, though, because the climate on

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11. The bright orange, spherical fruits of Juania australis are about 2 cm (0.8 inch) in diameter. Cultivated, LosCanelos, Viña del Mar, Chile.

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Easter Island is mildly tropical and coconutsare widely planted there. Jubaea chilensis doesnot grow well in a tropical climate and ratherperforms best or thrives in a Mediterraneanclimate. It will be interesting to track theprogress of the few J. chilensis on Easter Islandand see how well they grow in the years tocome. Tour guides would like to have real livepalms to show the tourists because of thecritical role the palm might have played in thedevelopment and demise of the Polynesianculture on Easter Island. All they could showus now were purported palm trunk lava moldson the walls and ceilings of a few caves.

Cultivated Juania australis

After two days enjoying the sites on EasterIsland Marianne and I returned to Santiago.Our departure for Los Angeles was late the nextevening, meaning we had a full day left inSantiago. We decided to visit the privategarden Los Canelos in the scenic and touristyViña del Mar near Valparaiso on the coast westof Santiago. Eduardo Sone, curator of thegarden, showed us several, old, mature, andheavily fruiting specimens of Juania australis.Pistillate plants are showy when carryingseveral infructescences with bright, red-orangefruits (Fig. 9). While emerging within theleaves, the relatively short but showyinfructescences are mostly held below themin fruit and typically retain several, large, thick-papery, tan bracts that persist over the clusterof fruits (Fig.10). The spherical fruits are about2 cm (0.8 inch) in diameter (Fig. 11). Seedlingeophylls are strap-like (Fig. 12). Other thanthese specimens, the only other cultivated J.australis I had ever seen were in the LakesidePalmetum in Oakland, California near SanFrancisco and in Dick Endt’s fabulous gardennear Auckland, New Zealand. The plants inCalifornia, which are growing steadily butslowly, have yet to form trunk but the one atDick Endt’s garden had a short trunk in 2005.Larger specimens, which I have not seen butare perhaps mature, are at Illeifa, a small islandin Lago Ranco, Valdivia in southern Chile.

After seeing Juania australis in the wild andthe few cultivated specimens on the Chileanmainland, and in California and New Zealand,I can understand and appreciate how rare this

palm is in cultivation and how slowly it grows.The rather narrow and exacting environmentalparameters in which it grows, with little dailyor even seasonal variance, make it one of themost difficult palms to cultivate. There are fewplaces in the world of palm cultivation thathave the same or similar climate as that ofRobinson Crusoe Island, and the narrowenvironmental parameters are difficult toduplicate artificially.

We hurried back to Santiago to do our finalpacking, gather our luggage, check out of thehotel, and head to the airport for our returnto Los Angeles. Because I dislike hastydepartures, we were much relieved and contentfinally to settle into our seats for the long flightto Los Angeles and fondly remember Chile’stwo endemic and very different palms.

Acknowledgments

Several people and institutions facilitated ourtravel and visits to see palms in Chile and allhave my sincere thanks. These includeVeronica Lopez of Hacienda las Palmas deCocalán; Patricio Novoa of the Jardín BotánicoNacional at Viña del Mar; Mauricio Moreno ofthe Reserva Ecológica Oasis de la Campana;and Eduardo Sone of Los Canelos, Renaca,Viña del Mar. Ceci Salas of Latin Trip andMichelangelo Trezza, owner of Hotel Pangal,made our trip to Robinson Crusoe Islandpossible and pleasurable.

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12. Seedling eophylls of Juania australis are strap like.Cultivated, Los Canelos, Viña del Mar, Chile.

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In Search ofJuania australiswith a FewObservations ofJubaea chilensisalong the Way

DONALD R. HODEL

University of CaliforniaCooperative Extension4800 E. Cesar Chavez Ave.Los Angeles, CA 90022 [email protected]

One of the most mysterious, enigmatic and fascinating palms must be Juania

australis. Its isolated habitat alone, on Robinson Crusoe Island (Juan Fernández)

off the coast of Chile, is more than sufficient to conjure up images of a remote,

far away, mysterious land, while the name of the island itself and its past role in

literary lore add immeasurably to this mystique. I visited Chile in November, 2010

with Marianne Hodel and Steve Daugherty, my former college roommate, to

explore for the rare J. australis in its isolated, island habitat and to observe the

famous and well known Jubaea chilensis in the wild.

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1. At theHacienda delas Palmas deCocalán southof Santiago,Chile, theextensivepopulation ofJubaea chilensisinhabits theflat valleybottom and issemi-managedfor thebountiful cropof edible seedscalled coquitos.

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After the all-night flight from Los Angeles toSantiago, Chile, we rented an auto and droveto our hotel where we checked in and relaxedfor awhile before meeting Steve’s friend, EvaOchoa, for lunch. Over a traditional Chileanseafood extravaganza, we planned ouractivities for the next two weeks. Our plan wasto spend about 10 days in and aroundSantiago, making day trips to several locales tosee the famous Chilean wine palm, Jubaeachilensis, in the wild and cultivated around thecity. We would then make a four-day trip toRobinson Crusoe Island to see Juania australisafter which Marianne and I would travel toEaster Island for a few days before returning toLos Angeles.

Jubaea chilensis

Like California, central Chile, includingSantiago, has a Mediterranean climatecharacterized by cool, moist winters and warm,dry summers. November is late spring inSantiago, and typically the weather is mostlypleasant with warm, sunny days and coolnights although we experienced severalunusually cool days with clouds and rain. Wewere amazed at the similarity of the terrainand vegetation around Santiago with that ofsouthern California. The rocky hillsides werevariously covered with xerophytic shrubs,small trees, cacti and, at this time of year,

seasonal wildflowers, just like our chaparral inCalifornia. It was all the more amazing,though, to see some of these hills and valleyscovered densely with vast stands of Jubaeachilensis.

We visited three areas with Jubaea chilensis,including Quebrada Siete Hermanas near theport and tourist destinations of Valparaiso andVina del Mar west of Santiago, the Haciendade las Palmas de Cocalán south of Santiago(Fig. 1), and Parque Nacional La Campananorth of Santiago. The last two sites have thelargest populations of J. chilensis, 35,000 and62,500 adults each, respectively. While thispalm is most abundant in valley bottoms,where soil is deep and moisture is moreplentiful and available, it frequently inhabitsor even thrives on dry, well drained, rockyhilltops and ridges (Fig. 2). I was surprised andhad a difficult time understanding how thispalm could grow in such a harsh environment.At the Hacienda de las Palmas de Cocalán,where the palms are semi-managed for thebountiful fruits containing the edible seeds,called coquitos (small coconuts), we observedseveral, still-living and healthy-appearingspecimens with burned-out trunks, evidence ofthe occasional fires that ravage the palms andsurrounding area. Some were burned soextensively that only a perimeter layer of

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2. While Jubaea chilensis is most abundant in valley bottoms, where soil is deep and moisture is more plentifuland available, it frequently inhabits or even thrives on dry, well drained, rocky hilltops and ridges, as here atParque Nacional La Campana north of Santiago, Chile.

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sound tissue about 10 cm (4 inches) thickremained and, in some cases, only partiallyenclose the trunk, easily enabling a person tostep inside. These burned-out trunks stillsupported a healthy, full canopy of leaves.

Juania australis and Robinson Crusoe Island

After spending a few days in Santiago visitingseveral of the well known tourist sites, manyof them with exemplary specimens of Jubaeachilensis, we were ready and excited to visitRobinson Crusoe Island (otherwise known asJuan Fernández) in our quest to see Juaniaaustralis. Unfortunately, our plans unraveledslightly when the day before our departure thetravel agent who had made our arrangementsfor Robinson Crusoe Island (air, lodging andlocal guide), e-mailed me to say that theregularly scheduled airline on which we werebooked had decided not to fly to RobinsonCrusoe Island that week! We were stunnedbecause we were locked-in to our departure toLos Angeles and Marianne and I still had our

short trip to Easter Island, precluding us fromadjusting our schedule. This discouraging newsreminded me painfully what others had toldme about travel to Robinson Crusoe Island: itis not an easy place to get to, the airline thatserves it is unreliable and flights are frequentlycancelled or rescheduled with little or nonotice.

Fortunately, our savvy and resourceful travelagent quickly, at no additional coast, chartereda small, two-engine aircraft to take us toRobinson Crusoe Island. On the morning ofNovember 9, when Steve, Eva, Marianne andI arrived at one of the charter hangers at theairport, an agent met and told us that oneadditional passenger would be accompanyingus to Robinson Crusoe Island. As it turned out,the additional passenger was none other thanMichelangelo Trezza, the owner of the hotelwhere we would be staying for three nightson the island. At the time of our visit there wasonly one hotel operating on Robinson Crusoe

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3. Cultivated specimens of Juaniaaustralis in San Juan Bautista onRobinson Crusoe Island typically arebetter looking than their wildcounterparts and have a fairly robust,smooth, lime-green, conspicuouslyand densely ringed trunk supporting acompact, nearly spherical canopy of25 to 35, stiffly ascending tospreading to drooping, dark green,pinnate leaves.

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Island because the tsunami spawned by thepowerful earthquake that struck Chile inFebruary 2010 devastated San Juan Bautista,the only village on the island. The tsunamikilled over 20 people and destroyed nearly halfthe small village, including all the hotelsexcept one. We were the first tourists to visitRobinson Crusoe Island since the tsunami.

The flight from Santiago to Robinson Crusoewas uneventful but as we neared the islandthe skies suddenly became cloudy and wewould not see the sun again until we returnedto Santiago in three days. Once our plane hadlanded and we had collected our gear, welearned that the pilot would be staying withus for our three nights rather than makinganother trip back to Santiago and then backto the island again. From the airport we tooka short truck ride down to a small bay thatwas home to several hundred noisy sea lionsfrolicking in the rough surf or lyingcontentedly on the mossy rocks. From thesmall bay we took a rough, wet, two-hour, 18-km (11-mile) ride in a small, open boat to SanJuan Bautista. If not for the rain coverings wewere given upon boarding the salt spray wouldhave thoroughly soaked us and our gear.

Prior to the tsunami about 500 people lived onRobinson Crusoe Island, nearly all in San Juan

Bautista on Cumberland Bay, and they wereengaged in fishing, primarily lobster, and abudding eco-tourism industry. Now about 350people live on the island and, while fishing isstill the primary source of income, there ishope that tourism can get back on its feet withreconstruction of hotels and other necessaryinfrastructure.

Formerly known as Juan Fernández Island orMás a Tierra, the Chilean government renamedthe island Robinson Crusoe Island in 1966 toreflect is purported literary past. Many peopletheorize that Daniel Defoe based his 1719novel, Robinson Crusoe, on the experiences ofa Scottish castaway, Alexander Selkirk, whovoluntarily asked to be left on the island in1704 because of doubts of the seaworthinessof the vessel on which he sailed. After fouryears on the island he was rescued in 1709and returned to Europe to tell his tale.However, several other real-life incidences mayvery well have served as Defoe’s inspiration.

About 675 km (415 miles) west of Chile,Robinson Crusoe Island is the largest of threethat make up the Juan Fernández Islandsarchipelago (Alexander Selkirk and Santa Claraare the other two islands in the archipelago).The island covers 93 km2 (36 miles2) and risesvery precipitously to 916 m (3005 feet) at the

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4. The congested leaf bases of Juania australis, deeply split opposite the petiole, are loosely overlapping, donot form a crownshaft, and, like the petioles, are densely covered with grayish to tan or even rusty brown,felt-like indumentum.

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top of El Yunque, the highest point. Theremains of an ancient volcano, RobinsonCrusoe Island is extremely mountainous andspectacularly eroded with steep valleys andnarrow, razor-like ridges and is reminiscent ofsome of the picturesque, older islands inHawaii or the South Pacific.

Like the Chilean mainland, Robinson CrusoeIsland has a Mediterranean climate but thecold Humboldt Current sweeping up fromAntarctica provides significant modifications.Thus, it has a more moderate climate, not aswarm or cold as Valparaiso at roughly similarlatitude on the Chilean coast, and with littleseasonal variation. However, because of thecold Humboldt Current, the weather isfrequently cool, cloudy, misty or drizzly, andwindy, and reminded me much of SanFrancisco on the central California coast.Daytime high and nighttime low temperaturesin January, the warmest month, average 22ºC(71ºF) and 16ºC (61ºF), respectively, while inAugust, the coolest month, they are 15ºC(60ºF) and 10ºC (50ºF). A low -2ºC (29ºF) hasbeen recorded in October. Rain averages 170mm (7 inches) in July, the wettest month, and26 mm (1 inch) in February, the driest month.

Humidity is always high and the rainiestmonths of June and July average about 15 daysper month of rain or drizzle while the driestmonths of December and January averageabout six days per month of rain or drizzle.These records are for San Juan Bautista at sealevel but certainly the higher parts of theisland, which are frequently hidden in clouds,experience cooler temperatures and higherrainfall and humidity.

Pasture land and disturbed forest with manyinvasive, weedy exotic species, like Eucalyptus,Cupressus and Pinus, occur from sea level toabout 200 meters elevation. Lower montaneforest ranges from 200 to 400 meters elevation.Upper montane forest occurs above 400 meterselevation. Juania australis is restricted tomontane forest and is most common in uppermontane forest. Upper montane forests onsome of the higher mountains, which arenearly always enveloped in clouds, support anintriguing cloud forest. Robinson Crusoe Islandis rich in endemics, with 101 of the 146 nativeplant species (nearly 70%) found nowhere else.Most of the plants have relatives in SouthAmerica, New Zealand and Australia. Severalmembers of the sunflower family, whoserelatives are typically herbs in other locations,are trees on Robinson Crusoe Island. The entireisland was designated a World BiosphereReserve in 1977 because of its unique andendangered flora and fauna.

As our small boat pulled up to the wharf at SanJuan Bautista, the destruction from thetsunami was stunning. The lower half of thevillage adjacent to Cumberland Bay was gone,as if a giant hand had simply wiped it from theearth’s surface. Only a few very large and oldtrees and house foundations remained. As wewaited for the ride to our hotel, I looked up tothe steep and narrow ridgelines towering overthe village and here and there I was just ableto pick out a few specimens of Juania australisclinging precariously to nearly vertical cliffsnot too far above San Juan Bautista. Seeing thepalms above and so near to San Juan Bautistawas encouraging but, being an eternalpessimist and somewhat experienced insearching for palms in difficult-to-access places,I checked my optimism because I knew thatwhat seemed like a rather easy walk up to thepalms could easily be just the opposite.

After checking into the hotel and eating lunch,we discussed our plans for the next two dayswith Michelangelo, who would also serve asour guide in our search for Juania australis. The

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5. Juania australis clings tenaciously to a cliff nearMirador de Selkirk above San Juan Bautista onRobinson Crusoe Island.

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next day we would take a walk up a trailbehind San Juan Bautista to Mirador de Selkirk,a viewpoint at the top of the ridge overlookingthe village and bay near to the J. australis Ihad seen upon our arrival. Our second day’sactivities would take us on a much longer walkover several ridges to the southeast of San JuanBautista. We spent the remainder of theafternoon exploring the steep hillsides aroundthe hotel, looking at ferns and admiring theviews of the ocean crashing into the base ofthe precipitous slopes.

Michelangelo was full of confidence the nextmorning as he, Eva, Steve, Marianne and I setout for Mirador de Selkirk. He was sure wewould find our quarry, Juania australis. As wewalked toward the village we passed throughgroves of the Australian native Eucalyptusglobulus, the blue gum, which reminded memuch of the central and northern Californiacoasts. Much to our surprise as we passedthrough San Juan Bautista, we found severalcultivated specimens of J. australis adorning afew dooryards. Known locally as chonta, it isan unusual palm, not likely to be confusedwith any other. The fairly robust, smooth,lime-green, conspicuously and densely ringedtrunk supports a compact, nearly spherical

canopy of 25–35, stiffly ascending to spreadingto drooping, dark green, pinnate leaves withrelatively short petioles (Fig. 3). Leaf scars onthe lower part of the trunk, which wereproduced when the palm was young andgrowing more vigorously and or perhapsshaded, are frequently uneven andasymmetrical, with one side higher than theother, reminding me of those of Howeaforsteriana. In contrast, leaf scars near the topof the trunk just below the leaves are severelyclose set and congested, reminding me of thoseof Rhopalostylis baueri or R. sapida. The stiffpinnae are glossy dark green above and grayishbelow. The congested leaf bases, deeply splitopposite the petiole, are loosely overlapping,do not form a crownshaft, and, like thepetioles, are densely covered with grayish totan or even rusty brown, felt-like indumentum(Fig. 4). Simply looking at the leaf bases easilyreminds one of its relatives Ceroxylon,Oraniopsis appendiculata and even Ravenea.Unfortunately, none of the plants had flowersor fruits although they looked sufficiently largeand old to be mature. Michelangelo wasdelighted, jauntily declaring that we hadattained our objective for the trip. His spiritswere not in the least bit dampened when Ireminded him that I had come to see these

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6. Above Mirador de Selkirk on Robinson Crusoe Island Juania australis is exposed and, with its wind-battered,torn and frayed leaves, is not nearly as handsome as its cultivated counterparts in San Juan Bautista.

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palms in the wild, and he assured me that wewould soon see them at Mirador de Selkirk.

The trail to Mirador de Selkirk, like all the othertrails on the island, was unusually steep butafforded spectacular views of San Juan Bautistaand adjacent Cumberland Bay. We zigzaggedup the steep slope, passing through moistforests with short trees heavily laden withepiphytic ferns and a dense groundcover ofshrubs and other ferns. As we neared the topof the ridge Juania australis seemed tantalizingclose as they clung tenaciously to the nearvertical slopes 25–50 meters above us (Fig. 5).Finally we arrived at the top of the ridge andMirador de Selkirk where we enjoyedpanoramic views of the village and bay on oneside and the western end of the island on theother. Unfortunately we realized that we wouldbe unable to access the palms from this sitebecause the razor-sharp ridges leading away tothe north and south to the palms were simplytoo steep to negotiate without being a goat orprofessional mountain climber, neither ofwhich applied to us. Thus, I had to be contentwith viewing the palms from a distance and

trying to take a few shots with a telephoto lens(Fig 6). Despite the distance it was easy to seethat these palms, with their wind-battered,torn and frayed leaves, were not nearly ashandsome as their cultivated counterparts wehad just admired in San Juan Bautista. Thesewild palms had a hemi-spherical canopy ofmany fewer leaves with necrotic, gray- tobrown-tipped pinnae. I am sure that mydisappointment at not being able to reach thepalms was clear because Michelangeloconfidently assured me that we would reachthem the next day.

Like everyday during our stay on the RobinsonCrusoe Island, the next day dawned cloudy,drizzly, cool and windy. Eva and Steve decidedto remain at the hotel, but the pilot and oneof the hotel’s gardeners would joinMichelangelo, Marianne and me for ourarduous trek to the southeast to see Juaniaaustralis. We zigzagged up a very steep ridgedirectly behind the hotel and then crossed twosmall valleys and ridges before finally arriving,several hours later, on a grassy, windsweptplateau and large ridge overlooking a deep

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7 (left). A thrifty, wind-battered staminate plant of Juania australis in lower montane forest is exposed abovethe surrounding vegetation at El Cordon Piedra Agujereada, Robinson Crusoe Island. 8 (right). Old staminateinflorescences of this Juania australis at El Cordon Piedra Agujereada on Robinson Crusoe Island are heldamong the leaves.

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valley, an area known as El Cordon PiedraAgujereada. Across this valley and higher upwe could see extensive lower and uppermontane forest with numerous J. australispoking their leaves above the canopy. Excitedlydown we went into the deep valley and upthe other side, passing through lower montaneforest and panting heavily from the exertionof the climb before finally gaining access toupper montane forest. This dense, mossy, high-elevation forest was a delightful place,supporting an extensive understory of thecycad-like fern Blechnum cycadifolium andseveral, handsome tree ferns. The moss andleaf litter on the forest floor formed a spongylayer 30–60 cm (1–2 feet) deep and gave us abouncy sensation as we maneuvered our waythrough the dense undergrowth. Scattered hereand there were several J. australis that we couldactually touch and look right up the trunk intotheir wind-battered canopies! However, thesepalms were difficult to photograph because ofthe densely encroaching forest and not muchbetter looking than the palms we had seenfrom a distance the day before. They had thesame wind-torn and shredded leaves with gray-

and brown-tipped pinnae. Because we couldexamine these palms closely, though, we couldsee that some type of insect predator was alsoseverely ravaging the leaves.

Juania australis is dioecious, meaning there areseparate staminate (male, pollen-bearing) andpistillate (female, seed-bearing) plants. We werefortunate to find one staminate plant with oldinflorescences emerging among the leaves buthanging below them in nearby lower montaneforest that was sufficiently clear to photograph(Figs. 7 & 8). In upper montane forest wefound a pistillate plant with torn, tattered andravaged leaves that was in young fruit.Unfortunately we found no plants with maturefruit. We also noticed that during thedevelopmental phases from seedling to adultplant the palms display saxophone-typeestablishment growth and produce a “heel,”like other palms including Chamaedorearadicalis, Ravenea xerophila, Rhopalostylis spp.and Sabal spp.

We were in a special place, one in which wewanted to linger and were in no hurry to leave.We simply wanted to “soak up” the ambiance

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9 (left). Infructescences of Juania australis are showy when heavily laden with bright, red-orange fruits.Cultivated, Los Canelos, Viña del Mar, Chile. 10 (right). The showy infructescences of Juania australis aremostly held below the leaves and typically retain several, large, thick-papery, tan bracts that persist over thecluster of fruits. Cultivated, Los Canelos, Viña del Mar, Chile.

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of the moment. But the day was getting lateand we had a strenuous, four-hour walk toreturn to the hotel. We were a happy group aswe descended and then ascended a seeminglynever-ending series of valleys and ridges.However, our happiness was temperedsomewhat when Michelangelo twisted hisankle descending into one of the valleys,necessitating a 45-minute hiatus to recoverbefore he was able to continue on. We wererelieved finally to stagger into the hotel, takea warm shower, enjoy a lobster dinner, andshare our day’s adventures with Eva and Steve.

The next day we said our goodbyes to theattentive hotel staff and, after braving the wet,two-hour boat ride back to the west end of theisland and the airport, we departed on ourcharter flight to Santiago. After saying fondfarewells to the pilot and Michelangelo inSantiago, we dropped Eva off at her house andSteve, Marianne and I returned to our hotel.

Easter Island

The next day Marianne and I departed forEaster Island. While we both wanted to seethe famous remnants of the ancient Polynesiancivilization that once thrived on the island, Iwas keen to see the Jubaea chilensis that hadbeen transported from the Chilean mainland

by boat a few years ago in an attempt to“reforest” Easter Island, which is a sensitivesubject in Chile. In 1984 John Dransfield andothers published the name Paschalococosdisperta for an extinct palm that once inhabitedEaster Island. The name was based upon somefruit endocarps (shells) found in a cave andthat indicated the extinct palm was related toJubaea chilensis. It is thought that thePolynesians deforested Easter Island and in theprocess drove P. disperta to extinction. Theymay have cut the palms for food or shelter, andor used the trunks as rollers to move the largeand heavy moais (giant statues) from thequarries to various sites around the island.

A small controversy is raging in Chile aboutPaschalococos disperta and Jubaea chilensis. Onegroup believes that these two species are oneand the same and, thus, has made an effort toreestablish J. chilensis on Easter Island. Theother group believes that the two are distinctand, thus, there should be no efforts to reforestEaster Island with J. chilensis. At least one initialplanting of J. chilensis has been made, though,and small, still trunkless plants to 2 meters (6feet) overall height can be seen at theagriculture department arboretum and theairport. It seems unlikely that the two speciesare the same, though, because the climate on

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11. The bright orange, spherical fruits of Juania australis are about 2 cm (0.8 inch) in diameter. Cultivated, LosCanelos, Viña del Mar, Chile.

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Easter Island is mildly tropical and coconutsare widely planted there. Jubaea chilensis doesnot grow well in a tropical climate and ratherperforms best or thrives in a Mediterraneanclimate. It will be interesting to track theprogress of the few J. chilensis on Easter Islandand see how well they grow in the years tocome. Tour guides would like to have real livepalms to show the tourists because of thecritical role the palm might have played in thedevelopment and demise of the Polynesianculture on Easter Island. All they could showus now were purported palm trunk lava moldson the walls and ceilings of a few caves.

Cultivated Juania australis

After two days enjoying the sites on EasterIsland Marianne and I returned to Santiago.Our departure for Los Angeles was late the nextevening, meaning we had a full day left inSantiago. We decided to visit the privategarden Los Canelos in the scenic and touristyViña del Mar near Valparaiso on the coast westof Santiago. Eduardo Sone, curator of thegarden, showed us several, old, mature, andheavily fruiting specimens of Juania australis.Pistillate plants are showy when carryingseveral infructescences with bright, red-orangefruits (Fig. 9). While emerging within theleaves, the relatively short but showyinfructescences are mostly held below themin fruit and typically retain several, large, thick-papery, tan bracts that persist over the clusterof fruits (Fig.10). The spherical fruits are about2 cm (0.8 inch) in diameter (Fig. 11). Seedlingeophylls are strap-like (Fig. 12). Other thanthese specimens, the only other cultivated J.australis I had ever seen were in the LakesidePalmetum in Oakland, California near SanFrancisco and in Dick Endt’s fabulous gardennear Auckland, New Zealand. The plants inCalifornia, which are growing steadily butslowly, have yet to form trunk but the one atDick Endt’s garden had a short trunk in 2005.Larger specimens, which I have not seen butare perhaps mature, are at Illeifa, a small islandin Lago Ranco, Valdivia in southern Chile.

After seeing Juania australis in the wild andthe few cultivated specimens on the Chileanmainland, and in California and New Zealand,I can understand and appreciate how rare this

palm is in cultivation and how slowly it grows.The rather narrow and exacting environmentalparameters in which it grows, with little dailyor even seasonal variance, make it one of themost difficult palms to cultivate. There are fewplaces in the world of palm cultivation thathave the same or similar climate as that ofRobinson Crusoe Island, and the narrowenvironmental parameters are difficult toduplicate artificially.

We hurried back to Santiago to do our finalpacking, gather our luggage, check out of thehotel, and head to the airport for our returnto Los Angeles. Because I dislike hastydepartures, we were much relieved and contentfinally to settle into our seats for the long flightto Los Angeles and fondly remember Chile’stwo endemic and very different palms.

Acknowledgments

Several people and institutions facilitated ourtravel and visits to see palms in Chile and allhave my sincere thanks. These includeVeronica Lopez of Hacienda las Palmas deCocalán; Patricio Novoa of the Jardín BotánicoNacional at Viña del Mar; Mauricio Moreno ofthe Reserva Ecológica Oasis de la Campana;and Eduardo Sone of Los Canelos, Renaca,Viña del Mar. Ceci Salas of Latin Trip andMichelangelo Trezza, owner of Hotel Pangal,made our trip to Robinson Crusoe Islandpossible and pleasurable.

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12. Seedling eophylls of Juania australis are strap like.Cultivated, Los Canelos, Viña del Mar, Chile.

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Increasingly, the health and survival of palmsin southern U.S. landscapes is being challengedby diseases, both by new pathogens (Elliott etal. 2010) and by geographic or host expansionof established palm pathogens (Harrison et al.,2008, Harrison et al. 2009, Elliott et al. 2011,Singh et al. 2011). Unfortunately, palms thatare properly managed to reduce environmentalstresses appear to be just as vulnerable todiseases, especially the lethal diseases, asimproperly managed palms, which limits theuse of cultural methods as a means to managethese diseases and suggests a need for chemicalcontrol methods. However, only two lethaldiseases of mature, large palms have beensuccessfully managed with systemic pesticides– Phytophthora bud rot and lethal yellowing.Interestingly, trunk injection of the pesticidesis the most effective application method formanaging these two diseases.

Phytophthora bud rot control in Cocos nuciferahas been observed in Africa and Asia usingtrunk injections of the phosphonatecompounds fosetyl-Al or phosphorous acid aspreventive treatments (Thevenin et al. 1995,Pohe et al. 2003). Two or three trunk injectionapplications per year appear to be necessary foradequate disease control in Africa (Pohe et al.2003). Distribution of the phosphonatecompounds in palms has not been determined,but it is known that, in general, phosphonatecompounds are translocated via xylem andphloem tissue, a unique characteristic forfungicides (Guest & Grant 1991).

In the continental U.S., the only lethal palmdisease for which a successful managementplan using a pesticide has been developed islethal yellowing (LY) caused by a phytoplasma(McCoy 1974, McCoy 1976). The pesticide

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Detection ofThiabendazoleFungicide inCoconutPalms Using a Bioassay

MONICA L. ELLIOTT

AND

TIMOTHY K. BROSCHAT

University of Florida –IFAS, Fort Lauderdale Researchand Education Center, 3205 College Avenue,Fort Lauderdale, FL33314 USAE-mail addresses:[email protected] and [email protected]

A biological assay using the fungus Penicillium was developed for detecting

thiabendazole fungicide in palm canopies. Thiabendazole was provided to Cocos

nucifera via passive uptake infusion. Using the bioassay, the fungicide could be

consistently detected in the petiole and rachis tissue for up to 90 days after it

was applied. While the fungicide could be detected in leaflet tissue, it was not

consistently detected at any sampling date. Detection of the fungicide decreased

over time, but it did translocate into new leaves that emerged after the application.

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used is the antibiotic oxytetracycline. Variousmethods of applying the antibiotic to maturecoconut palms were tested in the 1970s, andit was determined that only a liquid trunkinjection (one injection site per palm) waseffective in moving this material into thephloem tissue of the palm canopy (McCoy1974, McCoy 1976). Soil drenches, foliar spraysand trunk implantation of solid tablets wereineffective. It was also determined that repeatapplications (2 to 6.5 ml per palm, dependingon size) were necessary every 4 months fordisease management because foliarconcentrations of the antibiotic slowlydeclined.

Use of both phosphonates and oxytetracyclinein palms is significantly different from theiruse in dicot trees (Timmer et al. 1982, Darvaset al. 1984, Kostka et al. 1985, Guest et al.1994). Multiple applications within a year arerequired for palms (monocots), whereas onlyone application per year is required for dicottrees. Only one trunk injection site perapplication is required for palms, but multipleinjection sites per application are required fordicot trees. These differences can be explainedbased on the morphology of the trees. Mostpalms have a vascular bundle pattern referredto as the “Rhapis principle,” wherein a bundlemay start near the outside of the stem, thencurve to the middle of the stem and then curveback to the outside of the stem (Dransfield etal. 2008). At the same time, vascular bundlesproduce short branches that connect to othervascular bundles (Dransfield et al. 2008). Withthousands of vascular bundles in a palm stem,material injected into one side of the palmshould be easily distributed to the entire palm.

Large palms (those with more than 1.5 to 2 mof clear trunk) in the landscape present specialproblems for management of diseases wherethe pathogen is located in the leaf canopy.Foliar application of pesticides is impracticaldue to palm height and canopy spread, theirlocation within landscapes (often inaccessiblewithout a bucket truck or lift), andenvironmental and human health risks causedby spray drift. Therefore, trunk injectionswould be more convenient and safer. However,in contrast to our knowledge aboutphosphonates and oxytetracyline efficacy oruptake and movement in palms, there hasbeen minimal research conducted on thesesame topics for xylem-mobile fungicides thatmay have applicability for management offungal palm diseases in the landscape, such asFusarium wilts (Fusarium oxysporum ff. spp.)

and petiole/rachis blights (numerouspathogens).

The limited studies on uptake and movementof xylem-mobile fungicides in palms have beenconducted with benzimidazole fungicides, axylem-mobile fungicide chemical group (Erwin1973). One study applied benomyl (Benlate isa former trader name) to a mature Phoenixcanariensis (~7.5 m tall) via a soil (root) drench(Surico 1977). After 45 days, benomyl wasdetected in the youngest leaves and the highestlevel detected in any leaf was 0.178 µg/g. Astudy in California examined the uptake anddistribution of carbendazim phosphate(Lignasan is a former trade name) in maturePhoenix canariensis (~4.5 m of trunk) (Feather1982). The fungicide was injected into thetrunks. After 48–56 hours, the fungicide wasdetected in the trunk and the apical meristem,but not in the leaf tissue. This was in contrastto application of this same material in Ulmusamericana (American elm), where the fungicidewas detected in twigs and leaves. However, theelm samples were obtained at least 20 daysafter injections (McCain 1980, Stennes &French 1987).

The objectives of the study described hereinwere two-fold: a) to develop a protocol toexamine uptake, distribution and persistenceof xylem-mobile fungicides in tall palms; andb) to determine the uptake, distribution andpersistence of thiabendazole. This fungicide iscurrently labeled in the U.S. for managementof Dutch elm disease via trunk injections. Itbelongs to the benzimidazole fungicide group,so the results obtained could be compared tothose observed previously with benomyl andcarbendazim phosphate.

Materials and Methods

Cocos nucifera with at least 2 m of clear trunklocated at the University of Florida’s FortLauderdale Research and Education Centerwere used for this experiment. These palmsare growing in a uniform Margate fine sand soiland had not been subjected to pesticidetreatments prior to this experiment. All palmshad at least 16 leaves. Leaves used for samplingwere numbered by starting with the newestgrowth at the time the fungicides were applied.The emerging spear leaf was designated leaf 0,the next oldest leaf as leaf 1 and so on downthrough the canopy to the oldest leaf. Leavesthat emerged after the start of the experimentwere labeled with negative numbers (-1, -2,etc.) as the leaves emerged.

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Preliminary studies with the thiabendazolefungicide demonstrated a trunk infusiontechnique was a better method for fungicideuptake by palms when compared to trunkinjection under low pressure (172 kPa).Infusion allows for passive uptake of thefungicides into the palm. Therefore, pine treeinfusers provided by Rainbow TreecareScientific Advancements (http://www.treecarescience.com/arborceuticals/equipment/pine-infuser-system) were used. Two holes onopposite sides of the trunk at breast heightwere drilled 8.5 cm deep using a ~0.2 cm drillbit. The infuser nozzle was tapped into thetrunk with a rubber mallet to a 2.5 cm depth,and the capped tube attached to the nozzlewas tied upright to the trunk with flaggingtape. Each infuser held approximately 40 ml(Figure 1).

The fungicide formulation used was Arbotect20-S (0.22 kg thiabendazole per liter; SyngentaCrop Protection, Inc., Greensboro, NC). There

were four palms per fungicide treatment, andtwo palms for the untreated (water) controltreatment. Each palm received 120 ml of liquid(either undiluted fungicide or water), 60 mlper infuser. For Arbotect-20S, this is equivalentto 26 g of the active ingredient thiabendazole.Since there were no fungicide rates developedfor palms, the rate selected was the lowtherapeutic rate for an elm with 25 cm trunkdiameter at breast height (DBH). The meanDBH for the four treated palms was 18 cm.Since each infuser held only 40 ml, the liquidwas replenished in the infusers as the liquidwas taken up by the palm. Infusers wereremoved after 24 hours. No signs of leakagewere evident.

A bioassay method was used to detectthiabendazole in the leaf tissue sampled. Forthis study, two fungi were used: Fusariumoxysporum f. sp. palmarum, a palm pathogen(PLM-249A=NRRL 53543), and a Penicilliumsp., a non-pathogen (PLM-445). The latter ismore sensitive to thiabendazole than theformer. Both isolates were obtained from palmtissue in Florida. For each fungus, sporesuspensions were prepared in sterile deionizedwater, diluted to 10,000 spores per ml andadded to sterile water agar. A thin layer of thisagar-spore suspension was spread on thesurface of 1/5 strength potato dextrose agaramended with 300 µg/ml streptomycin sulfateto inhibit bacterial growth. The fungal-seededmedium was used immediately. After leaf tissueor paper discs were placed on the media, plateswere incubated at 25°C. Zones of fungalinhibition were measured in two directionsand the average recorded. This was done at 24hrs for Fusarium and 40 hrs for Penicillium.

Standard inhibition curves were developedusing sterile filter paper discs (6-mm diameter)saturated with a range of known con-centrations of thiabendazole. After drying,discs were placed on fungal seeded media,incubated and inhibition zones measured.Regression analysis was performed to obtainthe equation that best fit the data for thestandards at each sampling time. This equationwas then used to calculate the amount ofthiabendazole detected in the palm tissue.

For sampling leaflet tissue, 4 basal leaflets and4 distal leaflets (2 from each side of the rachis)were cut from the rachis, washed and blottedthoroughly dry. Leaflet tissue discs (6-mmdiameter) were cut out of the leaflets (8 discsper leaflet) from both sides of the mid-rib usinga paper hole punch and placed on the fungal-seeded medium.

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1. Example of system used for passive infusion ofthiabendazole fungicide into the palm trunk.

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For sampling petiole and rachis tissue, three10-cm segments were obtained from each leaf:a) petiole section (P), located half way betweenthe trunk and rachis, b) basal section of therachis, located about 45 cm from beginning ofthe rachis (B), and c) distal section of therachis, located about 45 cm from leaf tip (D).The epidermis of each segment was removedand a cross-section selected and cut into 5-mm by 5-mm pieces of ~2-mm thickness.There were 4 sections from each of the 3segments placed on each of the fungal seededmedia. Note that sampling the petiole andrachis was destructive sampling since the leafwas removed from the canopy. On each sampledate, one of the oldest (=lower) leaves, a mid-canopy leaf (=middle), and the youngest, fullyexpanded leaf (=upper) was sampled from eachpalm.

Arbotect 20-S was infused into the palms on21 September 2009. Ten days later on October1, only leaflets from leaves 1, 5 and 10 weresampled. Leaflets and petiole tissue of thesesame leaves were sampled 30 days post-application. At 60 days post-application(November 2: leaves 0, 4 and 9) and 90 dayspost-application (December 21: leaves -1, 3and 8), leaflets, petiole and rachis tissues weresampled. On all sampling dates, leaf tissuesamples were obtained from the two control(untreated) palms that were equivalent to leaftissue samples from the fungicide treatedpalms.

Results

For all sampling dates, there was no inhibitionof either fungus (Fusarium or Penicillium) byany leaflet, petiole or rachis tissue from thecontrol palms, indicating there was nothingnaturally present in the palm tissue thatinhibited these fungi. Thus, any inhibition ofthese fungi by tissue obtained from treatedpalms described below is assumed to be due tothiabendazole fungicide. No phytotoxicity wasobserved on any palm leaf, despite usingundiluted material.

The level of thiabendazole detected in eachtissue piece on each sampling date was basedon the results obtained with the fungicidesaturated sterile paper discs for that particularsampling date. As preliminary studies hadindicated, thiabendazole inhibition wasdetected at much lower levels for Penicilliumthan Fusarium. Penicillium was inhibited at 25µg/g, but not at 5 µg/g.

Detection of thiabendazole in leaflet tissue wasinconsistent among treated palms and among

the leaves of each palm (Fig. 2). For example,at 10 days post-fungicide application,thiabendazole was detected in 3 of 4 palms, butnot in all leaves assayed for the 3 palms. Thegreatest amount detected was 58 µg/g. At 30days post-fungicide application, the fungicidewas detected in all 4 palms but not in all leavesassayed from each palm. The greatest amountdetected was 88 µg/g. At 60 days post-fungicideapplication, it was detected in only one leaf ofone palm. No thiabendazole was detected inany leaflet tissue of any palm 90 days afterfungicide application. Detection of thia-bendazole could be determined only withPenicillium, since the concentrations were solow.

The original protocol included bioassay of onlyleaflets and petiole tissue. Thus, at 30 dayspost-fungicide application, only the leafletsand petiole tissue were sampled and assayedfor fungicide. Rachis tissue was not sampled.Thiabendazole was consistently detected inthe petiole tissue of all 3 leaves sampled fromall treated palms. This was in contrast tofungicide detection results in the leaflet tissue.Therefore, at 60 and 90 days post-fungicideapplication, rachis tissue from the basal anddistal ends of the leaf were also assayed todetermine if thiabendazole was beingtranslocated in the leaf, beyond the petiole(leaf base).

The amount of thiabendazole detected inpetiole and rachis tissue is shown in Table 1.The only time the fungicide was not detected

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2. Spore germination and growth of the Penicilliumfungus is inhibited by the fungicide present in therachis tissue of the palm leaf, defined by the blackcircle. The fungicide passively exudes into themedium from the palm tissue.

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was in the distal portion of the rachis sampledat 90 days post-fungicide application. Thegreatest amount of thiabendazole detected inthe palm canopy was at 30 days after fungicide

infusion (October 21). Thereafter, the levelsdropped. Of particular note is the detection ofthiabendazole in leaf -1 (“upper” leaf onDecember 21). While the fungicide was not

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Table 1. Quantity of thiabendazole detected in leaf tissue after coconut palms were infused with Arbotect 20-S on 21 September 2009.______________________________________________________________________________________

µg/g thiabendazolew________________________________________________________________________Location 30 daysx 60 days 90 days

in ____________________ _______________________ ______________________ Tree Canopy Py B D P B D P B D______________________________________________________________________________________

I Lowerz 215 NS NS 106 112 89 53 44 22

Middle 220 NS NS 108 56 50 88 86 90

Upper 217 NS NS 113 112 44 136 110 0

II Lower 208 NS NS 107 133 73 50 73 10

Middle 215 NS NS 61 108 97 64 46 0

Upper 210 NS NS 102 101 68 90 92 0

III Lower 215 NS NS 104 92 74 86 94 48

Middle 180 NS NS 90 89 94 66 65 36

Upper 186 NS NS 72 77 47 127 123 0

IV Lower 186 NS NS 59 51 48 8 0 0

Middle 193 NS NS 23 20 17 32 34 0

Upper 180 NS NS 42 46 35 50 40 0

Mean ± SD

Lower 206±14 94±23 97±35 71±17 49±32 53±41 20±20

Middle 202±19 71±37 68±39 65±39 63±23 58±23 32±43

Upper 198±18 82±32 84±29 49±14 101±39 91±36 0±0

______________________________________________________________________________________

wValues are mean of four sub-samples per tissue piece sampled and are based on fresh weightof sample tissue. NS = not sampled. The regression equations used to calculate these valueswere y = -0.0003x2 + 0.2671x + 2.2771 (R2 = 0.983; P = 0.0001); y = -0.0003x2 + 0.2377x +3.0759 (R2 = 0.951; P = 0.005); and y = -0.0003x2 + 0.2297x + 2.776 (R2 = 0.963; P = 0.003)for sampling at 30 days, 60 days and 90 days, respectively.

xDays after treatment on 21 September 2009.

yP = petiole (leaf base); B = basal portion of rachis; D = distal portion of rachis.

zLower = older leaf (leaves 8, 9 and 10); Middle = mid-canopy leaf (leaves 3, 4, and 5);

Upper = younger leaf (leaves 1, 0 and -1).

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detected in the distal portion of this leaf, itwas detected in the petiole and basal portionof this leaf and at levels equivalent to or greaterthan the older leaves. While Fusarium wasinhibited in the 30-day post-application assay,thereafter, the amount of thiabendazole wastoo low for detection with Fusarium and couldbe detected only with the Penicillium assay.

Discussion

This experiment demonstrated that it ispossible for a xylem-mobile fungicide to movepassively into the palm canopy (via trunkinfusion) and persist for at least 90 days,although at low levels. These low levelsjustified using the Penicillium isolate in thebioassay. Although the thiabendazole levelspresent in the leaves (leaflets, petiole or rachis)were usually not great enough to inhibit sporegermination and growth of one of our targetpathogens, Fusarium oxysporum f. sp. palmarum,it is important to remember this is an in vitrobioassay. Further testing will be necessary todetermine the levels of thiabendazolenecessary to either prevent diseasedevelopment or significantly reduce the speedof disease development in living palms.

An important aspect of this study is the factthe fungicide thiabendazole was moving intoleaf tissue that was in development at the timeof the fungicide application, as it was detectedin a leaf that emerged after the fungicide hadbeen applied (leaf -1). The level of thia-bendazole in this newly emerged leaf wasequivalent to levels in leaves present at thetime of the application. Longer term studieswould be useful to determine just how manydeveloping leaves are affected by a singleapplication of the fungicide, and whethermultiple applications per year are required tomaintain inhibitory levels.

A primary hindrance to the application offungicides such as thiabendazole via the trunkis the amount of material that must be used.The rate selected for this study required theinfusion of 120 ml per palm. If applied asspecified for dicot trees, the formulatedmaterial should have been diluted with water,which was not feasible. In contrast, theamount of the most commonly usedformulated oxytetracyline material (Tree-Saver®) being injected into coconut palms formanagement of lethal yellowing is never morethan 6.5 ml per palm. Thus, a single antibioticdose can be easily injected into a palm.Likewise, with phosphonate injections into

coconut palms for bud rot, the amount offormulated material does not exceed 25 ml perpalm (Thevenin et al. 1995).

Thiabendazole levels appear to decline overtime, which would be similar to oxy-tetracycline. This indicates there would be aneed to treat palms more than once a yearwith xylem-mobile fungicides. It also appearsthat it might take time for thiabendazole tomove into the canopy. There was moreconsistent detection of thiabendazole in theleaflet tissue at 30 days (all 4 treated palms)than at 10 days post-application (only 3 of 4palms). This might explain why anotherbenzimidazole fungicide, carbendazin phos-phate, was not detected in palm leaf tissue ina California study in the 1970s (Feather 1982).In that study, researchers trunk injectedcarbendazim phosphate into a Phoenixcanariensis (Canary Island date palm) withabout ~4.5 m of trunk. After 48–56 hours,palms were felled, and trunk, bud and leaftissue were bioassayed for the fungicide, whichwas detected in the trunk and bud tissue butnot in the leaf tissue. In our study, a verylimited amount of thiabendazole was detectedin leaflet tissue and it was detected in leafletsof only a few leaves during the first twosampling dates. This is in stark contrast to theconsistent detection of thiabendazole in thepetiole and rachis tissue of the same leaf. Thismay be a methodology issue as there isprobably more exposure of vascular tissue inthe internal petiole and rachis tissue than inthe leaflet disc tissue.

In summary, passive uptake of thiabendazole,a xylem-mobile fungicide, into the palmcanopy after trunk infusion was demonstratedbased on a bioassay with a Penicillium isolatesensitive to this fungicide. The fungicide couldbe consistently detected in petiole and rachistissue, but not leaflet tissue, for at least 90 daysafter fungicide application.

Acknowledgments

Funding for this project was provided by agrant from the International Palm Society. Wethank Elizabeth Des Jardin and Susan Thor fortheir support in this research project.

LITERATURE CITED

DARVAS, J.M., J.C. TOERIEN AND D.L. MILNE. 1984.Control of avocado root rot by trunkinjection with phosethyl-Al. Plant Disease68: 691–693.

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DRANSFIELD, J., N.W. UHL, C.B. ASMUSSEN, W.J.BAKER, M.M. HARLEY AND C.E. LEWIS. 2008.Genera Palmarum: The Evolution andClassification of Palms. Kew Publishing,Royal Botanic Gardens, Kew, Surrey, U.K.

ELLIOTT, M.L., E. HONEYCUTT, J. WEST AND P.FRANKLIN. 2011. First report of Fusarium wiltcaused by Fusarium oxysporum f. sp.canariensis on Canary Island date palm inTexas and South Carolina. Plant Disease 95:358.

ELLIOTT, M.L., E.A. DES JARDIN, K. O’DONNELL,D.M. GEISER, N.A. HARRISON AND T.K.BROSCHAT. 2010. Fusarium oxysporum f. sp.palmarum, a novel forma specialis, causinga lethal disease of Syagrus romanzoffiana andWashingtonia robusta in Florida. Plant Disease94:31–38.

ERWIN, D. C. 1973. Systemic fungicides: diseasecontrol, translocation, and mode of action.Annual Review of Phytopathology 11:389–422.

FEATHER, T.V. 1982. Occurrence, Etiology andControl of Wilt and Dieback of Phoenixcanariensis in California. Ph.D. Thesis,University of California, Riverside. 119 pp.

GUEST, D. AND B. GRANT. 1991. The complexaction of phosphonates as antifungal agents.Biological Reviews 66:139–187.

GUEST, D.I., R.D. ANDERSON, H. J. FOARD, D.PHILLIPS, S. WORBOYS AND R.M. MIDDLETON.1994. Long-term control of Phytophthoradiseases of cocoa using trunk-injectedphosphonate. Plant Patholology 43:479–492.

HARRISON, N.A., E.E. HELMICK AND M.L. ELLIOTT.2008. Lethal yellowing-type diseases ofpalms associated with phytoplasmas newlyidentified in Florida, USA. Annals of AppliedBiology 153: 85–94.

HARRISON, N.A., E.E. HELMICK AND M.L. ELLIOTT.2009. First report of a phytoplasma-associated lethal decline of Sabal palmetto inFlorida, USA. Plant Pathology 58: 792.

KOSTKA, S.J., T.A. TATTAR AND J.L. SHERALD. 1985.Suppression of bacterial leaf scorchsymptoms in American elm through

oxytetracyline microinjection. Journal ofArboriculture 11: 54–58.

MCCAIN, A.H. 1980. The influence of site onthe distribution of benzimidole fungicidesin elm. Journal of Arboriculture 61: 153–155.

MCCOY, R.E. 1974. Techniques for treatment ofpalm trees with antibiotics. Proceedings ofthe Florida State Horticultural Society 87:537–540.

MCCOY, R.E. 1976. Uptake, translocation, andpersistence of oxytetracycline in coconutpalm. Phytopathology 66: 1039–1042.

POHE, J., B.K. DONGO AND N. N’GORAN. 2003.Effectiveness of aluminum-fosetyl in thecontrol of early nutfall of coconut tree dueto Phytophthora katsurae (Pythiaceae).Agronomie Africaine 3: 123–133.

SINGH, R., A. CASTRO, D.M. FERRIN, R. S. HARRIS

III AND B. OLSON. 2011. First report ofFusarium wilt of Canary Island date palmcaused by Fusarium oxysporum f. sp.canariensis in Louisiana. Plant Disease 95:1192.

STENNES, M.A. AND D.W. FRENCH. 1987.Distribution and retention of thiabendazolehypophosphite and carbendazim phosphateinjected into mature American elms.Phytopathology 77: 707–712.

SURICO, G. 1977. Sul possibile uso del benomylnella lotta contro il “bayoud” (indotto daFusarium oxysporum f. sp. albedenis) dellapalma da dattero. II. Assorbimento edistribuzione del benomyl in piante adultee resultati di lotta in serra. PhytopathologiaMediterranea 16: 69–74.

THEVENIN, J.M., H.F.J. MOTULO, S. KHARIE AND J.L.RENARD. 1995. Lutte chimique contre lapourriture du coeur à Phytophthora ducocotier en Indonésie. Plantations,Recherche, Développement 2: 41–50.

TIMMER, L.W., R.F. LEE AND L.G. ALBRIGO. 1982.Distribution and persistence of trunk-injected oxytetracycline in blight-affectedand healthy citrus. Journal of the AmericanSociety for Horticultural Science 107:428–432.

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PALMS Dransfield et al.: Dypsis robusta Vol. 56(1) 2012

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In June 1994, people from Masomanga, avillage 2 km east of the town of Ranomafananear Ranomafana National Park in easternMadagascar, found a palm seedling with leavesless than a meter long growing at a site beingprepared for a growth trial of native Malagasytrees. As it was the only palm growing at thesite, the seedling was protected. As the palmgrew, it became apparent that it was probablya species of Dypsis but different from Dypsismananjarensis, the only other similar largeDypsis known from the area. Dan Turk’s effortsto identify the palm using The Palms ofMadagascar (Dransfield and Beentje 1995) didnot yield a match. The flora of the area nearbyis quite well known; the Ranomafana NationalPark has been the center of intensive studiesof lemurs and the flora and vegetation, yet noone who has seen the palm knows its localname or knows of other palms like it.

Fast forward to October 12th 2008, when agroup of palm enthusiasts lead by John

Dransfield came to the site and contemplatedthe palm that was beginning to flower for thefirst time. As he looked at it, Jeff Marcus, oneof the group, suggested the palm might beDypsis robusta and John Dransfield concurred.They were in a position to know, being two ofthe three authors who named Dypsis robustaHodel, J. Marcus & J. Dransf. (Hodel et al. 2005)from a palm growing on Jeff Marcus’s propertyon the island of Hawai’i. That tree had grownfrom seeds that came from an unknownlocation in Madagascar. The following monthDan Turk collected a proper herbariumspecimen from the palm and when iteventually reached Kew, John Dransfieldconfirmed the identification by comparing thespecimen with the type of Dypsis robusta.

As the only individual of its species knowngrowing in the wild (Fig. 1), the specimen ofDypsis robusta at Masomanga has a legitimateclaim to the title “Rarest Tree in the World inthe Wild.” Fortunately, Dypsis robusta is not

Dypsis robustaFound in theWild

JOHN DRANSFIELDHerbarium, Royal BotanicGardens, Kew, Richmond,Surry, TW9 3AE, [email protected]

JEFF MARCUS

Floribunda Palms, P.O. Box 635, MountainView, Hawai’i, HI96771,[email protected]

AND

DAN TURKPC(USA) - SAF/FJKM, B.P.623, Antananarivo 101,[email protected]

Dypsis robusta, a large palm named in 2005 from a specimen grown in Hawai’i

but from seed that came from an unknown location in Madagascar, has been

found in the wild, just east of Ranomafana National Park.

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in immediate danger of extinction becauseseedlings from Jeff Marcus’s tree in Hawai’ihave been widely distributed, and seeds fromthe Masomanga tree also have yielded about50 seedlings that will be planted at protectedlocations around Madagascar. We feel sure thatat some time in the future it will be foundelsewhere in eastern Madagascar in the wild.

In March 2007, the site of the 1994 tree trialwas officially opened as the RanomafanaArboretum, a place for tourists and local people

to appreciate Madagascar’s amazing nativetrees. Located on a beautiful 4 ha siteoverlooking the Namorona river, theArboretum has over 180 species of native treesincluding many, like Dypsis robusta, thatarrived at the site on their own, withouthuman intervention. The Arboretum serves asan ex situ protection site for rare Malagasypalms such as Dypsis scandens, Dypsis basilongaand Tahina spectabilis. Since 2009, theRanomafana Arboretum also has the largestcollection of fruit trees at one location in

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1. Dypsis robusta and Germain Andrianaivoson at the Ranomafana Arboretum, October 2011.

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Madagascar (over 170 different varieties),including low-chill varieties of peaches andapples and ultra-tropicals such as mangosteen,pulasan, and breadfruit. The fruit trees arecontributing to efforts to improve food securityand increase income for farmers insoutheastern Madagascar. The RanomafanaArboretum is owned by the Commune ofRanomafana and managed by a localcommittee with technical assistance from theDevelopment Department of the FJKM church.

Dypsis robusta is a very ornamental palm withone of the largest inflorescences in the genus.In October 2011, Dypsis robusta at theRanomafana Arboretum had a tremendousinflorescence, 2.8 m wide and over 3 m long(Fig. 2).

Dypsis robusta is among a group of fiveMalagasy palms that were first described fromspecimens cultivated outside Madagascarwithout knowledge of the species’ locationsin the wild. Along with Dypsis robusta, D.albofarinosa, D. carlsmithii and D. leptocheiloshave now been found in the wild (although D.albofarinosa has yet to be documented with aherbarium specimen), leaving only the naturalhabitat of D. plumosa yet to be discovered.

LITERATURE CITED

DRANSFIELD, J. AND H. BEENTJE. 1995. The Palmsof Madagascar. Royal Botanic Gardens, Kewand the International Palm Society.

HODEL, D.R., J. MARCUS AND J. DRANSFIELD. 2005.Dypsis robusta, a large new palm fromcultivation. Palms 49: 128–130.

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2. The enormous inflorescence of Dypsis robusta at the Ranomafana Arboretum. Germain Andrianaivosonprovides scale.

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The genus Ceroxylon is a characteristic elementof the Andean mountains and includes theworld’s tallest palm, Ceroxylon quindiuense,growing up to 60 m tall, and the palm thrivingat the highest elevation, Ceroxylon parvifrons,which occurs at altitudes up to 3500 m inEcuador (Borchsenius & Moraes 2006).

Ceroxylon comprises twelve species (Sanín &Galeano 2011), and is most diverse inColombia, where seven species occur (Galeano& Bernal 2010). Four of the species occurringin Colombia are considered threatened(Galeano & Bernal 2005, Bernal & Galeano2006), mostly as a result of habitat loss. Threeof these species are categorized as endangered— Ceroxylon alpinum, disjunct in Colombiaand Venezuela, C. quindiuense, disjunct inColombia and Northern Peru (Galeano et al.2008) and C. ventricosum, ranging fromsouthern Colombia to Ecuador. The fourthspecies, Ceroxylon sasaimae is endemic to

Colombia and is considered to be criticallyendangered.

Ceroxylon sasaimae was described in the late20th Century from palms growing amongcoffee plantations on the western slopes of theEastern Cordillera near Bogotá (Galeano 1995),and no more than 100 adult individuals wereknown in the first years of this Century [thefigure mistakenly given as 200 by Galeano andBernal (2010)], mostly in the municipalities ofSasaima and San Francisco (Galeano & Bernal2005). Many young plants are now grown onfarms near the type locality and elsewhere, asinterest in this critically endangered endemichas grown in the country.

The former distribution of this species isunknown. Its original habitat, premontaneforest, is one of the most severely alteredecosystems in Colombia, as it is the idealclimate for cultivating coffee, one of the

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The CriticallyEndangeredCeroxylonsasaimaeRediscoveredin the Wild

RODRIGO BERNALInstituto de Ciencias Naturales,Universidad Nacional deColombia, Apartado 7945, Bogotá, [email protected]

HÉCTOR FAVIO MANRIQUEJardín Botánico del Quindío,Calarcá, Quindío, [email protected]

The critically endangered wax palm Ceroxylon sasaimae was previously known

only from adult palms surviving in agricultural areas on the Eastern Cordillera

of Colombia. A wild population has been discovered in a forest fragment on the

Central Cordillera, 144 km northwest of its known locality, and across the deep

Magdalena river valley.

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country’s major crop plants. Most extant palmsnear the type locality are probably survivors offormer forest rather than cultivated plants. Noplants had been recorded in forest habitats.

During recent field work in the CentralCordillera of Colombia, in the Department ofAntioquia, we discovered the first recordedwild populations of Ceroxylon sasaimae (Figs.

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1. Ceroxylon sasaimae (foreground, left) in recently cleared forest near San Luis, Antioquia,Colombia, with Euterpe precatoria and Wettinia kalbreyeri.

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1 & 2), ca. 144 km northwest of its currentlyknown distribution, and across the warmMagdalena River valley. The palm grows inpremontane forest on the eastern slope of the

Cordillera near the town of San Luis, an areathat remained off limits to botanists duringthe last 25 years due to warfare but is now atpeace and accessible. We spotted eight

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2. Crown of Ceroxylon sasaimae near San Luis, Antioquia, Colombia.

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individuals in a forest remnant and in adjacentareas that have been cleared for pasture andgrowing coffee, at an elevation of 1350–1460m (Fig. 3). The forest in that remnant reachesup to 1952 m and harbors other palm speciescommon in premontane forests at thenorthern end of the Central Cordillera, suchas Euterpe precatoria, Pholidostachys synanthera,Welfia regia and Wettinia kalbreyeri (Fig. 1).

Forest remnants near this locality with thesuitable elevation for C. sasaimae cover an areaof ca. 2800 ha in two separate blocks (Fig. 4).However, we do not know the extent of thearea where the palm actually grows withinthese remnants. The species does not grow inforests at the same elevation farther north orfarther west on the same slopes of theCordillera. It might occur in a big forestremnant ca. 30 km south of San Luis, but thatarea has not been explored for palms, as it wasalso inaccessible during the last two decades.

We were not able to estimate the number ofadult individuals of C. sasaimae at the newlocality but judging from palms left in pasturesand crowns spotted in the forest canopy, thepalm is not abundant. It is certainly far lesscommon than the three other large palms seenin the area, Euterpe precatoria, Welfia regia andWettinia kalbreyeri.

We have made no attempt to re-categorize thespecies under IUCN Red List parameters (IUCN2001), awaiting a detailed exploration of the

area and a better understanding of thepopulation’s structure. However, the finding ofthis new population probably will not alterthe conservation status of the species asCritically Endangered (CR), considering thesmall size of the forest remnant where it grows,the low density of the palm and thecontinuing deforestation in the area, whichwill probably increase now that peace returnedto this zone and people who had fled fromthe area are returning and expanding theagricultural frontier. There were clear signs ofrecent deforestation at the place.

SPECIMEN EXAMINED. COLOMBIA. Anti-oquia. Municipio de San Luis, VeredaManizales, Finca San Judas, 7 km NW of SanLuis, on the left margin of Río Dormilón, 6°04’50.9’’N, 75°01’34.9’’W, 1459 m alt., 28August 2011, Bernal & Manrique 4766 (COL).

Acknowledgments

Field work was supported by Instituto deInvestigación de Recursos Biológicos Alexandervon Humboldt and Jardín Botánico delQuindío. We thank Juan Lázaro Toro for helpduring field work and for enlighteningdiscussion, and Gloria Galeano and María JoséSanín for critically reading the manuscript.

LITERATURE CITED

BERNAL, R. & G. GALEANO. 2006. Endangermentof Colombian Palms (Arecaceae): change

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3. Forest and clearing with Ceroxylon sasaimae near San Luis, Antioquia, Colombia.

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over 18 years. Botanical Journal of theLinnean Society 151: 151–163.

BORCHSENIUS F. & M. MORAES. 2006. Diversidady usos de palmeras andinas (Arecaceae). Pp.412–433, in MORAES, M., B. ØLLGAARD, F.BOCHSENIUS & H. BALSLEV (eds.). BotánicaEconómica de Los Andes Centrales.Universidad Mayor de San Andrés, La Paz.

GALEANO, G. 1995. Novedades en el géneroCeroxylon (Palmae). Caldasia 17: 395–408.

GALEANO, G. & R. BERNAL. 2005. Palmas (familiaArecaceae o Palmae). Pp. 59–223 in E.CALDERÓN, G. GALEANO & N. GARCÍA (eds.).Libro Rojo de Plantas de Colombia, Volumen2. Ministerio de Ambiente, Vivienda yDesarrollo Territorial/ Instituto Alexandervon Humboldt/Instituto de CienciasNaturales, Bogotá.

GALEANO, G. & R. BERNAL. 2010. Palmas deColombia. Guía de Campo. EditorialUniversidad Nacional de Colombia, Bogotá.688 pp.

GALEANO, G., M.J. SANÍN, K. MEJÍA, J.-C. PINTAUD& B. MILLÁN. 2008. Novelties in the genusCeroxylon (Arecaceae) from Peru, withdescription of a new species. Revista peruanade biología 15(supl. 1): 65–72.

IUCN. 2001. IUCN Red List categories andcriteria: Version 3.1. IUCN, The WorldConservation Union, Gland, Switzerland.

SANÍN, M. J. & G. GALEANO. 2011. A revision ofthe Andean wax palms, Ceroxylon (Are-caceae). Phytotaxa 34: 1–64.

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4. Google Earth image of the forest fragments where Ceroxylon sasaimae grows near San Luis,Antioquia, Colombia. The yellow and green lines mark the contour lines of 1350 and 1800 m,respectively, the altitudinal range where the species is expected to occur. Arrows show therelevant forest fragments within this range. The red dot marks the place where the palm wasphotographed and collected.

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PALMS Ruppert et al.: Calamus Inflorescence Vol. 56(1) 2012

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New ShootsfromInflorescencesin Calamuscastaneus inPeninsularMalaysia

NADINE RUPPERT, ASYRAF MANSORAND

SHAHRUL ANUAR MOHD SAH

School of Biological Sciences,Universiti Sains Malaysia, 11800 Penang, Malaysia,[email protected]

Calamus castaneus (subfamily Calamoideae) is one of the most common rattan

species in Peninsular Malaysia yet little is known about its reproductive behavior.

Although C. castaneus is known to produce new shoots from its stem, here, we

present evidence of the formation of a new shoot from the inflorescence apex.

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1. Acaulescent non-climbingrattan Calamus castaneus.

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Calamus castaneus (Calamoideae) is one ofseveral non-climbing rattan species inPeninsular Malaysia. With its acaulescenthabit, its chestnut-colored fruits, bright yellow-based spines and broad lush green leaves thatare gray on the undersurface, it is easilyrecognizable and helps shape the undergrowthvegetation of primary lowland forests in theregion (Fig. 1).

Calamus castaneus usually produces inflor-escences up to about 45 cm long that are bornelow on the abaxial surface of the leaf sheathimmediately above the subtending axil, theorigin obscured by other leaf sheaths. Femaleinflorescences have about 15 rather stiffcrowded rachillae covered with dense bracts.Male inflorescences are more highly branched,more lax and sinuous (Dransfield 1979). The

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2. Normal male inflorescence of Calamus castaneus with closed flowers towards its distal end.

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apex seems to continue growing for a whileproducing new rachillae towards the end ofthe inflorescence (Fig. 2). Normally, growthstops and after single flowers undergo anthesis,subsequently the flowers fade and the wholeinflorescence becomes dry and drops off.

Here we record a male individual of C.castaneus that produces a new vegetative shootfrom the apex of the inflorescence. It wasfound growing in a primary forest site in SegariMelintang Forest Reserve on the west coast ofPeninsular Malaysia (4°18–19’N, 100°34–35’E).The whole reserve has a size of 4566 ha andcontains mainly primary forest and alluvialfresh water swamp vegetation. It hosts a

relatively high number of individuals of C.castaneus with an average of approximately 60per hectare along its western edge (a total of5 ha is being sampled at the moment). Thedescribed male individual was found at a drylowland site growing next to a small seasonalstream (at 04°19.581’N, 100°34.988’E). Threeother male individuals were found in veryclose proximity (less than 0.5 m from stem tostem) with all of them flowering but none ofthem bearing similar shoots.

This male flower-bearing individual was foundproducing a vegetative shoot arising from theapex of its inflorescence (Figs. 3–5). The shootseemed already mature and well developed

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3. Vegetative shoot arising from the apex of a male inflorescence of Calamus castaneus.

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during the observation period (9 Nov 2011 to27 Jan 2012), although no roots were present.All the male flowers of this particularinflorescence had faded and no longerproduced fresh pollen. Other inflor-escenceson the same plant were producing fresh pollenand buds were present.

Other individuals of C. castaneus growing inthe 1-ha study plot were closely examined ina survey walk after the shoot was discoveredbut none of them showed a similarphenomenon so far. Two out of 62 samplesindividuals, however, were bearing axillaryshoots growing at the base of the stem of themother plant (Fig. 6).

A local villager living near the forest andhaving vast experience in entering the studyarea reported to us that he already foundexamples of new shoots developing frominflorescences in C. castaneus in former times.Sometimes one plant would produce up tofour shoots at a time. Although we have noreason to doubt him, further investigation isrequired to verify his statement.

With the current results at hand, the specificecological role of this shoot proliferation is

unclear. As more individuals of C. castaneus ina 1-ha study plot were examined and none ofthem showed similar behavior to date, we donot know whether this shoot proliferationrepresents an alternative to sexual repro-duction in the species or if it is a one-offmutant individual. Furthermore, we do notknow whether these vegetative shoots havethe ability to root and establish new plantsonce in contact with the ground.

Asexual reproduction is quite common inmany seed plant species in general and thisreproductive method might be of advantage ifthe environment has been stable for manygenerations and genetic variability may play aminor role for species survival.

Many rattan species are clustered, but in thesethe production of axillary shoots only adds tothe size of the individual cluster, not to theestablishment of independent plants. Inrattans, unusual asexual reproduction has beenreported in some species in Borneo, with thedevelopment of new axes at the tips of theinflorescences; these eventually root and, withthe rotting of the old inflorescence, developinto independent individuals. Examples areDaemonorops ingens, Calamus pygmaeus and a

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4. Vegetative shoot arising from the apex of a male inflorescence of Calamus castaneus.

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form of Calamus nematospadix (Dransfield1992). Asexual reproduction can also occur ina few palm species in the Peninsular Malaysia,e.g. Salacca flabellata (Furtado 1949). A moredetailed and longer-termed survey of thisphenomenon needs to be undertaken to clarifyits role in the ecology and reproductive biologyC. castaneus.

Acknowledgments

The authors thank John Dransfield for hiscomments on the manuscript. This study wasfinanced by RU USM-Postgraduate ResearchGrant (1001/-PBIOLOGI/843098) and

Universiti Sains Malaysia Research UniversityGrant (1001/PBIOLOGI/811131).

LITERATURE CITED

DRANSFIELD, J. 1979. A Manual of the Rattansof the Malay Peninsula. Malayan ForestRecords 29. Forest Department, Ministry ofPrimary Industries, Malaysia.

DRANSFIELD, J. 1992. The Rattans of Sarawak.Royal Botanic Gardens Kew and SarawakForest Department.

FURTADO, C.X. 1949. Palmae Malesicae X. TheMalayan species of Salacca. Gardens’Bulletin, Singapore 12: 378–403.

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5 (left). Vegetative shoot arising from the apex of a male inflorescence of Calamus castaneus. 6(right). Vegetative shoots of Calamus castaneus arising from its stem.

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The 600-acre Nong Nooch Tropical Gardenthat lies some 163 km southeast of Bangkok,is perhaps one of the world’s largest privately

owned gardens. The land was originallypurchased to create a mango and other fruitorchard for Mr. Pisit and Mrs. Nongnooch

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Nong Noochand the IPSBiennial 2012

LELAND LAI

Topanga, CA 90290 USA

The 2012 Biennial will take place in Nong Nooch Tropical Garden in September,

2012. The palm collection at Nong Nooch promises to be dazzling (Fig. 1).

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1. Bromeliads andCyrtostachys rendaare part of thespectacular gardensat Nong Nooch.

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Tansacha. The Garden formally opened to thepublic in 1980, and the orchard wastransformed into themed sub-gardens. NongNooch has evolved through the years, andunder the guidance of Kampon Tansacha, theGarden, dedicated to preservation, researchand conservation, has now taken on another

primary goal of education for generations tocome.

For those IPS members lucky enough to haveattended the 1998 Biennial in Thailand, NongNooch comprised six gardens displaying theartistry of landscaping, palm collections, floral

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2. Nong Nooch’s grounds include temples and other landscape features.

3. Biennial participants will want to spend time in the Palm Shadehouse.

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and theme-based gardens (Figs. 2 & 3). Sincethen, an aerial walkway over one kilometerlong has been established over part of thecollection for canopy viewing, and severalmore venues have been developed includingone of the world’s most extensive collectionsof cycads, a lake where one can feed giantcatfish and a reproduction of Stonehenge inthe English garden (Fig. 4). Transformation hasincluded non-plant related venues (expandedcultural shows, rides and exhibits) that havebeen added to broaden the interest base foryounger children, who often accompanygrandparents during day visits while parentswork. Education, conference and hotelfacilities make the garden a haven foreverything botanical.

The 2012 Biennial will be the 28th IPS Biennialsince the first one in 1958 (Miami). The 2012IPS Biennial starts (Day I) on Tuesday, 11thSeptember 2012, and will be a seven-day,seven night Thai extravaganza endingTuesday, 18th September. The pre-Biennialtour will go to southern Thailand and will endin Bangkok at the start of the Biennial. The

post-Biennial tour to Vietnam is beingorganized by the New York Botanical Garden’sDr. Andrew Henderson ([email protected]), starting on Tuesday, 18th September (seeannouncement in the Supplement to Palms55(4) Dec. 2011).

Information on registration will be posted inthe March Supplement to Palms, on the IPSwebsite (www.palms.org) and on PalmTalkshortly (www.palmtalk.org/forum). Space islimited, so register early to take advantage ofearly registration discount and to reserve yourplace.

Day I: Tuesday 11th September: Arrival atBangkok (Suvannaphum Airport), hotel check-in and the welcoming dinner will be held inBangkok. Those of you deciding to arriveearlier can do so over the weekend, leavingyou ample time to recover and explore thewonders of Bangkok, its temples, klongs(canals), shops and open markets.

Day II: Wednesday, 12th September: Visit toa private palm garden within Bangkokfollowed by viewing Pinanga sylvestris, Licuala

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4. Stonehenge at Nong Nooch. Photo by Paul Craft.

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poonsakii and other palm species in theirnatural habitat to the north in the Khao YaiNational Park, the oldest and second largestnational preserve in Thailand. We will be thereduring the rainy season (May to October)when on most days there is a high chance ofprecipitation and high humidity with averagetemperatures of 27°C (80°F) during the day,dropping to 13°C (55°F) at night; bring

appropriate clothes and rain gear. There areabundant waterfalls, as the park is locatedwithin three mountain ranges that are hometo 3,000 species of plants, 320 species of birdssuch as red jungle fowl and green peafowl and67 species of mammals including Asiatic blackbear, Asian elephant, gaur, tiger, gibbon, Indiansambar deer, pig-tailed macaque, Indianmuntjac, dhole and wild pig. The park

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5. The hotel in Nong Nooch in which Biennial attendees will stay. Photo by Paul Craft.

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encompasses forests and grasslands, rangingfrom 400 to 1000 m above sea level. Dinnerand overnight will be at the Juldis Hotel, KhaoYai.

Day III: Thursday, September 13th: In themorning a visit to view wild populations ofCorypha lecomtei. Lunch will be taken on ourarrival at Nong Nooch Garden 2 in

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6. Copernicia fallaensis, one of the many rare species in the Nong Nooch collection.

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Prachinburi, where we will see plantings inthis new garden extension before going on toNong Nooch Tropical Garden in Pattaya,where the 1998 event was held. IPS Biennialguests will stay in NNTG’s own hotel (Fig. 5).

Day IV: Friday, 14th September: Tour thewonders of Nong Nooch Tropical Garden,starting from the Orchid House, Palm Gardenat the Thai House, French Garden, VarietyGarden and ending at the Cactus Garden

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7. Carpoxylon macrospermum, another rare species. Photo by Paul Craft.

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before lunch. The afternoon brings us to thePalms of the World (Figs. 6, 7 & 8). Of theestimated 2,400 species of palms existing in theworld, NNTG has approximately 1,100 species.The idea that NNTG will become a livingrepository of palms has credibility, for factorsof climate, care and maintenance and itsmanagement’s enthusiasm for collecting palms

have joined to assure this continuing objective.With the further advancement of palm studiesworldwide and rapid destruction of forestswhere palms formerly dwelled, both visitorsand scientists have yet another option atNNTG of a primary source of palm species forwhich they would otherwise not be able to seeor to collect specimens.

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8. Saribus rotundifolia. Photo by Paul Craft.

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Growth of palms has been spectacular,sometimes surprisingly so. For exampleLodoicea maldivica, often cited as not floweringand fruiting until at least 30 years old, has, inNong Nooch, started to flower at 18 years old,with seed being produced in year 23. A fruit,still somewhat immature, was x-rayed at a localhospital to examine seed and embryodevelopment (Fig. 9).

The day will conclude at Cart Cross Arboretumfor our first series of guest speakers followedby dinner at Nong Nooch.

Day V: Saturday 15th September: Free daywhere attendees will be given a multitude ofsports, beach, and tour activities on the coast,or in nearby villages, or just a day to relax andrevisit parts of the garden. Members of the IPSBoard of Directors will hold the annualmeeting.

Day VI: Sunday 16th September: Our tour ofNNTG continues with the Cycad Collectionand Hortus Botanicus plant collection, withafternoon visit to the themed gardens. We endthe day with our second series of guest speakersfollowed by dinner.

Day VII: Monday17th September: Morningevents with Thai cultural show and theElephant performances at NNTG. Lunch andafternoon is on your own, but our FarewellDinner will start at 6:30pm at the Nanta Lawn.

Day VIII: Tuesday 18th September: Attendeesdepart Nong Nooch for Suvannaphum airport(BKK) and the start of the Post Biennial Tourto Vietnam.

Stay tuned to the Supplement, PalmTalk andthe IPS website for updated announcementsconcerning this not-to-be missed event. Seeyou in September!

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9. An x-ray of a mature fruit of Lodoicea maldivica reveals the four chambers partially filled with endosperm.

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PalmsJournal of the International Palm Society Vol. 56(1) Mar. 2012