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Journal articles on the topic 'Hebe – new zealand'

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Published: 26 July 2024

Last updated: 26 July 2024

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1

Garnock-Jones, PJ. "Phylogeny of the Hebe Complex (Scrophulariaceae: Veroniceae)." Australian Systematic Botany 6, no. 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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2

Clarkson, Bruce D., and Phil J. Garnock-Jones. "Hebe tairawhiti(Scrophulariaceae): a new shrub species from New Zealand." New Zealand Journal of Botany 34, no. 1 (March 1996): 51–56. http://dx.doi.org/10.1080/0028825x.1996.10412692.

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3

Norton, D. A., and 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, no. 4 (December 1998): 531–38. http://dx.doi.org/10.1080/0028825x.1998.9512593.

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4

ARMSTRONG, TRISTAN T. J., and PETER J. DE LANGE. "Conservation genetics of Hebe speciosa (Plantaginaceae) an endangered New Zealand shrub." Botanical Journal of the Linnean Society 149, no. 2 (October 2005): 229–39. http://dx.doi.org/10.1111/j.1095-8339.2005.00437.x.

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5

Garnock‐Jones, P. J., M. J. Bayly, W. G. Lee, and B. D. Rance. "Hebe arganthera(Scrophulariaceae), a new species from calcareous outcrops in Fiordland, New Zealand." New Zealand Journal of Botany 38, no. 3 (September 2000): 379–88. http://dx.doi.org/10.1080/0028825x.2000.9512690.

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6

de Lange, P. J., and J. R. Rolfe. "Hebe saxicola(Plantaginaceae)—a new threatened species from western Northland, North Island, New Zealand." New Zealand Journal of Botany 46, no. 4 (December 2008): 531–45. http://dx.doi.org/10.1080/00288250809509783.

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7

Watson, M. C., T. M. Withers, and R. L. Hill. "Twophase openfield test to confirm host range of a biocontrol agent Cleopus japonicus." New Zealand Plant Protection 62 (August 1, 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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8

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, no. 3 (September 1998): 399–406. http://dx.doi.org/10.1080/0028825x.1998.9512578.

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9

Widyatmoko, D., and D. A. Norton. "Conservation of the threatened shrub Hebe cupressoides (Scrophulariaceae), eastern South Island, New Zealand." Biological Conservation 82, no. 2 (November 1997): 193–201. http://dx.doi.org/10.1016/s0006-3207(97)00016-5.

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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, no. 2 (June 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, no. 1 (March 1997): 1–8. http://dx.doi.org/10.1080/0028825x.1997.10410668.

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12

Shields, Morgan W., Jean-Marie Tompkins, David J. Saville, Colin D. Meurk, and Stephen Wratten. "Potential ecosystem service delivery by endemic plants in New Zealand vineyards: successes and prospects." PeerJ 4 (June 22, 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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13

Polizzi, G., A. Vitale, and G. Parlavecchio. "First Occurrence of Downy Mildew on Boxleaf Veronica Caused by Peronospora grisea in Italy." Plant Disease 88, no. 4 (April 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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14

CLARK, RYAN D., RENAUD MATHIEU, and PHILIP J. SEDDON. "Selection for protection from insolation results in the visual isolation of Yellow-eyed Penguin Megadyptes antipodes nests." Bird Conservation International 25, no. 2 (October 8, 2014): 192–206. http://dx.doi.org/10.1017/s0959270914000082.

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SummaryThe concealed and widely dispersed nests of the rare and endangered Yellow-eyed Penguin Megadyptes antipodes, or “hoiho”, have been considered to reflect an essential requirement for the visual isolation of nest sites from conspecifics. However, this may be a consequence of selection for habitat features that provide protection from insolation, thereby minimising the risk of heat stress. To help improve the understanding of hoiho nesting requirements and the effectiveness of habitat restoration, we aimed to determine whether visual isolation from conspecifics or protection from insolation is the primary driver of hoiho nest site selection. We compared the mean maximum distance of visibility and the mean percentage insolation cover of active nests with randomly sampled unused sites in flax Phormium tenax and Hebe elliptica coastal scrub at Boulder Beach, and in coastal forest at Hinahina Cove, New Zealand, 2006–2007. Results of univariate tests and the evaluation of logistic regression models suggested that the amount of insolation cover was more important than visibility for hoiho nest site selection, particularly in flax and scrub. In addition, Spearman's correlations indicated that decreasing insolation cover significantly increased the visibility of nests in the forest habitat, and had a similar effect on inter-nest distance in flax. We infer that hoiho nest site selection and distribution are influenced primarily by the location and density of micro-habitat features (particularly within 1 m of the ground) that provide optimal protection from insolation, possibly along with other important features such as a firm backing structure. Strong selection for these features results in the typical but non-essential visual isolation of nest sites from conspecifics. Restoration of nesting habitats with a relatively high density and diversity of vegetation and solid structures within 1 m of the ground may eventually provide an optimal availability and quality of suitable nest sites.

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15

Wagstaff, Steven J., Michael J. Bayly, Philip J. Garnock-Jones, and Dirk C. Albach. "Classification, Origin, and Diversification of the New Zealand Hebes (Scrophulariaceae)." Annals of the Missouri Botanical Garden 89, no. 1 (2002): 38. http://dx.doi.org/10.2307/3298656.

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16

Taskova, Rilka M., Tetsuo Kokubun, Phil J. Garnock-Jones, and Søren R. Jensen. "Iridoid and phenylethanoid glycosides in the New Zealand sun hebes (Veronica; Plantaginaceae)." Phytochemistry 77 (May 2012): 209–17. http://dx.doi.org/10.1016/j.phytochem.2012.02.001.

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17

Perry, Nigd B., Eleanor G. Becker, John W. Blunt, Robin J. Lake, and Murray H. G. Munro. "Diyne Enol Ethers of Glycerol from a New Zealand Sponge, Petrosia hebes." Journal of Natural Products 53, no. 3 (May 1990): 732–34. http://dx.doi.org/10.1021/np50069a036.

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18

Taskova, Rilka M., Tetsuo Kokubun, Ken G. Ryan, Phil John Garnock-Jones, and Soren Rosendal Jensen. "Phenylethanoid and Iridoid Glycosides in the New Zealand Snow Hebes (Veronica, Plantaginaceae)." CHEMICAL & PHARMACEUTICAL BULLETIN 58, no. 5 (2010): 703–11. http://dx.doi.org/10.1248/cpb.58.703.

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19

Meudt, Heidi M. "Taxonomic revision of Australasian snow hebes (Veronica, Plantaginaceae)." Australian Systematic Botany 21, no. 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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20

Scott, JM, IM Turnbull, MW Sagar, AJ Tulloch, TE Waight, and JM Palin. "Geology and geochronology of the Sub-Antarctic Snares Islands/Tini Heke, New Zealand." New Zealand Journal of Geology and Geophysics 58, no. 2 (April 3, 2015): 202–12. http://dx.doi.org/10.1080/00288306.2015.1023810.

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21

Taskova, Rilka M., Tetsuo Kokubun, Ken G. Ryan, Phil John Garnock-Jones, and Soren Rosendal Jensen. "ChemInform Abstract: Phenylethanoid and Iridoid Glycosides in the New Zealand Snow Hebes (Veronica, Plantaginaceae)." ChemInform 41, no. 45 (October 14, 2010): no. http://dx.doi.org/10.1002/chin.201045193.

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22

Delph, Lynda F. "Functional precocious protogyny in New Zealand sun hebes (Veronica sect. Hebe, Plantaginaceae)." New Zealand Journal of Botany, June 16, 2021, 1–9. http://dx.doi.org/10.1080/0028825x.2021.1936574.

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23

Kinsey, G. C. "Phoma terrestris. [Descriptions of Fungi and Bacteria]." IMI Descriptions of Fungi and Bacteria, no. 151 (August 1, 2002). http://dx.doi.org/10.1079/dfb/20056401509.

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Abstract A description is provided for Phoma terrestris. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: Pink root of Allium spp., principally onion but also affecting leek, shallot, garlic and chive. Possibly also a soil-borne saprobe and opportunistically pathogenic on other plants. HOSTS: From roots of Allium spp. Many other hosts reported, including Agropyron, Agrostis, Andropogon, Apostasia, Arctostaphylos, Artemisia, Arthraxon, Asparagus, Avena, Bambusa, Bouteloua, Bromus, Calamovilfa, Cenchrus, Chrysothamnus, Citrus, Clermontia, Cordia, Cucumis, Cucurbita, Cymbopogon, Cynodon, Dactylis, Dioscorea, Distichlis, Echinochloa, Elymus, Eragrostis, Eucalyptus, Festuca, Fragaria, Gentiana, Glycine, Hebe, Holcus, Hordeum, Ipomoea, Juniperus, Kentia, Koeleria, Lepidium, Linum, Lycospersicon, Medicago, Melilotus, Muhlenbergia, Musa, Oryza, Oryzopsis, Panicum, Phaseolus, Phleum, Pinus, Piper, Pisum, Poa, Populus, Purshia, Ribes, Rumex, Saccharum, Salix, Salvinia, Schedonnardus, Setaria, Sitanion, Solanum, Sorghum, Spinacia, Stipa, Trifolium, Triticum, Verbascum, Vigna, Vulpia and Zea. Also from soil, air, plant debris, cysts of the beet (Beta) cyst-nematode Heterodera and nasal swab of horse (Equus). GEOGRAPHICAL DISTRIBUTION: Worldwide. Records on Allium spp. include AFRICA: Egypt, Senegal, Sierra Leone, South Africa, Sudan, Uganda. NORTH AMERICA: Canada, USA. SOUTH AMERICA: Argentina, Brazil, Venezuela. ASIA: Brunei, China (Hong Kong), Israel, Mauritius, Pakistan. AUSTRALASIA: Australia, New Zealand. EUROPE: Germany, Great Britain, Greece, Netherlands, Poland. TRANSMISSION: Soil-borne.

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24

"Pseudomonas cichorii. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2006). http://dx.doi.org/10.1079/dmpd/20063191811.

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Abstract A new distribution map is provided for Pseudomonas cichorii (Swingle) Stapp. Hosts: lettuce (Lactuca sativa), chicory (Cichorium spp.) and many others. Information is given on the geographical distribution in Europe (Belgium, Bulgaria, France, Germany, Greece, Italy, Macedonia, Portugal, Serbia and Montenegro, Spain, UK, Ukraine), Asia (China, Hebei, Nei Menggu, India, Delhi, Iran, Japan, Hokkaido, Shikoku, Korea Republic, Taiwan, Turkey), Africa (Burundi, South Africa, Tanzania), North America (Canada, Alberta, Ontario, Mexico, USA, Alabama, California, Florida, Georgia, Illinois, Louisiana, Montana, New York, Washington), Central America and Caribbean (Barbados, Cuba, Puerto Rico), South America (Argentina, Brazil, Minas Gerais, Parana, Rio de Janeiro, Rio Grande do Sul, Sao Paulo, Chile, Colombia), Oceania (Australia, New South Wales, Queensland, New Caledonia, New Zealand).

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25

"Little cherry virus 1. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2017). http://dx.doi.org/10.1079/dmpd/20173342624.

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Abstract A new distribution map is provided for Little cherry virus 1. Closteroviridae: Velarivirus. Hosts: Prunus spp. Information is given on the geographical distribution in Europe (Belgium, Czech Republic, France, Germany, Greece, Italy, Mainland Italy, Poland, Romania, Slovakia, Spain, Switzerland, UK, England and Wales), Asia (Hebei, China, Liaoning, Shandong, India, Japan, Honshu, Korea Republic, Turkey), North America (Canada, British Columbia, USA, California, Oregon, Washington), Oceania (New Zealand).

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26

CABI and EPPO. "Cherry green ring mottle virus. [Distribution map]." Distribution Maps of Plant Diseases, May 31, 2022. http://dx.doi.org/10.1079/dmpd/20220233382.

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Abstract A new distribution map is provided for Cherry green ring mottle virus. Tymovirales: Betaflexiviridae: Robigovirus. Hosts: Prunus spp. Information is given on the geographical distribution in Africa (South Africa), Asia (China, Beijing, Fujian, Hebei, Shandong, Xinjiang, Japan, Honshu, Lebanon, Pakistan, Korea Republic, Turkey), Europe (Belgium, Bulgaria, Czechia, France, Germany, Hungary, Italy, Montenegro, Poland, Russia, Serbia, Slovenia, Switzerland), North America (Canada, British Columbia, Ontario, USA, California, Idaho, Michigan, New York, Oregon, Washington, Wisconsin), Oceania (Australia, New Zealand), South America (Chile).

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27

"Botryotinia squamosa. [Distribution map]." Distribution Maps of Plant Diseases, no. 4) (August 1, 2000). http://dx.doi.org/10.1079/dmpd/20066500164.

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Abstract A new distribution map is provided for Botryotinia squamosa Vien.-Bourg. Fungi: Ascomycota: Leotiales Hosts: Allium spp. Information is given on the geographical distribution in EUROPE, Belgium, Bulgaria, Czech Republic, France, Mainland France, Germany, Italy, Mainland Italy, Netherlands, Poland, UK, England and Wales, Scotland, ASIA, China, Hebei, Hong Kong, Japan, Hokkaido, Honshu, North Korea, Korea Republic, AFRICA, Mauritius, NORTH AMERICA, Canada, Ontario, Quebec, USA, Florida, Hawaii, Idaho, Illinois, Indiana, Iowa, Louisiana, Maine, Massachusetts, New York, Ohio, Texas, Wisconsin, SOUTH AMERICA, Brazil, Santa Catarina, Sao Paulo, OCEANIA, Australia, New South Wales, New Caledonia, New Zealand.

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28

"Little cherry virus 1. [Distribution map]." Distribution Maps of Plant Diseases, April (August 1, 2020). http://dx.doi.org/10.1079/dmpd/20203227938.

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Abstract A new distribution map is provided for Little cherry virus 1 (Closteroviridae: Velarivirus). Hosts: Prunus spp. Information on the geographical distribution in Europe (Belgium, Czech Republic, France, Germany, Greece, Hungary, Italy, Mainland Italy, Poland, Romania, Slovakia, Spain, Switzerland, UK, England and Wales), Asia (China, Hebei, Liaoning, Shandong, India, Japan, Honshu, Korea Republic, Turkey), Africa (Morocco), North America (Canada, British Columbia, USA, California, Oregon, Washington), South America (Chile) and Oceania (Australia, Queensland, Tasmania, New Zealand) is also given.

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29

"Callidiellum rufipenne. [Distribution Map]." Distribution Maps of Plant Pests, No.June (August 1, 2009). http://dx.doi.org/10.1079/dmpp/20093167381.

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Abstract A new distribution map is provided for Callidiellum rufipenne (Motschulsky). Coleoptera: Cerambycidae. Hosts: Cupressaceae and Pinaceae, including Chamaecyparis spp., Cryptomeria spp., Cupressus spp., Juniperus spp. and Thuja spp. Information is given on the geographical distribution in Europe (Italy (Mainland Italy), Russia (Far East)), Asia (China (Hebei), Japan (Hokkaido, Honshu, Kyushu, Ryukyu Archipelago, Shikoku) Korea Democratic People's Republic, Korea Republic, Taiwan), North America (Canada (British Columbia), USA (Connecticut, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Rhode Island, Washington)), Central America and Caribbean (Puerto Rico), South America (Argentina), Oceania (New Zealand).

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30

"Puccinia hemerocallidis. [Distribution map]." Distribution Maps of Plant Diseases, No.April (August 1, 2014). http://dx.doi.org/10.1079/dmpd/20143156822.

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Abstract A new distribution map is provided for Puccinia hemerocallidis Thüm. Pucciniomycetes: Pucciniales: Pucciniaceae. Host: Daylily (Hemerocallis sp.). Information is given on the geographical distribution in Europe (Russia, Siberia), Asia (China, Anhui, Fujian, Guangxi, Guizhou, Hainan, Hebei, Heilongjiang, Henan, Hubei, Hunan, Jiangsu, Jiangxi, Nei Mongol, Shaanxi, Shandong, Sichuan, Yunnan, Zhejiang, Japan, Hokkaido, Honshu, Kyushu, Ryukyu Archipelago, Shikoku, Korea Republic, Taiwan and Thailand), Africa (South Africa), North America (Canada, Ontario, Quebec, USA, Alabama, Arkansas, California, Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Vermont, Virginia and Wisconsin), Central America and Caribbean (Panama), South America (Brazil, Bahia, Minas Gerais, Rio de Janeiro, Santa Catarina, Sao Paulo, Colombia and Venezuela) and Oceania (Australia, Queensland and New Zealand).

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31

"Chrysomyxa rhododendri. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2012). http://dx.doi.org/10.1079/dmpd/20123367483.

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Abstract A new distribution map is provided for Chrysomyxa rhododendri De Bary. Basidiomycota: Pucciniales. Hosts: spruce (Picea); Rhododendron. Information is given on the geographical distribution in Europe (Austria, Belgium, Czech Republic, Finland, France, Germany, Ireland, Italy, Luxembourg, Netherlands, Norway, Portugal, Romania, Russia, Serbia, Spain, Switzerland, England and Wales, Scotland, UK, and Ukraine), Asia (Hebei, Heilongjiang, Jilin, Liaoning, Qinghai, Shaanxi, Sichuan, Xinjiang, Xizhang [Tibet], Yunnan, China, Korea Republic, Mongolia, and Taiwan), North America (British Columbia, Manitoba, Newfoundland, Northwest Territories, Ontario, Canada, and Greenland), Oceania (New South Wales, Tasmania, Victoria, Australia, and New Zealand).

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32

"Didymella fabae. [Distribution map]." Distribution Maps of Plant Diseases, no. 3) (August 1, 1993). http://dx.doi.org/10.1079/dmpd/20046500513.

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Abstract A new distribution map is provided for Didymella fabae Jellis & Punith. Hosts: Broad bean (Vicia faba). Information is given on the geographical distribution in Africa, Egypt, Ethiopia, Morocco, Tunisia, Asia, China, Hebei, Fujian, Guangxi, Zhejiang, Xizhang, Iraq, Israel, Japan, Korea, Pakistan, Saudi Arabia, Syria, Turkey, Australasia, Australia, New South Wales, Tasmania, Victoria, South Australia, New Zealand, Europe, Byelorussia, Czechoslovakia, Czech Republic, Denmark, Finland, France, Germany, Hungary, Italy, Lithuania, Netherlands, Norway, Poland, Russia, Spain, Sweden, Switzerland, UK, England, Scotland, Ukraine, North America, Canada, Nova Scotia, Manitoba, British Columbia, Saskatchewan, South America, Argentina.

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33

"Strawberry mottle virus. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2011). http://dx.doi.org/10.1079/dmpd/20113314304.

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Abstract A new distribution map is provided for Strawberry mottle virus. Virus: Secoviridae. Hosts: strawberry (Fragaria x ananassa). Information is given on the geographical distribution in Europe (Bulgaria, Czech Republic, Germany, Italy, Lithuania, Netherlands, Poland, Serbia, Spain (Mainland Spain), UK (England and Wales)), Asia (China (Hebei, Heilongjiang, Hubei, Jiangsu, Jiangxi, Jilin, Liaoning, Shaanxi, Shandong, Zhejiang), Israel, Japan (Honshu), Kazakhstan, Turkey), North America (Canada (British Columbia, New Brunswick, Nova Scotia, Ontario, Prince Edward Island, Quebec), USA (Arkansas, California, Maryland, Oregon)), South America (Brazil (Sao Paulo), Chile), Oceania (Australia (Queensland), New Zealand).

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34

CABI and EPPO. "Erwinia rhapontici . [Distribution map]." Distribution Maps of Plant Diseases, May 31, 2022. http://dx.doi.org/10.1079/dmpd/20220233390.

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Abstract A new distribution map is provided for Erwinia rhapontici (Millard) Burkholder. Gammaproteobacteria: Enterobacteriales: Erwiniaceae. Hosts: rhubarb ( Rheum rhaponticum ), wheat ( Triticum ), and onion ( Allium cepa ) among others. Information is given on the geographical distribution in Asia (China, Hebei, Hubei, Sichuan, Iran, Israel, Japan, Honshu, Korea Republic, Turkey), Europe (Belgium, France, Hungary, Italy, Sardinia, Lithuania, Netherlands, Poland, Portugal, Russia, Switzerland, Ukraine, United Kingdom), North America (Canada, Alberta, Manitoba, Saskatchewan, Mexico, USA, California, Colorado, Idaho, Kentucky, Montana, Nebraska, North Dakota, Oklahoma, Oregon, South Dakota), Oceania (New Zealand).

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35

"Rathayibacter rathayi and Rathayibacter tritici. [Distribution map]." Distribution Maps of Plant Diseases, no. 43) (August 1, 1996). http://dx.doi.org/10.1079/dmpd/20046500156.

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Abstract A new distribution map is provided for Rathayibacter rathayi (Smith) Zgurskaya, Evtushenko, Akimov & Kalakoutskii and Rathayibacter tritici (ex Hutchinson 1917) Zgurskaya, Evtushenko, Akimov & Kalakoutskii. Hosts: cocksfoot (Dactylis), rye (Secale), wheat (Triticum), weed grasses, etc. Information is given on the geographical distribution in Africa, Egypt, Ethiopia, Zambia, Asia, Afghanistan, China, Hebei, Guizhou, India, Delhi, Iran, Japan, Pakistan, Australiasia & Oceania, Australia, Western Australia, New Zealand, Europe, Austria, Cyrpus, Denmark, Germany, Norway, Romania, Sweden, UK, England, Scotland, North America, Canada, Quebec, USA, OR and VA.

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36

"Strawberry mild yellow edge virus. [Distribution map]." Distribution Maps of Plant Diseases, no. 1) (August 1, 2004). http://dx.doi.org/10.1079/dmpd/20066500937.

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Abstract A new distribution map is provided for Strawberry mild yellow edge virus Virus: Flexiviridae: Potexvirus Hosts: Strawberry (Fragaria ananassa). Information is given on the geographical distribution in EUROPE, Belgium, Bulgaria, Czech Republic, France, Germany, Ireland, Italy, Luxembourg, Netherlands, Poland, Serbia and Montenegro, Slovakia, Switzerland, UK, ASIA, China, Hebei, Heilongjiang, Hubei, Jiangsu, Jiangxi, Jilin, Liaoning, Shandong, Shanxi, Zhejiang, Israel, Japan, Hokkaido, Honshu, Kazakhstan, AFRICA, South Africa, NORTH AMERICA, Canada, British Columbia, USA, California, Maryland, North Carolina, Oregon, Washington, SOUTH AMERICA, Brazil, Chile, Paraguay, OCEANIA, Australia, Queensland, Tasmania, Victoria, Western Australia, New Zealand.

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37

"Strawberry crinkle virus. [Distribution map]." Distribution Maps of Plant Diseases, no. 1) (August 1, 2004). http://dx.doi.org/10.1079/dmpd/20066500936.

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Abstract A new distribution map is provided for Strawberry crinkle virus Virus: Rhabdoviridae: Cytorhabdovirus Hosts: Strawberry (Fragaria ananassa). Information is given on the geographical distribution in EUROPE, Belgium, Bulgaria, Czech Republic, France, Germany, Italy, Moldova, Netherlands, Poland, Serbia and Montenegro, Slovakia, UK, ASIA, China, Hebei, Heilongjiang, Hubei, Jiangxi, Jilin, Liaoning, Shandong, Shanxi, Zhejiang, Israel, Japan, Honshu, Kazakhstan, Korea Republic, AFRICA, South Africa, NORTH AMERICA, Canada, British Columbia, Mexico, USA, California, Indiana, Maine, Maryland, Massachusetts, Oregon, Pennsylvania, Washington, SOUTH AMERICA, Brazil, Minas Gerais, Rio Grande do Sul, Sao Paulo, Chile, OCEANIA, Australia, New South Wales, Queensland, Tasmania, Victoria, Fiji, New Zealand.

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38

"Chrysanthemum stunt viroid. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2017). http://dx.doi.org/10.1079/dmpd/20173342632.

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Abstract A new distribution map is provided for Chrysanthemum stunt viroid. Pospiviroidae: Pospiviroid. Hosts: Asteraceae especially Dendranthema [Chrysanthemum] spp. Information is given on the geographical distribution in Europe (Austria, Belgium, Czech Republic, France, Germany, Italy, Netherlands, Norway, Poland, Slovenia, Spain, Canary Islands, Sweden, UK, England and Wales), Asia (China, Anhui, Hainan, Hebei, Jiangsu, India, Assam, Himachal Pradesh, Karnataka, Rajasthan, Sikkim, Uttar Pradesh, Japan, Hokkaido, Honshu, Kyushu, Ryukyu Archipelago, Shikoku, Korea Republic, Taiwan, Turkey), Africa (Egypt, South Africa), North America (Canada, Ontario, USA, Kansas, Minnesota, New York), South America (Brazil, Sao Paulo), Oceania (Australia, Queensland, South Australia, New Zealand).

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39

"Botryotinia squamosa. [Distribution map]." Distribution Maps of Plant Diseases, No.April (August 1, 2007). http://dx.doi.org/10.1079/dmpd/20073069777.

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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).

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40

"Pectobacterium carotovorum subsp. brasiliense. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2018). http://dx.doi.org/10.1079/dmpd/20183337981.

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Abstract A new distribution map is provided for Pectobacterium carotovorum subsp. brasiliensis (Duarte et al.) Nabhan et al. Gammaproteobacteria: Enterobacteriales: Enterobacteriaceae. Hosts: various, especially potato (Solanum tuberosum). Information is given on the geographical distribution in Europe (Austria, Germany, Italy, mainland Italy, Netherlands, Poland and Switzerland), Asia (China, Fujian, Hebei, Henan, Liaoning, Shandong, Shanxi, Israel, Japan, Hokkaido, Korea Republic, Syria and Turkey), Africa (Algeria, Egypt, Kenya, South Africa and Zimbabwe), North America (Canada, Alberta, British Columbia, Manitoba, Quebec, USA, Florida, Minnesota, North Dakota and Wisconsin), South America (Brazil, Pernambuco, Rio Grande do Sul, Colombia, Peru and Venezuela) and Oceania (New Zealand).

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41

Minter, D. W. "Nitschkia broomeana. [Descriptions of Fungi and Bacteria]." IMI Descriptions of Fungi and Bacteria, no. 174 (August 1, 2007). http://dx.doi.org/10.1079/dfb/20083005532.

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Abstract A description is provided for Nitschkia broomeana, which are found on cracks in bark. Details are given of its hosts, geographical distribution (Gambia, Ghana, Malawi, Sierra Leone, Zimbabwe, USA (Alabama, Florida, Georgia, Idaho, Louisiana, Nebraska, New Jersey, North Carolina, Ohio, Oklahoma, South Carolina, Tennessee and Virginia), Guatemala, Nicaragua, Panama, Argentina, Brazil, Venezuela, China (Beijing, Fujian, Hebei, Hunan, Jiangsu, Sichuan, Yunnan and Zhejiang), India (Andhra Pradesh, Chhattisgarh, Madhya Pradesh and Maharashtra), Japan, South Korea, Pakistan, Sri Lanka, Taiwan, Australia (South Australia), New Zealand, Czech Republic, France, UK, Italy, and Serbia and Montenegro), transmission, diagnostic features and conservation status.

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42

"Pepper mild mottle virus. [Distribution map]." Distribution Maps of Plant Diseases, No.April (August 1, 2009). http://dx.doi.org/10.1079/dmpd/20093074270.

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Abstract A new distribution map is provided for Pepper mild mottle virus. Tobamovirus. Hosts: Peppers (Capsicum spp.), tomato (Lycopersicon esculentum) and cutleaf groundcherry (Physalis angulata). Information is given on the geographical distribution in Europe (Belgium, Bulgaria, Czech Republic, Denmark, France, Greece (Crete), Hungary, Iceland, Italy (Sicily), Netherlands, Spain (Mainland Spain), UK), Asia (China (Hebei, Hubei, Liaoning, Ningxia, Xinjiang), Japan (Hokkaido, Honshu), Korea Republic, Taiwan), Africa (Egypt, Senegal, South Africa, Tunisia, Zambia), North America (Canada (British Columbia, Ontario), Mexico, USA (Colorado, Florida, Georgia, Oregon, South Carolina)), Central America and Caribbean (Antigua and Barbuda, Barbados, Haiti, Jamaica, Montserrat, Panama, Trinidad and Tobago), South America (Argentina, Suriname), Oceania (Australia (New South Wales), New Zealand).

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43

"Pseudomonas viridiflava. [Distribution map]." Distribution Maps of Plant Diseases, no. 1) (August 1, 2004). http://dx.doi.org/10.1079/dmpd/20066500917.

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Abstract A new distribution map is provided for Pseudomonas viridiflava (Burkholder) Dowson Bacteria A wide host range including bean (Phaseolus vulgaris), tomato (Lycopersicon esculentum), various Cucurbitaceae, onion (Allium cepa) and celery (Apium spp.). Information is given on the geographical distribution in EUROPE, Belgium, Bulgaria, Czech Republic, France, Germany, Greece, Hungary, Italy, Macedonia, Netherlands, Poland, Portugal, Serbia and Montenegro, Slovakia, Spain, Switzerland, UK, ASIA, China, Hebei, Hunan, Yunnan, Iran, Japan, Honshu, Kyushu, Ryukyu Archipelago, Shikoku, Jordan, Korea Republic, Nepal, Turkey, AFRICA, Egypt, Kenya, Morocco, Tanzania, Uganda, NORTH AMERICA, USA, California, Florida, Georgia, Illinois, New York, Oregon, Washington, SOUTH AMERICA, Argentina, Brazil, Minas Gerais, Pernambuco, Venezuela, OCEANIA, Australia, New South Wales, Queensland, New Zealand.

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44

"Valsa sordida. [Distribution map]." Distribution Maps of Plant Diseases, April (August 1, 2006). http://dx.doi.org/10.1079/dmpd/20063115672.

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Abstract A new distribution map is provided for Valsa sordida Nitschke. Ascomycota: Diaporthales. Hosts: Populus spp., Salix spp. and, more rarely, other woody angiosperms. Information is given on the geographical distribution in Europe (Austria, Belgium, Bulgaria, Czech Republic, Denmark, Estonia, France, Germany, Greece, Ireland, Italy, Netherlands, Norway, Poland, Portugal, Romania, Russia (Central Russia, Eastern Siberia, Southern Russia), Serbia and Montenegro, Slovakia, Spain, Sweden, Switzerland, UK, Ukraine), Asia (Armenia, Azerbaijan, China (Anhui, Gansu, Guizhou, Hebei, Heilongjiang, Henan, Hubei, Hunan, Jiangsu, Jiangxi, Jilin, Liaoning, Nei Menggu [Nei Mongol], Ningxia, Qinghai, Shandong, Shanxi, Sichuan, Xinjiang, Yunnan, Zhejiang), Georgia, India (Delhi, Himachal Pradesh, Uttar Pradesh), Iran, Iraq, Israel, Japan, Kazakhstan, Korea Republic, Turkey, Turkmenistan, Uzbekistan), Africa (Morocco, South Africa), North America (Canada (Alberta, British Columbia, Manitoba, New Brunswick, Newfoundland, Nova Scotia, Ontario, Quebec, Saskatchewan), Mexico, USA (Alaska, Arizona, California, Colorado, Connecticut, Florida, Idaho, Illinois, Iowa, Kansas, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, North Dakota, Oklahoma, Oregon, Rhode Island, South Dakota, Texas, Utah, Washington, Wisconsin, Wyoming)), South America (Argentina, Bolivia, Chile, Uruguay), and Oceania (Australia (New South Wales, Victoria), New Zealand).

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45

"Fusarium oxysporum f.sp. niveum. [Distribution map]." Distribution Maps of Plant Diseases, No.April (July 1, 2011). http://dx.doi.org/10.1079/dmpd/20113091536.

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Abstract A new distribution map is provided for Fusarium oxysporum f.sp. niveum W.C. Snyder & H.N. Hansen. Ascomycota: Hypocreales. Hosts: watermelon (Citrullus lanatus). Information is given on the geographical distribution in Europe (Bulgaria, Croatia, Cyprus, Greece, Mainland Greece, Hungary, Italy, Montenegro, Poland, Serbia, Spain, Mainland Spain, UK, Ukraine), Asia (Armenia, Azerbaijan, Bangladesh, China, Anhui, Fujian, Gansu, Guangdong, Guangxi, Guizhou, Hebei, Heilongjiang, Henan, Hunan, Jiangsu, Jiangxi, Jilin, Liaoning, Nei Menggu, Ningxia, Qinghai, Shaanxi, Shandong, Sichuan, Xinjiang, Yunnan, Zhejiang, India, Karnataka, Punjab, Rajasthan, Uttar Pradesh, Iran, Iraq, Israel, Japan, Korea Republic, Malaysia, Sabah, Pakistan, Philippines, Taiwan, Turkey, Vietnam), Africa (Egypt, South Africa, Tunisia), North America (Canada, Alberta, British Columbia, Manitoba, Ontario, Quebec, Mexico, USA, California, Colorado, Delaware, Florida, Georgia, Hawaii, Idaho, Indiana, Iowa, Maryland, Michigan, Mississippi, Montana, New Mexico, North Carolina, Oklahoma, Oregon, South Carolina, Texas, Washington, Wisconsin), Central America and Caribbean (Panama), South America (Argentina, Brazil, Pernambuco, Sao Paulo, Chile), Oceania (Australia, Western Australia, Federated States of Micronesia, New Zealand, Palau).

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46

"Pectobacterium brasiliense. [Distribution map]." Distribution Maps of Plant Diseases, April (August 1, 2021). http://dx.doi.org/10.1079/dmpd/20210251692.

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Abstract A new distribution map is provided for Pectobacterium brasiliense Portier et al. Gammaproteobacteria: Enterobacterales: Pectobacteriaceae. Hosts: potato (Solanum tuberosum) and other Solanaceae; wide variety of economically important crops. Information is given on the geographical distribution in Africa (Algeria, Egypt, Kenya, Morocco, Reunion, South Africa, Zimbabwe), Asia (China, Fujian, Guangdong, Hebei, Henan, Inner Mongolia, Liaoning, Shandong, Shanxi, Israel, Japan, South Korea, Syria, Thailand, Turkey), Europe (Austria, France, Germany, Italy, Sicily, Netherlands, Poland, Russia, Serbia, Spain, Switzerland), North America (Canada, Alberta, British Columbia, Manitoba, Quebec, Martinique, Mexico, USA, Florida, Georgia, Hawaii, Minnesota, North Dakota, Wisconsin), Oceania (New Zealand), South America (Brazil, Pernambuco, Rio Grande do Sul, Colombia, Peru, Venezuela).

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47

"Aphelenchoides fragariae. [Distribution map]." Distribution Maps of Plant Diseases, no. 1) (July 1, 2002). http://dx.doi.org/10.1079/dmpd/20066500863.

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Abstract A new distribution map is provided for Aphelenchoides fragariae (Ritzema-Bos) Christie Nematoda: Aphelenchida: Aphelenchoididae Hosts: mostly strawberry (Fragaria ananassa), ferns and members of Liliaceae, Primulaceae and Ranunculaceae. Information is given on the geographical distribution in EUROPE, Belgium, Bulgaria, Denmark, Estonia, France, Germany, Hungary, Ireland, Italy, Latvia, Moldova, Netherlands, Norway, Poland, Portugal, Azores, Madeira, Central Russia Russia, Eastern, Russian Far East, Southern Russia, Western Siberia, Slovakia, Spain, Canary Islands, Mainland Spain, Sweden, Switzerland, UK, Ukraine, ASIA, China, Anhui, Guangdong, Hebei, Jiangsu, Sichuan, India, Himachal Pradesh, Israel, Japan, Hokkaido, Honshu, Korea Republic, Kyrgyzstan, Turkey, NORTH AMERICA, Canada, British Columbia, Ontario, Mexico, USA, California, Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Maryland, Massachusetts, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Virginia, OCEANIA, Australia, New South Wales, Queensland, Victoria, New Zealand, Papua New Guinea.

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48

"Heterodera avenae. [Distribution map]." Distribution Maps of Plant Diseases, no. 1) (August 1, 2001). http://dx.doi.org/10.1079/dmpd/20066500823.

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Abstract A new distribution map is provided for Heterodera avenae Wollenweber Nematoda: Tylenchida: Heteroderidae Hosts: Cereals of the Poaceae including triticale, barley (Hordeum vulgare), rye (Secale cereale), wheat (Triticum) and oat (Avena sativa). Information is given on the geographical distribution in EUROPE, Belgium, Bulgaria, Czech Republic, Denmark, Estonia, France, Germany, Greece, Ireland, Italy, Latvia, Malta, Netherlands, Norway, Poland, Portugal, Central Russia Russia, Southern Russia, Western Siberia, Slovakia, Spain, Sweden, Switzerland, UK, Ukraine, Yugoslavia, (former) ASIA, China, Hebei, Henan, Hubei, NeiMenggu, Qinghai, Shanxi, India, Delhi, Haryana, Punjab, Rajasthan, Uttar Pradesh, Iran, Israel, Japan, Honshu, Kazakhstan, Pakistan, Saudi Arabia, Turkey, AFRICA, Algeria, Libya, Morocco, South Africa, Tunisia, NORTH AMERICA, Canada, Ontario, USA, Idaho, Oregon, SOUTH AMERICA, Peru, OCEANIA, Australia, New South Wales, South Australia, Victoria, Western Australia, New Zealand.

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49

"Pseudomonas syringae pv. mori. [Distribution map]." Distribution Maps of Plant Diseases, No.October (August 1, 2009). http://dx.doi.org/10.1079/dmpd/20093245828.

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Abstract A new distribution map is provided for Pseudomonas syringae pv. mori (Boyer & Lambert) Young et al., Bacteria. Hosts: mulberry (Morus spp.), hemp (Cannabis sativa) and Lima bean (Phaseolus lunatus). Information is given on the geographical distribution in Europe (Czechoslovakia, France, Mainland France, Germany, Hungary, Italy, Mainland Italy, Romania, Serbia), Asia (China, Anhui, Fujian, Guangdong, Guangxi, Hebei, Hong Kong, Hubei, Jiangsu, Shandong, Sichuan, Zhejiang, Georgia, India, Andhra Pradesh, Karnataka, Kerala, Tamil Nadu, West Bengal, Iran, Japan, Honshu, Korea Democratic People's Republic, Korea Republic, Pakistan, Turkey), Africa (South Africa, Tanzania, Uganda), North America (Canada, Ontario, Prince Edward Island, USA, Connecticut, Massachusetts, Ohio), South America (Brazil, Minas Gerais), Oceania (Australia, New South Wales, Queensland, South Australia, Tasmania, Victoria, Western Australia, New Zealand).

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50

"Botrytis fabae. [Distribution map]." Distribution Maps of Plant Diseases, no. 5) (August 1, 1995). http://dx.doi.org/10.1079/dmpd/20046500162.

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Abstract A new distribution map is provided for Botrytis fabae Sardiña. Hosts: Broad bean (Vicia faba). Information is given on the geographical distribution in Africa, Algeria, Angola, Egypt, Ethiopia, Morocco, South Africa, Sudan, Tunisia, Asia, Burma, China, Fuijian, Gansu, Guangxi, Guizhou, Hubei, Hebei, Heilonghiang, Hunan, Jilin, Jiangsu, Jiangxi, Liaoning, Sichuan, Yunnan, Zheijiang, India, w. Bengal, Sikkim, Iran, Israel, Japan, Korea, Pakistan, Russia, Caucasus, Far East, Transcaucasus, Bashkiria, central and NW European regions, Syria, Turkey, Australasia & Oceania, Australia, Western Australia, Tasmania, South Australia, New Zealand, Europe, Cyprus, Denmark, Estonia, France, Germany, Hungary, Italy, Latvia, Lithuania, Netherlands, Norway, Poland, Spain, UK, England, Scotland, Wales, Ukraine, North America, Canada, Nova Scotia, Saskatchewan, Manitoba, South America, Argentina, Chile, Colombia, Uruguay.

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