Diarylpropanes from Iryanthera coriacea

The trunk wood of Iryanthera coriacea Ducke (Myristicaceae) contains six compounds which belong to the recently discovered 1,3-diarylpropane type of flavonoids, 1-(2-hydroxy-4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)-propane, 1-(2,4-dihydroxyphenyl)-3-(3,4-methylenedioxyphenyl)-propane, 1-(4-methoxyphenyl)-3-(2-hydroxy-4,5-methylenedioxyphenyl)-propane, 1-(4-hydroxy-2-methoxy-phenyl)-3-(4-hydroxy-3-methoxyphenyl)-propane, 1-(2,4-dihydroxyphenyl)-3-(2-methoxy-4,5-methylene-dioxyphenyl)-propane, 1-(2,4-dihydroxy-3,5-methylphenyl)-3-(2-hydroxy-4,5-methylenedioxyphenyl)-propane.     

Flavonoids from the leaves and twigs of Knema elegans

Knema elegans, a tropical evergreen plant, belongs to Myristicaceae family. Phytochemical investigation on the leaves and twigs of K. elegans led to the isolation and identification of two new flavonoids knemavones A and B (1 and 2), along with fifteen known analogues (3–17). These compounds belong to four subtypes of flavonoids, including chalcones, flavanes, flavones, and isoflavones. The structures of 1 and 2 were elucidated by means of spectroscopic techniques, including HRESIMS, 1D, and 2D NMR experiments. Compounds 3–17 are isolated from the title plant for the first time. Moreover, the new chalcones 1 and 2 could serve as chemotaxonomic markers of K. elegans.     

Sieve-element characters of Myristicaceae: Nuclear crystals, S-and P-type plastids, nacreous walls

The phloem of the Myristicaceae is composed of sieve elements, parenchymatous cells, and fibers. Within the metaphloem and secondary phloem parenchymatic layers including prominent secretory elements alternate with tangential bands of fibers and layers composed of sieve elements, companion cells and phloem-parenchyma cells. among the latter the sieve elements are most abundant and easily identified by the presence of thick (nacreous) walls. The most characteristic feature of the sieve elements of Myristicaceae (and found nowhere else among the Magnoliiflorae) are nuclear crystals, which are released into the lumen during nuclear degeneration and persist in the mature cell. P-and S-type sieve-element plastids were recorded for the 18 species investigated. Both types of the plastid are characterized by large diameters and many medium-sized starch grains. The sizes and contents (small protein crystals only) of the P-type plastids of the Myristicaceae do not conform to the tiny P-type plastids (with large protein crystals) of the Annonaceae, a family to which the Myristicaceae is traditionally allied.     

Gynoecium diversity and systematics of the Magnoliales and winteroids

Carpel and ovule structure was compared in representatives of all 11 families of the Magnoliales (Annonaceae, Canellaceae, Degeneriaceae, Eupomatiaccae, Himantandraceae, Magnoliaceae, Myristicaceae) and winteroids (Austrobaileyaceae, Illiciaceae, Sehisandraceae, Winteraceae). Special attention was paid to features that are constant at family level. Bisexual flowers are always protogynous. In all representatives studied the carpels are closed at anthesis. Caipel closure is attained in three different ways: (1) postgenital fusion of inner surfaces (Degeneriaceae, Eupomatiaccae. Winteraceae), or (2) occlusion by secretion (Austrobaileyaceae, Sehisandraceae), or (3) a combination of (1) and (2): in Annonaceae, Canellaceae, Myristicaceae there is a conspicuous secretory canal in the innermost part of the ventral slit; in Illiciaceae and Magnoliaceae there is a narrow canal in the innermost part of the ventral slit; and in Himantandraceae the ventral slit is postgenilally fused in the style but completely open in the ovary. In most families the carpels have a double stigmalic crest or they have two tips in the transversal symmetry plane (i.e. at right angles to the median plane). Stigmas are unicellular papillate in most families but the papillae are bi-to multicellular (uniseriate) in Degeneriaceae and Eupomatiaceae. An unusual cryptic exlracarpellary compitum was found in Himantandraceae and Sehisandraceae. Intrusive oil cells were found in the carpel epidermis of Illiciaceae and Sehisandraceae. Mature ovules vary in length between 0.15 and 1.1 mm. The outer integument is fully annular (not semiannular) in Degeneriaceae, Himantandraceae, Canellaceae, Myristicaceae, and Illiciaceae. A rudimentary aril occurs in Canellaceae, and originates at the same site as in arillate Annonaceae and Myristicaceae. The results most strongly support an Annonaceae-Myristicaceae-Canellaceae alliance, to some degree also an Eupomatiaccac-Degeneriaceae-Himantandraceae-Magnoliaceae alliance, and an Illiciaceae-Schisandraceae-Winteraccae-Austrobaileyaceae alliance.     

Two new neotropical species of compsoneura (Myristicaceae)

Brittonia - Two new species ofCompsoneura (Myristicaceae) from recent collections are described, discussed, and illustrated:Compsoneura rigidifolia, a species from the wet forest along the...     

Phylogenetic analysis of Magnoliales and Myristicaceae based on multiple data sets: implications for character evolution

Magnoliales, consisting of six families of tropical to warm-temperate woody angiosperms, were long considered the most archaic order of flowering plants, but molecular analyses nest them among other eumagnoliids. Based on separate and combined analyses of a morphological matrix (115 characters) and multiple molecular data sets (seven variable chloroplast loci and five more conserved genes; 14 536 aligned nucleotides), phylogenetic relationships were investigated simultaneously within Magnoliales and Myristicaceae, using Laurales, Winterales, and Piperales as outgroups. Despite apparent conflicts among data sets, parsimony and maximum likelihood analyses of combined data converged towards a fully resolved and well-supported topology, consistent with higher-level molecular analyses except for the position of Magnoliaceae: Myristicaceae + (Magnoliaceae + (( Degeneria + Galbulimima ) + ( Eupomatia + Annonaceae))). Based on these results, we discuss morphological evolution in Magnoliales and show that several supposedly plesiomorphic traits are synapomorphies of Magnoliineae, the sister group of Myristicaceae (e.g. laminar stamens). Relationships within Annonaceae are also resolved with strong support ( Anaxagorea basal, then ambavioids). In contrast, resolution of relationships within Myristicaceae is difficult and still incomplete, due to a very low level of molecular divergence within the family and a long stem lineage. However, our data provide good evidence that Mauloutchia is nested among other Afro-Malagasy genera, contradicting the view that its androecium and pollen are plesiomorphic  © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society , 2003, 142 , 125–186.     

1,3-diaryl-propanes and propan-2-ols from Virola species

The trunk woods of two Amazonian Myristicaceae, Virola minutiflora and V. elongata, contain respectively 1-(2-hydroxy-4-methoxyphenyl)-3-(3,4-m     

Androecium diversity and evolution in Myristicaceae (Magnoliales), with a description of a new Malagasy genus, Doyleanthus gen. nov

Myristicaceae (Magnoliales) consist of 20 genera and nearly 500 species of lowland rainforest trees with a pantropical distribution. They are distinctive in having small, unisexual flowers with stamens fused into a synandrium, which consists of a single whorl of sessile anthers borne around a sterile central column. With its short filaments and more complex anther phyllotaxy, the Malagasy genus Mauloutchia represents a notable exception to this pattern. New scanning electron microscope (SEM) examinaitons of Brochoneura, Cephalosphaera, Knema, Mauloutchia, and Staudtia are incorporated into a broader review of androecium diversity across the family. These new results are discussed in the context of a phylogenetic study of the family, based on combined molecular and morphological data. The unusual synandrium of Mauloutchia, nested among genera with strictly sessile anthers fused to the column, appears to be secondarily derived. Furthermore, the diversity of patterns observed within the genus may be interpreted as the result of a stepwise transformation involving reappearance and elongation of filaments, increase of anther number, and modification of anther phyllotaxy. However, the question of the origin of stamen fusion in Myristicaceae remains unanswered and requires more developmental studies. Finally, a new Malagasy genus of Myristicaceae (Doyleanthus) is described, which is similar to Mauloutchia in most characters but fundamentally different in androecial traits.     

Implications of collection patterns of botanical specimens on their usefulness for conservation planning: an example of two neotropical plant families (Moraceae and Myristicaceae) in Peru

We evaluated the usefulness of herbarium collection databases for assessing patterns of species diversity and distribution based on a dataset from the flowering plant families Moraceae and Myristicaceae from the Peruvian Amazon. For Moraceae, a total of 3523 collections were used representing 134 species. The Myristicaceae were represented by 2113 collections of 46 species. We evaluated the distribution of collections based on 252 grid cells (0.5° size) covering all lowland rainforest in the Peruvian Amazon. We found that collections were concentrated in a few cells and that species diversity clearly increases in relation to collection density. Moraceae were collected in only 45% and Myristicaceae in only 31% of the 252 grid cells. Fifty percent of the collections came from just six and three cells, respectively. Most species were represented by only a small number of collections and collected only in a few grid cells, meaning a few widespread common species tend to dominate the collection records. Not surprisingly, most collections were made close to towns and transport routes. We evaluated the usefulness of rarefaction curves and diversity estimators for comparing diversity between regions. These techniques seem to be of little use for botanical collections due to violations of underlying assumptions. Problems such as accuracy of geographic and taxonomic data and strong bias in the spatial representation of the whole dataset are important to consider when basing conservation analysis, planning, and decision-making on seemingly large databases of biodiversity collections and are discussed in detail.     

Isoflavones from Virola caducifolia

The Myristicaceae must be added to the small number of families which contain isoflavonoids; the previously unknown 5,7,2′-trihydroxy-4′-methoxyisoflavone and 5,7-dihydroxy-2′,4′-dimethoxyisoflavone having been found to co-occur with biochanin A in Virola caducifolia W. Rodr.     

Diet of a Group of Callicebus torquatus lugens (Humboldt, 1812) During the Annual Resource Bottleneck in Amazonian Colombia

A group of Callicebus torquatus lugens using a territory of 22.25 ha in eastern Colombia showed a varied diet throughout the annual period of lowest fruit availability. This is a time when the females are usually pregnant. During a 6-month period the study group's diet consisted of 59.4% fruits, 26.9% immature seeds, 6.4% leaves, 3.9% flowers, and 3.4% insects and spiders. At the fruit bottleneck, consumption of seeds and flowers increased, while consumption of leaves and insects showed no particular trend. They ate 62 species of plants: 45 for flesh, 6 for seeds, 2 for flowers, and 13 for foliage. The most important families in terms of species chosen are Moraceae (8 species, or 11 species if Cecropiaceae is included), Myristicaceae (7), Arecaceae (4), Chrysobalanaceae (4), and Euphorbiaceae. The most important families in terms of feeding time are Myristicaceae (25%), Euphorbiaceae (15%), Moraceae (14%), and Arecaceae (9%). Of 440 marked feeding trees in the territory of the group, 41.1% are represented by Sandwithia heterocalyx (Euphorbiaceae). This species is the most important food in the diet and has the highest density of all food trees in the home range. It followed by Heterostemon conjugates (Caesalpiniaceae) (10%), Iryanthera ulei (Myristicaceae) (6.1%), Anaxagorea brachycarpa (Annonaceae) (5.9%), and Iryanthera crassifolia (Myristicaceae) (3.4%). The remaining 33.5% of the marked trees are represented by the other 57 species. In terms of time spent feeding, the important trees in the diet include Sandwithia heterocalyx (13.9%), Virola melinonii (10%), Iryanthera ulei (8.35%), Oenocarpus bataua (7.06%), and Heterostemon conjugates (6.53%). We suggest that Callicebus torquatus should be described as a frugivore–granivore; they share with the Pitheciin an immature seed-eating adaptation.     

Constitutions of diarylpropanoids from Virola multinervia

The wood of Virola multinervia Ducke (Myristicaceae) contains sitosterol, stigmasterol and two novel diarylpropanoids virolane [1-(2-hydroxy-4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)-propane] and virolanol [2-hydroxy-1-(2-hydroxy-4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)-propane].     

Osteophloeum platyspermum andVirola duckei (myristicaceae): newly reported as hallucinogens from Amazonian Ecuador

Quijos Quichua collaborators identifiedOsteophloeum platyspermum andVirola duckei (Myristicaceae) as sources of a psychoactive sap. This is the first reported hallucinogenic use of Myristicaceae from Ecuador. Species in Malpighiaceae and Solanaceae are more common sources of hallucinogens, but older Quichua still employ these myristicaceous species.Virola is used widely as a hallucinogen in other parts of Amazonia but there are no previous reports on the psychoactive use ofO. platyspermum. Field tests for the presence of alkaloids using Dragendorffs reagent were positive for both species. Like the Bora and Witoto in Peru, the Quijos Quichua consume myristicaceous hallucinogens orally. Most other indigenous peoples prepare psychoactive snuffs from the bark and sap.     

Systematic revision of Myristicaceae (Magnoliales) in Madagascar, with four new species of Mauloutchia

The systematics of Malagasy Myristicaceae is revised to take into account new collections made since the work by Capuron in the 1970s, as well as improved knowledge from fieldwork and two scanning electron microscopy studies by the author. Four new species are described: Mauloutchia annickiae Sauquet, M. capuronii Sauquet, M. echinocarpa Capuron ex Sauquet, and M. sambiranensis (Capuron) Sauquet. In addition, basic information is given for each remaining Malagasy species of the family (synonymy, type specimen, updated distribution and main distinctive features). According to this treatment, Malagasy Myristicaceae now consist of four endemic genera and 15 species: Brochoneura Warb. (three species), Doyleanthus Sauquet (one species), Haematodendron Capuron (one species) and Mauloutchia (Baill.) Warb. (ten species). Two identification keys to these species are provided: one based primarily on fruit characters and one based primarily on male flower and inflorescence characters. Putative phylogenetic relationships among these species are also indicated, based on a previous combined morphological and molecular study by the author.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 146 , 351–368.     

Biodiversity of Asterina species on Neotropical host plants: new species and records from Panama

Two new species of the genus Asterina are described from living leaves collected in provinces Chiriquí and Bocas del Toro in western Panama. Asterina alloplecti on Alloplectus ichtyoderma (Gesneriaceae) differs from other Asterina on Gesneriaceae by its stalked appressoria and host relationship. Asterina compsoneurae on Compsoneura sprucei (Myristicaceae) can be distinguished from other members of Asterina on Myristicaceae by its larger ascomata, larger, prominently spinose ascospores and host relationship. New records for Panama are Asterina corallopoda from a new host plant species (Solanum trizygum, Solanaceae), A. diplopoda, A. ekmanii from a new host plant species (Gonzalagunia rudis, Rubiaceae), A. siphocampyli from a new host plant genus and species (Burmeistera vulgaris, Campanulaceae) and A. styracina from a new host-plant species (Styrax argenteus, Styracaceae). This study increases the number of species of Asterina known for Panama from 12 to 19 and the number of Asterinaceae from 14 to 21. Asterina corallopoda, A. diplopoda, A. ekmanii, A. siphocampyli and A. styracina are illustrated for the first time. A phylogeny inferred from the analysis of LSU rDNA sequences of species of Asterina is presented. The diversity and host-plant patterns of known Neotropical species of Asterina are discussed.     

Diarylpropanoids from Iryanthera polyneura

The trunk wood of Iryanthera polyneura Ducke (Myristicaceae) contains pinocembrin, 1-(2′,4′-dihydroxyphenyl)-3-(3″,4″-methylenedioxyphenyl)-propane, 1-(2′,4′-dihydroxy-3′-methylphenyl)-3-(2″-methoxy-4″, 5″-methylenedioxyphenyl)-propane and 4,2′,4′-trihydroxy-3-methoxydihydrochalcone.     

Lipophyllic antioxidants from Iryanthera juruensis fruits

The phytochemical investigation of the hexane extract of Iryanthera juruensis (Myristicaceae) fruits led to the isolation of two tocotrienols and four lignans which exhibited antioxidant activity towards beta-carotene on TLC autographic assay. Two inactive quinones and three omega-arylalkanoic acids were also isolated. The isolates were investigated for their redox properties using cyclic voltammetry. The structure elucidation of the new compounds (one tocotrienol. one quinone and three omega-arylalkanoic acids) was based on analysis of spectroscopic data.     

Acylresorcinols from Virola sebifera and Virola elongata

The fruits of Virola sebifera and V. elongata (Myristicaceae) contain three ω-phenylundecanoyl-substituted compounds, a 2,6-dihydroxybenzene, a 2,6-dihydroxy-4-methoxybenzene and a 3-hydroxycyclohexan-2,6-dione. Three additional 2,6-dihydroxybenzenes are substituted by hexadecanoyl, hexadec-4Z-enoyl and 8-hydroxyoctadec-4Z-enoyl groups.