Dating topographic evolution in New Zealand using mitochondrial DNA

2006 ◽  
Vol 70 (18) ◽  
pp. A115
Author(s):  
D. Craw ◽  
R. Norris ◽  
C. Burridge ◽  
J. Waters
Keyword(s):  
Mitochondrial Dna ◽  
New Zealand ◽  
Topographic Evolution

Study of COI sequences from endemic New Zealand aphids highlights high mitochondrial DNA diversity in Rhopalosiphina (Hemiptera: Aphididae)

2018 ◽  
Vol 46 (2) ◽  
pp. 107-123
Author(s):  
Colleen Podmore ◽  
Ian D. Hogg ◽  
Gabrielle M. Drayton ◽  
Barbara I. P. Barratt ◽  
Ian A. W. Scott ◽  
...  
Keyword(s):  
Mitochondrial Dna ◽  
New Zealand ◽  
Dna Diversity ◽  
Coi Sequences

Variation in the mitochondrial DNA of the potential biological control agent Chondrostereum purpureum

2000 ◽  
Vol 77 (10) ◽  
pp. 1490-1498 ◽  
Author(s):  
Tod D Ramsfield ◽  
Simon F Shamoun ◽  
Zamir K Punja ◽  
William E Hintz
Keyword(s):  
Biological Control ◽  
British Columbia ◽  
Mitochondrial Dna ◽  
New Zealand ◽  
Cytochrome B ◽  
Biological Control Agent ◽  
Gene Diversity ◽  
Restriction Enzymes ◽  
Sample Population ◽  
Chondrostereum Purpureum

The mitochondrial DNA (mtDNA) of Chondrostereum purpureum (Pers.:Fr.) Pouzar was extracted and purified, and the size ranged from 51.8 to 66.4 kb. One isolate each from British Columbia, Alberta, Finland, the Netherlands, and New Zealand were found to have identical BamHI mtDNA restriction patterns, resulting in a mitochondrial genome of 63.8 kb. An additional isolate from British Columbia and one from Switzerland had different banding patterns, however, resulting in mitochondrial genomes of 66.4 kb and 51.8 kb, respectively. A sequence-characterized amplified region (SCAR) assay, based on a polymerase chain reaction, was developed to rapidly screen a larger population of 84 isolates from North America, Europe, and New Zealand. Two SCARs, one encoding the NADH 4 gene (3 kb) and the second encoding the ATPase VI and cytochrome b genes (5.1 kb), were digested with 24 restriction enzymes. There were no polymorphisms in the NADH 4 containing SCAR, while a single polymorphism was detected by NsiI in the ATPase VI - cytochrome b containing SCAR. Two mitochondrial haplotypes that were distributed throughout the sample population were thus identified. The coancestry coefficient (<$Q7A0D00000010446D80BFFEFF88A524F5343905055B98C420120907B4DDA9ECB1F0>) for all subpopulations of the sample population was calculated to be 0.0353. The level of gene diversity in the mtDNA ofC. purpureum suggested that the chance introduction of novel mitochondrial genes following biological control applications of the fungus is relatively low.

Status of the New Zealand cave weta (Rhaphidophoridae) genera Pachyrhamma, Gymnoplectron and Turbottoplectron

2010 ◽  
Vol 24 (2) ◽  
pp. 131 ◽  
Author(s):  
Lorraine D. Cook ◽  
Steven A. Trewick ◽  
Mary Morgan-Richards ◽  
Peter M. Johns
Keyword(s):  
Mitochondrial Dna ◽  
New Zealand ◽  
Sequence Data ◽  
Taxonomic Revision ◽  
Spatial Diversity ◽  
Species Level ◽  
Dna Sequence Data ◽  
Poorly Differentiated ◽  
Single Genus ◽  
Endemic Genera

The New Zealand Rhaphidophoridae Walker, 1869 comprise 18 endemic genera (including 8 that are monotypic). Although there are many new species to be described, rationalisation at the genus level is also required due to inconsistencies in their current systematics. Even the largest and best known taxa, including those that occupy cave systems and are the most frequently encountered by people, require taxonomic revision. These cave weta include species assigned to three poorly differentiated genera, Pachyrhamma Brunner v. Wattenwyl, 1888, Gymnoplectron Hutton, 1897 and Turbottoplectron Salmon, 1948, that are best known from North Island New Zealand. We used mitochondrial DNA sequence data to examine their relationships using representatives of each genus. The results indicate that a single genus Pachyrhamma would be appropriate for all, as Gymnoplectron and Turbottoplectron nest phylogenetically within it. There are insufficient morphological, spatial or ecological reasons to justify retention of all three. However, we also note that species level diversity does not correlate with genetic or spatial diversity; some species are genetically well partitioned and widespread while others have narrow ranges in single cave systems and are closely related to one another.

Australian fur seals establish haulout sites and a breeding colony in South Australia

2010 ◽  
Vol 58 (2) ◽  
pp. 94 ◽  
Author(s):  
Peter D. Shaughnessy ◽  
Jane McKenzie ◽  
Melanie L. Lancaster ◽  
Simon D. Goldsworthy ◽  
Terry E. Dennis
Keyword(s):  
Mitochondrial Dna ◽  
New Zealand ◽  
South Australia ◽  
Breeding Colony ◽  
Mitochondrial Dna Control Region ◽  
Sea Lions ◽  
Neophoca Cinerea ◽  
Fur Seals ◽  
Fur Seal ◽  
New Zealand Fur Seal

Australian fur seals (Arctocephalus pusillus doriferus) breed on Bass Strait islands in Victoria and Tasmania. They have been recorded in South Australia (SA) for many years as non-breeding visitors and on Kangaroo Island frequently since 1988, mostly in breeding colonies of the New Zealand fur seal (A. forsteri) which is the most numerous pinniped in SA. Australian fur seals have displaced New Zealand fur seals from sections of the Cape Gantheaume colony on Kangaroo Island. North Casuarina Island produced 29 Australian fur seal pups in February 2008. Australian fur seal pups were larger than New Zealand fur seal pups in the same colony and have been identified genetically using a 263-bp fragment of the mitochondrial DNA control region. North Casuarina Island has been an important breeding colony of New Zealand fur seals, but pup numbers there decreased since 1992–93 (contrary to trends in SA for New Zealand fur seals), while numbers of Australian fur seals there have increased. This study confirms that Australian fur seals breed in SA. The two fur seal species compete for space onshore at several sites. Australian fur seals may compete for food with endangered Australian sea lions (Neophoca cinerea) because both are bottom feeders.

Mitochondrial DNA variability and geographic origin of the sheep blowfly, Lucilia cuprina (Diptera: Calliphoridae), in New Zealand

1997 ◽  
Vol 87 (3) ◽  
pp. 265-272 ◽  
Author(s):  
D. M. Gleeson ◽  
S. Sarre
Keyword(s):  
Mitochondrial Dna ◽  
New Zealand ◽  
Phylogenetic Analyses ◽  
Geographic Origin ◽  
Restriction Endonucleases ◽  
Lucilia Cuprina ◽  
Multiple Introductions ◽  
Gene Coi ◽  
Mitochondrial Dna Variability ◽  
Mitochondrial Cytochrome Oxidase

AbstractVariation in the sheep blowfly, Lucilia cuprina (Weidemann), mitochondrial DNA (mtDNA) was assessed using restriction endonucleases. Ten individuals from 13 localities throughout New Zealand and Australia were examined using 18 restriction endonucleases. Only two localities exhibited polymorphism, suggesting historical events have contributed to this low level of mitochondrial variability in L. cuprina from these regions. A 472 base pair region of the mitochondrial cytochrome oxidase I gene (COI) was sequenced from six Australasian regions and samples from South Africa and Malaysia. Phylogenetic analyses using both parsimony and neighbor-joining methods indicates possible multiple introductions of L. cuprina in New Zealand.

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