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BULLETIN OF THE UNITED STATES FISH COMMISSION 1901
Page 415 MARINE PROTOZOA FROM WOODS HOLE.
Comparatively little has been done in this country upon marine Protozoa. A few observations have been made by Kellicott, Stokes, and Peck, but these have not been at all complete. With the exception of Miss Stevens's excellent description of species of Lichnophora I am aware of no single papers on individual forms. Peck ('93 and '95) clearly stated the economic position of marine Protozoa as sources of food, and I need not add to his arguments. It is of interest to know the actual species of various groups in any locality and to compare them with European forms. The present contribution is only the beginning of a series upon the marine Protozoa at Woods Hole, and the species here enumerated are those which were found with the algæ along the edge of the floating wharf in front of the Fish Commission building and within a space of about 20 feet. Many of them were observed in the water and algae taken fresh from the sea; others were found only after the water had been allowed to stand for a few day, in the laboratory. The tow-net was not used, the free surface Protozoa were not studied, nor was the dredge called into play. Both of these means of collecting promise excellent results, and at some future time I hope to take advantage of them. My observations cover a period of two months, from the 1st of July to the 1st of September. During that time I was able to study and describe 72 species representing 55 genera, all from the limited space mentioned above. In addition to these there are a few genera and species upon which I have insufficient notes, and these I shall reserve until opportunity comes to study them further. I take this opportunity to express my thanks to Dr. Hugh M. Smith for many favors shown me while at Woods Hole. In dealing with these marine forms from the systematic standpoint, two courses are open to the investigator. He may make numerous new species based upon minor differences in structure, or he may extend previous descriptions until they are elastic enough to cover the variations. The great majority of marine Protozoa have been described from European waters, and the descriptions are usually not elastic enough to embrace the forms found at Woods Hole. I have chosen, however, to hold to the conservative plan of systematic work, and to make as few new species as possible, extending the older descriptions to include the new forms. --------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION. Page 416 The different classes of Protozoa, and orders within the classes, are distributed more or less in zones. Thus the Infusoria, including the Ciliata and the Suctoria, are usually littoral in their habitat, living upon the shore-dwelling, or attached, water plants and upon the animals frequenting them. It is to be expected, therefore, that in forms here considered there should be a preponderance of Infusoria. Flagellated forms are also found in similar localities, but on the Surface of the sea as well; hence the number described in these pages is probably only a small proportion of the total number of Mastigophora in this region. The Sarcodina, including the Foraminifera and the Radiolaria, are typically deep-sea forms and would not be represented by many types in the restricted locality examined at Woods Hole. Two species, Gromia lagenoides and Truncatulina lobatula, alone represent the great order of Foraminifera, while the still larger group of Radiolaria is not represented at all. The Protozoa described are distributed among the different orders as follows: (Note: this classification includes only the orders and families represented at Woods Hole.) [Click on page numbers to visit each species] See Image Gallery (courtesy University of Washington Library Digital Collection)
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------------------------------------------------------------- Page 417 GENUS AMOEBA Auct The pseudopodia are lobose, sometimes 'absent, the body then progressing by a flowing movement; the body consists of ectoplasm and endoplasm, the latter being granular and internal, the former hyaline and external. There is always one nucleus and one vacuole, but both may be more numerous. Reproduction takes place by division or by spore formation. Fresh-water and marine. IMAGE Fig. 1 Fig.3 Trichosphaerium Sieboldi Amoeba guttula Duj. Fig.1
Amoeba sp.
Fig. 2
--------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 418 GENUS TRICHOSPHAERIUM Schneider 1878
Marine rhizopods, globular or irregular in form, and slow to change shape. Dimorphic. Both forms multinucleate during vegetative life. Pseudopodia are long, thin, and thread-form, with rounded ends. Their function is neither food-getting nor locomotion, but probably tasting. The plasm of both forms is inclosed in a soft gelatinous membrane. In one form the jelly is impregnated with needles of magnesium carbonate (Schaudinn), but these are absent in the other form. The membrane is perforated by clearly defined and permanent holes for the exit of the pseudopodia. Reproduction occurs by division, by budding or by fragmentation, but the parts are invariably multinucleate. At the end of vegetative life the needle-bearing form fragment-9 into numerous mononucleate parts; these develop into adults similar to the parent, but without the spines. At the end of its vegetative life this new individual fragments into biflagellated swarm-spores which may conjugate, reproducing the form with needles. Size up to 2 mm. Trichosphaerium sieboldi Schneider. Fig. 3.
Only one specimen of this interesting form was seen, and I hesitate somewhat in placing it on such a meager basis. It is so peculiar, however, that attention should be called to it in the hope of getting further light upon its structure and mode of life. Its membranous disk recalls the genus Plakopus; its mononucleate condition, its membranous disk, and the short, sometimes branched, ---------------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE. Page 419 pseudopodia make it difficult to identify with any phase in the life-history of Trichosphaerium. I shall leave it here provisionally, with the hope that it may be found more abundantly another time. GENUS GROMIA Dujardin '35.
The form is ovoid or globular, and the body is covered by a tightly fitting, plastic, chitin shell, which, in turn, is covered by a fine layer of protoplasm. The flexibility of the shell makes the form variable as in the amoeboid types. The thickness of the shell is quite variable. The pseudopodial opening is single and terminal. The pseudopodia are very fine, reticulate, granular, and sharply pointed, and form a loose network outside of the shell opening. Nucleus single or multiple. Contractile vacuole is usually absent. Fresh and salt water.
Gromia lagenoides Gruber '84. Fig. 4. Length of shell 245u; largest diameter 125u. GENUS TRUNCATULINA D'Orbigny.
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forms. The characters are very inconstant, and Brady gives up the attempt to distinguish the group by precise and constant characters.
Truncatulina lobatula GENUS ACTINOPHRYS Ehr.
Actinophrys sol Ehr., variety. Fig. 5. Click for image
The single specimen that I found looked much like a Suctorian of the genus Sphaerophrya, but the absence of a firm cuticle and the presence of food-taking pseudopodia with granule-streaming makes it a very questionable Suctorian, and 1 place it here until further study throws more light upon it. Diameter of body 40u; length of pseudopodia 120 to 140u. --------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901.
GENUS HETEROPHRYS Archer.
Heterophrys myriapoda Archer. Fig. 6. Click for image.
Diameter 25 to 80u pseudopodia twice as long as the body diameter; the plasm often contains chlorophyll bodies (Zoochlorella). The granular part of the gelatinous layer is thick (up to 10u). The spine-like processes are very thin and short. (Schaudinn '95.) The marine form found at Woods Hole probably belongs to this species, as described by Schaudinn. The short pseudopodia which give to the periphery a fringed appearance are quite regularly placed in connection with the pseudopodia. The latter are not so long as twice the body diameter, the longest being not more than equal to the diameter of the sphere. The body inside of the gelatinous covering is thickly coated with bright yellow cells similar to those on Radiolaria. The animal moves slowly along with a rolling motion similar to that described by Penard '90, in the case of Acanthocystis. Diameter of entire globe 35u; of the body without the jelly 18u. The extremely fine granular pseudopodia are 8 to 35u long. Common among algae. This form was probably meant by Peck '95, when be figured "a heliozoon." Key to orders of Flagellidia. * Presence at Woods Hole indicated by asterisk.
Key to the families of Monadida.
Key to marine genera of Monadida.* Family Rhizomastigidae
Family Codonacidae:
Family Heteromonadidae:
Key to marine qenera of Choanoflagellida. 1. Without gelatinous or membranous test...3
* Presence at Woods Hole indicated by asterisk.
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Key to families and marine genera of Heteromastigida.
Family Bodonidae:
Family Trimastigidae:
Key to marine genera of Polymastigida.
Key to familiar and marine genera of Euglenida.
Family Euglenidae:
Family Astasiidae:
Family Peranemidae:
GENUS MASTIGAMOEBA F. E. Schultze '78.
In some cases the flagellum turns into a pseudopodium, and, conversely, the pseudopodium at one end may become a flagellum (see below). In some rare cases the ectoplasm secretes a gelatinous mantle. Reproduction not observed. Fresh and salt water. Mastigamoeba simplex, n. sp. Fig. 7.
Several of them were seen at different times during the summer, and they were always of the same size and form in the flagellated or amoeboid condition. I did not make out their reproduction, and I shall not be satisfied that this is a good species until their life history is known. In decaying algae. Length 10u. ----------------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE. Page 423 CODONOECA
Codonoeca gracilis, n. sp. Fig. 8.
IMAGE Fig. 7. Mastigamoeba simplex ... Fig. 8 Codonoecea gracilis. GENUS MONAS (Ehr.) Stein '78
Monas sp. Fig. 9.
GENUS MONOSIGA Kent '81.
Small colorless forms of Choanoflagellida, always naked and solitary. The posterior end is attached directly to the substratum, or there is a short stalk not exceeding the body in length. Kent '81 distinguished nine species, but Butschli questioned the accuracy of many of these, and in this he was ----------------------------------------------------------------- Page 424 BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. followed by France' '97, who recognized three species--Monosiga ovata, M. fusiformis, and M. augustata. Fresh and salt water. Monosiga ovata S. Kent '81. Fig. 10.
The individuals are unstalked or provided with a very short stalk less than the body in length. The form is spherical or ovate, broadest at the base and tapering to the extremity. The collar is somewhat variable in size. In the Woods Hole forms it was about the length of the body. Oil particles present. Contractile vacuole posterior, nucleus anterior. Fresh and salt water. Length of body without the collar 5u. Monosiga fusiformis S. K. Fig. 11.
IMAGE Fig 9, 10, 11, 12,
GENUS CODONOSIGA (Jas. Clark '67).
This genus, as modified by France', is distinguished from the preceding by the possession of an unbranched stalk much longer than the body length. The body is naked and of various shapes, and the individuals are solitary or colonial upon a single stalk. Kent '81 enumerates no less than 10 species, which were cut down by Butschli to 1. France' admits 4--C. botrytis Jas. Clark; C. grossularia; C. pyriformis, and C. furcata, all S. Kent--but regards the second and third as merely form varieties of the first. Codonosiga botrytis (Ehr. sp.) Jas. Clark '67. Fig. 12.
The individuals are small and provided with a long unbranched, or terminal, simply split stalk. The individuals are single or colonial. The Woods Hole form measured 22u over all; the body was 5u, the collar 3u, and the stalk 14u. No colonies were seen, and only a few individuals upon red algae. GENUS BODO (Ehr.) Stein.
The body is naked, usually amoeboid in its changes, and provided with two flagella, one of which is usually trailed along under and behind the animal. The anterior end is usually pointed, with the flagella arising from a minute depression; the posterior end is rounded. Specific characters very difficult to analyze. Fresh and salt water. ----------------------------------------------------------------- UNITED STATES FISH COMMISSION Page 425 MARINE PROTOZOA FROM WOODS HOLE. Bodo globosus Stein. Fig. 13.
Bodo caudatus (Duj.) Stein. Fig. 14.
The body is variable in shape, but usually flattened and pointed posteriorly. An anterior process is almost always present, and below this the flagella are inserted in a minute depression. The contractile vacuole is close to the base of the flagella. The flagella are about the same size, the anterior one usually somewhat longer. Common. Length 12 to 18u. This species was seen by Peck '95 and described as a small flagellate. IMAGE Fig. 13: Bodo globosus FIG. 14. Bodo caudatus. Fig 15. Oxyrrhis marina. GENUS OXYRRHIS Duj.
Oxyrrhis marina Duj. Fig. 15.
GENUS ASTASIA Ehr.
----------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901 Page 426. Astasia contorta Duj. Fig. 16.
Common in decaying algae. Length 60u; greatest diameter 30u. IMAGE FIG. 16. Two aspects of Astasia contorta. GENUS ANISONEMA Butschli Flagellates with two flagella, of which one is directed forwards and is concerned with the locomotion of the animal, while the other is directed backwards and drags after the animal when in motion. Body slightly compressed dorso-ventrally (fig. 17, section). An oral furrow is present on the ventral side and the two flagella originate in it (fig. 17, at left). The vacuole is on the left side. Food vacuoles are present in the posterior part. The nucleus is central. Movement creeping. Fresh and salt water. IMAGE Fig. 17 Anisonema vitrea (Duj.) Anisonema vitrea (Duj.) Fig 17.
---------------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE Page 427 its peculiar furrowed surfaces, and, above all, its perfectly transparent, vitreous appearance, were well described by Dujardin. Stein's Tropidoscyphus octocostatus is a fresh-water form which may possibly be a distinct species, especially as it is described with both flagella directed forwards. GENUS DISTEPHANUS Stohr.
Dictyocha Speculum Stohr; Dictyocha Auc.
Key to families of Dinoflagellidia.
Key to marine genera of Prorocentridae. Diagnostic characters: The transverse furrow is absent and the two flagella arise from the anterior end of the body. The shell may be bivalved. 1. No tooth-like process dorsal to the flagellum...Genus Exuviaella, p. 428
Key to marine genera of Peridinidae. Diagnostic characters: The cross-furrow is nearly central (see, however, Oxytoxum); the body may or may not have a shell; the shell may or may not be composed of distinct plates; the plates are distinguished as equatorial (i.e., bordering the cross-furrow), apical, and antapical, while still another, the "rhombic plate", may be present, extending from the cross-furrow to the apex. 1. Without distinct shell...Genus * Gymnodinium, P. 429
=============================================================== BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 428 Key to marine genera of Dinophysidae. Diagnostic characters: The cross-furrow is above the center of the body, and its edges, as well as the left edge of the longitudinal furrow, are usually produced into characteristic ledges; those of the cross-furrow usually form great funnel-like anterior processes, while those of the longitudinal furrow usually form great, lateral, wing-like processes ornamented by ribs and other markings. 1. Without shell; longitudinal furrow may open & close...Genus *Amphidinium, p. 432
IMAGE FIG. 18 Exuviaella lima. FIG. 19.Exuviaella marina GENUS EXUVIAELLA Cienkowsky '82.
Exuviaella lima Ehr. Fig. 18.
========================================================= Page 429 MARINE PROTOZOA FROM WOODS HOLE Exuviaella marina Cienkowsky. Fig. 19.
GENUS GYMNODIUM Stein '78.
They are also frequently flattened dorso-ventrally. The transverse furrow may be either circular and straight around the body or may describe a spiral course, passing even twice around the body. The flagella arise near cross-furrow or, in some cases, in longitudinal furrow. Chromatophores may or may not be present and food-taking is holozoic, in many cases at least. In some cases ectoplasm and endoplasm can be distinguished. Fresh and salt water. Gymnodinium gracile Bergh '82, var. sphaerica, n.
IMAGES
GENUS GLENODINIUM (Ehr.), Stein '83.
======================================================= BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 430 Glenodinium compressa n. sp. Fig. 21, a,b,c.
The posterior end of the animal is often somewhat pointed and this point frequently becomes attached, so that the animal whirls around upon it as upon a pivot. Glenodinium cinctum Ehr. Fig. 22.
IMAGE FIG. 23._Peridinium digitale.
GENUS PERIDINIUM Ehr.'32, Stein'83.
-------------------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE. Page 431 the body. The two halves of the body are similar, the posterior being somewhat shorter; the anterior half has seven equatorial plates, an oral plate, two lateral apical plates, and one or two dorsal plates. The two antapical plates frequently have a tooth-like process. The bodies are colorless, green or brown. Fresh and salt water. Peridinium digitale Pouchet. Fig. 23.
Although the description of Pouchet's P. digitale differs in some respects from a careful description of the Woods Hole form, I think the species are the same. The chief difference is in the single horn of the posterior half; in Pouchet's form this is furrowed by a narrow groove which runs to the S-shaped longitudinal furrow. In the Woods Hole form I was unable to make out such a furrow. The flagella, also, were not seen. This same form was pictured by Peck '95 as P. divergens. Peridinium divergens Ehr. Fig. 24.
IMAGE FIG. 25. Ceratium tripos. GENUS CERATUM (Schrank).
-------------------------------------------------------------------- Page 432 BULLETIN OF THE UNITED STATES FISH COMMISSION anterior half of the shell. The shell is thick, reticulate or striped, and sometimes provided with short spines; often distinctly porous. The anterior half is composed of 3 equatorial and 3 apical plates, the latter being continued into the horn-like process. The posterior half is composed of 3 equatorial and one apical plate continued into the posterior horn. The right posterior plate is continued into a similar horn which may remain rudimentary or be continued into a considerable process. Similarly the left posterior horn is usually developed, but remains small. There may be from 2 to 3, 4, and 5 horns. Chromatophores usually present, green to yellow brown. Fresh and salt water. Ceratium tripos Ehr. Fig. 25.
IMAGE FIG. 26. Ceratium fusus. Ceratium fusus Ehr. Fig. 26.
Both of these species are common in the tow and in the algae at the edge of the wharf. Both of them are mentioned by Peck in '93 and ' 95. The body is ovoid to globular and usually much flattened dorso-ventrally. The anterior portion is very much reduced and is somewhat head-like or cap-like. The longitudinal furrow extends through the entire posterior body length and is apparently capable of widening and narrowing. It is probably naked (see here Klebs, Pouchet, Butschli), although Stein maintained that there is a delicate cuticle-like shell. Chromatophores of brown or green colors present and usually grouped radially about a central amylum granule. The nucleus is posterior. Fresh and salt water. Amphidinium operculatum Clap. & Lach.
IMAGE Fig 27 Amphidinium operculatum. Klebs maintains that the two furrows are not connected, but in this he is certainly mistaken, provided we have the same species under consideration. Very common about Woods Hole. Length from 40 to 50u; width 30u; thickness 15u. ------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE. Page 433 Key to Infusoria.
1. Gymnostomina.
2. Trichostomina.
Key to marine genera of Enchelinidae
1. Body naked...3
GENUS LACRYMARIA Ehr. '30.
Lacrymaria lagenula Clap. & Lach. Fig. 28, a, b.
-------------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901 434 body cilia are not thickly placed except around the proboscis. The endoplasm is thickly packed with large granules (food particles) in the anterior half and with finely granular particles in the posterior half. The elongate macronucleus lies a little above the center among the larger granules; the contractile vacuole is double, one on each side of the median line and at the posterior end of the body among the finer granules. The anus is posterior. Length 90m to 160u; greatest width assumed 65m. When fully expanded the posterior end assumes a curious polyhedral form. (Fig. 28 b.) This form differs slightly from others of the same species as described by different observers, the most striking difference being the presence of two contractile vacuoles in place of the usual one. These are very slow to fill and grow to a large size before diastole. The membrane is very tough and retains its form easily under pressure of the cover glass. Another characteristic feature is the flattening of the surfaces between the striae. Decaying algae. Lacrymaria coronata Cl. & Lach. '58. Fig. 29.
This species is not very different from L. lagenula, but I noted that in addition to the elongate nucleus, the body striae are much more apparent here and seem to sink into the cuticle, giving the periphery, especially at the collar region, a curious crenulated effect. The endoplasm is very densely granular and colored a blue-green, probably from food particles. The number of striae is much larger than in the preceding species. The membrane is very tough and retains the shape of the body, even with the full pressure of the cover glass. Micronucleus and trichocysts were not observed. ------------------------------------------------------------ MARINE PROTOZOA FROM WOODS HOLE. 1901 Page 435 GENUS TRACHELOCERCA (Ehr. '83) Cohn '66.
Trachelocerca phoenicopterus Cohn '66. Fig. 30.
In one instance I noticed a very large form with the anterior end under some debris, which evidently held it tight, for the body of the ciliate was thrashing back and forth and twisting itself into knots, etc., like a nematode worm. Finally, the anterior end broke off with about one-tenth of the body; the remainder, in an hour, had regenerated a new anterior end with long cilia, but with no indication of four sides. The small anterior piece was also very lively, IMAGE Figure 30. Trachelocerca phoenicopterus moving about and eating like the normal animal; its history, however; was not followed. This species appears to be variable in other ways as well; thus, in some cases the posterior end is rounded (cf. Entz '84); in others it is pointed (cf. Kent '81, Cohn '66, et al.). Again, the macronucleus may be a single round body (Entz '84, Butschli' 88) or in two parts (Kent '81), or in many parts scattered about the body (Gruber). In the Woods Hole forms the tail is distinctly pointed and turned back sharply, forming an angle at the extremity. The cilia on this angular part are distinctly longer than the rest. The function of this posterior part is apparently to anchor the animal while it darts here and there upon the tail as a pivot, contracting and expanding the while. The body is finely striated with longitudinal markings; when contracted there are no transverse markings nor annulations. The nucleus is in the form of many fragments scattered throughout. Length of large specimen 1.7 mm. GENUS MESODINIUM Stein '62.
The main part of the body is globular or conical, with a short, platform-like oral region, and a deep annular groove about the middle of the body. The esophagus is rather long, and smooth or longitudinally striped. One or more rings of cirri rise in the groove. If more than one ring of cirri are present, the anterior set usually point forward and lie close to the anterior part of the body. The posterior set, on the other hand, cling close to the posterior region of the body and give to it a peculiar encapsuled appearance. The most characteristic feature is the presence of four short tentacle-like processes which can be protracted and retracted from the oral region. (Mereschowsky says that the entire anterior half is more or less contractile.) The macronucleus is horseshoe-shaped or ovoid and is situated in the posterior half of the body. The contractile vacuole is also posterior. ------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 436 Movement consists in rapid swimming, with rotation on its axis, or in creeping by means of its anterior cirri, or in sudden jumping, by which it apparently clears a distance of 20 times its diameter in one bound. Mouth parts may also be used for attachment to foreign bodies. The moving periods alternate with quiescent periods, during which the organisms with their outstretched and radiating cirri resemble the heliozoon Actinophrys. Mesodinium cinctum, n. sp. Fig. 31.
There are two sets of cirri and one of cilia; the latter stand out radially from the girdle and are usually in motion. The cirri of one set, the anterior, extend forward about twice the length of the anterior half; those of the posterior set closely engirdle the lower half, reaching not quite to the posterior extremity. These are somewhat hyaline and are closely approximated, giving the impression of a tight-fitting crenulate casing about the lower half. The cirri are sharply pointed, much broader at IMAGE Fig. 31. Side and top views of Mesodinium cinctum. the base, and the two sets are so placed that, looked at from above, they have the appearance of a twisted cord. (Fig. 31 b.) Movement erratic; sometimes the animal swims steadily forward with mouth in front; again it shoots across the field of the microscope, either backward or forward or sideways, through the action of its powerful cirri. It is often quiet, usually mouth downward, and is held in place by adhesion of the tentacles. In this position it looks strikingly like a heliozoon. Length 35u; greatest width 30u. Not uncommon. The chief features by which this species is distinguished from the frequently described M. pulex of Europe are the number of anterior cirri and the ring of true cilia in place of the central girdle of cirri. The European form is described with four anterior bristles; the present form has from 28 to 32. The radial cilia differ decidedly from the more powerful cirri and they are not in one plane, so that counting is difficult; they are not closely set. The presence of tentacles makes these forms of especial theoretical interest, especially in the light of the origin of Suctoria. GENUS TIARINA R.S. Bergh '79.
...................................................... MARINE PROTOZOA FROM WOODS ROLE. Page 437 Tiarina fusus (Cl. & Lach. ) emend R.S. Bergh.
Key to marine genera of Trachelinidae. Diagnostic characters: Body bilateral, or asymmetrical by local prolongations; usually compressed or flattened laterally, the left side more convex than the right. The essential feature is the position and character of the mouth. This is either a long slit extending from the anterior end well down the ventral surface, or the posterior part only of a ventral furrow remains open as a round or elongate mouth some distance from the anterior end. The entire mouth region of the body is usually drawn out into an elongate tapering proboscis which is generally curved dorsally at the extremity. An oesophagus is short or absent altogether; when present it is supported by a stiff buccal armature. Cilia are uniform about entire body or limited to the flat right side. Food is swallowed. 1. a. Proboscis easily distinguished from the main body...2
IMAGE Fig. 32. Loxophyllum setigerum, var. armatum. a,b,c = ventral, dorsal, and lateral aspects. GENUS LOXOPHYLLUM Dujardin '41
The body is flat and somewhat leaf-shape, flexible, and elastic. The anterior end is somewhat proboscis-like and flexible, but is not sharply demarcated as in lionotus. The central portion of the body is developed into a more or less arched dorsal mass, which usually contains the nuclei and contractile vacuoles. As a result of this local thickening, the body is surrounded by a thin hyaline margin. This, however, may be absent on the right side in some species. The mouth reaches from the anterior --------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 438 extremity to a short distance from the end, and usually approaches the left edge. An anus is present near the posterior end of the dorsal swelling. Trichocysts are numerous on the ventral surface, and often on the dorsal surface, where they are inclosed in minute papilla-like swellings. Cilia-distribution controverted. Maupas and Butschli hold that ventral surface alone is ciliated; others (Kent and Dujardin)that cilia are uniformly distributed. The entire body, dorsal and ventral surfaces alike, are uniformly striated. The contractile vacuole lies posteriorly, on the right side and in the dorsal swelling. In the fresh-water form h. meleagris, it is connected with a long canal whose swellings are frequently taken for additional contractile vesicles (Butschli); in the marine form described below the canal is not developed and a series of vacuoles takes its place; these are all contractile. The macronucleus may be single, double, quadruple, band-formed, or rosette-formed. Movement is steadily progressive and peculiarly gliding. Fresh and salt water. Loxophyllum setigerum Quenn. '67.
Variety armatum (Cl. & Lach.)(Fig. 32.)
For this reason I include the Woods Hole form under the tentative name armatum, as a variety of Quennerstedt's L. Setigerum. The flat margins are distinctly striated longitudinally, and faintly marked radially, on the dorsal surface. Longitudinal elevated striae also run the length of the dorsal hump and upon the entire ventral surface. The ventral surface is alone ciliated. Upon the edges of the flat border are sharp-pointed, colorless, spine-like processes, situated at equal distances around the entire periphery except at the anterior end. Each spine is thick at the base and tapers to a full point which is curved upward--i.e., dorsally (fig. 32, a,b). The entire body is plastic and contractile, turning its leaf-like edge readily over objects upon which it creeps. The cilia are fine and uniform, with a tendency to lengthen in the oral region.
GENUS LIONOTUS Wrzesniowski '70.
Movement: free-swimming or gliding, with especial tendency to get under clumps of foreign matter. Fresh and salt water. Lionotus fasciola Ehr. Fig. 33.
---------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE. Page 439 and is not sharply marked from the rest of the body but tapers gradually, its base being equal to the diameter of the body at its middle point. The body is slightly contractile and the posterior end is carried to a rounded point, but not into a distinct tail. Unlike the fresh-water variety, this one has no hyaline margin nor hyaline caudal region, and the contractile vacuole is double or multiple on the dorsal side near the posterior end. Cilia are present only on the under (right) side, with, however, a row of large cilia marking the course of the elongate mouth, upon its left side. The right side is striated, the left arched and without markings. The endoplasm is finely granular with, however, larger food particles in the process of digestion, while specimens are occasionally seen with the natural form completely lost through distortion caused by over-large captures (Cf. also Wrzesniowski '70, p. XXIII, fig. 32). Movement continuous, slow, and gliding; very little tendency to jerking movements. Macronucleus double, both parts spherical, and placed in about the center of the larger part of the body; closely approximated but not, as Schewiakoff described, connected. In conjugation, a large form unites with a smaller one, the mouth parts being connected. Details of conjugation and macronuclei not made out. Length 200u to 600u. IMAGE Fig. 33. Lionotus fasciola. Key to marine genera of Chlamydodontidae.
Body cylindrical. Cilia about entire body ...Genus * Nassula p. 440
------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 440 GENUS NASSULA Ehr, '33
The entire body is marked by clearly defined spiral stripes. The mouth is circular and the esophagus is supported by a considerable armature, which usually extends dorsally and to the left, rarely to the right. In some cases the structure of this armature is indistinct; again it can be clearly seen to consist of definite rods (Stabchen). The anus is probably always terminal. Contractile vacuoles are variable in different species. In some cases there is but one, which is placed at the posterior end or centrally on the ventral side; in others there may be four--two dorsal and two ventral. In many cases trichocysts are uniformly distributed. Sometimes the body is colorless; again, and more often, it is brightly colored with red, blue, brown, or black pigment. The macronucleus is globular and central, occasionally bandform and with numerous attached micronuclei. Food substance varied, usually vegetable matter, see, however, below. Cysts are globular. Movement is a steady progression, combined with rolling. Nassula microstoma Cohn'66. Fig. 34.
GENUS CHILODON Ehr.
------------------------------------------------------ MARINE PROTOZOA FROM WOODS HOLE. Page 441 usually single, elliptical in form, and centrally placed; one micronucleus. Reddish granular pigment and trichocysts are occasionally present. Chilodon cucullulus Mull., sp. Fig. 35.
GENUS DYSTERIA Huxley '57.
IMAGE FIG. 35. Ventral and dorsal aspects of chilodon cucullulus.
opening lies in the anterior widened portion of the ventral surface and is connected with a smooth tubular pharynx. The right half of the dorsal side, i.e., the apparent dorsal side, is arched and bears longitudinal ridges. Two to four contractile vacuoles are placed on the ventral side. The macronucleus is usually dorsal, elliptical, and cleft, with one micronucleus attached. Fresh and salt water. Dysteria lanceolata Cl. et Lach. Fig. 36.
The mouth lies between the two valves and is surrounded by a long and smooth buccal armature which passes downward and backward to the left a distance equal to about half the entire body length. The macronucleus is situated in the dorsal region in the central part of the body. There are two contractile vacuoles, one behind the center of the buccal armature, the other near the inner end of this organ. Movement is in circles, the animal moving around quite rapidly when not attached by its posterior process. It is colorless and measures 45u in length by 27u in width. Claparede & Lachmann and Shevyakov describe it as 70u long. ------------------------------------------------------------- Page 442 BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Key to marine genera of Chiliferidae. Diagnostic characters: Mouth never lies behind the middle of the body; the oesophagus is but slightly developed. The undulating membranes are placed either on the edge of the mouth or in the oesophagus. A peristomial depression leading to the mouth is absent or very slightly indicated. 1. Mouth in the anterior half, undulating membrane on left edge only; right edge Continued in a long ventral furrow...Genus Frontonia, p. 242 2. Two undulating membranes; mouth central; no caudal bristles ...Genus * Colpidium, p. 443 3. Two undulating membranes; caudal bristle...Genus * Uronema, p. 443 GENUS FRONTONIA Ehr. (Cl. & Lach. '58)(?). (Ehrenberg, subgenus of Bursaria '38; Claparede & Lachmann '58; Butschli '88; Shevyakov '96.) Form elongate and cylindrical, or often flattened dorso-ventrally, with round or pointed ends. It is usually plastic and contractile. Cilia are evenly distributed about the body and are similar in length. The large, open mouth lies on the anterior half of the ventral surface, and is elongate and oval in outline. On its left edge is a well-defined membrane which stretches across to the right side of the mouth. On the right edge is a small, longitudinally striped tract which is free from trichocysts and smooth in appearance. This tract is continued posteriorly in a long furrow, which in some cases reaches the posterior end of the animal IMAGES Fig.37. Frontonia Leucas. FIG. 38. Colpidium colpoda. FIG. 39.Uronema marina. A few rows of cilia in this furrow vibrate differently from the others and give the effect of a membrane (Butschli). The oesophagus is extremely short and hard to make out. The body is usually covered uniformly with trichocysts, often of considerable size. There are 1 or 2 vacuoles with long canals radiating throughout the endoplasm. The macronucleus is oval and centrally placed. Micronuclei vary from one to many. An anal opening is placed at the end of the long ventral furrow. The plasm is colorless or green by the presence of Zoochlorella, or colored brown or black by pigments. In these cases there is a considerable pigment mass on the anterior end. Movement is regular, forward, and combined with rotation. Food consists of foreign objects, diatoms, other protozoa and the like. Fresh and salt water. Frontonia leucas Ehr. Fig. 37.
----------------------------------------------------- Page 443 MARINE PROTOZOA FROM WOODS HOLE. covered with fine cilia, and the periphery is uniformly studded with large trichocysts, except along the furrow. Food consists of dinoflagellates and other small forms. Color dark brown to black. Length 330u; width 200u. This form differs considerably from the fresh-water Frontonia leucas as described by Schewiakoff '89, especially in the extreme length of the peristomial furrow, in the position of the nucleus and contractile vacuole, and in the nature of the water canals. These in the Woods Hole form are very irregular in size and very much branched, not uniform as in Lieberkuhn's (see Butschli) figure of Frontonia leucas, nor radiating as in Schewiakoff's description. This may be the same species as Frontonia marina, of Fabre-Domergue '91, whose description and figure I have not seen. The general form is oval, slightly compressed laterally with the dorsal side strongly arched. The ventral side is slightly incurved. The anterior end is somewhat smaller than the posterior end, which is broadly rounded. The mouth is placed some distance from the anterior end in an oral depression and opens into a tubular oesophagus. There are usually two undulating membranes which do not extend beyond the mouth borders. The right undulating membrane extends down into the oesophagus and appears to he attached to the walls of the latter. The body stripes in front of the mouth are twisted to the left. The anus is terminal and the contractile vacuole may be terminal or situated forwards in the dorsal region. The macronucleus is spherical and has one micronucleus attached. Food consists mainly of bacteria. Movement rapid, but interrupted. Fresh and salt water, common in infusions. Colpidium colpoda Ehr., sp. Fig. 38.
The body is oval, somewhat larger posteriorly, and a little compressed dorso-ventrally. The anterior end is twisted a little from the right to the left (more evident in fresh-water forms), and leans somewhat toward the ventral side. Under this portion, on the ventral side, lies the mouth in a large depression just above the middle of the body. The entire body is covered with uniform and delicate cilia, which are placed in longitudinal rows. These rows are almost straight on the dorsal side, but bend on the ventral surface, following the contour of the twisted anterior portion. The endoplasm is finely granular; the oesophagus leading into it is very distinct. Schewiakoff ('89) describes two membranes, an inner and an outer; Maupas ('83) describes them as right and left. In the present species I was able to make out only one. The macronucleus is central, spherical in form, and bears a single minute micronucleus. The contractile vacuole is posterior and dorsal to the long axis of the body. The anus is ventral to this axis and also posterior. Length 45u, width 20u. Common. This marine variety is much smaller than the fresh-water form and the form differs in a number of respects, viz, in the anterior torsion and in the structure of the mouth. These may be, however, only individual variations of a widely spread species, and I believe it is perfectly safe to describe this as Colpidium colpoda. GENUS URONEMA Duj. '41.
--------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION.
MARINE PROTOZOA FROM WOODS HOLE. Uronema marina Duj. Fig. 39.
The most characteristic feature is the long caudal bristle, which is extremely delicate and about two-thirds the length of the body. Schewiakoff thinks this bristle has a sensory function. I could not make this out, for although other protozoa ran against this bristle, often bending it well over to one side, the animal showed no sign of irritability but lay quiescent. A spherical macronucleus with attached micronucleus lies in the center of the body. The contractile vacuole is posterior in front of the bristle. The macronucleus was found to be double, as though just divided, in a large percentage of cases. This may be a precocious division of the nucleus long before signs of the body division are evident. Such a phenomenon, however, is rare, the macronucleus usually dividing at a late stage of cell division. Length 30 to 50u; width 15 to 20u. Common in decomposing algae. Key to marine genera of Pleuronemidae.
Body small; not produced into neck-like elongation...Genus *Pleuronema, p.444
GENUS PLEURONEMA Dujardin '41.
Upon the left edge of the peristome is a high, undulating membrane, sail-like in appearance when extended. This may stretch around the posterior edge of the peristome and upon the right aide, thus forming a pocket by means of which the food particles are directed into the mouth. IMAGE FIG 40. Pleuronema chrysalis. The rest of the right edge of the peristome is occupied by closely approximated powerful cilia (Butschli) or a second undulating membrane (Stein). The body cilia are relatively long. Trichocysts and caudal bristles may be present. The contractile vacuole is subterminal and dorsal; it is questionable whether there are canals leading to it. A round macronucleus with one micronucleus is in the anterior half of the body. The anus is terminal. Food is chiefly bacteria. Movement combines springing with swimming and rotation. Fresh and salt water. Pleuronema chrysalis Ehr., sp. Fig. 40.(ABOVE)
----------------------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE: Page 445 anterior end posteriorly three-quarters of the body length. The posterior end of the peristome is straight, the left curved, following the depressed portion. The body is covered with fine cilia in longitudinal lines, except on the peristome. The mouth is small and situated in the hollow of the peristome near the left border. On the left peristome edge is a large undulating membrane. It begins near the anterior end of the body and increases in height posteriorly following the peristome edge around on the right side. This posterior bend of the membrane causes the appearance of a full sail, so often seen. It can be entirely withdrawn and folded together in the peristome. On the right edge of the peristome are large, powerful cilia. The contractile vacuole is central and dorsal; the macronucleus is in the anterior half of the body, with one attached micronucleus. Food consists of bacteria. Not very common. Fresh and salt water. It often remains quiet, with membrane and cilia outstretched, as though dead, but suddenly gives a spring and is gone. Pleuronema setigera, n. sp. Fig. 41.
IMAGE: Fig 41 Pleuronema setigera This is small and without an oesophagus. The body is clothed with long setose cilia which are frequently fully outstretched when the animal is resting, a slight tremor of the large membrane alone indicating vitality. Posteriorly these appendages are drawn out into long filiform setae, the number varying in different individuals from three to nine or ten. These are extremely fine and difficult to see without a high power (e.g. 1/12 oil) and careful focussing of the substage condensor. Like P. chrysalis, the resting periods are terminated by sudden springs, otherwise the movements are steady and forward. The macronucleus is central, and the contractile vacuole posterior and terminal. Length 45u to 50u; greatest diameter 17u. In decaying algae. It was this form, I believe, that Peck '95 described as a "ciliate." GENUS LEMBUS Cohn 1866.
Free-swimming animals of elongate form, more or less elastic, and flexible, bending readily to avoid obstacles, etc. The anterior half is usually drawn out into a slightly curved neck-like portion. The peristome is a small groove leading from the anterior end to the mouth about midway down the ventral side of the body. Butschli, following Quennerstedt, describes an undulating membrane on each side of the peristome groove. Other observers, however, usually describe but one, the left, which is clearly defined and stretches out some distance from the body, while the right border is described as having smaller but very active cilia. The general body surface is clothed with fine, uniform cilia, and body striae are usually absent. One or more caudal bristles may be present. The --------------------------------------------------------- BULLETIN OF THE UNITED STATE FISH COMMISSION PAGE 446 contractile vacuole is posterior and terminal, and may be multiple. The macronucleus is spherical and perhaps double (Kent). Food is chiefly bacteria, and the animals are frequently found with the anterior end embedded in zoogloea masses. Salt water, usually in infusions. Lembus infusionum, n. sp. Fig. 42.
The endoplasm is colorless and finely granular, not regionally differentiated. The ectoplasm consists of a relatively thick cortical plasm specially noticeable in the posterior half of the body and a delicate cuticle which bears almost imperceptible longitudinal markings--the insertion points of the fine cilia. The body is covered with uniform cilia except at the anterior extremity. Here they are much larger and bristlelike. I was unable to find any cilia in the peristome. One long caudal bristle, one-quarter of the length of the body, trails out behind. The macronucleus is spheroidal and placed near the center of the body; a conspicuous micronucleus lies near it. A row of contractile vacuoles extends from the posterior end. I have seen as many as six of nearly equal size and one or two smaller ones. The intervals of contraction are quite long. Length 70 to 75u; greatest diameter 10 to 12u. IMAGE FIG. 42. Lembus infusionum.
Lembus pusillus Quennerstedt 1869. Fig. 43.
Habitat similar to that of L. infusionum, in zoogloea masses. Length 26 to 30u; diameter 7 to 8u. -------------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE. Page 447 Although Quennerstedt's description of L. pusillus makes no mention of a caudal bristle, the size and other characters are so closely similar that I hesitate to make a new species. The bristle is extremely delicate, scarcely thicker than a cilium, and easily overlooked, yet with proper focussing of the condenser I found it on every specimen examined. IMAGE Fig. 43. Lembus pusillus. Key to marine genera of Opalinidae. Diagnostic characters: The form is oval, and the body may be short or drawn out to resemble a worm. They are characterized mainly by the absence of mouth and pharynx. Anterior end not pointed; body cylindrical; tapering...Genus * Anoplophrya. p.447
GENUS ANOPLOPHRYA Stein 1860.
IMAGE FIG. 44. Anoplophrya branchiarum. Anoplophrya branchiarum. Stein '52. Fig. 44.
----------------------------------------------------------- Page 448 BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. I was much surprised to find this form swimming about freely in the water; its mouthless condition showed it to belong to the family of parasites, the Opalinidae. As the name indicates, however, this species is an ectoparasite upon the gills, and Stein gave the name branchiarum to a fresh water form parasitic upon Gammarus pulex. The Woods Hole form is so strikingly similar to the figure of G. Branchiarum that, although the name was given to a fresh-water form, it obviously applies to this marine variety. One important difference is the presence of only one contractile vacuole in the marine form. Key to families of Heterotrichida.
1. Polytrichina.
2. Oligotrichina.
b. Thecate forms; the body is attached by a stalk to the cup; within the adoral zone is a ring of cilia...Family Tintinnidae c. The peristomial depression is deep and funnel-like; cuticle thick, with posterior spine-like processes...Family Ophryoscolecidae; Key to the marine genera of Plagiotomidae. Diagnostic characters: The peristome is a narrow furrow which begins, as a rule, close to the anterior end and runs backward along the ventral side, to the mouth, which is usually placed between the middle of the body and the posterior end. A well-developed adoral zone stretches along the left side of the peristome, and is usually straight. 1. Body cylindrical; size medium; peristome long and turns sharply to the left at the extremity...Genus Metopus
Key to the marine genera of Bursaridae. Diagnostic characters: The body is usually short and pocket-like, but may be elongate. The chief characteristic is the peristome, which is not a furrow, but a broad triangular area deeply insunk and ending in a point at the mouth. The adoral zone is usually confined to the left peristome edge, or it may cross over to the right anterior edge. 1. The anterior half of the body tapers to nearly a point in front; the peristome is narrowest at the apex; the mouth is the entire peristome base...Genus Balantidium 2. The anterior end does not taper; the peristome is widest at the end of the body; the mouth is clearly defined...Genus* Condylostoma., p: 448 GENUS CONDYLOSTOMA (KONDYLOSTOMA) Bory de St. Vincent 1824 Dujardin'41.
Colorless and more or less flexible animals of medium size. The general form is elongate and cylindrical or somewhat smaller anteriorly. The posterior end is broadly rounded, the anterior end somewhat truncate and oblique. The peristome is broad and triangular, the base of the triangle being the entire anterior end of the body. The entire length of the peristome is one-fourth or less of the body length. The mouth is large and placed at the apex of the peristomial triangle and opens into a comparatively small oesophagus. The right edge of the peristome is lamellate and bears a clearly defined undulating membrane. The adoral zone is well developed upon the left edge of the peristome, from which it passes around anteriorly to the right edge. The surface of the peristome is free from cilia, but the rest of the body is uniformly coated with small active cilia. Contractile vacuoles are not safely determined. Butschli thinks there is probably one terminal vacuole, but some observers deny this (e.g. Maupas). Others describe them on the dorsal side of the posterior end (Quennerstedt). The macronucleus is long and beaded and placed upon the right side. Micronuclei are numerous and scattered along the macronucleus. The anus is terminal and dorsal. Food consists of large and small particles. Movement rapid, free swimming, alternating with resting periods; in some cases an undulating or wriggling movement is seen, showing clearly the flexibility of the body. Fresh and salt water. ============================================================ MARINE PROTOZOA FROM WOODS HOLE. Page 449 Condylostoma patens Muller. (Fig. 45.)
IMAGE Figure 45. Condylostoma patens. Length 400u; diameter at widest part 105u. Maupas gives the length from 305u to 495u; and Stein 376u to 564u. Very common. For a more extended account of the structures, see the excellent, description by Maupas '83. Key to the marine genera of Stentoridae Diagnostic characters: The peristome is relatively short and limited to the front end of the animal, so that its plane is nearly at right angles to that of the longitudinal axis of the body. The adoral zone of cilia either passes entirely around the peristome edge or ends at the right-hand edge. The surface of the peristome is spirally striated and provided with cilia. Undulating membranes are absent. 1. Peristome circular in outline; limited to the anterior end...Genus Stentor
GENUS STROMBIDIUM Cl. & Lach. 1858.
The latter is surrounded by a complete circle of the adoral zone, the oral end of which passes into a peristomial depression which extends deep into the middle of the body. The mouth, with a very small oesophagus, lies at the bottom of the inturned peristome. The region surrounded by the adoral zone is frequently drawn out into an anterior process, occasionally bearing a pigment mass. The ventral surface in some cases bears cilia, which may be distributed or restricted to a row of large cilia. Trichocysts are usually present and ===================================================== BULLETIN OF THE UNITED STATES FISH COMMISSION 1901.
may be widely spread, limited to the posterior region, or arranged in a girdle about the middle. The contractile vacuole is simple, and posterior in position. The macronucleus is spherical and usually central in position. Movement is rapid swimming, combined with resting and floating periods, the latter usually terminated by a sudden leap. Fresh and salt water; more common in the latter. Strombidium caudatum Fromentel '74. Fig. 46, a,b,c.
FIG. 46. Strombidium caudatum. It splits up into a bundle of fine fibers upon treatment with caustic potash (c). The cirri emerge from minute hollows in the edge of the anterior border. The cortical plasm contains peculiar rod-like bodies, which look more like lines or markings than like rods or trichocysts. The nucleus is large, spherical, and placed in the center of the body. The contractile vacuole is posterior. Length without appendage is about 35u; greatest diameter 15 to 18u. In decaying vegetable matter. Common. Although Fromentel's species is Incompletely described, it is very evident that the organism corresponds fairly well with the Woods Hole variety. His was a fresh-water type; this is marine, but the caudal filament and the contractile vacuole are similar. Certainly in this case the organism can not be regarded as a Vorticella broken off its stalk, as Kent '81 suspected. The anterior process with its pigment spot; the cirri, the spherical nucleus, the position of the vacuole, etc., are all opposed to such an interpretation which Kent applied to the original species. Neither can it be a Tintinnoid. I place it provisionally as S. caudatum. ========================================================== MARINE PROTOZOA FROM WOODS HOLE. Page 451 Key to the marine genera of Tintinnidae. Diagnostic characters: Body attached by a stalk to a cup. Inside the zone of membranelles is a ring of cilia (par-oral).
GENUS TINTINNOPSIS Stein '87.
The entire body is covered with cilia, but as the lorica is always opaque these can be made out only when the animal is induced to leave the house. The only difference between this genus and Tintinnus is the covering of foreign bodies-usually sand crystals. Movement is rapid and restless, and peculiarly vibratory, owing to the apparent awkwardness in moving the house. Salt water. IMAGE Fig 47. Tintinnopsis beroidea. Fig. 48 Tintinnopsis davidoff. Tintinnopsis beroidea Stein, var. plagiostoma Daday. Fig. 47.
Var. compressa Daday'87.
Tintinnopsis davidoffi Daday. Fig. 48.
The variations of these species are considerable, and as the internal structures, such as the nucleus, are essential in fixing their systematic position, I place them as above, provisionally, and until further observations can be made. ================================================ BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. P age 452 Key to families of Hypotrichida.
b. Peristome more or less indistinct; cilia reduced to a few rows on the ventral surface; anal and frontal cirri present...Family Oxytrichidae c. Cilia entirely reduced; frontal and anal cirri present or reduced; macronucleus band-formed or spherical...Family Euplotidae. d. Peristome reduced to left edge and does not reach over the anterior margin...Family Aspidiscidae One genus, *Aspidisca...p. 458 GENUS PERITROMUS Stein '62.
(Maupas describes bristles on the back, but this is not corroborated.) The adoral zone is fairly well developed, but not distinctly marked off from the remaining ventral surface. It begins on the right side and extends entirely around the frontal margin and down the left side below the middle of the body, where it turns suddenly to the right, entering the slightly insunk peristome. The mouth leads into a short, indistinct (esophagus. One contractile vacuole is situated in the dorsal swelling at the posterior end of the animal. Macronucleus double, one in each side of the dorsal swelling. Movement is slow and creeping, with a peculiar method of contracting the more hyaline edge, which may turn upward or around a foreign object. Fresh (?) and salt water. IMAGE FIG. 49. Peritromus emmae, ventral and lateral aspects. Peritromus emmae Stein. Fig. 49.
Key to the marine genera of Oxyrtrichidae.
1. The posterior end is pointed or tail-like...2
2. The front end is pointed...8
3. Frontal and anal cirri absent; often tube-forming...Genus Stichotricha
4. Anal cirri present; with or without short lateral bristles...Genus *Epiclintes, p. 453;
5. With frontal cirri...8
============================================================== MARINE PROTOZOA FROM WOODSHOLE. PAGE 453 6: Right margin of peristome straight as far as the anterior end; 5 rows ventral cirri; b anal cirri...Genus oxytricha
7. Five rows or less of ventral cirri...8
8. Membranelles normal; 5-10 anal cirri; no caudal cirri...Genus *Amphisia, p.453
GENUS EPICLINTES Stein'62,
The peristome is short and stretches around the front end of the animal. In the frontal region are from one to three rows of cirri. The ventral surface is covered with longitudinal rows of cilia, the number of rows being in dispute (6 to 7 according to Stein; 9 according to Mereschowsky and Rees) Some of these cilia project from the lateral edges and from the posterior end, where they are slightly elongated. The anus is dorsal and placed at the beginning of the posterior process. Macronucleus probably double. Movement is rapid and restless, the tail process contracting to jerk the body backward. Salt water. Epiclintes radiosa Quenn. Fig. 50.
The peculiar nervousness of this form made it extremely difficult to study, and the oral region was imperfectly made out. The anterior cirri appear to line the upper left border of the peristome, which is marked by a row of large cilia. The peristome begins upon the right side of the anterior end and passes backward and to the left, narrowing at this point. IMAGE FIG. 50. Epiclintes radiosa. The mouth is very small and difficult to see. It is apt to stay in one locality under zoogloea, switching back and forth with great vivacity, or hanging on by the posterior cilia while the anterior end stretches out in the surrounding medium. Nucleus and contractile vacuole were not observed. Length 45u. GENUS AMPHISIA Sterki '78.
================================================= BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 454 side. The peristome is long and rather narrow and carries an undulating membrane on its right margin. Fresh and salt water. Amphisia kessleri Wrzes. '77. Fig. 51.
This variety differs from O. kessleri as described by Wrzesniowski in having three frontal cirri instead of four. Another difference is in the structure of the nuclei and in their position. These IMAGE Fig. 51. Amphisia kessleri. differences are too minute to warrant a specific name. O. velox of Quennerstedt is probably the same as 0. kessleri, but differs in having three complete rows of ventral cirri. O. relox has three frontal cirri in a line, thus differing from the Woods Hole form. Key to the marine genera of Euplotidae. Diagnostic characters: Cilia, as well as the frontal, marginal, and ventral cirri, very much reduced; the anal cirri, on the other hand, are always present. The macronucleus is band-form. 1. Frontal cirri more than 8...2
2. Eleven marginal cirri on the left side; 11 frontal cirri...Genus Certesia
3. Seven frontal, 6 anal, 3 right marginal, and 2 left marginal cirri...Genus *Diophrys, p.456
GENUS EUPLOTES (Ehr. 1851) Stein '59.
==================================================== MARINE PROTOZOA FROM WOODS HOLE. Page 455 below. The anus is posterior and on the right side. The characteristic macronucleus is long and band-form, its main portion being usually on the left side with an anterior and a posterior arm toward the right. Movement is rapid swimming, which, however, is frequently broken by creeping periods, during which the animals appear to be examining the foreign body on which they creep. Fresh and salt water. Euplotes charon Ehr. Fig. 52.
IMAGE FIG. 52. Euplotes charon, dorsal and ventral aspects. There are 5 posterior cirri and 4 anal cirri, of much smaller size. The cirri may or may not be fimbriated, the latter condition indicating the approaching disintegration of the body and is abnormal. The macronucleus is long and band-formed or horseshoe shape. The contractile vacuole lies on the right side dorsal to the posterior cirri. Fresh and salt water. Length 45u; diameter 25u. Euplotes harpa Stein. Fig. 53.
Seven of the 10 ventral cirri are situated at the anterior extremity; the remainder are arranged in a triangle on the right edge. The anal cirri, 5 in number, are long and stiff; the marginal cirri smaller and finer. The nucleus and contractile vacuole are similar to those of the preceding species. Length 95u; width 54u. ================================================================ BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 456 GENUS DIOPHRYS Dujardin '41.
Medium size, colorless to yellow, rigid in form. The body contour is oval, the anterior end being rounded or slightly reduced, the posterior end usually cut in on the right side. The peristome is broad but less extensive than in Euplotes, and may extend beyond the middle of the body. Its right edge is convex toward the right side, extends forward and does not turn again to the right. The anterior ventral surface has 7 to 8 scattered cirri and just behind the mouth is a transverse row of large anal cirri. In the sharp in-cut of the posterior end are three great angular cirri. Two lateral IMAGE Fig. 53.Euplotes harpa. Fig. 54. Diophrys appendiculatus. cirri are placed on the left of the median line between the mouth and the anal cirri, and usually in a slight hollow. The contractile vacuole is on the right side in the vicinity of the anal cirri. The macronucleus is in two parts, each band-form, one anterior, the other posterior in position. Movement is rapid and steady. Salt water. Diophrys (Styloplotes) appendiculatus Stein '59. Fig. 54. Synonyms: Styloplotes appendiculatus Stein '59; Kent '81; Quennerstedt '67, etc. The general form resembles Euplotes. Its outline is oval and regular except at the posterior end on the right side, where there is a considerable indentation. The frontal margin is characterized by a row of powerful membranelles, which become smaller at the peristome and at the mouth they are of characteristically small size. The ventral cirri are 7 in number. Five of them are in one row from the anterior end down the right side nearly to the anal cirri; one is on the frontal border between the first two; one lies just anterior to the second anal cirrus from the right side. The 5 anal cirri are large and powerful and extend some distance beyond the posterior end of the body. In all specimens observed these cirri curve to the left. Dorsal to the anal cirri and placed deep into the dorsal pit are 3 large, sharply curved cirri, which in most cases are fimbriated, but when the specimens are ============================================================== MARINE PROTOZOA FROM WOODS HOLE. Page 457 normal these are painted and curve abruptly to the right. Two smaller cirri lie to the left of the group of anal cirri. The peristome is well-marked by the adoral zone, and upon its right border there is a row of cilia, and a similar row of cilia runs along the base of the oral membranelle. The macronucleus is double and consists of two elongate cylindrical masses lying parallel with one another. One of these is in the anterior region; the other is posterior. The contractile vacuole lies dorsal to the anal cirri and anterior to the three dorsal cirri. The movement and general activities resemble those of Euplotes. Length 50u; diameter 25u. GENUS URONYCHIA Stein '52.
Above the 5 right-side cirri, i.e., dorsal to them, but in the same depression, are 3 angular cirri. A few edge cirri are found to the left of them and another to the right of the 5 cirri. The contractile vacuole is on the left side between the main groups of cirri. The macronucleus is band-form or spherical, and is situated in the middle region of the body. Movement consists in forward swimming with sudden springs. Salt water. Uronychia setigera. Fig. 55
IMAGE Uronychia setigera, n. sp. Fig. 55. The ventral surface is flat and has two excavations in the posterior end. The right hollow is larger and contains 5 great cirri of unequal size, the extreme right one being the largest. The left hollow contains 2 cirri, also of dissimilar size. Dorsal to the 5 right cirri are 3 sickle-formed cirri, which are usually fimbriated. These are pointed and curve regularly to the left. The peristome is wide and open, and a small pocket-like hollow on its left border indicates the region of the mouth. The adoral zone runs into this pocket and the mouth is located in its lower right-hand corner. In U. transfuga the right border is generally described as having a membrane of extreme delicacy. I was unable to see such a membrane in this form, but in its place there are 2 flagella-like cirri extending from the margin of the mouth-opening into the peristome, and these vibrate slowly. I do not believe these could be the moving edge of an undulating membrane, for they are quite distinct. The macronucleus is spherical instead of band-form, and a single micronucleus is closely attached. This is unlike the European species U. transfuga, in which the nucleus is elongate. The contractile vacuole lies between the two sets of posterior cirri. There are no marginal folds like those of the European species. Length 40u; width 25u. Common. ================================================================== BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 458 GENUS ASPIDISCA Ehr. 1830.
Aspidisca hexeris Quennerstedt '67. Fig. 56.
IMAGE Fig. 56 Aspidisca hexeris The extreme right cirrus is the largest, and they become progressively smaller to the opposite end. Dorsal to these lies the contractile vacuole. The peristome is in the posterior half of the body and an undulating membrane extends from it into the oesophagus. The dorsal surface is longitudinally striated by 5 or 6 lines, which are usually curved. The nucleus is horseshoe-shaped and lies in the posterior half of the body. Length 68u; diameter 48u. This form was incorrectly mentioned as Mesodinium sp. by Peck '95: In the figure given by Quennerstedt there are only 7 ventral cirri. In the Woods Hole form there are 8, 7 of which are anterior, 6 of them about one central one. The eighth cirrus is by itself, near the base of the largest posterior cirrus. These cirri, in spite of their size, are easily overlooked and more easily confused, but by using methylene blue they can be seen and counted. Aspidisca polystyla Stein. Fig. 57.
============================================================= MARINE PROTOZOA FROM WOODS HOLE. Page 459 close together and one at some distance, near the largest anal cirrus. The peristome contractile vacuole, and nucleus are similar to the preceding. Length 36u; width 22u. Stein assigns only 7 ventral cirri to this species, but he also describes 2 very fine bristle like cilia (page 125) and pictures them in figs. 18, 19, 20, and 21 of his Taf. iii in the same relative position as my eighth cirrus. I am positive that cilia do not occur on the ventral face of this form, and that the characteristic cirri are the sole locomotor organs. Key to families of Peritrichida. a. Peristome drawn out into funnel-like process; parasitic...Family Spirochonidae
GENUS LICHNOPH0RA Claparede '67.
IMAGE Fig.57. Aspidisca polystyla. Fig.58. Lichnophora macfarlandi. A well-developed adoral zone incloses the peristome; it begins at the mouth on the left side and includes nearly all of the peristome in its left-wound spiral, the extremity approaching closely the end near the mouth. The macronucleus is a long-beaded structure, or it may be in several parts connected by strands (Gruber). The contractile vacuole is on the left side in the region of the mouth. Salt water. Lichnophora macfarlandi Stevens. Fig. 58.
On the egg capsules of Crepidula plana; also reported upon annelids at Woods Hole. Length 60u from disk to extremity of the peristomial disk. This form does not agree in all respects with Stevens's species, but the agreement is so close in other respects that I believe it can be safely identified as L. macfarlandi. The mode of life is different, and the macronucleus is different, there being from 25 to 30 fragments in Stevens's form and only 5 or 6 in the present one. There is, however, the same evidence of chain formation in both of them. The length of the oral cilia in Stevens's form is 18u in fixed and 30u in living forms. In the Woods Hole form the cilia are not more than half that length. ============================================================= BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 460 Key to the marine genera of Vorticellidae Diagnostic characters: Attached or unattached forma of peritrichous ciliates in which the adoral zone seen from above forms a right-wound spiral. A secondary circlet of cilia around the posterior end may be present either permanently or periodically. 1. Posterior ciliated girdle permanent around an attaching disk ...3
IMAGE: Fig.59. Vorticella patellina. FIG. 60. Vorticella marina. FIG. 61. Zoothamnium elegans. GENUS VORTICELLA (Linnaeus 1767) Ehr. '38
Contractile vacuole, single or double, usually connected with a sac-like reservoir. The macronucleus is invariably long and band-formed, with attached micronucleus. Fresh and salt water. PAGE 460 ------------------------------------------------ MARINE PROTOZOA FROM WOODS HOLE. Page 461 so many species of Vorticella have been described that the task of collecting data and of arranging the synonyms is extremely irksome and difficult. Stokes enumerates 66 species, inhabiting fresh and salt water, and several other new species have been added since his work. I am impressed with the fact that new species have been created without proper regard for the manifold variations which nearly all of the Ciliata show, and I believe the 66 species might be safely reduced to 12 or 15. Vorticella patellina Muller. Fig. 59.
Vorticella marina Greeff. Fig. 60.
Small, but common, and grows in small social groups. Length 35u. IMAGE Fig. 62. Cothurnia crystallina. GENUS ZOOTHAMNIUM (Bory de St. Vincent 1824) Stein '38, '54.
The colonies are usually richly branched upon the dichotomous plan and the entire colony is contractile. The main character is that with each division of the individual the stalk also divides, each daughter cell getting one-half of the parent stem. The stems therefore remain in communication, so that a simultaneous contraction results, and the colony as a whole is withdrawn. In some species so-called macrogonidia, or larger sexual individuals, are developed alongside the usual ones. Fresh and salt water. Zoothamnium elegans D'Udekem '64? Fig. 61.
GENUS COTHURNIA (Ehr.'31) Clap. & Lach.'58.
----------------------------------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 462 brownish lorica of quite variable form but always attached. These houses may be finger-formed, with widened center, or widened mouth, or constricted mouth, and the like. Ring-formed swellings are frequently developed. Sometimes the mouth becomes twisted and the lorica is therefore bilateral. The houses are attached either directly to some foreign object or by means of a short stalk. The animals are similarly fastened to the lorica, sometimes directly, sometimes by means of a short stalk. When they contract they draw back to the bottom of the lorica; when expanded they usually stretch out of the mouth opening. In some forms there is an operculum, by means of which the opening of the shell can be closed when the animal is retracted. Fresh and salt water. The number of species of Cothurnia has become so great that the difficulty in placing forms is almost sufficient to discourage the systematist; as Butschli well remarks, the variations in the theca have been made the basis of new species so many times that the genus is almost as confused as Difflugia among the rhizopods or Campanularia among the hydroids. The length of cup, of stalk, the presence of annulations on stalk or cup, etc., have given rise to many specific names, the majority of which I believe can be discarded. According to such differentials the same branch of an alga holding a hundred specimens of Cothurnia crystallina yield 10 or 12 species, whereas they are merely growth stages of one and the same form. Cothurnia crystallina Ehr. Fig. 62.
The form of the cup shows the greatest differences; sometimes it is cylindrical, sometimes elongate thimble-shape, sometimes pouch-shape, corrugated or smooth on the sides, and wavy or smooth on border. Frequently the basal part becomes stalk-like, but this is very short. When present, the stalk may or may not have a knob-like swelling. The animal within the cup may or may not be borne on a stalk, and this stalk may or may not be knobbed. The cups are colorless or brown. The animal is very contractile and may stretch half its length out of the cup or retract well into it. There is no operculum. The length of the cup varies from 70u to 200u (C. gigantea; Vag. grandis, etc. ). From Entz. There is nothing to add to Entz's characterization of this species, which is found both in fresh and saltwater. The variability of the cup and stalk is quite noticeable in the Woods Hole forms. Cothurnia imberbis Ehrenberg, var. curvula Entz. Fig. 63.
IMAGE FIG. 63 Cothurnia imberbis. FIG. 64. Cothurnia nodosa. It is perfectly smooth and without annulations. The animal itself has no definite stalk. When fully expanded the animal emerges but slightly from the margin of the cup. Fresh and salt water. On red algae. Dimensions of Woods Hole form: Cup 50 to 55u long; greatest diameter 22u; length of stalk 4 to 5u. ------------------------------------------------------- MARINE PROTOZOA FROM WOODS HOLE, Page 463 Cothurnia nodosa Claparede & Lachmann. Fig.64.
The cup is elongated, swollen centrally, tapering at oral end and conical at base or rounded. Oral opening either circular or elliptical. Cross rings may or may not be present, and the cup is either smooth or annulate. Length of cup 70u to 80u. The stalk which supports the cup is extremely variable in length. The animal is borne upon a stalk of variable length within the cup. Entz states that the many variations which this species exhibits run into each other so gradually that he does not believe it wise to separate them. The Woods Hole forms which I found on algae of various kinds were nearly of a size, and did not vary much from the one figured. Kellicott '94 described a Cothurnia from Woods Hole under the name of C. longipes, which I believe is only a long-stemmed variety of C. nodosa. My form has the following dimensions: Cup 75u; cup stalk 38u; animal stalk 14u. SUBCLASS SUCTORIA
GENUS PODOPHRYA Ehr. '33.
Podophrya gracilis, n. sp. Fig. 65.
GENUS EPHELOTA 8tr. Wright '78,
Some are long and sharp-pointed and adapted for piercing; others are short, cylindrical, usually retracted and capitate, adapted for sucking. Contractile vacuoles vary from one to many. The macronucleus is nearly central in position and usually of horseshoe shape, Page 463 ------------------------------------------------------ BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 464 but is frequently branched and irregular. Reproduction is accomplished by external multiple budding, usually from the anterior half of the body. Salt water. Ephelota coronata Str. Wright. Fig. 66.
IMAGE FIG. 65. Podophrya gracilis.
GENUS ACINETA Ehr. '33, Butschli'88.
MARINE PROTOZOA FROM WOODS HOLE. Page 465 Acineta divisa Fraipont '79. Fig. 67.
Length of body 27u; of stalk 100u; of extended tentacle 65u. Acineta tuberosa Ehr. Fig. 68.
Length of body 330u. ------------------------------------------------------------------ BULLETIN OF THE UNITED STATES FISH COMMISSION 1901. Page 466 GENUS TRICHOPHBYA Map. & Lach,'58.
Small forms to medium size; no cups or stalks. The body is spherical to elongate, usually, however, more or less irregularly lobed and changeable. The tentacles are in fascicles which are usually borne upon lobed or swollen places. The body is always more or less spread out. Contractile vacuoles variable. The macronucleus is spherical, elongate, band-formed or horseshoe-shaped. Reproduction takes place by endogenous budding, and the swarm spores are flat or lenticular with a distinct ciliary girdle. They are frequently parasitic. Fresh and salt water. Trichophrya salparum Entz'84.
IMAGE FIG. 69. Trichophrya salparum. These maybe continued internally as far as the nucleus (Sand). The cytoplasm is uncolored, but may contain some brilliant granules. The nucleus is granular, and spherical, band or horseshoe formed. This species was found by Dr. G. Hunter on the branchial bars of the Ascidian Molgula manhattensis, where great numbers of them are often parasitic. LIST OF REFERENCES. AUERBACH, L. '54. Ueber Encystierung von Oxytricha pellionella. Zeit. wiss. Zool., v, 1854. AUERBACH, L. '55. Ueber die Einzelligkeit der Amoeben. Zeit. wiss. Zool., vii, 1855. BALBIANI E. G. '61. Recherches sur les phenom~nes sexuelles des Infusoires. Jour. de la phy siol:, iv, 1891. BALBIANI E. G. '85. Sur un Infusoire parasite du sang de l'Aselle aquatique. Rec. zool. Suisse, II, 1885. BERGH, R. S. '79. Tiarina fusus Cl. & Lach. Vid. Med. f d. Nat. Foren. Kjobenhavn. BERGH, R. S. '82. Der Organismus der Cilioflagellaten. Morph. Jahr., vii, p. 177. BRADY, H. B. '79. Report on the Foramnifera dredged by H. M. S. Challenger during the years 1873-1876. Challenger Reports, Zoology, ix. BRANDT, K. '96. Die Tintinnodeen. Bibliot. zoolog., xx, 1896. BUTSCHLI, O. '76. Studien uber die ersten Entwickelungsvorg. der Eizelle, die Zelltheilung, und die Conjugation der Infusorien. Abhand. der Senck. naturf. Ges. Freiburg, x, 1876. BUTSCHLI, O. '83-'88. Die Protozoen. Bronn's Klassen u. Ord. des Tierreichs. CARPENTER, W. B. '56. Researches on the Foraminifera. Phil. Trans. (2), p. 547. CARTER, H. J. '56. Notes on the fresh-water Infusoria of the island of Bombay. Ahn. Mag. Nat. Hist. (2), xviii. CARTER, H. J. '63. On the coloring matter of the Red Sea. Id. (3), xii. CARTER, H. J. '63a. On Amceba princeps and its reproductive cells. Id. (3), xii. CARTER, H. J. '64. On fresh-water Rhizopods of England and India. Id. (3), xiii, p. 13. CARTER, H. J. '65. On the fresh- and salt-water Rhizopods of England and India. Id. (3), xv, p. 277. CIENKOWSKY, L. '55. Bemerkungen uber Stein's Acinetenlehre. Bull. Phys. Math. Acad., St. Petersburg, xiii, p. 297 (also in Ann. Mag. Nat. Hist.(3), xiii). CIENKOWSKY, L. '55. Ueber Cystenbildung bei Infusorien. Zeit. wiss. Zool., vi, p. 301. CIENKOWSKY, L. '61. Beitrage zur Kenntniss der Monaden. Arch. f. mik. Anat., I, 1865, p. 203. CLAPAREDE, E. '54. On Actinophrys sol. Ann. Mag. Nat. Hist. (2), xv, 1854. CLAPAREDE, E. '60. Recherches sur les annelides, etc., observes dans les Hebrides. Mem. Soc. phys. d'hist. nat., Geneve, xvi, 1860. CLAPAREDE, E. '67. Miscellanees zoologiques. Ann. d. sc. nat. zool. (5), viii, 1867. CLAPAREDE ET LACHMANN '58-'60. Etudes sur les Infusoires et les Rhizopodes. Mem. Inst. genevoise, v vi, vii. =========================================================== MARINE PROTOZOA FROM WOODS HOLE. PAGE 467 COHN, F. '54. Beitrage z. Entwicklungsges. der Infusorien. Zeit. wiss. Zool. iii, 1851; iv, 1853. COHN, F. '57. Ueber Fortpflanzung von Nassula elegans Ehr. Zeit. wiss. Zool., ix, 1857, p. 143. COSTE, M. '64. Developpement des Infusoires cilies dans une maceration de foin. Ann. d. ac. nat. zool.(5), ii. DADAY, E. v. '86. Ein kleiner Beitrag der Infusorien-Fauna des Golfes v. Neapel. Mitt. Zool. St. Neap., vi, p. 481. DADAY, E. v. '88. Monographie der Familie der Tintinnodeen. Mitt. Zool. St. Neap., viii, p. 473. DAVIS, J. '79. On a new species of Cothurnia. Jour. Roy. Mic. Soc., ii, 1879. DUJARDIN, F. '35. Recherches sur les organismes inferieures. Ann. d. sc. nat. zool. (2), iv, p. 343. DUJARDIN, F. '41. Histoire naturelle des Zoophytes infusoires. Paris, 1841. EHRENBERG, C. G. '31. Ueber die Entwickelung und Lebensdauer d. Infusionsthiere. Abhand. d. Berlin Ak., 1831, p. 1. EHRENBERG, C. G. '38. Die Infusionsthierchen als vollkommne Organismen. Leipzig, 1838. ENGELMANN, Th. W. '78. Zur Physiologie der Contractilen Vacuolen der Infusionsthiere. Zool. Anz., 1, p. 121. ENTZ, G. '84. Ueber Infusorien d. Golfes v. Neapel. Mitt. Zool. St. Neap., v, p. 289. ENTZ, G. '85. Zur naheren Kenntniss der Tintinnodeen. Mitt. Zool. St. Neap., vi, p. 185. FABRE-DOMERGUE, P. '85. Note sur les Infusoires cilies de la baie de Concarneau. Jour. d. l'anat. et de la phys., xxi, p. 554. FABRE-DOMERGUE, P. '91. Materiaux pour servir a l'histoire des Infusoires cilies. Ann. d. mic., III, 1890-91, p. 49. FOL, H. '83. Further contribution to the knowledge of the Tintinnodea. Ann. Mag. Nat. Hist. (5), xii p.73. FRANCE', R. H. '97. Der organismus der Craspedomonaden. Budapest. FROMENTEL. E. DE. '74. Etudes sur les microzoaires, etc. Paris, 1874. GOURRET ET ROESER. '88. Contributions a l'etude des Protozoaires de la Corse. Archi. d. biol., viii p. 139. GREEFF, R. '66. Ueber einige in der Erde lebende Amoeben und andere Rhizopoden. Arch. f. mik. Anat., ii, p. 299. GREEFF, R. '70. Untersuchungen ueber den Bau u. d. Naturgeschichte d. Vorticellen. Arch. f. Naturges., xxxvi, xxxvii. GREEFF, R. '71. Ueber die Actinophryens oder Sonnenthierchen des Sussenwassers als echte Radiolarien. Sitz. Ber. d. Niederrh. Ges. i. Bonn, xxviii, p. 4. GREEFF, R. '75. Ueber Radiolarien u. Radiolarienartige Rhizopoden des Sussenwassers 2. Arch. f. mik. Anat., xi. GREEFF, R. '88. Studien uber Protozoen. Sitz. Ber. Ges. z. Bef. d. ges. Nat., Marburg, 1888, p. 91. GRENACHER, H. '68. Ueber Actinophrys sol Ehr. Verh. phys.-med. Ges. Freiburg (n. F.), I. GRUBER, A. '83. Beobachtungen an Chilodon curvidentis n. sp. Festschr. 56. Vers. Deutsch. Naturf. gewid. v. d. Naturf. Ges. Freiburg, ii, p. 1. GRUBER, A. '84. Die Protozoen des Hafens v. Genua. Nova Act. d. K. Leop.-Car. Deutsch. Akad. d. Naturf., xlvi, p. 475. GRUBER, A. '87. Ueber der Bedeutung der Conjugation bei den Infusorien.Ber, d. Naturf. Ges. Freiburg, ii, p. 31. HAECKEL, E. '73. Zur Morphologie der Infusorien. Jena Zeit., vii, p. 516. HERTWIG, R. '76. Ueber Podophrya gemmipara, nebst Bemerkungen, zum Ban u. d. systemat. Stellung d. Acineten. Morph. Jahr., iv, p. 20. HERTWIG U. LESSER. Ueber Rhizopoden u. denselben nahe stehende Organismen. Arch. F. mik. Anat., x, Suppl., p. 35. HUXLEY, T. H. '57. On Dysteria, a new genus of Infusoria. Jour. Mic. Sci., v, p. 78. ISHIKAWA, C. Ueber eine in Misaki vorkommende Art v. Ephelota, etc. Journ. Coll. Sci. Imp. Univ. Tokyo, Japan, x, pt. 2. JAMES-CLARK, H. '66. On the Spongiae ciliatae as Infusoria flagellata, etc. Mem. Bost. Soc. Nat. Hist. (3), I, p. 1. KENT, W. SAVILLE. '81. Manual of the Infusoria. London, 1881. KLEBS, G. '84. Ein kleiner Beitrag z. Kenntniss d. Peridineen. Bot. Zeit., xlii, p. 721. KLEBS, G. '92. Flagellaten Studien 1. Zeit. wiss. Zool., lv. LABBE', A. '95. Sur les Protozoaires marins de Roscoff. Arch. d. zool. exper. (3), N. et R., p. xiv. LAUTERBORN, R. '94. Beitrage z. Susswasserfauna der Insel Helgoland. Wiss. Meeresunt. Komm. wiss. Unt. d. Meere Kiel (2), I, p. 215. LEIDY, J. '77. Remarks upon Rhizopods and notice of a new form. Proc. Ac. Sci. Phila., 1877, p. 293. LEIDY, J. '79. Fresh water Rhizopods of North America. Washington, 1879. LIEBERKUHN, N. '56. Ueber Protozoen. Notes from a letter to C. Th. v. Siebold. Zeit. wiss. Zool., viii, p. 307. MAUPAS, E. '81. Contributions a l'etude des Acinetiens. Arch. d. zool. exper. (1), ix, p. 299. MAUPAS, E. '83. Contributions a l'etude morphologique et anatomique des Infusoires cilies. Id. (2), I. MAUPAS, E. '83a. Les sucto-cilies de M. Mereschowsky. Comp. Ren., xcv, p. 1381. MAUPAS, E. '88. Recherches experimentales sur la multiplication des Infusoires cilies. Arch. d. zool. exper. (2), vi, p. 165. MERESKOWSKY, C. '78. Studien Uber Protozoen des nordlichen Russland. Arch. f. mik. Anat., xvi p. 163. ----------------------------------------------- BULLETIN OF THE UNITED STATES FISH COMMISSION. Page 468 MERESKOWSKY, C. '81. On some new or little-known Infusoria. Ann. Mag. Nat. Hist. (5), vii, 1881. MOEBIUS, K. '88. Bruchstucke einer Infusorien fauna der Kieler Bucht. Arch. f. Naturg., 1888. PECK, J. I. '93. On the food of the menhaden. Bull. U. S. Fish Com., 1893, p. 113. PECK, J. I. '95. The sources of marine food. Bull. U. S. Fish Com., 1895, p. 351. PERTY, M. '49. Mikrosk. Organ. der Alpen u. d. Italien. Schweiz. Mitt. d. Naturf. Ges. in Bern, 164-165. PERTY, M. '52. Zur Kenntniss kleinster Lebensformen, etc., Bern. POUCHETTE, G. '83; '85. Contributions a l'histoire des Peridiniens marins. Jour. de l'anat. et de la phys., xix, xxi. QUENNERSTEDT, A. '65; '67; '69. Bidrag till Sveriges Infusorie-fauna. Lunds Univ. Arsskrift, ii, IV, VI. SAND, R. 1901. Etude monographique sur le groupe des Infusoires tentaculiferes. Ann. d. la Soc. belge de microscopie, xxiv, xxv, xxvi. SCHAUDINN, F. '95. Die Heliozoen. Das Tierreich, 1895. SCHEWIAKOFF, W. '89. Beitrage z. Kenntniss der Holotrichen Ciliaten. Bib. Zool.; v, p. 1. SCHEWIAKOFF, W. '93. Ueber einige ecto- u. ento-parasitische Protozoen der Cyclopiden. Bull. Soc. nat. Moscou, 1893. i. SCHUETTE, F. '95. Die Peridineen d. Plankton-Expedition, 1. Kiel u. Leipzig. SCHULTZE, F. E. '74; 75. Rhizopodenstudien. Arch. f. mik. Anat., x, xi, xiii. SCHULTZE, M. '62. Ueber d. Organismus d. Polythalamien. Leipzig, 1862. SHEVYAKOV ?. '96. Monograph on Holotrichous ciliates. (In Russian.) Mem. of the St. Petersburg Acad., VII. STEIN, F. '59; 78; '83. Der Organismus der Infusionsthiere. I. Infusoria, '59; II. Infusoria, '78; III. Flagellata, '83. STEIN, F. '49. Untersuchung uber die Entwicklungs d. Infusorien. Arch. f. Natur., I, p. 92. STEIN, F. '54. Die Infusionsthiere auf ihre Entwicklungsgeschichte untersucht: Leipzig, 1854. STEIN, F. '60. Ueber Leucophrys patula u. uber 2 neue Infusoriengattungen Gyrocoris u. Lophomonas. Sitz. Ber. d. K.-bohm. Ges. d. Wiss. d. Prag, 1860, p. 4. STEIN, F. '64. Ueber die neue Gattung Epiclintes. Id., 1864, I. STERKI, V. '78. Beitrage z. Morphologie der Oxytrichinen. Zeit. wiss. Zool., xxxi, p. 29. STERKI, V. '98. On the classification of ciliate Infusoria. Amer. Natur., xxxii, p. 425. STEVENS, N. M. 1901. Studies on ciliate Infusoria. Proc. Calif. Acad. Sciences, III, 1. STOKES, A. C. '84. Notices of some new parasitic Infusoria. Amer. Nat., xviii, p. 1081. STOKES, A. C. '85. Some apparently undescribed Infusoria from fresh water. Id., xix, p. 18. STOKES, A. C. '87. Some new hypotrichous Infusoria from American fresh waters. Ann. Mag. Nat. Hist. (5), 20. TATEM, T. G. '67. New species of microscopic animals. Q.J.M.S. (n.s.), vii, p. 251. VEJDOWSKY, F. '79. Monographie der Enchytraeiden. Prag, 1869. WALLENGREN, H. '94. Studier ofver ciliata Infusorier, 1. Slagtet Lichnophora. Lund, 1894. WALLICH, G. C. '63. Observations on an undescribed indigenous Amoeba. Ann. Mag. Nat. Hist. (3), xi, xii. WESTON, J. '56. On the Actinophrys sol. Q.J.M.S., iv, p. 116. WRZESNIOWSKI A. '61. Observations stir quelques Infusoires. Ann. d. ac. nat. zool. (6), xvi. WRZESNIOWSKI A. '69. Ein Beitrag zur Anatomie der Infusorien. Arch. f. mik. Anat., v, p. 25. WRZESNIOWSKI A. '70. Beobachtungen uber Infusorien a. d. Umgebung v. Warschau. Zeit. wiss. Zool., xx, p. 467. END ----------------------------------------------------------- |