scholarly journals Impact of Puccinia psidii on M257;ori taonga plant species

2014 ◽  
Vol 67 ◽  
pp. 324-324
Author(s):  
T.T. Alipia ◽  
D.A.J. Teulon ◽  
M.G. Cromey ◽  
A.T. Marsh ◽  
S.L.H. Viljanen-Rollinson
Keyword(s):  
New Zealand ◽  
Environmental Impact ◽  
South America ◽  
New Caledonia ◽  
Indigenous Species ◽  
Plant Family ◽  
Puccinia Psidii ◽  
Myrtle Rust ◽  
The World ◽  
Potential Impact

Myrtle rust caused by the pathogen Puccinia psidii sensu lato is a disease of species in the plant family Myrtaceae that is not found in New Zealand It originates in South America but it has steadily spread around the world and is now found in Australia and New Caledonia While the potential economic and environmental impact of myrtle rust establishment in New Zealand has been well documented the potential sociocultural consequences including those for M257;ori have not All New Zealand Myrtaceae species including indigenous species are at risk from P psidii infection but the potential impact on their health is not known All indigenous Myrtaceae species can be considered as Taonga (or treasure) by M257;ori who have utilised the properties (eg spiritual medicinal construction tools food) of some species in many ways both tangible and intangible Optimally preparedness and response plans for a myrtle rust incursion in New Zealand should consider the unique spiritual and other values that M257;ori associate with these plants

scholarly journals The threat of myrtle rust to M257;ori taonga plant species in New Zealand

2015 ◽  
Vol 68 ◽  
pp. 66-75 ◽  
Author(s):  
D.A.J. Teulon ◽  
T.T. Alipia ◽  
H.T. Ropata ◽  
J.M. Green ◽  
S.L.H. Viljanen- Rollinson ◽  
...  
Keyword(s):  
New Zealand ◽  
South America ◽  
Environmental Impacts ◽  
Plant Species ◽  
Indigenous Species ◽  
Rust Infection ◽  
Myrtle Rust ◽  
The World ◽  
The Impact ◽  
Central South

Myrtle rust caused by the pathogen Puccinia psidii is a disease of plants in the Myrtaceae that is currently not known to be present in New Zealand Its origin is Central/ South America but it has steadily spread around the world and is now found in Australia All New Zealand Myrtaceae species including indigenous species are at risk from myrtle rust infection but the extent of the impact on plant health is not known While the potential economic and environmental impacts of myrtle rust establishment in New Zealand have been well documented this paper explores potential sociocultural consequences for M257;ori All indigenous Myrtaceae species can be considered as taonga (or treasure) by M257;ori who have and continue to use the properties of some species in many ways (both tangible and intangible) Preparedness and response plans for a myrtle rust incursion in New Zealand should consider the values that M257;ori derive from these plants

Alternaria passiflorae. [Distribution map].

2014 ◽  
Author(s):  
Keyword(s):  
South Africa ◽  
New Zealand ◽  
North America ◽  
South America ◽  
Papua New Guinea ◽  
West Bengal ◽  
New Caledonia ◽  
Distribution Map ◽  
Norfolk Island ◽  
New Distribution

Abstract A new distribution map is provided for Alternaria passiflorae Simmonds. Dothideomycetes: Pleosporales: Pleosporaceae. Host: passionflower (Passiflora sp.). Information is given on the geographical distribution in Asia (Bhutan, China, Guangdong, India, Kerala, Sikkim, West Bengal), Africa (Kenya, Malawi, Mauritius, South Africa, Tanzania, Uganda, Zambia, Zimbabwe), North America (Canada, British Columbia, Florida, Hawaii), South America (Brazil, Sao Paulo, Colombia, Venezuela), Oceania (Australia, Queensland, Western Australia, Fiji, New Caledonia, New Zealand, Niue, Norfolk Island, Papua New Guinea, Tonga).

Botryotinia squamosa. [Distribution map].

2007 ◽  
Author(s):  
Keyword(s):  
New York ◽  
Czech Republic ◽  
New Zealand ◽  
South America ◽  
New Caledonia ◽  
Rio Grande ◽  
Rio Grande Do Sul ◽  
Distribution Map ◽  
New Distribution ◽  
Distribution In Europe

Abstract A new distribution map is provided for Botryotinia squamosa Vienn.-Bourg. Fungi: Ascomycota: Helotiales. Hosts: Allium spp. Information is given on the geographical distribution in Europe (Belgium, Bulgaria, Czech Republic, France (mainland France), Germany, Ireland, Italy (mainland Italy), Netherlands, Poland, UK (England and Wales, Scotland)), Asia (China (Hebei, Hong Kong), Japan (Hokkaido, Honshu), Korea Democratic People's Republic, Korea Republic), Africa (Mauritius), North America (Canada (Alberta, British Columbia, Ontario, Quebec), USA (Florida, Hawaii, Idaho, Illinois, Indiana, Iowa, Louisiana, Maine, Massachusetts, New York, Ohio, Texas, Washington, Wisconsin)), South America (Argentina, Brazil (Rio Grande do Sul, Santa Catarina, Sao Paulo), Peru), Oceania (New Caledonia, New Zealand).

A molecular phylogeny of the circum-Antarctic Opiliones family Neopilionidae

2021 ◽  
Author(s):  
Gonzalo Giribet ◽  
Kate Sheridan ◽  
Caitlin M. Baker ◽  
Christina J. Painting ◽  
Gregory I. Holwell ◽  
...  
Keyword(s):  
New Zealand ◽  
South America ◽  
Morphological Study ◽  
18S Rrna ◽  
New Caledonia ◽  
Sister Group ◽  
28S Rrna ◽  
South American ◽  
Australian Species ◽  
The Family

The Opiliones family Neopilionidae is restricted to the terranes of the former temperate Gondwana: South America, Africa, Australia, New Caledonia and New Zealand. Despite decades of morphological study of this unique fauna, it has been difficult reconciling the classic species of the group (some described over a century ago) with recent cladistic morphological work and previous molecular work. Here we attempted to investigate the pattern and timing of diversification of Neopilionidae by sampling across the distribution range of the family and sequencing three markers commonly used in Sanger-based approaches (18S rRNA, 28S rRNA and cytochrome-c oxidase subunit I). We recovered a well-supported and stable clade including Ballarra (an Australian ballarrine) and the Enantiobuninae from South America, Australia, New Caledonia and New Zealand, but excluding Vibone (a ballarrine from South Africa). We further found a division between West and East Gondwana, with the South American Thrasychirus/Thrasychiroides always being sister group to an Australian–Zealandian (i.e. Australia + New Zealand + New Caledonia) clade. Resolution of the Australian–Zealandian taxa was analysis-dependent, but some analyses found Martensopsalis, from New Caledonia, as the sister group to an Australian–New Zealand clade. Likewise, the species from New Zealand formed a clade in some analyses, but Mangatangi often came out as a separate lineage from the remaining species. However, the Australian taxa never constituted a monophyletic group, with Ballarra always segregating from the remaining Australian species, which in turn constituted 1–3 clades, depending on the analysis. Our results identify several generic inconsistencies, including the possibility of Thrasychiroides nested within Thrasychirus, Forsteropsalis being paraphyletic with respect to Pantopsalis, and multiple lineages of Megalopsalis in Australia. In addition, the New Zealand Megalopsalis need generic reassignment: Megalopsalis triascuta will require its own genus and M. turneri is here transferred to Forsteropsalis, as Forsteropsalis turneri (Marples, 1944), comb. nov.

scholarly journals Brucellosis and tuberculosis in cattle in South America

2018 ◽  
Vol 55 (2) ◽  
pp. e141139
Author(s):  
José Soares Ferreira Neto
Keyword(s):  
New Zealand ◽  
South America ◽  
Epidemiological Data ◽  
Review Article ◽  
South American ◽  
Cattle Population ◽  
High Quality ◽  
The World ◽  
Meat Market ◽  
Epidemiological Situation

In general, European and North American countries, as well as Australia and New Zealand, have already eradicated or reached good levels of control of brucellosis and tuberculosis in cattle. In the rest of the world, however, the epidemiological situation of these two diseases is frequently poorly understood. In this review article, quantified data on these diseases in the South American countries are presented. Initially, the aspects that led the continent to host 25% of the world cattle population are presented, in addition to the aspects that placed the continent at a prominent position in the international meat market. Subsequently the continent was divided into three country groups, considering the size of the cattle population and how well the epidemiological situation of brucellosis and tuberculosis in cattle is quantified. It is argued that countries that do not generate high-quality quantitative epidemiological data on these diseases have serious limitations in outlining and managing control or eradication strategies. Thus, for successful outcomes, at least methodologies to estimate the prevalence of infected herds should be employed.

Corrigendum to: Systematics and distribution of world hyptiogastrine wasps (Hymenoptera : Gasteruptiidae)

2002 ◽  
Vol 16 (6) ◽  
pp. 957 ◽  
Author(s):  
J. T. Jennings ◽  
A. D. Austin
Keyword(s):  
New Species ◽  
New Zealand ◽  
South America ◽  
New Caledonia ◽  
Cladistic Analysis ◽  
Taxonomic Revision ◽  
Morphological Characters ◽  
The Family ◽  
New Hebrides ◽  
New Britain

This study examines the phylogeny, taxonomy, distribution and biology of the gasteruptiid subfamily Hyptiogastrinae and, at the same time, presents an overview of the family. Following a cladistic analysis of 35 discrete morphological characters, two monophyletic genera are recognised, Hyptiogaster Kieffer and Pseudofoenus s. l. Kieffer. As a consequence, the genera Aulacofoenus Kieffer, Crassifoenus Crosskey, and Eufoenus Szépligeti are synonymised with Pseudofoenus. A total of 88 species are recognised for the subfamily, 10 species of Hyptiogaster, which are restricted to mainland Australia, and 78 species of Pseudofoenus, 40 of which are described as new. Pseudofoenus has a restricted Gondwanan distribution and is found in Australia including Tasmania (65 spp.), New Guinea and New Britain (5 spp.), the south-west Pacific (New Caledonia, New Hebrides and Fiji – 2 spp.), New Zealand (4 spp.) and South America (2 spp.). No new species have been recorded from either New Zealand or South America. For Pseudofoenus, information on the distribution of each species, their biology (if known) and an identification key are presented.Following a taxonomic revision, the following new species are described: P. baileyi, sp. nov., P. baitetaensis, sp. nov., P. beverlyae, sp. nov., P. caperatus, sp. nov., P. cardaleae, sp. nov., P. carrabinensis, sp. nov., P. claireae, sp. nov., P. collessi, sp. nov., P. coorowensis, sp. nov., P. crosskeyi, sp. nov., P. douglasorum, sp. nov., P. eliseae, sp. nov., P. ericae, sp. nov., P. eustonensis, sp. nov., P. feckneri, sp. nov., P. gressitti, sp. nov., P. gullanae, sp. nov., P. hackeri, sp. nov., P. imbricatus, sp. nov., P. iqbali, sp. nov., P. kadowi, sp. nov., P. karimuiensis, sp. nov., P. kelleri, sp. nov., P. leinsterensis, sp. nov., P. macdonaldi, sp. nov., P. malkini, sp. nov., P. marshalli, sp. nov., P. masneri, sp. nov., P. mitchellae, sp. nov., P. morganensis, sp. nov., P. nalbarraensis, sp. nov., P. pumilis, sp. nov., P. schmidti, sp. nov., P. stevensi, sp. nov., P. tasmaniensis, sp. nov., P. taylori, sp. nov., P. umboiensis, sp. nov., P. walkeri, sp. nov. and P. zborowskii, sp. nov. The synonymy of Aulacofoenus, Crassifoenus and Eufoenus with Pseudofoenus result in the following new combinations: from Aulacofoenus: P. bungeyi (Jennings & Austin), comb. nov., P. deletangi (Schletterer), comb. nov., P. fallax (Schletterer), comb. nov., P. fletcheri (Jennings & Austin), comb. nov., P. goonooensis (Jennings & Austin), comb. nov., P. infumatus (Schletterer), comb. nov., P. kurmondi (Jennings & Austin), comb. nov., P. loxleyi (Jennings & Austin), comb. nov., P. marionae (Jennings & Austin), comb. nov., P. perenjorii (Jennings & Austin), comb. nov., P. swani (Jennings & Austin), comb. nov., P. thoracicus (Guérin Menéville), comb. nov., P. whiani (Jennings & Austin), comb. nov. and P. wubinensis (Jennings & Austin), comb. nov.; from Crassifoenus: P. houstoni (Jennings & Austin), comb. nov., P. grossitarsis (Kieffer), comb. nov and P. macronyx (Schletterer), comb. nov.; and from Eufoenus: P. antennalis (Schletterer), comb. nov., P. australis (Westwood), comb. nov., P. crassitarsis (Kieffer), comb. nov., P. darwini (Westwood), comb. nov., P. extraneus (Turner), comb. nov., P. ferrugineus (Crosskey), comb. nov., P. floricolus (Turner), comb. nov., P. inaequalis (Turner), comb. nov., P. melanopleurus (Crosskey), comb. nov., P. minimus (Turner), comb. nov., P. nitidiusculus (Turner), comb. nov., P. patellatus (Westwood), comb. nov., P. pilosus (Kieffer), comb. nov., P. reticulatus (Crosskey), comb. nov., P. rieki (Crosskey), comb. nov., P. ritae (Cheesman), comb. nov. and P. spinitarsis (Westwood), comb. nov. Pseudofoenus microcephalus (Crosskey), comb. nov. is transferred from Hyptiogaster and Eufoenus flavinervis (Kieffer) remains incertae sedis.

scholarly journals Molecular Ecology and Systematics of Blue  Mussels (Genus Mytilus) (Mytilidae; Bivalvia;  Mollusca) in the Southern Hemisphere

2021 ◽  
Author(s):  
◽  
Kristen Marie Westfall
Keyword(s):  
Gene Flow ◽  
New Zealand ◽  
South America ◽  
Southern Hemisphere ◽  
Northern Hemisphere ◽  
Molecular Ecology ◽  
Population Subdivision ◽  
Kerguelen Islands ◽  
Blue Mussels ◽  
The World

<p>The Mytilus edulis species complex, comprised of M. edulis, M. galloprovincialis and M. trossulus, is antitropically distributed in temperate coastal regions of all oceans and main seas of the world. This genus has been heavily studied in the Northern hemisphere but Southern hemisphere populations have received much less attention. This thesis aims to place Southern hemisphere blue mussels into global evolutionary relationships among Mytilus species and investigate aspects of their molecular ecology, including, effects of non-native Northern hemisphere species introductions, biogeography across the Southern hemisphere, regional phylogeographic patterns and population genetics within New Zealand. Southern hemisphere blue mussel phylogenetic reconstruction resulted in the detection of a monophyletic M. galloprovincialis lineage. Two new molecular markers developed with specificity for this lineage and congruence among phylogenetic investigations indicates a panhemispheric distribution of this M. galloprovincialis lineage with implications for naming a new sibling species of the M. edulis complex. This proposed new species, M. meridianus, is distributed in South America, the Kerguelen Islands, New Zealand and Australia at latitudes between ~ 30°S and ~ 55°S. Non-native M. galloprovincialis introduced from the Northern hemisphere have been present in NZ, Australia and Chile for at least ten years and hybridise with native blue mussels. Introgression is observed in New Zealand and Australian but not Chilean hybrid regions. The limited number of introduced mussels in Australia induces hybrid swamping of non-native alleles but an interlineage gender bias towards non-native maternal parents may result in eventual loss of the unique genomic content of native blue mussels in NZ. Southern hemisphere blue mussels form a monophyletic sister clade to a haplogroup shared by Northern hemisphere M. edulis and M. galloprovincialis. Although single gene histories are not congruent with respect to evolutionary relationships within the Northern hemisphere due to introgressive hybridisation after speciation, it is clear that Southern hemisphere blue mussels arose from a species native to the northeast Atlantic Ocean after speciation of the three ‘M. edulis complex’ members. Within the Southern hemisphere monophyletic clade lies three reciprocally monophyletic clades restricted to the geographic regions South America/Kerguelen Islands, New Zealand and Australia. Phylogeographic analysis indicates past gene flow between South American/Kerguelen Islands and New Zealand populations that has ceased at present day and ongoing gene flow between South America and the Kerguelen Islands likely via the West Wind Drift. Within NZ, population subdivision inferred from mtDNA indicates genetic variation is distributed within an east-west phylogeographic split on the North Island. These populations experienced gene flow in the past that has ceased at present day. Microsatellite allele frequencies indicate a different population subdivision within the northwest North Island that has been narrowed down to a 15 km stretch of coastline in a sheltered bay. The abrupt discontinuity within a small geographic area does not conform to classic population subdivision in this broad-cast spawning species, therefore, further investigation into the genomic content of northwest North Island mussels with respect to introgressed non-native genes is warranted. Resolving complex phylogenetic patterns from interspecific introgression is key to understanding the evolutionary history of Southern hemisphere M. galloprovincialis. Further characterisation of hybrid introgression would increase accuracy of (1) inferences of processes contributing to hybridisation dynamics and (2) population subdivision in NZ. Probing the basis for variation of hybridisation dynamics would help to predict the outcomes of Northern hemisphere M. galloprovincialis introductions in other areas of the world.</p>

New species of Psychodidae (Diptera) from Australasia, with a checklist of the world species of Bruchomyiinae and Sycoracinae

Zootaxa ◽  
2012 ◽  
Vol 3552 (1) ◽  
pp. 43 ◽  
Author(s):  
GREGORY R. CURLER ◽  
AMANDA J. JACOBSON
Keyword(s):  
New Species ◽  
New Zealand ◽  
Genital Tract ◽  
New Caledonia ◽  
Male Genital Tract ◽  
World Species ◽  
The World ◽  
One New Species ◽  
Male Genital

Adults of one new species of Bruchomyiinae and five new species of Sycoracinae were collected from Australia and New Caledonia, respectively.  Nemopalpus glyphanos sp. nov., Sycorax furca sp. nov., S. sinuosa sp. nov., S. spina sp. nov., S. tridentata sp. nov., and S. webbi sp. nov. are described, and Sycorax dispar Satchell from New Zealand is redescribed.  A key to males of Sycorax species known to occur in New Caledonia, and a checklist of the world species of Bruchomyiinae and Sycoracinae are provided.  Characters of the male genital tract, and relationships among Australasian Bruchomyiinae and Sycoracinae are discussed.

Systematics and host relationships of Australasian Diolcogaster (Hymenoptera : Braconidae : Microgastrinae)

1999 ◽  
Vol 13 (1) ◽  
pp. 117 ◽  
Author(s):  
A. Saeed ◽  
P. C. Dangerfield ◽  
A. D. Austin
Keyword(s):  
New Zealand ◽  
New Caledonia ◽  
Key To Species ◽  
The World ◽  
Species Groups ◽  
Host Relationships ◽  
Braconid Wasp ◽  
First Time ◽  
Australasian Region ◽  
World Fauna

The braconid wasp genus Diolcogaster Ashmead is revised for the Australasian region, and is recorded from New Zealand and New Caledonia for the first time. A key to species is presented, the relationships within the Microgastrinae and among species-groups of the genus, the size of the world fauna, the biology and host relationships, and the distribution of Australasian species are discussed. The connexus-group sensu Nixon is expanded and redefined to include two monotypic, non-Australasian groups (D. ippis Nixon and D. reales Nixon), while the spretus-group sensu Nixon is expanded to include the monotypic group for D. coenonymphae (Watanabe) from Japan. Twenty-six species are recognised from Australasia:D. adiastola, sp. nov., D. alkingara, sp. nov., D. ashmeadi, sp. nov., D. dichromus, sp. nov., D. eclectes (Nixon), D. euterpus (Nixon), D. hadrommatus, sp. nov., D. harrisi, sp. nov., D. iqbali, sp. nov., D. lucindae, sp. nov., D. masoni, sp. nov., D. merata, sp. nov., D. muzaffari, sp. nov., D. naumanni, sp. nov., D. newguineaensis, sp. nov., D. nixoni, sp. nov., D. notopecktos, sp. nov., D. perniciosus(Wilkinson), D. rixosus (Wilkinson), D. robertsi, sp. nov., D. sons (Wilkinson), D. tearae (Wilkinson), D. tropicalus, sp. nov., D. vulpinus (Wilkinson), D. walkerae, sp. nov. and D. yousufi, sp. nov.

Ireland and New Zealand: a legacy and an assault from within

2017 ◽  
Author(s):  
Ben Worthy
Keyword(s):  
New Zealand ◽  
South America ◽  
Controversial Issue ◽  
Court Cases ◽  
Consensus Model ◽  
The Core ◽  
The World

This chapter looks at two countries that offer deviant cases-one where the legislation was passed through a consensual process and one where it was ‘imposed’ upon a new government by its predecessor. • The Consensus Model in New Zealand: agreement between senior politicians and officials led to a consensual process around developing policy, driven by those who, elsewhere, frequently formed the core resistance to the process (White 2007; Snell 2001). This led to a step-by-step, conciliatory process and a dynamic and flexible law, frequently judged one of the strongest in the world (White 2007; Aitken 1998). • The Imposed Model in Ireland: a series of controversial court cases and a scandal over infected beef in 1990s placed FOI on the agenda of two successive reformist governments. In 1997 legislation was passed as a ‘legacy’ policy in the dying days of a government which was then replaced with a successor deeply sceptical of FOI (Kearney and Stapleton 1998). The process meant FOI became a contentious and controversial issue from its inception (Felle and Adshead 2008). This represents another reason for FOI being passed, seen also in South America, whereby legislation is fostered upon a government as a legacy issue (Michener 2010).

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