Basidiomycetous endophytes in New Zealand Aneuraceae (simple thalloid liverworts, Metzgeriidae) and the derived status of the monotypic genus Verdoornia

Botany ◽  
2008 ◽  
Vol 86 (4) ◽  
pp. 346-358 ◽  
Author(s):  
Jeffrey G. Duckett ◽  
Roberto Ligrone

The ultrastructure of endophytic basidiomycetes in two New Zealand species of Aneura and the endemic genus Verdoornia is compared with that in northern hemisphere members of the Aneuraceae. The discovery of a basidiomycete colonization in Verdoornia and a reappraisal of earlier morphological data confirms molecular evidence that this is a derived genus nested within the Aneuraceae rather than a primitive isolated taxon, as considered previously. Throughout the Aneuraceae, the basidiomycetes exhibit similar colonization patterns; initial proliferation of dikaryotic, non-clamp-forming hyphal coils within the host cells is followed by senescence and aggregation of collapsed hyphae into large masses. Multiple cycles of colonization are common. Dolipores with imperforate parenthesomes indicate that the fungi are all heterobasidiomycetes. In line with earlier cross-colonization experiments showing complete host specificity, differences in hyphal diameters and dolipore dimensions suggest that the fungi belong to different taxa. The New Zealand aneuracean fungi have multilayered walls similar to their northern hemisphere counterparts. Within the Aneuraceae there appears to be a trend from very limited or no endophyte colonization in Riccardia to colonization of the entire thallus in Cryptothallus. The cytology of the fungal associations in Aneura and Verdoornia is highly suggestive of mixotrophy.

Author(s):  
Mathias Jaschhof ◽  
Catrin Jaschhof

Glemparon Jaschhof, 2013, a previously monotypic genus confined to Sweden, is shown here to be considerably richer in species, with most species found to occur in the Australasian region. Eighteen new species are described: G. tomelilla sp. nov. (from Sweden); G. aotearoa sp. nov., G. birhojohmi sp. nov., G. cervus sp. nov., G. didhami sp. nov, G. kaikoura sp. nov., G. nativitas sp. nov., G. orautahi sp. nov., G. otago sp. nov., G. pureora sp. nov., G. rakiura sp. nov., G. rotoiti sp. nov., G. rotoroa sp. nov., G. tewaipounamu sp. nov., G. waipapa sp. nov., G. waipoua sp. nov. (all from New Zealand); G. manuka sp. nov. and G. warra sp. nov. (both from Tasmania, Australia). Glemparon sagittifer Jaschhof, 2013 is redescribed. Genitalic illustrations are provided allowing for the effective identification of all the species known thus far. Morphological data obtained here are used for revising the generic definition. Dicerura Kieffer, 1898 is hypothesized as the sister group to Glemparon. The case of Glemparon is discussed as a perfect example of the fact that our collective ignorance of porricondyline diversity in most parts of the world is a major impediment to a better understanding of the European species.


1992 ◽  
Vol 70 (1) ◽  
pp. 58-72 ◽  
Author(s):  
Jeffrey G. Duckett ◽  
Roberto Ligrone

The ventral epidermal cells of the photosynthetic, surface-living gametophytes of Lycopodium cernuum, collected from moist shaded banks in Peninsular Malaysia, contain an aseptate fungus. In some cells the hyphae are thick walled and form coils encapsulated by a thin layer of host wall material. In others the fungus is thin walled and shows limited differentiation into larger trunk hyphae and arbuscules. The adjacent host cytoplasm, separated from the fungus by a granular interfacial matrix, contains numerous chloroplasts, mitochondria, and microtubules. The hyphae contact the substratum via the ventral walls of the epidermal cells and the rhizoids are free from infection. In the protocorm and root nodules, aseptate hyphae initially colonize mucilage-filled schizogenous intercellular spaces. Subsequent invasion of the host cells is associated with the development of massive overgrowths of host wall material. The fungal associations in L. cernuum share a mixture of attributes otherwise found in different angiosperm mycorrhizae and in mycotrophic relationships in liverworts. Wall ingrowths are present in both the gametophyte and sporophyte cells in the placenta of L. cernuum. The very limited development of the placenta, compared with L. appressum, certain bryophytes and ferns, the diminutive size, and early senescence of the gametophytes of L. cernuum are all linked to the presence of the protocorm. This massive absorptive organ, homologous to a foot, in terms of its position in sporophyte ontogeny, but external to the parent gametophyte, derives its nutrition partly from photosynthesis and partly from its fungal endophyte. Key words: chloroplasts, Lycopodium, mycorrhiza, pteridophytes, root nodules, symbiosis, transfer cells.


Author(s):  
J. Walker

Abstract A description is provided for Melampsora medusae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Pycnia and aecia on Coniferae, especially Larix and Pseudotsuga, less commonly on Pinus and other genera (Ziller, 1965). Uredinia and telia on species of Populus, especially Populus deltoides, and its varieties and hybrids P. balsamifera, P. nigra var. italica and others. Its exact host range on species of Populus is not known due to confusion with other species of Melampsora and to uncertainty in the reported identity of some species of Populus and clones (Walker, Hartigan & Bertus, 1974). DISEASE: Leaf rust of poplars, causing severe leaf damage and early defoliation on susceptible species and clones. Continued defoliation of successive flushes of growth predisposes trees to winter injury and dieback (Peace, 1962) and can cause death of trees, especially nursery stock and trees 1-2 yr old (25, 204; 47, 241; Walker Haitigan & Bertus, 1974). Reduction in incremental growth of timber occurs with susceptible varieties. Some damage can occur to the conifer hosts. It is often severe on Pseudotsuga menziesii (45, 459; 47, 126) and in nurseries Pinus spp. and Larix spp. can be heavily attacked (Ziller, 1965). GEOGRAPHICAL DISTRIBUTION: North America (Canada, USA), Asia (Japan); Australasia and Oceania (Australia, New Zealand); Europe (France, Spain). Reports of Melampsora spp. on poplars (including P. deltoides and P. canadensis) from South America (Argentina, 21, 173), Uruguay (Lindquist & de Rosengurtt, 1967) may refer in part to M. medusae. TRANSMISSION: By air-borne urediniospores, often over long distances (suspected from eastern Australia to New Zealand). Urediniospores survive the winter in milder climates on semi-evergreen lines and on green sucker growth of deciduous trees. This is probably the main method of overwintering in the Southern Hemisphere and in warmer parts of the Northern Hemisphere. The possibility of bud carryover as occurs with M. epitea on Salix in Iceland (Jorstad, 1951) and the Canadian Arctic (Savile, 1972) should be investigated. Telia survive the winter and basidiospores formed in spring infect susceptible conifers in parts of the Northern Hemisphere (Ziller, 1965) but no conifer infection has so far been found in Australia.


1962 ◽  
Vol 12 (1) ◽  
pp. 25-42
Author(s):  
Paul Woldstedt

Abstract. The Pleistocene sequence of Wanganui (North Island of New Zealand) and the succession of glaciations in the South Island are shortly reviewed. The Last Glaciation and the Postglacial time in New Zealand were, as C14 determinations definitly show, contemporaneous with those of the Northern Hemisphere. If the Last Glaciation was contemporaneous on the two Hemispheres, then the older ones must also have been contemporaneous. This does not agree with the MILANKOVITCH-curve, which in the form, as it has been given by M., cannot have been the cause of the ice ages.


2016 ◽  
Author(s):  
Jocelyn C. Turnbull ◽  
Sara E. Mikaloff Fletcher ◽  
India Ansell ◽  
Gordon Brailsford ◽  
Rowena Moss ◽  
...  

Abstract. We present 60 years of Δ14CO2 measurements from Wellington, New Zealand (41° S, 175° E). The record has been extended and fully revised. New measurements have been used to evaluate the existing record and to replace original measurements where warranted. This is the earliest atmospheric Δ14CO2 record and records the rise of the 14C "bomb spike", the subsequent decline in Δ14CO2 as bomb 14C moved throughout the carbon cycle and increasing fossil fuel CO2 emissions further decreased atmospheric Δ14CO2. The initially large seasonal cycle in the 1960s reduces in amplitude and eventually reverses in phase, resulting in a small seasonal cycle of about 2 ‰ in the 2000s. The seasonal cycle at Wellington is dominated by the seasonality of cross-tropopause transport, and differs slightly from that at Cape Grim, Australia, which is influenced by anthropogenic sources in winter. Δ14CO2 at Cape Grim and Wellington show very similar trends, with significant differences only during periods of known measurement uncertainty. In contrast, Northern Hemisphere clean air sites show a higher and earlier bomb 14C peak, consistent with a 1.4-year interhemispheric exchange time. From the 1970s until the early 2000s, the Northern and Southern Hemisphere Δ14CO2 were quite similar, apparently due to the balance of 14C-free fossil fuel CO2 emissions in the north and 14C-depleted ocean upwelling in the south. The Southern Hemisphere sites show a consistent and marked elevation above the Northern Hemisphere sites since the early 2000s, which is most likely due to reduced upwelling of 14C-depleted and carbon-rich deep waters in the Southern Ocean. This developing Δ14CO2 interhemispheric gradient is consistent with recent studies that indicate a reinvigorated Southern Ocean carbon sink since the mid-2000s, and suggests that upwelling of deep waters plays an important role in this change.


2009 ◽  
Vol 34 (3) ◽  
pp. 580-594 ◽  
Author(s):  
Anthony R. Magee ◽  
Ben-Erik van Wyk ◽  
Patricia M. Tilney ◽  
Stephen R. Downie

Generic circumscriptions and phylogenetic relationships of the Cape genera Capnophyllum, Dasispermum, and Sonderina are explored through parsimony and Bayesian inference analyses of nrDNA ITS and cpDNA rps16 intron sequences, morphology, and combined molecular and morphological data. The relationship of these genera with the North African genera Krubera and Stoibrax is also assessed. Analyses of both molecular data sets place Capnophyllum, Dasispermum, Sonderina, and the only southern African species of Stoibrax (S. capense) within the newly recognized Lefebvrea clade of tribe Tordylieae. Capnophyllum is strongly supported as monophyletic and is distantly related to Krubera. The monotypic genus Dasispermum and Stoibrax capense are embedded within a paraphyletic Sonderina. This complex is distantly related to the North African species of Stoibrax in tribe Apieae, in which the type species, Stoibrax dichotomum, occurs. Consequently, Dasispermum is expanded to include both Sonderina and Stoibrax capense. New combinations are formalized for Dasispermum capense, D. hispidum, D. humile, and D. tenue. An undescribed species from the Tanqua Karoo in South Africa is also closely related to Capnophyllum and the Dasispermum–Sonderina complex. The genus Scaraboides is described herein to accommodate the new species, S. manningii. This monotypic genus shares the dorsally compressed fruit and involute marginal wings with Capnophyllum, but is easily distinguished by its erect branching habit, green leaves, scabrous umbels, and fruit with indistinct median and lateral ribs, additional solitary vittae in each marginal wing, and parallel, closely spaced commissural vittae. Despite the marked fruit similarities with Capnophyllum, analyses of DNA sequence data place Scaraboides closer to the Dasispermum–Sonderina complex, with which it shares the erect habit, green (nonglaucous) leaves, and scabrous umbels.


Zootaxa ◽  
2019 ◽  
Vol 4623 (3) ◽  
pp. 401-440
Author(s):  
WAYNE N. MATHIS ◽  
TADEUSZ ZATWARNICKI

Two genera of the shore-fly tribe Hyadinini, Hyadina Haliday and Parahyadina Tonnoir & Malloch, are revised, and all species treated, save P. lacustris Tonnoir & Malloch, are described for the first time. The phylogenetic position of both genera within Hyadinini is presented along with confirming, morphological evidence. The New Zealand fauna of Hyadina is now limited to the single new species H. breva, and Parahyadina is expanded from being a monotypic genus based on P. lacustris to also include the following 9 endemic new species: P. angusta, P. atra, P. bifurcata, P. bulla, P. debilis, P. edmistoni, P. hennigi, P. irwini, and P. latistylis. For both genera, emphasis is given to structures of the male terminalia, which are fully illustrated. Detailed locality data and distribution maps for all species are provided, and structures of the male terminalia are fully illustrated. For perspective and to facilitate recognition of genera, the tribe Hyadinini is diagnosed and a key to genera from New Zealand is provided. 


2013 ◽  
Vol 26 (6) ◽  
pp. 408 ◽  
Author(s):  
Matt A. M. Renner ◽  
Nicolas Devos ◽  
Elizabeth A. Brown ◽  
Matt J. von Konrat

The current paper presents molecular data from three chloroplast markers (atpB–rbcL spacer, trnG G2 intron, trnL–trnF intron and spacer); morphological data, and geographic data to support the recognition of nine species belonging to Radula subg. Odontoradula in Australasia. R. ocellata, the subgeneric type from the Wet Tropics bioregion, is maintained as distinct from its sister species, R. pulchella, from south-eastern Australian rainforests; both species are Australian endemics. Reinstatement of R. allisonii from synonymy, under R. retroflexa, is supported by molecular data and morphological characters, including the absence of triradiate trigones on leaf-lobe cell walls, the apex of lobules on primary shoots not being turned outwards, the oblong-elliptic female bracts, and the perianths having a pronounced wing. Reinstatement of R. weymouthiana, from synonymy under R. retroflexa, is also supported by molecular data and morphological characters, including the presence of a single low dome-shaped papilla over each leaf-lobe cell, and the large imbricate lobules on primary shoots. R. weymouthiana occurs in Tasmania and New Zealand, whereas R. allisonii is a New Zealand endemic. Australian R. retroflexa exhibits differentiation into epiphytic and rheophytic morphs, interpreted as ecotypes. Australian individuals, comprising both epiphytic and rheophytic morphs, are monophyletic and nested within a clade containing individuals from other regions. R. novae-hollandiae is newly reported for the New Zealand Botanical Region, from Raoul Island in the Kermadecs. R. novae-hollandiae exhibits decoupling of morphological and molecular divergence, with Australian individuals forming two clades reflecting geography (a Wet Tropics bioregion clade and a south-eastern Rainforest clade). These clades exhibit equivalent levels of molecular divergence, as observed in R. pulchella and R. ocellata, but no morphological differences. Similar levels of molecular divergence were observed in trans-Tasman populations of R. tasmanica. The New Zealand endemic, R. plicata, is excluded from the Australian flora, and R. cuspidata replaces R. dentifolia for the New Zealand endemic species formerly known by both names.


Zootaxa ◽  
2019 ◽  
Vol 4646 (3) ◽  
pp. 461-500 ◽  
Author(s):  
PETER S. CRANSTON

Riethia Kieffer, known previously from New Zealand for a species stated to be also in Australia plus several Australian and South American species, is revised for the Austro-Pacific region. The three previously-described Australian species Riethia stictoptera Kieffer (the genotype), Riethia cinctipes Freeman and Riethia plumosa Freeman are distinct and valid, and are redescribed in all stages. In contrast, Riethia zeylandica Freeman now is restricted to New Zealand: Australian specimens previously allocated to R. zeylandica belong to several new species recognised on morphology of adult male, pupa and larva, with guidance from molecular data. Most belong to a widespread eastern Australian Riethia azeylandica sp. n.: others are allocated to Riethia hamodivisa sp. n., Riethia paluma sp. n., Riethia phengari sp. n. and Riethia queenslandensis sp. n., each with a more restricted range. From Western Australia three species, Riethia donedwardi sp. n., Riethia noongar sp. n. and Riethia wazeylandica sp. n., are described as new from adult male, pupa and larva. Riethia kakadu sp. n. is described from the monsoonal tropics of Northern Territory from the adult male and tentatively associated pupa. From New Caledonia a reared species is described as Riethia neocaledonica sp. n.. Illustrated identification keys are provided for the males, pupae and larvae. Unassociated larvae that key to reared described species are excluded from type status, and based on morphology and molecular evidence three unreared larval types, ‘A’, ‘B’ and ‘C’, are also described and keyed. Previously reported molecular vouchers are reviewed, and certain Genbank accessions re-identified. Extensive data shows Riethia are distributed almost throughout Australia from standing and flowing waters, from tropics and subtropics to cool temperate Tasmania, but probably only in permanent and standing waters. The immature stages of several taxa can co-occur: as many as four can be found simultaneously in one site. Terminology of the volsellae of the male genitalia and the dorsal head and maxilla of the larva is reviewed. 


Phytotaxa ◽  
2019 ◽  
Vol 391 (2) ◽  
pp. 122 ◽  
Author(s):  
MURAT KOÇ ◽  
ERGIN HAMZAOĞLU ◽  
AHMET AKSOY

The genus Minuartia is represented in Turkey by 34 taxa. Some interesting specimens were collected from Antalya province, and examined. These specimens resemble Minuartia meyeri, and M. multinervis from which differ by characters (macro-, and micromorphological) of inflorescence, alar pedicels, petals, sepals, capsules and seeds. Moreover, by using the DNA sequences of the ITS genes, phylogenetic relationships between this collected species, and the related species were investigated. As a result of the evaluation of molecular, and morphological data, we proposed to described the population from Antalya as a new species for the science. A description, pictures, distribution, habitat, and IUCN category are given.


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