Carbon Fixation by Paphiopedilum insigne and Paphiopedilum parishii (Orchidaceae),{dagger}

Measurements of stomalal conductance, ¹⁴CO₂ fixation and aciditylevels indicate that Paphiopedilum insigne (Walhch) and P parishii(Rchb f) Stein, Orchidaceae, do not fix carbon via the Crassulaceanacid metabolism pathway Acidity, C₂ pathway, CAM, stomatal conductance     

Bee size and pollen transfer in Cypripedium calceolus (Orchidaceae)

In Denmark Cypripedium calceolus is found in only two small and isolated populations, and its fruit set is suspected to be pollinator-limited. Collection and observations of flower visitors were carried out between 1995 and 1997, and fruit set were estimated. Forty-four visitors were collected. The majority belonged to the genera Halictus, Lasioglossum and Andrena . The latter is known as pollinator of C. calceolus in other parts of Europe, but in this study Andrena spp. were both not regular visitors and too large to function as efficient pollinators. Medium-sized halictine species, especially females of Halictus tumulorum and Lasioglossum calceatum , were the most regular and frequent pollen vectors. Andrena jacobi and Lasioglossum rufitarse are recorded for the first time in Denmark.     

Ontogenesis of monad pollen inPterostylis plumosa (Orchidaceae,Neottioideae)

Pterostylis plumosa (Neottioideae) is an orchid with monosulcate monad pollen. Tetrads may be isobilateral, decussate, tetrahedral, rhomboid or T-shaped, but all pollen grains have a similar shape. Those belonging to the same tetrads are contiguous from microspore release to opening of the anther, with the furrow oriented inwards. Sporophytic proteins are present outside the furrow. The tapetum is of the parietal type without orbicles. The increase in pollen grain size between meiosis and maturity is only three-fold. The generative cell is spherical when the pollen is mature. These features are discussed in relation to the primitive nature of the species.     

The pollinium ofLoroglossum hircinum (Orchidaceae) between pollination and pollen tube emission

The structure of the massulae composing the pollinium ofLoroglossum hircinum was studied before pollination and 12 and 24 hours afterwards. The grains are grouped in tetrads closely packed in massulae. The exine is only present on the outside of the massulae. The intine consists of two layers: a compact layer surrounding the pollen grain and a looser layer surrounding the pollen grain and a looser layer surrounding the tetrad. Twelve hours after pollination, pollen volume and the space between the tetrads increase due to vacuolization. Twenty-four hours after pollination, pollen volume and tetrad spacing are higher due to vacuolization and some grains have emitted pollen tubes. Pollen growth due to vacuole formation, and the absence of common walls between adjacent tetrads lead to crumbling of the massulae. The mature pollen grain does not have apertures: the site of pollen tube emission is determined after pollination. The first grains to germinate are those in the centre of the massula. The vegetative cell nucleus is the first to enter the pollen tube; the generative cell elongates and undergoes the second haploid mitosis shortly after entering the pollen tube.     

Anther wall and pollen development in Ophrys mammosa L. (Orchidaceae)

The objective of this study was to investigate anther wall and pollen development in Ophrys mammosa. Primary sporogen tissue resembles longitudinal cells with divided archeosporal cells. Thereafter these primary sporogen tissue cells re-divide anticlinally and periclinally forming secondary sporogen tissue. Microsporogenesis was successive type. Microgametogenesis occurred at the distal poles of the microspores. In addition, dense starch accumulation was detected in the pollen. Pollinia and massulae are separated from each other by dead cells filled with callose, according to histochemical preparations. The anther wall was a four-layered “monocotyledon” type. There was ring-like wall thickening in the endothecium. The tapetum is of the glandular type. When these two developmental processes are compared, it is seen that the anther wall has become mature by the sporogen tissue phase and is composed of only epidermis and endothecium at the beginning of microgametogenesis.     

The generaGlomera andGlossorhyncha (Orchidaceae)

In the discussion aboutGlomera andGlossorhyncha reasons are give how to delimit and redefine the two genera. The genusGiulianettia is merged intoGlossorhyncha. A list of species belonging to each genus is included resulting in several new combinations.     

Taxonomy of barkeria (Orchidaceae)

The genusBarkeria (Orchidaceae) consists of four species and eight subspecies (the treatment includes a key) of epiphytic plants endemic to Mexico and Central America.Barkeria is separated from the genusEpidendrum on the structure of the rostellum and column in the flower, plus shape of the pseudobulbs. The authors suggest thatBarkeria is most closely related toCaularthron based on the general shape of the flowers, widely spreading fleshy column wings, and structure of the rostellum.     

Adventitious embryony inNigritella (Orchidaceae)

The embryology of diploid and polyploidNigritella species is described. The development of the adventitious embryos of the polyploids in relation to the sexual embryos of the diploids has been given special consideration. Partial sexuality in the apomicticN. nigra has been proven for the first time by chromosome counts in proembryos after pollination of a tetraploid plant with pollen from a diploid species.     

The genus Chamaegastrodia (Orchidaceae)

A merger of the genera Evrardia and Chamaegastrodia is proposed, and an annotated enumeration of five species so far recognized is proposed.     

Incompatibility in Dendrobium (Orchidaceae)

JOHANSEN, B., 1990. Incompatibility in Dendrobium (Orchidaceae). A unique self-incompatibility system in Dendrobium is demonstrated by more than 1700 pollination experiments. The majority (72%) of the 61 species that were self-pollinated showed self-sterility. In contrast with many other orchid genera Dendrobium showed high incompatibility in interspecific pollinations. Self-and interspecific incompatibility is expressed by flower abscission and not by inhibition of pollen germination or pollen tube growth. The incompatibility system is gametophytic and complementary, and it is likely that the auxin content in the pollinia triggers the incompatibility reaction. Microscopical investigations on the detached cells of the stigma (here called eleutherocytes) after compatible and incompatible pollinations, suggest that the incompatibility response is probably controlled by these cells.     

始兴斑叶兰(兰科)的订正

通过仔细研究藏于中国科学院植物研究所标本馆(PE)以及中国科学院华南植物园标本馆(IBSC)的始兴斑叶兰Goodyera shixingensis K. Y. Lang的模式及等模式标本, 并同作者野外观察和采集的小小斑叶兰G. yangmeishanensis T. P. Lin的新鲜植物和文献描述以及标本进行比较, 证实始兴斑叶兰应为小小斑叶兰的异名。     

Anthecology of Orchis mascula (Orchidaceae)

Interactions between Orchis mascula L. ssp. mascula and anthophilous insects were studied mainly on the island of Öland, Sweden. The species is nectarless and acts by deceiving various bees (Hymenoptera, Apoidea). Temporary seeking/exploratory drives of bees for food–sources were exploited by means of superiority in floral display. A floral reflectance maximum at 440 nm (blue) largely determines the colour in the visual spectrum of bees. The floral scent is composed to about 90% of mono–terpenes. Nothing suggested mimesis of concurrent food–flowers either in colour or in scent. Anthesis covered a time period in late spring when (a) concurrent food–flowers for bees were rather few, (b) many bumble–bee queens (Bombus Latr. spp.) were inexperienced as regards food–flowers and had no foraging routines, (c) cuckoo bumble–bee females (Psithyrus Lep. spp.) recovery–fed on flowers after hibernation, (d) males of Eucera longicornis (L.) (Anthophoridae) patrolled far out from their nest–area, and when (e) many solitary bee species flew about. The pollinator fauna differed between sites, viz. either Bombus queens, Psithyrus females or E. longicornis males transported the majority of the pollinaria. The pollination system does not seem to be stabilised in the study areas. Floral morphology indicates that the plant's anthecological specialisation to bees as a group implies a graded unspecialisation to each species of bee in the legitimate pollinator group.     

Pollination ofOphrys (Orchidaceae) in Cyprus

In the southern part of Cyprus the pollinator —Ophrys (Orchidaceae) relationships and its specifity have been investigated from the end of February until the middle of March 1986. 12Ophrys spp. were found. To date, only a single pollinator reference has been reported from this island. We found the following pollinators:Melecta tuberculata (Ophrys kotschyi),Eucera dimidiata (Ophrys flavomarginata),Eucera gaullei (Ophrys umbilicata),Eucera paulusi (Ophrys bornmuelleri),Anthophora erschowi (Ophrys elegans),Andrena torda (Ophrys sicula =O. lutea subsp.minor),Andrena cinereophila (Ophrys fusca, small-flowered),Andrena flavipes (Ophrys israelitica),Andrena morio (Ophrys iricolor andOphrys transhyrcana),Andrena bimaculata (Ophrys sphegodes aggr., probably formerly confused withO. transhyrcana). Most interestingly, it could be verified thatO. flavomarginata/O. umbilicata, O. bornmuelleri/O. levantina andO. transhyrcana/O. sphegodes aggr. (possiblyO. sintenisii) are different biospecies. This is a result of genetic isolation due to varying pollinators, and of differences in flower morphology.     

Floral mimesis inThelymitra nuda (Orchidaceae)

Insect pollination occurred inThelymitra nuda R. Br. on sunny days when the ambient temperature exceeded 20 °C. The flower buds on a raceme opened subsynchronously displaying the brightly-colored, actinomorphic perianth and exposed the contrastingly-colored, scented and ornamented column. InT. nuda the staminodes and the filament of the fertile stamen are fused to one another producing an inflated hood over the anther. This staminodal hood is terminated in two non-ornamental, but brightly-colored, central lobes and two terete lateral lobes bearing approximately 400 white trichomes. Each trichome bears a double chain of 30–40 spherical, rugulose cells. Female bees, in the genusLasioglossum (Halictidae), were observed to land directly on the hood and curled their bodies around the four lobed tip of the staminodal complex. The bees attempted to forage on the lobes as if they were collecting pollen from fertile, poricidal stamens. These bees applied thoracic vibration to the yellowish central lobes and actively scraped the trichome clusters (Pseudopollen) with their forelegs. Bees carried the pollinaria ofT. nuda dorsally on their abdomens. Abdominal contact with the rostellum appeared to occur when the female bee disengaged herself from the staminodal hood. Observations made of bees on co-blooming flowers, and analyses of pollen loads collected by bees suggested that the orchid flower mimics the guild of blue-purple flowers that lack floral nectar but offer pollen in poricidal anthers. The models ofT. nuda are co-bloomingLiliaceae in the generaDichopogon andThysanotus. However, nectarless, buzz-pollinated flowers are also extensively distributed over the orchid’s range. More than 30% of the flowers in theT. nuda population had their pollinaria removed, suggesting a high capacity for cross-pollination in an orchid genus usually considered to be self-pollinated via mechanical autogamy. This study confirmed previous predictions that column modifications represented a trend towards pseudanthery.     

The pollination ecology ofBletilla striata (Orchidaceae)

Anthecological observations of an orchidBletilla striata were carried out in Kobe, Japan. The purplish pink flowers were visited by 26 species of insects belonging to Hymenoptera, Diptera and Lepidoptera, although the flower did not offer food rewards of any kind. Candidates for pollination were seven species of aculeate Hymenoptera with a body size that well fitted the space in between the column and labellum. The most effective candidate was the male of the longhorn beeTetralonia nipponensis, judging from its abundance and legitimate intrafloral behavior. The female ofT. nipponensis and the other six species also contributed to promote out-crossing, but to a lesser extent than the maleT. nipponensis, since they occasionally exhibited illegitimate intrafloral behaviors for pollination and also, their flower visitation rate was lower.     

Vegetative anatomy of subtribe Habenariinae (Orchidaceae)

Leaves of Habenariinae are characterized by anomocytic stomatal apparatuses, homogeneous mesophyll, collateral vascular bundles in a single series, and thin-walled bundle sheath cells. There is no foliar sclerenchyma nor a hypodermis. Cauline cortex consists of thin-walled living cells among which are large and numerous intercellular spaces. The ground tissue is bordered externally by a layer of thick-walled living cells, except in Habenaria repens. Central ground tissue cells are living, and usually thin-walled surrounding intercellular spaces of various dimensions. These are conspicuously large in H. repens. Collateral vascular bundles are scattered across the ground tissue. Sclerenchyma is absent. Absorbing roots are generally velamentous, exodermal dead cells are diin-walled, and passage cells usually have a thickened outer wall. A regular vascular cylinder is present, and vascular tissue is embedded in parenchyma. Root tubers are velamentous, exodermal cells are usually thin-walled, and passage cells frequently have thickened outer walls. Vascular tissue of root tubers is organized into two classes: (1) those with a single vascular cylinder surrounded by a cortex and (2) those with a series of meristeles dispersed throughout the ground tissue. In group (1) cortex is homogeneous either with or without mucilage cells except in Stenoglattis where the cortex is heterogeneous, consisting of water-storage and assimilatory cells, and lacks mucilage cells. In group (2) the ground tissue consists of larger mucilage-containing cells and smaller assimilatory cells.     

Systematic leaf anatomy of Caladeniinae (Orchidaceae)

Leaf anatomy of 25 species in 15 genera of Caladeniinae (Diurideae, Orchidaceae), excluding Caladenia, was investigated to determine diagnostic characters to be used in forthcoming, broad-based cladistic analyses of the subtribe and to assess interspecific and intergeneric relationshipS. Of the characters examined, those that show the most variation among the study taxa are presence and types of trichomes, cuticular sculpturing, anticlinal walls of epidermal cells, heterogeneity of chlorenchyma, distribution and length: width ratios of stomata. Anatomical evidence supports the generic concept of Leptoceras Lindley but contradicts that of Drakonorchis Hopper & A.P. Brown. Paracaleana is not sufficiently distinct from Caleana to warrant generic status. Lyperanthus serratus and L.suaveolens are hyperstomatic, a rare condition in Orchidaceae. On the basis of these and other characters, Lyperanthus, as currently circumscribed, is polyphyletic. From leaf structure Caladeniinae as now conceived is polyphyletic and comprises seven groups: (1) Caladenia, Leptoceras, Elythranthera, Eriochilus, Glossodia, Aporostylis; (2) Adenochilus, Rimacola; (3) Arthrochilus, Chiloglottis, Spiculaea, Leporella; (4) Caleana (including Paracaleana); (5) Bumettia; (6) Lyperanthus suaveolens and L.serratus; (7) Lyperanthus nigricans.     

Comparative labellar micromorphology of Zygopetalinae (Orchidaceae)

Background and Aims

Molecular evidence indicates that the Neotropical sub-tribe Zygopetalinae is sister to Maxillariinae. Most members of the latter sub-tribe have deceit pollination strategies, but some species produce rewards such as nectar, pseudopollen, resin and wax, and are pollinated by a range of pollinators that include stingless bees (Meliponini), wasps and hummingbirds. By contrast, relatively little is known about the pollination of Zygopetalinae species. However, some are pollinated by fragrance-gathering, male euglossine bees or employ nectar deceit strategies. The aim of this study is to describe the labellar micromorphology of Zygopetalinae and to compare it with that of Maxillariinae sensu lato (s.l.) as part of an ongoing project to record the range of labellar characters found within the tribe Maxillarieae, and to assess whether these characters represent synapomorphies or homoplasies resulting from similar pollination pressures.

Methods

The labella of 31 species of Zygopetalinae, including Cryptarrhena R. Br. and representatives of the Zygopetalum, Huntleya and Warrea clades, were examined using light microscopy and scanning electron microscopy, and the range of labellar characters was recorded. These characters were subsequently compared with those of Maxillariinae s.l. which formed the subject of our previous investigations.

Key Results and Conclusions

The labellar micromorphology of Zygopetalinae is less diverse than that of Maxillariinae and does not reflect the currently accepted phylogeny of the former sub-tribe based on molecular studies. Instead, the relative uniformity in labellar micromorphology of Zygopetalinae is probably due to homoplasies resulting from similar pollinator pressures. Labellar trichomes are relatively uncommon in Zygopetalinae, but occur in certain members of both the Zygopetalum and Huntleya clades. Trichomes are unbranched, uniseriate and multicellular with rounded apices, or unbranched and unicellular, with tapering, pointed and flexuose apices. Hitherto, unicellular trichomes of this kind have been observed only for euglossophilous orchid taxa, and the adoption of a relatively limited range of pollination strategies by Zygopetalinae may have resulted in reduced investment in micromorphological labellar characters.