Common Names
Thông lá det, Ngo rí (Vietnamese) (21).Taxonomic notes
Syn: Ducampopinus krempfii (Lecomte) A.Chev. (20). On purely morphological grounds, this is probably the most unusual species in the genus due to its flattened, ribbed, blade-like needles. The needles have a singular vascular bundle, thus the species is commonly assigned to Subgen. Strobus (22), but Little and Critchfield (23) assigned it to a distinct subgenus, Ducampopinus (A. Cheval.) de Ferré. The composition of heartwood phenolics is very typical of haploxyon pines (22), but recent work in DNA sequencing suggests the species may be basal to both haploxyl and diploxyl pines (24). In conclusion, the precise placement of this species in Pinus is still very much an open question.The taxon Pinus krempfii var. poilanei Lecomte (2) was described on the basis of its needles being longer, 6–7 cm, and much broader, 4–5 mm, than the material Lecomte had first described (1). Increased knowledge of the growth pattern of the species (4, 5, 14) shows it to be the normal immature (not juvenile) foliage of the species, retained until the tree is at least to 12 m tall and 25 cm in diameter, while growing in shade.
Description
Tree to 35-55 m tall and 200 cm dbh (12, 13, 21), with a monopodial bole, often buttressed (21), and a broad domed crown with many large branches (12, 14, 21).Bark is silvery grey, scaly-flaky (2), peeling off into irregular fragments, having resin ducts (21), similar to the species of section Gerardiana (12).
Needles are lanceolate-falcate, 3-6 cm long, 2-4 mm wide on adult trees, much larger on juvenile trees. The fascicle sheath is composed of few broad acute scales in an alternate arrangement (2), with each scale markedly longer than the previous, the longest to 15 mm, to 40% of the full length of the fascicles examined (12, 14). The sheath is early deciduous; similar to that of P. bungeana, though in that species the scales are arranged in a loose spiral. Foliage is flattened on weak shoots (12), with fascicles flattened and held flat in a single plane, unique in Pinus. On stronger shoots foliage is all around the shoot (15, 18). The shoots are glabrous, with small (1 mm) decurrent scale-leaf bases deciduous by the second to fourth year. This gives the leafless shoot a strong similarity to some piñons, and most notably to P. pinceana, and later, after the scale leaf bases are shed, to P. bungeana. Shoots low on old trees (12) and young trees in shade (13) are very slender and slow-growing (1-4 cm long, 1.3 mm thick), with 2-10 scattered fascicles on each year's growth, here again resembling P. pinceana; stronger, coning shoots are more typical for a pine, 5-10 cm long and 3-5 mm thick with numerous fascicles (15).
Male cones are sometimes carried on small weak, ± pendulous, tassel-like shoots with few to no needle fascicles (12), a feature shared with P. pinceana. Immature pollen lacks the air bladders seen on pollen of all other pines, though this may be due to the immaturity of the pollen, dissected out of c. 2-3 months premature male cones (19). Mature pollen still undescribed.
Mature seed cones 3.5-6 cm long (ovate, 4-9 cm in (21)), glossy orange-brown when freshly mature (15). Fertile scales 12-20 with a well-defined dorsal umbo and no sealing band. The apophysis has a raised transverse ridge to 3-4 mm thick, the umbo small and unarmed, with a minute (less than 0.5 mm) mucro. Scales are similar to those of P. rzedowskii. Cone peduncle 7-15 mm long, 4-5 mm thick, curved so that cone is pendulous; similar to that of P. squamata. Cones produced cones in April-May; seeds mature in July-September (21).
The seed (infertile seed in 15, and cone scale seed cavities of 13 & 14) are 4-5 mm long with a 10-15 mm articulate wing, similar to seed of P. balfouriana and P. longaeva. Seedlings are typical of many other pines, with glaucous single needles; as in other species in this subgenus and in sect. Pinea of subgenus Pinus, they are produced for several years before mature foliage appears (14).
Buchholz (5) and Little & Critchfield (23) reported the absence of ray tracheids, but Greguss (6) and Van der Burgh (11) found them to be present, as in all other pines. Erdtman et al. (7) analysed wood chemistry and found heartwood polyphenols similar to other haploxyl pines in both subsect. Strobi and subsect. Gerardianae.
Range
Vietnam: local in Khanh Hoa and Lam Dong, principally around Bi Doup mountain. The species is locally frequent, with 200 trees in one population (12). Grows emergent above the evergreen monsoon forest canopy on steep slopes at elevations of 1500-2000 m, often in mixed stands with Fokienia hodginsii, Pinus dalatensis, Dacrydium elatum and other broad-leaved trees such as Symingtonia populnea and Rhodoleia championii. Pinus kesiya forest grows at relatively higher and tropical rainforest at lower elevations (14, 21). It often grows in sites having black-grey, deep humus soils or humus-rich loamy soils along streams (21). Reportedly, natural regeneration on the site is very low (24). Regeneration can occur in deep shade on deep, humus-rich soil (12) but is better in more open situations (14).Big Tree
Oldest
Dendrochronology
Ethnobotany
Wood soft, light and slightly resinous, having good physical and mechanical properties. Can be used as Pinus kesiya (21).Observations
Can only be seen in the wild within its exceedingly limited range. I have a report that the Vietnamese a" are very proud of the few trees that are left" and it is difficult to secure permission to visit the site (24). I have yet to find it in a botanical garden.Remarks
P. krempfii can best be regarded as a primitive but otherwise fairly typical pine with a number of special adaptations to moist subtropical climate and dense forest not found elsewhere in the genus, other pines being of recent immigration to subtropical areas (9) and confined to drier substrates.Listed as threatened in Vietnam by the World Conservation Monitoring Centre. This species has attracted the interests of many Vietnamese and foreign scientists.
Citations
(1) Lecomte, H. 1921. Un pin remarquable de l'Annam, Pinus krempfii. Bull. Mus. Hist. Nat. Paris 27: 191-192.(2) Lecomte, H. 1924. Additions au sujet de Pinus krempfii H Lec. Bull. Mus. Hist. Nat. Paris 30: 321-325.
(4) Ferré, Y de. 1948. Quelques particularités anatomiques d'un pin indochinois P. krempfii. Trav. Lab. Forest. Toulouse T.1 vol.4 art.25: 1-6. (5) Buchholz, J T. 1951. A flat-leaved pine from Annam, Indo-China. American Journal of Botany 38: 245-252.
(6) Greguss, P. 1962. Le genre Ducampopinus est-il valable en vertu de sa xylotomie? Trav. Lab. Forest. Toulouse T.1 vol.6 art.13: 1-6.
(7) Erdtman, H, B Kimland & T Norin. 1966. Wood constituents of Ducampopinus krempfii (Lecomte) Chevalier (Pinus krempfii Lecomte). Phytochemistry 5: 927-931.
(8) Critchfield & Little 1966.
(9) Mirov 1967.
(11) Burgh, J van der. 1973. Hölzer der Niederrheinischen Braunkohlenformation 2. Rev. Palaeobot. Palynol. 15: 73-275.
(12) M Newman, field notes and herbarium specimens at Edinburgh RBG.
(13) K-H zur Mühlen, herbarium material at Potsdam.
(14) K Rushforth, field notes and herbarium specimens at Edinburgh RBG.
(15) Vu van Dung, herbarium specimens at Oxford Forestry Institute.
(18) Vidakovic 1991.
(19) C N Page, pers. comm. to M P Frankis, based on study of M Newman material.
(20) Silba 1986.
(21) Forest Inventory and Planning Institute 1996 (as Ducampopinus krempfii).
(22) Price et al. 1998.
(23) Little & Critchfield 1969.
(24) E-mail communication from Jerry W. Leverenz, 13-Oct-1998, reporting hearsay information.
Much of the text for this page was prepared by Michael P. Frankis.
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Edited by Christopher J. Earle
E-mail:earlecj@earthlink.net
Last modified on 2-Jan-99