Morphology of Chondrophycus undulata and C. parvipapillata and its implications for the taxonomy of the Laurencia (Ceramiales,Rhodophyta) complex

Laurencia Lamouroux subgenus Chondrophycus Tokida et Saito was recently raised to generic status as Chondrophycus (Tokida et Saito) Garbary et Harper (Ceramiales, Rhodophyta). The previously unknown morphology and anatomy of two Chondrophycus species, C. undulata (Yamada) Garbary et Harper and C. parvipapillata (C.K. Tseng) Garbary et Harper, were studied in specimens from Korea, Japan and Hawaii. These species share some features, such as a strongly compressed thallus, vegetative axes with two pericentral cells, tetrasporangial production from pericentral cells and spermatangial development of the trichoblast type. However, they differ from each other in the position of the first pericentral cell relative to the trichoblast in axial segments and in the position of the tetrasporangial pericentral cell. In C. undulata, the first pericentral cell is always produced at one side of the basal cell of a trichoblast, whereas in C. parvipapillata it is formed underneath this cell. While tetrasporangia in C. undulata are produced only from three (occasionally four) additional pericentral cells, in C. parvipapillata they are formed by the existing second pericentral cell and two (occasionally three) additional pericentral cells, so the resulting tetrasporangial axial segment has only one sterile pericentral cell rather than two as in C. undulata. C. undulata produces spermatangial branches from two laterals on the suprabasal cell of trichoblasts but one of the two remains partly sterile, whereas in C. parvipapillata a spermatangial branch develops from only one of the two laterals. These two species also differ distinctly from each other in some vegetative features, such as presence or absence of (1) secondary pit connections between epidermal cells, (2) a palisade structure of epidermal cells with conical projections and (3) corps en cerise. The taxonomic implications of these vegetative and reproductive features of Chondrophycus and those of other genera of the Laurencia complex necessitate changes to the generic delineations of Osmundea Stackhouse, Laurencia and Chondrophycus. The required new combinations in Chondrophycus are made, mainly for species from the western Pacific. An infrageneric classification scheme is also proposed for Chondrophycus including Kangjaewonia subgen. nov., Palisada (Yamada) subgen. stat. nov., Yuzurua subgen. nov. and Parvipapillatae sect. nov.     

Species diversity of the genus Osmundea (Ceramiales,Rhodophyta) in the Macaronesian region

Species diversity within the genus Osmundea in the Macaronesian region was explored by conducting a comprehensive sampling in the Azores, the Canary, and the Madeira archipelagos. Toward identification, all specimens were first observed alive to verify the absence of corps en cerise, a diagnostic character for the genus and morphometric data were measured (thallus length and width, first‐order branches length and width, branchlets length and width, cortical cell length and width in surface view, cortical cell length and width in transverse section). Specimens were sequenced for COI‐5P (39 specimens) and three species delimitation methods (Generalized Mixed Yule Coalescent, Automatic Barcode Gap Discovery method, and Poisson Tree Processes) were used to assess the threshold between infra‐ and interspecific relationships. Subsequently, one or several sequences of plastid‐encoded large subunit of RuBisCO (21 specimens) per delimited species were generated to assess the phylogenetic relationships among Macaronesian Osmundea. Moreover, for each delineated species, vegetative and reproductive anatomy was thoroughly documented and, when possible, specimens were either assigned to existing taxa or described as novel species. This integrative approach has provided data for (i) the presence of O. oederi, O. pinnatifida, and O. truncata in Macaronesia; (ii) the proposal of two novel species, O. prudhommevanreinei sp. nov. and O. silvae sp. nov.; and (iii) evidence of an additional species referred as “Osmundea sp.1,” which is a sister taxon of O. hybrida.     

Phylogenetic Re-Evaluation of the Laurencia Complex (Rhodophyta) with a Description of L. Succulenta Sp. Nov. from Korea

Laurencia succulenta sp. nov. (Rhodophyta) is described from Korea. This species exhibits vegetative and reproductive structures typical of the genus, but is distinct from similar species in its epiphytic habitat and the fleshy, robust, thick and subcompressed thalli with basically distichous branching. In addition, it is readily distinguished from the most similar species, such as L. nipponica Yamada and L. okamurae Yamada, by the cystocarps with a somewhat protuberant ostiole. In a phylogenetic analysis of 47 species of the Laurencia Lamouroux complex from various localities around the world based on 49 morphological characters, four major clades (Laurencia, Chondrophycus palisadus (Yamada) Nam group, C. cartilagineus (Yamada) Garbary et Harper group and Osmundea Stackhouse assemblage), each of which forms a monophyletic group, were recognized. Among these, the Laurencia clade is basal to the overall assemblage, and is defined by the vegetative axis with four rather than two pericentral cells. The Osmundea clade is supported by autapomorphic characters for the genus, features associated with spermatangial formation of the filament type and tetrasporangial production from epidermal cells. By contrast, Chondrophycus, a genus characterized by a combination of features (vegetative axis with two pericentral cells, trichoblast-type spermatangial development and tetrasporangial production from pericentral cells), is paraphyletic, and the species were separated into two well-supported clades, the C. palisadus group and C. cartilagineus group. These clades are distinguished from each other by the position of the first pericentral cell relative to the trichoblast, the presence or absence of fertility at the second pericentral cells and number of sterile pericentral cells in the tetrasporangial axis, the pattern of formation of spermatangial branches on trichoblasts, post-fertilization feature associated with the formation time of the auxiliary cell, and, probably, the number of pericentral cells in the procarp-bearing segment. Of these features, the side position of the first pericentral cell in the latter group (a synapomorphy for the C. cartilagineus group plus Osmundea) suggests that the C. cartilagineus group is more closely related to Osmundea than to the C. palisadus group. This cladistic analysis indicates that Chondrophycus is not monophyletic, suggesting that the C. palisadus group should be separated from Chondrophycus at the genus level. Based on this result, Palisada (Yamada) stat. nov. is proposed for the group, together with an emendation of the generic delineation of Chondrophycus, and relevant nomenclatural changes for several Chondrophycus species are also included. In addition, Corynecladia J. Agardh is reinstated for the type species L. clavata Sonder.     

Morphology of Laurencia clavata and L. elata (Ceramiales,Rhodophyta) in relation to generic circumscription in the Laurencia complex

Laurencia Lamouroux (Rhodophyta) was recently separated into three genera–Laurencia, Chondrophycus (Tokida et Saito) Garbary et Harper and Osmundea Stackhouse – each of which was newly defined based on vegetative and reproductive structures. In this study, the previously unknown vegetative and reproductive morphology of two Australian endemic species of Laurencia, L. clavata Sonder and L. elata (C. Agardh) Harvey, was studied, particularly in the context of the revised generic delineation. These species exhibit vegetative axes with four pericentral cells and trichoblast-type spermatangial development. Tetrasporangia are abaxially produced from the existing third and fourth pericentral cells. L. clavata has terete thalli with distinctive verticillate branching and is similar to Chondria C. Agardh, rather than to Laurencia, in having an unusually marked constriction at the base of the branches and starch accumulation in subcortical and medullary cells. Compared to Laurencia, apical cells of this species exhibit a less oblique division ; the resulting recognizable axial cell rows extend somewhat below the branches, and particularly at a young stage they are also clear throughout branchlets. However, other vegetative and spermatangial structures show that L. clavata is more closely allied to Laurencia than to Chondria, and it is placed in Laurencia. By contrast, L. elata exhibits morphology typical of Laurencia and is characterized by large, robust, compressed thalli with fastigiately distichous branching and an extensive secondary cortex. Furthermore, it appears to be distinct from similar species in sometimes having a parasitic species of Janczewskia Solms-Laubach (Rhodophyta). Taxonomy of Laurencia is discussed on the basis of these and previous studies.     

New records of Gelidiella pannosa, Pterocladiella caerulescens and Pterocladiella caloglossoides (Rhodophyta, Gelidiales) from Japan

Three gelidialean species, Gelidiella pannosa (Feld‐mann) Feldmann et Hamel, Pterocladiella caerulescens (Kutzing) Santelices et Hommersand and Pterocladiella caloglossoides (Howe) Santelices, are newly reported from Japan, and their characteristic features are described. Monoecious plants of P. caerulescens produce spermatangial sori on: (i) fertile cystocarpic branchlets; (ii) special spermatangial branchlets on a cystocarpic axis; and (iii) branchlets of a special spermatangial axis. The latter two are newly reported in this species. Gelidiella pannosa has numerous unicellular independent points of attachment, whereas P. caerulescens and P. caloglossoides have the peg type of secondary rhizoidal anchorage. In the molecular phylogenetic study using small subunit ribosomal DNA sequences, G. pannosa is included in the Gelidiella clade with 100% bootstrap support in neighbor‐joining (NJ) analysis and 99% in maximum parsimony (MP) analysis. Pterocladiella caerulescens and P. caloglossoides are included in the Pterocladiella clade with 99.7% bootstrap support in NJ analysis and 100% in MP analysis. Each type of secondary rhizoidal attachment is completely consistent with the respective genus clade, which suggests that this morphological characteristic reflects phylogeny within the order Gelidiales.     

Ultrastructure of trichoblasts in the red alga Osmundea spectabilis var. spectabilis (Rhodomelaceae,Ceramiales)

The apex of the tetrasporangial branches of Osmundea spectabilis var. spectabilis (= Laurencia spectabilis var. spectabilis) exhibits cavities in which tufts of multicellular trichoblasts occur. Trichoblast development in Osmundea spectabilis var. spectabilis begins with the differentiation of an epidermal cell within the crypt. This cell differentiates into a trichoblast mother cell (TMC). The TMC divides to form a two-celled incipient trichoblast. Successive periclinal divisions of the apical cell of the young trichoblast result in the formation of a multicellular developing trichoblast. With the exception of the apical cell all trichoblast cells are at the same developmental stage. They possess a large nucleus, abundant plastids with peripheral and some internal thylakoids and dictyosomes. Daughter chloroplasts result from one constriction or multiple fission of a single chloroplast. Dictyosomal cisternae and mucilage sacs contribute material to wall formation. Each differentiating trichoblast cell is surrounded by a bi-layered wall. The outer wall layer represents the trichoblast mother cell wall and the inner wall layer is the trichoblast cell wall. Mature trichoblast cells have thin walls, probably as a consequence of mucilage extrusion, the most likely function of trichoblasts in Osmundea.     

REASSESSMENT OF THE LITTLE‐KNOWN CRUSTOSE RED ALGAL GENUS POLYSTRATA (GIGARTINALES), BASED ON MORPHOLOGY AND SSU rDNA SEQUENCES1

The taxonomic distinctiveness of the crustose red algal genus Polystrata Heydrich (Peyssonneliaceae) is confirmed on the basis of morphological and molecular data. The vegetative and reproductive morphology of the type species Polystrata dura Heydrich is newly described. Polystrata thalli are thick multi‐layered crusts, each crust of which is composed of a mesothallus, a superior perithallus, and an inferior perithallus. P. dura is characterized by a poorly developed inferior perithallus consisting of single‐celled perithallial filaments and each layer of multi‐layered crusts being closely adherent to the parental layer. This Polystrata species is identical to Peyssonnelia species, the type genus of the Peyssonneliaceae in the morphology of sexual reproductive organs: a carpogonial branch and an auxiliary cell branch are formed laterally on respective nemathecial filaments; the gonimoblasts are developed from connecting filaments and auxiliary cells; the spermatangia are produced in male and female nemathecia; and the spermatangial filament produces a series of one to four paired spermatangia that form a whorl surrounding each central cell (the Peyssonnelia dubyi‐type development). Polystrata fosliei (Weber‐van Bosse) Denizot is clearly distinguished from P. dura by an inferior perithallus as well‐developed as the superior perithallus, and each layer of multi‐layered crusts being loosely adherent to the parental layer. In our small subunit rDNA trees of the Peyssonneliaceae, these Polystrata species formed a clade with low to medium supports, although the phylogenetic position of Polystrata was unresolved in this family. Therefore, the thallus structure of Polystrata may be regarded as an important taxonomic character at the genus rank.     

Two species of Dasya (Ceramiales, Rhodophyta) from Bonin Islands, southern Japan, with the description of Dasya boninensis sp. nov.

Two species of Dasya in the Dasyaceae (Ceramiales, Rhodophyta) are reported from Bonin Islands, southern Japan. Dasya murrayana Abbott et Millar, new to Japan, is characterized by the following set of features: the tufted habit (up to 30 erect axes developing from a basal disc), small‐sized (6–10 mm high and 350–500 μm in diameter in the middle region), thinly but completely corticated axes, rigid and incurved pseudolaterals forming corymbose heads at the apices of axes and branches, the absence of adventitious monosiphonous filaments, a large number of tetrasporangial stichidia and spermatangial branches per fertile pseudolateral and slender spermatangial branches (35–45 μm in diameter). Dasya boninensis Masuda, Kurihara et Kogame, sp. nov. is characterized by short but thick (10–30 mm high and 600–1000 μm in diameter at the middle portion), heavily corticated axes, indistinct pericentral cells except for the upper portion in transverse sections, soft, straight pseudolaterals and adventitious monosiphonous filaments densely covering the axis and branches, a small number of tetrasporangial stichidia and spermatangial branches per fertile pseudolateral, thick spermatangial branches (65–90 μm in diameter), and short‐necked cystocarps. A dichotomous key to the taxa found in Japanese waters is given.     

Species concept and morphological differentiation of strains traditionally assigned to Micrasterias truncata

The morphological and molecular differentiation of the Micrasterias truncata (Corda) ex Bréb species complex was investigated. In total, 17 strains traditionally assigned to M. truncata were isolated from different European localities (Czech Republic, southwest France, Ireland), and obtained from public culture collections. In addition, strains of the morphologically similar species, M. decemdentata (Nägeli) W. Archer and M. zeylanica F. E. Fritsch, were also included. Molecular phylogenetic analysis based on trnG^ucc intron sequences revealed five well supported clades. Two Australian strains assigned to M. truncata var. pusilla G. S. West formed a lineage sister to M. zeylanica. This was evident from a concatenated phylogeny based on small subunit rDNA and trnG^ucc intron sequences. The isolated position of these strains was also illustrated by parallel landmark‐based geometric morphometric analysis of cell shapes. The strains NIES 783 and NIES 784 probably represent a separate species. Particular analysis, including additional strains, is needed to resolve the relationship inside this lineage. The second phylogenetic lineage, containing two strains of M. truncata var. semiradiata (Kützing) Wolle, was also different from other strains on the basis of morphometric data. We suggest recognizing this variety as a separate species, Micrasterias semiradiata L.A. Brébisson ex F. T. Kützing. The remaining three clades formed a firmly supported group of the ‘core’M. truncata recognized by both molecular markers. However, neither any morphological, morphometric, nor geographical pattern was detected among members of these three clades. This pattern could be caused by a relatively recent origin of these lineages that may represent a sympatric, truly cryptic species. Strains attributable to traditional morphologically defined variety M. truncata var. neodamensis were nested within the ‘core’M. truncata.     

The contribution of foliar micromorphology and anatomy to the circumscription of species within the <Emphasis Type="Italic">Chusquea ramosissima</Emphasis> informal group (Poaceae,Bambusoideae, Bambuseae)

Chusquea is a diverse but monophyletic genus of Neotropical woody bamboos from primarily montane forests that comprises four well-supported lineages: subg. Magnifoliae, subg. Platonia, subg. Rettbergia, and the Euchusquea clade (comprising subg. Swallenochloa and subg. Chusquea). However, the relationships among clades or taxa within the Euchusquea clade inferred from molecular data are mostly not congruent with those inferred from morphological evidence, consequently limiting our ability to understand species relationships. In this study we generated foliar micromorphological and anatomical data for the Chusquea ramosissima informal group (Chusquea ramosissima, C. tenella, and C. tenuiglumis), and for the putative new species from Bolivia in this group, in order to test the value of these types of data for defining species and to seek potential synapomorphies for this group. Our results demonstrate that epidermal features, mainly with regard to the stomatal apparatus, proved to be more valuable in distinguishing species than anatomical characters. The presence of horizontally elongated silica cells over the veins and adaxial arm cells with invaginations from the abaxial side was shared by all the studied species but is not unique to this group. The type of trichomes, shape of silica bodies, type of arm cells, and midrib structure may be useful to lesser degree. All four species exhibited intraspecific variation in development of the papillae on the long cells. Support for the recognition of the new species from Bolivia is provided by micromorphological characters. An identification key based on leaf blade features is provided for the four studied species.     

Nutritional value of selected macroalgae

Macroalgae are traditionally used in human and animal nutrition. Their protein and fiber content have been widely studied and differ according to the species, their geographic origin and their seasonal conditions. In addition to their value for human nutrition, seaweeds have multiple therapeutically applications (e.g., weight control, hypocholesterolemic, antioxidant and antitumor activities, others) and, in general, contribute and promote human health. In the archipelago of the Azores, the consumption of seaweeds is widespread and accepted as a common practice in some islands. This work is aimed at providing information on the protein and fiber content of the locally consumed species, to promote this regional food product that can be potentially profitable from the biotechnology and commercial perspective, and also benefit public health, particularly, taking into account the low level of marine pollution in the Azores archipelago. Protein and fiber content of eight seaweeds (Porphyra sp., Osmundea pinnatifida, Pterocladiella capillacea, Sphaerococcus coronopifolius, and Gelidium microdon, Rhodophyta; Cystoseira abies-marina and Fucus spiralis, Phaeophyta; Ulva compressa, Chlorophyta) were determined using the Kjeldahl method and the Weende method, respectively. The protein content ranged from 6.81 to 26.62 of dry weight for C. abies-marina and U. compressa, respectively. Fiber content was generally higher as compared with that in seaweeds from other origins and ranged from 33.82 to 63.88 for O. pinnatifida and F. spiralis, respectively.     

Reproductive morphology of Gastroclonium pacificum (Champiaceae,Rhodymeniales) from Japan

Morphological studies were undertaken on Gastroclonium pacificum (E.Y. Dawson) C.F. Chang et B.M. Xia (Champiaceae, Rhodymeniales) from Japan. We describe the details of male reproductive structures, the procarp and early post‐fertilization stages. This species has a solid axis, with both tetrasporangia and polysporangia, spermatangia are cut off from spermatangial parent cells, and a procarp is composed of a 4‐celled carpogonial branch and two 2‐celled auxiliary cell branches. The mature cystocarp lacks a conspicuous ostiole, a characteristic of the genus Gastroclonium. The most distinctive characteristic of the species is the tela arachnoidea, which is lacking in other species of Gastroclonium.     

Growth and water relations of Tamarix ramosissima and Populus euphratica on Taklamakan desert dunes in relation to depth to a permanent water table

The hypothesis that water relations and growth of phreatophytic Tamarix ramosissima Ledeb. and Populus euphratica Oliv. on dunes of varying height in an extremely arid Chinese desert depend on vertical distance to a permanent water table was tested. Shoot diameter growth of P. euphratica was inversely correlated with groundwater depth (GD) of 7 to 23 m (adj. R² = 0.69, P = 0.025); growth of T. ramosissima varied independent of GD between 5 and 24 m (P = 0.385). Pre‐dawn (pd) and midday (md) water potentials were lower in T. ramosissima (minimum pd ?1.25 MPa, md ?3.6 MPa at 24 m GD) than in P. euphratica (minimum pd ?0.9 MPa, md ?3.05 MPa at 23 m GD) and did not indicate physiologically significant drought stress for either species. Midday water potentials of P. euphratica closely corresponded to GD throughout the growing season, but those of T. ramosissima did not. In both species, stomatal conductance was significantly correlated with leaf water potential (P. euphratica: adj. R² = 0.84, P < 0.0001; T. ramosissima: adj. R² = 0.64, P = 0.011) and with leaf‐specific hydraulic conductance (P. euphratica: adj. R² = 0.79, P = 0.001; T. ramosissima: adj. R² = 0.56, P = 0.019); the three variables decreased with increasing GD in P. euphratica. Stomatal conductance of P. euphratica was more strongly reduced (> 50% between ?2 and ?3 MPa) in response to decreasing leaf water potential than that of T. ramosissima (30% between ?2 and ?3 MPa). Tolerance of lower leaf water potentials due to higher concentrations of leaf osmotically active substances partially explains why leaf conductance, and probably leaf carbon gain and growth, of T. ramosissima was less severely affected by GD. Additionally, the complex below‐ground structure of large clonal T. ramosissima shrub systems probably introduces variability into the assumed relationship of xylem path length with GD.     

PHYLOGENY OF AULACOSEIRA (BACILLARIOPHYTA) BASED ON MOLECULES AND MORPHOLOGY1

The phylogeny of 67 populations representing 45 species of Aulacoseira Thwaites was estimated by maximum parsimony methods using a combination of nucleotide sequence data and qualitative and quantitative morphological characteristics of the silica cell wall gathered primarily from original observation by LM and SEM. A new type of character using continuous quantitative variables that describe the ontogenetic‐allometric trajectories of cell wall characteristics over the life cycle (size range) of diatoms is introduced. In addition to the 45 Aulacoseira species, the phylogeny also incorporated one Miosira Krammer, Lange‐Bertalot, and Schiller species and two outgroup species (Melosira varians Agardh and Stephanopyxis nipponica Gran & Yendo). Fifteen species, represented by 24 populations, also contained molecular data from the nuclear genome (18S rDNA), and 11 of these species (18 populations) contained data from the chloroplast genome (rbcL) as well, which were sequenced or downloaded from GenBank. The phylogeny of Aulacoseira is composed of five major clades: 1) an A. crenulata (Ehrenburg) Thwaites and A. italica (Ehrenburg) Simonsen clade, which is the most basal; 2) an A. granulata (Ehrenburg) Simonsen complex clade; 3) an A. ambigua (Grunow) Simonsen clade; 4) an A. subarctica (O. Müller) Haworth and A. distans (Ehrenburg) Simonsen clade; and 5) an A. islandica (O. Müller) Simonsen clade that also contained endemic species from Lake Baikal, Siberia and many extinct Aulacoseira taxa. Monophyly of Aulacoseira can only be achieved if Miosira is no longer given separate generic status.     

Molecular data reveal cryptic lineages within the northeastern Atlantic and Mediterranean small mussel drills of the Ocinebrina edwardsii complex (Mollusca: Gastropoda: Muricidae)

We used a molecular phylogenetic approach to investigate species delimitations and diversification in the mussel drills of the Ocinebrina edwardsii complex by means of a combination of nuclear (internal transcribed spacer 2, ITS2) and mitochondrial [cytochrome oxidase subunit I (COI) and 16S] sequences. Our sample included 243 specimens ascribed to seven currently accepted species from 51 sites. Five of the samples were from either the type locality of a nominal species or a close nearby locality (O. edwardsii from Corsica, O. carmelae and O. piantonii from the Kerkennah Islands, O. hispidula from the Gulf of Gabès and O. leukos from the Canary Islands), one from the inferred original locality (O. ingloria from Venice Lagoon), and specimens assigned in the recent literature to O. nicolai. We used a combination of distance‐ and tree‐based species delimitation methods to identify Molecular Operational Taxonomic Units (MOTUs) to compare with the a priori species identifications. The consensus tree obtained by BEAST on the COI alignment allows the recognition of several distinct clades supported by the three species delimitation methods employed. The eight‐MOTUs scenario, shared by the Automatic Barcode Gap Discovery (ABGD) and Generalized Mixed Yule‐Coalescent (GMYC) methods, comprises the following major clades: clade A contains the south Tunisian species Ocinebrina piantonii Cecalupo, Buzzurro & Mariani from which the sympatric taxon O. carmelae Cecalupo, Buzzurro & Mariani (new synonym) cannot be separated; clades B and C bring together all populations from the Aegean Sea and some from the Ionian Sea, respectively; clade D groups, on the one hand, the south Tunisian samples morphologically assigned to O. hispidula Pallary and, on the other, Atlantic and Alboran Sea samples (including the Canarian taxon O. leukos Houart); clade E includes a sample from the type locality of O. edwardsii and several samples from the Tyrrhenian Sea; clades F and G correspond to a few samples from the Venice Lagoon and the Tyrrhenian Sea, respectively; clade H groups the bulk of samples from the Adriatic Sea, including samples from the Venice Lagoon morphologically identified as Ocinebrina ingloria (Crosse), and some from the Ionian Sea. No final conclusions could be reached to reconcile the currently recognized morphological taxa with the clades suggested by the COI data. The geographical structure proposed by the mitochondrial markers is similar to that found in other marine invertebrates and partially corresponds to the species defined by shell characters. We propose here a framework for the revision of the Ocinebrina edwardsii species complex, suggesting a geographical pattern for the diversification of this group in the studied area. © 2013 The Linnean Society of London     

Oligoneuria Pictet: phylogenetic analysis and description of three new species from Brazil (Ephemeroptera: Oligoneuriidae)

For 150 years O. anomala has been the only known species of Oligoneuria, the type genus of the Oligoneuriidae (Ephemeroptera). However, two species have been recently described and Oligoneuria has been proposed as a senior synonym of the genus Oligoneurioides. In the present paper, based on material from the Amazon and Brazilian Atlantic Forest, three new species are described, including information on all life stages. Given these new species, as well as the lack of cladistic support for the proposed synonymy between Oligoneuria and Oligoneurioides, a phylogenetic analysis was performed in order to address the relationships between all species and to test the status of Oligoneurioides. Our results show that the status of the genus is uncertain, mainly due to the lack of knowledge of the type species of O. anomala, known exclusively from a female subimago. Taking into account phylogenetic as well as taxonomic arguments, we propose that the genus Oligoneuria should be divided into three subgenera: Oligoneuria s.s., for O. anomala; Oligoneuria (Yawari) new subgenus, for Oligoneuria truncata sp.n. ; and Oligoneuria (Oligoneurioides) for the remaining five species, including O. amandae sp.n. and O. mitra sp.n. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:A2AEE4B7‐FEA8‐4067‐8F3B‐666095EDB997 .     

TWO TYPES OF AUXILIARY CELL AMPULLAE IN GRATELOUPIA (HALYMENIACEAE,RHODOPHYTA), INCLUDING G. TAIWANENSIS SP. NOV. AND G. ORIENTALIS SP. NOV. FROM TAIWAN BASED ON rbcL GENE SEQUENCE ANALYSIS AND CYSTOCARP DEVELOPMENT1

Few species in the genus Grateloupia have been investigated in detail with respect to the development of the auxiliary cell ampullae before or after diploidization. In this study, we document the vegetative and reproductive structures of two new species of Grateloupia, G. taiwanensis S.‐M. Lin et H.‐Y. Liang sp. nov. and G. orientalis S.‐M. Lin et H.‐Y. Liang sp. nov., plus a third species, G. ramosissima Okamura, from Taiwan. Two distinct patterns are reported for the development of the auxiliary cell ampullae: (1) ampullae consisting of three orders of unbranched filaments that branch after diploidization of the auxiliary cell and form a pericarp together with the surrounding secondary medullary filaments (G. taiwanensis type), and (2) ampullae composed of only two orders of unbranched filaments in which only a few cells are incorporated into a basal fusion cell after diploization of the auxiliary cell and the pericarp consists almost entirely of secondary medullary filaments (G. orientalis type). G. orientalis is positioned in a large clade based on rbcL gene sequence analysis that includes the type species of Grateloupia C. Agardh 1822 , G. filicina. G. taiwanensis clusters with a clade that includes the generitype of Phyllymenia J. Agardh 1848 , Ph. belangeri from South Africa; that of Prionitis J. Agardh 1851 , Pr. lanceolata from Pacific North America; and that of Pachymeniopsis Y. Yamada ex Kawab. 1954, Pa. lanceolata from Japan. A reexamination of the type species of the genera Grateloupia, Phyllymenia, Prionitis, and Pachymeniopsis is required to clarify the generic and interspecific relationships among the species presently placed in Grateloupia.     

Developmental anatomy of seedlings of Indodalzellia gracilis (Podostemaceae)

In Tristichoideae, aquatic angiosperms in the family Podostemaceae, Terniopsis, Tristicha, Indotristicha and Cussetia have creeping roots with flanking (sub)cylindrical shoots, while Dalzellia is rootless and has crustose shoots. Indodalzellia gracilis, sister to a clade of Dalzellia zeylanica and Indotristicha ramosissima, has subcrustose shoots on the side of creeping roots, suggesting that I. gracilis may be a key species to reveal how saltational evolution of the body plan occurred in these three species. We investigated developmental morphology of I. gracilis seedlings grown in culture, using scanning electron microscopy and semi‐thin serial sections. As in D. zeylanica, the plumular apical meristem in the seedling gives rise to two shoot apical meristems, which develop into horizontal subcrustose shoots with dorsal and marginal leaves. Neither radicle nor adventitious root is produced from the hypocotyl, but an adventitious root arises endogenously from the juvenile shoot and from some shoots of adult plants. These results, together with the phylogenetic relationships, suggest that the Indodalzellia seedling evolved by loss of the adventitious root derived from the hypocotyl, appearance of shoots in the axil of cotyledons, and appearance of adventitious roots from adventitious shoots. The difference in place of origin of the root between Indodalzellia and I. ramosissima suggests differing evolutionary origin of the root in Tristichoideae.