Tubular Hairs Research Articles

Microhair on the adaxial leaf surface of salt secreting halophytic Oryza coarctata Roxb. show distinct morphotypes: Isolation for molecular and functional analysis

Halophytic Oryza coarctata is a good model system to examine mechanisms of salinity tolerance in rice. O. coarctata leaves show the presence of microhairs in adaxial leaf surface furrows that secrete salt under salinity. However, detailed molecular and physiological studies of O. coarctata microhairs are limited due to their relative inaccessibility. This work presents a detailed characterization of O. coarctata leaf features. O. coarctata has two types of microhairs on the adaxial leaf surface: longer microhairs (three morphotypes) lining epidermal furrow walls and shorter microhairs (reported first time) arising from bulliform cells. Microhair morphotypes include (i) finger-like, tubular structures, (ii) tubular hairs with bilobed and flattened heads and (iii) bi-or trifurcated hairs. The unicellular nature of microhairs was confirmed by propidium iodide (PI) staining. An efficient method for the isolation and enrichment of O. coarctata microhairs is presented (yield averaging ˜2 × 105/g leaf tissue). The robustness of the microhair isolation procedure was confirmed by subsequent viability staining (PI), total RNA isolation and RT-PCR amplification of O. coarctata trichome-specific WUSCHEL-related homeobox 3B (OcWox3B) and transporter gene-specific cDNA sequences. The present microhair isolation work from O. coarctata paves the way for examining genes involved in ion secretion in this halophytic wild rice model.

Tubular Hair Casts in Trichoscopy of Hair and Scalp Disorders.

Introduction:Hair casts have been reported in a variety of hair and scalp disorders. Trichoscopy allows a quick and noninvasive method for the evaluation of hair and scalp disorders in high magnification. However, the study of hair casts seen in trichoscopy is lacking.Objective:The main objective is to study the occurrence and patterns of tubular hair cast (THC) in different hair and scalp disorders.Patients and Methods:The patients with hair and scalp disorders presenting at the dermatology department of our hospital were evaluated using trichoscopy. Cases of primary parakeratotic disorders and behavioral disorders were excluded. After a detailed history and evaluation of the hair and scalp, histopathology, light microscopic examination, potassium hydroxide examination, and fungal culture were done when necessary.Results:THC was seen in total 21 cases of seven different hair and scalp disorders. Of these, the majority of cases were of discoid lupus erythematosus (DLE) (5/21) and maximum frequency of THCs within a disorder was seen in cases of pemphigus foliaceus (PF) (50%). Proximal casts occurred in 90.47% of cases. Single cast involving two shafts was seen in a case of PF, and two casts within a single shaft were seen in two cases of DLE and one case of alopecia areata.Conclusions:THCs in trichoscopy can be seen in various hair and scalp disorders and their study may help during the diagnosis of those disorders when combined with other trichoscopic features.

Characterisation of Stramenopile-specific mastigoneme proteins in Phytophthora parasitica.

Mastigonemes, tripartite tubular hairs on the anterior flagellum of Phytophthora zoospores, are instrumental for disease dissemination to new host plants. A previous study showed that PnMas2 was part of the tubular shaft of Phytophthora parasitica mastigonemes. In the current study, genes encoding two related proteins, PnMas1 and PnMas3, were identified in the genome of P. parasitica. PnMas1 interacts with PnMas2 and also occurs along the mastigoneme shaft. RNA-Seq analyses indicate that PnMas1 and PnMas2 genes have similar expression profiles both in vitro and in planta but that PnMas3 is expressed temporally prior to PnMas1 and PnMas2 during asexual development and plant infection. Immunocytochemistry and GFP-tagging document the occurrence of all three PnMas proteins within the specialised compartments of the ER during mastigoneme formation, but only PnMas1 and PnMas2 occur in mature mastigonemes on the flagellar surface. Anti-PnMas1 and anti-PnMas2 antibodies co-labelled two high-molecular-weight (~400kDa) protein complexes in native gels but anti-PnMas3 antibodies labelled a 65kDa protein complex. Liquid chromatography-mass spectrometry analysis identified PnMas1 and PnMas2 but not PnMas3 in flagellar extracts. These results suggest that PnMas3 associates with mastigonemes during their assembly within the ER but is not part of mature mastigonemes on the anterior flagellum. Phylogenetic analyses using homologues of Mas genes from the genomes of 28 species of Stramenopiles give evidence of three Mas sub-families, namely Mas1, Mas2 and Mas3. BLAST analyses showed that Mas genes only occur in flagellate species within the Stramenopile taxon.

Identification of a Mastigoneme Protein from Phytophthora nicotianae

Tripartite tubular hairs (mastigonemes) on the anterior flagellum of protists in the stramenopile taxon are responsible for reversing the thrust of flagellar beat and for cell motility. Immunoprecipitation experiments using antibodies directed towards mastigonemes on the flagella of zoospores ofPhytophthora nicotianaehave facilitated the cloning of a gene encoding a mastigoneme shaft protein in this Oomycete. Expression of the gene, designatedPnMas2, is up-regulated during asexual sporulation, a period during which many zoospore components are synthesized. Analysis of the sequence of the PnMas2 protein has revealed that, like other stramenopile mastigoneme proteins, PnMas2 has an N-terminal secretion signal and contains four cysteine-rich epidermal growth factor (EGF)-like domains. Evidence from non-denaturing gels indicates that PnMas2 forms large oligomeric complexes, most likely through disulphide bridging. Bioinformatic analysis has revealed thatPhytophthoraspecies typically contain three or four putative mastigoneme proteins containing the four EGF-like domains. These proteins are similar in sequence to mastigoneme proteins in other stramenopile protists including the algaeOchromonas danica,Aureococcus anophagefferensandScytosiphon lomentariaand the diatomsThalassiosira pseudonana and T. weissflogii.

INTERGENERIC HYBRIDIZATION BETWEEN DENDRANTHEMA CRASSUM AND AJANIA MYRIANTHA

Intergeneric cross has been made between Dendranthema crassum (2n=10x=90; ♀) and Ajania myriantha (2n=2x=18; ♂). Using ovule rescue, only one embryo germinated and produced the plantlet showing 2n=6x=54. Leaf length, petiole length, tubular florets number and epidermal hair density of the hybrid are intermediate between that of the parents. Leaf width and epidermal hair length of the hybrids are less than that of the parents. While ligulate florets number, flower diameter and epidermal hair height exceed that of the parents and showed transgressive inheritance. A genomic in situ hybridization approach was able to distinguish between the parental genomes of mitotic metaphase chromosomes in the unique hybrid plant.

A TUBULAR MASTIGONEME‐RELATED PROTEIN, OCM1, ISOLATED FROM THE FLAGELLUM OF A CHROMOPHYTE ALGA,OCHROMONAS DANICA1

The phylogenetic group stramenopiles refers to the systematic groups that possess tripartite tubular hairs (stramenopiles) on their flagella. There have been a number of studies describing the fine structure of these mastigonemes and a few studies isolating the component proteins; however, these proteins and their gene sequences have not yet been identified. In the present study, we identified a mastigoneme protein (Ocm1) of the chrysophycean algaOchromonas danicaPringsh. (UTEX LB1298). Its corresponding gene,Ocm1, was identified by using degenerate primers that correspond to the partial amino acid sequences of a protein (85 kDa) obtained from a mastigoneme‐rich fraction of isolated flagella. The polypeptide encoded byOcm1has four cysteine‐rich, epithelial growth factor (EGF)–like motifs, potentially involved in protein–protein interactions. It lacks obvious hydrophobic regions characteristic of transmembrane domains, suggesting that this polypeptide is not likely a protein for anchoring the mastigoneme. In addition, a polyclonal antibody against Ocm1 labeled the area where the tubular shafts of the mastigonemes are located, but not the basal portion or the terminal filaments.

Phylogenetic position of Karotomorpha and paraphyly of Proteromonadidae

The taxon Slopalinida (Patterson, 1985) comprises two families of anaerobic protists living as commensals in the intestine of vertebrates. The proteromonadids are small Xagellates (ca. 15 m) with one nucleus, a single large mitochondrion with tubular cristae, Golgi apparatus and a Wbrillar rhizoplast connecting the basal bodies and nucleus (Brugerolle and Mignot, 1989). The number of Xagella diVers between the two genera belonging to the family: Proteromonas, the commensal of urodelans, lizards, and rodents, has two Xagella, whereas Karotomorpha, the commensal of frogs and other amphibians, has four Xagella. The surface of the cell is folded, the folds are supported by single microtubules (Proteromonas) or by ribbons of several laterally interconnected microtubules (Karotomorpha). The transitional Xagellar region contains double transitional helix. The posterior part of Proteromonas cell is covered with Wne tubular hairs— the somatonemes (Brugerolle and Joyon, 1975). The representatives of the second family—Opalinidae— are quite diVerent from the proteromonadid Xagellates. They are multinucleated and multiciliated, often large (up to several mm). They are common commensals of frogs, some can inhabit the intestine of urodelans or Wsh. The family comprises three binucleated genera (Protoopalina, Protozelleriella, Zelleriella) and two genera with up to hundreds of nuclei (Cepedea, Opalina). Besides nuclei the cell contains a large number of mitochondria with tubular cristae, Golgi complexes and small digestive vacuoles (Delvinquier and Patterson, 1993). The cell surface is heavily folded, the folds are supported by ribbons of microtubules in a very similar way as in Karotomorpha. The ultrastructure of Xagellar transi-

An ultrastructural study of development and reproduction in the nematode parasite Myzocytiopsis vermicola

An isolate of Myzocytiopsis vermicola, a holocarpic parasite of Rhabditis nematodes, was studied with transmission electron microscopy (TEM) to follow development during infection, asexual and sexual reproduction. Nematodes became infected after attachment of apical cystospore buds to the nematode cuticle. Apical buds were packed with vesicles with dense fibrillar contents, which were absent from the thallus. Some thalli developed into sporangia while others became paired gametangial cells. Zoospore cleavage was often intrasporangial, although during the early stages of an epidemic partially differentiated zoospores usually were released via an exit tube into a fine vesicle. Packets of tripartite tubular hairs (TTH) were not observed in the cytoplasm of either developing or mature sporangia. TEM of sectioned material and whole mounts of zoospores revealed biflagellate zoospores, some without hairs and others with a proximal row of very short hairs on the anterior flagellum. Gametangial contact was via a short, walled fertilization tube and surplus antheridial and oogonial nuclei remained in their respective gametangial cells until disintegration of the periplasm. The mature oospores had a scalloped, electron opaque, epispore wall layer. These observations will be discussed in relation to the likely phylogenetic position of the Myzocytiopsidales within the oomycetes.

An ultrastructural study of development and reproduction in the nematode parasite Myzocytiopsis vermicola

An isolate of Myzocytiopsis vermicola, a holocarpic parasite of Rhabditis nematodes, was studied with transmission electron microscopy (TEM) to follow development during infection, asexual and sexual reproduction. Nematodes became infected after attachment of apical cystospore buds to the nematode cuticle. Apical buds were packed with vesicles with dense fibrillar contents, which were absent from the thallus. Some thalli developed into sporangia while others became paired gametangial cells. Zoospore cleavage was often intrasporangial, although during the early stages of an epidemic partially differentiated zoospores usually were released via an exit tube into a fine vesicle. Packets of tripartite tubular hairs (TTH) were not observed in the cytoplasm of either developing or mature sporangia. TEM of sectioned material and whole mounts of zoospores revealed biflagellate zoospores, some without hairs and others with a proximal row of very short hairs on the anterior flagellum. Gametangial contact was via a short, walled fertilization tube and surplus antheridial and oogonial nuclei remained in their respective gametangial cells until disintegration of the periplasm. The mature oospores had a scalloped, electron opaque, epispore wall layer. These observations will be discussed in relation to the likely phylogenetic position of the Myzocytiopsidales within the oomycetes.

Morphological Studies on Zoospores of Aphanomyces cochlioides and Changes during Interaction with Host Materials

The behavioral and morphological diversity of intact zoospores of Aphanomyces cochlioides and their dynamic morphological changes when interacting with the host or a host-specific zoospore attractant were studied by light and electron microscopy. The reniform-ovate zoospore has two heterokont flagella, both inserted in a ventral groove. The anterior flagellum possesses two rows of tripartite tubular hairs (TTHs) distributed throughout its length, whereas the posterior flagellum was ornamented with two rows of highly dense fine tubular hairs, except on its tapered terminal part. The tip of the posterior flagellum has a bunch of similar fine hairs like those on the flagellum shaft. The biflagellated zoospores quickly aggregated on the host (spinach) root, adhered to the root surface, encysted by shedding or retracting the flagella, germinated at a fixed point to form germ tubes, and finally invaded the root tissues via the appressoria within 50–60 min. This precise homing response of A. cochlioides zoospores reflects guidance by a host-specific signal(s) for locating potential infection sites, differentiation of zoospores to cystospores, formation of infection structures and/or germ-tube tropism for completing pre-infection events in haste. Prior to the encystment, the posterior flagellum may be involved in successful docking on the root surface by tip contact followed by shedding or retraction.

Cell structure and asexual reproduction in Lagynion delicatulum (Stylococcaceae, Chrysophyceae)

Lagynion delicatulum Skuja is a first record for New Zealand freshwaters. Individual vegetative cells in nature and culture were sessile, aflagellate, and surrounded by a hyaline lorica lacking mineral deposits. Cells were uninucleate, had one or two chloroplasts with girdle lamellae and ring nucleoids, several mitochondria, and two to four basal-body-like centrioles. Cell division was followed by the release of one or both progeny from the parent lorica as biflagellate zoospores without eyespots. The anterior flagellum bore a tomentum of fine fibrils and two balanced rows of tripartite tubular hairs. The posterior flagellum was short, scarcely visible with light microscopy. A paraflagellar rod and paraflagellar vanes were associated with its axoneme. The flagellar apparatus consisted of two basal bodies and three microtubular roots. The coplanar basal bodies diverged from each other at an angle of approximately 130°. Simple transitional helices were present. No root that could be identified with the R3 root of other stramenopiles was present. Settling zoospores produced a few long pseudopods, and lost flagella by abscission. Cells forming loricas had a circumferential array of numerous short pseudopodia. Similarities in morphology and reproduction suggest that at least those Stylococcaceae with apparently uniflagellate swarmers form a monophyletic group. Flagellar apparatus similarities between Lagynion and Hibberdia suggest a relationship, but this is not supported by previously-published phylogenies reconstructed from molecular sequences. Convergent evolution of flagellar apparatus architecture is a possibility.

Cell structure and asexual reproduction in Lagynion delicatulum (Stylococcaceae, Chrysophyceae)

Lagynion delicatulum Skuja is a first record for New Zealand freshwaters. Individual vegetative cells in nature and culture were sessile, aflagellate, and surrounded by a hyaline lorica lacking mineral deposits. Cells were uninucleate, had one or two chloroplasts with girdle lamellae and ring nucleoids, several mitochondria, and two to four basal-body-like centrioles. Cell division was followed by the release of one or both progeny from the parent lorica as biflagellate zoospores without eyespots. The anterior flagellum bore a tomentum of fine fibrils and two balanced rows of tripartite tubular hairs. The posterior flagellum was short, scarcely visible with light microscopy. A paraflagellar rod and paraflagellar vanes were associated with its axoneme. The flagellar apparatus consisted of two basal bodies and three microtubular roots. The coplanar basal bodies diverged from each other at an angle of approximately 130°. Simple transitional helices were present. No root that could be identified with the R3 root of other stramenopiles was present. Settling zoospores produced a few long pseudopods, and lost flagella by abscission. Cells forming loricas had a circumferential array of numerous short pseudopodia. Similarities in morphology and reproduction suggest that at least those Stylococcaceae with apparently uniflagellate swarmers form a monophyletic group. Flagellar apparatus similarities between Lagynion and Hibberdia suggest a relationship, but this is not supported by previously-published phylogenies reconstructed from molecular sequences. Convergent evolution of flagellar apparatus architecture is a possibility.

Ultrastructure and 18S rDNA Sequence Analysis of Wobblia lunata gen. et sp. nov., a New Heterotrophic Flagellate (Stramenopiles, Incertae Sedis)

A new heterotrophic flagellate Wobblia lunata gen. et sp. nov. is described. This organism usually attaches to the substratum showing a wobbling motion, and sometimes glides on the substratum or swims freely in the medium. W. lunata has various features characteristic of the stramenopiles. These include a hairy flagellum with tripartite tubular hairs, a mitochondrion with tubular cristae, arrangement of flagellar apparatus components and a double helix in the flagellar transition zone. W. lunata shares a double helix with heterotrophic stramenopiles, including Developayella elegans, oomycetes, hyphochytrids, opalinids and proteromonads, and could be placed in the phylum Bigyra Cavalier-Smith. However, from 18S rDNA tree analysis, these organisms form two distantly-related clades in the stramenopiles, and Wobblia appears at the base of the stramenopiles. Evaluation of morphological features and comparison of 18S rDNA sequences indicate that W. lunata is a member of the stramenopiles, but it is distinct from any other stramenopiles so far described. Its phylogenetic position within the stramenopiles is uncertain and therefore W. lunata is described as a stramenopile incertae sedis.

Symbiomonas scintillans gen. et sp. nov. and Picophagus flagellatus gen. et sp. nov. (Heterokonta): Two New Heterotrophic Flagellates of Picoplanktonic Size

Two new oceanic free-living heterotrophic Heterokonta species with picoplanktonic size (< 2 microm) are described. Symbiomonas scintillans Guillou et Chrétiennot-Dinet gen. et sp. nov. was isolated from samples collected both in the equatorial Pacific Ocean and the Mediterranean Sea. This new species possesses ultrastructural features of the bicosoecids, such as the absence of a helix in the flagellar transitional region (found in Cafeteria roenbergensis and in a few bicosoecids), and a flagellar root system very similar to that of C. roenbergensis, Acronema sippewissettensis, and Bicosoeca maris. This new species is characterized by a single flagellum with mastigonemes, the presence of endosymbiotic bacteria located close to the nucleus, the absence of a lorica and a R3 root composed of a 6+3+x microtubular structure. Phylogenetical analyses of nuclear-encoded SSU rDNA gene sequences indicate that this species is close to the bicosoecids C. roenbergensis and Siluania monomastiga. Picophagus flagellatus Guillou et Chrétiennot-Dinet gen. et sp. nov. was collected in the equatorial Pacific Ocean. Cells are naked and possess two flagella. This species is characterized by the lack of a transitional helix and lateral filaments on the flagellar tubular hairs, the absence of siliceous scales, two unequal flagella, R1 + R3 roots, and the absence of a rhizoplast. SSU rDNA analyses place this strain at the base of the Chrysophyceae/Synurophyceae lineages.

BOLIDOMONAS: A NEW GENUS WITH TWO SPECIES BELONGING TO A NEW ALGAL CLASS, THE BOLIDOPHYCEAE (HETEROKONTA)

A new algal class, the Bolidophyceae (Heterokonta), is described from one genus, Bolidomonas, gen. nov., and two species, Bolidomonas pacifica, sp. nov and Bolidomonas mediterranea, sp. nov., isolated from the equatorial Pacific Ocean and the Mediterranean Sea, respectively. Both species are approximately 1.2 μm in diameter and have two unequal flagella; the longer flagellum bears tubular hairs, whereas the shorter is smooth. The flagellar basal apparatus is restricted to two basal bodies, and there is no transitional helix. Cells are naked, devoid of walls or siliceous structures. The internal cellular organization is simple with a single plastid containing a ring genophore and a girdle lamella, one mitochondrion with tubular cristae, and one Golgi apparatus close to the basal bodies. The Mediterranean and the Pacific species differ in the insertion angle between their flagella and their pattern of swimming, these differences possibly being linked to each other. Analyses of the SSU rDNA gene place the two strains as a sister group to the diatoms. Moreover, pigment analyses confirm this position, as fucoxanthin is found as the major carotenoid in both lineages. These data strongly suggest that the ancestral heterokont that gave rise to the diatom lineage was probably a biflagellated unicell.

Pirsonia, phagotrophic nanoflagellates incertae sedis, feeding on marine diatoms: attachment, fine structure and taxonomy

Summary After being chemotactically attracted by its host, marine diatoms of the genus Coscinodiscus, the Pirsonia flagellates are guided by the topography of the host cell surface to the rimoportulae through which the trophosome, a basally formed pseudopodium, penetrates into the diatom. Cytochalasin D does not disturb the chemotaxis of the flagellates but inhibits their attachment. Pirsonia diadema and P. guinardiae, feeding on Coscinodiscus and on Guinardia flaccida, respectively, are very similar in their fine structure. The anterior flagellum has tubular hairs which seem to belong to the tripartite, stramenopile type. They are synthesized within the ER and exocytosed by the Golgi apparatus. In certain developmental stages the posterior flagellum and the cell body bear „knotted hairs“ which differ in length. The mode of their formation is unknown. The mitochondria have unique non-contorted tubular cristae which are parallel to each other. The few dictyosomes have a parabasal position. The flagellar root apparatus consists of fibrillar bands which connect the basal body of the anterior flagellum with the nucleus and with the basal body of the posterior flagellum. Other fibrillar bands and a few microtubules run from the basal bodies to the cell surface. The organization of the flagellar root apparatus thus differs from that of typical stramenopiles. The taxonomic position of Pirsonia is discussed.

16S-like rDNA sequences from Developayella elegans, Labyrinthuloides haliotidis, and Proteromonas lacertae confirm that the stramenopiles are a primarily heterotrophic group

Summary A phylogenetic analysis of the 16S-like ribosomal RNA coding regions from Labyrinthuloides haliotidis, Developayella elegans, Proteromonas lacertae and other organisms corroborates morphological evidence that proteromonads and other eukaryotes with tripartite tubular hairs form a monophyletic group of organisms, the stramenopiles. Within the stramenopiles, the heterotrophic groups (proteromonads, Labyrinthulida, bicosoecids, Developayella and oomycetes) diverge before the radiation of the “heterokont algae”, the autotrophic stramenopiles. The stramenopiles were initially “protozoan” but their ecological success is largely attributable to the late symbiotic acquisition of chloroplasts. The stramenopiles and other taxa with chlorophyll a+c containing chloroplasts (cryptomonads, dinoflagellates, and haptophytes) do not share a common autotrophic ancestor. These photosynthetic assemblages acquired their plastids independently.

KATABLEPHARIS OVALIS, A COLORLESS FLAGELLATE WITH INTERESTING CYTOLOGICAL CHARACTERISTICS1

ABSTRACT Katablepharis ovalis Skuja, isolated from an impoundment in Colorado, has a cell covering composed of two layers over the cell body and flagella. The outer component of the cell covering contains 25‐nm‐diameter hexagonal scales arranged in rows. The inner component of the cell covering is composed of a layer of interwoven microfibrils. The inner component of the cell covering is joined to the plasma membrane by one or more attachment strips that always occur outside, and along, one of the microtubular groups of the outer array. The attachment strips resemble hemidesmosomes and are composed of rows of electron‐dense material, 12 nm apart, that protrude through the plasma membrane into the extracellular space, to attach to the inner wall. The two flagella are inserted subapically into a raised area of the cell. The flagella do not have any fibrillar or tubular hairs and are covered only by the two‐layered cell covering. The cell has an inner and outer array of microtubules, both of which are spindle‐shaped, arising at the anterior end of the cell and continuing into the posterior end of the cell. A single large Golgi apparatus occurs in the anterior cytoplasm. The nucleus is in the center of the cell. Two rows of large ejectisomes occur posterior to the area of flagellar attachment. Smaller ejectisomes occur under the plasma membrane in the posterior and medial areas of the cell. Each ejectisome is composed of a single body containing a spirally wound, tapered ribbon. On discharge, the ejectisome ribbon rolls inward, creating a tubular structure. The possible relationship between Katablepharis, the green algae, and the cryptophytes is discussed.

Insights into the evolution of heliozoa (Protozoa, Sarcodina) as provided by ultrastructural studies on a new species of flagellate from the genus Pteridomonas

The fine structure of Pteridomonas danica, a new species of helioflagellate (protozoa), is described. The organism has a single apical flagellum which bears two rows of tripartite tubular hairs. There are two kinetosomes which are bound to each other and to the surface of the single nucleus by amorphous electron-dense material. The flagellum is surrounded by a wreath of fine arms, which are supported internally by triads of microtubules. The triads terminate on the nucleus. The mitochondria have tubular cristae which contain wisps of intracristal material. The dictyosomes are located in the posterior part of the cell, being clustered around the internal element of the contractile stalk. Extrusomes are present. Pteridomonas has substantial similarities with the colourless flagellate Ciliophrys and with the pedinellid algal flagellates. As Ciliophrys resembles the actinophryid heliozoa in several important respects, the evidence supports the contention that these heliozoa have a common ancestry with the heterokont algae and have evolved along a line involving the pedinellids and some colourless helioflagellates. If the perceived relationships are to be reflected in their taxonomy, then a substantial reclassification of these organisms is required.

The Genus Parisia in New Caledonia

In New Caledonia, three species of the genus Parisia are known: P. neo-caledonica, P. ciliata and P. laevipila, the latter two species were formerly in the genus Eucamptodon. In 1875, Bescherelle described Eucamptodon cil- iatus, characterized by a rough, tubular hair at the apex of the leaf. Montagne described the genus Eu- camptodon with multicellular spores, meanwhile Bescherelle wrote spores sph6riques (and unicel- lular). Brotherus (1906) defined a new monotypic genus Parisia in which the leaf has the configuration of an E. ciliatus leaf with unicellular and spherical spores. Some years after, Cardot and Th6riot (1908) added a new species near E. ciliatus, E. laevipilus (with a Latin diagnosis of two lines). In the second edition of Pflanzenfamilien, Brotherus put E. cil- iatus and E. laevipilus in a subgenus of the genus Eucamptodon: Blepharacis. All the material known to the author (PC, z, and Rennes herbarium including the recent collections of Huerlimann and MacKee) was seen and all three species viz: Parisia neocaledonica, Eucamptodon ciliatus and E. laevipilus have spherical spores.