Showing posts with label Sturtevant. Show all posts
Showing posts with label Sturtevant. Show all posts

Wednesday, March 1, 2017

1886 - E. Lewis Sturtevant's "A Study of the Dandeliion"

I really can't tell you why I enjoy Sturtevant's works so much...but I do. 
 And! - now that
spring is fast approaching it is the right time to share his A Study of the Dandelion 

He is putting forth the idea that all stable forms of a plant in cultivation are merely forms which could be found in nature.  Too be frank, I don't know what his point is...or maybe, why is he making this point.  

No matter, dandelions make a charming botanical illustration and this is the place to share them!

The following article has illustrations I like, only one plain line drawing was in the original.  

The comments in brown italics are mine as well.




A STUDY OF THE DANDELION.



BY E. LEWIS STURTEVANT, M.D.

THE dandelion is a plant of northern climates, especially found growing amidst the herbage of meadows, and as a weed in gardens. Its common name is a corruption of dent de leon, a word which is met with in the Welsh Dant y Llew of the 13th century.  (Interesting link related to ancient botanical names - 1815Antiquæ Linguæ Britannicæ Thesaurus; being a British or Welsh-English.)

Its vernacular names in various languages have usually reference to the peculiar indentation of the leaves, or to some other resemblance or character of the plant. By commentators it has been identified with the 

  • aphake of Theophrastus, a in composition signifying absence of, and phake lentils, or the name perhaps signifying that the plant can be used as a green before lentils appear in the spring (?);
  • the ambubeia of Pliny may suggest the scattering of the seed, ambulo meaning the going backward and forward, but some commentators assign this name to the wild endive or chicory;
  • the hedypnois of Pliny is but doubtfully identified with our dandelion, and appears to be derived from two Greek words signifying sweet breath, and may refer to the sweet smell of the flowers.
  • Pinaeus, 1561, calls it Dens Leonis, Dens Caninus, caput Monachi, Rostruporcinum or Ambubeia, the aphake of Theophrastus;
     
  • by the French, Pissenlit or Dent de Lyon
  • by the Germans, Pfaffen roerlin.
  • Pena and Lobel, 1570, give additional names of Urinaria,
  • German, Korlkraut und Phaffenblat,  (I love this name!)
  • Belgian, Pappen cruyt,
  • English, Dent de Lyon


The modern vernacular names are: 

(I put in my blog comments in brown italics.)

  • English -  dandelion, swine's snout (Prior);  (Ah ha!! A chance search return yields this: Proverbs.11:22 As a jewel of gold in a swine's snout, so is a fair woman which is without discretion.  Perhaps the dandelion is the "jewel of gold"? )
  • France  - pissenlit, dent-de-lion (Vilm.);  (Pissenlit/Piss In Bed -Etymology. The vulgar name by which it is familiar to children, the French Pissenlit, and equivalent synonyms in other languages, indicate the long and general acquaintance of the people with its diuretic qualities.)
  • German -  löwensahn (Lenz); (?)
  • Flanders  - molsalaad (Vilm.); (?)
     
  • Danish -  moelkebtte (Vilm.); (Yup, that's a dandelion.)
  • Italian -  tarassaco (Lenz), dente de leone, virasole dei prati (Vilm.); (The first one translates.)
  • Spanish -  diente de leon, Amargon (Vilm.); (This first one translates, too!)
  • Greek -  agriomaroulia (Sibth.), pikraphake (Fraas); (Hmm...none of these turn up as a translation for dandelion. Are they phonetic?  πικραλίδα = dandelion)
  • Japanese fosei or usually fudsina or tsugumi gusee or tampopo (Pick.). (The only one that Google translates nowadays as dandelion is tampopo.)


Bauhin, in his Pinax, edition of 1623, enumerates two varieties of dandelion, one the Dens Leonis latiore filio carried back in his synonomy to Brunselsius, 1539; the other, Dens Leonis angustiore folio, carried back in like manner to Caesalpinus, 1583.

The first kind, he says, has a large and a medium variety, the leaves sometimes pointed,  sometimes obtuse.

In the Flore Naturelle et Economique, Paris, 1803, the same varieties, apparently, are mentioned, one with narrow leaves and the other with large and rounded leaves.



In Martyn's Millers Dictionary, 1807, the leaves of the dandelion are said to vary from pinnatifid or deeply runcinate in a very dry situation to nearly entire in a very moist one, generally smooth, but sometimes a little rough, and Leontodon palustre is described as scarcely more than a variety, as varying very much in its leaves which have few notches or are almost entire, the plant smoother, neater, more levigated and more glaucous than the common dandelion. (Wow, he does like a long sentence!)




In Geneva, N. Y., on the grounds of the New York Agricultural Experiment Station, a large number of varieties are to be commonly noted, both in the habit and appearance of the plant and irrespective of difference of soil or exposure, as varieties may readily be separated whose roots are intertwined.



Some plants grow with quite erect leaves, others with their leaves closely adpressed to the soil; some have broad, others narrow leaves; some have runcinate leaves, others leaves much cut and almost fringed, and yet others the leaves  nearly entire; 



some have almost sessile leaves, some have smooth leaves, others roughened leaves; some have thin, others thick leaves; some as varieties grow to a larger size, others are always dwarfer; some have an open manner of growth, others a close, etc.

These leaves are from here...
















The use of the wild plant as a vegetable seems to have been common from remote times, but its culture is modern.   



  • In 1836 a Mr. Corey, of Brookline, Mass., grew dandelions for the Boston market, the seed obtained from the largest of the wild plants (Mass. Hort. Soc. Trans., 1884, 128);
  • in 1863 dandelions are described among garden esculents by Burr (Field and Gard. Veg. of America, 345), but the context not indicating any especial varieties;
  • in 1828 Fessenden (New Am. Gardener) says the wild plant is used but never cultivated.
  • In 1874 the seed appears for sale in seed catalogues (Briggs Bros. Cat, 1874), perhaps earlier, and the various seed catalogues of 1885 offer six names, one of which is the " common." 


In England, dandelion culture is not mentioned in Mawe's Gardiner, 1778, nor in Martyn's Millers Dictionary, 1807; the first notice I find is in the Gardeners' Chronicle, 1846 (p. 340), where an instance of cultivation is noted, the herbage forming "a beautiful and delicate blanched salad." 
Pissenlit Mousse

In 1880 its culture had not become common, as this year its cultivation in France, and not in England, is noted (Jenkins Jour. R. A. S., xvi, 94). 

In France, Noisette, 1829 (Man. du Jard., 1829, 356) gives cultural directions, and says the wild plant furnishes a spring pot-herb; the plant is, however, not mentioned in L'Horticulteur Francais, 1824-5, nor in Nouveau Dictionnaire du Jardinage, 1826. 

Vilmorin (Bon Jardinier, 1882) states its culture in France as dating from 1868, and the firm of Vilmorin, Andrioux & Cie in 1885 offer four sorts of seed, one, the "improved moss" as new. 




In Vilmorin's Les Plantes Potageres, 1883, two forms are figured, Pissenlit ameliore a coeur plein and Pissenlit ameliore tres hatif. The first of these is named in Album de Cliches, Pissenlit ameliore frise, and a fourth name or third form is figured, the Pissenlit mousse.

  1. The type of the Pissenlit mousse can be readily found among the wild plants of the station grounds, very closely resembling Vilmorin's figure in every respect when growing on rich soil except that the leaf divisions are scarcely as much crowded.
  2. The type of the Pissenlit ameliore a coeur plein is perhaps to be recognized in Anton Pinaeus' figure, 156r, and is certainly to be found growing wild at the station.
  3. The Pissenlit-ameliore tres hatif is figured in 1616, the resemblance between the two figures, the one by Dodonaeus and the other by Vilmorin, is very close. It is also to be found growing wild on the station grounds.


Above illustrations from

The Vegetable Garden,
J. Murray, 1885



P.J. Redouté
The influence of rich soil and protected growth upon the dandelion is to give increased size and succulency to the plant, and to thicken the branching of the leaves, in the direction of answering the description of a coeur plein; but this influence appears to be limited by the heredity of the plant, as the types do not react to an equal extent. 


This fullness, or hearting, in No. 2 seems to come from the strong tendency in plants of this type to divide the root into a group of crowns; the leaves, also, in rich soil, grow rather upright with the upper portion curving outwards, giving a curled appearance to the plant, and thus justifying Vilmorin's alternate name "frise." 

The No. 3 form is more succulent in rich soil than the others, attains size distinctly earlier, is less crowded and less upright in growth, and in some cases is very closely adpressed to the ground. 

No. 1 type does not in all cases seem to be a depauperate (lacking in numbers or variety of species) form, as it is found on fertile soil along with the rest, it is usually small, but in some instances is of fair size and quite bunchy growth. A form with nearly entire leaves has not yet reached culture under a distinct name; this type is distinctly smaller than the rest, and some plants have sessile and thickened leaves, other plants long petioled and spatulate-like thin leaves. In all the forms some plants may be looked for with hairy and roughened leaves.
detail - P.J. Redouté




In view of the limited extent of the present culture of the dandelion, and the short time since its cultivation was first attempted, as well as to the fact that its present culture about Geneva (New York) seems unknown, it seems unreasonable to infer that our plants are escapes from cultivation, and much more so when it is considered that these same described types are common elsewhere in Western New York. 


If not escapes from cultivation the inference seems strongly established that our cultivated varieties did not originate under cultivation, but are simply selections from wild types. If this be granted it may be legitimately questioned whether other of our cultivated form-species in other plants are not likewise of natural origin.

A careful investigation into the history of the origin of our cultivated varieties fully justifies the statement that I have as yet secured no data which justifies the belief that form-species in culture are other than of natural origin, and I have secured much evidence in favor of the view that form-species are introductions from natural variations. Before, however, such a radical belief can receive countenance, much must be done in the herbarium study of varieties as collected from various sources, in order that we may have wild forms to which our cultivated types can be referred. 


Our so-called modern vegetables, introduced as novelties, often seem to be such only because we are unfamiliar with what our predecessors possessed. Thus the figure that Pinaeus gives, in 1561, of a lettuce answers to our stone tennis-ball variety as closely as do the figures in our seed catalogues to the varieties whose name they carry;   the deer-tongue lettuce introduced as a novelty in 1883 seems nearly identical with the Lactuca folio oblongo acuto of Bauhin's Prodromus, 1671; a large number of our capsicums or peppers seem to be identical with the varieties figured in Hortus Eystettensis, 1623; new types of squash followed the appearance of the Valparaiso from Chili in the early part of the present century, etc., etc.

Under the hypothesis that the form-species of cultivation are originally from nature, we can explain the permanency of these form-species, and their resistance to change from cross fertilization, the tendency seeming strongly towards trueness to type, and the purging themselves from contaminations unless restrained perhaps by human selection. Thus two form-species of maize, when crossed, have not produced intermediates in their crop, but the parent types without intermediates, and the continuous planting of the progeny tended toward a complete separation into the original types. Various crossings of a like kind, made at the Experiment station, seem confirmatory of this view, and seem to suggest in addition that seeming sports are often the result of atavism.


Appended are a few of the variations which are to be found in the leaves of the dandelion, selected rather as representative than as exceptional. A series could readily have been selected showing a passage from one type to another, as frequently leaves of quite different appearance appear on the same plant.





Want more? 


A FURTHER STUDY OF THE DANDELION; A PHASE OF EVOLUTION.

E. LEWIS STURTEVANT.
(Note: Any references by Sturtevant to colored plates were not supported by any of the 
sources available online that I found, which had no illustrations at all!)

January, 1886, I published a paper in the American Naturalist in which I claimed as 
Real Jardin Botanico, Madrid , Spain
probable that all our cultivated varieties of Dandelion were removes from nature and not garden originations, and I also implied that in the case of our cultivated vegetables in general, all the types were likewise derived from natural varieties or variations. 


The importance of this proposition is such that I may not seek excuse for offering a demonstration in the case of the Dandelion, and I can not refrain from also claiming that all the data gained by years of attention justifies the belief that in nature we are to seek and find the types of every cultivated vegetable, and that the modifications produced by protective culture and its concomitants are far less than usually credited, being always within the limits that are discoverable in the feral plant. 

From careful observation and study I think I can properly claim that varieties in nature are indicative of the varieties that appear under culture; that variations in nature are indicative of variations that shall appear under culture; that variation under cultivation furnishes guidance to variation to be sought for in nature; that varieties in cultivation have like varieties in the feral condition of the species. 

Should this generalization prove to be correct, as I firmly believe it will be, we are supplied a method by which the history of cultivated plants can be traced, and by which their geographical distribution can be correctly followed through the assistance of historical data.
Smithsonian Institute, Washington, D.C., U.S.A.

 To accomplish this, however, means herbarium collections which shall include varieties and variations of species, together with notes on the habitat.

 The influence of the factors which find concrete expression in the words climate, soil, culture, requires careful attention and study. The effect of these factors in their power to turn plants from their hereditary aptitudes seems far less than is usually allowed, and it is difficult to assign exact value to either the components or the totality, but the greater effect is undoubtedly either increase or diminution in size (including duplication of parts or its opposite), and tendency towards reversion to some earlier condition.
This is not the place, however, to discuss these propositions, as my object is but to demonstrate in the case of the Dandelion the variability of the wild species, and the practical identity between the wild forms and cultivated varieties. 

This brings us face to face with the question of the limitations of evolution as influenced by human control.

The Dandelion, Taraxacum dens-leonis of Gray's Manual is one of the most common spring plants at Nonquit, a summer resort on the west shore of Buzzard's Bay, six miles south of New Bedford.  

 It is there found flourishing not only in the lawns and dry plains, but notably in copses, occasionally in the forest, and quite abundantly on the borders of brackish swamps, less so in the edges; in the clear sand of the dunes bordering the line of high tide, and on piles of decaying eel-grass, in abandoned gardens, etc. 


Five types of varieties, or centers of variations within the species, are readily discernable, and to which as varieties a large number of variables can be readily assigned. While it is probable that a wider area of collections would connect these five variables through successive gradations, yet for the purpose of a local flora they may be considered as distinct. As I have not had access to herbariums, I prefer at the present time not to assign these varieties to described species (of some botanists) with which they appear to be synonymous. 

I have indicated them by letters of the alphabet. 

Variety A. 
  • This has pinnate (?) leaves; the scapes usually not longer than the leaves, and frequently with a bract upon the upper portion;the calyx scales usually upright or spreading, but often reflexed; size, small.

    It occurs abundantly in dry and moist pastures, often bordering on the beach, and does not attain a large size even when found alongside of larger samples of other varieties which indicate very fertile soil. The plant has either prostrate or erect foliage. The colored figures exhibited show the normal form and size; the herbarium specimens the variables as well.
Variety B.
  • This has pinnate (?) leaves, but the divisions linear triangular, or linear and pinnatifid (?) and distant. It obtains often a considerable size, and occurs in pastures, gardens, and on heaps of decaying eel-grass. It is little variable at Nonquit, but very variable at Geneva, N. Y.

    This variety is noticeable for its tendency to form clustered root stocks, and hence a clumpy appearance to the foliage. The midribs are usually slender. In very fertile soil the leaves become somewhat thickened with a tendency to curl on the borders. In Geneva the leaves often appear cut and laciniated, the laciniae occasionally curled and overlapping and crowded. The plant usually with rather erect foliage.

    The colored figure exhibited represents a less crowded form than is commonly found in rich soil, the herbarium samples a common form. 

Variety C. 

  • This form is abundant in copses, occasionally in dense woods, less common in localities exposed to full sunlight, and attains a great length of leaf when found in rich soil, among the high grass in the copses.

    The pinnae (?) are frequently alternate on some of the leaves. The root frequently supports many crowns, thus affording a dense clumpy plant. The leaves not observed to be clustered, usually very upright. The leaf often quite broad between the pinnae (?).

    One sample collected on the roadside had 52 leaves and 22 flowering scapes. There are quite a large number of variables within the type of this form. The colored figure represents the type, and the herbarium samples some of the variations. 

Variety D

  • This form, with somewhat entire leaves, is very frequent, and extremely variable, growing either in the sun or shade. In rich soil it often attains a large size, the leaf often very thick, bullate and crimpled, and up to six and one-half inches wide. In shaded position the leaf becomes narrower and elongated, approaching to spatulate at times. The petioles are frequently bordered to the base. The colored figure represents the type and the herbarium samples exhibit variations including leaves six and one-half inches wide. 

Variety E. 

  • This form, with long, broad leaves more or less triangular dentate, and with usually broadly bordered petioles, in rich soil, has the surface of the leaves strongly waved or bullate. It occurs in shaded locations, as in abandoned gardens, orchards, and under scattered trees, less common in sunny exposures, rarely in copses.

    The scapes often attain a length of thirty inches. The calyx scales are either in two or three rows. The colored figure represents the type, and the herbarium samples variations up to leaves twenty-two inches long.

    The cultivated Dandelion is of modern introduction. The earliest record I can find in America being in 1836, in the vicinity of Boston; in England an instance is dated 1846. Its market culture in France dates from 1868, according to Vilmorin, and its seed appeared in American seed catalogues in 1874, perhaps a few years earlier.

    The removal of the roots of the wild plants to gardens, annually, for the purpose of blanching for salad use, is mentioned by Stevenson in his Gardner's Kalendar for March, 1765, and by Miller, in his Gardner's Dictionary, edition of 1771.

    In 1885 Vilmorin describes five varieties as distinct, and certainly these varieties offer sufficient contrast to excite our interested attention, if, as is claimed, such have originated through art during the short period under which its culture has existed. This view is, however, a mistaken one, and that our cultivated varieties so apparently diverse are but feral varieties slightly modified by protected growth and fertile soil, is demonstrable; first, from the fact that the types of each variety are to be found growing wild; second, because any point or points noticed in descriptions (or in the growing plant as well), are discoverable in the wild plant.

    In support of these statements, I exhibit colored drawings of typical leaves from the cultivated variety of the Dandelion, as kindly furnished by Mr. E. S. Goff, of the New York Agricultural Experiment Station, to whom I am under obligation, and corresponding leaves from the Dandelion as found growing wild. I also exhibit in herbarium specimens a collection of variable leaves, taken from both wild and cultivated varieties, and which taken as a whole, exhibit the great number of variations which commonly occur in the species, and which, in the wild form, by selective effort, are subject to appearance as cultivated varieties in the future.

Thursday, November 3, 2016

1891 -Tomato (cont.) to Turnip - Sturtevant's HISTORY OF GARDEN VEGETABLES

THE HISTORY OF GARDEN VEGETABLES. BY E. L. STURTEVANT. (Continued from page 706, Vol. XXV., 1891.) 
https://archive.org/details/jstor-2452344 

Lycopersicum humboldtii Dun. 

 This is very like the preceding, but the racemes of the flowers smaller, the calycine segments being never the length of the corolla, and the berries one-half smaller, red, and, when cultivated, not less angular than those of L. esculentum. 
It was noticed by Humboldt  as under cultivation at La Victoria, Neuva Valencia, and everywhere in the valleys of Aragua, in South America, and is described by Kunth'in 1823, and by Willdenow, about 1806, from plants in the Berlin garden from seeds received from Humboldt. The fruit, although small, has a fine flavor.

 I suspect the Turban, Turk's Cap, or Turk's Turban of our seedsmen, a novelty of 1881, to be referable here, although this cultivated variety is probably a monstrous form.










 Lycopersicum pyriforme Dun. 

 This, which is to be classed as one of the fancy varieties under cultivation, occurs with both yellow, red, and pale yellow or whitish fruit. It was described by Dunalin 1813, and in Persoon's synopsis in 1805.  It is mentioned in England in 1819, and both the colors in the United States by Salisbury in 1848.
 It is liked by some for garnishing and pickling. 

The common names are pear-shaped and fig.





 Lycopersicum pimpinellifolium Dun. 


The currant tomato bears its red fruit, somewhat longer than a common currant, or as large as a very large currant, in two ranked racemes, which are frequently quite large and abundantly filled. It grows wild in Peru and Brazil, and is figured by Feuille  in 1725, but not as a cultivated plant, and is described by Linnaeus  in 1763.  The grape or cluster tomato is recorded in American gardens by Burr  in 1863, and as the red currant tomato by Vilmorin  in 1883 and 1885. It is an exceedingly vigorous and hardy variety, with delicate foliage, and fruits most abundantly. The berries make excellent pickles. 

 According to the test of cross-fertilization, few, if any, of the above are true species. Two only of the above named — the cherry and the currant tomato — do I find recorded in a truly wild condition. The tomato has, however, been under cultivation from a remote period by the Nahua and other Central American nations, and reached European and American culture, as all the evidence implies, in an improved condition. If there is any evidence that any of our so-called types arose spontaneously from the influences of culture, I have failed to note it. We may well ask, Why did not other forms appear during the interval from 1558 to 1623, when but one sort, and that figured as little variable, received the notice of the early botanists? 

 The modern names of the tomato, or love apple, are 

  • in France, tomate, pomme d 'amour, pomme d'or, pomme du Perou
  • in Germany, tomate, liebesapfel
  • in Flanders and Holland, tomaat
  • in Italy, pomo d'oro ;
  • in Spain and Portugal, tomate ;
  • in Norway, kjoerlighedsaeble
  • In Arabic, bydingan toumaten
  • in Burma, kha-yan-myae-phung
  • in Ceylon, maha-rata-tamattie
  • in the Deccan, wallwangee
  • in Egypt, bydingan toumaten
  • in Malaya, tomatte
  • in Tagalo, tomates, camatis
  • in Tamil, seemie-takalie-pidlam ;
  • in Indian gardens, goot-begoon, oou laeetee buengun
  • in Mexico, jomatl ;
  • in Japan, akanasu, red egg-plant



Turnip. Brassica sp. 

 Vilmorin in his "Les Plantes Potageres," 1883, classes all the turnips under Brassica napus L. ; but the older authors referred them, more correctly as we think, to Brassica napus and B. rapa.   
Decandolle, who makes this distinction, separates the first into three groups, based on color, the white, yellow, and black ; the second into groups, comprising the white, yellow, black, red, and green. 

In the thirteenth century Albertus Magnus describes the napus as with a long root, which is eaten, and the rapa as having a spherical compressed bulb, and sometimes red in the stalk. 

The turnip is of ancient culture. Columella, 18 a.d., says the napus and the rapa are both grown, and the latter the larger and greener for the use of man and beasts, especially in France; the former not having a swollen, but a slender, root. He also speaks of the Mursian gongylis, which may be the round turnip, as being especially fine. 


The distinction between the napus and the rapa was not always held, as Pliny  uses the word napus generically, and says that there are five kinds, the 
  • Corinthean, 
  • Cleonaeum, 
  • Liothasium, 
  • Boeoticum, and the 
  • Green. 
The Corinthean, the largest, with an almost bare root, grows on the surface, and not, as do the rest, under the soil. 
The Liothasium, also called Thracium, is the hardiest. 
The Boeoticum is sweet, of a notable roundness, and not very long as is the Cleonaeum. 

At Rome the Amiternian is in most esteem, next the Nursinian, and third our own kind (the green ?). 

In another place, under rapa he mentions two kinds, the one broad-bottomed (flat?), the other globular, and the most esteemed those of Nursia. The napus of Amiterninum, of a nature quite similar to the rapa, succeeds best in a cool place. He mentions that the rapa sometimes attain a weight of forty pounds. 

This weight has, however, been exceeded in modern times.  Matthiolus, in 1558, had heard of turnips that weighed a hundred pounds, and speaks of having seen long and purple sorts that weighed thirty pounds. Amatus Lusitanus, in 1524, speaks of turnips weighing fifty and sixty pounds. In England, in 1792, Martyn  says the greatest weight that he is acquainted with is thirty-six pounds. In California, about 1850, a turnip is recorded of one hundred pounds weight.  

Brassica napus esculenta DC.

Vilmorin
This differs from the Brassica rapa oblonga by its smooth and glaucous leaves. It surpasses other turnips by the sweetness of its flavor, and furnishes white, yellow, and black varieties. It is known as the Navet or French turnip.  It was apparently the napa of Columella.  It was certainly known to the early botanists, yet its synonymy is difficult to be traced from the figures. 

 I think, however, the following are correct: 
  •  Napus. Trag., 1552, 730; Matth., 1554, 240; Pin., 1561, 144; Cam. Epit, 1586, 222; Dod., 1616, 674; Fischer, 1646. 
  •  Bunias sive napus. Lob. ic, 1 591, I., 200. 
  •  Bunias silvestris lobelii. Ger., 1597, 181. 
  •  Napi. Cast. Dur., 161 7, 304. 
  •  Bunias. Bodaeus, 1644, 773. 
  •  Napus dulcis. Blackw., 1765, t. 410. 
  •  Navet petit de Berlin. Vilm., 18.83,360. 
  •  Teltow turnip. Vilm., 1885, 5 8 

 The navews are mentioned as under cultivation in England by Worlidge,  in 1683, as the French turnip by Wheeler, in 1763, and Miller's Dictionary, 1807.  Gasparin  says the navet de Berlin, which often acquires a great size, is much grown in Alsace and in Germany. In China, according to Bretschneider,  it was known in the fifth century. 




 Brassica rapa depressa DC. 

 This has a large root expanding under the origin of the stem into a thick, round, fleshy tuber, flattened at the top and bottom. It has white, yellow, black, red or purple, and green varieties. It seems to have been known from ancient times, and is described and figured in the earlier botanies. 
A.  Flattened both above and below; Vilmorin



 A. Flattened both above and below. 
 Rapum. Matth., 1554, 240; Cam. Epit., 1586, 218. 
 Rapum sive rapa. Pin., 1561, 143. 
 Rapa. Cast. Dur., 1617, 386. 
 Navet turnip. Vilm., 1883, 583. 





B. Flattened, but pointed below.
Rave d'Auvergne tardive




 B. Flattened, but pointed below. 
 Orbiculatum seu turbinatum rapum. Lob. ic., 1791, I., 197. 
 Rapum. Porta, Phytognom, 1591, 120. 
 Rapum vulgare. Dod., 16 16, 673. 
 Rave d'Auvergne tardive. Vilm., 1883., 369. 






Vilmorin





 C. Globular. 
 Rapum. Trag., 1552, 728. 
 Rapa, La Rave. Tourn., 1719, 113. 
 Navet jaune d'Hollande. Vilm., 1883, 370. 
 Yellow Dutch. Vilm., 1885, 588. . 









Brassica rapa oblonga DC. 

 This race differs from the preceding in having a long and oblong tuber tapering to the radicle. It seems an ancient form, — perhaps the Cleonaeum of Pliny. 

  •  Vulgare rapum alterum. Trag., 1532, 729.
  •  Rapum longum. Cam. Epit, 1586, 219. 
  •  Rapum tereti, rotunda, oblongaque radici. Lob. ic., 1591, I., 197. 
  •  Rapum oblongius. Dod., 1616, 673. 
  •  Rapum sativum rotundum and oblongum. J. Bauh., 165 1, II., 838.
  •  Rapa, La Rave. Tourn., 1719, 113. 
  •  Navet de Briollay. Vilm., 1883, 372. 
  • Briollay turnip. Vilm., 1885, 591.

 This representation by no means embraces all the turnips now known, as it deals with form only, and not with color and habits. In 1828 thirteen kinds were in Thorburn's American seed catalogue, and in 1887 thirty-three kinds. 

In France, twelve kinds were named by Pirolle in 1824, and by Petit in 1826. In 1887 Vilmorin's wholesale seed-list enumerates thirty-one kinds. 

 The turnip is believed to have reached England from Holland in 1550, but before this it had reached the New World. In 1540 Cartier sowed turnip seed at the present Montreal, in Canada. In 1609  turnips are mentioned in Virginia, as also in 1649; they are mentioned as cultivated in Massachusetts in 1629. 

In Peru they are said by Acosta, in 1604, to have increased so abundantly as to become a nuisance in the planting of grain. 

 The turnip is called 
  • in France, navet, gros navet, grosse rave, naveau, navet turnips, rabiole, rabioule, rave plate, tornep, turneps, turnip ;
  •  in Germany, herbst-rube, stoppel-rube
  • in Flanders and Holland, raap
  • in Denmark, roe;
  • in Italy, navone, rapa
  • in Spain and Portugal, nabo
  • in Arabic, lift,  luft
  • in Bengali, shalgram
  • in Persia, shalgram ;
  •  in Sindh, gokhru
  • in Japan, busei, aona (the round form). 

Hmmm...is this the end of Sturtevant's articles?  No vegetable after "T"?   As far as I have found it is the last installment, but I will look again!