The Different Forms of Flowers on Plants of the Same Species

haracter of het

in fertility between legi

ised p

ains, size of anthers and

rent

nera which include h

antages derived f

ich plants beca

ssion o

rieties of hete

l re

ins, or in the structure of the stigma. The individuals of many ordinary hermaphrodite plants habitually fertilise one another, owing to their male and female organs being mature at different periods, or to the structure of the parts, or to self-sterility, etc.; and so it is with many hermaphrodite animals, for instance, land-snails or earth-worms; but in all these cases any one individual can fully fertilise or be fertilised by any other individual of the same species. This is not so with heterostyled plants: a long-styled, mid-styled or short-styled plant cannot fully fertilise or be fertilised by any other individual, but only by one belonging to another form. Thus t

sed with its own-form pollen, I will append Table 6.33 giving a summary of the results in all the cases hitherto ascertained. The fertility of the unions may be judged by two standards, namely, by the proportion of flowers which, when ferti

red with that of the illegitimate unions together. The fertility of

: Name o

ions : proportional numbe

sul

unions : average numb

veris :

elatior

ulgaris :

inensis :

sis (second t

sis (Hildebra

icula (Scot

imensis (Sco

usoides (Sco

lucrata (Sco

inosa (Scot

ne species of Pri

stris (H. Mul

difference probably is

erenne

ne (Hildebr

lis (German stock,

angustifoli

repens :

Brazilian

fagopyru

alicaria

iana (Hildebr

egnelli

peciosa

ts colour. In the reproductive organs the differences are much greater and more important. In the one form the stamens may be all of the same length, and in the other graduated in length, or alternately longer and shorter. The filaments may differ in colour and thickness, and are sometimes nearly thrice as long in the one form as in the other. They adhere also for very different proportional lengths to the corolla. The anthers sometimes differ much in size in the two forms. Owing to the rotation of the filaments, the anthers, whe

n of the styles, the papillose surface of the stigma is turned outwards in one form of Linum perenne, and inwards in the other form. In flowers of the same age of Primula veris the ovules are larger in the long-styled than in the short-styled form. The seeds produced by the two or three forms often differ in number, and sometimes in size and weight; thus, five seeds from the long-styled form of Lythrum salicaria equal in weight six from the mid-styled and seven from the short-styl

forty-three cases in which this was ascertained. But it should be observed that some of the following measurements are only approximately accurate, as only a few grains were measured. In several cases, also, the grains had been dried and were then soaked in water. Whenever they

rom the forms of the same heterostyled species; thos

HIC SP

: Name o

long-styled form

a veri

vulgar

ensis (Hild

auricu

ustris (H. M

alustris (

andiflor

(diameter vari

flavum

a officin

a angusti

m fagopy

Burnetti

la elat

s trifoli

mum Indic

ia (sp.

a suspen

(sp.?

ulchell

icranth

acumina

ylum (sp

on formo

en-grains of the long-

a (sp.?

a (sp.

.?) (Fritz

a coerul

dia (sp.

s (sp.?

(sp.?) (Fritz

ma (sp.

micrant

PHIC S

the extreme differences in diameter of the pollen- g

salica

erticill

viana (Hilde

Regnell

specios

sensiti

ria (sp

between the diameters of the pollen-grains

ng-styled form (

ssa, short-st

p.?) short-st

er sp. mid-sty

la Distribuzione dei Sessi nelle Piante' etc 1867 page 17.) But the case of Linum, in which the grains of the two forms are of equal size, whilst the pistil of the one is about twice as long as that of the other, made me from the first feel very doubtful with respect to this view. My doubts have since been strengthened by the cases of Limnanthemum and Coccocypselum, in which the grains are of equal size in the two forms; whilst in the former genus the pistil is nearly thrice and in the latter twice as long as in the other form. In those species in which the grains are of unequal size in the two forms, there is no close relationship between the degree of their inequality and that of their pistils. Thus in Pulmonaria officinalis and in Erythroxylum the pistil in the long-styled form is about twice the length of that in the other form, whilst in the former species the polle

he conducting tissue of the pistil. It is hardly possible to doubt that this must occur in such cases as that of the Datura, in which the tubes have to grow down the whole length of the pistil, and therefore to a length equalling 3,806 times the diameter of the grains (namely, .00243 of an inch) from which they are protruded. I may here remark that I have seen the pollen-grains of a willow, immersed in a very weak solution of honey, protrude their tubes, in the course of twelve hours, to a length thirteen times as great as the diameter of the grains. No

n those of the long-styled. With Pulmonaria angustifolia they vary much in size, but from an average of seven measurements of each kind the ratio is as 100 to 91. In six genera of the Rubiaceae there is a similar difference, either slightly or well marked. Lastly, in the trimorphic Pontederia the ratio is 100 to 88; the anthers from the longest stamens in the short-styled form being compared with those from the shortest stamens in the long-styled form. On the other hand

d. With most of the species, if there is any difference in the size of the stigma of the two forms, that of the long-styled, whatever its shape may be, is larger than that of the short-styled. But here again there are some exceptions to the rule, for in the short-styled form of Leucosmia Burnettiana the stigmas are longer and much narrower than those of the long-styled; the ratio between the lengths of the stigmas in the two forms being 100 to 60. In the three Rubiaceous genera, Faramea, Houstonia and Oldenlandia, the stigmas of the short- st

-styled than in the short-styled form, for the papillae on the former compared with those on the latter are as 100 to 58 in length. The length of the pistil in the long-styled form of Linum grandiflorum varies much, and the stigmatic papillae vary in a corresponding manner. From this fact I inferred at first that in all cases the difference in length between the stigmatic papillae in the two forms was one merely of correlated growth; but this can hardly be the true or general explanation, as the shorter stigmas of th

a, widely distributed throughout the world. These genera are included in fourteen Families, most of which are very distinct from one

genera including h

TYLE

RICI

tox

HROX

hrox

th

NIAC

nu

al

HRA

th

se

IAC

cho

var

ett

yot

nlan

sto

ocyp

ost

ox

ra

cho

dg

te

che

od

rer

rma

ULAC

im

ton

ros

ACE

syt

IANA

yan

anth

lar

MONI

li

DIE

rd

AGI

mon

ENAC

iph

YGO

ygo

MEL

mel

OTYLE

DERIA

ted

es for the modified descendants of a common progenitor to have spread from a single centre to such widely remote and separated areas. The family of the Rubiaceae contains not far short of as many heterostyled genera as all the other thirteen families together; and hereafter no doubt other Rubiaceous genera will be found to be heterostyled, although a large majority are homostyled. Several closely allied genera in this family probably owe their heterostyled structure to descent in common; but as the genera thus characterised are distributed in no less than eight of the tribes into which this family has been divided by Bentham and Hooker, it is almost certain that several of them must have become heterostyled independently of one another. What there is in the constitution or structure of the members of this family which favours their becoming heteros

se to have their sexes separated, as the forms must mutually fertilise one another. Therefore it seemed worth while to ascertain what proportion of the genera in the Linnean classes, Monoecia, Dioecia and Polygamia, contained species which live "in water, marshes, bogs or watery places." In Sir W.J. Hooker's 'British Flora' 4th edition 1838, these three Linnean classes include 40 genera, 17 of which (i.e. 43 per cent) contain species inhabiting the just-specified stations. So that 43 per cent of those British plants which have their sexes

he former cannot be looked at as tending to become dioecious. With Lythrum salicaria, however, we have the curious and unique case of the mid-styled form being more feminine or less masculine in nature than the other two forms. This is shown by the large number of seeds which it yields in whatever manner it may be fertilised, and by its pollen (the grains of which are of smaller size than those from the corresponding stamens in the other two forms) when applied to the stigma of any form producing fewer seeds than the normal number. If we suppose the process of deteriorat

relation to the visits of insects. The wonderful diversity of the means for gaining the same end in this case, and in many others, depends on the nature of all the previous changes through which the species has passed, and on the more or less complete inheritance of the successive adaptations of each part to the surrounding conditions. Plants which are already well adapted by the structure of their flowers for cross-fertilisation by the aid of insects often possess an irregular corolla, which has been modelled in r

be discussed. Heterostyled species, however, have an advantage over dichogamous species, as all the flowers on the same heterostyled plant belong to the same form, so that when fertilised legitimately by insects two distinct individuals are sure to intercross. On the other hand, with dichogamous plants, early or late flowers on the same individual may intercross; and a cross of this kind does hardly any or no good. Whenever it is profitable to a species to produce a large number of seeds and this obviously is a very common case, heterostyled will have an advantage over dioecious plants,

the same form, and in this case they will not produce the full number of vigorous and fertile seedlings; all these, moreover, will tend strongly to belong to the same form as their parents. On the other hand, if two plants of the same trimor

LANTS MAY HAVE BEEN

roughout the whole vegetable kingdom, and that even within the family of the Rubiaceae they are dispersed in eight of the tribes. We may therefore conclude that this structure has been acquired

lana prostrata these organs differ so much in length in different individuals that, until experimenting on them, I thought both species heterostyled. The stigma of Gesneria pendulina sometimes protrudes far beyond, and is sometim

ny plants, though in different degrees and ways, to be cross- fertilised. It might well happen that our supposed species did not vary in function in the right manner, so as to become either dichogamous or completely self-sterile, or in structure so as to ensure cross-fertilisation. If it had thus varied, it would never ha

ered to the same part of the body of the insects which frequented the flowers, and would afterwards have been deposited without loss on the stigma, if it likewise stood on the same unvarying level in all the flowers. But as the stamens and pistils are supposed to have already varied much in length and to be still varying, it might well happen that they could be reduced much more easily through natural selection into two sets of different lengths in different individuals, than all to the same length and level in all th

es, that there is no difficulty in believing that it could be effected through natural selection. Our plant would then make a close approach in structure to a heterostyled dimorphic species; or to a trimorphic species, if the stamens were reduced to two lengths in the same flower in correspondence with that of the pistils in the other two forms. But we have not as yet even touched on the chief difficul

en from the long-styled flowers of Hottonia to the stigma of the same form, and that this illegitimate union was not nearly so sterile as the corresponding union in other heterostyled species. But this conclusion is directly opposed by some other cases, for instance by that of Linum grandiflorum; for here the long-styled form is utterly barren with its own-form pollen, although from the position of the anthers this pollen is invariably applied to the stigma. It is obvious that

minated in the case of the individuals which differed in the length of their pistils and stamens. It is, however, incredible that so peculiar a form of mutual infertility should have been specially acquired unless it were highly beneficial to the species; and although it may be beneficial to an individual plant to be sterile with its own pollen, cross-fertilisation being thus ensured, how can it be any advantage to a plant to be sterile with half its brethren, that is, with all the individuals belo

ture, the anthers in size, and the pollen-grains in diameter. It appears, therefore, at first sight probable that organs which differ in such important respects could act on one another only in some manner for which they had been specially adapted. The probability of this view is supported by the curious rule that the greater the difference in length between the pistils and stamens of the trimorphic species of Lythrum and Oxalis, the products of which are united for reproduction, by so much the greater is the infertility of the union. The same rule applies to the two illegitimate unions of some dimorphic species, namely, Primula vulgaris and Pulmonaria angustifolia; but it entirely fails in other cases, as with Hottonia palustris and Linum grandiflorum. We shall, however, best perceive the difficulty of understanding the nature and origin of the co-adaptation between the reproductive organs of the two forms of heterostyled plants, by considering the case of Linum gra

e that the species which have become heterostyled at first varied so that two or three sets of individuals were formed differing in the length of their pistils and stamens and in other co-adapted characters, and that almost simultaneously their reproductive powers became modified in such a manner that the sexual elements in one set were adapted to act on the sexual elements of another set; and consequently that these elements in the same set or form incidentally became ill-adapted for mutual interaction, as in the case of distinct species. I have elsewhere shown that the sterility of species when first crossed and of their hybrid offspring must also be looked at as merely an incidental result, following from the special co-adaptation of the sexual elements of the same species. (6/7. 'Origin of Species' 6th edition page 247; 'Variation of Animals and Plants under Domestication' 2nd edition volume 2 page 169; 'The Effects of Cross and Self-fertilisation' page 463. It may be well here to remark t

HE TWO FORMS BY H

throw some light on their manner of development. Hildebrand observed that seedlings from the long-styled form of Primula Sinensis when fertilised with poll

fspring from illegitimately

Species

er of long-sty

er of short-st

tilised by own-form pollen during fi

led form, fertilised by

fertilised by own-form pollen during

rm pollen, is said to produce during successive generatio

fertilised by own-form pollen during

form, fertilised by own-form

tyled form, fertilised by

g-styled form, fertilised b

styled form, fertilised by

-styled form, fertilised b

fspring from illegitimately

Species

er of long-sty

ber of mid-st

er of short-st

yled form, fertilised by o

tyled form, fertilised by

fertilised by pollen from mid-length s

led form, fertilised by ow

ertilised by pollen from shortest sta

ertilised by pollen from longest stam

ing several generations by own- form pollen, p

yled form, fertilised by ow

vulgaris similarly raised all were long-styled. So it was with 56 seedlings from the long-styled form of the trimorphic Lythrum salicaria, and with numerous seedlings from the long-styled form of Oxalis rosea. The offspring from the short-styled forms of dimorphic plants, and from both the mid-styled and short-styled forms of trimorphic plants, fertilised with their own-form pollen, likewise

hort-styled seedlings may be attributed to reversion to their short-styled progenitor. But it is a surprising fact in this case, and in other similar ones, that the number of the offspring which thus reverted was not larger. The fact is rendered still more strange in the particular instance of P. veris, for there was no reversion until four or five generations of long-styled plants had been raised. It may be seen in both tables that the long-styled form transmits its form much more faithfully than does the short-styled, when both are fertilised with their own-form pollen; and why this should be so it is difficult to conjecture, unless it be that the aboriginal parent-form of most heterostyled species possessed a pistil which exceeded its own stamens considerably in length. (6/8. It may be suspected that this was the case

TYLED V

lf- fertilisation of a legitimate nature and yield a full complement of seed, or even more than the number produced by ordinary flowers legitimately fertilised. With P. Sinensis, on the other hand, the stamens resemble in all respects the shorter ones proper to the long-styled form, whilst the pistil makes a near approach to that of the short-styled, but as it varies in length, it would appear as if a long-styled pistil had been reduced in length and modified in function. The flowers in this case as in the last are capable of spontaneous legitimate fertilisation, and are rather more productive than ordinary flowers legitimately fertilised. With P. auricula and farinosa the stamens resemb

d plants of P. Sinensis, I have observed the first appearance and subsequent stages of this variation. With some other plants of P. Sinensis of similar parentage the flowers appeared to have reverted to their original wild condition. Again, some hybrids between P. veris and vulgaris were strictly equal-styled, and others made a near approach to this structure. All these facts support the view that this variation results, at least in part, from reversion to the original state of the genus, before the species had become heterostyled. On the other hand, some considerations indicate, as previously remarked, that the aboriginal pare

L RE

solely on their structure. On the other hand, with heterostyled dimorphic species there are two females and two sets of males, and with trimorphic species three females and three sets of males, which differ essentially in their sexual powers. We shall, perhaps, best perceive the complex and extraordinary nature of the marriage arrangements of a trimorphic plant by the following illustration. Let us suppose that the individuals of the same species of ant always lived in triple communities; and that in one of these, a large-sized female (differing also in other characters) lived with six middle-sized and six small-sized males; in the second community a middle-sized female lived with six large- and six small-sized males; and in the third, a small-sized female lived with six large- and six middle-sized males. Each of these three females, though enabled to unite with any male, would be nearly sterile with her own two sets of males, and likewise with two other sets of males of the same size with her own which lived in the other two communities; but she would be fully fertile when paired with a male of her own size. Hence the thirty-six males, distributed by half-dozens in the three commun