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Manuel Halvelik<br />

<strong>the</strong><br />

<strong>TRIMERAL</strong> <strong>SYSTEM</strong><br />

<strong>in</strong><br />

<strong>BIOLOGICAL</strong><br />

<strong>TAXONOMY</strong><br />

A REVOLUTIONARY NEW APPROACH<br />

Version 2.1<br />

2002<br />

1


The present work is an application <strong>in</strong> actual practice<br />

of <strong>the</strong> <strong>the</strong>oretical analysis and <strong>the</strong> elements<br />

expounded <strong>in</strong> <strong>the</strong><br />

INTERNATIONAL TERMINOLOGICAL KEY<br />

by <strong>the</strong> same author<br />

which is a special feature of his world language project<br />

UNIESPO (Universal Esperanto).<br />

3


Manuel Halvelik<br />

The<br />

Trimeral System <strong>in</strong> Biological Taxonomy<br />

( “Universal Taxonomy” )<br />

Editorial Assistant: Derek Casselle, Newcastle, GB<br />

Kariljono Publications, 1996<br />

ISBN 90-75859-01-5<br />

D/1996/77471/1<br />

All rights reserved<br />

4


Ma<strong>in</strong> reference works<br />

Pres. F. BOERNER, horticulturist<br />

Taschenwörterbuch der Botanischen Pflanzennamen<br />

Paul Parey Verlag, Berl<strong>in</strong> 1951<br />

Prof. F.C. WERNER, zoologist<br />

Wortelemente late<strong>in</strong>isch-griechischer Fachausdrücke<br />

Max Niemeyer Verlag, Leipzig/Halle 1968<br />

Dr. W.M.A. DE SMET, zoologist<br />

Introduction to New Biological Nomenclature<br />

Association for NBN, Kalmthout (Belgium), 1974<br />

XV th International Congress of Zoology<br />

International Code of Zoological Nomenclature<br />

London 1964<br />

XII th International Botanical Congress<br />

International Code of Botanical Nomenclature<br />

Utrecht 1978<br />

International Committee on Bionomenclature<br />

Draft BioCode<br />

Taipei 1997<br />

Dr. C.A. BACKER, botanist<br />

Verklarend Woordenboek<br />

van Wetenschappelijke Plantennamen (660 pag.)<br />

Uitg. L.J. Veen, Amsterdam 2000<br />

5


6<br />

1 - The Key to <strong>the</strong> Key<br />

There can be no deny<strong>in</strong>g that change and discovery s<strong>in</strong>ce <strong>the</strong><br />

18 th Century <strong>in</strong>ception of L<strong>in</strong>naean Biological Nomenclature has<br />

left this system <strong>in</strong> a state of chaos. Its <strong>in</strong>adequacies are <strong>the</strong><br />

subject of many articles <strong>in</strong> scientific journals; and <strong>the</strong> topic<br />

absorbs unend<strong>in</strong>g time and energy at <strong>in</strong>ternational symposia and<br />

sem<strong>in</strong>ars. But ra<strong>the</strong>r than elaborate upon any of that, let it be<br />

“first th<strong>in</strong>gs first” by summariz<strong>in</strong>g <strong>the</strong> fundamental causes of this<br />

deplorable situation...<br />

First of all, <strong>in</strong> our own Anglo-Saxon technological era, knowledge<br />

and active use of Lat<strong>in</strong>, let alone Greek, has dropped to an alltime<br />

low <strong>in</strong> <strong>the</strong> academic world. And it is arguable that study of<br />

<strong>the</strong>se classic languages is best left to historians and philologists.<br />

But <strong>in</strong> any event many biologists — zoologists, botanists,<br />

virologists, and <strong>the</strong> like — are scarcely able to f<strong>in</strong>d <strong>the</strong> correct<br />

word forms among <strong>the</strong> labyr<strong>in</strong>th<strong>in</strong>e <strong>in</strong>tricacies of (neo)Lat<strong>in</strong><br />

grammar, when <strong>the</strong>y have to name or rename yet ano<strong>the</strong>r genus<br />

or species. Moreover, handbooks such as The International<br />

Code of Zoological Nomenclature, regarded as Gospel Truth, are<br />

<strong>the</strong>mselves such a web of rules — plus a host of exceptions to<br />

those rules — that even a spider would be hard put to f<strong>in</strong>d its way<br />

around this web. Topp<strong>in</strong>g this is <strong>the</strong> idiotic situation that <strong>the</strong> life<br />

sciences are apply<strong>in</strong>g five (yes five!) different sets of rules, valid<br />

only <strong>in</strong> <strong>the</strong> discipl<strong>in</strong>es concerned: botany, zoology, cultivated<br />

plants, bacteriology, virology.<br />

Then, <strong>the</strong>re is <strong>the</strong> explosive advance <strong>in</strong> Genetics (cladism) and<br />

similar new life sciences, which makes it ever more and more<br />

imperative not only to reconsider <strong>the</strong> whole phylogenetic<br />

ramification of liv<strong>in</strong>g th<strong>in</strong>gs, but also <strong>in</strong> fact to reorganize <strong>the</strong><br />

whole L<strong>in</strong>naean system — this still too hazy mirror of Evolution<br />

on Earth — from top to bottom!<br />

Only a few decades ago this very idea might have looked like a<br />

horrible nightmare to biologists, confronted by mounta<strong>in</strong>s of<br />

archives piled up <strong>in</strong> <strong>the</strong>ir temples dedicated to Natural History,<br />

and compiled by generations of researchers. But today we have<br />

a formidable tool at hand, brought about by <strong>the</strong> advances <strong>in</strong><br />

electronics: His Supremacy <strong>the</strong> Computer. Now we have


Databanks; now we have CD-Roms with sight and sound; and<br />

above all now we have <strong>the</strong> INTERNET with a limitless potential for<br />

<strong>in</strong>formation retrieval and exchange, mak<strong>in</strong>g it possible even to<br />

(quickly!) f<strong>in</strong>d <strong>the</strong> proverbial needle <strong>in</strong> a haystack ...<br />

So, what are we wait<strong>in</strong>g for?<br />

We are wait<strong>in</strong>g for a totally logical and easy-to-use system to<br />

replace <strong>the</strong> cumbersome and creaky L<strong>in</strong>naean one. A system<br />

which would do away with <strong>the</strong> onerous need to master dead and<br />

extremely complex languages. A system with a moderate<br />

number of simple rules, as free of exceptions as possible; so that<br />

<strong>the</strong>y can be remembered and adhered to without rack<strong>in</strong>g one’s<br />

bra<strong>in</strong> or spend<strong>in</strong>g valuable time on a complicated handbook. A<br />

system fully compatible with <strong>the</strong> computer. A system so coherent<br />

as to provide a solid <strong>in</strong>frastructure need<strong>in</strong>g no extension or<br />

modification, once mastered, and leav<strong>in</strong>g users free to apply<br />

complete attention to <strong>the</strong>ir objective study: liv<strong>in</strong>g th<strong>in</strong>gs and <strong>the</strong>ir<br />

evolution, without bo<strong>the</strong>r<strong>in</strong>g about l<strong>in</strong>guistics.<br />

Admittedly, many proposals to this end have already seen <strong>the</strong><br />

light of day, <strong>in</strong>clud<strong>in</strong>g representation by numbers <strong>in</strong>stead of<br />

names or by express<strong>in</strong>g everyth<strong>in</strong>g <strong>in</strong> pla<strong>in</strong> English. In fact, <strong>the</strong><br />

need for muck<strong>in</strong>g out <strong>the</strong>se Augean stables has become so<br />

urgent at this start of <strong>the</strong> 21 st Century, that a so-called Draft<br />

BioCode has been worked out by a special commission to that<br />

end — <strong>the</strong> International Committee on Bionomenclature (ICB) —<br />

which code must and undoubtedly will be discussed by<br />

representatives of all <strong>the</strong> life sciences. Well, here is yet ano<strong>the</strong>r<br />

proposal, but this time on an entirely new foot<strong>in</strong>g ... with many<br />

advantages, never seen before. A bold statement, <strong>in</strong>deed, but let<br />

<strong>the</strong> reader judge for himself <strong>in</strong> <strong>the</strong> follow<strong>in</strong>g chapters.<br />

The operat<strong>in</strong>g pr<strong>in</strong>ciple is essentially that of a constant, close<br />

engagement between three mechanical components analogous<br />

to <strong>the</strong> steer<strong>in</strong>g wheel, <strong>the</strong> gear box, and <strong>the</strong> accelerator pedal of<br />

a motor car. The steer<strong>in</strong>g wheel would be a new taxonomic<br />

framework proper, <strong>the</strong> gear box a new nomenclative wordlist, and<br />

<strong>the</strong> accelerator pedal a new l<strong>in</strong>guistic <strong>in</strong>frastructure, <strong>the</strong> latter<br />

be<strong>in</strong>g free of <strong>the</strong> complexities of Lat<strong>in</strong> and Greek. In fact, <strong>the</strong><br />

whole has a Tau-like <strong>in</strong>frastructure. This comb<strong>in</strong>ation is so easily<br />

7


mastered that it would scarcely be an exaggeration to call it<br />

child’s play resembl<strong>in</strong>g <strong>the</strong> Lego-concept. To tell <strong>the</strong> truth,<br />

automated registration (Rule2) is yet ano<strong>the</strong>r and important factor<br />

<strong>in</strong> <strong>the</strong> system, which we shall not enlarge upon here, s<strong>in</strong>ce it<br />

belongs to <strong>the</strong> world of computer software, but which constitutes<br />

no pr<strong>in</strong>cipal complication <strong>in</strong> itself.<br />

Ideally, <strong>the</strong> steer<strong>in</strong>g wheel — <strong>the</strong> Trimeral System 1 — should be<br />

dealt with first. But s<strong>in</strong>ce noth<strong>in</strong>g can be described or<br />

demonstrated without <strong>in</strong>volv<strong>in</strong>g verbal means, <strong>the</strong> gear box, alias<br />

<strong>the</strong> new vocabulary, must take precedence.<br />

Do not panic, dear reader, it will not be absolutely necessary to<br />

learn an entire new language, but only how to consult <strong>the</strong><br />

reference handbook compiled with its help: <strong>the</strong> International<br />

Term<strong>in</strong>ological Key (ITK) and, if desired for understand<strong>in</strong>g <strong>the</strong><br />

mean<strong>in</strong>g of a species name, an Esperanto dictionary. Certa<strong>in</strong>ly<br />

this is <strong>in</strong>f<strong>in</strong>itely easier than hav<strong>in</strong>g to wrestle with convoluted Lat<strong>in</strong><br />

declensions, conjugations, orthography, and even uncerta<strong>in</strong><br />

semantics !<br />

This ITK is a modest bil<strong>in</strong>gual dictionary, list<strong>in</strong>g over 5000<br />

scientific word roots, adapted from Lat<strong>in</strong> or Greek orig<strong>in</strong>als, <strong>in</strong><br />

which each root has both a fixed form and a fixed mean<strong>in</strong>g, and<br />

can <strong>the</strong>refore be easily l<strong>in</strong>ked to any o<strong>the</strong>r member of <strong>the</strong> group,<br />

or be given an appropriate affix, also of a fixed form and fixed<br />

mean<strong>in</strong>g. Thus <strong>the</strong> old Lat<strong>in</strong> and Greek stems are re<strong>in</strong>carnated,<br />

so to speak, <strong>in</strong> a modern simplified and streaml<strong>in</strong>ed form. There<br />

is no longer any need to worry about assimilative affix variations,<br />

such as syn becom<strong>in</strong>g sym, syr, syll, or even sy; or ad becom<strong>in</strong>g<br />

ac, af, ag, al, ap. No more wonder<strong>in</strong>g whe<strong>the</strong>r -us should not<br />

ra<strong>the</strong>r be -um or -ae or -os. Consequently, practitioners <strong>in</strong> any<br />

scientific discipl<strong>in</strong>e — not only biologists — which by tradition<br />

happens to be embedded <strong>in</strong> those dead languages, can now<br />

jettison <strong>the</strong>ir old burden.<br />

The ITK table of scientific word stems can dispose of <strong>the</strong><br />

traditional <strong>in</strong>tricacies of grammar, because it is embedded <strong>in</strong> a<br />

1 The term trimeral ("three-membered") has been co<strong>in</strong>ed to avoid<br />

confusion with tr<strong>in</strong>om<strong>in</strong>al (“three-named”).<br />

8


new “constructed” world language, called Uniespo, which lends<br />

its simple orthography and absolutely rational grammar to <strong>the</strong><br />

form<strong>in</strong>g of actual scientific terms from <strong>the</strong> build<strong>in</strong>g blocks<br />

presented. In o<strong>the</strong>r words: if one element provides <strong>the</strong> necessary<br />

build<strong>in</strong>g blocks, <strong>the</strong> o<strong>the</strong>r one provides mortar and tools. As yet,<br />

<strong>the</strong> ITK dictionary translates only from and to English, but that<br />

can of course be replaced by any liv<strong>in</strong>g language.<br />

Uniespo (or Universal Esperanto) is a considerably expanded<br />

and rationalized version of traditional Esperanto. The latter —<br />

despite popular op<strong>in</strong>ion to <strong>the</strong> contrary — is no pidg<strong>in</strong> at all and<br />

perfectly capable of produc<strong>in</strong>g high-flown literature, but has<br />

always been lack<strong>in</strong>g <strong>in</strong> <strong>the</strong> fields of sciences and technology. Not<br />

from any <strong>in</strong>herent <strong>in</strong>ability to absorb scientific loanwords, but<br />

because its traditional grammar is completely at a loss for a<br />

secure way to orqanize and digest purely scientific words. Its<br />

offspr<strong>in</strong>g Uniespo, however, rectifies this shortcom<strong>in</strong>g — mak<strong>in</strong>g<br />

“Language for Special Purposes” its broad-spectrum prime<br />

objective, with Bionomenclature a choice field of application.<br />

As stated before, <strong>the</strong>re is no <strong>in</strong>herent need to master this new<br />

language <strong>in</strong> any conventional sense, though a work<strong>in</strong>g<br />

knowledge would be useful, of course. But, where up to now<br />

consult<strong>in</strong>g a Lat<strong>in</strong> or Greek dictionary — for construct<strong>in</strong>g (or<br />

understand<strong>in</strong>g) a given scientific name — is like enter<strong>in</strong>g a<br />

labyr<strong>in</strong>th to non-philologists, <strong>the</strong> International Term<strong>in</strong>ological Key<br />

is completely regular <strong>in</strong> structure and usage (no exceptions!)<br />

Therefore, any <strong>in</strong>telligent person can employ this small handbook<br />

confidently and effectively, after memoriz<strong>in</strong>g only a couple of<br />

<strong>in</strong>troductory pages on composition and orthography. 2<br />

In fact, by simple analysis of <strong>the</strong> scientific names exampled<br />

fur<strong>the</strong>r on <strong>in</strong> this publication, many of its components and rules<br />

will become immediately apparent.<br />

2<br />

A volum<strong>in</strong>ous treatise will eventually be available (for free) as a PDFfile.<br />

9


At this po<strong>in</strong>t it is only right and reasonable to acknowledge that<br />

Dr. W.M.A. DE SMET, a renowned Belgian zoologist, has already<br />

devised a somewhat similar approach, called New Biological<br />

Nomenclature (NBN). This has been published (ma<strong>in</strong>ly <strong>in</strong><br />

Esperanto) under <strong>the</strong> impr<strong>in</strong>t of a scientific Association 3 with <strong>the</strong><br />

same name and which has already accomplished a significant<br />

reorder<strong>in</strong>g of zoological term<strong>in</strong>ology and taxonomy. But, s<strong>in</strong>ce<br />

<strong>the</strong> <strong>in</strong>itiator makes almost a clean sweep of established<br />

taxonomy, deny<strong>in</strong>g even <strong>the</strong> concept of genus (i.e. recogniz<strong>in</strong>g<br />

only families) and <strong>in</strong>sist<strong>in</strong>g that all generic and higher names be<br />

translated <strong>in</strong>to everyday traditional Esperanto, <strong>the</strong>re seems to be<br />

little po<strong>in</strong>t <strong>in</strong> pursu<strong>in</strong>g this tra<strong>in</strong> of thought, however meritorious<br />

<strong>the</strong> venture.<br />

Some o<strong>the</strong>r noteworthy workers <strong>in</strong> <strong>the</strong> same field but along<br />

divergent l<strong>in</strong>es, all esperantists, were: Prof. Carl Støp-Bowitz, a<br />

Norwegian biologist; Prof. Paul Neergaard, a Danish botanist,<br />

and B.Sc. G.F. Makk<strong>in</strong>k, a Dutch agricultural researcher.<br />

Uniespo, on <strong>the</strong> o<strong>the</strong>r hand, sets out to liberalise taxonomy by<br />

giv<strong>in</strong>g it a versatility which makes <strong>the</strong> go<strong>in</strong>g so easy — for<br />

“splitters” as well as “bumpers” — that biological nomenclature<br />

should cease to be plagued by vehement, time-wast<strong>in</strong>g<br />

discussions at sem<strong>in</strong>ars and <strong>in</strong> periodicals.<br />

Essentially, <strong>the</strong>n, this booklet presents a new (triple) tool and<br />

demonstrates how it should be applied; but noth<strong>in</strong>g more. If<br />

biologists 4 choose to accept it — a big “if “ — <strong>the</strong>n <strong>the</strong> actual<br />

3 Seat: NBN, Hertendreef 12, B-2920 Kalmthout (Belgium).<br />

4 In fact, it would be better to use <strong>the</strong> term "biontologists" <strong>in</strong> <strong>the</strong> very<br />

broad perspective of this new system, which can be applied by<br />

practitioners <strong>in</strong> all <strong>the</strong> life sciences (bacteriologists, horticulturists,<br />

breeders aso.) and even beyond.<br />

10


operational decisions rema<strong>in</strong> <strong>the</strong>irs. The examples given on<br />

subsequent pages thus are just examples and <strong>in</strong> no way<br />

immutable f<strong>in</strong>al forms! Nor are <strong>the</strong> rules <strong>the</strong> basis of any claim to<br />

some ultimate and absolute perfection. What <strong>the</strong>y should prove,<br />

though, is that <strong>the</strong> Trimeral System, <strong>the</strong> ITK, and its embedd<strong>in</strong>g<br />

Uniespo, constitute an enormous leap forward over <strong>the</strong> classical<br />

Lat<strong>in</strong>-based L<strong>in</strong>naean system... enough to justify <strong>the</strong> monumental<br />

task of completely rewrit<strong>in</strong>g all <strong>the</strong> textbooks on taxonomy or<br />

systematics.<br />

11


12<br />

2 - Nam<strong>in</strong>g <strong>the</strong> Child<br />

Let us beg<strong>in</strong> by do<strong>in</strong>g away with <strong>the</strong> ill-conceived<br />

1 Law of Priority !! Scientific discipl<strong>in</strong>es <strong>in</strong> general<br />

seek maximum objectivity and precision. Yet, with<br />

Taxonomy <strong>the</strong>re is acceptance of even <strong>the</strong> most ambiguous<br />

and nonsensical name for a species, <strong>in</strong> <strong>the</strong> misguided belief<br />

that this Law will make a paragon of <strong>the</strong> little monster,<br />

creat<strong>in</strong>g stability and clarity. But <strong>in</strong> this computerized day<br />

and age, this obsolete Law can much more efficiently and<br />

surely be replaced by enabl<strong>in</strong>g reference to a worldwide<br />

databank — a new k<strong>in</strong>d of “Zoological and Botanical<br />

Record” — literally at one’s f<strong>in</strong>gertips: a Central Biological<br />

Catalogue, and thus from now on governed by a Law of<br />

Reference ! To that end, a subject should be given that<br />

name which fits it best, and leave all o<strong>the</strong>r candidates out,<br />

regardless of how recently or long ago that name was first<br />

co<strong>in</strong>ed, and no matter whe<strong>the</strong>r it came from a dist<strong>in</strong>guished<br />

professional or an obscure amateur. Names of authors and<br />

dates of description — <strong>the</strong> so-called “<strong>in</strong>dications” — would<br />

appear <strong>in</strong> this Catalogue only as a supplement, not directly<br />

l<strong>in</strong>ked to <strong>the</strong> name itself, i.e. as <strong>in</strong>formation for people<br />

<strong>in</strong>terested <strong>in</strong> archives.<br />

A researcher, WALCKENAER, who published an extensive study<br />

about spiders <strong>in</strong> 1805, concluded that LINNAEUS had listed far<br />

too many disparate species under <strong>the</strong> same generic name, and<br />

that <strong>the</strong>y should <strong>the</strong>refore be distributed over a greater number<br />

of genera. So, e.g. he thought up <strong>the</strong> genus Epaira for <strong>the</strong><br />

cross or garden spider, nam<strong>in</strong>g it Epeira diadema. But no,<br />

because LINNAEUS’ work of 1758 preceded his, only <strong>the</strong> name<br />

Aranea diadema was considered worthy of official acceptance,<br />

thus perpetuat<strong>in</strong>g <strong>the</strong> confusion.<br />

Naturally, decid<strong>in</strong>g on <strong>the</strong> most appropriate name<br />

2<br />

should entail an accurate assessment of all <strong>the</strong>


elevant facts about <strong>the</strong> group under consideration.<br />

Includ<strong>in</strong>g a situation where new f<strong>in</strong>d<strong>in</strong>gs — ei<strong>the</strong>r <strong>the</strong>oretical<br />

or observed — may make it necessary to alter an exist<strong>in</strong>g<br />

and accepted name, despite its previous validity. Now,<br />

s<strong>in</strong>ce it rema<strong>in</strong>s essential to know exactly which species or<br />

genus is affected, this is where <strong>the</strong> Law of Reference comes<br />

<strong>in</strong>to play. It will, <strong>in</strong> all required <strong>in</strong>stances, also give <strong>the</strong><br />

Catalogue Number — a list<strong>in</strong>g procedure for which <strong>the</strong><br />

established Decimal Classification seems ready-made. The<br />

new CBC Databank could output a totality of detail on any<br />

taxon or species, or even subspecies. And if anyone is<br />

<strong>in</strong>terested <strong>in</strong> <strong>the</strong> historic background, all <strong>the</strong> names ever<br />

assigned, plus when and where and by whom, could be<br />

accessed too. Except that <strong>the</strong>re would no longer be any<br />

real need to preserve all those little known and often<br />

unpronounceable personal names.<br />

So <strong>the</strong> globeflower might be fully catalogued as:<br />

Trollius laxus CBC 34-1056.<br />

At <strong>the</strong> moment of publication, this system of catalogu<strong>in</strong>g all liv<strong>in</strong>g th<strong>in</strong>gs<br />

<strong>in</strong> a worldwide databank may appear like sciencefiction to some, not<br />

aware yet of <strong>the</strong> BioCode commotion. However, even <strong>the</strong>y cannot stay<br />

bl<strong>in</strong>d for <strong>the</strong> explosive growth of <strong>in</strong>formation technology nor for this<br />

practicability be<strong>in</strong>g near at hand. In fact, such catalogu<strong>in</strong>g would and<br />

should become a fully automated process, provided it is modelled on <strong>the</strong><br />

way <strong>the</strong> human bra<strong>in</strong> stores and accesses its <strong>in</strong>formation. 5 No formally<br />

constituted oversee<strong>in</strong>g authority (always lagg<strong>in</strong>g beh<strong>in</strong>d) would any<br />

longer be necessary if <strong>the</strong> CBC — through on-l<strong>in</strong><strong>in</strong>g with o<strong>the</strong>r<br />

databanks — cont<strong>in</strong>ually monitors all <strong>the</strong> relevant books and periodicals.<br />

If a given name allocation is found <strong>in</strong>, say, five (dist<strong>in</strong>ctly) different<br />

sources dur<strong>in</strong>g, say, three consecutive years, <strong>the</strong>n this name will<br />

become officially recognized and recorded as such — without any<br />

human <strong>in</strong>tervention! While no specialist could ever hope to consult each<br />

and every member of his profession, <strong>the</strong> CBC would be able to achieve<br />

total and simultaneous coverage and thus enable consensus to be<br />

reached as expeditiously as possible.<br />

5 The author also conceived a set of algorithms enabl<strong>in</strong>g a pars<strong>in</strong>g<br />

programme to automatically determ<strong>in</strong>e <strong>the</strong> subject of a given text.<br />

13


As <strong>the</strong> CBC would undoubtedly register any and all newcomers arriv<strong>in</strong>g<br />

<strong>in</strong> literature — or even over <strong>the</strong> Internet itself — as yet “immature<br />

names” would have to be labelled by <strong>the</strong> customary asterisk<br />

stand<strong>in</strong>g for “not official, hypo<strong>the</strong>tical”, until <strong>the</strong> above criterion were<br />

satisfied. Of course, <strong>in</strong> case a given proposal proves to be too<br />

ephemeral or unpopular to be reta<strong>in</strong>ed, also an “expiration date” should<br />

be implemented. And names which do not comply with <strong>the</strong> Rules of <strong>the</strong><br />

BioCode would be discarded automatically.<br />

Now, as to <strong>the</strong> language to be applied, we have to<br />

3 use a two-part methodology: <strong>the</strong> Key for recreat<strong>in</strong>g<br />

generic names and a new everyday (common)<br />

vocabulary for (re)creat<strong>in</strong>g specific names. Let us consider<br />

<strong>the</strong>m separately.<br />

Generic names, plus all higher taxons, are to be<br />

4<br />

(re)created <strong>in</strong> accordance with <strong>the</strong> International<br />

Term<strong>in</strong>ological Key (see <strong>the</strong> Introduction). Only a<br />

few grammatical rules, for l<strong>in</strong>k<strong>in</strong>g <strong>the</strong> scientific roots of this<br />

Key or mak<strong>in</strong>g derivations, have to be observed, all<br />

rigorously without exceptions. The roots <strong>the</strong>mselves have a<br />

fixed form never altered by declensions of any k<strong>in</strong>d.<br />

1. All generic names, be<strong>in</strong>g substantives, end <strong>in</strong> -O; no<br />

more arbitrar<strong>in</strong>ess, confusion, uncerta<strong>in</strong>ty about a host of<br />

Lat<strong>in</strong> suffixes for genders and cases:<br />

Lumbricus Lumbriko<br />

Jasm<strong>in</strong>um Jasmeno<br />

2. If a lead<strong>in</strong>g stem ends on a consonant, and <strong>the</strong> trail<strong>in</strong>g<br />

stem starts with one, <strong>the</strong>n <strong>the</strong> vowel -0 is to be <strong>in</strong>serted<br />

between <strong>the</strong> consonants:<br />

14<br />

Raphiolepis Rafjolepido from rafj• and lepid•<br />

D<strong>in</strong>osaurus D<strong>in</strong>osawro from d<strong>in</strong>• and sawr’


3. If <strong>the</strong> leader ends on a vowel or <strong>the</strong> trailer starts with it,<br />

<strong>the</strong>n that vowel takes <strong>the</strong> place of <strong>the</strong> above -0.<br />

Epimys Epi|muzho from epi• and muzh•<br />

Galanthus Galakt|anto from galakt• and ant•<br />

4. If leader stem and trailer stem meet one ano<strong>the</strong>r with<br />

DIFFERENT vowels, <strong>the</strong>n both vowels have to be written:<br />

Paronychia Para|onyxo from para• and onyx•<br />

Monodon Mona|odonto from mona• and odont•<br />

5. If leader and trailer meet one ano<strong>the</strong>r with <strong>the</strong> SAME<br />

vowel, <strong>the</strong>n both vowels comb<strong>in</strong>e <strong>in</strong>to one:<br />

Thelyper Tel|y|pero<br />

from tely• [“female”] and yper• [“serve”].<br />

This places some burden on <strong>the</strong> memory, but is noth<strong>in</strong>g compared to<br />

cop<strong>in</strong>g with <strong>the</strong> weld<strong>in</strong>g practised <strong>in</strong> traditional lat<strong>in</strong>ized names.<br />

Besides, <strong>the</strong> ITK-handbook will always be able to clarify <strong>the</strong><br />

“etymological” structure.<br />

Naturally, names handed down as a whole from <strong>the</strong><br />

5<br />

past, which perta<strong>in</strong> exclusively to <strong>the</strong> object, are<br />

considered sufficient <strong>in</strong> <strong>the</strong>mselves and need no<br />

revision o<strong>the</strong>r than that brought about by <strong>the</strong> new<br />

orthography (see Rule 18). After this it is only a matter of<br />

familiarisation...<br />

Fagus Fago<br />

Salix Saliko<br />

Vulpes Vulpo<br />

15


Cypr<strong>in</strong>us Tsipr<strong>in</strong>o<br />

In a relatively few number of cases, <strong>the</strong> elements of<br />

6 a compound generic name may, because of <strong>the</strong>ir<br />

purely Lat<strong>in</strong> orig<strong>in</strong>, have <strong>the</strong> consistency and form<br />

of a species name. This will be confus<strong>in</strong>g and conflict with<br />

ord<strong>in</strong>ary (popular) word<strong>in</strong>g. In such <strong>in</strong>stances it seems<br />

advisable to make a radical change over to <strong>the</strong> ITK-stems,<br />

while conserv<strong>in</strong>g <strong>the</strong> old mean<strong>in</strong>g(s). The same goes for<br />

words imported from some ethnic tongue:<br />

16<br />

Passiflora = “pasionfloro” <strong>in</strong> common language Algianto<br />

from <strong>the</strong> ITK-roots algi• (“pa<strong>in</strong>”) and ant• (“flower”).<br />

Phytolacca, irregularly composed of a Greek stem (“plant”) plus an<br />

Italian one (“lacquer”), might be rephrased as Fytoglojo, with exactly<br />

<strong>the</strong> same mean<strong>in</strong>g.<br />

Ano<strong>the</strong>r onion to peel is <strong>the</strong> nature of a word stem.<br />

7<br />

In numerous cases, it has no recognisable identity,<br />

but is ei<strong>the</strong>r a mean<strong>in</strong>gless stump or a personal<br />

name, both equally untranslatable and <strong>the</strong>refore immune to<br />

even our Universal Key. A nonsensical word may be<br />

thought up by some author, lack<strong>in</strong>g <strong>in</strong>spiration or just be<strong>in</strong>g<br />

lazy l<strong>in</strong>guistically (Lobivia anagrammed from <strong>the</strong> correct<br />

form Bolivia); it could be a mean<strong>in</strong>gful word where <strong>the</strong><br />

etymological orig<strong>in</strong> has been lost or become extremely<br />

archaic (Radymna, Mogulones); or it might be — worst of all<br />

— a personal name <strong>in</strong> honour of some high rank<strong>in</strong>g but long<br />

forgotten patron. (Whoever was <strong>the</strong> Baron W. von Sa<strong>in</strong>t-<br />

Paul Hilaire <strong>in</strong> Sa<strong>in</strong>tpaulia ?)<br />

* * * * * * *<br />

Now, with <strong>the</strong> object of mak<strong>in</strong>g everyth<strong>in</strong>g as clear and<br />

concise as possible, one should try <strong>in</strong> such cases to apply<br />

<strong>the</strong> follow<strong>in</strong>g criteria::


1. Reduce complex ethnic spell<strong>in</strong>gs.to a m<strong>in</strong>imum (ideally<br />

no more than four syllables), us<strong>in</strong>g only characters<br />

employed <strong>in</strong> Uniespo and <strong>the</strong> ITK, <strong>in</strong> accordance with<br />

Rule 18. And that goes of course for “Lat<strong>in</strong>” centipedes<br />

too!<br />

Saxegothaea Saksegotio<br />

Bouss<strong>in</strong>gaultia Bus<strong>in</strong>goltio<br />

Parapallaseakotylodermogammarus Kotylodermo<br />

Roberthoffstetteria nationalgeographica Robertusso<br />

2. If non-Lat<strong>in</strong> names are translatable — such as those<br />

lat<strong>in</strong>ized from Russian or Ch<strong>in</strong>ese — it is necessary,<br />

without exception, to turn <strong>the</strong>m <strong>in</strong>to comb<strong>in</strong>ations of<br />

correspond<strong>in</strong>g and <strong>in</strong>ternational ITK-roots.<br />

Krasnopoevaecejathus tyrgaensis REPINA, KHOMENTOVSKII,<br />

ZHURAULEVA & ROZANOV, 1964 Ruberosomfo turguja<br />

3. Provide <strong>the</strong>m with <strong>the</strong> end<strong>in</strong>g -(Z)IO which, though<br />

hav<strong>in</strong>g no mean<strong>in</strong>g <strong>in</strong> itself, does serve as a marker to<br />

denote <strong>the</strong> word <strong>in</strong> question foreign and <strong>the</strong>refore<br />

officially devoid of coherent <strong>in</strong>nate mean<strong>in</strong>g:<br />

Brosmius Brosmio<br />

(German) Pfrille Pfrilio<br />

Fuxsio, Panio, L<strong>in</strong>eio, Lamarkio... a.s.o.<br />

The difference between this rule and Rule 5, is that here we are<br />

deal<strong>in</strong>g with words hav<strong>in</strong>g no (tangible) mean<strong>in</strong>g, as opposed to<br />

those with at least some degree of comprehensibility<br />

4. Where tradition need not be observed — as <strong>in</strong> co<strong>in</strong><strong>in</strong>g a<br />

name for a new genus — but <strong>the</strong> author is determ<strong>in</strong>ed to<br />

use a proper name, it should be borrowed from a<br />

universally exist<strong>in</strong>g concept such as a country, lake,<br />

mounta<strong>in</strong>, city, ethnic group, mythological figure, or <strong>the</strong><br />

17


18<br />

like — never a person’s name and never forgett<strong>in</strong>g <strong>the</strong><br />

(Z)IO-end<strong>in</strong>g or a default suffix — and observ<strong>in</strong>g <strong>the</strong><br />

orthography of Uniespo! [see Rule 18]<br />

e.g. Kubio (from Cuba); Ikario (from lcarus); Panio (from Pan)...<br />

or Molukello (from <strong>the</strong> Moluccas).<br />

5. Hav<strong>in</strong>g become <strong>in</strong>tegrated with Uniespo, such names<br />

may <strong>the</strong>n be regarded as technically equivalent to ITKroots<br />

and applied <strong>in</strong> <strong>the</strong> same way.<br />

Baluchi<strong>the</strong>rium Balutshoterjo [terj• = “animal”]<br />

Turcmeniga Turkmenogeno [gen• = “produce”]<br />

Cub<strong>in</strong>colo Kubotsholo [tshol• = “dwell”]<br />

6. Instead of mak<strong>in</strong>g an anagram from a compound word, it is<br />

better to <strong>in</strong>verse <strong>the</strong> order of <strong>the</strong> constituent elements, or<br />

select synonymous roots from <strong>the</strong> ITK.<br />

Potamogeton/Aponogeton [potam• = “river”; geton• = “neighbour”]<br />

Potamogetono / Getonopotamo<br />

Fluviogetono / Amnjogetono<br />

Potamoxomro / Potamovitshno<br />

7. Where <strong>the</strong>re are apparently no constituents but only a<br />

monolithic name, select<strong>in</strong>g different default end<strong>in</strong>gs is aga<strong>in</strong><br />

preferable to co<strong>in</strong><strong>in</strong>g anagrams.<br />

Mitella / Tellima Mitjello / Mitjimmo<br />

from mitj• [“scull-cap”]<br />

8. Mak<strong>in</strong>g compounds with proper names, not with<strong>in</strong> <strong>the</strong><br />

category of 7.4, is not allowed. Derivations on <strong>the</strong> o<strong>the</strong>r<br />

hand are allowed, if made with <strong>the</strong> suffixes mentioned under<br />

Rule 8.1.<br />

Wattonithyris ei<strong>the</strong>r Watonio or (eventually) Kyklotyro<br />

Thomsonaria ei<strong>the</strong>r Tomsonio or (eventually) Hermesarro


It is also important to note that <strong>the</strong> Key does not permit<br />

8<br />

one of its OWN word roots to stand isolated <strong>in</strong> a text.<br />

Such roots must always be given a “plug” to seal <strong>the</strong>m<br />

off aga<strong>in</strong>st <strong>in</strong>advertent use as common words and to preserve<br />

<strong>the</strong>ir scientific (normoglot) character. So, if a generic name<br />

conta<strong>in</strong>s only one such scientific root and is not l<strong>in</strong>ked ei<strong>the</strong>r to<br />

ano<strong>the</strong>r stem or a MEANINGFUL suffix, <strong>the</strong>n <strong>the</strong> Key provides a<br />

number of special end<strong>in</strong>gs, called “default suffixes” —<br />

particularly applicable <strong>in</strong> biontology — conta<strong>in</strong><strong>in</strong>g any given<br />

vowel plus double consonant, and all hav<strong>in</strong>g <strong>the</strong> same general<br />

mean<strong>in</strong>g of “be<strong>in</strong>g, entity, liv<strong>in</strong>g th<strong>in</strong>g”. They enable us to form<br />

about a hundred different names with each of <strong>the</strong> ITK-roots!<br />

One may rightly object that this spell<strong>in</strong>g of default suffixes is aga<strong>in</strong>st <strong>the</strong><br />

pr<strong>in</strong>ciples stated <strong>in</strong> Rule 18. That is true, but it is <strong>the</strong> ONLY deviation<br />

necessitated by this l<strong>in</strong>guistic problem and justified by <strong>the</strong> great benefit it<br />

br<strong>in</strong>gs for differentiat<strong>in</strong>g between ever so many homonyms. The consonant<br />

doubles (gem<strong>in</strong>ations) will be pronounced with a little extra emphasis<br />

and/or duration, <strong>in</strong> order to make <strong>the</strong>m recognisable <strong>in</strong> spoken language.<br />

1. From among those default suffixes one can freely choose<br />

whichever seems <strong>the</strong> most appropriate element; that is<br />

closest to <strong>the</strong> orig<strong>in</strong>al or best suited for mak<strong>in</strong>g a dist<strong>in</strong>ction.<br />

This simple rule allows <strong>the</strong> bypass<strong>in</strong>g of a great quantity of<br />

complicated graecolat<strong>in</strong> suffixes, when deal<strong>in</strong>g with a real<br />

word.<br />

-ULL for -ulus, -ulum, -ula<br />

-ARR for -arius, -arium<br />

-IDD for -ide, -ides, -idus and so on<br />

The difference between this procedure and <strong>the</strong> one presented <strong>in</strong> 7.3<br />

is that we have here a mean<strong>in</strong>gful word stem; and <strong>in</strong> <strong>the</strong> o<strong>the</strong>r, ei<strong>the</strong>r<br />

a mean<strong>in</strong>gless person’s name or an ethnic term.<br />

19


2. Normally, <strong>the</strong>se suffixes are to be used ONLY with a lone<br />

root. If that root is (to be) l<strong>in</strong>ked with ano<strong>the</strong>r root, <strong>the</strong><br />

eventual default suffix should <strong>in</strong>variably be dropped.<br />

20<br />

Hymenaea Himenazzo<br />

but Hymenan<strong>the</strong>ra Himenantsero<br />

3. Default suffixes can also be used to differentiate between<br />

compounds which would o<strong>the</strong>rwise be homonymous.<br />

Microchaet<strong>in</strong>a Mikroshet<strong>in</strong>no<br />

Microchaetana Mikroshetanno<br />

4. The use of ord<strong>in</strong>ary Uniespo-roots, as with names of pure<br />

Lat<strong>in</strong> orig<strong>in</strong>, is permissible <strong>in</strong> <strong>the</strong> same situation, but us<strong>in</strong>g<br />

strictly ITK-material is by far preferable.<br />

Ocul<strong>in</strong>a Okul<strong>in</strong>no [okul’ = “eye”]<br />

but Omat<strong>in</strong>no [from omat•] is to be preferred.<br />

5. Only ONE such suffix should be used at a time, but not two<br />

or three <strong>in</strong> a row! If <strong>the</strong> orig<strong>in</strong>al name carries such a<br />

comb<strong>in</strong>ation, or may <strong>in</strong> pr<strong>in</strong>ciple give rise to it, only one of<br />

<strong>the</strong>se should be selected.<br />

Plumatella gives ei<strong>the</strong>r Plumatto or Plumello but not Plumattello<br />

Valerianella gives ei<strong>the</strong>r Valranno or Valrello, not Valrannello<br />

6. Where <strong>the</strong> orig<strong>in</strong>al end<strong>in</strong>g is unclear or absent, <strong>the</strong> suffix –<br />

AZZ should be chosen as representative.<br />

Sylvia Silvazzo [from silv• = “forest, woods”]


9<br />

Specific names, subspecies <strong>in</strong>cluded, are to be<br />

expressed <strong>in</strong> <strong>the</strong> everyday common vocabulary of<br />

Uniespo, as follows, with no exception to <strong>the</strong> rules: 6<br />

* * * * * * *<br />

Dear reader, we appreciate that tackl<strong>in</strong>g Everyday Uniespo as well,<br />

might be ra<strong>the</strong>r more than you’d barga<strong>in</strong>ed for! But do you really prefer<br />

to have to cope with both a Greek and a Lat<strong>in</strong> dictionary? The<br />

compilation of a translat<strong>in</strong>g list Lat<strong>in</strong>-Uniespo-English for epi<strong>the</strong>ts <strong>in</strong><br />

biontology is at <strong>the</strong> plann<strong>in</strong>g stage <strong>in</strong> <strong>the</strong> form of a database file, should<br />

this need really be felt. So, <strong>in</strong> <strong>the</strong> meantime, <strong>the</strong> best course would be to<br />

use <strong>the</strong> ITK handbook <strong>in</strong> conjunction with one of <strong>the</strong> many easily<br />

obta<strong>in</strong>able Esperanto dictionaries — such as <strong>the</strong> two-way The Esperanto-<br />

English Dictionary by Dr. J.C. WELLS, <strong>in</strong> <strong>the</strong> well-known Teach Yourself<br />

Books, published by The English Universities Press; guaranteed a lot<br />

easier to consult than a Lat<strong>in</strong> handbook! The “old” Esperanto will serve<br />

perfectly well for render<strong>in</strong>g epi<strong>the</strong>ts, until Uniespo-dictionaries become<br />

available, s<strong>in</strong>ce on <strong>the</strong> everyday level of usage <strong>the</strong>re’s not all that much<br />

difference between <strong>the</strong>m, except for spell<strong>in</strong>g. So, get gourself The Key<br />

and an Esperanto dictionary — a small one will do quite well — and <strong>the</strong>n<br />

donate those complex Lat<strong>in</strong> and Greek volumes to a teacher of those<br />

languages.<br />

1. All specific names, be<strong>in</strong>g adjectives, end <strong>in</strong> -A: so no more<br />

doubt over which Lat<strong>in</strong> declension form should be used —<br />

<strong>the</strong>y no longer apply.<br />

rampans rampanta [“crawl<strong>in</strong>g”]<br />

lacciferum lakoporta [“lacquer-carry<strong>in</strong>g”]<br />

gyratus shpirala [“spiral”]<br />

2. As a wedge / l<strong>in</strong>kage — obligatory for this particular<br />

application — between <strong>the</strong> common word roots of a<br />

compound vernacular word, use one of <strong>the</strong>se:<br />

6<br />

-A if <strong>the</strong> lead<strong>in</strong>g stem is an adjective:<br />

picrococcus amarakerna [“bitter kernel”]<br />

It is noteworthy that <strong>the</strong> NBN-Association has established a<br />

considerable number of useful and pert<strong>in</strong>ent new epi<strong>the</strong>ta for zoology.<br />

21


22<br />

-O if <strong>the</strong> lead<strong>in</strong>g stem is a substantive:<br />

harpophyllus harponofolia [“harpoon-leafed”]<br />

-I if <strong>the</strong> lead<strong>in</strong>g stem is a verb:<br />

flexibilis fleksikapabla [”capable of bow<strong>in</strong>g”]<br />

-E if <strong>the</strong> lead<strong>in</strong>g stem is an adverb:<br />

campylonascis kurbekreska [”curved-grow<strong>in</strong>g”]<br />

3. Compound words <strong>in</strong>corporat<strong>in</strong>g a numeral, preposition, or<br />

<strong>the</strong> like, are spelled without a juncture element. Numerals<br />

have to be written <strong>in</strong> full:<br />

<strong>in</strong>termedius <strong>in</strong>termeta [“<strong>in</strong>termediate”]<br />

redivivus revivanta [“reliv<strong>in</strong>g”]<br />

sexdentatus sisdenta [“six-too<strong>the</strong>d”]<br />

familiaris malsovadzha [“unwild”]<br />

4. Although ord<strong>in</strong>ary words are to be preferred for this specific<br />

nam<strong>in</strong>g, <strong>in</strong> contrast with generic word-form<strong>in</strong>g, it is still<br />

possible to use a strictly technical term, taken from<br />

chemistry or anatomy for <strong>in</strong>stance, or <strong>the</strong> usual<br />

geographical concepts or even a codenumber:<br />

Melanogrammus aeglef<strong>in</strong>a Melanogramo sensheligebla<br />

= “peelable”; for <strong>the</strong> haddock. [French: aiglef<strong>in</strong>]<br />

but:<br />

Uragoga ipecacuanha Uragogo ipekaka, for <strong>the</strong> vomit-nut<br />

Rosa ch<strong>in</strong>ensis Rozo tsh<strong>in</strong>uja<br />

Human Papilloma Virus #16 Papilomusso deksesa<br />

5. Trivial names for plants and animals, as designated <strong>in</strong><br />

Uniespo are considered equivalent to technical terms. That<br />

goes for self-conta<strong>in</strong>ed s<strong>in</strong>gular words [see Rule 5], but not<br />

for titles or metaphors, us<strong>in</strong>g more than one word. Such<br />

names are to be dist<strong>in</strong>guished by add<strong>in</strong>g -noma (“named”)<br />

as a pseudo-suffix.


Clupea harengus Klupeo harengonoma [herr<strong>in</strong>g]<br />

Turdus merula Turdo merlonoma [blackbird]<br />

Falco cherrug Falko tsherugonoma<br />

[We borrowed this standard procedure from NBN.]<br />

The cowslip, Primula offic<strong>in</strong>alis, is popularly named “majfloro”<br />

[mayflower] <strong>in</strong> traditional Esperanto, but is scientifically named<br />

only as Primullo medits<strong>in</strong>a; although “majelomonata” [”(In <strong>the</strong>)<br />

month of May”] may do just as well for this epitethon.<br />

6. A morphological or behavioural feature should override any<br />

purely geographical notion.<br />

nilotica mevobeka<br />

[”from <strong>the</strong> Nile”] [”hav<strong>in</strong>g a gull’s beak”]<br />

caspia kritshanta<br />

[”caspian”] [”screech<strong>in</strong>g”]<br />

7. The semantic elements of a compound word are considered<br />

to be of equal value and quality. They are normally cited <strong>in</strong><br />

alphabetic order; but this sequence may be <strong>in</strong>versed if a<br />

synonym has to be co<strong>in</strong>ed with <strong>the</strong> same elements and<br />

mean<strong>in</strong>g.<br />

blugriza [”blue-grey”] preferable to grizablua [“grey-blue”]<br />

8. Once attributed under <strong>the</strong> new Taxonomy, a specific<br />

name/word should never be changed, even if <strong>the</strong> species at<br />

stake needs to be moved to ano<strong>the</strong>r genus. [For eventually<br />

ensu<strong>in</strong>g homonymy see Rule 29.2]<br />

Fr<strong>in</strong>gilla domesticus Passer domesticus <br />

Pasero familiara<br />

Taenia dim<strong>in</strong>uta Hymenolepis dim<strong>in</strong>uta <br />

Himenolepido plieta<br />

23


Ano<strong>the</strong>r ill-advised custom is tautonymy between<br />

10 genus and epi<strong>the</strong>ton. This should certa<strong>in</strong>ly be<br />

avoided, unless <strong>the</strong> repetition is not formal but only<br />

semantic (same mean<strong>in</strong>g but o<strong>the</strong>r word). This goes for <strong>the</strong><br />

subspecies too. Translation <strong>in</strong>to Uniespo will more often<br />

than not automatically br<strong>in</strong>g <strong>the</strong> necessary differentiation,<br />

anyway.<br />

24<br />

Cygnus cygnus Tsigno sovadzha [”wild”]<br />

Pica pica Pigo samnoma [”same-name”]<br />

Chloris chloris Xlorisso verdula [”green-one”]<br />

Gallus gallus Galjusso kokonoma [”rooster”]<br />

Genus and species names of a particular nature,<br />

11<br />

such as “uncerta<strong>in</strong> determ<strong>in</strong>ation, hypo<strong>the</strong>tical reconstruction,<br />

reference to ano<strong>the</strong>r genus”, are to be<br />

marked by a special flag, to <strong>the</strong> right of <strong>the</strong> word concerned,<br />

as an exponential symbol (o, +, ).<br />

alfataktsa o (reference to o<strong>the</strong>r genus)<br />

[stands for “refero”]<br />

betataktsa + (fossil or ext<strong>in</strong>ct species)<br />

[stands for “fosilia”]<br />

deltataktsa * (uncerta<strong>in</strong> identification)<br />

[stands for “maltserta”]<br />

Arthonia nephromiaria Artonio nefromma o<br />

(as dwell<strong>in</strong>g on <strong>the</strong> particular genus Nefrommo).<br />

Lernaea lusci Lernio gadussa o and not Lernio unuokula<br />

(because it is a copepod parasite on Gadus luscus).


Reference to some generic name, related or un-<br />

12 related, should <strong>the</strong>oretically be avoided, but cannot<br />

be ruled out <strong>in</strong> practice (parasitism!). Even more<br />

undesirable is <strong>the</strong> habit of referr<strong>in</strong>g to ano<strong>the</strong>r species,<br />

related or unrelated. But, if it really cannot be avoided, one<br />

can resort to <strong>the</strong> mention -spetsia (“species”) added as a tail<br />

to <strong>the</strong> normal epi<strong>the</strong>ton. Its tape-worm aspect will make <strong>the</strong><br />

name stand out as Hobson’s choice by itself ...<br />

Phaeospora granulosae Fajosporo grajnetsospetsia<br />

Polycoccum bryonthae Polykoktso muskokotospetsia<br />

Any scientific species name must consist of only<br />

13 one word. If two or more concepts are at stake,<br />

<strong>the</strong>y must be merged <strong>in</strong>to a s<strong>in</strong>gle compound.<br />

However, one should avoid weld<strong>in</strong>g more than two concepts<br />

toge<strong>the</strong>r. In such a case it is advisable to create a new<br />

name altoge<strong>the</strong>r. [see Rule 25]<br />

14<br />

New-Zealandian novazilenda<br />

terrae novae novalanda<br />

kwerka + betula (oak + birch) betulokwerka<br />

Acronyms and codes — as <strong>in</strong> microbiology — are<br />

admissible on condition <strong>the</strong>y obey <strong>the</strong> general<br />

nam<strong>in</strong>g procedures of Universal Taxonomy. 7<br />

“laser prone” laserosentema<br />

HIV homimunetsa<br />

An extremely important matter, where specific<br />

15<br />

names are concerned, is <strong>the</strong> characteristic(s)<br />

which <strong>the</strong>y are to express for typify<strong>in</strong>g a given<br />

species. These are normally drawn — and <strong>in</strong> <strong>the</strong> follow<strong>in</strong>g<br />

7 Universal Esperanto provides special rules for realms such as<br />

geology, astronomy, chemistry... and even jargon.<br />

25


order — from morphology, habits, habitat, region, and<br />

(alas!) also substituted by proper names. The trouble is that<br />

such typify<strong>in</strong>g particulars usually are ra<strong>the</strong>r limited <strong>in</strong><br />

number, whereas <strong>the</strong> species may run <strong>in</strong>to scores. This is<br />

particularly true for plants and animals on <strong>the</strong> lower rungs of<br />

<strong>the</strong> evolutionary ladder. Or, if <strong>the</strong>re are sufficient<br />

characteristics to choose from, more often than not <strong>the</strong>y are<br />

commonly shared by several species. Or, such<br />

characteristics may be short-lived or be just too particular,<br />

because <strong>the</strong>y are l<strong>in</strong>ked to sex, season, age. Also, a typical<br />

trait may be quite hidden from view, and appear only on<br />

very close <strong>in</strong>spection (microbiology!). So, <strong>the</strong> biologist often<br />

faces a dilemma and will resort to nonsensical words<br />

(treated under Rule 7).<br />

In view of <strong>the</strong>se difficulties it is utopian to suppose one can<br />

and must always f<strong>in</strong>d <strong>the</strong> exclusive characteristic, and<br />

set it down <strong>in</strong> <strong>the</strong> specific name. Therefore we should<br />

radically shift <strong>the</strong> helm by prescrib<strong>in</strong>g that, when <strong>the</strong> few<br />

really prom<strong>in</strong>ent and exclusive characteristics have been<br />

judiciously allotted, a list be made of all possible o<strong>the</strong>r<br />

characteristics. Then, <strong>the</strong> as yet unnamed members of <strong>the</strong><br />

group (= those <strong>in</strong> need of renam<strong>in</strong>g) will receive <strong>the</strong>m<br />

accord<strong>in</strong>g to an arbitrary distribution of <strong>the</strong> characteristics,<br />

such as <strong>the</strong> alphabetical order. Moreover, s<strong>in</strong>ce Uniespo<br />

(as well as Esperanto) is an agglut<strong>in</strong>ative language, <strong>the</strong>re<br />

are usually several ways to comb<strong>in</strong>e <strong>the</strong> elements of a given<br />

specific compound word, mak<strong>in</strong>g synonyms feasible and, <strong>in</strong><br />

this respect, even desirable. Besides which, a mean<strong>in</strong>gful<br />

epi<strong>the</strong>ton — even if erroneous — is a lot easier to<br />

remember!<br />

26<br />

The only really important consideration here is to make<br />

sure that a given species carry a characteristic name<br />

attached to no o<strong>the</strong>r species with<strong>in</strong> <strong>the</strong> same genus, even<br />

though eventually all <strong>the</strong> members of that generic group<br />

may lay claim to <strong>the</strong> very same characteristic !


It is precisely this stumbl<strong>in</strong>g-block of characteristic exclusiveness which<br />

defeats <strong>the</strong> rival NBN-project, mentioned before. This has led its<br />

advocates to produce a number of anagrammatic proper names, <strong>in</strong><br />

absolute contradiction with <strong>the</strong>ir declared policy of turn<strong>in</strong>g scientific<br />

names <strong>in</strong>to everyday language, so even <strong>the</strong> layman may understand<br />

what is meant. (See <strong>the</strong> application specimens for examples.)<br />

What about <strong>the</strong> particular end<strong>in</strong>gs for taxons,<br />

16<br />

such as Family, Order, and Class? Well, <strong>in</strong> <strong>the</strong><br />

Trimeral System <strong>the</strong>y utterly lose <strong>the</strong>ir function of taxon<br />

<strong>in</strong>dicators and will be seen no more!<br />

1. To replace <strong>the</strong>m, we now have some mean<strong>in</strong>gful<br />

suffixes perta<strong>in</strong><strong>in</strong>g to <strong>the</strong> sort of name used:<br />

-ARO for (high) taxons with vernacular names:<br />

Birdaro, Algaro, Fungaro, Mikrobiaro<br />

(Birds, Seaweed, Mushrooms, Microbes)<br />

-ESKOJ for “related to a given genus”:<br />

Ericacea Erikeskoj<br />

Blattidae Blateskoj<br />

-OJDOJ for “merely look<strong>in</strong>g like”:<br />

Nematoda Nematojdoj<br />

Omphalodes Omfalojdoj<br />

-ITOJ for “fossils”:<br />

Trilobita Trylobitoj<br />

Pterisospermidae Ptersospermitoj<br />

-ULOJ for “hav<strong>in</strong>g this common characteristic”<br />

Bryozoa Bryozouloj<br />

Cormophytae Kormofytuloj<br />

27


2. For <strong>the</strong> level of Family it is mandatory — and for taxons<br />

up to <strong>the</strong> level of Order, recommendable — to use <strong>the</strong><br />

end<strong>in</strong>g -ESK based on one of <strong>the</strong> relevant generic names<br />

(<strong>the</strong> chosen holotype).<br />

28<br />

Dermatemydidae Dermatemyseskoj<br />

Apocynareae Apokyneskoj<br />

3. It is possible to comb<strong>in</strong>e some of <strong>the</strong>se determ<strong>in</strong>ation<br />

suffixes.<br />

-OJDESKOJ from -OJD and -ESK<br />

-ITESKOJ from -IT and -ESK<br />

4. If a particular genus needs to be split <strong>in</strong>to several<br />

subgenera, <strong>the</strong>n it is <strong>the</strong> orig<strong>in</strong>al generic name which will<br />

receive <strong>the</strong> end<strong>in</strong>g -ESKOJ.<br />

Alfataktso<br />

Alfataktso Alfataktseskoj {<br />

Betataktso<br />

5. If a fossil form should prove to be still <strong>in</strong> existence or,<br />

<strong>in</strong>versely, a taxon become utterly ext<strong>in</strong>ct, it is sufficient to<br />

just alter <strong>the</strong> correspond<strong>in</strong>g suffix and/or flag.<br />

Coelacanth Koelakanto+ Koelakanto<br />

Raphus solitarius Rafjusso izolita Rafjusso izolita +<br />

6. It is customary to use vernacular names along with<br />

scientific names for <strong>the</strong> highest taxons. Universal<br />

Taxonomy does not want to decide between <strong>the</strong>se two<br />

and leaves <strong>the</strong> alternatives open for <strong>the</strong> specialists to<br />

choose.


Animals Bestaro / Terjarzhuloj<br />

Birds Birdaro / Aviarzhuloj<br />

Insects Insektaro / Entomarzhuloj<br />

Mollusks Molbestaro / Moluskarzhuloj<br />

Mushrooms Fungaro / Mykarzhuloj<br />

Plants Plantaro / Fytarzhuloj<br />

Seaweed Algaro / Fykarzhuloj<br />

7. If a given subspecies or genus, hav<strong>in</strong>g a name of its own,<br />

proves to be just a particular life-form of some o<strong>the</strong>r<br />

subspecies or genus, <strong>the</strong>n it is to lose its prior name and<br />

acquire <strong>the</strong> name of <strong>the</strong> subspecies or genus it really<br />

belongs to. If <strong>the</strong> species name is apposite it can be<br />

conserved; o<strong>the</strong>rwise it must be changed too.<br />

[compare Rule 10.9]<br />

Siredon pisciformis Amblystoma tigr<strong>in</strong>um<br />

= Amblystomo tigretsa [axolotl]<br />

Leptocephalus morrisii Anguilla anguilla<br />

= Angwillo palengonoma [eel]<br />

On <strong>the</strong> o<strong>the</strong>r hand, for ease of application and<br />

17<br />

conciseness, taxon names above <strong>the</strong> elementary<br />

level of Genus, (or a genus hav<strong>in</strong>g subgenera)<br />

MAY_be abbreviated to just a couple of syllables, provided<br />

<strong>the</strong>re is no immediate danger of confusion between <strong>the</strong>m.<br />

By putt<strong>in</strong>g this superior taxon name — which is a s<strong>in</strong>gle<br />

word — before a given generic name, one can at once put<br />

this genus <strong>in</strong> its wider sett<strong>in</strong>g and thus directly po<strong>in</strong>t to <strong>the</strong><br />

true nature of <strong>the</strong> subject. This procedure is certa<strong>in</strong>ly not<br />

superfluous if two (or more) generic names are complete<br />

homonyms, and each perta<strong>in</strong>s to different higher taxons or<br />

even to completely different realms. After all, many names,<br />

left to <strong>the</strong>mselves, are equivocal about whe<strong>the</strong>r <strong>the</strong>y perta<strong>in</strong><br />

29


to a plant or an animal, a bacterium or an elephant. [see<br />

Rule 20.2]<br />

30<br />

Gastrop• for Gastropoduloj (Gastropodidae)<br />

Fanerog• for Fanerogamuloj (Phanerogamae)<br />

1. This abbreviated form has to be marked by a capital letter<br />

at <strong>the</strong> beg<strong>in</strong>n<strong>in</strong>g and a po<strong>in</strong>t at <strong>the</strong> end, preferably by a<br />

midway dot as used <strong>in</strong> ma<strong>the</strong>matics. The normal number<br />

of syllables goes from one to four, although exceptions<br />

may occasionally occur to avoid homonymy.<br />

18<br />

Fag• for Fageskoj Fagales<br />

Abi• for Abieskoj Abietacea<br />

Shelyker• for Shelykereskoj Chelyceratae<br />

Konusofor• for Konusoforuloj Coniferophyta, Coniferae<br />

F<strong>in</strong>ally we come to <strong>the</strong> not unimportant matter of<br />

Orthography, valid for <strong>the</strong> Key <strong>in</strong> particular as well<br />

as for common Uniespo.<br />

1. All characters are pronounced as <strong>the</strong>y are written, and<br />

written as <strong>the</strong>y are pronounced, whatever <strong>the</strong>ir<br />

position<strong>in</strong>g, whatever speech sound comes before or<br />

after. 8 So <strong>the</strong> antique C and Q(ue) are gone —<br />

supplanted by ei<strong>the</strong>r S or K or TS.<br />

Consequently, no more variations of <strong>the</strong> sort: sutchuenensis,<br />

setchuenensis, szechuanensis, szechwanensis, setchwanensis,<br />

szechuenensis... but uniformly and simply: setshwanuja.<br />

[The suffix -U J stands for “land, region”]<br />

8 Uniespo also provides a system for transliteration of names from non-<br />

Lat<strong>in</strong> alphabets, called “Universala Skribo” (Universal Writ<strong>in</strong>g).


2. The characters used are those to be found <strong>in</strong> <strong>the</strong><br />

International Phonetic Alphabet (def<strong>in</strong>itely not equivalent<br />

to English usage!) and have precisely <strong>the</strong> same<br />

pronunciations, except for <strong>the</strong> follow<strong>in</strong>g digraphs: SH and<br />

ZH correspond respectively to sh <strong>in</strong> English show, and j<br />

<strong>in</strong> French journal. In fact <strong>the</strong>y ought to be <strong>the</strong> s<strong>in</strong>gle<br />

characters S and Z with a cedilla. If <strong>the</strong>se letters are not<br />

(yet) available on a given typewriter or text editor, one can<br />

use <strong>the</strong> Chech equivalents with a caret, or most simply<br />

SH and ZH <strong>in</strong>stead — as is done throughout this paper<br />

— which will do just as well. The two vowels O and E<br />

have (for English-speak<strong>in</strong>g people) very much <strong>the</strong><br />

phonetic values of e <strong>in</strong> bed and of o <strong>in</strong> lock. 9<br />

3. Digraphs (a pair of different letters for one phoneme)<br />

have been made ext<strong>in</strong>ct: PH is now always F; TH is now<br />

T; AE is now simply E or A; and so on. Therefore, all<br />

letters have to be <strong>in</strong>dividually pronounced, except for <strong>the</strong><br />

just mentioned temporary ZH and SH.<br />

Phacophyceae Fajofukuloj<br />

Thalarctos Talasarkto<br />

Elaeagnus Elajagno<br />

4. Diphthongs are written with a vowel plus j or w,<br />

<strong>in</strong>stead of i or u : -aj, -oj, -uj, -aw, -ew, etc.<br />

5. Because of Rule 18.1, one should try to make names as<br />

easily pronounceable as possible, avoid<strong>in</strong>g <strong>in</strong> particular a<br />

9 Interl<strong>in</strong>guists should make a note of <strong>the</strong> fact, that <strong>the</strong> spell<strong>in</strong>gs of new<br />

Uniespo and traditional Esperanto don’t entirely match up; e.g. new<br />

/ts/w/dž/ aga<strong>in</strong>st customary /c/ŭ / ĝ/ .<br />

31


32<br />

succession of more than two or three consonants.<br />

Sandhi-rules should be obeyed: pv pf, vk fk, tz <br />

ts, etc. ra<strong>the</strong>r than just import<strong>in</strong>g <strong>the</strong> orig<strong>in</strong>al spell<strong>in</strong>g<br />

forms. Such adaptations can also be used as a means of<br />

fur<strong>the</strong>r differentiation between homonyms!<br />

G<strong>in</strong>kgo G<strong>in</strong>ko<br />

Abudefduf Abudevdo<br />

6. Emphasis goes <strong>in</strong>variably on <strong>the</strong> penultimate syllable.<br />

Only exception: fancy names for cross-breeds [Rule 26].<br />

KryptogamUloj, BalenotsEpso, p<strong>in</strong>tanAza, ventrostrIa<br />

7. If <strong>the</strong> spell<strong>in</strong>g of a particular name should afterwards be<br />

found wrong, <strong>the</strong>re is now no more need to completely<br />

rename <strong>the</strong> group, but only and simply to correct <strong>the</strong><br />

name <strong>in</strong> <strong>the</strong> CBC, which anyone can consult anytime.<br />

Ambystomo Amblystomo<br />

riveropuda riverapuda<br />

8. Gem<strong>in</strong>ation (doubl<strong>in</strong>g of a letter) <strong>in</strong> a word stem is no<br />

longer allowed and must be substituted by some<br />

“euphonic” adaptation. (Only <strong>the</strong> special suffixes<br />

referred to <strong>in</strong> 8.1 are allowed such a digression.)<br />

Pyrrhocactus Pyrokakto<br />

Gekko Gekxo


Because of recent evolutions, Taxonomy f<strong>in</strong>ds itself <strong>in</strong> a<br />

sort of crisis. The realizations of cladism and genetics,<br />

treatable with powerful computer programmes<br />

(manipulation of numerous data at <strong>the</strong> same time <strong>in</strong> <strong>the</strong><br />

form of matrices) make it possible and imperative to<br />

revise <strong>the</strong> whole of traditional Systematics.<br />

[LA RECHERCHE, Nr.212, p.864]<br />

33


34<br />

3 - A Wholesome Threesome<br />

The time-honoured custom of signall<strong>in</strong>g <strong>the</strong> genus<br />

name as a noun (by its capital letter) and <strong>the</strong><br />

species name as an adjective (with lower case<br />

letter) may be considered <strong>the</strong> core around which <strong>the</strong> whole<br />

of taxonomy is constructed. There is no <strong>in</strong>tention of do<strong>in</strong>g<br />

away with this vested build<strong>in</strong>g block — <strong>in</strong> spite of <strong>the</strong> fact<br />

that “genus” is an extremely vague and highly subjective<br />

concept 10 19<br />

— but <strong>in</strong>stead add<strong>in</strong>g a third element <strong>in</strong> between<br />

<strong>the</strong> two already used, namely a taxon symbol. The<br />

elements of this new trimeral sequence of “Genus-Taxon-<br />

Species” will be referred to respectively as: dependent -<br />

relator - governor.<br />

Thus Acer campestre gets to be Atsero S kampara,<br />

and Lithobius forficatus becomes Litobio S tondila.<br />

At first glance, this may look like a mere cosmetic operation,<br />

but under <strong>the</strong> follow<strong>in</strong>g rules <strong>the</strong> reader will see that <strong>the</strong> new<br />

relator becomes a powerful tool for easy nam<strong>in</strong>g and<br />

recognition of taxons on higher and lower levels.<br />

Instead of <strong>the</strong> customary Lat<strong>in</strong> suffixes for<br />

20<br />

<strong>in</strong>dicat<strong>in</strong>g <strong>the</strong> taxon level (-formes, -ales, -acea, -<br />

idae, -<strong>in</strong>ae...) now a convenient relator is placed<br />

<strong>in</strong> front of <strong>the</strong> name — whe<strong>the</strong>r written/spoken <strong>in</strong> full, or <strong>in</strong><br />

<strong>the</strong> abbreviated form mentioned under Rule 17. It carries<br />

no full stop.<br />

10 We trust <strong>the</strong> CBC-procedure of Rule 2 will br<strong>in</strong>g better agreement and<br />

more stability about generic names, through its automated “majority<br />

vote”.


S<strong>in</strong>ce it is estimated that evolutionary embranchments will<br />

eventually reach up to 40 or 50 hierarchical levels, <strong>the</strong>n<br />

<strong>the</strong>oretically a taxonomy should provide dist<strong>in</strong>guish<strong>in</strong>g<br />

elements equal to <strong>the</strong> worst-case-scenario. Traditional<br />

nomenclature has at its disposal only a meagre handful of<br />

suffixes with which to meet this challenge. And although<br />

<strong>the</strong>y can be divided and subdivided by means of<br />

“subtaxons” and “supertaxons”, that measure would be no<br />

more than a palliative. Therefore, <strong>the</strong> list of taxon symbols<br />

has been made as numerous as possible — while keep<strong>in</strong>g<br />

<strong>the</strong>m well diversified, ordered, and recognisable. Their<br />

attribution and distribution, <strong>in</strong> work<strong>in</strong>g practice, is up to <strong>the</strong><br />

specialist; who can now be as detailed or generalised as<br />

desired, or as <strong>the</strong> ever <strong>in</strong>sufficient data will permit.<br />

The biological committees should supervise <strong>the</strong> nam<strong>in</strong>g and<br />

distribution of ALL taxons, from variety up to k<strong>in</strong>gdom, <strong>in</strong><br />

order to br<strong>in</strong>g unity to handbooks and schoolbooks all over<br />

<strong>the</strong> world. But perhaps this exact<strong>in</strong>g task would be taken<br />

over by <strong>the</strong> CBC anyway. Moreover, it should be a<br />

welcome opportunity for fill<strong>in</strong>g <strong>in</strong> <strong>the</strong> all too numerous blank<br />

spaces on <strong>the</strong> taxonomic map of Evolution.<br />

By means of <strong>the</strong>se relators it is now possible to move a<br />

whole taxon upwards or downwards at will, without hav<strong>in</strong>g<br />

to change <strong>the</strong> taxon name, irrespective of its end<strong>in</strong>g!<br />

M Imperio k<strong>in</strong>gdom T Tribo tribe<br />

P Fylalo phylum F Familio family<br />

B Brantsho branch G Genro genus<br />

K Klaso class S Spetsio species<br />

L Kladalo cladus R Raso race<br />

O Ordo order V Vario variety<br />

35


36<br />

H Hibridulo hybrid<br />

X Taktsalo taxon (any)<br />

Y Artefarito artefact<br />

Z Synbiawzo symbiosis<br />

In between F and T may be added a fur<strong>the</strong>r taxon N for “nation”<br />

(Natsio). T replaces “suborder”; L replaces “subclass”. H for<br />

hybrid is used for denot<strong>in</strong>g cross-breeds (chimeras) <strong>in</strong>capable of<br />

reproduc<strong>in</strong>g <strong>the</strong>mselves <strong>in</strong> Nature.<br />

1. Evidently, <strong>the</strong> sequence(s) of an official representation must<br />

follow <strong>the</strong> normal hierarchical order, left-to-right <strong>in</strong> text for topto-bottom<br />

<strong>in</strong> <strong>the</strong> table.<br />

Dicotylae Fanerog• G Dykotiledonuloj<br />

Lepadogaster Gobiez• G Lepasogastro<br />

2. Which higher taxon(s) are to be mentioned, or which to be left<br />

out, will be freely decided by <strong>the</strong> specialist <strong>in</strong> each context.<br />

There are no absolute rules here, o<strong>the</strong>r than always keep<strong>in</strong>g<br />

<strong>the</strong> trimeral array well <strong>in</strong> m<strong>in</strong>d, if not explicitly <strong>in</strong> writ<strong>in</strong>g.<br />

EXCESSIVE: Mandibl• Entom• Pter• Ektopter• Izopter• G Termito<br />

SUFFICIENT: Entom• L Pterentomontjuloj for <strong>the</strong> cladus Pterygota<br />

3. When a given name is valid for several hiqher taxons, <strong>the</strong><br />

system allows for putt<strong>in</strong>g <strong>the</strong> relators concerned one after <strong>the</strong><br />

o<strong>the</strong>r. It seems preferable, though not imperative, to keep<br />

<strong>the</strong>m separated by a blank space.<br />

Synpet• O F Rubleskoj for order & family Rublaceae<br />

Axenarzh• T F Tserveskoj for tribe & family Cervidae<br />

All right — acceptance of this new arrangement and its extra<br />

differentiation will almost certa<strong>in</strong>ly call for a lot of reshuffl<strong>in</strong>g among<br />

<strong>the</strong> traditional taxons. But <strong>the</strong>n, we don’t get “owt for nowt”, do<br />

we? Besides, th<strong>in</strong>k of <strong>the</strong> peace, stability, and unity which must<br />

f<strong>in</strong>ally ensue !


4. In <strong>the</strong> spoken language it may prove practical to use <strong>the</strong><br />

alternative NBN-proposal of add<strong>in</strong>g -(taktsal)anoj (“taxon<br />

members”) to <strong>the</strong> basic name.<br />

O Delfeneskoj = “Delfenordanoj”<br />

When <strong>in</strong>corporat<strong>in</strong>g a scientific name <strong>in</strong>to a<br />

21 text, <strong>the</strong>re is no longer any need to make its<br />

particular status stand out aga<strong>in</strong>st <strong>the</strong> environment<br />

of normal language, by giv<strong>in</strong>g it a special emphasis such as<br />

(<strong>the</strong> usual) italics. The relator takes over this function<br />

perfectly well. One is now even at liberty to leave out <strong>the</strong><br />

genus name altoge<strong>the</strong>r and use only <strong>the</strong> species name<br />

preceded by its relator — provided, of course, that <strong>the</strong><br />

context makes it clear which genus it refers to.<br />

“Speak<strong>in</strong>g about Borago, its species name S medits<strong>in</strong>a (spec.<br />

offic<strong>in</strong>alis) gets its name from <strong>the</strong> ancient practice of us<strong>in</strong>g it to<br />

make wounds close up quickly.”<br />

“Snake birds, like G Anh<strong>in</strong>go (Anh<strong>in</strong>ga), pursue and catch fish<br />

under water.”<br />

As usual, subspecies are also def<strong>in</strong>ed by an extra<br />

22<br />

adjective put after <strong>the</strong> normal species adjective.<br />

Here, however, <strong>the</strong> taxon symbol is subdivided by<br />

an <strong>in</strong>dex<strong>in</strong>g cross. Everyth<strong>in</strong>g said about species names<br />

applies also to <strong>the</strong> subspecies names — particularly<br />

avoidance of tautonymy — except for <strong>the</strong> custom of<br />

employ<strong>in</strong>g mostly geographical concepts. [For varieties and<br />

races see Rule 27]. Decid<strong>in</strong>g, which subspecies has to be<br />

considered as typical of <strong>the</strong> whole group, is a very vexed<br />

question, which might better be left to <strong>the</strong> CBC-programme<br />

of Rule 2, mak<strong>in</strong>g a choice at random...<br />

37


38<br />

Motacilla flava flava Motatsillo gelba S+ belguja<br />

Motacilla thunbergi Motatsillo gelba S+ skand<strong>in</strong>ava<br />

Motacilla flavissima Motatsillo gelba S+ brituja<br />

Motacilla feldeggi Motatsillo gelba S+ balkana<br />

23<br />

Supertaxons are notated with an exponentially<br />

placed cross, and subtaxons with an <strong>in</strong>dexed<br />

cross.<br />

Thus K Kar<strong>in</strong>uloj (Car<strong>in</strong>ates) can, if one wishes, be degraded<br />

without more ado to subclass K+ Kar<strong>in</strong>uloj or be promoted to<br />

superclass K + Kar<strong>in</strong>uloj; <strong>the</strong> name itself never needs to be<br />

changed, <strong>in</strong> sharp contrast with today’s usage.<br />

1. If a species should become a (sub)genus <strong>in</strong> itself, <strong>the</strong>n<br />

<strong>the</strong> common language epi<strong>the</strong>ton has to be turned <strong>in</strong>to a<br />

standardized substantive.<br />

Anaso S platabeka (“flat-beak”) Anas• G+ Platyrynxo or<br />

(if homonymy threatens) G+ Rynxoplatyo [fictitious example]<br />

It rema<strong>in</strong>s a sound practice to select a given<br />

24<br />

species as representative for <strong>the</strong> whole genus (<strong>the</strong><br />

holotype); <strong>the</strong>n a given genus for <strong>the</strong> whole family, and so<br />

on up <strong>the</strong> scale. Obviously, whichever is selected as typical<br />

should be a precisely determ<strong>in</strong>ed and widely known<br />

species.<br />

1. In <strong>the</strong> present Universal Taxonomy this is expressed by<br />

plac<strong>in</strong>g <strong>the</strong> relator between square brackets, <strong>in</strong>dicative of<br />

“taxon type” (“genus type, family type, subspecies<br />

type”). This <strong>in</strong> turn facilitates unified representation <strong>in</strong><br />

general reference books, so that <strong>the</strong> same specimen of<br />

plant, animal, or m<strong>in</strong>eral will always be used for a<br />

representative illustration. Moreover <strong>the</strong> relators may be<br />

judiciously comb<strong>in</strong>ed.


Anas platyrhynchos Anaso [S] platabeka = “(genro)tipa”<br />

Accord<strong>in</strong>g to NBN, <strong>the</strong> best-known and described species among<br />

Cetacea (whales) is Tursiops truncatus, <strong>the</strong> bottle-nosed dolph<strong>in</strong>,<br />

mak<strong>in</strong>g it even typical for <strong>the</strong> whole order; <strong>the</strong>refore it should<br />

take <strong>the</strong> name Turshopsho [OS] trunkigita = “ordotipa” [from<br />

tursh• “shuttle” and opsh• “aspect”] <strong>in</strong> Universal Taxonomy.<br />

2. It seems preferable to name a superior taxon after still<br />

liv<strong>in</strong>g groups, ra<strong>the</strong>r than select a fossil for holotype,<br />

even if <strong>the</strong> fossils happen to be (far) more numerous.<br />

Platanacea [K] Plataneskoj “plane-trees”<br />

Xiphosura [O] Ksifuvreskoj “horseshoe-crabs”<br />

3. Of course, if a given generic holotype ought to be<br />

regarded as belong<strong>in</strong>g to ano<strong>the</strong>r family, <strong>the</strong>n it must be<br />

transferred <strong>the</strong>re and <strong>the</strong> former family name will have to<br />

be changed accord<strong>in</strong>g to a holotype newly selected from<br />

among its rema<strong>in</strong><strong>in</strong>g genera... and so on for higher<br />

taxons.<br />

F Alfataktseskoj<br />

changed to:<br />

| [G] Alfataktso<br />

| G Betataktso<br />

| G Gamataktso<br />

F Betataktseskoj | [G] Betataktso<br />

| G Gamataktso<br />

and:<br />

F Deltataktseskoj |<br />

|<br />

G Alfataktso<br />

[G] Deltataktso<br />

| G Zetataktso<br />

4. A subspecies can also be selected as holotype for <strong>the</strong><br />

species.<br />

S rudzhatiga S+ sibiruja [“red-twigged”]<br />

S rudzhatiga [S+] nordafrika = “spetsitipa”<br />

39


5. Group<strong>in</strong>gs by means of a holotvpe, hav<strong>in</strong>g <strong>the</strong> end<strong>in</strong>g<br />

–ESK, can go up to <strong>the</strong> level of order (Ordo), but this is<br />

not mandatory. Whenever a holotype of any hierarchical<br />

level is absent — i.e. has not yet been determ<strong>in</strong>ed — <strong>the</strong><br />

end<strong>in</strong>g -ESK becomes naturally unusable.<br />

6. If a family of genera is too loosely bound for determ<strong>in</strong><strong>in</strong>g<br />

a holotype, <strong>the</strong>n <strong>the</strong> family name will have to be a<br />

characteris<strong>in</strong>g word end<strong>in</strong>q on -ULOJ or a vernacular<br />

group name with simply -ARO as an end<strong>in</strong>g <strong>in</strong>stead of -<br />

ESKOJ. This applies also to taxons higher up.<br />

40<br />

Agamofilaria X Agamofiluloj<br />

Diplistomulum X Diplostomuloj<br />

From all <strong>the</strong> preced<strong>in</strong>g Rules it should be clear, that<br />

25 <strong>the</strong>re is no longer any need to <strong>in</strong>corporate <strong>the</strong><br />

name of <strong>the</strong> author who first determ<strong>in</strong>ed <strong>the</strong><br />

species, nor <strong>the</strong> year <strong>in</strong> which this memorable event took<br />

place, as demanded by <strong>the</strong> now obsolete Priority Rule.<br />

Biological Nomenclature has better purposes to serve than<br />

be a memorial to past human endeavour!<br />

Botany and Zoology both should accept race<br />

(Raso) as a (sub)form for a subspecies and, if yet<br />

ano<strong>the</strong>r deviation from this taxon occurs, <strong>the</strong><br />

conceptual symbol of variety (Vario) 11 26<br />

i.e. cultivar. The same<br />

goes for hybrids.<br />

11 A question to consider is whe<strong>the</strong>r or not <strong>the</strong> notion of "regional<br />

subspecies" should be abandoned, and "race" become used <strong>in</strong>stead.


Syr<strong>in</strong>ga vulgaris Charles X = Sir<strong>in</strong>go S ord<strong>in</strong>ara V KARLES’<br />

Clematis lanup<strong>in</strong>osa x viticella = Clematis Jackmani<br />

= Klematisso H DZHAKMAN’<br />

Race as well as Variety consists — just like <strong>the</strong><br />

27<br />

species — of a s<strong>in</strong>gle name, written <strong>in</strong> capital letters<br />

and end<strong>in</strong>g with an apostrophe to <strong>in</strong>dicate that stress<br />

now lies on <strong>the</strong> last syllable. Contrary to Rule 17.6, it is (to<br />

be) regarded as a fancy proper name and must be spelled as<br />

a true Uniespo-word; <strong>the</strong> orig<strong>in</strong>al (ethnic) orthography will be<br />

utterly disregarded and titles reduced to a s<strong>in</strong>gle word of two<br />

to three syllables. Its form can be taken ei<strong>the</strong>r from <strong>the</strong><br />

orig<strong>in</strong>al spell<strong>in</strong>g or from <strong>the</strong> orig<strong>in</strong>al pronunciation, depend<strong>in</strong>g<br />

on which is easiest to render.<br />

Narcissus pseudonarcissus var. Queen Victoria <br />

Nartsiso S shajna V VIKTORI ‘<br />

var. Amethyst V AMETYST ‘<br />

var. Chocolate Soldier V TSHOKLAT ‘<br />

1. If <strong>the</strong> orig<strong>in</strong>al name is too short or ends on a difficult array<br />

of consonants, <strong>the</strong> vowel -u should be added.<br />

var. Bosc V BOSKU ‘<br />

rac. Dogue R DOGU ‘<br />

2. Where practicable, a name or title may be translated <strong>in</strong>to<br />

common Uniespo. [Here too, eventual homonymy<br />

(isonymy) may be countered by Rule 29.2]<br />

var. Sunsh<strong>in</strong>e V SUNBRIL‘<br />

rac. Bouvier R BOVUL‘ [”ox-dog”]<br />

After all, changes brought about by humans (genetic eng<strong>in</strong>eer<strong>in</strong>g)<br />

are fundamentally no different from those worked by Mo<strong>the</strong>r Nature.<br />

41


3. For fur<strong>the</strong>r differentiations (at this level!), all sorts of<br />

anagrams are permissible — contrary to Rule 7.6 —<br />

which is made possible by <strong>the</strong> particular nature of <strong>the</strong>se<br />

names.<br />

42<br />

var. Alexander V ALEKSANT ‘<br />

var. Alexandra V LEKSANDRA ‘<br />

var. Alexandr<strong>in</strong>a V KSANDRINA ‘<br />

4. Such adaptations of fancy orig<strong>in</strong>als should be reta<strong>in</strong>ed<br />

even if an orig<strong>in</strong>al name has been patented as “trade<br />

name” for a cultivar or breed <strong>in</strong> commercial respect. Of<br />

course, it would be a great bonus if <strong>the</strong> Patent Office(s)<br />

as well as horticulturists and breeders agreed to<br />

accept<strong>in</strong>g only norm-abid<strong>in</strong>g names!<br />

28<br />

Real synonyms (different names for one and <strong>the</strong><br />

same subject) must and will no doubt become<br />

impossible through <strong>the</strong> automated CBC [Rule 2].<br />

Ei<strong>the</strong>r Natrix natrix or Coluber natrix or Tropidonotus natrix<br />

for <strong>the</strong> r<strong>in</strong>g-snake, but not all three considered valid, as actually<br />

found <strong>in</strong> three different handbooks!<br />

29<br />

Last but not least, homonyms (<strong>the</strong> same name for<br />

different subjects) are not allowed with<strong>in</strong> <strong>the</strong> SAME<br />

taxon, but are to be tolerated if each belongs to a DIFFERENT<br />

superior taxon. It is to be expected that this sort of conflict<br />

will become of particular importance <strong>in</strong> <strong>the</strong> co-ord<strong>in</strong>ated<br />

BioCode. In such a case it is advisable to put <strong>the</strong> superior<br />

taxon name <strong>in</strong> front of <strong>the</strong> homonymic name, at least once.


That is to say: whichever superior taxon really makes <strong>the</strong><br />

difference.<br />

Meropsheskoj G Meropsho Insekt• G Meropsho<br />

Meropsheskoj G Meropsho Bird• G Meropsho<br />

1. Homonyms result<strong>in</strong>g from a mere misspell<strong>in</strong>g will be<br />

corrected without any more fuss.<br />

G Ambystomo G Amblystomo<br />

S blankodenta S blankadenta<br />

2. Whenever homonymy becomes <strong>in</strong>evitable, for lack of<br />

sufficient dist<strong>in</strong>guish<strong>in</strong>g features (compressible to a<br />

s<strong>in</strong>gle word), it can easily be neutralised by apply<strong>in</strong>g<br />

Greek numerals as prefixes plus a hyphen.<br />

30<br />

Larus fuscus Larusso -nigradorsa [“black-backed”]<br />

Larus mar<strong>in</strong>us Larusso -nigradorsa<br />

var. Fantasie V -FANTAZI ‘<br />

var. Fantasy V -FANTAZI ‘<br />

var. Phantasy V -FANTAZI ‘<br />

As to trivial names, which need not be as rigorous<br />

as scientific names, <strong>the</strong> task must be left to...<br />

creative poets.<br />

Aletris & Liatris brilsteleto [“blaz<strong>in</strong>g star”]<br />

Cocc<strong>in</strong>ella Di-skarabeto [“ladybird”]<br />

43


44<br />

4.1 – Specimens for Botany<br />

MOULDS, FUNGI, MUSHROOMS<br />

High taxon layout based on:<br />

Encyclopédie Bordas, Paris - Volume 10 - “La vie des plantes”<br />

> Barr<strong>in</strong>g mistakes and omissions <<br />

FUNGI B MYKOFYTULOJ / FUNGARO<br />

Ascomycetes K Askomykuloj<br />

Discomycetidae L Kyklomykuloj<br />

Heliotales O Hevlotteskoj<br />

Helotiacea [F] Hevlotteskoj<br />

Phacidiacea F Pfakedjeskoj<br />

Pezizales O Pezizeskoj<br />

Helvellacea F Helvelleskoj<br />

Pezizacea [F] Pezizeskoj<br />

Rhiz<strong>in</strong>acea F Ridz<strong>in</strong>neskoj<br />

Tuberales O Tuberulleskoj<br />

Tuberacea [F] Tuberulleskoj<br />

Loculomycetidae L Loklomykuloj<br />

Dothiorales O Dotjorruloj<br />

Myriangiales O Mirjangiuloj<br />

Pseudosphaeriales O Psewdosferuloj<br />

Pyrenomycetidae L Pirenemykuloj<br />

Laboulbeniales O Entomomykuloj<br />

Clavicipitales O Klavjotsepseskoj<br />

Sphaeriales O Sferuloj<br />

Plectomycetidae L Pleksomykuloj<br />

Erysiphales O Erysifneskoj<br />

Erysiphacea [F] Erysifneskoj<br />

Plectascales O Pleksaskuloj


Aspergillacea F Spergilleskoj<br />

Protascomycetidae L Protaskomykuloj<br />

Saccharomycetidae O Saxaromykeskoj<br />

Saccharomycetacea [F] Saxaromykeskoj<br />

Taphr<strong>in</strong>ales O Tafr<strong>in</strong>neskoj<br />

Taphr<strong>in</strong>acea [F] Tafr<strong>in</strong>neskoj<br />

Basidiomycetes K Bashedjomykuloj<br />

Exobasidiales L Ektobashedjeskoj<br />

Exobasidiacea [F] Ektobashedjeskoj<br />

Phragmobasidiomyce L Fragmobashedjomykuloj<br />

tidae Auriculariales O Awrikkeskoj<br />

Auriculariacea [F] Awrikkeskoj<br />

Tremellales O Tremelleskoj<br />

Tremellacea [F] Tremelleskoj<br />

Ured<strong>in</strong>ales O Ured<strong>in</strong>neskoj<br />

Endophyllacea F Endofyleskoj<br />

Melampsoracea F Melanopsoreskoj<br />

Pucc<strong>in</strong>iacea F Putsh<strong>in</strong>ieskoj<br />

Ustilag<strong>in</strong>ales O Ustilaggeskoj<br />

Tilletiacea F Tiletieskoj<br />

Ustilag<strong>in</strong>acea [F] Ustilaggeskoj<br />

Gasteromycetes L Gastromykuloj<br />

Hynenogasteracea F Himenogastreskoj<br />

Hysterangiacea F Hystrangieskoj<br />

Lycoperdacea F Lykoperdneskoj<br />

Nidulariacea F Nidulleskoj<br />

Phallacea F Pfalusseskoj<br />

Holobasidiomycetes L Holobashedjeskoj<br />

Hymenomycetales O Himenomykuloj<br />

Agaricacea F Agarikeskoj<br />

Hydnaceae F Hydnezzeskoj<br />

45


Clavariacea F Klavjarreskoj<br />

Polyporaceae F Polyporeskoj<br />

Thelephoraceae F Teljoforeskoj<br />

Phycomycetes K Fykomykuloj<br />

Blastocladiales O Blastokladeskoj<br />

Blastocladiaceae [F] Blastokladeskoj<br />

Endogonales O Endogoneskoj<br />

Endogonaceae [F] Endogoneskoj<br />

Entomophtorales O Entomoftoreskoj<br />

Entomophtoraceae [F] Entomoftoreskoj<br />

Hyphochytriales O Hyfoxytreskoj<br />

Hyphochytriaceae [F] Hyfoxytreskoj<br />

Monoblepharidales O Monablefareskoj<br />

Monoblepharidaceae [F] Monablefareskoj<br />

Mucorales O Mukorreskoj<br />

Mucoraceae [F] Mukorreskoj<br />

Pilobolaceae F Piluboluseskoj<br />

Peronosporales O Pernosporeskoj<br />

Albug<strong>in</strong>aceae F Albugeskoj<br />

Peronosporaceae [F] Pernosporeskoj<br />

Plasmodiophorales O Plasmodoforeskoj<br />

Plasmodiophoraceae [F] Plasmofoforeskoj<br />

Saprolegniales O Saprolegneskoj<br />

Saprolegniaceae [F] Saprolegneskoj<br />

Chytridiales O Xytrisseskoj<br />

Chytridiaceae [F] Xytrisseskoj<br />

46


4.2 NON-LICHENIZED LICHEN-DWELLING FUNGI<br />

Low taxon list based on <strong>the</strong> well detailed and illustrated<br />

determ<strong>in</strong>ation handbook by<br />

Clauzade, Diederich, & Roux: Nelikeniĝ<strong>in</strong>taj fungoj likenloĝaj<br />

Société l<strong>in</strong>néenne de Provence, Marseille 1989<br />

> Barr<strong>in</strong>g mistakes and omissions <<br />

Ascomycot<strong>in</strong>a Klaso Askomykuloj<br />

Abrothallus acetabuli Abrotsalo S atsetabla<br />

Abrothallus bertianus Abrotsalo S kalvidzh<strong>in</strong>ta<br />

Abrothallus cetrariae Abrotsalo S gajlestiga<br />

Abrothallus chrysanthus Abrotsalo S avrumaflora<br />

Abrothallus cladoniae Abrotsalo S senranda<br />

Abrothallus mairei Abrotsalo S ebenadiska<br />

Abrothallus microspermus Abrotsalo S etasema<br />

Abrothallus parmelianum Abrotsalo S shildaro<br />

Abrothallus parmotrematis Abrotsalo S trushilda<br />

Abrothallus peyritshii Abrotsalo S senprujnuma<br />

Abrothallus prodiens Abrotsalo S elstara<br />

Abrothallus suecicus Abrotsalo S -brunaspora<br />

Abrothallus usneae Abrotsalo S bartohava<br />

Abrothallus welwitzchii Abrotsalo S -brunaspora<br />

Act<strong>in</strong>opelis peltigericola Akt<strong>in</strong>opeltso S peltsogera o<br />

Adelococcus alpestris Aedelokoktso S alpomonta<br />

Adelococcus groedensis Aedelokoktso S arafrukta<br />

Adelococcus lecanorae Aedelokoktso S raravanda<br />

Agyr<strong>in</strong>a crozalsii Egyr<strong>in</strong>no S verdetafrukta<br />

Agyrium cephalodioides Egyrummo S dukapa<br />

Anthostomella apogyra Antostomo S netavanda<br />

Apiosporella mongolica Apisporo S mongoluja<br />

Arthonia amylospora Artonio S amelospora<br />

47


Arthonia atropunctata Artonio S nigrapunta<br />

Arthonia basidiospora Artonio S bashedjospora<br />

Arthonia caerulescens Artonio S profundeblua<br />

Arthonia c<strong>in</strong>nabar<strong>in</strong>ula Artonio S ts<strong>in</strong>abra<br />

Arthonia circ<strong>in</strong>ata Artonio S tsirklostara<br />

Arthonia clemens Artonio S dekliveta<br />

Arthonia crypto<strong>the</strong>ciae Artonio S kashateka<br />

Arthonia curreyi Artonio S renospora<br />

Arthonia destruens Artonio S detrua<br />

Arthonia epimela Artonio S pirotshela<br />

Arthonia epiphyscia Artonio S surkolbasa<br />

Arthonia ericetorum Artonio S falsaranda<br />

Arthonia excentrica Artonio S ekstera<br />

Arthonia far<strong>in</strong>acea Artonio S farunetsa<br />

Arthonia fuscopurpura Artonio S brunapurpura<br />

Arthonia galact<strong>in</strong>aria Artonio S melkablanka<br />

Arthonia gelidae Artonio S frostama<br />

Arthonia glaucomaria Artonio S verdashultra<br />

Arthonia <strong>in</strong>sidiens Artonio S entruda<br />

Arthonia <strong>in</strong>sitiva Artonio S pleneshtopita<br />

Arthonia <strong>in</strong>texta Artonio S enplektita<br />

Arthonia lepidophila Artonio S bastoshata<br />

Arthonia mazoziae Artonio S konuseta<br />

Arthonia microsticta Artonio S makuleta<br />

Arthonia molendoi Artonio S v<strong>in</strong>omembrana<br />

Arthonia neglectula Artonio S nerimarkebla<br />

Arthonia nephromiaria Artonio S nefromma o<br />

Arthonia nideri Artonio S magraspora<br />

Arthonia oligospora Artonio S raraspora<br />

Arthonia oxyspora Artonio S p<strong>in</strong>taspora<br />

Arthonia peltigera Artonio S -shildoporta<br />

48


Arthonia peltiger<strong>in</strong>a Artonio S -shildoporta<br />

Arthonia pelvetii Artonio S tutamonda<br />

Arthonia phlyctidicola Artonio S fliktidda o<br />

Arthonia punctella Artonio S puntohava<br />

Arthonia rubescens Artonio S rudzhidzhanta<br />

Arthonia sphyridii Artonio S elipsospora<br />

Arthonia subconveniens Artonio S malkonvena<br />

Arthonia subvelut<strong>in</strong>ae Artonio S velureta<br />

Arthonia tabescens Artonio S sekidzhanta<br />

Arthonia urceolata Artonio S pokaletsa<br />

Arthonia varia Artonio S variema<br />

Arthopyrenia microspila Artapirno S makuleta<br />

Arthrorhaphis citr<strong>in</strong>ella Artrorafjo S tsitrona<br />

Arthrorhaphis grisea Artrorafjo S griza<br />

Ascohansfordiellopsis <strong>in</strong>sectivora Askokarpello S <strong>in</strong>sektomandzha<br />

Bacidia killiasi Batsidio S rondafrukta<br />

Barya lichenophila Baryazzo S likenoshata<br />

Broomella leptogiicola Brumelio S shp<strong>in</strong>ilospora<br />

Buellia adjuncta Buelio S aldona<br />

Buellia badia Buelio S dikavanda<br />

Buellia brachyspora Buelio S kurtaspora<br />

Buellia destructans Buelio S detruanta<br />

Buellia imshaugii Buelio S bluidzha<br />

Buellia leptolepis Buelio S maldikaskwama<br />

Buellia nivalis Buelio S nedzhablanka<br />

Buellia pseudosaxatilis Buelio S malaper<strong>in</strong>ta<br />

Buellia pulverulenta Buelio S polvoplena<br />

Buelliella m<strong>in</strong>imala Bueliello S m<strong>in</strong>imala<br />

Buelliella physciicola Bueliello S fyskizza O<br />

Buelliella pusilla Bueliello S malgrandeta<br />

Buelliella trype<strong>the</strong>lii Bueliello S truhawta<br />

49


Caliciella parasitica Kalyksello S parazita<br />

Calicium corynellum Kalyksummo S nigrafrukta<br />

Calicium ret<strong>in</strong>ens Kalyksummo S firmetena<br />

Calicium subparoicum Kalyksummo S lepratsala<br />

Capronia peltigerae Kapronio S shildoporta<br />

Carbonea supersparsa Karbonno S disestara<br />

Carbonea vitell<strong>in</strong>aria Karbonno S ovogelbaspetsia<br />

Catillaria mediterranea Katlarro S mediteranea<br />

Cercidospora caudata Kerkosporo S vosta<br />

Cercidospora collematum Kerkosporo S koljemma o<br />

Cercidospora epipolytropa Kerkosporo S multadirekta<br />

Cercidospora lichenicola Kerkosporo S surlikena<br />

Cercidospora stereocaulorum Kerkosporo S sterekawla o<br />

Cercidospora ulothii Kerkosporo S shp<strong>in</strong>ilospora<br />

Chaeno<strong>the</strong>copsis brevipes Xaenotekopsho S kurtapieda<br />

Chaeno<strong>the</strong>copsis consociata Xaenotekopsho S komunuma<br />

Chaeno<strong>the</strong>copsis epithall<strong>in</strong>a Xaenotekopsho S surtsala<br />

Chaeno<strong>the</strong>copsis exserta Xaenotekopsho S elstara<br />

Chaeno<strong>the</strong>copsis haematopus Xaenotekopsho S sangapieda<br />

Chaeno<strong>the</strong>copsis koerberi Xaenotekopsho S nigrakapa<br />

Chaeno<strong>the</strong>copsis nigra Xaenotekopsho S nigra<br />

Chaeno<strong>the</strong>copsis nigropedata Xaenotekopsho S nigrapieda<br />

Chaeno<strong>the</strong>copsis pusilla Xaenotekopsho S malgrandeta<br />

Chaeno<strong>the</strong>copsis pusiola Xaenotekopsho S brunapodiska<br />

Chaeno<strong>the</strong>copsis rubescens Xaenotekopsho S rudzhidzha<br />

Chaeno<strong>the</strong>copsis rub<strong>in</strong>a Xaenotekopsho S rudzha<br />

Chaeno<strong>the</strong>copsis sagenidii Xaenotekopsho S sagnedja o<br />

Chaeno<strong>the</strong>copsis sangu<strong>in</strong>ea Xaenotekopsho S sangofarba<br />

Chaeno<strong>the</strong>copsis savonica Xaenotekopsho S -brunaspora<br />

Chaeno<strong>the</strong>copsis tasmanica Xaenotekopsho S -brunaspora<br />

50


Chaeno<strong>the</strong>copsis treichelianum Xaenotekopsho S lentokapa<br />

Chaeno<strong>the</strong>copsis va<strong>in</strong>oana Xaenotekopsho S verdahypoteka<br />

Chaeno<strong>the</strong>copsis viridialba Xaenotekopsho S verdablanka<br />

Chaeno<strong>the</strong>copsis viridireagens Xaenotekopsho S verdareaga<br />

Clypeococcum cladonema Klypekoktso S brantshidzha<br />

Clypeococcum grossum Klypekoktso S dika<br />

Clypeococcum hypocenomyces Klypekoktso S hypotsenomyka o<br />

Clypeococcum placopsiphilum Klypekoktso S plakopsha o<br />

Cyphelium sessile Tsyfello S sidanta<br />

Dactylospora acarosporae Daktylosporo S akarospora<br />

Dactylospora athall<strong>in</strong>a Daktylosporo S rudzhepiteka<br />

Dactylospora frigida Daktylosporo S malvarma<br />

Dactylospora glaucomarioides Daktylosporo S verdashultra<br />

Dactylospora hafellneriana Daktylosporo S unuvanda<br />

Dactylospora homocl<strong>in</strong>ella Daktylosporo S samekl<strong>in</strong>a<br />

Dactylospora <strong>in</strong>quil<strong>in</strong>a Daktylosporo S hejmesida<br />

Dactylospora lamyi Daktylosporo S kupolodiska<br />

Dactylospora lobariella Daktylosporo S bruneksipura<br />

Dactylospora parasitica Daktylosporo S parazita<br />

Dactylospora parellaria Daktylosporo S brunepiteka<br />

Dactylospora pertusaricola Daktylosporo S pertsarra o<br />

Dactylospora placophylla Daktylosporo S tabulofolia<br />

Dactylospora porphyrea Daktylosporo S purpura<br />

Dactylospora protothall<strong>in</strong>a Daktylosporo S prototsala<br />

Dactylospora rimulicola Daktylosporo S fendolodzha<br />

Dactylospora saxatilis Daktylosporo S rokoshata<br />

Dactylospora tegularum Daktylosporo S tegoletsa<br />

Dactylospora urceolata Daktylosporo S krutsheta<br />

Decampia engeliana Dekampio S miskoloriga<br />

Decampia hookeri Dekampio S shp<strong>in</strong>ilospora<br />

Decampia rufescentis Dekampio S rufidzhaspetsia<br />

51


Dichosporium glomeratum Dixosporo S glomeridzha<br />

Didymella aipoliae Didmello S tshiamgriza<br />

Didymella berengeriana Didmello S bruneksipura<br />

Didymella brunii Didmello S shwelaska<br />

Didymella cladoniae Didmello S kladonna o<br />

Didymella crozalsiana Didmello S malmultafrukta<br />

Didymella epicarph<strong>in</strong>ea Didmello S surpajla<br />

Didymella epimelanostola Didmello S surnigravesta<br />

Didymella mart<strong>in</strong>atiana Didmello S simplaparafiza<br />

Didymella parvispora Didmello S etaspora<br />

Didymella perigena Didmello S tshirkawnaska<br />

Didymella sph<strong>in</strong>ctr<strong>in</strong>oides Didmello S kunpremitetsa<br />

Didymella weillii Didmello S anastoma<br />

Diplonaevia parmeliae Diplonajvo S parmella o<br />

Diploschistes act<strong>in</strong>ostomus Diplosxizo S radibusha<br />

Diploschistes scruposus Diplosxizo S raspa<br />

Discocera lichenicola Kyklokerato S likenolodzha<br />

Disco<strong>the</strong>cium <strong>in</strong>festans Kykloteko S damadzha<br />

Dothidea lichenum Dotidio S likena<br />

Ech<strong>in</strong>otecium cladoniae Ex<strong>in</strong>oteko S kladonna o<br />

Ech<strong>in</strong>otecium reticulatum Ex<strong>in</strong>oteko S retoforma<br />

Endococcus alectoriae Endokoktso S alektorra o<br />

Endococcus alpestris Endokoktso S alpomonta<br />

Endococcus araneosus Endokoktso S aranereta<br />

Endococcus exerrans Endokoktso S elmigra<br />

Endococcus gyrophorarum Endokoktso S tsirkloporta<br />

Endococcus nanellus Endokoktso S naneta<br />

Endococcus pariet<strong>in</strong>arius Endokoktso S paried<strong>in</strong>na o<br />

Endococcus prop<strong>in</strong>quus Endokoktso S parentsa<br />

Endococcus ramal<strong>in</strong>arius Endokoktso S ramnalla o<br />

52


Endococcus rugulosus Endokoktso S fajnafalda<br />

Endococcus stigma Endokoktso S stigma<br />

Endococcus zahlbrucknerellae Endokoktso S zalbruknella o<br />

Epilichen clauconigellus Epilikeno S blunigra<br />

Epilichen scabrosus Epilikeno S krudega<br />

Guignardia ahlesiana Gignardio S brunafrukta<br />

Guignardia fimbriatae Gignardio S frandzha<br />

Guignardia micro<strong>the</strong>lia Gignardio S etatsala<br />

Guignardia olivieri Gignardio S gajlovezika<br />

Guignardia psoromoides Gignardio S skabietsa<br />

Guignardia verrucicola Gignardio S verukolodzha<br />

Hemigrapha astericus Hemigrafo S stelara<br />

Homostegia encaustica Xomostego S enbruligita<br />

Homostegia parmeliana Xomostego S parmelia o<br />

Homostegia piggotii Xomostego S trivanda<br />

Karschia l<strong>in</strong>itaria Karshio S brunepiteka<br />

Karschia pertusariae Karshio S pertsarra o<br />

Karschia santessonii Karshio S brunamedola<br />

Karschia sordidae Karshio S malpura<br />

Karschia talcophila Karshio S polvoshata<br />

Keratosphaera batistae Keratosfero S kashamykura<br />

Koordersiella deightonii Kordersio S senparafiza<br />

Lachnella tetraspora Laxnello S kwarspora<br />

Lasiosphaeriopsis salisburyi Lasisferopsho S tsharbostroma<br />

Lasiosphaeriopsis stereocaulicola Lasisferopsho S sterekawla o<br />

Lecidea aggregantula Letsidio S kunvena<br />

Lecidea associata Letsidio S asotsia<br />

Lecidea cladoniaria Letsidio S kladonna o<br />

Lecidea dispersula Letsidio S dissemita<br />

Lecidea frigidella Letsidio S fridoshata<br />

Lecidea <strong>in</strong>qu<strong>in</strong>ans Letsidio S makuliza<br />

53


Lecidea <strong>in</strong>sidiosa Letsidio S <strong>in</strong>sidega<br />

Lecidea neglecta Letsidio S nerimarkitaspetsia<br />

Lecidea oroantarctica Letsidio S sudapolusamonta<br />

Lecidea perforans Letsidio S traboritaspetsia<br />

Lecidea punctum Letsidio S punteta<br />

Lecidea superjecta Letsidio S surkovrita<br />

Lecidea thallicola Letsidio S tsalolodzha<br />

Lecidea umbonella Letsidio S dzhibeta<br />

Lecidea verrucariae Letsidio S veruketsa<br />

Leciographa associata Lekshografo S grupigita<br />

Leciographa attendenda Lekshografo S atent<strong>in</strong>da<br />

Leciographa dubia Lekshografo S dub<strong>in</strong>da<br />

Leciographa furfuracea Lekshografo S argiletsa<br />

Leciographa gyrolophii Lekshografo S turnikresta<br />

Leciographa nephromatis Lekshografo S renogloba<br />

Leciographa parvula Lekshografo S malgrandeta<br />

Leciographa physciaria Lekshografo S veziketsa<br />

Leciographa rhyparizae Lekshografo S rapidoradika<br />

Leciographa stigma Lekshografo S makula<br />

Leciographa weissii Lekshografo S nigrafrukta<br />

Leciographa zwackhii Lekshografo S dikepiteka<br />

Leptosphaeria clarkii Leptosferazzo S helabrunaspora<br />

Leptosphaeria crozalsii Leptosferazzo S sporokwaropa<br />

Leptosphaeria geographicola Leptosferazzo S ridzokarpa o<br />

Leptosphaeria maheui Leptosferazzo S r<strong>in</strong>od<strong>in</strong>a o<br />

Leptosphaeria pycnostigma Leptosferazzo S densamakula<br />

Leptosphaeria ramal<strong>in</strong>ae Leptosferazzo S ramnalla o<br />

Leptosphaerul<strong>in</strong>a peltigera Leptosferullo S peltsogera o<br />

Lethariicola siperi Letarrotsholo S radifenda<br />

Lichenostigma maureri Likenostigmo S falsahista<br />

Lichenostigma rugosa Likenostigmo S faldoplena<br />

54


Melanopsamma lettauiana Melanopsamo S diferentsospora<br />

Melaspilea canariensis Melanoshpilo S kanari<strong>in</strong>sula<br />

Melaspilea epigena Melanoshpilo S surnaskidzha<br />

Melaspilea leciographoides Melanoshpilo S sternidiska<br />

Melaspilea lentig<strong>in</strong>osa Melanoshpilo S lentugara<br />

Melaspilea rhododendri Melanoshpilo S rjododendra o<br />

Melaspilea tenellula Melanoshpilo S malmola<br />

Merismatium coccisporum Merisso S kuglospora<br />

Merismatium lecanorae Merisso S senr<strong>in</strong>ga<br />

Merismatium nigritellum Merisso S nigretsa<br />

Metasphaeria plurisepta Metasfero S pluravanda<br />

Metasphaeria superveniens Metasfero S supredvena<br />

Metasphaeria tartar<strong>in</strong>a Metasfero S <strong>in</strong>fera<br />

Microcalicium arenarium Mikrokalykso S sablogrunda<br />

Microcalicium conversum Mikrokalykso S renversita<br />

Microcalicium dissem<strong>in</strong>atum Mikrokalykso S dissemita<br />

Micropeltopsis cetrariicola Mikropeltsopsho S ketraria o<br />

Microtelia m<strong>in</strong>or Mikroteljo S malgranda<br />

Microthyrium cetrariae Mikrotyrso S ketraria o<br />

Microthyrium maculans Mikrotyrso S makulara<br />

Mollisia collematis Molisio S koljemma o<br />

Mollisia lesda<strong>in</strong>ii Molisio S lekanora o<br />

Muellerella atricola Myleriello S nigraspetsia o<br />

Muellerella hospitans Myleriello S gastanta<br />

Muellerella lichenicola Myleriello S likenolodzha<br />

Muellerella polyspora Myleriello S multspora<br />

Muellerella pygmaea Myleriello S pigmea<br />

Muellerella stict<strong>in</strong>ae Myleriello S stiktazza o<br />

Muellerella triseptata Myleriello S trivanda<br />

Muellerella vesicularia Myleriello S vezika<br />

Mycobilimbia acervata Mykob<strong>in</strong>alembo S stakita<br />

55


Mycobilimbia amoldiana Mykob<strong>in</strong>alembo S briladiska<br />

Mycobilimbia endocarpicola Mykob<strong>in</strong>alembo S enfrukta<br />

Mycobilimbia subfuscae Mykob<strong>in</strong>alembo S bruneta<br />

Mycobilimbia tetramera Mykob<strong>in</strong>alembo S kwarparta<br />

Myxotrichum bicolor Mykotrixo S dukolora<br />

Nanostictis peltigerae Pumelostikto S peltsogera o<br />

Nectria epicallopisma Neksarro S epikaliopsha o<br />

Nectria <strong>in</strong>sidiosa Neksarro S <strong>in</strong>sidega<br />

Nectria lecanodes Neksarro S harofrukta<br />

Nectria <strong>in</strong>digens Neksarro S enlanda<br />

Nectria lichenophila Neksarro S likenoshata<br />

Nectria parmeliae Neksarro S almiela<br />

Nectria rigidiuscula Neksarro S rigideta<br />

Nectria rubefasciens Neksarro S rudzhaspekta<br />

Nectriella erythr<strong>in</strong>ella Neksello S eritr<strong>in</strong>na o<br />

Nectriella leptaleae Neksello S leptalla<br />

Nectriella ornamentata Neksello S ornamita<br />

Nectriella robergei Neksello S orandzhafrukta<br />

Nectriella santessoni Neksello S rudzhafrukta<br />

Nectriella subimperspicua Neksello S nekomprenebla<br />

Nectriella tenacis Neksello S tenatsa<br />

Nectriella tenuispora Neksello S fajnaspora<br />

Nectriella t<strong>in</strong>cta Neksello S punta<br />

Nectriella verrucariae Neksello S hevlarra o<br />

Neolamya peltigerae Neolamio S peltsogera o<br />

Nesolechia ceras<strong>in</strong>a Nezolekto S brunepiteka<br />

Nesolechia coccocarpiae Nezolekto S koktsokarpa o<br />

Nesolechia diversispora Nezolekto S diversaspora<br />

Nesolechia oxyspora Nezolekto S -shp<strong>in</strong>ilospora<br />

Nesolechia oxysporiza Nezolekto S -shp<strong>in</strong>ilospora<br />

Nesolechia xenophona Nezolekto S verdepiteka<br />

56


Niesslia cladoniicola Nislio S kladonna o<br />

Niptera lichenicola Niptero S kladonna o<br />

Niptera microscopica Niptero S malgrandeta<br />

Nitschkiopsis stictarum Nitshkiopsho S stiktazza o<br />

Norrl<strong>in</strong>ia peltigericola Norl<strong>in</strong>io S peltsogera o<br />

Obryzum corniculatum Obryzo S korniketsa<br />

Opegrapha brevis Opegrafo S mallonga<br />

Opegrapha brigant<strong>in</strong>a Opegrafo S brigantia o<br />

Opegrapha maculans Opegrafo S makula<br />

Opegrapha melanospila Opegrafo S nigramakula<br />

Opegrapha pulv<strong>in</strong>ata Opegrafo S remburazha<br />

Opegrapha quaternella Opegrafo S kwaropa<br />

Opegrapha r<strong>in</strong>od<strong>in</strong>ae Opegrafo S kirlileda<br />

Opegrapha saxatilis Opegrafo S rokoshata<br />

Opegrapha stigmodes Opegrafo S tsikatra<br />

Opegrapha <strong>the</strong>lotrematis Opegrafo S teljotremta o<br />

Ophiobolus aspiciliae Ofibolo S harashilda<br />

Ophiobolus barbarus Ofibolo S barbara<br />

Ophiobolus thallicola Ofibolo S tsalolodzha<br />

Orbicula buellia Orbikko S buelia o<br />

Orbicula variolariae Orbikko S pustula<br />

Orbilia cocc<strong>in</strong>ella Orbilio S purpurakerna<br />

Orbilia peltigerae Orbilio S peltsogera o<br />

Paranectria aff<strong>in</strong>is Paranekso S parentsa<br />

Paranectria oropensis Paranekso S shp<strong>in</strong>ilospora<br />

Paranectria superba Paranekso S superba<br />

Pezizella epithall<strong>in</strong>a Pezizio S surtsala<br />

Phacopsis campestricola Pfakopsho S kamparaspetsia<br />

Phacopsis crustulosae Pfakopsho S krustoplenaspetsia<br />

Phacopsis ericetorum Pfakopsho S erikeja<br />

Phacopsis geographici Pfakopsho S teroglobospetsia<br />

57


Phacopsis huuskonenii Pfakopsho S helahimenura<br />

Phacopsis lesda<strong>in</strong>ii Pfakopsho S purpurahimenura<br />

Phacopsis usneae Pfakopsho S usnea o<br />

Phacopsis vulp<strong>in</strong>a Pfakopsho S vulporudzhaspetsia<br />

Phaespora can<strong>in</strong>ae Fajosporo S ord<strong>in</strong>aregaspetsia<br />

Phaespora catolechiae Fajosporo S kawtolekta o<br />

Phaespora consocians Fajosporo S kunligidzha<br />

Phaespora corae Fajosporo Spupila<br />

Phaespora decolorans Fajosporo S senkoloriga<br />

Phaespora exoriens Fajosporo S entruda<br />

Phaespora fritzei Fajosporo S densagrupa<br />

Phaespora granulosae Fajosporo S grajnetsaspetsia<br />

Phaespora parasitica Fajosporo S parazita<br />

Phaespora parmeliarum Fajosporo S parmelia o<br />

Phaespora peltigericola Fajosporo S peltsogera o<br />

Phaespora peregr<strong>in</strong>a Fajosporo S fremda<br />

Phaespora rimosicola Fajosporo S fendolodzha<br />

Phaespora subantarctica Fajosporo S sudapolusa<br />

Phaespora supersparsa Fajosporo S dissemita<br />

Phaespora triplicantis Fajosporo S trioblidzha<br />

Phaesporis <strong>in</strong>terlatens Fajosporisso S <strong>in</strong>terkshitaspetsia<br />

Phaesporis melasperma Fajosporisso S nigrasemaspetsia<br />

Phaesporis phaeosperma Fajosporisso S rudzhasemaspetsia<br />

Phaesporis podzimekii Fajosporisso S kwartsita<br />

Pharcidia arthoniae Farkiddo S artonia o<br />

Pharcidia coarctate Farkiddo S kunpremita<br />

Pharcidia collematis Farkiddo S gluifita<br />

Pharcidia coniodes Farkiddo S konusetsa<br />

Pharcidia constrictella Farkiddo S kunligita<br />

Pharcidia cupularis Farkiddo S pokaletsa<br />

Pharcidia dealbans Farkiddo S kurbaspora<br />

58


Pharcidia ephebes Farkiddo S belajunula<br />

Pharcidia epiramal<strong>in</strong>a Farkiddo S -ramnalla o<br />

Pharcidia epiramal<strong>in</strong>a Farkiddo S -ramnalla o<br />

Pharcidia frigida Farkiddo S fridama<br />

Pharcidia haesitans Farkiddo S alglua<br />

Pharcidia hygrophila Farkiddo S humidoshata<br />

Pharcidia lacustris Farkiddo S lagoshata<br />

Pharcidia lichenicola Farkiddo S likenolodzha<br />

Pharcidia maritima Farkiddo S tshemara<br />

Pharcidia microspora Farkiddo S etaspora<br />

Pharcidia porocyphi Farkiddo S kurbaspora<br />

Pharcidia punctillum Farkiddo S puntizita<br />

Pharcidia ramal<strong>in</strong>ae Farkiddo S -ramnalla o<br />

Pharcidia rivolorum Farkiddo S rivereta<br />

Pharcidia thall<strong>in</strong>a Farkiddo S tiga<br />

Pharcidia verrucarium Farkiddo S veruka<br />

Phragmonaevia fuckelii Fragmonajvo S najlospora<br />

Phragmonaevia peltigerae Fragmonajvo S peltsogera o<br />

Physalospora aspiciliae Fysosporo S aspidotsilia o<br />

Physalospora collematis Fysosporo S koljemma o<br />

Physalospora friesii Fysosporo S senvandaspora<br />

Physalospora lecanorae Fysosporo S lekanora o<br />

Physalospora leptogiophila Fysosporo S sekagrunda<br />

Physalospora xanthoriae Fysosporo S ksantorra o<br />

Plagiostoma cahirensis Plagjostomo S egitpuja<br />

Plagiostoma conductrix Plagjostomo S kunigita<br />

Plagiostoma prasiolae Plagjostomo S ajletsa<br />

Plagiostoma solor<strong>in</strong>ae Plagjostomo S solor<strong>in</strong>a o<br />

Plectocarpon lichenum Pleksokarpo S likena<br />

Plectocarpon pseudosticta Pleksokarpo S shajnamakula<br />

Pleoscutula arsenii Pleiskutlo S heteroderma o<br />

59


Pleospilis ascaridiella Pleishpilo S vermoforma<br />

Pleosphaeria lichenothricis Pleisfero S likenotrixa o<br />

Pleospora collematum Pleisporo S koljemma o<br />

Pleospora crozalsii Pleisporo S disstarafrukta<br />

Pleospora leptogiicola Pleisporo S leptogga o<br />

Pleospora peripherica Pleisporo S tshirkawanta<br />

Plowrightia mereschkowskyi Plorixtio S surshela<br />

Polyblastia dim<strong>in</strong>uta Polyblasta S malgrandigita<br />

Polyblastia discrepans Pleisporo S malakorda<br />

Polycoccum arnoldii Polykoktso S netavanda<br />

Polycoccum bryonthae Polykoktso S muskokotaspetsia<br />

Polycoccum cartilag<strong>in</strong>osum Polykoktso S kartilaga<br />

Polycoccum cladoniae Polykoktso S kladonia o<br />

Polycoccum crassum Polykoktso S ornamispora<br />

Polycoccum dzieduszyckii Polykoktso S elipsaspora<br />

Polycoccum epicrassum Polykoktso S surdikazha<br />

Polycoccum galligenum Polykoktso S gajlofara<br />

Polycoccum gelidarium Polykoktso S glatsiejaspetsia<br />

Polycoccum <strong>in</strong>natum Polykoktso S ennaskita<br />

Polycoccum jamesii Polykoktso S multafrukta<br />

Polycoccum kerneri Polykoktso S tsaljodetrua<br />

Polycoccum marmoratum Polykoktso S marmora<br />

Polycoccum microsticticum Polykoktso S etapuntara<br />

Polycoccum opulentum Polykoktso S fruktoplena<br />

Polycoccum peltigerae Polykoktso S peltsogera o<br />

Polycoccumrugulosarium Polykoktso S fajnafalda<br />

Polycoccum sporastatiae Polykoktso S sporostatsa<br />

Polycoccum squamarioides Polykoktso S skwametsa<br />

Polycoccum t<strong>in</strong>antii Polykoktso S verukospora<br />

Polycoccum trype<strong>the</strong>lioides Polykoktso S tsalobora<br />

Polycoccum umbilicarae Polykoktso S omfalarra o<br />

60


Polycoccum vermicularium Polykoktso S vermetsa<br />

Polycoccum versisporum Polykoktso S diversaspora<br />

Polyschistes mairei Polysxizo S elstarafrukta<br />

Proto<strong>the</strong>lenella crocae Prototeljenno S safrana<br />

Proto<strong>the</strong>lenella santessoni Prototeljenno S surskwama<br />

Pyrenidium act<strong>in</strong>ellum Pirnedjo S radiara<br />

Pyrenidium hetairizans Pirnedjo S okopaspora<br />

Pyrgidium montellicum Pyrgedjo S montetaspetsia<br />

Rhagadostoma lichenicola Ragostomo S likena<br />

Rhizocarpon advenulum Ridzokarpo S zhusven<strong>in</strong>ta<br />

Rhizocarpon malenconianum Ridzokarpo S galjlofara<br />

Rhizocarpon schedomyces Ridzokarpo S apudfunga<br />

Rhynchomeliola lichenicola Rynxomelyo S surlikena<br />

R<strong>in</strong>od<strong>in</strong>a <strong>in</strong>sularis R<strong>in</strong>od<strong>in</strong>o S surlikena<br />

Rosell<strong>in</strong>ia aspera Rosel<strong>in</strong>io S kruda<br />

Rosell<strong>in</strong>ia cladoniae Rosel<strong>in</strong>io S kladonna o<br />

Rosell<strong>in</strong>ia nephromatis Rosel<strong>in</strong>io S nefromma o<br />

Rosell<strong>in</strong>ula frustulosae Rosel<strong>in</strong>iullo S disspetsigitaspetsia<br />

Rosell<strong>in</strong>ula haplospora Rosel<strong>in</strong>iullo S simplaspora<br />

Rosell<strong>in</strong>ula kalbii Rosel<strong>in</strong>iullo S multaspora<br />

Rosell<strong>in</strong>ula lopadii Rosel<strong>in</strong>iullo S multabrantsha<br />

Sarcopyrenia gibba Sarxopirno S dzhiba<br />

Sarea aurellae Sareo S avrumaspetsia<br />

Scutula aff<strong>in</strong>is Skutlazzo S parentsa<br />

Scutula aggregata Skutlazzo S amasigita<br />

Scutula aspicilliae Skutlazzo S aspidotsilia o<br />

Scutula cristata Skutlazzo S kombila<br />

Scutula epicladonia Skutlazzo S kladonna o<br />

Scutula epiphylla Skutlazzo S surfolia<br />

Scutula episema Skutlazzo S sursema<br />

Scutula krempelhuberi Skutlazzo S brunepiteta<br />

61


Scutula leptogica Skutlazzo S maldiketsa<br />

Scutula leptogii Skutlazzo S leptogea o<br />

Scutula miliaris Skutlazzo S etagrajna<br />

Scutula ramal<strong>in</strong>ae Skutlazzo S ramnalla o<br />

Scutula solor<strong>in</strong>aria Skutlazzo S solor<strong>in</strong>arra o<br />

Scutula stereocaulorum Skutlazzo S sterekawla o<br />

Scutula tuberculosa Skutlazzo S tuberara<br />

Skyttea cruciata Skytio S krutsigita<br />

Skyttea fusispora Skytio S shp<strong>in</strong>ilospora<br />

Skyttea hawksworthii Skytio S striofrukta<br />

Skyttea nitschkei Skytio S turbanospora<br />

Skyttea sp<strong>in</strong>osa Skytio S dorsa<br />

Skytella muelleri Skytiello S elipsospora<br />

Sphaerul<strong>in</strong>a chlorococca Sferullo S verdaglobeta<br />

Sphaerul<strong>in</strong>a dolichotera Sferullo S longaspetsia<br />

Sphaerul<strong>in</strong>a dubiella Sferullo S maltserta<br />

Sphaerul<strong>in</strong>a endococcoidea Sferullo S englobetsa<br />

Sphaerul<strong>in</strong>a <strong>in</strong>termedia Sferullo S enmeza<br />

Sphaerul<strong>in</strong>a lepidiotae Sferullo S skwametsa<br />

Sphaerul<strong>in</strong>a parvipuncta Sferullo S punteta<br />

Sphaerul<strong>in</strong>a tabac<strong>in</strong>ae Sferullo S tabaka<br />

Sph<strong>in</strong>ctr<strong>in</strong>a anglica Sf<strong>in</strong>t<strong>in</strong>no S angluja<br />

Sph<strong>in</strong>ctr<strong>in</strong>a leucopoda Sf<strong>in</strong>t<strong>in</strong>no S blankapieda<br />

Sph<strong>in</strong>ctr<strong>in</strong>a tubiformis Sf<strong>in</strong>t<strong>in</strong>no S tuboforma<br />

Sph<strong>in</strong>ctr<strong>in</strong>a turb<strong>in</strong>ata Sf<strong>in</strong>t<strong>in</strong>no S tsirkla<br />

Spolver<strong>in</strong>ia punctum Spolverio S punta<br />

Stegia vermicularis Stegazzo S vermetospetsia<br />

Stictis cladoniae Stiktisso S kladonna o<br />

Stigmidium aggregatum Stigmedjo S kungrupa<br />

Stigmidium allogenum Stigmedjo S malegala<br />

Stigmidium dispersum Stigmedjo S dissemita<br />

62


Stigmidium eucl<strong>in</strong>e Stigmedjo S belekl<strong>in</strong>a<br />

Stigmidium fuscatae Stigmedjo S malhelaspetsia<br />

Stigmidium glebarum Stigmedjo S alglua<br />

Stigmidium hageniae Stigmedjo S konusofrukta<br />

Stigmidium icmadophilae Stigmedjo S ikmofila o<br />

Stigmidium mar<strong>in</strong>um Stigmedjo S tshemara<br />

Stigmidium peltidae Stigmedjo S peltsogera o<br />

Stigmidium schaereri Stigmedjo S malegalatshela<br />

Stigmidium solor<strong>in</strong>arium Stigmedjo S soljor<strong>in</strong>a o<br />

Stigmidium stygnospilum Stigmedjo S makulatsha<br />

Stigmidium superpositum Stigmedjo S supresida<br />

Stratisporella episemoides Stratsosporo S sursema<br />

Strongyleuma albipes Strongolewso S blankapieda<br />

Synaptospora tartaricola Synapsosporo S tartaruja<br />

Telimena foreaui Telmenno S longaspora<br />

Teratoschaeta rondoniensis Tatrosheto S multabrantsha<br />

Thamnogalla crombei Tamnogalgo S vezikiza<br />

Thelidium parvum Teljedjo S malgranda<br />

Thelocarpon epibolum Teljokarpo S surholtsa<br />

Thelocarpon epithall<strong>in</strong>um Teljokarpo S surtsalja<br />

Thelocarpon lichenicola Teljokarpo S surlikena<br />

Trematosphaeria dermatocaponis Tremtosfero S dermatokarpa o<br />

Trematosphaeria lophiostoma Tremtosfero S vertotrua<br />

Trichonectria hirta Trixonekso S hirta<br />

Trichosphaeria lichenum Trixosfero S surlikena<br />

Tryblidaria capensis Trybliddo S sudafrika<br />

Tryblidaria lusitanica Trybliddo S portugaluja<br />

Unguiculariopsis lichenicola Unglopsho S surlikena<br />

Verrucaria congestula Hevlarro S kunprema<br />

Weddellomyces epicallopisma Wedelio S kalopia o<br />

63


64<br />

4.3 RACES (VARIETIES) OF PEARS<br />

Alexander Lucas R LYKAS ‘<br />

André Desportes R DEPORT '<br />

Beurré Hardy R BERARDI '<br />

Bonne Louise d’Avranches R DAVRANTSH '<br />

Bosc R BOSKU '<br />

Bristol Cross R BRISTOS '<br />

Charnue R KARNUL ' “fleshy one”<br />

Clapp’s Favourite R FAVORIT '<br />

Clara Frijs R KLARAF '<br />

Colorée de juillet R JULIKOLOR ' “July’s colour”<br />

Comte de Chambord R DESHAMBOR '<br />

Comtesse de Paris R PARIZULIN ' “Parisian woman”<br />

Conférence R KONFERENTS '<br />

Conseiller de la Cour R KONSILIST ' “councellor<br />

Doyenné de Comice R DUKOMIS '<br />

Doyenné de juillet R JULIDEKAN ' “July’s deacon”<br />

Doyenné de Mérode R DEMEROT '<br />

Dr. Jules Huyot R WIJOT '<br />

Durandeau R DURANDU '<br />

Early Market R FRUMERKAT '<br />

Épargne R ELSHPAR '’ “sav<strong>in</strong>gs”<br />

Eva Baltet R EVABALT '<br />

Gieser Wildemanspeer R SOVADZHUL ' “savage one”<br />

Giffard R GIFART '<br />

Gøteborgs Diamant R DIAMANT ' “diamond”<br />

Gråpäron R GRIZPIR ' “grey pear”<br />

Hodge R HODZHU '<br />

Hofstade R HOFSTAT '<br />

Höstbergamott R HOSTAMOT '<br />

Joséph<strong>in</strong>e de Mal<strong>in</strong>es R JOSMALIN '<br />

Laxton’s Superb R LAKSTON '<br />

Légipont R LEGIPONT '<br />

Lübecker Bergamott R LYBEKOT '


Marguerite Marillat R MARILAT '<br />

Marie-Louise R MARILIS '<br />

Moltke R MOLKE '<br />

Påskpäron R PASKOPIR ' “Easter pear”<br />

Précoce de Trévoux R FRUAPER ' “early arrival”<br />

Sa<strong>in</strong>t-Rémy R SANTREM '<br />

Seckel R SETSKEL '<br />

Skånskt R PLEJBEL ' “loveliest”<br />

Sockerpäron R SUKERPIR ' “sugar pear”<br />

Souvenir du Congrès R KONGRESAN ' “Congressist”<br />

Triomphe de Vienne R VIENAVENK ' “Viennese triumph”<br />

Tyson R TAJSON '<br />

Williams R WILIAMS '<br />

W<strong>in</strong>ter Williams R WINTERWIL '<br />

Worden Seckel R WORDENSEK '<br />

The only rule for [spell<strong>in</strong>g correctly] <strong>the</strong> gender of<br />

generic names, it appears to me, is:<br />

one must memorise <strong>the</strong> genders case by case !<br />

[The same goes for] different gender term<strong>in</strong>ations of<br />

nouns from <strong>the</strong> classic languages.<br />

[F BOERNER]<br />

65


66<br />

5.1 – Specimens for Zoology<br />

BIRDS<br />

High taxon layout based on:<br />

Encyclopédie Bordas, Paris - Volume 1 - “La vie animale”<br />

> Barr<strong>in</strong>g mistakes and omissions ! <<br />

AVES B AVJARZHOJ / BIRDOJ<br />

Archaeorni<strong>the</strong>s L Arxornituloj<br />

Archaeopterygiformes O + Arxoptereskoj<br />

Neorni<strong>the</strong>s L Neornituloj<br />

Leptopterygales O + Leptopteruloj<br />

Sphenisciformes O Sfenikkeskoj<br />

Spheniscidae [F]Sfenikkeskoj<br />

Struthioniformes O Struteskoj<br />

Apterygidae F Aeptereskoj<br />

Casuariidae F Kaswareskoj<br />

Dromalidae F Dromalleskoj<br />

Rheidae F Rejazzeskoj<br />

Struthionidae [F]Struteskoj<br />

T<strong>in</strong>amiformes O T<strong>in</strong>ameskoj<br />

T<strong>in</strong>amiidae [F]T<strong>in</strong>ameskoj<br />

Stenopterygales O + Stenopteruloj<br />

Anseriformes O Ansereskoj<br />

Anatidae F Anaseskoj<br />

Anhimidae F Anhimeskoj<br />

Anseridae [F] Ansereskoj<br />

Apudiformes O Apuseskoj<br />

Apodidae [F]Apuseskoj<br />

Caprimulgiformes O Erifomulgeskoj<br />

Caprimulgidae [F]Erifomulgeskoj


Charadriiformes O Xaradrusseskoj<br />

Alcidae F Alkeskoj<br />

Charadriidae [F]Xaradrusseskoj<br />

Laridae F Larusseskoj <br />

Scolopacidae F Sklopakkeskoj<br />

Ciconiiformes O Tsikonieskoj<br />

Ardeidae F Ardeeskoj<br />

Balaenicipitidae F Tsetotsepseskoj<br />

Ciconiidae [F] Tsikonieskoj<br />

Coliiformes O Kolieskoj<br />

Coliidae [F] Kolieskoj<br />

Columbiformes O Kolombeskoj<br />

Columbidae [F] Kolombeskoj<br />

Pterochidae F Pteroxeskoj<br />

Coraciiformes O Korakeskoj<br />

Alced<strong>in</strong>idae F Altsedeskoj<br />

Coraciidae [F]Korakeskoj<br />

Meropidae F Meropeskoj<br />

Upupidae F Upupeskoj<br />

Cuculiformes O Kukoleskoj<br />

Cuculidae [F]Kukoleskoj<br />

Falconiformes O Falkeskoj<br />

Accipitridae F Aktsipitreskoj<br />

Cathartidae F Kataresseskoj<br />

Falconiidae [F] Falkeskoj<br />

Sagittariidae F Sagitarreskoj<br />

Galliformes O Galjusseskoj<br />

Galliidae [F] Galjusseskoj<br />

Megapodidae F Megapodeskoj<br />

Phasianidae F Fazaneskoj<br />

Tetraonidae F Tetronneskoj<br />

67


Gaviifomres O Gavieskoj<br />

Gaviidae [F] Gavieskoj<br />

Gruiformes O Gruseskoj<br />

Gruidae [F] Gruseskoj<br />

Rallidae F Raluseskoj<br />

Passeriformes O Pasereskoj<br />

Alaudidae F Alawdeskoj<br />

Bombycillidae F Bombikilleskoj<br />

Certhiidae F Tsertieskoj<br />

Corvidae F Korveskoj<br />

Fr<strong>in</strong>gillidae F Fr<strong>in</strong>geskoj<br />

Hirund<strong>in</strong>idae F Hirundeskoj<br />

Laniidae F Laniusseskoj<br />

Menuridae F Menuvreskoj<br />

Motacillidae F Ts<strong>in</strong>okawdeskoj<br />

Muscicapidae F Musxotsapseskoj<br />

Oriolidae F Avrolleskoj<br />

Paradisaeidae F Paradizezzeskoj<br />

Paridae F Parueskoj<br />

Passeridae [F] Pasereskoj<br />

Prunellidae F Prunelleskoj<br />

Regulidae F Redzhulleskoj<br />

Sittidae F Sititeskoj<br />

Sturnidae F Sturneskoj<br />

Sylviidae F Silvazzeskoj<br />

Troglodytidae F Troglodyteskoj<br />

Turdidae F Turdeskoj<br />

Pelecaniformes O Pelikaneskoj<br />

Pelecanidae [F] Pelikaneskoj<br />

Phalacrocoracidae F Falakrokorakeskoj<br />

Sulidae F Sulaeskoj<br />

68


Phoenicopteriformes O Fenitsoptereskoj<br />

Phoenicopteridae [F] Fenitsoptereskoj<br />

Piciformes O Pigeskoj<br />

Indicatoridae F Indikatteskoj<br />

Picidae [F] Pigeskoj<br />

Ramphastidae F Ramfasseskoj<br />

Podicipediformes O Poditsopodeskoj<br />

Podicipedidae [F] Poditsopodeskoj<br />

Procellariiformes O Protselarreskoj<br />

Diomedeidae F Diomedeskoj<br />

Hydrobatidae F Hidrobasheskoj<br />

Procellariidae [F] Protselarreskoj<br />

Psittaciformes O Psitakeskoj<br />

Psittacidae [F] Psitakeskoj<br />

Strigiformes O Strigeskoj<br />

Strigidae [F] Strigeskoj<br />

Trochiliformes O Troxilleskoj<br />

Trochilidae [F] Troxilleskoj<br />

Trogoniformes O Trogoneskoj<br />

Trogonidae [F] Trogoneskoj<br />

69


70<br />

5.2 - SEA GULLS<br />

Low taxon list based on <strong>the</strong> award w<strong>in</strong>n<strong>in</strong>g<br />

determ<strong>in</strong>ation handbook by<br />

Peter Harrison: Seabirds, an identification guide<br />

Christopher Helm, London 1983<br />

> Barr<strong>in</strong>g mistakes and omissions ! <<br />

Laridae Familio Larusseskoj<br />

Anous m<strong>in</strong>utus Aenoho S blankakufa<br />

Anous stolidus Aenoho S fajnabeka<br />

Anous tenuirostris Aenoho S brunakrura<br />

Chlidonias hybridus Xlidonno S hibrida<br />

Chlidonias leucopterus Xlidonno S blankaflugila<br />

Chlidonias niger Xlidonno S nigra<br />

Gygis alba Gygeso S blanka<br />

Larosterna <strong>in</strong>ca Laroshterno S blanka<br />

Larus argentatus Larusso S ardzhenta<br />

argentatus argentatus S+ ardzhentetsa<br />

argentatus atlantis S+ lardzhagonura<br />

argentatus cach<strong>in</strong>nans S+ pliblanka<br />

argentatus heugl<strong>in</strong>i S+ gelbakrura<br />

argentatus michahellis S+ pligriza<br />

argentatus mongolicus S+ pligranda<br />

argentatus smithsonianus S+ nordamerika<br />

argentatus taimyrensis S+ rozakrura<br />

argentatus vegae S+ plivigla<br />

Larus atricilla Larusso S ridanta<br />

Larus audou<strong>in</strong>ii Larusso S rudzhokula<br />

Larus belcheri Larusso S rubandovosta<br />

Larus brevirostris Larusso S kurtabeka<br />

Larus brunnicephalus Larusso S brunakapa


Larus bulleri Larusso S nigrabeka<br />

Larus californicus Larusso S rudzhafemura<br />

Larus canus Larusso [S] mildarigarda<br />

canus brachyrhynchus S+ kurtanaza<br />

canus kamtschatschensis S+ kamtshatka<br />

Larus cirrocephalus Larusso S grizakapa<br />

cirrocephalus cirrocephalus S+ ts<strong>in</strong>drokolora<br />

cirrocephalus poiocephalus S+ herbokolora<br />

Larus crassirostris Larusso S nigravosta<br />

Larus delawarensis Larusso S bendobeka<br />

Larus dom<strong>in</strong>icanus Larusso S gelbokula<br />

Larus fulig<strong>in</strong>osus Larusso S fulgoplena<br />

Larus furcatus Larusso S forkovosta<br />

Larus fuscus Larusso S nigramantela<br />

fuscus graellsii S+ sweltaflugila<br />

Larus genei Larusso S gratsilabeka<br />

Larus glaucescens Larusso S glakalaflugila<br />

Larus glaucoides Larusso S blankaflugila<br />

glaucoides kumlieni S+ brunareta<br />

Larus heermanni Larusso S buntabeka<br />

Larus hemprichi Larusso S fulgetsa<br />

Larus hyperboreus Larusso S gelbomatorba<br />

Larus ichtyaethus Larusso S fishagla<br />

Larus leucophthalmus Larusso S blankokula<br />

Larus macullipennis Larusso S brunatshapa<br />

Larus mar<strong>in</strong>us Larusso S nigradorsa<br />

Larus melanocephalus Larusso S nigrakapa<br />

Larus m<strong>in</strong>utus Larusso S malgranda<br />

Larus modestus Larusso S griza<br />

Larus novaehollandiae Larusso S purpurabeka<br />

novaehollandiae forsteri S+ awstralia<br />

71


72<br />

novaehollandiae hartlaubii S+ koloshnura<br />

novaehollandiae scopol<strong>in</strong>us S+ novzilenda<br />

Larus occidentalis Larusso S rozomatorba<br />

occidentalis livens S+ gelbakrura<br />

Larus pacificus Larusso S bekega<br />

Larus philadelphia Larusso S blankazona<br />

Larus pipixcan Larusso S b<strong>in</strong>okla<br />

Larus relictus Larusso S longapieda<br />

Larus ridibundus Larusso S ridatshanta<br />

Larus sab<strong>in</strong>i Larusso S trikolora<br />

Larus saundersi Larusso S nigrapolma<br />

Larus schistisagus Larusso S ardezodorsa<br />

Larus scoresbi Larusso S rudzhabeka<br />

Larus serranus Larusso S montara<br />

Larus thayeri Larusso S grizokula<br />

Larus tridactyla Larusso S trif<strong>in</strong>gra<br />

tridactyla pollicaris S+ nigraprimala<br />

tridactyla tridactyla S+ (subspets<strong>in</strong>oma)<br />

Pagophila eburnea Pagosofilo S ebura<br />

Phaetusa spec. Fajtusso S {spets<strong>in</strong>oma)<br />

Procelsterna cerulea Protseloshterno S blugriza<br />

Rhodostetia rosea Rjodosteto S roza<br />

Sterna albifrons Shternazzo S blankafrunta<br />

Sterna albostriata Shternazzo S blankastria<br />

Sterna aleutica Shternazzo S aleutuja<br />

Sterna anae<strong>the</strong>tus Shternazzo S brunaflugila<br />

Sterna aurantia Shternazzo S orandzhabeka<br />

Sterna balaenarum Shternazzo S nigrakapa<br />

Sterna bengalensis Shternazzo S tufeta<br />

Sterna bergii Shternazzo S nukotufa


Sterna bernste<strong>in</strong>i Shternazzo S nigrap<strong>in</strong>ta<br />

Sterna caspia Shternazzo S sangobeka<br />

Sterna dougalli Shternazzo S rozetsa<br />

Sterna elegans Shternazzo S eleganta<br />

Sterna eurygnatha Shternazzo S lardzhamaksela<br />

Sterna forsteri Shternazzo S nigramaska<br />

Sterna fuscata Shternazzo S brunega<br />

Sterna hirund<strong>in</strong>acea Shternazzo S hirundetsa o<br />

Sterna hirundo Shternazzo S hirunda o<br />

Sterna lorata Shternazzo S zonizita<br />

Sterna lunata Shternazzo S maskoporta<br />

Sterna maxima Shternazzo S redzha<br />

Sterna melanogastra Shternazzo S nigraventra<br />

Sterna nereis Shternazzo S orandzhakrura<br />

Sterna nilotica Shternazzo S mevobeka<br />

Sterna paradisaea Shternazzo S paradiza<br />

Sterna repressa Shternazzo S blankavanga<br />

Sterna sandvicensis Shternazzo S palap<strong>in</strong>ta<br />

Sterna striata Shternazzo S sulketa<br />

Sterna sumatrana Shternazzo S nukobenda<br />

Sterna superciliaris Shternazzo S gelbabeka<br />

Sterna trudeaui Shternazzo S nedzhotshapa<br />

Sterna virgata Shternazzo S rubanda<br />

Sterna vittata Shternazzo S girlanda<br />

73


74<br />

5.3 - RACES (VARIETIES) OF DOGS<br />

Airedale R ARDAL ‘<br />

Barbet R BARBET ' “little beard”<br />

Basset R BASET '<br />

Barzoï R BARZOJ '<br />

Basenji R BASENZHU '<br />

Beagle R BIGEL '<br />

Bobtail R NODVOST ' “knot-tail”<br />

Boston-terrier R BOSTER '<br />

Boxer R BOKSIST ' “fist-fighter”<br />

Bull-terrier R BULTER '<br />

Cairn-terrier R KERNTER '<br />

Chihuahua R TSHIWAN '<br />

Chow-chow R TSHOTSHO '<br />

Collie R KOLI '<br />

Deerhound R TSERVUL ' “deer-one”<br />

Doberman-p<strong>in</strong>cher R DOBERPINTSH '<br />

Dogue R DOGU '<br />

Fox-terrier R FOKSTER '<br />

Griffon R GRIFON '<br />

Hushpuppy R HUSHPUP ‘<br />

Husky R HUSKI '<br />

Kerryblue R KERIBLU '<br />

K<strong>in</strong>g Charles R KINTSHAR '<br />

Lévrier R LEPORUL ' “hare-one”<br />

Loulou R LULU '<br />

Mastiff R MASTIF '<br />

Molosse R MOLOS '<br />

Newfoundlander R NJUFON '<br />

Papillon R PAPILIUL ' “butterfly-one”<br />

P<strong>in</strong>cher R PINTSHIST ' “p<strong>in</strong>cher”<br />

Po<strong>in</strong>ter R MONTRIST ' “<strong>in</strong>dicator”<br />

Pomeranian R POMERAN '


Poodle R PUDEL '<br />

Pug-dog R MOPS '<br />

Retriever R REAKIR ' “w<strong>in</strong>-back”<br />

Ridge-back R KRESTODORS ' “ridge-back”<br />

Sa<strong>in</strong>t-Bernard R BERNARDUL ' “Bernard-one”<br />

Samoyede R SAMOJED '<br />

Schipperke R SHIPIST ' “boat-man”<br />

Schnauzer R MUZELUL ' “snout-one”<br />

Sealyham-terrier R SILIHAM '<br />

Setter R METIST ' “putter”<br />

Shepherd R SHAFHUND ' “sheep-dog”<br />

Skye-terrier R TSHIELTER ' “sky-earth”<br />

Spaniel R HISPANUL ' “Spaniard”<br />

Terrier R TERJER '<br />

Welsh Corgi R WELKOR '<br />

Wippet R WIPET '<br />

L<strong>in</strong>guists, who didn’t know biology,<br />

and biologists, who didn’t know l<strong>in</strong>guistics,<br />

have created a situation harmful to both discipl<strong>in</strong>es.<br />

[F.C. WERNER]<br />

75


76<br />

6 - Read<strong>in</strong>g Coffee Grounds<br />

Extremely simple and efficient though <strong>the</strong> new Trimeral<br />

System may be, we cannot disguise from ourselves <strong>the</strong> fact<br />

that a wide gap yawns between mere exposition and actual<br />

application. What steps are <strong>the</strong>re to take? What obstacles<br />

might be encountered?<br />

Presumably <strong>the</strong> first step would be to organize a worldwide<br />

th<strong>in</strong>k-tank of specialists from ALL <strong>the</strong> biological discipl<strong>in</strong>es<br />

— none left out — <strong>in</strong>clud<strong>in</strong>g people from Asia and Africa,<br />

not just from <strong>the</strong> Western World, but all will<strong>in</strong>g to undertake<br />

<strong>the</strong> great change-over. May we see <strong>the</strong> advent of this<br />

dream <strong>in</strong> <strong>the</strong> com<strong>in</strong>g BioCode Symposium, planned <strong>in</strong><br />

Greece for <strong>the</strong> year 2002? Surely <strong>the</strong> existence of INTERNET<br />

makes such an undertak<strong>in</strong>g <strong>the</strong>oretically feasible and<br />

exchange of ideas, if not task division, fast and efficient.<br />

Whatever <strong>the</strong> way of launch<strong>in</strong>g <strong>the</strong> ship, that Body should<br />

absolutely <strong>in</strong>clude accomplished philologists, for runn<strong>in</strong>g a<br />

f<strong>in</strong>e comb through <strong>the</strong> enormous amount of lat<strong>in</strong>ized names,<br />

<strong>in</strong> order to establish <strong>the</strong>ir etymological mean<strong>in</strong>gs — or <strong>the</strong>ir<br />

lack of such. These people know how to say it, where<br />

biologists know what to say ...<br />

F<strong>in</strong>ally, with (about) all <strong>the</strong> old names reframed or replaced<br />

by better ones, and <strong>the</strong> taxon structures reconsidered,<br />

expanded, consolidated, unified, <strong>the</strong>re looms <strong>the</strong> longw<strong>in</strong>ded<br />

labour of pa<strong>in</strong>stak<strong>in</strong>gly feed<strong>in</strong>g all <strong>the</strong>se data <strong>in</strong>to<br />

<strong>the</strong> Central Databank mentioned at <strong>the</strong> beg<strong>in</strong>n<strong>in</strong>g. Or,<br />

perhaps more probably, this compilation might progress<br />

parallel to <strong>the</strong> drafts submitted and... agreed upon by some<br />

majority of participants.


Anyway, oppositions will certa<strong>in</strong>ly be numerous and fierce,<br />

from many directions. There will be <strong>the</strong> celebrated<br />

academicians who spent a lifetime among <strong>the</strong> classic<br />

names, produc<strong>in</strong>g important works of reference based on<br />

<strong>the</strong>m, and now see<strong>in</strong>g <strong>the</strong>ir work apparently outstripped.<br />

There will be <strong>the</strong> bookworms: heart and soul devoted to<br />

sift<strong>in</strong>g through endless shelves of archives, for establish<strong>in</strong>g<br />

whoever was first <strong>in</strong> l<strong>in</strong>e for <strong>the</strong> cherished Law of Priority,<br />

and whose endeavours will become null and void or at least<br />

reduced to life <strong>in</strong> <strong>the</strong> marg<strong>in</strong>. There will be even those<br />

publishers and bookshops kick<strong>in</strong>g back, because of <strong>the</strong>ir<br />

valuable stocks of handbooks grow<strong>in</strong>g obsolete almost<br />

overnight.<br />

So, we do not cherish high hopes about <strong>the</strong> established<br />

Scientific Community, bound by age-old traditions. More<br />

likely than not <strong>the</strong> <strong>in</strong>itiative would come from enthusiastic<br />

outsiders. Time will tell. That is... if this small brochure<br />

succeeds <strong>in</strong> reach<strong>in</strong>g public attention, s<strong>in</strong>ce Conspiracy of<br />

Silence is a very powerful means for keep<strong>in</strong>g even <strong>the</strong> most<br />

promis<strong>in</strong>g project <strong>in</strong> solitary conf<strong>in</strong>ement.<br />

* * * * * * *<br />

77


Whoever gets confronted with <strong>the</strong> subject, cannot avoid at<br />

present to make his or her personal choice between <strong>the</strong><br />

follow<strong>in</strong>g old and new items:<br />

Over ¾ trouble with<br />

Less than ¼ trouble with<br />

<strong>in</strong>flectional Lat<strong>in</strong> grammar. agglut<strong>in</strong>ative Uniespo grammar.<br />

Very <strong>in</strong>tricate and even<br />

Very simple and<br />

chaotic spell<strong>in</strong>g.<br />

regular spell<strong>in</strong>g.<br />

Complicated pronunciations. Clear prononciation scheme.<br />

Different end<strong>in</strong>gs for different A typical symbol for each taxon<br />

taxons with uncerta<strong>in</strong>ty.<br />

without special end<strong>in</strong>gs.<br />

Never secure Law of Priority<br />

Stable Law of Reference<br />

(m<strong>in</strong>ority vote).<br />

(majority vote).<br />

Capricious rules<br />

Logical rules<br />

with many exceptions.<br />

with hardly any exceptions.<br />

Complicated Lat<strong>in</strong> dictionary. Easy to use ITK word-lists.<br />

Memory stra<strong>in</strong><strong>in</strong>g handbooks. Memory help<strong>in</strong>g handbook.<br />

A host of uncontrollable<br />

Well organized<br />

name variations.<br />

name variabilities.<br />

Almost impossible material<br />

Highly adapted material<br />

for automatic treatment<br />

for automatic treatment<br />

by computer.<br />

by computer.<br />

Taxonomy restricted to<br />

Taxonomy operative for any<br />

botany or to zoology or to<br />

and all liv<strong>in</strong>g th<strong>in</strong>gs...<br />

virology or to ...<br />

and beyond.<br />

Dear reader, th<strong>in</strong>k about it!<br />

79


80<br />

Excerpt from <strong>the</strong> International Key<br />

ae• not bry•2 flower<strong>in</strong>g<br />

agan• charm daktyl•1 f<strong>in</strong>ger<br />

akant•1 thorn daktyl•2 datefruit<br />

akant•2 rub del•1 apparent<br />

akt<strong>in</strong>•1 bright del•2 allure<br />

akt<strong>in</strong>•2 needle dermat• fur<br />

ambly• blunt didm•1 couple<br />

amnj• river didm•2 testicle<br />

angw• serpent d<strong>in</strong>•1 frighten<strong>in</strong>g<br />

ant•1 flower d<strong>in</strong>•2 roll<strong>in</strong>g<br />

ant•2 decoration dipl• double<br />

ap•1 away dix• divide<br />

ap•2 extremity dots• girder<br />

api• berry drom•1 arena<br />

aps+ absolute drom•2 port<br />

arta• bread dy• two<br />

artr• jo<strong>in</strong>t egyr• collective<br />

arx• master ekt• outward<br />

arž• person entom• <strong>in</strong>sect<br />

aski• exercice epi•1 add<br />

avj• bird epi•2 em<strong>in</strong>ent<br />

awr•1 hear<strong>in</strong>g erif• goat<br />

awr•2 ear ery• pull<br />

bary• heavy ex<strong>in</strong>• viper<br />

baš• foundation faj•1 brown<br />

bi• life faj•2 happy<br />

b<strong>in</strong>a• two fajt• bright<br />

blast• bud falakr• barren<br />

blefar• eyelid faner• display<br />

bol•1 drive fark• furrow<br />

bol•2 current fenits• purple<br />

bry•1 moss fil•1 adept<br />

fil•2 fiber kawd• tail<br />

fluvj• river kerat• horn


for• carry kerk•1 tail<br />

fragm•1 break kerk•2 shuttle<br />

fragm•2 wall klad• branch<br />

ftor• damage klavj•1 bludgeon<br />

fyk• seaweed klavj•2 bolt<br />

fys•1 balloon klemat• branch<br />

fys•2 <strong>in</strong>flation klype• shield<br />

fyt• plant koel• cavity<br />

galg• chicken kokts• berry<br />

gam• marriage koris• bug<br />

gastr• belly krypt•1 bury<br />

gen• product krypt•2 cover<br />

ger•1 carry ksif• dagger<br />

ger•2 old kykl• wheel<br />

geton• neighbour kyn• dog<br />

graf• design lani• kill<br />

gram• draw<strong>in</strong>g lar•1 gull<br />

helv•1 revel lar•2 agreeable<br />

helv•2 nail lasi• bristl<strong>in</strong>g<br />

hemi• half laxn•1 fluff<br />

hevl•1 bog laxn•2 burrow<br />

hevl•2 wart legn• fr<strong>in</strong>ge<br />

hidr•1 water lekš• read(<strong>in</strong>g)<br />

hidr•2 sweat lekt•1 bed<br />

hol• all lekt•2 idiom<br />

hydn• truffle lemf• glanders<br />

hyf• filament lepid• bast<br />

hystr•1 womb lept•1 slender<br />

hystr•2 recent lept•2 trifle<br />

ixtj• fish lews• flat<br />

iz• equal lit• stone<br />

kalyks• chalice lokl• chamber<br />

katl• dish lyk• wolf<br />

meg• big ort•1 square<br />

melan• black ort•2 correct<br />

mely• honey pagos•1 freeze<br />

81


82<br />

mer•1 part pagos•2 hill<br />

mer•2 sh<strong>in</strong>bone para•1 beside<br />

meta•1 across para•2 obligatory<br />

meta•2 less water pelts• protection<br />

mikr• small perdn•1 bladder<br />

mirj• multitude perdn•2 fart<br />

mitj• sweet pern•1 thigh<br />

mona• one pern•2 nail<br />

mulg• milk pfak• freckle<br />

myk• mushroom pfal• penis<br />

myš• closed pikr•1 bitter<br />

najv• sign pikr•2 sharp<br />

ne• new pirn• gist<br />

nefr•1 kidney plagj•1 slant<strong>in</strong>g<br />

nefr•2 horrible plagj•2 steal<br />

neks•1 proportion platy• flat<br />

neks•2 knotted plei• augment<br />

nemt• thread pleks•1 net(work)<br />

nez• island pleks•2 basket<br />

od• direction pod• foot<br />

ofi• serpent podits• arse<br />

olog•1 phenomenon poly• many<br />

olog•2 knowledge potam• stream<br />

omat• eye prot• orig<strong>in</strong>al<br />

omfal• navel protsel• gale<br />

onim• name psam• sand<br />

ope• needle psewd• apparent<br />

opš•1 appearence psitak• parrot<br />

opš•2 exam<strong>in</strong>e psor• eczema<br />

orb•1 circle pter• w<strong>in</strong>g<br />

orb•2 ball pters• fern<br />

ornit• bird pyr•1 fire<br />

pyr•2 gra<strong>in</strong> strats•2 army<br />

pyrg• tower strong• tube<br />

rafj•1 needle sxiz• split<br />

rafj•2 seam syn+ toge<strong>the</strong>r


ag•1 cleave tafr• furrow<br />

rag•2 berry takts•1 diligent<br />

ramf• beak takts•2 arrange<br />

rej•1 flow tatr• bogey<br />

rej•2 juice telj•1 nipple<br />

ridz• root telj•2 sk<strong>in</strong><br />

r<strong>in</strong>•1 nose telm• marsh<br />

r<strong>in</strong>•2 lea<strong>the</strong>r terj• animal<br />

rjod•1 rose tremt• perforation<br />

rjod•2 splash trix•1 hair<br />

rynx• snout trix•2 cotton<br />

sagit• arrow trogl• cavern<br />

sapr• putrefy trox• disk<br />

sarx• flesh try• three<br />

saxar• sugar trybl• plate<br />

šet• tail tsamp•1 meander<br />

sfen• wedge tsamp•2 caterpillar<br />

sf<strong>in</strong>t• compressed tseps• head<br />

sifn• mole tset• whale<br />

silv• forest ts<strong>in</strong>• move<br />

sklop• mole tšol•1 dwell<br />

skutl• lozenge tšol•2 hill<br />

špil•1 sta<strong>in</strong> tsyf• hump<br />

špil•2 cape turš• shuttle<br />

steg• roof tyr•1 door<br />

sten•1 narrow tyr•2 cheese<br />

sten•2 <strong>in</strong>tense tyrs•1 bush<br />

stet• breast tyrs•2 w<strong>in</strong>dow<br />

stikt• po<strong>in</strong>t ungl• hoof<br />

stom• mouth ured•1 burn<br />

strats•1 echelon ured•2 coal<br />

ustil• rust xlor•2 fresh<br />

uvr• tail xom• equal<br />

valr• eagle xomr• nearby<br />

xaen• yawn xytr• box<br />

xaradr• abyss zo• animal<br />

83


84<br />

xers• desert -edj small<br />

xlid• impose -isk t<strong>in</strong>y<br />

xlor•1 green -ojk period<br />

Sketch by Darw<strong>in</strong>


"If it cannot be accomplished <strong>in</strong> <strong>the</strong> com<strong>in</strong>g decades that <strong>the</strong><br />

tools of term<strong>in</strong>ology (term<strong>in</strong>ological pr<strong>in</strong>ciples, methods and<br />

formats) are fully applied on both national and <strong>in</strong>ternational<br />

levels, so that term<strong>in</strong>ologies become reliable, <strong>the</strong>n serious<br />

difficulties <strong>in</strong> regard to subject communication can occur,<br />

and even a complete breakdown can be expected. This<br />

situation is ma<strong>in</strong>ly due to <strong>the</strong> rapid progress achieved <strong>in</strong> all<br />

areas of human activity, which caused an abundance of<br />

new concepts. These concepts, however, have to be<br />

expressed by a very limited number of terms and possible<br />

comb<strong>in</strong>ations of term elements <strong>in</strong> <strong>the</strong> various languages.<br />

These tremendous dynamics with<strong>in</strong> term formation and<br />

evolution stand <strong>in</strong> contrast to a static stock of word elements<br />

from which terms can actually be formed. The stems that<br />

are available <strong>in</strong> <strong>the</strong> various languages amount to a few<br />

thousand, while <strong>the</strong> number of concepts known can only be<br />

expressed <strong>in</strong> millions. The limits of assign<strong>in</strong>g terms to<br />

concepts <strong>in</strong> an unambiguous way will be reached very<br />

quickly if this development proceeds fur<strong>the</strong>r at such a rate."<br />

86<br />

[Professor H. Felber, former director of UNESCO's<br />

INFOTERM, <strong>in</strong>:<br />

Infoterm; Ten years of activities – Vienna 1982]<br />

It is to this predicament, that <strong>the</strong> International<br />

Term<strong>in</strong>ological Key and its system try to br<strong>in</strong>g<br />

an efficient and radical solution, far beyond <strong>the</strong><br />

scope and reach of any present day<br />

proposal; a solution truly tailored to <strong>the</strong> needs<br />

of <strong>the</strong> 21st Century…

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