INDEX.

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  • Fall weaver, 197.
  • Fire fly, 202.
  • Flea, 86.
  • Forceps Tail, 171.
  • Forficula, 136.
  • Fossil insects, 158.
  • Myriopods, 158.
  • Scorpion, 158.
  • Foul brood, 40.

  • Gad fly, 74.
  • Galley worm, 149.
  • Gall flies, 193.
  • Gall fly, 72, 203.
  • Gall fly, two-winged, 196.
  • Gamasus, 120.
  • Ganin on embryology of insects, 161.
  • Gegenbaur on tracheÆ, 172.
  • Generalized types, 154.
  • Generation, alternate, 168.
  • Gerris, 210.
  • Gerris, egg-parasite of, 166.
  • Gills of insects, 172.
  • Gnat, 71, 189.
  • Gonocerus, 204.
  • Gordius, 46.
  • Gortyna, 215.
  • Grain Aphis, 209.
  • Grape insects, 57.
  • Grape leaf roller, 205.
  • Grape saw fly, 207.
  • Grapta, 189, 204, 207.
  • Grasshopper, 181, 211.
  • Green head, 74.
  • Grimm on parthenogenesis, 168.

  • HÆckel, Ernst, on ancestry of insects, 156.
  • Hairs of insects, 185.
  • Hair worm, 46.
  • Halictus, 31, 192.
  • Handily, A. H., on Thysanura, 133.
  • Hartt's discovery of fossil insects in New Brunswick, 158.
  • Harvest bugs, 122.
  • Haustellate insects, 183.
  • Hawk moth, 194, 200.
  • Head of insects, mode of formation of, 174.
  • Heart, iv.
  • Hemiptera, 209.
  • Hemipterous larvÆ, 175.
  • Hessian fly, 72, Nebalia, 182.
  • Nephelis, 166.
  • Nephopteryx, 49.
  • Neuropterous larvÆ, 175.
  • New Brunswick, fossil insects of, 158.
  • Newport, on embryology of Julus, 164.
  • Nicoletia, 131.
  • Nomada, 38.
  • Notonecta, 209.
  • Nova Scotia, fossil insects of, 159.

  • Ocypete, 159.
  • Odynerus, 207.
  • Œcanthus, 216.
  • Oil beetle, 188.
  • Onion fly, 49.
  • Ophioneurus, embryology of, 165.
  • Orchesella, 143.
  • Ornithomyia, 84.
  • Orthopterous larvÆ, 175.
  • Osmia, 27.
  • Otiorhynchus, 199.
  • Ovipositor of Cicada, 185.

  • Palpus, vi.
  • Origin of, 174.
  • Pangus, 191.
  • Panorpa, 171, 209.
  • Paper wasp, 207.
  • Papilio Asterias, 200.
  • Papirins, 142.
  • Parasite of insect eggs, 164.
  • Parsnip butterfly, 200.
  • Parthenogenesis, 168.
  • Pasteur on the silk worm disease, 63.
  • Pauropus, 149, 154, 158, 171.
  • Peach borer, 206.
  • Pear slug, 207.
  • Pea weevil, 188.
  • Peck, W. D., on the habits of Stylops and Xenos, 45, 46.
  • PelopÆus, 207.
  • Pentastoma, 148, 160.
  • Peripatus, 161.
  • Perla, 154.
  • Phora, 40.
  • Phymata, 211.
  • Phytocoris, 211.
  • Pickle worm, 57.
  • Pieris, 55, 197, 207.
  • Pieris brassicÆ, egg parasite of, Wasp, 206.
  • Water bear, 150.
  • Water boatman, 166, 209.
  • Waterhouse, G. R., on habits of Osmia, 27.
  • Weevil, 179, 188, 194.
  • Weismann on growth of insects, 164.
  • West, Tuffen, on the foot of the fly, viii.
  • Wheat midge, 197.
  • Wine fly, 83.
  • Wingless insects, 171.
  • Wings of insects as respiratory organs, 165.
  • Wings, origin of, 172.
  • Worthen's discovery of fossil insects in Illinois, 158.
  • Worms, the ancestors of insects, 160, 169.
  • Wyman, Jeffries, on the cells of the honey bee, 17.

  • Xenos, 46.
  • Xylobius, 159.
  • Xylocopa, 21.

  • Zaddach on development of worms, insects and crustaceans, 169.
  • ZoËa, 156.

  • [1] The cells are not perfectly hexagonal. See the studies on the formation of the cells of the bee, by Professor J. Wyman, in the Proceedings of the American Academy of Arts and Sciences, Boston, 1866; and the author's Guide to the Study of Insects, p 123.

    [2] Notes on the Habits of the Humble Bee (Proceedings of the Essex Institute, vol. iv, 1864, p. 101).

    Mr. Angus also writes us as follows concerning the habits of the Wandering Humble bee (Bombus vagans): "I have found the males plentiful near our garden fence, within a hole such as would be made by a mouse. They seem to be quite numerous. I was attracted to it by the noise they were making in fanning at the opening. I counted at one time as many as seven thus employed, and the sound could be heard several yards off. Several males were at rest, but mostly on the wing, when they would make a dash among the fanners, and all would scatter and play about. The workers seem to be of a uniform size, and full as large as the males. I think the object of the fanning was to introduce air into the nest, as is done by the Honey bees."

    [3] "Since writing the above I have opened one of the new holes of Xylocopa, which was commenced between three and four weeks ago, in a pine slat used in the staging of the greenhouse. The dimensions were as follows:—Opening fully 3-8 wide; depth 7-16; whole length of tunnel 6 5-16 inches. The tunnel branched both ways from the hole. One end, from opening, was 2 5-8, containing three cells, two with larva and pollen, the third empty. The other side of the opening, or the rest of the tunnel, was empty, with the exception of the old bee (only one) at work. I think this was the work of one bee, and, as near as I can judge, about twenty-five days' work. Width of tunnel inside at widest 9-16 inch.

    "I have just found a Xylocopa bobbing at one of the holes, and in order to ascertain the depth of the tunnel, and to see whether there were any others in them, I sounded with a pliable rod, and found others in one side, at a depth of five and one half inches; the other side was four inches deep without bees. The morning was cool, so that the object in bobbing could not have been to introduce fresh currents of air, but must have had some relation to those inside. Their legs on such occasions are, as I have noticed, loaded with pollen."

    [4] The External and Internal Parasites of Man and Domestic Animals. By Prof. A. E. Verrill, 1870. We are indebted to the author for the use of this and the figures of the Bot fly of the horse, the turkey, duck and hog louse, the Cattle tick, the itch insect and mange insect of the horse.

    [5]

    Ha! whare ye gaun, ye crowlin ferlie!
    Your impudence protects you sairly:
    I canna say but ye struift rarely,
    Owre gauze and lace;
    Tho' faith, I fear ye dine but sparely
    On sic a place.

    Ye ugly, creepin, blastic wormer,
    Detested, shunn'd by saunt and sinner,
    How dare ye set your fit upon her
    Sae fine a lady!
    Gae somewhere else and seek your dinner
    On some poor body.

    (To a Louse.—Burns.)

    [6] We notice while preparing this article that a journal of Parasitology has for some time been issued in Germany—that favored land of specialists. It is the "Zeitschrift fur Parasitenkunde," edited by Dr. E. Hallier and F A. Zurn. 8vo, Jena.

    [7] Figure 111 represents the parts of the mouth in a large specimen of Pediculus vestimenti, entirely protruding, and seen from above, magnified one hundred and sixty times; aa, the summit of the head with four bristles on each side; bb, the chitinous band, and c, the hind part of the lower lip, such as they appear through the skin by strong transmitted light; dd, the foremost protruding part of the lower lip (the haustellum); ee, the hooks turned outwards; f, the inner tube of suction, slightly bent and twisted; the two pairs of jaws are perceived on the outside as thin lines; a few blood globules are seen in the interior of the tube.

    [8] The figure at the bottom on the left represents the adult, fully-gorged tick.

    [9] Nicolet, in the "Annales de la Societe Entomologique de France" (tome v, 1847), has given us the most comprehensive essay on the group, though Latreille had previously published an important essay, "De l'Organization Exterieure des Thysanoures" in the "Nouvelles Annales du Museum d'Histoire Naturelle, Paris, 1832," which I have not seen. Gervais has also given a useful account of them in the third volume of "Apteres" of Roret's Suite a Buffion, published in 1844.

    The Abbe Bourlet, Templeton, Westwood, and Haliday have published important papers on the Thysanura; and Meinert, a Danish naturalist, and Olfers, a German anatomist, have published important papers on the anatomy of the group. In this country Say and Fitch have described less than a dozen species, and the writer has described two American species of Campodea, C. Americana, our common form, and C. Cookei, discovered by Mr. C. Cooke in Mammoth Cave, while Humbert has described in a French scientific journal a species of Jupyx (J. Saussurii) from Mexico.

    [10] The direct homology of these parts of the head (the occiput and the epicranium) with Perla, Forficula, etc., seems to me the best evidence we could have that the PodurÆ are not an independent group. In these most fundamental characters they differ widely from the Myriopods. I am not aware that this important relation has been appreciated by observers.

    [11] As we descend to the soft, tube-like, suctorial (?) mouth of Anura, which is said not to have hard mouth-parts, we see the final point of degradation to which the mouth of the Thysanura is carried. I think that this gradual degradation of the mouth-parts in this group indicates that the appendages in these animals are not formed on an independent type, intermediate, so to speak, between the mandibulate and haustellate types, but are simply a modification (through disuse) of the mandibulate type as seen in Neuropterous insects.

    [12] Lubbock considers that Papirius should be placed in a distinct family from Smynthurus, because it wants tracheÆ. Their presence or absence scarcely seems to us to be a family character, as they are wanting in the PoduridÆ, and are not essential to the life of these animals, while in other respects Papirius seems to differ but slightly from Smynthurus.

    [13] Dr. LaboulbÈne has recently, and we think with good reason, separated Anura maritima from the genus Anura, under the name of Anurida maritima.

    [14] Memoirs of the Peabody Academy of Science, II. Embryological Studies on Diplax, Perithemis, and the Thysanurus genus Isotoma. Salem, 1871.

    [15] Translated in 1859 by Mr. Dallas under the title "Facts for Darwin."

    [16] "Whether that common stem-form of all the Tracheata [Insects, Myriopods and Spiders] which I have called Protracheata in my 'General Morphology' has developed directly from the true Annelides (Coelminthes), or, the next thing to this (zunachst), out of Zoea-form Crustacea (Zoepoda), will be hereafter established only through a sufficient knowledge and comparison of the structure and mode of growth of the Tracheata, Crustacea and Annelides. In either case is the root of the Tracheata, as also of the Crustacea, to be sought in the group of the true jointed worms (Annelides, Gephyrea and Rotatoria." He considers the first insect to have appeared after the Silurian period, viz., in the Devonian.

    [17] The ZoËa is born with eight pairs of jointed appendages belonging to the head, and with no thoracic limbs, while in insects there are but four pairs of cephalic appendages and three pairs of legs. Correlated with this difference is the entirely different mode of grouping the body segments, the head and thorax being united into one region in the crab, but separate in the insects, the body being as a rule divided into a head, thorax and abdomen, while these regions are much less distinctly marked in the crabs, and liable in the different orders to great variations. The great differences between the Crustacea and insects are noticeable at an early period in the egg.

    [18] Considerations on the Transmutation of Insects in the Sense of the Theory of Descent. Read before the Imperial Zoological-botanical Society in Vienna, April 3, 1869.

    [19] American Naturalist, vol. 3, p. 45, March, 1869.

    [20] See Prof. Torell's discovery of Eophyton LinnÆanum, a supposed land plant allied to the rushes and grasses of our day, in certain Swedish rocks of Lower Cambrian age. The writer has, through the kindness of Prof. Torell, seen specimens of these plants in the Museum of the Geological Survey at Stockholm. Mr. Murray, of the Canadian Geological Survey, was the first to discover in America (Labrador, Straits of Belle Isle) this same genus of plants. They are described and figured by Mr. Billings, who speaks of them as "slender, cylindrical, straight, reed-like plants," in the "Canadian Naturalist" for August, 1872.

    Should the terrestrial nature of these plants be established on farther evidence, then we are warranted in supposing that there were isolated patches of land in the Cambrian or Primordial period, and if there was land there must have been bodies of fresh water, hence there may have been both terrestrial and aquatic insects, possibly of forms like the Podurids, May flies, PerlÆ, mites and Pauropus of the present day. There was at any rate land in the Upper Silurian period, as Dr. J. W. Dawson describes land plants (Psilophyton) from the Lower Heiderberg Rocks of Gaspe, New Brunswick, corresponding in age with the Ludlow rocks of England.

    We might also state in this connection that Dr. Dawson, the eminent fossil botanist of Montreal, concludes from the immense masses of carbon in the form of graphite in the Laurentian rocks of Canada, that "the Laurentian period was probably an age of most prolific vegetable growth. * * * Whether the vegetation of the Laurentian was wholly aquatic or in part terrestrial we have no means of knowing." In 1855, Dr. T. Sterry Hunt asserted "that the presence of iron ores, not less than that of graphite, points to the existence of organic life even during the Laurentian or so-called Azoic period." In 1861 he went farther and stated his belief in "the existence of an abundant vegetation during the Laurentian period." The Eophyton in Labrador occurs above the Trilobite (Paradoxides) beds, while in Sweden they occur below.

    [21] In a communication made to the Boston Society of Natural History, Oct. 17, 1870 (see also "American Naturalist" for Feb. and Sept., 1871).

    [22] On the Origin of Insects, a paper read before the LinnÆan Society of London Nov. 2, 1871, and reported in abstract in "Nature," Nov. 9, 1871.

    [23] This reminds us (though Ganin does not mention it) of the development of the embryo of Julus, the Thousand legs, which, according to Newport, hatches the 25th day after the egg is laid. At this period the embryo is partially organized, having faint traces of segments, and is still enveloped in its embryonal membranes and retains its connection with the shell. In this condition it remains for seventeen days, when it throws off its embryonal membrane, and becomes detached from the shell.

    [24] It is a suggestive fact that these deciduous forms give way through histolysis to true larval forms, just as in some flies (Musca vomitoria) the true larval form goes under, and the adult form is built up from the imaginal disks of the larva. In an analogous manner the deciduous, pluteus-condition of the young Echinoderm perishes and is absorbed by the growing body of the permanent adult stage. This deciduous stage of the ichneumon may accordingly be termed the prelarval stage. Now as we find insects with and without this prelarval stage, and in the radiates quite different degrees of metamorphoses, the inquiry arises how far these differences are correlated with, and consequently dependent upon, the physical surroundings of these animals in the free swimming condition. Merely to point out the differences in the mode of development of animals is an interesting matter, and one could do worse things, but the philosophical naturalist cannot rest here. He must seek how these differences were brought about.

    [25] Leuckart, in his great work, "Die Menschlichen Parasiten," p. 700, after the analogy of Hirudo, which develops a primitive streak late in larval life, ventures to consider the first indications of the germ of Nemertes in its larval, Pilidium form as a primitive streak. He also suggests that the development of the later larval forms of the Echinoderms is the same in kind.

    Moreover, nearly twenty years ago (1854) Zaddach, a German naturalist, contended that the worms are closely allied in their mode of development to the insects and crustaceans. He compares the mode of development of a leech (Clepsine) and certain bristle-bearing worms (SÆnuris, Lumbricatus and Uaxes); and we may now from Kowalensky's researches (1871) add the common earth worm (Lumbricus), in which there is no such metamorphosis as in the sea Nereids, to that of insects; the mode of formation of the primitive band in the leeches and earth worms being much like that of insects. This confirms the view of Leuckart and Ganin, who both seem to have overlooked Zaddach's remarks. Moreover, the rings of the harder bodied worms, as Zaddach says, contain chitine, as in the insects. Zaddach also enters into farther details, which in his opinion ally the worms nearer to the insects than many naturalists at his time were disposed to allow. The singular Echinoderes has some remarkable Arthropod characters.

    [26] Vergleichende Anatomie, 2te Auflage, 1870, p. 437. I should, however, here add that I am told by Mr. Putnam that some fishes which have no swim-bladder, are surface-swimmers, and vice versa.

    [27] Reported In "Nature" for Nov. 9, 1871.

    [28] The Embryology of Chrysopa, and its bearings on the Classification of the Neuroptera, "American Naturalist," vol. v. Sept., 1871.

    [29] "It is my opinion that the 'incomplete metamorphosis' of the Orthoptera is the primitive one, inherited from the original parents of all insects, and the 'complete metamorphosis' of the Coleoptera, Diptera, etc., a subsequently acquired one." Fuer Darwin, English Trans., p. 121.

    [30] The right side represents the under side of the wings.

    [31]The lower side of the wings is figured on the right side of this and figures 228. and 229.

    [32] See "Proceedings of the Essex Institute," vol. iv, p. 105.

    [33] Naturalist on the River Amazons, vol. 1, p. 32.

    [34] Transformations of Insects, p. 205.


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