NATURE AND AFFINITIES OF THE SPONGES. 179in the same specific type, would there seem to be much prospect of arrivalat a more definite result.The Metazoic nature of the sponges, in deference to the authoritativedictum of Professor Haeckel, being accepted d priori as an article of creed,it has been rendered necessary to indicate, in one and all of those diverseso-called ciliated sponge-embryos, the existence of the two primary andabsolutely essential constituents of the Metazoic embryo, the ectodermand endoderm, as produced by the segmentation and subsequent metamorphosisof a primitive unicellular impregnated ovum. Deferring for awhile the consideration of the presumed identity of this earliest or initialphase, it may be first observed that the structural type, out of the threerespective series just enumerated, which has been accepted as conformingitself most conveniently to the Metazoic formula, is exhibited by that onein which the apical pole or segment of the reproductive body is composedof more minute columnar flagellate cells, and the opposite one of largerbut simply subspheroidal elements. Here, as typically represented in thecalcareous sponge, Grantia compressa (PI. IX. Fig. 27), there certainly, atfirst sight, appears to be a remarkable structural correspondence with thesegmented holoblastic ovum of the Mammalia, Amphibia, and various fishes,including Amphioxus, and numerous higher Invertebrata in which one-halfof the primitive ovum, dividing more rapidly and abundantly, becomes convertedinto numerous minute columnar blastomeres, and the opposite half,Dividing more slowly and less extensively, into fewer larger and subspheroidalblastomeres. Out of these two elemental series, distinguishedrespectively as the epiblast and hypoblast, the future ectoderm and endodermare subsequently developed, the former from the minute columnar blastomeresor epiblast, and the latter from the larger blastomeres or hypoblast.The identity of the segmentation process in the Metazoic embryo and inthe so-called sponge-larva being so far regarded as complete, the apparentcorresponding factors in either case have also been accepted as homologousectodermic and endodermic elements. Supposing, for the time, that thesetwo structural elements could be consistently correlated, what should bethe next step?In the Metazoic embryo it invariably happens that either by theinvagination or falling inwards, as in Amphioxus, upon the primitivecentral segmentation cavity or archenteron of the hypoblast or endodermicelement, or by the encroachment upon or growing over the latter, as inthe Amphibia, of the epiblast or ectodermal element, it comes to pass thatthe endoderm is enclosed within the ectoderm, and a bilaminate structureisproduced roughly resembling the double-walled sac-like body or so-called" "gastrula of Professor Haeckel. The outer lamina or wall of this saclikebody is now the ectoderm, the inner one, closely applied to it, theendoderm. The central cavity most usually enclosed within these layersrepresents the primitive alimentary tract or archenteron, and the apertureplacing the latter in communication with the outer world the primitive analN 2
l8oNATURE AND AFFINITIES OF THE SPONGES.aperture or blastopore. The question at issue is whether similar or equivalentdevelopmental steps are traceable in the ciliated sponge-gemmule ?F. E. Schulze, writing of Sycandra raphanus in the year 1875, deposes thatthere are, giving in demonstration the figures reproduced at PI. IX. Fig. 33.The same authority reports, however, as the result of a more recent investigationof this species, an entirely opposite plan of structure. According tohis later interpretation,* it is not the larger and apparent endodermic blastomeresthat become invaginated or enclosed within the more minuteectodermal elements, but, as indicated at Fig. 34 of the same plate, thelatter that sink down into, and are enclosed by, the former. By Metschnikoff,a second chronicler of the developmental phases of this identical species,the so-called ciliated larvae are described as presenting, in addition to theordinary form having dissimilar hemispheres of large, subspheroidal, nonflagelliferous,and more minute columnar flagellate cells, examples that aremade up entirely of flagellate columnar elements, which, however, towardsthe basal region, are of somewhat larger size. This slight modification ofthe first of the three structural types enumerated in a preceding page, asobserved by Metschnikoff, of Sycandra raphanus, represents the dominantform found in other closely allied calcareous species, as also in theMyxospongiae and the majority of the Siliceospongiae, where the characteristicamphiblastuloid type previously considered is not known to occur.This so to say homoblastic embryonic form, produced by the entire and evensegmentation of the primitive so-called ovum, and exhibiting in its characteristicstate the structure and condition only of a monoblastic or simplesingle-cell-walled morula, with a more or less extensive segmentation cavity,does not subsequently, by direct or indirect invagination, as occurs with themonoblastic morulae of the Metazoa, attain to the higher diploblastic formula ;it cannot therefore be consistently compared with the typical and characteristicdiploblastic embryo of any Metazoic organism. Nevertheless, variousmore or less arduous attempts have been made to demonstrate that evenin this simpler monoblastic reproductive body, the essential Metazoicelements, " ectoderm," " endoderm," and in some cases even " mesoderm,"are substantially represented.By some, including Professor Haeckel, it has been suggested that theendoderm is indirectly produced through the process of delamination,instead of that of invagination, as most usually obtains. Such an interpretation,however, is entirely upset by some highly remarkable results ofrecent investigation. It has been shown, in fact, by Oscar Schmidt, f withrelation to the calcareous type Ascetta primordialis, that the elements usuallyaccepted as representing the endoderm are produced neither by delaminationnor by invagination, but creep into the central segmentation cavityas separate and independent amcebiform units from the circumjacentso-called ectodermal layer, of which latter they are the metamorphosed'* 'Zeitschrift fur Wissenschaftliche Zoologie, Bel. xxxi., 1878.t ' Archiv fiir Mikroskopische Anatomic,' Bd. xiv., 1877.
- Page 3:
aoamoa
- Page 6 and 7:
"Our little systems have their day,
- Page 9:
TOTHOMAS HENRY HUXLEY, LL.D.,F.R.S.
- Page 12 and 13:
viiiPREFACE.experience some disappo
- Page 14 and 15:
XPREFACE.ready and valuable assista
- Page 16 and 17:
LEEUWENHOEtfS OBSERVATIONS. 3relate
- Page 18 and 19:
LEEUWENHOEICS OBSERVATIONS.5spatter
- Page 20 and 21:
LEEUWENHOEK'S OBSERVATIONS.Jstopped
- Page 22 and 23:
SIfi E. KING, 1693. JOHN HARRIS, 16
- Page 24 and 25:
STEPHEN GRA Y, 1696. LEEUWENHOEK, 1
- Page 26 and 27:
HENRY BAKER, 1742, 1753.13"Oct. 6th
- Page 28 and 29:
O. F. MULLER, 1773-1786. 15ledge of
- Page 30 and 31:
EHRENBERG, 1836. 17Notwithstanding
- Page 32 and 33:
F. DUJARDIN, 1841. T. VON SIEBOLD,
- Page 34 and 35:
FRIEDRICH STEIN, 1849-1854. 21cules
- Page 36 and 37:
CLAPAREDE AND LACHMANN, 1858-1860.
- Page 38 and 39:
F. STEIN, 1859. R. M. DIES ING, 184
- Page 40 and 41:
ANDREW PRITCHARD, 1861. H. JAMES-CL
- Page 42 and 43:
DALLINGER AND DRYSDALE, 1873-1875.
- Page 44 and 45:
CHAPTER II.THE SUB-KINGDOM PROTOZOA
- Page 46 and 47:
AFFINITIES OF THE SPONGIDA. 33ordin
- Page 48 and 49:
PRIMARY SUBDIVISIONS A UTHOKS S YST
- Page 50 and 51:
AUTHORS PHYLOGENETIC SCHEME. 37DIAG
- Page 52 and 53:
FLA CELLA TA -PANTOS TOMA TA ; FLA
- Page 54 and 55:
CHOANO-FLAGELLATA; MYCETOZOA. 41acc
- Page 56 and 57:
MYCETOZOAj LABYRINTHULIDA. 43From t
- Page 58 and 59:
GROUPS PROTISTA AND MONERA. 45of th
- Page 60 and 61:
DISTINCTION BETWEEN PROTOZOA AND PR
- Page 62 and 63:
( 49 )CHAPTER III.NATURE AND ORGANI
- Page 64 and 65:
AUTHORS CLASSIFICATORY TABLE.TABULA
- Page 66 and 67:
UNICELL ULAR NA TURE. 5 3dissolutio
- Page 68 and 69:
UN1CELL ULAR NA TURE. 5 5of the ent
- Page 70 and 71:
CUTICULAR ELEMENTS. 57substance the
- Page 72 and 73:
EXCRETED ELEMENTS. 59by the interca
- Page 74 and 75:
EXCRETED ELEMENTS. 6 1transparent,
- Page 76 and 77:
ENCYSTMENT. 63corresponding type of
- Page 78 and 79:
LOCOMOTIVE AND PREHENSILE APPENDAGE
- Page 80 and 81:
ORAL APERTURE. 67Oral Aperture or C
- Page 82 and 83:
CONTRACTILE VESICLES. 69shadowed. A
- Page 84 and 85:
CONTRACTILE VESICLES.71in the major
- Page 86 and 87:
NUCLEUS OR ENDOPLAST. 73to indicate
- Page 88 and 89:
NUCLEUS OR ENDOPLAST. 75Spirostomit
- Page 90 and 91:
NUCLEOLUS OR ENDOPLASTULE. 77with t
- Page 92 and 93:
COLOURING SUBSTANCES. 79held to ind
- Page 94 and 95:
TRICHOCYSTS. 8 1crowded together an
- Page 96 and 97:
TRICHOCYSTS. 83follow it,and being
- Page 98 and 99:
BINARY DIVISION. 85that remain, red
- Page 100 and 101:
EXTERNAL GEMMATION. 87entire oblite
- Page 102 and 103:
SPORULAR MULTIPLICATION. 89four, ei
- Page 104 and 105:
GENE TIC REPROD UCTION. 9 1and the
- Page 106 and 107:
GENETIC REPRODUCTION. 93illustrated
- Page 108 and 109:
GENETIC REPRODUCTION. 95capsules we
- Page 110 and 111:
GENETIC REPRODUCTION. 97be essentia
- Page 112 and 113:
ZOOLOGICAL AFFINITIES.90as known, i
- Page 114 and 115:
ZOOLOGICAL AFFINITIES.IOIunicellula
- Page 116 and 117:
ZOOLOGICAL AFFINITIES. 103position.
- Page 118 and 119:
ZOOLOGICAL AFFINITIES. 105forming t
- Page 120 and 121:
DIS TRIE UTION. \ O 7plete covering
- Page 122 and 123:
DISTRIBUTION.IOQIn an enumeration o
- Page 124 and 125:
DISTRIBUTION. I Ihunting grounds. A
- Page 126 and 127:
PRESER VA TION. I 13Preservation of
- Page 128 and 129:
ME THODS OF INVES TIGA TION. I I5fo
- Page 130 and 131:
METHODS OF INVESTIGA TION.1 1^only
- Page 132 and 133:
RED I; TUBERVILLE NEEDHAM. 119simil
- Page 134 and 135:
JOHN HARRIS ; SPALLANZANI.l 2 rfor
- Page 136 and 137:
LORENZ OKEN; EHRENBERG. 123moment w
- Page 138 and 139:
POUCHET ; PASTEUR. 125Director of t
- Page 140 and 141:
PROFESSOR TYNDALL. 127now to be sup
- Page 142 and 143: PROFESSOR TYNDALL. I29needle-dip fr
- Page 144 and 145: PROFESSOR TYNDALL. 131tubes, as giv
- Page 146 and 147: DALLINGER AND DRYSDALE. 133four day
- Page 148 and 149: A UTHOKS INVESTIGA TIONS. 13 5and D
- Page 150 and 151: A UTHORS INVESTIGA TIONS. 13 7or le
- Page 152 and 153: AUTHOR'S INVESTIGATIONS. 139and lai
- Page 154 and 155: A UTHORS INVESTIGA TIONS. 1 4 1clos
- Page 156 and 157: ( 143 )CHAPTER V.NATURE AND AFFINIT
- Page 158 and 159: NATURE AND AFFINITIES OF THE SPONGE
- Page 160 and 161: NATURE AND AFFINITIES OF THE SPONGE
- Page 162 and 163: NATURE AND AFFINITIES OF THE SPONGE
- Page 164 and 165: NATURE AND AFFINITIES OF THE SPONGE
- Page 166 and 167: NATURE AND AFFINITIES OF THE SPONGE
- Page 168 and 169: NATURE AND AFFINITIES OF THE SPONGE
- Page 170 and 171: NATURE AND AFFINITIES OF THE SPONGE
- Page 172 and 173: NATURE AND AFFINITIES OF THE SPONGE
- Page 174 and 175: NATURE AND AFFINITIES OF THE SPONGE
- Page 176 and 177: NATURE AND AFFINITIES OF THE SPONGE
- Page 178 and 179: NATURE AND AFFINITIES OF THE SPONGE
- Page 180 and 181: NATURE AND AFFINITIES OF THE SPONGE
- Page 182 and 183: NATURE AND AFFINITIES OF THE SPONGE
- Page 184 and 185: NATURE AND AFFINITIES OF THE SPONGE
- Page 186 and 187: NATURE AND AFFINITIES OF THE SPONGE
- Page 188 and 189: NATURE AND AFFINITIES OF THE SPONGE
- Page 190 and 191: NATURE AND AFFINITIES OF THE SPONGE
- Page 194 and 195: NATURE AND AFFINITIES OF THE SPONGE
- Page 196 and 197: NATURE AND AFFINITIES OF THE SPONGE
- Page 198 and 199: NATURE AND AFFINITIES OF THE SPONGE
- Page 200 and 201: NATURE AND AFFINITIES OF THE SPONGE
- Page 202 and 203: NATURE AND AFFINITIES OF THE SPONGE
- Page 204 and 205: NATURE AND AFFINITIES OF THE SPONGE
- Page 206 and 207: NATURE AND AFFINITIES OF THE SPONGE
- Page 208 and 209: ( 195 )CHAPTER VI.SYSTEMS OF CLASSI
- Page 210 and 211: CLASSIFICATION OF THE INFUSORIA.197
- Page 212 and 213: MULLERS CLA SSIPICA TOR Y S YSTEM.
- Page 214 and 215: EHRENBERG'S CLASSIFICATORY SYSTEM.2
- Page 216 and 217: CLASSIFICATORY SYSTEMS OF SIEBOLD A
- Page 218 and 219: CLAPAREDE AND LACHMANWS CLASSIFICAT
- Page 220 and 221: DIESINGS CLASSIFICATORY SYSTEM. 207
- Page 222 and 223: S TEIN'S CLA SSIFICA TOR Y S Ki TEM
- Page 224 and 225: A UTHOKS CLASSIFICA TOR Y S YSTEM.
- Page 226 and 227: A UTHOR'S CLA SSIPICA TOR Y S YSTEM
- Page 228 and 229: A UTHOKS CLASSIPICA TOR Y S YSTEM.
- Page 230 and 231: CLASS FLAGELLA TA. 2 I7more extensi
- Page 232 and 233: GENUS TRYPANOSOMA. 219Trypanosoma s
- Page 234 and 235: GENUS MASTIGAMCEBA . 221The some ha
- Page 236 and 237: ;,HAB.GENUS REPTOMONAS. 22$immediat
- Page 238 and 239: ORDER RA DIO-FLA CELLA TA.225Podost
- Page 240 and 241: Body subspherical orGENUS ACTINOMON
- Page 242 and 243:
GENUS SPONGASTERISCUS. 229Spongocyc
- Page 244 and 245:
Cladomonas.ipidodendrtSpongomonas.D