such intermediate links?  Geology assuredly does not reveal any such 
 finely-graduated | finely-graduated 1861 1866 1869 1872 |  | finely graduated 1859 1860 |  
  
organic chain; and 
 this, | this, 1859 1860 1861 1869 1872 |  | this 1866 |  
  
perhaps, is the most obvious and 
 serious | serious 1861 1866 1869 1872 |  | gravest 1859 1860 |  
  
objection which can be urged against 
 the | the 1869 1872 |  | my 1859 1860 1861 1866 |  
  
 theory | theory 1872 |  | theory. 1859 1860 1861 1866 1869 |  
   The explanation lies, as I believe, in the extreme imperfection of the geological record.  | 
 | 
 In the first 
 place, | place, 1866 1869 1872 |  | place 1859 1860 1861 |  
  
it should always be borne in mind what sort of intermediate forms must, on 
 the | the 1869 1872 |  | my 1859 1860 1861 1866 |  
  
theory, have formerly existed.  I have found it difficult, when looking at any two species, to avoid picturing to 
 myself | myself 1869 1872 |  | myself, 1859 1860 1861 1866 |  
  
forms 
 
directly
 | 
directly
 1859 1860 1866 1869 1872 |  | directly 1861 |  
  
intermediate between them.  But this is a wholly false view; we should always look for forms intermediate between each species and a common but unknown progenitor; and the progenitor will generally have differed in some respects from all its modified descendants.  To give a simple illustration: the fantail and pouter pigeons 
 are | are 1872 |  | have 1859 1860 1861 1866 1869 |  
  
both descended from the rock-pigeon; if we possessed all the intermediate varieties which have ever existed, we should have an extremely close series between both and the rock-pigeon; but we should have no varieties directly intermediate between the fantail and pouter; none, for instance, combining a tail somewhat expanded with a crop somewhat enlarged, the characteristic features of these two breeds.  These two breeds, moreover, have become so much modified, 
 that, | that, 1866 1869 1872 |  | that 1859 1860 1861 |  
  
if we had no historical or indirect evidence regarding their origin, it would not have been possible to have 
 determined, | determined, 1866 1869 1872 |  | determined 1859 1860 1861 |  
  
from a mere comparison of their structure with that of the 
 rock-pigeon, | rock-pigeon, 1859 1860 1866 1869 1872 |  | rock-pigeon 1861 |  
  
 C. livia, whether | C. livia, whether 1866 1869 1872 |  
| whether 1859 1860 |  
| (C. livia), whether 1861 |  
  
they had descended from this species or from some other allied 
 form, | form, 1872 |  | species, 1859 1860 1861 1866 1869 |  
  
such as C. oenas.  | 
 | 
 So with natural species, if we look to forms very distinct, for instance to the horse and tapir, we have no reason to suppose that links 
 directly intermediate between them ever existed, | directly intermediate between them ever existed, 1872 |  
| ever existed directly intermediate between them, 1859 1860 1861 1866 1869 |  
  
but between each and an unknown common parent.  The common parent will have had in its whole organisation much general resemblance to the tapir and to the horse; but in some points of structure may have differed considerably from both, even perhaps more than they differ from each other. 
 Hence, | Hence, 1866 1869 1872 |  | Hence 1859 1860 1861 |  
  
in all such cases, we should be unable to recognise the parent-form of any two or more species, even if we closely compared the structure of the parent with that of its modified descendants, unless at the same time we had a nearly perfect chain of the intermediate links.  | 
 | 
 It is just possible by 
 the | the 1869 1872 |  | my 1859 1860 1861 1866 |  
  
theory, that one of two living forms might have descended from the other; for instance, a horse from a tapir; and in this case 
 
direct
 | 
direct
 1859 1860 1866 1869 1872 |  | direct 1861 |  
  
intermediate links will have existed between them.  But such a case would imply that one form had remained for a very long period unaltered, whilst its descendants 
 |