|Watson, L., Dallwitz, M.J., Gibbs, A.J., and Pankhurst, R.J. 1988. Automated taxonomic descriptions. In ‘Prospects in systematics’, pp. 292–304. (Ed. D.L. Hawksworth.) Clarendon Press, Oxford. Also available at http://delta-intkey.com.|
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1 Research School of Biological Sciences, The Australian National University, Canberra, Australia.
2 Division of Entomology, CSIRO, Canberra, Australia.
3 British Museum (Natural History), Cromwell Road, London, UK.
Automation of taxonomic descriptions has progressed to the extent that several large-scale, functional accounts operable from microcomputers are now available. They permit automated generation of typeset and microfiche descriptions and keys, which are readily updated and relatively easily translated into different natural languages. They also permit direct information retrieval, are conveniently accessible for classificatory experiments, and provide online identificatory facilities superior to printed keys (extending, for example, the possibilities for identifying fragmentary material). Their general applicability and present capabilities are illustrated by applications of the DELTA system to the genera of grasses and legumes, plant viruses, species of beetles, and a floristic account of the Paniceae of Australia.
We illustrate here the versatility and practicability of methods for preparing and using automated taxonomic descriptions, with reference to fully operational sets of data which are available to potential users. The given examples are all organized under the DELTA system (Dallwitz 1980a; Dallwitz and Paine 1986), which is itself freely available accompanied by a small, operational set of data, working examples of all directives files, and a ‘Primer’ (Partridge et al. 1986). DELTA was designed to satisfy the need for a generalized system capable of accommodating all the different kinds of descriptive data used by taxonomists, without information loss, in an easy-to-use format chosen to minimize coding errors; and for facilities to translate data into the diversity of special formats required by programs (e.g. KEYGEN, Pankhurst 1970; MULTBET, Lance and Williams 1967) for classification and identification (cf. Watson and Milne 1972; Clifford and Watson 1977).
DELTA in its present form handles unordered and ordered multistate (including two-state) characters, counts, measurements, and text. Intermediates, ranges, combinations, and alternatives can be represented in a natural way, and distinction is made between ‘variable’, ‘unknown’, and ‘inapplicable’. With all character types, comments can be used to qualify or amplify the coded information. An associated program, CONFOR, translates the coded descriptions into natural language, offering a choice of formats; produces summarized descriptions of specified sets of taxa, giving numbers of taxa exhibiting each character state and for numeric characters giving means, ranges, and the names of taxa representing the extremes of ranges; and carries out various data maintenance operations — for example, changing the sequences of characters and character states, while automatically keeping all the files consistent with one another. Data coded in DELTA format can also be translated into the formats used by various other taxonomic programs, of which the following are currently available via CONFOR:
KEY. Generation of tabular and sequential printed keys (Dallwitz 1974; Dallwitz and Paine 1986).
PABTRAN. Punched card keys (Higgins 1979).
DCR. The TAXON numerical taxonomy package developed by CSIRO Division of Computing Research (Ross et al. 1985).
GENKEY. Key generation (Payne 1975).
EXIR/TAXIR. Information retrieval (Estabrook and Brill 1969).
DIST. Generation of distance matrices (M. J. Dallwitz and T. A. Paine unpubl.).
PAUP. Phylogenetic analysis (Swofford 1984).
INTKEY. Interactive identification and information retrieval (M. J. Dallwitz and T. A. Paine unpubl.)
DELTA format is used directly by programs of the PANKEY package for key generation, interactive key construction, polyclaves, interactive identification, identification by matching, description printing, and diagnostic descriptions (Pankhurst 1970, 1975, 1978a,b, 1983, 1986; Pankhurst and Aitchison 1975; Dallwitz and Paine 1986, Appendix 4). Of particular interest are the programs for interactive identification, ONLINE and INTKEY. These are similar in many ways to an ‘expert system’. The latest version of ONLINE includes colour graphics, and was demonstrated at the meeting using a data set for British orchids with leaf and flower characters illustrated by high resolution colour drawings.
The appended examples, and the publications associated with them, demonstrate the applicability of DELTA at different levels of the taxonomic hierarchy, to prepare and present printed descriptions and keys. They also illustrate its ability to cope with diverse materials (flowering plants, beetles, viruses). Automation can streamline the exacting and time-consuming operations which have always been required by taxonomic work, and facilitates operations which surely would long have been routine had they been practicable. It also provides access to novel taxonomic services, in the form of interactive facilities. The advantages may be summarized as follows.
Boswell, K. and Gibbs, A.J. 1983. Viruses of Legumes 1983. Descriptions and keys from VIDE. Australian National University, Canberra.
Boswell, K. and Gibbs, A.J. 1986. The VIDE data bank for plant viruses. In ‘Development and applications in virus testing’, pp. 283–7. (Eds. R.A.C. Jones and L. Torrance.) Association of Applied Biologists, UK.
Boswell, K.F., Dallwitz, M.J., Gibbs, A.J. and Watson, L. 1986. The Vide (Virus Identification Data Exchange) project: a data bank for plant viruses. Rev. Pl. Path. 65: 221–31.
Britton, E.B. 1986. A revision of the Australian chafers (Coleoptera: Scarabaeidae: Melalonthinae). Vol. 4. Tribe Liparetrini: genus Colpochila. Aust. J. Zool., Suppl. ser. 118: 1–135.
Clifford, H.T. and Watson, L. 1977. Identifying grasses. Data, methods and illustrations. University of Queensland Press, Brisbane.
Dallwitz, M.J. 1974. A flexible program for generating identification keys. Syst. Zool. 23: 50–7.
Dallwitz, M.J. 1980a. A general system for coding taxonomic descriptions. Taxon 29: 41–6.
Dallwitz, M.J. 1980b. User’s guide to TYPSET — a computer typesetting program. Division of Entomology Report No. 18. CSIRO, Canberra.
Dallwitz, M.J. and Paine, T.A. 1986. User’s guide to DELTA System. A general system for coding taxonomic descriptions. Division of Entomology Report No. 13. 3rd edition. CSIRO, Canberra.
Estabrook, G.F. and Brill, R.C. 1969. The theory of the TAXIR accessioner. Math. Biosci. 5: 327–40.
Higgins, J.P. 1979. User’s guide to PABTRAN — a computer program for translating a character-taxon matrix from peekaboo cards into KEY and DELTA format. Division of Entomology Report No. 6. CSIRO, Canberra.
Lance, G.N. and Williams, W.T. 1967. Mixed-data classificatory programs. I. Agglomerative systems. Aust. Comput. J. 1: 15–20.
Lazarides, M. and Watson, L. 1986. Cyperochloa: a new genus in the Arundinoideae Dumortier (Poaceae). Brunonia 9: 215–21.
Pankhurst, R.J. 1970. A computer program for generating diagnostic keys. Computer J. 13: 145–51.
Pankhurst, R.J. 1975. Identification by matching. In ‘Biological identification with computers’, pp. 79–91. (Ed. R.J. Pankhurst.) Academic Press, London.
Pankhurst, R.J. 1978a. Biological identification: the principles and practice of identification methods in biology. Edward Arnold, London.
Pankhurst, R.J. 1978b. The printing of taxonomic descriptions by computer. Taxon 27: 35–8.
Pankhurst, R.J. 1983. An improved algorithm for finding diagnostic taxonomic descriptions. Math. Biosci. 65: 209–18.
Pankhurst, R.J. 1986. A package of computer programs for handling taxonomic databases. CABIOS 2: 33–9.
Pankhurst, R.J. and Aitchison R.R. 1975. An on-line identification program. In ‘Biological Identification with Computers’, pp. 181–94. (Ed. R.J. Pankhurst.) Academic Press, London.
Partridge, T.R., Dallwitz, M.J. and Watson, L. 1986. A primer for the DELTA system on VMS, MS-DOS, and PRIMOS. Division of Entomology Report No. 38. CSIRO, Canberra.
Payne, R.W. 1975. Genkey: a program for constructing diagnostic keys. In ‘Biological identification with computers, pp. 65–72. (Ed. R.J. Pankhurst.) Academic Press, London.
Ross, D., Dale, M., Shields, K. and Hulett, C. 1985. TAXON User’s manual, 4th edn. Division of Computing Research CSIRONET Manual No. 6. CSIRO, Canberra.
Swofford, D.L. 1984. PAUP. Phylogenetic analysis using parsimony. Version 2.3. Illinois Natural History Survey, Champaign.
Watson, L. 1981. An automated system of generic descriptions for Caesalpinioidea, and its application to classification and key-making. In ‘Advances in legume systematics, pp. 65–81. (Eds R.M. Polhill and P.H. Raven.) Royal Botanic Gardens, Kew.
Watson, L. 1987. Automated descriptions of grass genera. In ‘Grass systematics and evolution’, pp. 343–351. (Eds T.R. Soderstrom, K.W. Hilu, C.S. Campbell and M.E. Barkworth). Smithsonian Institution, Washington.
Watson, L. and Dallwitz, M.J. 1981. An automated data bank for grass genera. Taxon 30: 424–9.
Watson, L. and Dallwitz, M.J. 1983. The genera of Leguminosae-Caesalpinioideae. Anatomy, morphology, keys and classification. Australian National University, Canberra.
Watson, L. and Dallwitz, M.J. 1985. Australian grass genera. Anatomy, morphology, keys and classification, 2nd edn. Australian National University, Canberra.
Watson, L. and Milne, P.W. 1972. A flexible system for automatic generation of special purpose dichotomous keys and its application to Australian grass genera. Aust. J. Bot. 20: 331–52.
Watson, L., Clifford, H.T. and Dallwitz, M.J. 1985. The classification of Poaceae: subfamilies and supertribes. Aust. J. Bot. 33: 433–84.
Watson, L. Aiken, S.G., Dallwitz, M.J., Lefkovitch, L.P. and Dubé, M. 1986a. Canadian grass genera: keys and descriptions in English and French from an automated data bank. Can. J. Bot. 64: 53–70.
Watson, L. and Dallwitz, M.J. and Johnston, C.R. 1986b. Grass genera of the world: 728 detailed descriptions from an automated database. Aust. J. Bot. 34: 223–30.
Webster, R.D. 1987. The Australian Paniceae (Poaceae). J. Cramer, Berlin & Stuttgart.
These sample descriptions and key (Examples 1–6) exemplify CONFOR and KEY output, reproduced without subsequent editing. They have been automatically typeset on a III COMp80 phototypesetter, using the program TYPSET (Dallwitz 1980b). Each complete data set is available on magnetic tape, or on MS-DOS discs. They can all be processed by CONFOR and employed for interactive identification via the programs ONLINE (Pankhurst 1978a) and INTKEY using MS-DOS microcomputers. All other operations can also be run on microcomputers using the smaller data sets, or subsets of the large sets. Example 7 shows use of ONLINE for a purpose other than that for which it was primarily intended.
One of 177 generic descriptions, prepared, maintained by and obtainable from Watson (Watson 1981; Watson and Dallwitz 1983).
Caesalpinia L. Tropical and sub-tropical, 100 species
Habit and leaf form. Trees, or shrubs, or herbs, or climbers or scramblers; without tendrils; armed (with prickly branchlets and rachides), or unarmed. Leaves and inflorescences crowded on short shoots, or not crowded on short shoots. Phyllotaxy spiral. Leaves compound; pinnate (rarely, in Chile and Cuba; = Balsamocarpon), or bipinnate; with opposite or sub-opposite pinnae; with opposite or sub-opposite leaflets, or with alternate leaflets; paripinnate; with rachides adaxially ridged. Leaflets many per leaf, or few per leaf; with markedly twisted petiolules, or with petiolules not noticeably twisted. Stipules absent or early caducous or very inconspicuous, or present, persistent and conspicuous; leafy, or spinescent, or neither leafy nor spinescent. Stipels present, or absent.
Inflorescence and floral morphology. Flowers small, or large and showy; hermaphrodite; pentamerous; coloured; in panicles (of racemes); not distichous. Inflorescences axillary, or terminal. Inflorescence of racemose units. Bracts absent at anthesis, or persistent beyond anthesis. Bracteoles absent. Hypanthium present. Length of floral tube relative to total hypanthium plus calyx length, about 0.25. Calyx polysepalous; covering the rest of the flower in bud, or not covering the rest of the flower in bud; markedly zygomorphic; 5 partite (the lowest tooth outside); imbricate. Corolla present; slightly zygomorphic, or very zygomorphic; polypetalous; without greatly reduced petals. Petals yellow, or red; 5; imbricate; imbricate-ascending. Clawed petals present. Disk absent. Androecium of ten parts; members all free of one another; without staminodia. Fertile stamens 10. Anthers attached well above base of connective. Dehiscence introrse; longitudinal. Ovary sessile or subsessile; free. Stigma not peltate (the style filiform). Ovules few, or numerous, or solitary.
Fruit, seed and seedling. Fruit a two-valved pod, or indehiscent (sometimes spiny); not becoming woody; straight, or distinctly curved; not internally septate; not winged; without markedly twisting or enrolling valves. Seeds endospermic, or non-endospermic; with a straight or slightly oblique radicle; amyloid-negative; with galactomannan. Cotyledons flat; Type 2, or Type 3, or Type 4; with a vascular system in one plane; epigeal, or hypogeal.
Transverse section of lamina. Leaves without conspicuous phloem transfer cells in the minor veins. Druses common in the mesophyll. Mesophyll secretory cavities (gland-dots) common, or absent; when present, without a lining of epithelium. Adaxial hypodermis absent. Leaf girders absent or very rare (the veins embedded). Laminae dorsiventral. Mesophyll without unaligned fibres or sclereids. Minor veins with no or very scanty accompanying fibrous tissue.
Leaf lamina epidermes. Epidermal crystals not seen either adaxially or abaxially. Simple unbranched hairs common, or not seen; when present scabrid, or smooth. No compound or branched eglandular hairs seen. Capitate glands present, or not seen. Hooked hairs not seen. Cassieae-type leaf pseudo-glands not seen. Expanded and embedded hair-feet absent. Adaxial interveinal epidermal cell walls straight in optical section, or markedly sinuous in high-focus optical section; conspicuously pitted, or not conspicuously pitted. Stomata adaxially common and widespread, or adaxially very rare. Abaxial stomata predominantly paracytic, or not predominantly paracytic. Abaxial epidermis not papillate. Abaxial interveinal epidermal cell walls straight, or gently undulating; conspicuously pitted in optical section, or not conspicuously pitted in optical section; scarcely staining with safranin; medium-thin.
Wood anatomy. Wood without septate fibres; storied, or not storied; without normal intercellular canals; without traumatic canals. Intervascular pits very small, or medium to large.
Pollen ultrastructure. Tectum punctate (rarely), or reticulate; smooth punctate, or puncticulate; strongly irregularly coarse-reticulate. Length of colpi greater than one half pole to pole distance (with a margocolpus). Foot layer of pollen wall with obvious projections.
Cytology, cultivation. Basic chromosome number, x = 12. Widely cultivated.
Not coded: 14 16–17 22 36–38 59 71 74–75 79 110
Portion of one of 761 generic descriptions, from data gathered by Watson and collaborators. Database maintained by and obtainable from Watson (Watson and Dallwitz 1981, 1985; Watson et al. 1985, 1986; Watson 1987).
References. S.T. Blake 1972; (for leaf anatomy and photosynthetic pathways) Hattersley et al 1982, Hattersley and Roksandic 1983.
Habit, vegetative morphology. Perennial; caespitose (from short rhizomes). Culms 15 to 50 cm high; herbaceous. Nodes hairy, or glabrous. Culm internodes solid. Young shoots extravaginal and intravaginal (primary shoots extravaginal, each terminating in a tuft of intravaginal culm shoots). Leaves mostly basal; without auricles. Leaf blades linear (to very narrowly so); narrow; 0.9 to 3.5 mm wide; not setaceous; flat, or rolled; without readily visible transverse veins; not disarticulating; rolled in bud. Adaxial ligule a fringe of hairs.
Reproductive organization. Plants bisexual, with bisexual spikelets; with hermaphrodite florets. The spikelets of sexually distinct forms on the same plant (the lowermost being reduced).
Inflorescence. Inflorescence a single spike (almost, in N. munroi), or a single raceme (spike-like, or even capitate to ovoid in N. alopecuroidea and N. minor); espatheate. Spikelet-bearing axes persistent. Spikelets solitary; not secund; not two-ranked (spiralled). The spikelets subsessile to having pedicellate spikelets. Pedicel apices oblique, or discoid, or cupuliform.
Female-sterile spikelets. Several of the lowermost spikelets generally much reduced, closer together and more persistent.
Female-fertile spikelets. Spikelets 5 to 13 mm long (erect); abaxial; compressed dorsiventrally; falling with the glumes; without an apically prolonged rachilla. Hairy callus present (with very conspicuous long white hairs).
Glumes two; more or less equal; long relative to the adjacent lemmas (exceeding them); dorsiventral to the rachis; hairy (especially marginally); pointed (acuminate); awned, or awnless; very dissimilar to similar (both rigidly membranous, ovate-acuminate to lanceolate-subulate, becoming hardened towards the base. The lower ciliate or not, the upper with a dense narrow sub-marginal beard of long white hairs on each side below). Lower glume 3 to 7 nerved. Upper glume 7 to 13 nerved. Spikelets with incomplete florets. The incomplete florets proximal to the female-fertile florets. Proximal incomplete florets 1; paleate; with the palea fully developed (except occasionally in N. alopecuroidea); male. The proximal lemmas awnless; ...
Descriptions in English and French of 109 genera, derived with some modifications from Example 2. This sample of part of the French version represents another of the output formats available from CONFOR, in which the numbers in parenthesis cross-reference with the character list. Available from S. G. Aiken, National Museums of Canada, Ottawa, Ontario Canada, K1A OM8 (Watson et al. 1986).
Festuca <L.> <Plus de 170, régions tempérées du monde entier et montagnes, environ 20 au Canada.>
Port, caractères végétatifs. (2) Plantes vivaces. (3) Hélophytes <rarement>; ou mésophytes; ou xérophytes. (7) À longs rhizomes; ou à longs stolons; ou à port cespiteux; ou à port décombant. (10) Chaume herbacé. (14) Hauteur du chaume à maturité 2 à 200 cm. (15) Jeunes pousses extravaginales; ou jeunes pousses intravaginales. (16) Chaume non ramifié végétativement dans la partie supérieure. (18) Chaume tubéreux à la base; ou chaume non ...
Descriptions of 177 species, subspecies and varieties, prepared by R. D. Webster for the Flora of Australia. The two samples illustrate applications with synonymy and Latin diagnoses. Available from Webster (U.S.D.A., Bldg. 265, BARC East, Beltsville, Maryland, U.S.A.) or from Watson (Webster 1987).
Yakirra australiensis (Domin) Lazarides & R. Webster var. australiensis, Brunonia 7(2): 293 (1985). — Ichnanthus australiense (Domin) Hughes, Kew Bull. 1923: 329 (1923). — Panicum australiense Domin, J. Linn. Soc. (Bot.) 41: 271 (1912); Lazarides, Aust. J. Bot. 7(3): 333 (1959), p.p.. — Type: Western Australia, between the Ashburton and Yule Rivers, Clement s.n. (K, holo).
Panicum pauciflorum var. fastigiatum Benth., Fl. Austral. 7: 483 (1878). — Type: upper Victoria River, Mueller s.n. (K, iso).
Plants annual, or perennial; rhizomes absent; stolons absent. Cataphylls absent. Flowering culms erect; clumped; 5–30 cm tall (rarely to 35 cm); copiously branched; 5–10 noded. Nodes hairy (occasionally with a few scattered hairs), or glabrous. Mid-culm internodes solid or spongy; glabrous, or scabrous; shorter than the associated leaf sheaths. Mid-culm leaves with neither sheath nor blade auricles. Mid-culm sheaths rounded on the back; hairy; with non-ciliate ...
(Variant) Y. australiensis var. intermedia R. Webster, var. nov.
Planta annua, culmis floriferis 15–35 mm altis, copiose ramosis. Foliorum ligula 0.5–1.0 mm longa; lamina 30–70 mm longa, 0.5–4 mm lata. Inflorescentia intoto vel exparte exserta; ramis primariis patentibus, 20–40 mm longis. Spiculae 3.2–3.9 mm longae, 1–1.3 mm latae; gluma inferior 1.7–2.4 mm long, 5-nervis; gluma superior 3.2–3.9 mm longa, 7-nervis; lemma inferius 3.2–3.8 mm longum, 7-nerve; lemma superius 2.3–3.7 mm longum. — Typus. Western Australia, Near Lucky Hill 23 km NNE of Dunham River, M. Lazarides 8547 (CANB, holo).
Plants annual. Flowering culms 15–30 cm tall (–35 cm); copiously branched. Ligule 0.5–1 mm long. Mid-culm leaf blades 30–70 mm long; 0.5–4 mm wide.
Inflorescence not fully exserted. Primary branches spreading; 20–40 mm long.
Spikelets 4–7 on a typical lowermost primary branch; 3.2–3.9 mm long; 1–1.3 mm wide. First glume 1.7–2.4 mm long; 3–5 nerved. Second glume 3.2–3.9 mm long; 7 nerved. Lower lemma 3.2–3.8 mm long; 7 nerved. Upper lemma 2.3–3 mm long.
Western Australia, Northern Territory, and Queensland. Geobotanical distribution: Kimberley, Arnhem, Carpentaria, and Barkly. Distribution by vegetation region: tropical and subtropical sub-humid woodlands, arid and semi-arid low woodlands, arid hummock grasslands, and tropical sub-humid grasslands.
Intermediate in appearance between Y. australiensis var. australiensis and Y. pauciflora. Generally more profusely branched and with smaller spikelets than Y. pauciflora, while the more exserted inflorescence and the spreading primary branches separate it from var. australiensis.
Representative specimens: W.A.: Bindoola Creek, M. Lazarides 8624 (CANB); 5 km N of Point Coulomb, K.F. Kenneally 5905 (CANB, PERTH); Camballin, Y. Power 799 (PERTH). N.T.: 20.8 miles W of Invervay, G. Chippendale 5951 (CANB); near Echo Waterhole, R. Pullen 9228 (CANB). Qld.: 25 mile hut on Normanton-Croydon road, H.G. Bishop 264 (BRI).
Not coded: 196 200
Portion of one of over 500 plant virus descriptions. Complete for those of legumes (about 150) and for those of Australian plants; being extended to cover all plant viruses, commencing with those of tropical crops. Data provided by over 300 international contributors; organized and maintained by, and available from Gibbs and coworkers (Boswell and Gibbs 1983, 1986; Boswell et al. 1986).
Kennedya yellow mosaic tymovirus
INTRODUCTION. First found in Kennedya rubicunda. Reported in 1975 from Murrays Beach, Jervis Bay, in Australia. Dale et al. (1975, 1976); Gibbs (1978). Strains: Port Douglas (Mount Jukes), Jervis Bay, Wapengo; these are the type members of three geographically separate strains found in north Queensland, central coast N.S.W. and south coast N.S.W. respectively.
Data collated by A.J. Gibbs, 1981, Australia. Revised 1985.
MORPHOLOGY OF PARTICLES. Isometric; not enveloped; 28 nm in diameter; profiles rounded; capsomere arrangement readily discernible. Leaf sap contains many particles.
STABILITY IN SAP. Thermal inactivation point 65–70 °C. Longevity in vitro 10–100 days. Dilution end point 10–5 to 10–6. Infectivity of sap not changed by treatment with di-ethyl ether.
GEOGRAPHICAL DISTRIBUTION. Spreads in coastal eastern Australia.
Natural host species and symptoms:
Kennedya rubicunda, Desmodium triflorum, D. scorpiurus, Indigofera australis - bright blotchy yellow mosaic. Symptoms shown by naturally infected plants persist (and are often bright).
Diagnostic host species and symptoms:
Glycine max - chlorotic local lesions, bright yellow blotchy systemic mosaic.
Kennedya rubicunda - chlorotic local lesions, systemic yellow mosaic.
Phaseolus vulgaris cv. Redland Pioneer - chlorotic local lesions; systemic yellow mosaic.
Pisum sativum - chlorotic local lesions; systemic yellow mosaic.
Vigna radiata - necrotic lesions; systemic leaf shape distortion.
Datura stramonium - chlorotic local lesion; not systemic.
Nicotiana glutinosa - chlorotic local lesions; not systemic.
Diagnostically insusceptible: Lycopersicon esculentum, Nicotiana clevelandii.
Maintenance and propagation host species: Pisum sativum cv. Early Massey, Glycine max.
Species for Local lesion or Whole plant assay: Phaseolus vulgaris cv. Redland Pioneer (L), Pisum sativum cv. Massey (W), Vigna radiata (L).
HOST PLANTS. Experimental host range narrow. Species are recorded as Susceptible or Insusceptible to infection by any means. Dicotyledons: Cajanus cajan (S); Chenopodium amaranticolor (I); Chenopodium quinoa (I); Clitoria ternatea (S); Cucumis sativus (I); Datura stramonium (S); Glycine max (S); Gomphrena globosa (I); Lotus corniculatus (I); Lupinus angustifolius (S); Lycopersicon esculentum (I); Macrotyloma uniflorum (S); Medicago sativa (I); Nicotiana clevelandii (I); Nicotiana glutinosa (S); Phaseolus vulgaris (S); Pisum sativum (S); Trifolium incarnatum (I); Trifolium pratense (I); Trifolium repens (I); Vicia faba (I); Vicia sativa (I); Vigna angularis (S); Vigna radiata syn. Phaseolus aureus (S); Vigna unguiculata syn. sinensis (S); Vigna unguiculata ssp. sesquipedalis (S).
Sources of host range data: Dale et al. (1976); Gibbs (1978) unpublished data.
REFERENCES. CMI/AAB Description of Plant Viruses No (193 by A.J. Gibbs (1978)).
Blok, Gibbs & Mackenzie (1987). Arch. Virol. (in press).
Dale et al. (1975). Aust. Pl. Path. Newsl. 4: 13.
Dale et al. (1976). Aust. J. biol. Sci. 29: 397.
Gibbs et al. (1979). Aust. Pl. Path. Newsl. 8: 49.
Part of key a generated from descriptions of the 127 species. Prepared by and available from E. B. Britton, CSIRO Division of Entomology, G. P. O. Box 1700, Canberra, A. C. T. Australia (Britton 1986).
(A) A plant pathologist wants a list of C4 NADP-ME grasses, possessed of certain other characteristics demanded by his equipment and working conditions. Using a set of grass generic descriptions (see Example 2) in association with the interactive identificatory program ONLINE (Pankhurst 1978a), we find (user’s responses in bold face):
: auto 0
: exclude i u
744 TAXA REMAIN
CHARACTER 275: photosynthetic pathway
307 TAXA REMAIN
CHARACTER 276: C4 biochemical type as determined by enzyme assay
25 TAXA REMAIN
(B) We are not attempting an identification here, so the program is set (exclude i u) to exclude taxa for which any particular character is unknown or inapplicable; and auto 0 overrides calculation of ‘best’ characters (an identificatory aid). We see that of the 744 genera in the data bank, 307 are known to consist of or include C4 species. Of these, 25 contain species which have been typed biochemically as NADP-ME. Our physiologist’s gas exchange experiments involve use of a leaf chamber, calling for a fairly large leaf area, and he sees experimental advantages in plants with a relatively short generation time:
CHARACTER 29: whether maximum leaf blade width exceeds 1cm
1 leaf blades broad maximum (flattened) width greater than lcm
2 leaf blades narrow maximum (flattened) width no more than lcm
14 TAXA REMAIN
CHARACTER 2: longevity of plants
1 annual or biennial without remains of old sheaths or culms
2 perennial with remains of old sheaths or culms
11 TAXA REMAIN
Sadly, his establishment is short of funds, and the genetic engineers have priority over glasshouses and growth cabinets. He will have to grow his material outside:
CHARACTER 324: geographical occurrence, in Australasian terms
2 New South Wales
3 Australian Capital Territory
5 Western Australia
7 Northern Territory
8 South Australia
9 New Guinea
10 New Zealand
11 not known in Australasia
6 TAXA REMAIN
DIFFS NO. NAME
0 200 Digitaria
0 223 Echinochloa
0 484 Panicum
0 495 Pennisetum
0 625 Setaria
0 736 Zea
Should further suggestions be required, and assuming that Zea is not selected, the possibilities offered by the first 5 genera could be explored at species level using Webster’s automated descriptions of Paniceae (see Example 4).
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