Phylogenetic implications of the mesofurca in Chalcidoidea (Hymenoptera), with emphasis on Aphelinidae

The skeletomusculature of the mesofurcal–mesopostnotal complex is surveyed within the Chalcidoidea. Four internal character systems are assessed for their phylogenetic significance: the mesofurcal bridge, the structure and position of the furcal–laterophragmal muscle, the structure of the lateral arms of the mesofurca, and the supporting structures for the interfurcal muscles. Among Hymenoptera, Chalcidoidea are unique in having the furcal–laterophragmal muscle attached along the entire length of the laterophragmal apodeme. Also the furcal–laterophragmal muscle originates medial to the junction of the mesofurcal bridge and lateral mesofurcal arm in most Chalcidoidea. Mymarommatidae do not share either of these apomorphic states with Chalcidoidea. Within Chalcidoidea, apomorphic character states were found in each of Aphelinidae, Encyrtidae, Eulophidae, Mymaridae, Rotoitidae, Signiphoridae, Tanaostigmatidae and Trichogrammatidae. For taxa classified as Aphelinidae, the plesiomorphic complement of structures and muscle attachments is retained in Eriaphytinae and Eriaporinae. The mesofurcal bridge is considered to have been lost at least twice in each of Aphelininae and Coccophaginae. Similar interfurcal processes, resulting from loss of the mesofurcal bridge, support the monophyly of Aphelininae (Aphelinini, Aphytini and Eutrichosomellini). Azotinae are placed as the sister group of Aphelininae because of a similar lateral origin of the laterophragmal muscle and the shape of the mesofurcal arms. Other than loss of the mesofurcal bridge, no character states were shared by Azotinae and Coccophaginae. Coccophaginae (Coccophagini and Pteroptricini) are regarded as monophyletic based on the loss of the mesofurcal bridge, the peculiar shape of the mesofurca, and a unique modification of the laterophragmal muscle. Euxanthellus is removed from synonomy with Coccophagus and may be best treated as a separate tribe of Coccophaginae based on the shape of the lateral mesofurcal arms and the presence of a mesofurcal bridge. The shape of the mesofurca suggests a monophyletic grouping of Cales, Eretmocerus and Trichogrammatidae that could render Aphelinidae paraphyletic.     

Revision of the Cales noacki species complex (Hymenoptera,Chalcidoidea, Aphelinidae)

The genus Cales (Hymenoptera: Aphelinidae) includes 13 species worldwide, of which 10 form a highly morphologically uniform species complex with a native range in the Neotropical region. We recognize ten species previously attributed to a single Neotropical species, Cales noacki Howard, which in the strict sense is a species broadly disseminated to control woolly whitefly. A neotype is designated for C. noacki, and it is redescribed based on specimens molecularly determined to be conspecific with the neotype. Newly described species include: C. bicolor Mottern, n.sp ., C. breviclava Mottern, n.sp ., C. brevisensillum Mottern n.sp ., C. curvigladius Mottern, n.sp ., C. longiseta Mottern, n.sp ., C. multisensillum Mottern n.sp ., C. noyesi Mottern, n.sp ., C. parvigladius Mottern, n.sp . and C. rosei Mottern, n.sp . Species are delimited based on a combination of morphological and molecular data (28S‐D2 rDNA and COI). Additional specimens are included in the phylogenetic analyses and although these likely represent several new species, we lack sufficient specimen sampling to describe them at this time. Cales are highly morphologically conserved and character‐poor, resulting in several cryptic species. A molecular phylogeny of the known Neotropical species based on 28S‐D2–5 rDNA and a 390‐bp segment of COI is included, and identification keys to males and females are provided. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:7FEB0479‐9B2E‐48E8‐8603‐4B7C2759D4EC .     

A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera)

Chalcidoidea (Hymenoptera) is extremely diverse with an estimated 500 000 species. We present the first phylogenetic analysis of the superfamily based on both morphological and molecular data. A web‐based, systematics workbench mx was used to score 945 character states illustrated by 648 figures for 233 morphological characters for a total of 66 645 observations for 300 taxa. The matrix covers 22 chalcidoid families recognized herein and includes 268 genera within 78 of 83 subfamilies. Morphological data were analysed alone and in combination with molecular data from ribosomal 18S (2105 bp) and 28S D2–D5 expansion regions (1812 bp). Analyses were analysed alone and in combined datasets using implied‐weights parsimony and likelihood. Proposed changes in higher classification resulting from the analyses include: (i) recognition of Eriaporidae, revised status; (ii) recognition of Cynipencyrtidae, revised status; (iii) recognition of Azotidae, revised status; (iv) inclusion of Sycophaginae in Agaonidae, revised status; (v) reclassification of Aphelinidae to include Aphelininae, Calesinae, Coccophaginae, Eretmocerinae and Eriaphytinae; (vi) inclusion of Cratominae and Panstenoninae within Pteromalinae (Pteromalidae), new synonymy; (vii) inclusion of Epichrysomallinae in Pteromalidae, revised status. At a higher level, Chalcidoidea was monophyletic, with Mymaridae the sister group of Rotoitidae plus the remaining Chalcidoidea. A eulophid lineage was recovered that included Aphelinidae, Azotidae, Eulophidae, Signiphoridae, Tetracampidae and Trichogrammatidae. Eucharitidae and Perilampidae were monophyletic if Eutrichosomatinae (Pteromalidae) was included, and Eupelmidae was monophyletic if Oodera (Pteromalidae: Cleonyminae) was included. Likelihood recovered a clade of Eupelmidae + (Tanaostigmatidae + (Cynipencyrtus + Encyrtidae). Support for other lineages and their impact on the classification of Chalcidoidea is discussed. Several life‐history traits are mapped onto the new phylogeny.     

On the parasitoid complex (Hymenoptera: Chalcidoidea) of Anophococcus abaii (Hemiptera: Eriococcidae), with description of Metaphycus anophococcusi Lotfalizadeh,n. sp.

The parasitoid community of Anophococcus abaii (Danzig, 1990) – one of the main pests of Haloxylon in Iran – was studied. Four species of Chalcidoidea, belonging to the families Aphelinidae, Encyrtidae, Pteromalidae, and Signiphoridae, were found. Metaphycus anophococcusi Lotfalizadeh, n. sp. is described in the zebratus species group and compared with closely allied species of Metaphycus.     

Support for vicariant origins of the New Zealand Onychophora

Aim The distribution of Onychophora across the southern continents has long been considered the result of vicariance events. However, it has recently been hypothesized that New Zealand was completely inundated during the late Oligocene (25–22 Ma) and therefore that the entire biota is the result of long-distance dispersal. We tested this assumption using phylogenetic and molecular dating of DNA sequence data from Onychophora. Location New Zealand, Australia, South Africa, Chile (South America). Methods We obtained DNA sequence data from the nuclear genes 28S and 18S rRNA to reconstruct relationships among species of Peripatopsidae (Onychophora). We performed molecular dating under a Bayesian relaxed clock model with a range of prior distributions using the rifting of South America and South Africa as a calibration. Results Our phylogenetic trees revealed that the New Zealand genera Ooperipatellus and Peripatoides, together with selected Australian genera (Euperipatoides, Phallocephale and an undescribed genus from Tasmania), form a monophyletic group that is the sister group to genera from Chile (Metaperipatus) and South Africa (Peripatopsis and Opisthopatus). The relaxed clock dating analyses yielded mean divergence times from 71.3 to 78.9 Ma for the split of the New Zealand Peripatoides from their Australian sister taxa. The 0.95 Bayesian posterior intervals were very broad and ranged from 24.5 to 137.6 Ma depending on the prior assumptions. The mean divergence of the New Zealand species of Ooperipatellus from the Australian species Ooperipatellus insignis was estimated at between 39.9 and 46.2 Ma, with posterior intervals ranging from 9.5 to 91.6 Ma. Main conclusions The age of Peripatoides is consistent with long-term survival in New Zealand and implies that New Zealand was not completely submerged during the Oligocene. Ooperipatellus is less informative on the question of continuous land in the New Zealand region because we cannot exclude a post-Oligocene divergence. The great age of Peripatoides is consistent with a vicariant origin of this genus resulting from the rifting of New Zealand from the eastern margin of Gondwana and supports the assumptions of previous authors who considered the Onychophora to be a relict component of the New Zealand biota.     

The biogeography of Gunnera L.: vicariance and dispersal

Aim The genus Gunnera is distributed in South America, Africa and the Australasian region, a few species reaching Hawaii and southern Mexico in the North. A cladogram was used to (1) discuss the biogeography of Gunnera and (2) subsequently compare this biogeographical pattern with the geological history of continents and the patterns reported for other Southern Hemisphere organisms. Location Africa, northern South America, southern South America, Tasmania, New Zealand, New Guinea/Malaya, Hawaii, North America, Antarctica. Methods A phylogenetic analysis of twenty‐six species of Gunnera combining morphological characters and new as well as published sequences of the ITS region, rbcL and the rps16 intron, was used to interpret the biogeographical patterns in Gunnera. Vicariance was applied in the first place and dispersal was only assumed as a second best explanation. Results The Uruguayan/Brazilian Gunnera herteri Osten (subgenus Ostenigunnera Mattfeld) is sister to the rest of the genus, followed sequentially upwards by the African G. perpensa L. (subgenus Gunnera), in turn sister to all other, American and Australasian, species. These are divided into two clades, one containing American/Hawaiian species, the other containing all Australasian species. Within the Australasian clade, G. macrophylla Blume (subgenus Pseudogunnera Schindler), occurring in New Guinea and Malaya, is sister to a clade including the species from New Zealand and Tasmania (subgenus Milligania Schindler). The southern South American subgenus Misandra Schindler is sister to a clade containing the remaining American, as well as the Hawaiian species (subgenus Panke Schindler). Within subgenus Panke, G. mexicana Brandegee, the only North American species in the genus, is sister to a clade wherein the Hawaiian species are basal to all south and central American taxa. Main conclusions According to the cladogram, South America appears in two places, suggesting an historical explanation for northern South America to be separate from southern South America. Following a well‐known biogeographical pattern of vicariance, Africa is the sister area to the combined southern South America/Australasian clade. Within the Australasian clade, New Zealand is more closely related to New Guinea/Malaya than to southern South America, a pattern found in other plant cladograms, contradictory to some of the patterns supported by animal clades and by the geological hypothesis, respectively. The position of the Tasmanian G. cordifolia, nested within the New Zealand clade indicates dispersal of this species to Tasmania. The position of G. mexicana, the only North American species, as sister to the remaining species of subgenus Panke together with the subsequent sister relation between Hawaii and southern South America, may reflect a North American origin of Panke and a recolonization of South America from the north. This is in agreement with the early North American fossil record of Gunnera and the apparent young age of the South American clade.     

Leaf hoppers of New Zealand: Subfamilies Aphrodinae,Jassinae, Xestocephalinae,Idiocerinae, and Macropsinae (Homoptera: Cicadellidae)

The cosmopolitan subfamilies Aphrodinae, Jassinae, Xestocephalinae, Idiocerinae, and Macropsinae are diagnosed and the New Zealand species described and illustrated. Each subfamily is represented in New Zealand by only one or two species, those in Idiocerinae having been introduced from Europe or North America. The species Euacanthella brunnea Evans (Aphrodinae) is synonymised with the Australian species E. insularis Evans (new synonymy).     

Hyperparasitoids of the gum leaf skeletoniser, Uraba lugens Walker (Lepidoptera: Nolidae), with implications for the selection of a biological control agent for Uraba lugens in New Zealand

Abstract  The hyperparasitoids reared from three species of primary parasitoids of the gum leaf skeletoniser, Uraba lugens Walker (Lepidoptera: Nolidae) collected in South Australia and Tasmania are recorded and discussed. Seven hyperparasitoids were reared. Diatora sp. and ? Paraphylax sp. (Ichneumonidae: Cryptinae); Tetrastichus sp. (Chalcidoidea: Eulophidae); Megadicylus dubius (Girault) (Chalcidoidea: Pteromalidae) and Elasmus sp. (Chalcidoidea: Eulophidae) were reared from Cotesia urabae Austin and Allen (Braconidae: Microgastrinae). Megadicylus dubius , Elasmus sp. and Anastatus sp. (Chalcidoidea: Eupelmidae) were reared from Dolichogenidea eucalypti Austin and Allen (Braconidae: Microgastrinae). Pediobius bruchicida (Rondani) (Chalcidoidea: Eulophidae) was reared from Euplectrus sp. (Chalcidoidea: Eulophidae). This appears to be the first record of the cryptine ichneumonid genus Diatora Förster from Australia. Of the seven hyperparasitoid species reared, only one ( P. bruchicida ) is known to be present in New Zealand. Implications for the selection of a biological control agent for U. lugens in New Zealand are discussed. Some prior misidentifications of associated hyperparasitoids are noted.     

Phylogeny and biogeography of Chinese and Australasian Polystichum ferns as inferred from chloroplast trnL-F and rps4-trnS sequence data

Polystichum, one of the largest genera of ferns, occurs worldwide with the greatest diversity in southwest China and adjacent regions. Although there have been studies of Chinese Polystichum on its traditional classification, geographic distributions, and even a few on its molecular systematics, its relationships to other species outside China remain little known. Here, we investigated the phylogeny and biogeography of the Polystichum species from China and Australasia. The evolutionary relationships among 42 Polystichum species found in China (29 taxa) and Australasia (13 taxa) were inferred from phylogenetic analyses of two chloroplast DNA sequence data sets: rps4-trnS and trnL-F intergenic spacers. The divergence time between Chinese and Australasian Polystichum was estimated. The results indicated that the Australasian species comprise a monophyletic group that is nested within the Chinese diversity, and that the New Zealand species are likewise a monophyletic group nested within the Australasian species. The divergence time estimates suggested that Chinese Polystichum migrated into Australasia from around 40 Ma ago, and from there to New Zealand from about 14 Ma. The diversification of the New Zealand Polystichum species began about 10 Ma. These results indicated that Polystichum probably originated in eastern Asia and migrated into Australasia: first into Australia and then into New Zealand.     

Records of Carulaspis juniperi (Homoptera: Diaspididae) in New Zealand

Abstract

Previous reports of Carulaspis visci (Schrank) in New Zealand are considered to be misidentifications of C. juniperi (Bouché), the juniper scale. The known hosts (Cupressaceae and Taxodiaceae), distribution (all South Island localities), and a record of a parasite (Aspidiotiphagus citrinus (Craw), Aphelinidae) of C. juniperi in New Zealand are given.     

Biogeography of temperate Australasian Polystichum ferns as inferred from chloroplast sequence and AFLP

Aim and location New Zealand began to separate from Gondwana c. 85 Ma, and has been isolated from the nearest large landmass, Australia, by some 2000 km of the Tasman Sea since c. 60 Ma. Given New Zealand's long geographical isolation, there has been considerable interest in explaining the origins of its different biotic elements. Here we investigate the biogeography of the fern genus Polystichum from temperate Australasia. Six species are found in New Zealand, four in Australia, and two on Lord Howe Island. Methods The evolutionary relationships between the twelve Polystichum species found in temperate Australasia were inferred from phylogenetic analyses of two molecular data sets: DNA sequence from the chloroplast rps4–trnS spacer locus; and AFLP DNA‐fingerprinting. The timing of the separation between Australian and New Zealand Polystichum was estimated by using the fossil record to temporally calibrate the rbcL sequence differentiation between representative species from these regions. Results Species of Polystichum from New Zealand appear to comprise a monophyletic group. This suggests that Polystichum crossed the Tasman only once. Temporal calibration of the rbcL sequence differentiation between Australian and New Zealand Polystichum indicates that a vicariant explanation for their separation can be rejected in favour of trans‐oceanic dispersal. Main conclusions The extant diversity within New Zealand Polystichum appears to have been derived from a single, trans‐oceanic dispersal event (within the last c. 20 Myr), followed by a relatively extensive in situ ecological radiation.     

Welcome back New Zealand: regional biogeography and Gondwanan origin of three endemic genera of mite harvestmen (Arachnida, Opiliones, Cyphophthalmi)

Aim Biogeographers have long been intrigued by New Zealand’s biota due to its unique combination of typical ‘continental’ and ‘island’ characteristics. The New Zealand plateau rifted from the former supercontinent Gondwana c. 80 Ma, and has been isolated from other land masses ever since. Therefore, the flora and fauna of New Zealand include lineages that are Gondwanan in origin, but also include a very large number of endemics. In this study, we analyse the evolutionary relationships of three genera of mite harvestmen (Arachnida, Opiliones, Cyphophthalmi) endemic to New Zealand, both to each other and to their temperate Gondwanan relatives found in Australia, Chile, Sri Lanka and South Africa. Location New Zealand (North Island, South Island and Stewart Island). Methods A total of 94 specimens of the family Pettalidae in the suborder Cyphophthalmi were studied, representing 31 species and subspecies belonging to three endemic genera from New Zealand (Aoraki, Neopurcellia and Rakaia) plus six other members of the family from Chile, South Africa, Sri Lanka and Australia. The phylogeny of these taxa was constructed using morphological and molecular data from five nuclear and mitochondrial genes (18S rRNA, 28S rRNA, 16S rRNA, cytochrome c oxidase subunit I and histone H3, totalling c. 5 kb), which were analysed using dynamic as well as static homology under a variety of optimality criteria. Results The results showed that each of the three New Zealand cyphophthalmid genera is monophyletic, and occupies a distinct geographical region within the archipelago, grossly corresponding to palaeogeographical regions. All three genera of New Zealand mite harvestmen fall within the family Pettalidae with a classic temperate Gondwanan distribution, but they do not render any other genera paraphyletic. Main conclusions Our study shows that New Zealand’s three genera of mite harvestmen are unequivocally related to other members of the temperate Gondwanan family Pettalidae. Monophyly of each genus contradicts the idea of recent dispersal to New Zealand. Within New Zealand, striking biogeographical patterns are apparent in this group of short‐range endemics, particularly in the South Island. These patterns are interpreted in the light of New Zealand’s turbulent geological history and present‐day patterns of forest cover.     

A review of the New Zealand Chirostylidae (Anomura: Galatheoidea) with description of six new species from the Kermadec Islands

Prior to the present study, seven species of deep‐sea Chirostylidae (‘squat lobsters’), were known from New Zealand: Gastroptychus novaezelandiae, Uroptychodes spinimarginatus, Uroptychus australis, Uroptychus maori, Uroptychus novaezelandiae, Uroptychus politus, and Uroptychus tomentosus. All species are examined from type material and discussed, original illustrations supplemented, and new records provided where available. Uroptychus maori and Uroptychus novaezelandiae are re‐described. The chirostylid fauna of the Kermadec Islands, a remote group of islands north‐east of New Zealand, is studied. Uroptychus alcocki and Uroptychus scambus are reported for the first time from New Zealand, and six new species of the genus Uroptychus are described. Distributional patterns of New Zealand species are discussed and a key to New Zealand Uroptychus species is presented. © 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 155 , 542–582.     

Crossing the Tasman Sea: Inferring the introduction history of Litoria aurea and Litoria raniformis (Anura: Hylidae) from Australia into New Zealand

Abstract The amphibian fauna of New Zealand consists of three native species (Leiopelma spp.), and three Litoria species introduced from Australia in the last 140 years. We conducted a molecular phylogeographical study that aimed to identify the Australian origins of two species, Litoria aurea and Litoria raniformis. We used partial sequences of the mitochondrial cytochrome oxidase I (cox1) gene from 59 specimens sampled from across the range of both species to identify the probable source populations for the New Zealand introductions, and to describe the current genetic diversity among New Zealand Litoria populations. Our genetic data suggest that L. aurea was introduced into the North Island of New Zealand from two regions in Australia, once from the northern part of coastal New South Wales and once from the southern part of coastal New South Wales. Our data indicate that L. raniformis introductions originated from the Melbourne region of southern Victoria and once established in the South Island of New Zealand, the species subsequently spread throughout both islands. In addition, we found a distinct haplotype in L. raniformis from Tasmania that strongly suggests, contrary to earlier reports, that this species was not introduced into New Zealand from Tasmania. Finally, we identified two very distinctive mitochondrial lineages of L. raniformis within the mainland Australia distribution, which may be previously unrecognized species.     

From East Gondwana to Central America: historical biogeography of the Alstroemeriaceae

Aim The Alstroemeriaceae is among 28 angiosperm families shared between South America, New Zealand and/or Australia; here, we examine the biogeography of Alstroemeriaceae to better understand the climatic and geological settings for its diversification in the Neotropics. We also compare Alstroemeriaceae with the four other Southern Hemisphere families that expanded from Patagonia to the equator, to infer what factors may have permitted such expansions across biomes. Location South America, Central America, Australia and New Zealand. Methods Three chloroplast genes, one mitochondrial gene and one nuclear DNA region were sequenced for 153 accessions representing 125 of the 200 species of Alstroemeriaceae from throughout the distribution range; 25 outgroup taxa were included to securely infer evolutionary directions and be able to use both ingroup and outgroup fossil constraints. A relaxed‐clock model relied on up to three fossil calibrations, and ancestral ranges were inferred using statistical dispersal–vicariance analysis (S‐DIVA). Southern Hemisphere disjunctions in the flowering plants were reviewed for key biological traits, divergence times, migration directions and habitats occupied. Results The obtained chronogram and ancestral area reconstruction imply that the most recent common ancestor of Colchicaceae and Alstroemeriaceae lived in the Late Cretaceous in southern South America/Australasia, the ancestral region of Alstroemeriaceae may have been South America/Antarctica, and a single New Zealand species is due to recent dispersal from South America. Chilean Alstroemeria diversified with the uplift of the Patagonian Andes c. 18 Ma, and a hummingbird‐pollinated clade (Bomarea) reached the northern Andes at 11–13 Ma. The South American Arid Diagonal (SAAD), a belt of arid vegetation caused by the onset of the Andean rain shadow 14–15 Ma, isolated a Brazilian clade of Alstroemeria from a basal Chilean/Argentinean grade. Main conclusions Only Alstroemeriaceae, Calceolariaceae, Cunoniaceae, Escalloniaceae and Proteaceae have expanded and diversified from Patagonia far into tropical latitudes. All migrated northwards along the Andes, but also reached south‐eastern Brazil, in most cases after the origin of the SAAD. Our results from Alstroemeria now suggest that the SAAD may have been a major ecological barrier in southern South America.     

Small but not ephemeral: newly discovered species of Aphelinidae and Trichogrammatidae (Insecta: Hymenoptera: Chalcidoidea) from Eocene amber

New species of fossil Aphelinidae and Trichogrammatidae are described from middle Eocene (Lutetian) Baltic amber (41.3–47.8 Ma). A new subfamily, two new genera and three new species of Aphelinidae are described, with comments on their placement: Phtuaria fimbriae gen.n. , sp.n. in Phtuariinae subf.n. , Glaesaphytis interregni gen.n. , sp.n. and Centrodora brevispinae sp.n. These represent the first described true fossil Aphelinidae. Four new species of Trichogrammatidae are described: Mirufens illusionis sp.n. , Palaeogramma eos gen.n. , sp.n. , Pterandrophysalis plasmans sp.n. and Szelenyia terebrae sp.n. , thus expanding our knowledge of fossil Trichogrammatidae beyond the single previously described species. The presence of recognizable extant genera of Aphelinidae and Trichogrammatidae in the Eocene suggests that the morphology of these genera has been relatively invariant despite highly variable conditions during and since the Eocene. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:E9AD60B6‐3D56‐4E74‐AA54‐F7B91F4FDC79 .     

STUDIES OF PACIFIC ISLAND PLANTS. XXIX. BLEASDALEA AND RELATED GENERA OF PROTEACEAE

The genus Kermadecia (Proteaceae), originally described as endemic to New Caledonia, has been expanded in recent decades to include three species from the New Hebrides and Fiji. Specialists on the Proteaceae have suggested that the three Melanesian species were generically misplaced, and careful reexamination supports this viewpoint. It is now apparent that a distinct group within the subfamily Grevilleoideae is composed of the genera Euplassa (endemic to South America), Sleumerodendron (a monotypic New Caledonian genus), Gevuina (based on a single South American species but recently expanded to include two other species from Queensland and New Guinea), and the three questionable Melanesian species. A review of this cluster of taxa indicates that Gevuina should again be interpreted as restricted to South America and that the generic name Bleasdalea F. v. Muell. ex Domin should be adopted for a group of five species extending from Queensland and New Guinea to the New Hebrides and Fiji. The relationships of the four genera are discussed and within Bleasdalea four new combinations are proposed: B. bleasdalei (F. v. Muell.), B. ferruginea (A. C. Sm.), B. vitiensis (Turrill), and B. lutea (Guillaumin). Kermadecia, very distinct from the four genera under present consideration, is again interpreted as a New Caledonian endemic.     

Bryophyte Tree of Life: the current state of phylogenetic reconstruction in mosses

Abstract

A Holantarctic species, the inter-subgeneric allopolyploid Sphagnum ×falcatulum s.l. is a cryptic species complex composed of allodiploid and allotriploid cytotypes. The allotriploid plants are double allopolyploids (one of just two reported for bryophytes), with the allodiploid cytotype being one parent. Using a combination of microsatellites, nucleotide sequences, and morphological characters, allotriploid S. ×falcatulum is shown to be the most widespread Sphagnum species in the Holantarctic, with genetically documented populations in South America (Tierra del Fuego), New Zealand (South Island), and Australia (Macquarie Island, Tasmania). It is further concluded that six Sphagnum species described from the Tierra del Fuego Archipelago (TDF) of South America and a seventh described from South Island, New Zealand are synonymous with the allotriploid cytotype of S. ×falcatulum. The synonymized species include five named by Heikki Roivainen in 1937, S. ×ehyalinum, and S. subditivum. Allotriploid S. ×falcatulum is the predominant, perhaps the only, subgenus Cuspidata species present in TDF and immediate vicinity. The combination of low genetic diversity and an apparent absence of sexual reproduction indicate that the TDF population of the dioicous allotriploid S. ×falcatulum was likely founded by one or a limited number of individuals. The same is apparently the case for Macquarie I. and Tasmanian populations of allotriploid S. ×falcatulum. Several lines of evidence, including high genetic diversity, frequent sporophyte production, and the occurrence of the allodiploid parent, suggest that allotriploid S. ×falcatulum likely evolved in New Zealand.     

The first records of Stylodrilus heringianus (Oligochaeta: Lumbriculidae) from the Southern Hemisphere

Abstract

The oligochaete family Lumbriculidae is well represented in the Northern Hemisphere, but for the Southern Hemisphere only Lumbriculus variegatus (Müller) is recorded, from Africa, Australia, and New Zealand; no species are known from South America (Brinkhurst & Jamieson 1971). According to Brinkhurst (1971), L. variegatus may be a recent introduction to New Zealand, where it is now widely distributed in a range of inland waters.