Savory - Arachnida 1977
Savory - Arachnida 1977 Savory - Arachnida 1977
228 III. PROLES ARACHNES and tarsus ( telotarsus) fuse, forming a compound miotarsus, and sometimes the two parts of the femur are united. In the Heterosphyronida the forelegs have miotarsi and the hind legs have separate metatarsi and tarsi. In the Diplosphyronida all the metatarsi and tarsi are separate and in the :\Ionosphyronida all have miotarsi. The pretarsus consists of two claws and a membranous arolium between them. The latter is a short sucking pad, which enables the false scorpion to climb perpendicularly and to walk or rest on the underside of smooth horizontal surfaces. The tarsal claws are not toothed. In the forelegs of the males of most Cheliferidae the anterior claw is distorted and is slenderer than its fellow. The tip of the miotarsus is often produced into a distinct spine, which is used in mating to open the female genital operculum and assist the entry of the spermatophore. The mouth parts of pseudoscorpions lie between the maxillae or gnathobases of the pedipalpi. The mouth itself is an aperture at the end of a tube or rostrum formed from dorsal and ventral projections. The latter, the labium or lophognath, is convex or crested dorsally, and is immovable. The upper lip, epipharynx or taphrognath, fits over the lower. By a slight upward movement of the taphrognath, the tube which they form can be enlarged, thus exerting a slight sucking effect. The true mouth, however, does not directly touch the food. The coxae of the pedipalpi enclose the rostrum in a trough-like chamber. Within this the laminae superiores and laminae inferiores lie closely below the rostrum, forming a compound tube which touches the prey in feeding and conducts the juices to the mouth. In the rostrum is an internal expansion forming a pharyngeal pump similar to, but not homologous with, the sucking stomach of spiders. Weygoldt (1972) has described the action of the effective muscle, which in a Chelifer made 160 vibrations per minute. At intervals, peristalsis could be seen, forcing the food onwards from the mesenteron. Indigestible particles were ejected between the palpal coxae, which were then cleaned by rubbing them on the ground. The ventral surface of the prosoma (Fig. 98) of pseudoscorpions is never protected by a large sternum, though a vestige may be found in certain species. This region is generally composed of the coxae of the legs and pedipalpi, which touch each other and meet in the middle line. However, in certain Chthonioidea a chitinous tubercle or platelet bearing one or two setae is found between the third and fourth coxae. This is a vestige of the true sternum. A secondary sternum is found in Garypidae, a mere membranization between the fourth coxae, and there is a larger secondary sternum in the small family Sternophoridae. The coxae extend further back than the carapace, and as a result the ventral surface of the first opisthosomatic segment is reduced. 28. THE ORDER PSEUDOSCORPIONES 229 FIG. 98. Pseudoscorpion. Species Chelifer cancroides, ventral aspect. The opisthosoma, more or less oval in form, is always broadly attached to the prosoma. It is fully segmented, with 12 tergites and ten sternites. The first sternite is either missing or fused with the second, which, with the third, forms the genital opercula. These enclose the genital chamber, which opens in the constant place on the second segment. The terminal somite is reduced to form the anal tubercle. Tracheae open on the third and fourth sternites. These hard plates of the opisthosoma are united by an extensible membrane. Since the abdomen contains the digestive and reproductive organs, whose bulk is liable to change, the size of the opisthosoma varies a good deal according to season and circumstances. In many genera the tergites are medially divided into two parts. The male organs within the second and third somites are an amazingly complex invagination of these two sternites. The slit leads to a uterus masculinus externus, and thence to a uterus masculinus internus.
230 Ill. PROLES ARACHNES From the former arise three large extensible chambers, the median and lateral genital sacs. The lateral ones are the protrusible "ram's horn organs" ~f Cheliferinae, which apparently function in sexual display. The median sac may serve as a seminal receptacle or as a reservoir for the secretions of the accessory glands. The female genitalia are much simpler. The uterus receives the oviduct, ~nd a pair o~spermathecae also open into it. Legg (1975), in an analysis of the vanous forms of spermathecae, has pointed out that the possibility of storing spermatozoa "has enabled the pseudoscorpions to escape from the stable, static and humid habitat of soil and decaying veg:tab~: debris a?d to exploit less favourable, non-static and temporary habita_ts .. A median and a pair of lateral perforated plates, known as the cnbiform plates, are found in association with the spermathecae. Their function is doubtful. The bodies and limbs of all Pseudoscorpiones carry sensory spines and setae, and are well supplied with lyriform organs. DISTRIBUTION Fals: scorpions are found everywhere except in the frigid regions of the Arct~c and Antarctic. When the distribution of the separate families is considered some degree oflocalization is found, but several of them are cosmopolitan or nearly so. The following summary offamily distribution is taken from Chamberlin's work. FAMILY Dithidae Chthoniidae Syarinidae N eobisiidae Hyidae Ideoroncidae Olpiidae Menthidae Garypidac Feaellidae Pseudogarypidae Cheiridiidae Sternophoridae Pseudoch eiridiidae M yrmochernetidae Chernetidae Atemnidae Cheliferidae DISTRIBUTION West lndies, S.E. United States, Brazil Cosmopolitan Rocky Mountains and Pacific Coasts of North America Cosmopolitan Philippine Islands Brazil, Paraguay, Mexico, W. United States Sumatra Siam Tropical ' ' Deserts of W. Mexico and S.W. United States Tropical Africa, India, Seychelles, Madagascar Wyoming, Utah, Idaho, Oregon and California Cosmopolitan, except Australasia Western Mexico and Australia Nicobars, India, Burma and South Africa Africa Cosmopolitan Oriental and Ethiopian, rare in America Cosmopolitan 28. THE ORDER PSEUDOSCORPIONES 231 PALAEONTOLOGY No fossil false scorpions of the earlier epochs have been discovered, but a fairly large number of species preserved in amber have been described. Some of these have been assigned to recent genera, and it is of particular interest to note that even in those remote times false scorpions had adopted the same method of securing dispersal that they use today. One specimen was found in am her attached to the leg of an ichneumon just as it might have been found at the present. Amber-enclosed pseudoscorpions have come from the Baltic and from Burma, showing a wide dispersal comparable to the present condition. A Miocene species, Garypus birmiticus, has also been described from Burma. CLASSIFICATION When Eugene Simon produced his account of the French false scorpions in 1879 he grouped them all in a single family, Cheliferidae, with three sub-families and six genera. Simple as this system was, it was the foundation of all modern methods. In 1891 there first appeared, in a work by L. Balzan, the division of the order into two sub-orders, Panctenodactyli and Hemictenodactyli, based on the complete or partial attachment of the serrula to the chelicera. In this scheme there were four families and 13 genera, and it provided the foundation of all the systematic work on the group. It was greatly improved as a result of the labours of Hansen ( 1893) and With ( 1908) and in this modified form is adopted in the work of Berland (1932). In 1931 there appeared the striking monograph ofJ. C. Chamberlin; the result of many years of intensive study, in which the whole order is subjected to a thorough scrutiny, and a full and comparative account is given of the structure of these Arachnida. An alternative system, is that due to Beier in "Das Tierreich", 1933. He proposed a separation into three sub-orders, including 14 families with about 160 genera. I (2) Legs I and 2 with tarsus undivided, legs 3 and 4 with tarsus of two parts CHTHONIINEA 2 (I) All legs have similar tarsi, i.e. of one or of two parts (3) 3 (4) All legs with tarsus undivided; eyes never four in number CHELIFERINEA 4 (3) All legs with tarsus in two parts NEOBISINEA. (With the exception of the Feaellidae which have four eyes) The most recent system is that ofWeygoldt ( 1969), in which there are two "groups", three sub-orders and six super-families. In outline it reads as follows:
- Page 69 and 70: 126 III. PROLES ARACHNES 14. THE OR
- Page 71 and 72: 130 Ill. PROLES ARACHXES The lowly
- Page 73 and 74: 134 Ill. PROLES ARACHNES to be seen
- Page 75 and 76: 16. THE ORDER SCHIZOMIDA 139 16 The
- Page 77 and 78: 142 Ill. PROLES ARACHKES power, an
- Page 79 and 80: 146 III. PROLES ARACHNES DISTRIBUTI
- Page 81 and 82: 150 III. PROLES ARACHNES chelicerae
- Page 83 and 84: 154 Ill. PROLES ARACHNES FIG. 53. S
- Page 85 and 86: 158 Ill. PROLES ARACHNES (vi) Lobed
- Page 87 and 88: 162 III. PROLES ARACHNES is found i
- Page 89 and 90: 166 III. PROLES ARACHNES 4 (3) Chel
- Page 91 and 92: 20. THE ORDER TRIGONOTARBI 171 20 T
- Page 93 and 94: 174 Ill. PROLES ARACHNES 22 The Ord
- Page 95 and 96: 178 III. PROLES ARACHNES The family
- Page 97 and 98: 182 III. PROLES ARACHNES are above
- Page 99 and 100: 186 Ill. PROLES ARACHNES opisthosom
- Page 101 and 102: 190 Ill. PROLES ARACHNES Sub-order
- Page 103 and 104: 194 III. PROLES ARACIINES 25. THE O
- Page 105 and 106: 26 The Order Acari 26. THE ORDER AC
- Page 107 and 108: 202 III. PROLES ARACHNES Tetrastigm
- Page 109 and 110: 206 Ill. PROLES ARACHNES 26. THE'.
- Page 111 and 112: 210 Ill. PROLES ARACHNES ( 1) Notos
- Page 113 and 114: 214 Ill. PROLES ARACHNES The sevent
- Page 115 and 116: 218 Ill. PROLES ARACHNES family, Ho
- Page 117 and 118: 222 Ill. PROLES ARACHNES posterior
- Page 119: 226 III. PROLES ARACHNES 28. THE OR
- Page 123 and 124: 234 Ill. PROLES ARACHNES 29. THE OR
- Page 125 and 126: 238 Ill. PROLES ARACHNES The chelic
- Page 127 and 128: 242 IlL PROLES ARACHNES 29. THE ORD
- Page 129 and 130: 30 Economic Arachnology The Arachni
- Page 131 and 132: 250 IV. DE ARACHNOLOGIA Although th
- Page 133 and 134: ··~~- -..... 254 IV. DE ARACHNOLO
- Page 135 and 136: 31 Historical Arachnology The histo
- Page 137 and 138: 262 IV. DE ARACHNOLOGIA spiders qui
- Page 139 and 140: 266 IV. DE ARACHNOLOGIA little was
- Page 141 and 142: 32 Practical Arachnology The practi
- Page 143 and 144: 274 IV. DE ARACHNOLOGIA hard. In th
- Page 145 and 146: 278 IV. DE ARACHNOLOGIA EXCURSUS A
- Page 147 and 148: 33 Chemical Arachnology In the stud
- Page 149 and 150: 286 IV. DE ARACHNOLOGIA not very pl
- Page 151 and 152: 290 IV. DE ARACHNOLOGIA seventeenth
- Page 153 and 154: 294 IV. DE ARACHNOLOGIA A new aspec
- Page 155 and 156: 298 IV. DE ARACHNOLOGIA For more th
- Page 157 and 158: 36 The Spider's Web The webs that s
- Page 159 and 160: 306 V. HETEROGRAPHIA a number ofver
- Page 161 and 162: 310 V. HETEROGRAPHIA dramatically p
- Page 163 and 164: 314 ( i) ( ii) ( iii) (iv) (v) V. H
- Page 165 and 166: 318 V. HETEROGRAPHIA this may be ad
- Page 167 and 168: 322 V. HETEROGRAPHlA .1\Jenge in 18
- Page 169 and 170: 326 VI. EPILEGO:VIENA Vellard, J.,
228 III. PROLES ARACHNES<br />
and tarsus ( telotarsus) fuse, forming a compound miotarsus, and sometimes<br />
the two parts of the femur are united. In the Heterosphyronida<br />
the forelegs have miotarsi and the hind legs have separate metatarsi and<br />
tarsi. In the Diplosphyronida all the metatarsi and tarsi are separate and<br />
in the :\Ionosphyronida all have miotarsi.<br />
The pretarsus consists of two claws and a membranous arolium<br />
between them. The latter is a short sucking pad, which enables the<br />
false scorpion to climb perpendicularly and to walk or rest on the<br />
underside of smooth horizontal surfaces. The tarsal claws are not<br />
toothed. In the forelegs of the males of most Cheliferidae the anterior<br />
claw is distorted and is slenderer than its fellow. The tip of the miotarsus<br />
is often produced into a distinct spine, which is used in mating to open<br />
the female genital operculum and assist the entry of the spermatophore.<br />
The mouth parts of pseudoscorpions lie between the maxillae or<br />
gnathobases of the pedipalpi. The mouth itself is an aperture at the end<br />
of a tube or rostrum formed from dorsal and ventral projections. The<br />
latter, the labium or lophognath, is convex or crested dorsally, and is<br />
immovable. The upper lip, epipharynx or taphrognath, fits over the<br />
lower. By a slight upward movement of the taphrognath, the tube which<br />
they form can be enlarged, thus exerting a slight sucking effect. The<br />
true mouth, however, does not directly touch the food. The coxae of the<br />
pedipalpi enclose the rostrum in a trough-like chamber. Within this<br />
the laminae superiores and laminae inferiores lie closely below the<br />
rostrum, forming a compound tube which touches the prey in feeding<br />
and conducts the juices to the mouth. In the rostrum is an internal<br />
expansion forming a pharyngeal pump similar to, but not homologous<br />
with, the sucking stomach of spiders.<br />
Weygoldt (1972) has described the action of the effective muscle,<br />
which in a Chelifer made 160 vibrations per minute. At intervals,<br />
peristalsis could be seen, forcing the food onwards from the mesenteron.<br />
Indigestible particles were ejected between the palpal coxae, which<br />
were then cleaned by rubbing them on the ground.<br />
The ventral surface of the prosoma (Fig. 98) of pseudoscorpions is<br />
never protected by a large sternum, though a vestige may be found in<br />
certain species. This region is generally composed of the coxae of the<br />
legs and pedipalpi, which touch each other and meet in the middle line.<br />
However, in certain Chthonioidea a chitinous tubercle or platelet<br />
bearing one or two setae is found between the third and fourth coxae.<br />
This is a vestige of the true sternum. A secondary sternum is found in<br />
Garypidae, a mere membranization between the fourth coxae, and<br />
there is a larger secondary sternum in the small family Sternophoridae.<br />
The coxae extend further back than the carapace, and as a result the<br />
ventral surface of the first opisthosomatic segment is reduced.<br />
28. THE ORDER PSEUDOSCORPIONES 229<br />
FIG. 98. Pseudoscorpion. Species Chelifer cancroides, ventral aspect.<br />
The opisthosoma, more or less oval in form, is always broadly<br />
attached to the prosoma. It is fully segmented, with 12 tergites and ten<br />
sternites. The first sternite is either missing or fused with the second,<br />
which, with the third, forms the genital opercula. These enclose the<br />
genital chamber, which opens in the constant place on the second segment.<br />
The terminal somite is reduced to form the anal tubercle.<br />
Tracheae open on the third and fourth sternites.<br />
These hard plates of the opisthosoma are united by an extensible<br />
membrane. Since the abdomen contains the digestive and reproductive<br />
organs, whose bulk is liable to change, the size of the opisthosoma varies<br />
a good deal according to season and circumstances. In many genera the<br />
tergites are medially divided into two parts.<br />
The male organs within the second and third somites are an amazingly<br />
complex invagination of these two sternites. The slit leads to a<br />
uterus masculinus externus, and thence to a uterus masculinus internus.