It will be seen that this
arrangement
of the order does not differ materiallyfrom
thosewhich have
beenmost
generally in use (for asummary
of the principal attempts at classifying the cetaceans see W'inge, Smithsonian Misc. Coll., Vol. 72,No.
8, pp. 58-62) exceptin the greaterindependencenow
attributed to allthreeof the suborders, and,among
themembers
ofthe Odontoceti, inthewide
separation of the ziphiidsfrom
the physeteroids,and
especially in the separation of the rather primitive iniidsfrom
Platanista, thegenus which
Iregard as presenting the greatest total of modifications
known
inany
cetacean.Aside from
these admittedly controversial details the departuresfrom
accepted usage, so far as such usage can be said toexist, chiefly pertain to questions ofjudgment
with regard to the limits of theminor
groupsand
the relative importance assigned tosome
of thesegroups.That
aclassificationbasedon
a mostlyuntried set of characters should coincide in themain
with the classifications already in existence indicates the general soundness of the broader results ofwork on
cetaceantaxonomy. The
differences in detail are mostly the result oftwo
causes: first, thatsome
of the char- acters hitherto regarded as indices to relationshipnow
appear to be paralleland
independent modifications, and, second, thatcompara-
tively
few
of the extinctmembers
of the order areknown from
re-mains
completeenough
toshow
the featureswhich
arenow
seen to beneeded
for a natural classification.Examples
of the first are furnishedby
the beakform
supposed to bring together the other- wise excessively different Platanistaand
Inia or Lipotcs; the tusk- like tooth structure supposed to indicate relationship to thesperm
whales on thepart of various fossilcetaceansknown from
teeth only (this structurenow
appears to be merelya mechanical strengthening of the teeth bymeans which have
been independently adopted in thesperm
whale, the whitewhale and
the ziphiids; probably elsewhere
under
the influence of appropriate stimulus) ; the unusual relation- ship of the hindermost ribs to the vertebraesupposed
to be evidence in favor of placing the ziphiids in thesame group
with thesperm whale
notwithstanding thefundamental
differences presentedby
the structure of the skulls.Examples
of the second are sonumerous
that detailed listing is scarcely necessary in the present connection.A few
characteristic instances are furnished by the remainswhich
formed
the bases of the following 30 genericnames
: Agriocetus, Cetophis, Cetorliynchus, Delphinaviis, Delphinopsis, Dinoziphius, Eucetiis,Hcspcrocctus, Hoplocetus,Iniopsis,IxacantJins,Kekenodon,
Metasqnalodon, Microcetus, Microseuglodon, Outocetus, Orycetero-42 SMITHSONIAN MISCELLANEOUS COLLECTIONS
VOL. 76 cetus, Palccodclphis, Patriocctus', Phocanopsis, Phocagcnius,Physo-
don, Priseodelphinus, Prophysetef, Prosqualodon, Protophoccena, Rhabdostciis, Scaldicetus, Stcnodofi, Tretosphys.Most
of the supergeneric groups here recognizedhave
already been sufficiently discussed for the purposes of this paper. Concern- ingsome
ofthem
further observationsmay
not be out of place.Arcliccoccti.
—
Cabrera(Manual
de Mastozoologia, p. 316, 1922) has recently placed the zeuglodonts in an order separatefrom
themodern
cetacea. Thismay
be the firststeptoward
the eventual ele- vation of all three of the currently recognizedmajor
groups to the rank of orders.According
toPompeckj
(Senckenbergiana, Vol. 4,pp. 43-100,Oc-
tober 20, 1922) the structure of the perioticbone
in the zeuglodonts resembles thatnow found
in the baleen whales.The
presence of such conditions is not likely tomean
anythingmore
than a paralleldevelopment
of the ear in thetwo
groups, ormore
probably, the existence of similar ear structure in thetwo
ancestral stocksfrom which
these groups took their origin.The
difficulties in theway
of deriving a mysticeteskullfrom
onewhich had
firstassumed
theform
present in allknown
zeuglodonts appear to be little short of in- superable.A g
orophiidcc—'The
threeAmerican
generanow
placedin thisfam-
ily are well dififerentiated
from
each otherthough
they probably represent one stage of the telescoping process.Whether
the genus Patriocetus belongs in thesame
family orwhether
it represents a distinctgroup
are questionswhich
the descriptionsand
figuresdo
not furnish the data for answering.The
photographs publishedby Abel
(Denkschr. kais.Akad.
Wissensch.Wien,
math.-naturw. Kl., Vol. 90, pis. 1-4, 1914) indicate (a) that the generalform
of the skull in both dorsaland
lateralview
is essentially likethat ofAgoro-
phius (Smithsonian Inst., Special Publ.,No.
1694, pi. 6, 1907),and Archao
delphis (Bull.Mus. Comp.
Zool.,Vol. 65,No.
i,figs, i, 2and
plate, 1921), (b) that the braincase is similarly small as
compared
withthe restof the skull,and
(c) that adeeppostorbital constrictionis present. Apparently the maxillary
may have formed
part of the anterior orbital wall as in Arehceodelphis.The most
obvious differ- encefrom Agorophius
clearlyshown by
Abel's photographs is the presence of a thin overhanging ledge slopingupward and backward
from
the hindermargin
of the orbit,and
partly obscuring the post- orbital constriction.The
surface of the fossilis thickly covered with grains ofsandwhich
obscuremost
of thefiner details. (Seeremarks
NO. 5
TELESCOPING
OFTHE CETACEAN SKULL 43 by
Koriig, Jahres-Ber.Mus.
Franc.-Carol., Linz, Vol. 69, p. iii, 1911.)Such
details as can be seen are, however, in accord with the conditions present in both the kindand
stage of telescoping repre- sentedby Agorophiiisand
Archcrodclphis.The
reconstructionsgivenby
Abel in plates6 and
11 show,on
the contrary, a structurewhich
differs fundamentally
from
thatknown
to occurinany
other cetacean.The
maxillar}- is represented as broadly united with the frontal by a straight suture extending directlyinward
to the intermaxillaryfrom
a point situatedon
the side of therostrum
in front of the anteriormargin
of the orbit.No
part of the maxillary extends behind this level eitherabove
orbelow
the frontal; yet the intermaxillary runs farback
behind both maxillaryand
orbit, its extremity touching the parietal.The
fronto-maxillary suture, if correctly interpreted, isnot very different
from
that usually seen in the zeuglijdonts.The
relative degree of
backward
extension of the maxillaryand
inter- maxillary is,on
the contrary,something unknown
either in zeu- glodonts or in cetaceans wnth telescoped skulls. It should furtherbe noticed that essentiallynormal
conditions, not very differentfrom
thosewhich
appear tohave
been present inAgorophms were
de- scribedby Konig
as occurring in the specimen afterward interpretedby
Abel. Inthezeuglodontsthe relationships ofthesetw^oboneshave remained
normal,and
the posterior border of the maxillary lies be- hind the extremity of the intermaxillary (pi. 5, fig. i).During
the process of telescoping in allknown
cetaceans it appears to be the maxillarywhich
leads in thebackward move,
sothatin rareinstances only does the intermaxillary attain themore
posteriorlevel,and
thenby
such amere
trifle as toform no
real exception to the general rule (seediagram
of Rhachianectes, pi. 8, fig. 3).That
the inter- maxillary inany
cetacean shouldhave extended backward
to the parietal whilethe maxillaryremained
stationary in front of the orbit is so contrary to probability that the evidence ofan
unusually well preserved specimenwould
be necessary before anything of the kind could be believed tohave
taken place. If such a condition should ever be demonstrated to occur itwould
indicate the existence of a third type of telescoping not directly related to or derivablefrom
either of thosenow known. That
the genus Patriocetns as inter- pretedby Abel would
be unlikely torepresent a stage ancestral to themodern
baleen whales appears to be clearlyenough
indicatedby
the character justmentioned
; it ismade
practically certainby
the absenceof theorbital plateof the maxillary,no
trace ofwhich
appears either in Abel's photographs or restoration (based chieflyon
theI
44 SMITHSONIAN MISCELLANEOUS COLLECTIONS
VOL. 76
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