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1

Meudt, Heidi M. "Taxonomic revision of Australasian snow hebes (Veronica, Plantaginaceae)". Australian Systematic Botany 21, n.º 6 (2008): 387. http://dx.doi.org/10.1071/sb08034.

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The snow hebes, formerly comprising the genus Chionohebe, are here included within Veronica (Plantaginaceae). The five species (including two subspecies) of snow hebes recognised here are cushions or subshrubs that occur exclusively in high-elevation habitats of Australia and the South Island of New Zealand. Species delimitation among the cushion snow hebes is very difficult because of the reduced pulvinate habit, solitary flowers and few gross-morphological characters useful for identification. To address species limits, investigate intraspecific patterns and revise the taxonomy of the snow hebes, morphological analyses were conducted and the results compared with previously published molecular phylogenetic data. Ordination and clustering analyses of morphological data showed some taxonomic structuring; however, species clusters were not widely separated from one another. Morphological and amplified fragment length polymorphism (AFLP) data show that the cushion species are clearly distinguished from the subshrub species, V. densifolia (F.Muell.) F.Muell. Among the four cushion species (V. chionohebe Garn.-Jones, V. ciliolata (Hook.f.) Cheeseman, V. pulvinaris (Hook.f.) Cheeseman, V. thomsonii (Buchanan) Cheeseman), the distribution of leaf trichomes is important for species identification, particularly when used in conjunction with ovary vestiture, capsule size, and/or seed size. One new combination V. ciliolata subsp. fiordensis (Ashwin) Meudt is proposed, and V. uniflora Kirk is treated as a naturally occurring hybrid V. × uniflora (V. densifolia × V. thomsonii). Complete synonymies, descriptions, illustrations and range maps are provided for each species, as well as a key to all species and a discussion of putative hybrids.
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2

Garnock-Jones, PJ. "Phylogeny of the Hebe Complex (Scrophulariaceae: Veroniceae)". Australian Systematic Botany 6, n.º 5 (1993): 457. http://dx.doi.org/10.1071/sb9930457.

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The southern segregates of Veronica (Hebe, Parahebe, Chionohebe, Dementia, and Detzneria) form a monophyletic assemblage of c. 144 species found in New Guinea, Australia, New Zealand, Rapa, and South America. Most of the species occur in New Zealand, where Hebe is the largest genus and a characteristic member of many vegetation types. Cladistic analysis of the Hebe complex, based on 45 characters and 22 terminal taxa, indicates that: (1) Hebe is monophyletic if Hebe 'Paniculatae' is excluded and H. formosa is included; (2) Parahebe is paraphyletic; (3) Chionohebe is monophyletic, but is part of a larger clade which includes alpine Parahebe and possibly the monotypic Detzneria; (4) Hebe 'Paniculatae', Derwentia, and New Guinea Parahebe are monophyletic basal groups in the complex. According to this study, recognition of monophyletic genera would require six genera in the complex, supporting the recognition of Derwentia and separation of Hebe 'Paniculatae' from Hebe. Leonohebe Heads is considered polyphyletic and is not accepted; new combinations are provided for two species of Leonohebe with no name at species rank in Hebe. Competing biogeographic hypotheses have implied (1) a Gondwanan origin, or (2) migration from South-east Asia via New Guinea. An origin in Australasia from Asian ancestors best explains the topology of the basal parts of the cladogram, but at least seven dispersal events from New Zealand are postulated to explain the occurrence of species of Hebe in South America and Rapa and Parahebe, Hebe, and Chionohebe in Australia. An hypothesis which did not allow dispersal would require that nearly all the evolution in the complex occurred before the Tertiary, and hardly any since.
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3

Clarkson, Bruce D., e Phil J. Garnock-Jones. "Hebe tairawhiti(Scrophulariaceae): a new shrub species from New Zealand". New Zealand Journal of Botany 34, n.º 1 (março de 1996): 51–56. http://dx.doi.org/10.1080/0028825x.1996.10412692.

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4

Norton, D. A., e P. J. De Lange. "Hebe paludosa(Scrophulariaceae)—a new combination for an endemic wetland Hebe from Westland, South Island, New Zealand". New Zealand Journal of Botany 36, n.º 4 (dezembro de 1998): 531–38. http://dx.doi.org/10.1080/0028825x.1998.9512593.

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5

ARMSTRONG, TRISTAN T. J., e PETER J. DE LANGE. "Conservation genetics of Hebe speciosa (Plantaginaceae) an endangered New Zealand shrub". Botanical Journal of the Linnean Society 149, n.º 2 (outubro de 2005): 229–39. http://dx.doi.org/10.1111/j.1095-8339.2005.00437.x.

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6

Garnock‐Jones, P. J., M. J. Bayly, W. G. Lee e B. D. Rance. "Hebe arganthera(Scrophulariaceae), a new species from calcareous outcrops in Fiordland, New Zealand". New Zealand Journal of Botany 38, n.º 3 (setembro de 2000): 379–88. http://dx.doi.org/10.1080/0028825x.2000.9512690.

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7

de Lange, P. J., e J. R. Rolfe. "Hebe saxicola(Plantaginaceae)—a new threatened species from western Northland, North Island, New Zealand". New Zealand Journal of Botany 46, n.º 4 (dezembro de 2008): 531–45. http://dx.doi.org/10.1080/00288250809509783.

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8

Widyatmoko, D., e D. A. Norton. "Conservation of the threatened shrub Hebe cupressoides (Scrophulariaceae), eastern South Island, New Zealand". Biological Conservation 82, n.º 2 (novembro de 1997): 193–201. http://dx.doi.org/10.1016/s0006-3207(97)00016-5.

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9

De Lange, P. J. "Hebe perbella(Scrophulariaceae)—a new and threatened species from western Northland, North Island, New Zealand". New Zealand Journal of Botany 36, n.º 3 (setembro de 1998): 399–406. http://dx.doi.org/10.1080/0028825x.1998.9512578.

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10

De Lange, P. J. "Hebe bishopiana(Scrophulariaceae) — an endemic species of the Waitakere Ranges, West Auckland, New Zealand". New Zealand Journal of Botany 34, n.º 2 (junho de 1996): 187–94. http://dx.doi.org/10.1080/0028825x.1996.10410682.

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11

de Lange, P. J. "Hebe brevifolia(Scrophulariaceae) — an ultramafic endemic of the Surville Cliffs, North Cape, New Zealand". New Zealand Journal of Botany 35, n.º 1 (março de 1997): 1–8. http://dx.doi.org/10.1080/0028825x.1997.10410668.

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12

Watson, M. C., T. M. Withers e R. L. Hill. "Twophase openfield test to confirm host range of a biocontrol agent Cleopus japonicus". New Zealand Plant Protection 62 (1 de agosto de 2009): 184–90. http://dx.doi.org/10.30843/nzpp.2009.62.4776.

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The buddleia leaf weevil Cleopus japonicus was released in New Zealand in 2006 as a biological control agent for the weed Buddleja davidii A twophase openfield design was used to confirm laboratory host range and examine nontarget impacts in the field This was the first field trial undertaken in New Zealand and included six nontarget plant species Feeding and dispersal of the agent on the test species and B davidii were compared Cleopus japonicus strongly preferred B davidii Larvae were recorded on Verbascum virgatum and Scrophularia auriculata during the choice stage of the trial Killing the B davidii plants in the second phase resulted in adults feeding on the two exotic species V virgatum and S auriculata Minor exploratory feeding was recorded on the natives Hebe speciosa and Myoporum laetum These results confirm that laboratory tests conducted to assess the safety of this agent for release in New Zealand accurately predicted field host range
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13

Walsh, Delwynne, Gordon Sharfe, Trish James, Jess Owen, David Boot, Nicole Walker e Margaret Hill. "Handwriting Identification". Journal of Forensic Document Examination 27 (31 de dezembro de 2017): 57–59. http://dx.doi.org/10.31974/jfde27-57-59.

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The authors are all practicing forensic document examiners for the New Zealand Police. However, this review was prepared by them in their personal capacity. The views and opinions expressed in this review are those of the authors and do not necessarily reflect the view of the New Zealand Police. Receive Book Review - $0
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14

Niederer, Kate, R. John Irwin, Kathryn C. Irwin e Ivan L. Reilly. "Identification of Mathematically Gifted Children in New Zealand". High Ability Studies 14, n.º 1 (junho de 2003): 71–84. http://dx.doi.org/10.1080/13598130304088.

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15

Parfitt, RL. "Allophane in New Zealand - a review". Soil Research 28, n.º 3 (1990): 343. http://dx.doi.org/10.1071/sr9900343.

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Studies of allophanes from New Zealand are reviewed, and a definition of the allophane group of minerals is suggested. Three types of allophane are identified, and their structures are discussed under headings Al-rich soil allophanes, Si-rich soil allophanes and stream deposit allophanes. Examples from New Zealand soils and tephras are discussed in relation to properties, identification and weathering processes.
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16

McConkey, Shaun D. "Photographic identification of the New Zealand sea lion: A new technique". New Zealand Journal of Marine and Freshwater Research 33, n.º 1 (março de 1999): 63–66. http://dx.doi.org/10.1080/00288330.1999.9516857.

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17

MOUND, LAURENCE A., e ANNETTE K. WALKER. "The Australia-New Zealand connection re-visited, with two new species of Cartomothrips (Thysanoptera, Phlaeothripinae)". Zootaxa 3487, n.º 1 (18 de setembro de 2012): 58. http://dx.doi.org/10.11646/zootaxa.3487.1.4.

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The distribution of the six species in Cartomothrips is considered, and a key provided for their identification. C. tofti sp.n. is described from New Zealand; manukae is widespread in New Zealand but also found in Tasmania; neboissi is infrequent in New Zealand but common in southern Australia; laughlini is known only from South Australia; browni breeds in the seed capsules of some Eucalyptus species and thus presumably is an Australian species but has also been found in Brazil, California, Kenya and New Zealand; C. abrsi sp.n. is described from Tasmania.
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18

BROWN, BRIAN V., e HUGH OLIVER. "Two new genera of Phoridae (Diptera) from New Zealand". Zootaxa 1933, n.º 1 (14 de novembro de 2008): 1–11. http://dx.doi.org/10.11646/zootaxa.1933.1.1.

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Two new genera, Wharia and Minicosta, are diagnosed and specimens of their included species, W. willcocksorum and M. mollyae, described. The relationships of both genera are unknown, although they do not belong in subfamily Metopininae. Modifications to the latest key to World phorid genera are given to allow identification of the new taxa.
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19

Guy, P. L. "New Zealand grasslands revisited: identification ofCocksfoot mild mosaic virus". Australasian Plant Pathology 35, n.º 4 (2006): 461. http://dx.doi.org/10.1071/ap06048.

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20

Young, J. M., C. N. Chilcott, A. Broadwell, P. J. Wigley e M. M. Lecadet. "Identification of serovars ofBacillus thuringiensisBerliner 1915 in New Zealand". New Zealand Journal of Crop and Horticultural Science 26, n.º 1 (março de 1998): 63–68. http://dx.doi.org/10.1080/01140671.1998.9514041.

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21

Goguel, R. L., e D. A. St John. "Chemical identification of portland cements in New Zealand concretes". Cement and Concrete Research 23, n.º 2 (março de 1993): 283–93. http://dx.doi.org/10.1016/0008-8846(93)90093-o.

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22

Goguel, R. L., e D. A. St. John. "Chemical identification of portland cements in New Zealand concretes". Cement and Concrete Research 23, n.º 1 (janeiro de 1993): 59–68. http://dx.doi.org/10.1016/0008-8846(93)90136-w.

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23

Patty, OA, e RTM Cursons. "The molecular identification ofStreptococcus equisubsp.equistrains isolated within New Zealand". New Zealand Veterinary Journal 62, n.º 2 (24 de outubro de 2013): 63–67. http://dx.doi.org/10.1080/00480169.2013.841536.

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24

CRANSTON, PETER S. "Identification guide to genera of aquatic larval Chironomidae (Diptera) of Australia and New Zealand". Zootaxa 4706, n.º 1 (6 de dezembro de 2019): 71–102. http://dx.doi.org/10.11646/zootaxa.4706.1.3.

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Identification keys are provided for the final (4th) instar larvae of genera of Chironomidae (Diptera), from aquatic habitats in Australia and New Zealand. Morphological features of taxonomic utility are discussed and illustrated by line drawings. Summaries of described species for each genus and their distribution is provided, with reference to means of further identification where available. In the subfamily Podonominae, 5 genera are keyed of which 3 are recorded from New Zealand; the 4 genera of Aphroteniinae are from Australia (absent from New Zealand); in Diamesinae 1 genus is Australian, 2 are from New Zealand; in the Tanypodinae 21 genera are found in Australia and 4 are from New Zealand; in Orthocladiinae 31 genera are reported from Australia, 14 from New Zealand; and in Chironominae 43 genera are keyed from Australia, 9 from New Zealand. Larvae of Axarus Roback, Chernovskiia Sæther and Omisus Townes (Chironomini) are recognised in Australia for the first time. The undescribed larva of Paucispinigera Freeman, endemic to New Zealand, is keyed and several other New Zealand taxa are included based on unpublished records. Genera reported from Australia and New Zealand as adults, but unknown as larvae, are listed.
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25

Liu, Y. N., N. Nan, B. H. Lu, W. Y. Xia, X. Y. Wu, Q. R. Bai e J. Gao. "First Report of Phoma rhei as a Pathogen of Rheum rhabarbarum in China". Plant Disease 98, n.º 8 (agosto de 2014): 1154. http://dx.doi.org/10.1094/pdis-01-14-0019-pdn.

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Rheum rhabarbarum L., rhubarb, is a perennial herb planted mainly in Hebei, Hubei, Shanxi, Heilongjiang, and Jilin provinces as well as Inner Mongolia, China. The plant grows about 1,000 meters above sea level (4), and is used widely in China to treat constipation and gout. From June to September 2012, a leaf spot was observed on R. rhabarbarum in the medicinal garden of Jilin Agricultural University, Changchun, Jilin Province, causing significant effects on the leaves of all infected plants. In the early stage of disease development, small red lesions were visible on infected leaves, which subsequently developed into irregularly shaped or circular necrotic spots, each with a light colored center, pink-red alternating concentric rings, and surrounded by a chlorotic halo. Some lesions became perforated in the center. Lesions ranged from 1 to 15 mm in diameter. Extensive spotting resulted in general browning and yellowing of entire leaves. As lesions enlarged and coalesced, some leaves died from the margin inwards. Lesions on the stem were fusiform and sunken. Small pieces of diseased leaves and stems were surface-disinfested in 75% ethanol for 60 s, rinsed twice in distilled water, dried, and plated on potato dextrose agar (PDA). A Phoma species was isolated that produced a gray or dark gray colony after 5 to 7 days. The isolate was transferred to oatmeal agar (OA) (3). Pycnidia were dark brown to black, globose to subglobose, and 121 to 354 × 100 to 262 μm. Conidia were ellipsoidal or reniform, colorless, unicellular, and 3.8 to 6.5 × 1.7 to 4.1 μm. On the basis of these characteristics, the fungus was identified as Phoma rhei (1). A PCR assay with the ITS4 and ITS5 primers was used to amplify the internal transcribed spacer (ITS) region of ribosomal DNA (rDNA) (2). The amplified product (567 bp) was sequenced and the sequence submitted to GenBank (Accession No. KF531831). The ITS sequence exhibited 99% identity to that of a P. rhei isolate in GenBank (GU237743.1), confirming the morphological identification. Pathogenicity of eight isolates on rhubarb was confirmed by spraying a spore suspension (1 × 106 spores/ml) produced on PDA on the leaves of each 6-year-old R. rhabarbarum (cv. Boyedahuang) plant. Each isolate was inoculated onto five plants, and five plants were sprayed similarly with sterilized water as a control treatment. The plants were then covered with plastic bags for 48 h, and kept in a greenhouse (20 to 30°C with a 12-h photoperiod/day). Initial symptoms on inoculated leaves were observed 3 to 4 days after inoculation, while the control plants remained healthy. Re-isolations from lesions on the inoculated leaves, using the same protocol as the original isolations, produced fungal colonies with the same morphological characteristics as the original isolates of P. rhei, but no fungi were re-isolated from the control plants. This fungus has been found on R. rhaponticum in New Zealand (1), but to our knowledge this is the first report of P. rhei on R. rhabarbarum in China. References: (1) G. H. Boerema et al. Phoma Identification Manual. Diffferentiation of Specific and Infra-Specific Taxa in Culture. CABI Publishing. Wallingford, UK, 2004. (2) D. E. L. Cooke et al. Mycol. Res. 101:667, 1997. (3) Z. D. Fang. Research Method of Phytopathology. China Agricultural Press (In Chinese), 1998. (4) A. J. Li et al. Flora Reipublicae Popularis Sinicae. Tomus 25:171, 1998.
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Hui, C. T. Justine, Hinako Masuda, Yusuke Hioka e Catherine I. Watson. "Word identification of New Zealand English by native Japanese listeners with and without exposure to New Zealand English". Acoustical Science and Technology 44, n.º 1 (1 de janeiro de 2023): 29–32. http://dx.doi.org/10.1250/ast.44.29.

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27

James, T. K., A. F. Leslie, A. I. Popay e P. D. Champion. "A Lucidtrade; key for common weeds of New Zealand". New Zealand Plant Protection 57 (1 de agosto de 2004): 277–80. http://dx.doi.org/10.30843/nzpp.2004.57.6972.

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An Illustrated Guide to Common Weeds of New Zealand was published by the New Zealand Plant Protection Society in 1998 and a second edition in 2004 This book has a key that uses flower colour and size and plant form for identification of broadleaf weeds However when no flowers are present the only recourse is to go through the book looking at the photographs Lucid Professionaltrade; is a software package produced by the University of Queensland for the production of identification or diagnostic keys The resultant Lucidtrade; key is a multiaccess key that allows identification to begin with any of the plants main characters As soon as the characters state is identified all the taxa that do not match are discarded and the process repeated until the plant is identified The information in the second edition of the book has been converted into a Lucidtrade; key that contains descriptions and illustrations for 333 taxa
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28

Shields, Morgan W., Jean-Marie Tompkins, David J. Saville, Colin D. Meurk e Stephen Wratten. "Potential ecosystem service delivery by endemic plants in New Zealand vineyards: successes and prospects". PeerJ 4 (22 de junho de 2016): e2042. http://dx.doi.org/10.7717/peerj.2042.

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Vineyards worldwide occupy over 7 million hectares and are typically virtual monocultures, with high and costly inputs of water and agro-chemicals. Understanding and enhancing ecosystem services can reduce inputs and their costs and help satisfy market demands for evidence of more sustainable practices. In this New Zealand work, low-growing, endemic plant species were evaluated for their potential benefits as Service Providing Units (SPUs) or Ecosystem Service Providers (ESPs). The services provided were weed suppression, conservation of beneficial invertebrates, soil moisture retention and microbial activity. The potential Ecosystem Dis-services (EDS) from the selected plant species by hosting the larvae of a key vine moth pest, the light-brown apple moth (Epiphyas postvittana), was also quantified. Questionnaires were used to evaluate winegrowers’ perceptions of the value of and problems associated with such endemic plant species in their vineyards. Growth and survival rates of the 14 plant species, in eight families, were evaluated, withLeptinella dioica(Asteraceae) andAcaena inermis‘purpurea’ (Rosaceae) having the highest growth rates in terms of area covered and the highest survival rate after 12 months. All 14 plant species suppressed weeds, withLeptinella squalida, Geranium sessiliforum(Geraniaceae),Hebe chathamica(Plantaginaceae),Scleranthus uniflorus(Caryophyllaceae) andL. dioica, each reducing weed cover by >95%. Plant species also differed in the diversity of arthropods that they supported, with the Shannon Wiener diversity index (H′) for these taxa ranging from 0 to 1.3.G. sessiliforumandMuehlenbeckia axillaris(Polygonaceae) had the highest invertebrate diversity. Density of spiders was correlated with arthropod diversity andG. sessiliflorumandH. chathamicahad the highest densities of these arthropods. Several plant species associated with higher soil moisture content than in control plots. The best performing species in this context wereA. inermis‘purpurea’ andLobelia angulata(Lobeliaceae). Soil beneath all plant species had a higher microbial activity than in control plots, withL. dioicabeing highest in this respect. Survival proportion to the adult stage of the moth pest,E. postvittana, on all plant species was poor (<0.3). When judged by a ranking combining multiple criteria, the most promising plant species were (in decreasing order)G. sessiliflorum, A. inermis‘purpurea’,H. chathamica, M. axillaris, L. dioica, L. angulata, L. squalidaandS. uniflorus. Winegrowers surveyed said that they probably would deploy endemic plants around their vines. This research demonstrates that enhancing plant diversity in vineyards can deliver SPUs, harbour ESPs and therefore deliver ES. The data also shows that growers are willing to follow these protocols, with appropriate advice founded on sound research.
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Sparks, G. A., D. B. MacGibbon, G. D. Coles e C. R. Slack. "Identification of New Zealand grown barley cultivars by grain characters". New Zealand Journal of Experimental Agriculture 13, n.º 4 (outubro de 1985): 359–67. http://dx.doi.org/10.1080/03015521.1985.10426104.

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Attwood, G. T., e K. Reilly. "Identification of proteolytic rumen bacteria isolated from New Zealand cattle". Journal of Applied Bacteriology 79, n.º 1 (julho de 1995): 22–29. http://dx.doi.org/10.1111/j.1365-2672.1995.tb03119.x.

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Garkavenko, O., R. B. Elliott e M. C. Croxson. "Identification of pig circovirus type 2 in New Zealand pigs". Transplantation Proceedings 37, n.º 1 (janeiro de 2005): 506–9. http://dx.doi.org/10.1016/j.transproceed.2004.12.301.

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32

Russell, K. M., P. C. Molan, A. L. Wilkins e P. T. Holland. "Identification of some antibacterial constituents of New Zealand manuka honey". Journal of Agricultural and Food Chemistry 38, n.º 1 (janeiro de 1990): 10–13. http://dx.doi.org/10.1021/jf00091a002.

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Khan, M. Ikram, Virginia Marroni, Sandi Keenan, Ian A. W. Scott, Suvi L. H. Viljanen-Rollinson e Simon Bulman. "Enhanced molecular identification of Botrytis spp. from New Zealand onions". European Journal of Plant Pathology 136, n.º 3 (16 de março de 2013): 495–507. http://dx.doi.org/10.1007/s10658-013-0182-y.

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Blouin, Arnaud G., Sandi Keenan, Kathryn R. Napier, Roberto A. Barrero e Robin M. MacDiarmid. "Identification of a novel vitivirus from grapevines in New Zealand". Archives of Virology 163, n.º 1 (12 de outubro de 2017): 281–84. http://dx.doi.org/10.1007/s00705-017-3581-0.

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Garkavenko, O., R. B. Elliott e M. C. Croxson. "IDENTIFICATION OF PIG CIRCOVIRUS TYPE 2 IN NEW ZEALAND PIGS." Transplantation 78 (julho de 2004): 579. http://dx.doi.org/10.1097/00007890-200407271-01560.

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JOCQUE, M., e W. BLOM. "Mysidae (Mysida) of New Zealand; a checklist, identification key to species and an overview of material in New Zealand collections". Zootaxa 2304, n.º 1 (4 de dezembro de 2009): 1–20. http://dx.doi.org/10.11646/zootaxa.2304.1.1.

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Mysida are small, mostly marine crustaceans that are an important element of food webs, specifically as prey for several commercially important fish species. Taking their ecological and economical importance into account, relatively little attention is attributed to these organisms, and they are often neglected in biodiversity surveys and studies. To draw attention to these animals and stimulate research in New Zealand, we summarize information available for New Zealand Mysidae. We present a checklist of the 17 species recorded in New Zealand waters as well as a preliminary identification key to species based on the existing literature. We also provide an overview of mysid material available in collections in New Zealand.
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BOYER, STEPHANE, ROBERT J. BLAKEMORE e STEVE D. WRATTEN. "An integrative taxonomic approach to the identification of three new New Zealand endemic earthworm species (Acanthodrilidae, Octochaetidae: Oligochaeta)". Zootaxa 2994, n.º 1 (12 de agosto de 2011): 21. http://dx.doi.org/10.11646/zootaxa.2994.1.2.

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This work adds three new species to the ca. 200 currently known from New Zealand. In Acanthodrilidae is Maoridrilus felix and in Octochaetidae are Deinodrilus gorgon and Octochaetus kenleei. All three are endemics that often have restricted ranges; however, little is yet known of their distribution, ecology nor conservation status. DNA barcoding was conducted, which is the first time that New Zealand endemic holotypes have been so characterized. The barcoding region COI (cytochrome c oxidase subunit 1) as well as the 16S rDNA region were sequenced using tissue from the holotype specimen to provide indisputable uniqueness of the species. These DNA sequences are publically available on GenBank to allow accurate cross checking to verify the identification of other specimens or even to identify specimens on the basis of their DNA sequences alone. Based on their 16S rDNA sequences, the position of the three newly described species in the phylogeny of New Zealand earthworms was discussed. The description of new species using this approach is encouraged, to provide a user-friendly identification tool for ecologists studying diverse endemic faunas of poorly known earthworm species.
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HEENAN, PETER B. "A taxonomic revision of Cardamine L. (Brassicaceae) in New Zealand". Phytotaxa 330, n.º 1 (5 de dezembro de 2017): 1. http://dx.doi.org/10.11646/phytotaxa.330.1.1.

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A taxonomic revision of the cosmopolitan genus Cardamine is presented for New Zealand. Previous systematic research and the taxonomic history of Cardamine in New Zealand is reviewed, and a phylogenetic analysis of DNA sequences shows most of the species of Cardamine in New Zealand and Australia are closely related. Forty one taxa indigenous to New Zealand are recognised, with thirty-one species newly named and described, ten previously named taxa are accepted, including C. depressa with two subspecies and a new name is provided for one species. An additional four species are accepted as naturalised in New Zealand. Descriptions are presented for all taxa, along with information on distribution, habitats and conservation status. All taxa are illustrated, distribution maps provided, and a dichotomous key presented to assist with identification.
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39

Polizzi, G., A. Vitale e G. Parlavecchio. "First Occurrence of Downy Mildew on Boxleaf Veronica Caused by Peronospora grisea in Italy". Plant Disease 88, n.º 4 (abril de 2004): 424. http://dx.doi.org/10.1094/pdis.2004.88.4.424b.

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Boxleaf veronica (Hebe buxifolia (Benth.) Cockayne & Allan), native to New Zealand, is an annual or perennial shrub widely cultivated in Mediterranean zones. During late spring 2003, after seasonably wet and cool weather, a downy mildew epidemic occurred on potted, overhead irrigated, 1-year-old seedlings at a commercial nursery in eastern Sicily (southern Italy). Infections affected boxleaf veronica at first, but spread to variegated boxleaf (H. buxifolia cv. variegata). Initial symptoms on the upper side of leaves were small, gray brown patches that gradually spread, eventually resulting in necrosis in the center of infected areas. At that point, brown patches were evident on both sides of the leaves. Lesions on the lower leaf surface became covered with a fairly dense, pale gray-to-brown layer of conidia and conidiophores. As the disease progressed, these spots coalesced into large and conspicuous brown lesions. The youngest, most succulent shoots withered and died. The large brown lesions on the leaves were disfiguring and affected 95 to 100% of plants in the nursery. All diseased nursery stock had to be discarded. Oospores were not observed in leaf tissues. The fungus recovered from leaves with abundant gray brown sporulation was identified as Peronospora grisea (Unger) Unger. Microscopic observations revealed conidiophores that branched dichotomously five to seven times with branch ends 6 to 10 × 2 to 3 μm, slightly curved, and tapered to a blunt apex. Hyaline conidia were ellipsoid, brownish when mature, and measured 23 to 27 × 15 to 18 μm (mean = 25.2 × 17.1 μm), falling within the range of those reported for P. grisea (1). Pathogenicity was confirmed by inoculating 10 1-yr-old seedlings (10 cm tall) by gently pressing infected leaves with abundant sporulation onto healthy leaves and maintaining inoculated plants in a humid chamber at 21°C. An equal number of noninoculated plants served as controls. After 9 to 11 days, symptoms similar to those originally observed developed onto inoculated plants, and after 12 to 15 days, grayish mildew grew on leaves. Microscopic examination of the developing mycelium confirmed that leaves were infected with P. grisea. Uninoculated control plants did not develop any symptoms. The disease was also confirmed in this way on variegated boxleaf veronica (H. buxifolia cv. variegata). Downy mildew of Hebe spp. has been recorded in New Zealand, Britain, France, Germany, and more recently, West Sussex (2). Heavy rainfall during the spring of 2003 in eastern Sicily could have favored disease development. To our knowledge, this is the first report of downy mildew of boxleaf veronica and variegated boxleaf veronica caused by P. grisea in Italy. References: (1) S. M. Francis and A. M. Berrie. Peronospora grisea. No. 766 in: Descriptions of pathogenic fungi and bacteria. CMI, Kew, Surrey, UK. 1983. (2) J. M. Whipps and C. A. Linfield. Plant Pathol. 36:216, 1987.
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40

Tinsley, Yvette. "Identification Procedures and Options for Reform". Victoria University of Wellington Law Review 31, n.º 1 (3 de abril de 2000): 117. http://dx.doi.org/10.26686/vuwlr.v31i1.5959.

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This article was presented as a Victoria University of Wellington Centennial Lecture during Law Festival Week in 1999. The author notes that while the identification parade is officially the preferred method of identification in New Zealand, very few live parades are organised. Police officers prefer to use photographic identification, for which there is little procedural guidance or training resulting in an ad hoc development of police practice. It is argued in this article that regardless of the method used, a review of the supervision and training of police officers in the area of witness identification is urgently required.This article incorporates qualitative research on identification procedures in New Zealand, funded by a Victoria University Internal Grant. More extensive research in the United Kingdom was completed for the author’s doctoral thesis.
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41

Broman, Patrick, e Tahu Kukutai. "Fixed not fluid: European identification in the Aotearoa New Zealand census". Journal of Population Research 38, n.º 2 (23 de abril de 2021): 103–38. http://dx.doi.org/10.1007/s12546-021-09262-4.

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42

Smith, Kirsty F., Hernando Acosta, Judith E. Broom e Lesley L. Rhodes. "Identification of non-indigenous marine macroalgae from New Zealand aquaria outlets". New Zealand Journal of Marine and Freshwater Research 44, n.º 1 (março de 2010): 29–37. http://dx.doi.org/10.1080/00288331003641679.

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43

Lamb, G., K. L. Choi, C. Selwyn, A. Wheeler, L. Hammond, J. Morgan e P. P. J. Dunn. "Identification of seven novel HLA class I alleles in New Zealand". International Journal of Immunogenetics 42, n.º 5 (24 de julho de 2015): 361–63. http://dx.doi.org/10.1111/iji.12221.

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44

Lancaster, J. E., E. P. McCartney, W. A. Jermyn e J. V. Johnstone. "Identification of onion cultivars for commercial production in Canterbury, New Zealand". New Zealand Journal of Crop and Horticultural Science 23, n.º 3 (setembro de 1995): 299–306. http://dx.doi.org/10.1080/01140671.1995.9513902.

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45

Gatley, Julia. "The heritage identification of modern public housing: the New Zealand example". Journal of Architecture 15, n.º 5 (outubro de 2010): 683–96. http://dx.doi.org/10.1080/13602365.2010.519960.

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46

Todd, Angela, Susan Taylor e Q. Sue Huang. "Identification of Enterovirus C105 for the first time in New Zealand". Western Pacific Surveillance and Response Journal 6, n.º 1 (10 de janeiro de 2015): 60–61. http://dx.doi.org/10.5365/wpsar.2014.5.4.003.

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47

King, Carolyn M., David G. Chapple, Rod A. Hitchmough e Tony Jewell. "Dynamic taxonomy versus field identification: A dilemma for New Zealand herpetologists". New Zealand Journal of Zoology 36, n.º 1 (janeiro de 2009): 59–71. http://dx.doi.org/10.1080/03014220909510140.

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48

Bell, Nigel, e Richard Watson. "Identification and host range assessment of Paratylenchus nanus (Tylenchida: Tylenchulidae) and Paratrichodorus minor (Triplonchida: Trichodoridae)". Nematology 3, n.º 6 (2001): 483–90. http://dx.doi.org/10.1163/156854101753389095.

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AbstractAdult and juvenile characters were used to identify Paratylenchus nanus Cobb, 1923 and Paratrichodorus minor (Colbran, 1956) Siddiqi, 1974 from soils under pasture in New Zealand. In glasshouse tests of 15 pasture plants, common in New Zealand, all good hosts (ratio of final to initial population >1) of P. nanus were grasses, namely Dactylis glomerata , Lolium multiflorum and L. perenne (Neotyphodium endophyte-infected and-free), all new host records for this species. Good hosts of P.minor included those listed for P.nanus and Festuca arundinacea (endophyte-free) , Poa annua , Trifolium pratense , T. repens and T. subterraneum. Except for T. repens, these are all new host records for P.minor in New Zealand.
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49

James, T. K., P. D. Champion, C. A. Dowsett, M. R. McNeill e G. J. Houliston. "Identification of weed seeds in soil samples intercepted at the New Zealand border". New Zealand Plant Protection 67 (8 de janeiro de 2014): 26–33. http://dx.doi.org/10.30843/nzpp.2014.67.5740.

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Identification of weed seeds from overseas countries can be problematic particularly when diagnostic tools are lacking or incomplete A well trained seed analyst will usually be able to identify seed to generic level but not always to the species level Resources for identification of mature plants are usually more complete Using a seed germination method for intercepted soil samples achieved two goals; it provided an easier route to identification and a measure of viable seed The drawback of this method is the need to grow the plants through to flowering DNA identification is an emerging method for more rapid identification but it relies on availability of matching sequences in an existing database and validation of source plant identification with reliable voucher specimens The limitations and advantages of both techniques are discussed and ways in which timely and accurate identification can be provided for biosecurity practitioners are suggested
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50

Mcconkey, SD, S. Heinrich, C. Lalas, H. Mcconnell e N. Mcnally. "Pattern Of Immigration Of New Zealand Sea Lions Phocarctos Hookeri To Otago, New Zealand: Implications For Management". Australian Mammalogy 24, n.º 1 (2002): 107. http://dx.doi.org/10.1071/am02107.

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The present management strategy for New Zealand sea lions Phocarctos hookeri assumes that kills in a squid trawl fishery around Auckland Islands, the species population base, have prevented an increase in abundance of sea lions. This strategy also assumes that emigration will be initiated as the population reaches carrying capacity, and that emigration rates will be density dependent. We used the combination of photographic identification of individuals and diagnostic features of age classes to estimate immigration rates of P. hookeri to Otago, South Island, New Zealand. Most immigrants were males = 2 years old at arrival, and included animals tagged as pups at Auckland Islands. Estimates for total numbers of immigrants to Otago from four consecutive cohorts, 1991/92 - 1994/95, varied three-fold through a period of constant annual pup production at Auckland Islands. The greatest influx was from the 1993/94 cohort, a breeding season that predated the enforcement of early closures of the squid fishery. We suggest published records from the Auckland Islands indicate that this population is already at carrying capacity. If so, then factors other than, or in addition to, pup production and fishery mortality have an impact on emigration rates.
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