TL;DR: The hypothesised, but never formally recognised, close association between the genera Garuga and Boswellia is reinforced and the position of the recently discovered Beiselia is resolved as a distant sister to the rest of the Anacardiaceae.
Abstract: Summary. The intron of the plastid rpsl6 gene was sequenced for 13 species in 11 genera of Burseraceae and three genera of Anacardiaceae. Parsimony analysis produced just three strongly supported trees. Canarieae and Protieae are shown to be monophyletic with 100% bootstrap support. Bursereae, however, are paraphyletic with two distinct clades corresponding to the subtribes. The hypothesised, but never formally recognised, close association between the genera Garuga and Boswellia is reinforced. The close association between the South American genus Bursera and African genus Commiphora is clearly demonstrated. The position of the recently discovered Beiselia is resolved as a distant sister to the rest of
TL;DR: Two new species of Encyrtidae from Dehradun, Uttarakhand, India, that parasitize Phacopteron lentiginosum Buckton (Hemiptera: Psyllidae), a leaf-galler of Garuga pinnata Roxburgh (Burseraceae), are described.
Abstract: Two new species of Encyrtidae, Psyllaephagus phacopteron sp. nov. and Psyllaephagus garuga sp. nov. (Hymenoptera: Chalcidoidea) from Dehradun, Uttarakhand, India, that parasitize Phacopteron lentiginosum Buckton (Hemiptera: Psyllidae), a leaf-galler of Garuga pinnata Roxburgh (Burseraceae), are described. The two species are differentiated from other known Indian species of the genus through modifying a previously published key to species.
TL;DR: This work is extended to a revision of the whole genus Floribunda because the species of this genus are not easily distinguishable when sterile and the identification of such specimens is all too often made on geographical evidence.
Abstract: Tn the Malaysian area proper this small genus is represented by one species only (G. floribunda), but it seemed preferable to extend this work to a revision of the whole genus. The species of this genus are not easily distinguishable when sterile and the identification of such specimens is all too often made on geographical evidence.
TL;DR: The present paper gives only additions to and alterations of Lam’s monograph, and descriptions, synonyms, litterature, specimens cited, ecological and other notes are only mentioned insofar as they are not given by Lam.
Abstract: Of this series of preparations to the definite publication of the Burseraceae in “Flora Malesiana”, the present part is giving an additional note on VI. Garuga and dealing with the genera VII. Triomma, VIII. Dacryodes and IX. Santiria (and a new combination in Protium).
The present paper gives only additions to and alterations of Lam’s monograph (H. J. Lam, Bull. Jard. Bot. Buitenz., Ser. 3, 12, 1932, 281— 561); descriptions, synonyms, litterature, specimens cited, ecological and other notes are only mentioned insofar as they are not given by Lam.
TL;DR: It is evidenced both by the characters and by area disjunction that Haplolobus must have originated bi- or polytopically from Santiria in Eastern Malaysia, and three different areas are in the way of genorheithra, migrating either eastward or westward in Malaysia.
Abstract: The Burseraceae comprise 3 tribes which show an increasing differentiation from West to East and have, accordingly, their points of gravity in America ( Protieae), Africa (Bursereae) and Asia to Australia-Polynesia (Canarieae) respectively. An eastward migration of the order is probable. The easternmost tribe comprises 5 genera, viz. Scutinanthe, Canarium, Santiria, Dacryodes and Haplolobus. These are tested regarding their fundamental characters, in order to calculate their ”phase indices“. In these calculations 1 (of the series 1, 1½, 2, 2½, 3) means the most primitive, 3 the most advanced condition of a feature. From the figures thus obtained and from geographical data, it is concluded that Haplolobus (area: Borneo to New Guinea inclusive; map 1) is the youngest genus of the five, whilst the four others must have originated in East Asia more or less simultaneously from the ”Procanarieae“ which where at that time still closely related to the ancestors of Garuga (Protieae). It is further evidenced both by the characters and by area disjunction that Haplolobus must have originated bi- or polytopically from Santiria in Eastern Malaysia. Santiria shows a recent species explosion in the Sunda Land, Haplolobus in New Guinea (map 2). In ”Wallacea“ the last-named genera are apparently either in regression (Santiria) or scantily developing (Haplolobus). The paper proceeds with considerations on migration tracks in Malaysia and adjacent regions (map 3), checked by a short survey of the geological history since the early Tertiary. From the last-named survey it is concluded that three different areas are in the way of genorheithra, migrating either eastward or westward in Malaysia, viz. 1. the old and large continental Sunda Land which enabled rapid migrations and large ”species explosions“; 2. ”Wallacea“ which with its continuous insular character has always been a serious impediment to migrations and which consequently is to be considered as a sieve for potentialities; and 3. the Sahul Land which is also continental, but younger and smaller than the Sunda Land. These conditions (among others) are responsible for the fact that so much more Asiatic types have reached Australia and Polynesia than Australian types reached Asia. The paper closes with a tentative reconstruction of the tertiary and quaternary phylogeny of the Canarieae in the region under discussion (fig. 1).