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Marine Protozoa from Woods Hole / Bulletin of the United States Fish Commission 21:415-468, 1901 cover

Marine Protozoa from Woods Hole / Bulletin of the United States Fish Commission 21:415-468, 1901

Chapter 10: Genus ACTINOPHRYS Ehr.
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A detailed systematic survey catalogs marine protozoan diversity sampled from algae and nearby waters at Woods Hole during a two-month summer interval. Seventy-two species representing fifty-five genera are recorded, with arranged accounts by major groups (Sarcodina, Mastigophora, Infusoria), notes on habitat distribution, morphological descriptions, figures, and several proposed new species. The work explains collecting limits and methods, adopts a conservative taxonomic approach extending existing European descriptions, and reserves uncertain or insufficiently documented forms for further investigation.

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Title: Marine Protozoa from Woods Hole

Author: Gary N. Calkins

Release date: May 5, 2006 [eBook #18320]
Most recently updated: November 9, 2023

Language: English

Credits: E-text prepared by Ronald Calvin Huber, while serving as Penobscot Bay Watch, Rockland, Maine,

*** START OF THE PROJECT GUTENBERG EBOOK MARINE PROTOZOA FROM WOODS HOLE ***



E-text prepared by Ronald Calvin Huber,
while serving as Penobscot Bay Watch, Rockland, Maine,
and Joseph E. Loewenstein, M.D.







From the Bulletin of the United States Fish Commission 21:415-468, 1901






Contributions from the Biological Laboratory of
the U. S. Fish Commission, Woods Hole, Massachusetts.




MARINE PROTOZOA
FROM WOODS HOLE.



by

GARY N. CALKINS,

Department of Zoology, Columbia University.





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 algæ taken fresh from the sea; others were found only after the water had been allowed to stand for a few days 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.

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:*

Class SARCODINA.
Subclass Rhizopoda.
Order Amœbida.
1. Amœba guttula Duj
2. Amœba sp.
3. Trichosphærium sieboldi Schn.
Order Reticulariida.
Suborder Imperforina.
4. Gromia lagenoides Gruber.
Suborder Perforina.
5. Truncatulina lobatula Walker & Jacob.
Subclass Heliozoa.
Order Aphrothoracida.
6. Actinophrys sol Ehr.
Order Chlamydophorida.
7. Heterophrys myriapoda Archer.
Class Mastigophora.
Subclass Flagellidia.
Order Monadida.
8. Mastigamœba simplex, n. sp.
9. Codonœca gracilis, n. sp.
10. Monas sp.
Order Choanoflagellida.
11. Monosiga ovata S. Kent.
12. Monosiga fusiformis S. Kent.
13. Codonosiga botrytis (Ehr.) J. Cl.
Order Heteromastigida.
14. Bodo globosus Stein.
15. Bodo caudatus (Duj.) Stein.
16. Oxyrrhis marina Duj.
Order Euglenida.
17. Astasia contorta Duj.
18. Anisonema vitrea Duj.
Order Silicoflagellida.
19. Distephanus speculum Stöhr.
Subclass Dinoflagellidia.
Order Adinida.
20. Exuviælla lima Clenk.
21. Exuviælla marina Clenk.
Order Diniferida.
22. Gymnodinium gracile Bergh.
23. Glenodinium cinctum Ehr.
24. Glenodinium compressa, n. sp.
25. Peridinium digitale Pouchet.
26. Peridinium divergens Ehr.
27. Ceratium tripos Nitsch.
28. Ceratium fusus Ehr.
29. Amphidinium operculatum Clap. & Lach.
Class Infusoria.
Subclass Ciliata.
Order Holotrichida.
Family Enchelinidæ.
30. Lacrymaria lagenula Cl. & Lach.
31. Lacrymaria coronata Cl. & Lach.
32. Trachelocerca phœnicopterus Cohn.
33. Tiarina fusus Cl. & Lach.
34. Mesodinium cinctum, n. sp.
Family Trachylinidæ.
35. Lionotus fasciola Ehr.
36. Loxophyllum setigerum Quenn.
Family Chlamydodontidæ.
37. Nassula microstoma Cohn.
38. Chilodon cucullulus Müll.
39. Dysteria lanceolata Cl. & Lach.
Family Chiliferidæ.
40. Frontonia leucas Ehr.
41. Colpidium colpoda Ehr.
42. Uronema marina Duj.
Family Pleuronemidæ.
43. Pleuronema chrysalis Ehr.
44. Pleuronema setigera, n. sp.
45. Lembus infusionum, n. sp.
46. Lembus pusillus Quenn.
Family Opalinidæ.
47. Anoplophrya branchiarum Stein.
Order Heterotrichida.
Family Bursaridæ.
48. Condylostoma patens Müll.
Family Halteridæ.
49. Strombidium caudatum From.
Family Tintinnidæ.
50. Tintinnopsis beroidea Stein.
51. Tintinnopsis davidoffi Daday.
Order Hypotrichida.
Family Peritromidæ.
52. Peritromus emmæ Stein.
Family Oxytrichidæ.
53. Epiclintes radiosa Quenn.
54. Amphisia kessleri Wrzes.
Family Euplotidæ.
55. Euplotes charon Ehr.
56. Euplotes harpa Stein.
57. Diophrys appendiculatus Stein.
58. Uronychia setigera, n. sp.
59. Aspidisca hexeris Quenn.
60. Aspidisca polystyla Stein.
Order Peritrichida.
Family Lichnophoridæ.
61. Lichnophora macfarlandi Stevens.
Family Vorticellidæ.
62. Vorticella marina Greeff.
63. Vorticella patellina Müller.
64. Zoothamnium elegans D'Udek.
65. Cothurnia crystallina Ehr.
66. Cothurnia nodosa Cl. & Lach.
67. Cothurnia imberbis Ehr.
Subclass Suctoria.
Family Podophryidæ.
68. Podophrya gracilis, n. sp.
69. Ephelota coronata Wright.
Family Acinetidæ.
70. Acineta divisa Fraip.
71. Acineta tuberosa Ehr.
Family Dendrosomidæ.
72. Trichophrya salparum Entz.

* This classification includes only the orders and families represented at Woods Hole



Genus AMŒBA 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.


Fig. 1.—
Amœba guttala.

 ENLARGE 

Amœba guttala Duj. Fig. 1.

A minute form without pseudopodial processes, extremely hyaline in appearance, and characterized by rapid flowing in one direction. The body is club-shape and moves with the swollen end in advance. A comparatively small number of large granules are found in the swollen portion, while the smaller posterior end is quite hyaline. Contractile vacuole absent, and a nucleus was not seen. Frequent in decomposing vegetable matter. Length 37µ. Traverses a distance of 160µ in one minute.

The fresh-water form of A. guttula has a vacuole, otherwise Dujardin's description agrees perfectly with the Woods Hole forms.


Fig. 2.—Amœba sp.
 ENLARGE 

Amœba ? Fig. 2.

A more sluggish form than the preceding, distinguished by its larger size, its dense granulation, and by short, rounded pseudopodia, which, as in Amœba proteus, may come from any part of the body. A delicate layer of ectoplasm surrounds the granular endoplasm, and pseudopodia formation is eruptive, beginning with the accumulation of ectoplasm. Movement rapid, usually in one direction, but may be backwards or sideways, etc. Contractile vacuole absent; the nucleus is spherical and contains many large chromatin granules. Length 80µ; diameter 56µ.




Genus TRICHOSPHÆRIUM Schneider '78

Synonym: Pachymyxa hystrix Gruber.

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 fragments 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.


Trichosphærium sieboldi Schneider. Fig. 3.

With the characters of the genus. A form which I have taken to be a young stage of this interesting rhizopod is described as follows:


Fig. 3.—
Trichosphærium sieboldi.


 ENLARGE 

A minute, almost quiescent, form which changes its contour very slowly. The membrane is cap-like and extends over the dome-shaped body, fitting the latter closely. The endoplasm is granular and contains foreign food-bodies. Nucleus single, spherical, and centrally located. Pseudopodia short and finger-form, emerging from the edge of the mantle-opening and swaying slowly from side to side or quiescent. The most characteristic feature is the presence of a broad, creeping sole, membranous in nature and hyaline in appearance. This membrane is the only evidence of ectoplasm, and it frequently shows folds and wrinkles, while its contour slowly changes with movements of body. The pseudopodia emerge from the body between this membrane and the shell margin. Contractile vacuole absent. Length 42µ, width 35µ. In decomposing seaweeds, etc.

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, pseudopodia make it difficult to identify with any phase in the life-history of Trichosphærium. I shall leave it here provisionally, with the hope that it may be found more abundantly another time.




Genus GROMIA Dujardin '35.

(Dujardin 1835; M. Schultze '62; F. E. Schultze '74;
Leidy '77; Bütschli '83; Gruber '84.)

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 amœboid 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.

This species is not uncommon about Woods Hole, where it is found upon the branches of various types of algæ. The body is pyriform, with the shell opening at the larger end. The chitinous shell is hyaline and plastic to a slight extent, so that the body is capable of some change in shape. The shell is thin and turned inwards at the mouth-opening, forming a tube (seen in optical section in fig. 4) through which the protoplasm passes to the outside. The walls of this tube are thicker than the rest of the shell, and in optical section the effect is that of two hyaline bars extending into the body protoplasm. A thin layer of protoplasm surrounds the shell and fine, branching, pseudopodia are given off in every direction. The protoplasm becomes massed outside of the mouth-opening and from here a dense network of pseudopodia forms a trap for diatoms and smaller Protozoa. The nucleus is spherical and contains one or two large karyosomes. The protoplasm is densely and evenly granular, without regional differentiation. I have never observed an external layer of foreign particles, such as Gruber described in the original species.

Length of shell 245µ; largest diameter 125µ.


Fig. 4.—Gromia lagenoides.    ENLARGE 



Genus TRUNCATULINA D'Orbigny.

A group of extremely variable foraminifera in which the shell is rotaline; i. e., involute on the lower side and revolute on the upper (Brady). The shell is calcareous and coarsely porous in older forms. The characters are very inconstant, and Brady gives up the attempt to distinguish the group by precise and constant characters.


Truncatulina lobatula Walker & Jacob.

Synonyms: See Brady '84 for a long list.

"It is impossible to define by any precise characters the morphological range of the present species. Its variations are infinite." (Brady, p. 660.)

This very common form, which occurs in all latitudes, was found frequently among the algæ at Woods Hole. Its characters are so difficult to define that for the present I shall limit my record to this brief notice. Size of shell 230µ by 270µ.




Genus ACTINOPHRYS Ehr.

The body is spherical and differentiated into granular endoplasm and vacuolated ectoplasm, but the zones are not definitely separated. There is one central nucleus and usually one contractile vacuole. The pseudopodia have axial filaments that can be traced to the periphery of the nucleus. Fresh and salt water.


Actinophrys sol Ehr., variety. Fig. 5.

Synonyms: See Schaudinn '95.


Fig. 5.—Actinophrys sol.

 ENLARGE 

The diameter is about 50µ; the vacuolated ectoplasm passes gradually into the granular endoplasm. This is the characterization given A. sol by Schaudinn, and it applies perfectly to the freshwater forms. If I am correct, however, in placing an Actinophrys-like form found at Woods Hole in this species, the description will have to be somewhat modified. In this form (fig. 5) there is no distinction between ectoplasm and endoplasm, and there is an entire absence of vacuoles. The nucleus is central, and axial filaments were not seen. The single specimen that I found looked much like a Suctorian of the genus Sphærophrya, 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 40µ; length of pseudopodia 120 to 140µ.




Genus HETEROPHRYS Archer.

The body is globular with but slight differentiation into ectoplasm and endoplasm; one nucleus in the latter; contractile vacuoles one or many; pseudopodia on all sides, thin, and with peripheral granule-streaming; surrounded by a globular, rather thick coat of jelly, which is hyaline inside and granular on the periphery. Fresh and salt water.


Heterophrys myriapoda Archer. Fig. 6.

Synonym: H. marina Hert. & Less. '74.


Fig. 6.—Heterophrys myriapoda.
 ENLARGE 

Diameter 25 to 80µ; 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 10µ). 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 Pènard '90, in the case of Acanthocystis. Diameter of entire globe 35µ; of the body without the jelly 18µ. The extremely fine granular pseudopodia are 8 to 35µ long. Common among algæ.

This form was probably meant by Peck '95, when be figured "a heliozoön."



Key to orders of Flagellidia.
Small, body usually amœboid; 1 or more flagella; no mouth Order Monadida.
Small; plasmic collar around the flagellum Order Choanoflagellida.
With 2 or more flagella; one trails behind Order Heteromastigida.
With 3 or more flagella, none of which trails Order Polymastigida.
Large; firm body wall; 1 or 2 flagella; mouth or pharynx, or both Order Euglenida.
Medium size; with chlorophyll, no mouth, usually colonial Order Phytoflagellida.
Small; silicious skeleton; parasitic on Radiolaria or free Order Silicoflagellida.
(One genus,
Distephanus Stöhr)


Key to the families of Monadida.
No mouth; 1 or 2 flagella: amœboid with lobose or ray-like pseudopodia Family Rhizomastigidæ
Mouth at base of single flagellum; plastic; no pseudopodia Family Cercomonadidæ
One flagellum; inclosed in gelatinous or membranous cups Family Codonœcidæ
One flagellum; tentacle like process at base of flagellum; inclosed in cup Family Bikœcidæ
One main flagellum and 1 or 2 accessory flagella Family Heteromonadidæ


Key to marine genera of Monadida.*
Family Rhizomastigidæ:  
1. Flagellum repeatedly thrown off and reassumed Genus *Mastigamœba in part
2. Flagellum never thrown off 3
3. a. Pseudopodia lobose Genus Mastigamœba
  b. Pseudopodia ray-like Genus Mastigophrys
Family Codonœcidæ:  
1. Goblet-shaped cups adherent by stalk Genus *Codonœca
Family Heteromonadidæ:  
1. The long flagellum vibratory Genus *Monas
2. The long flagellum rigid; shorter one vibrates Genus Sterromonas
* Presence at Woods Hole indicated by asterisk.


Key to marine genera of Choanoflagellida.
1. Without gelatinous or membranous test 3
2. With gelatinous or membranous test 4
3. a. Attached forms:  
      1. Without a stalk, or with a very short one Genus *Monosiga
      2. With a long, simple stalk Genus *Codonosiga
      3. With a long, branched, stalk Genus Codonocladium
  b. Free-swimming Genus Desmarella
4. Colonial, and with a gelatinous covering Genus Proterospongia
* Presence at Woods Hole indicated by asterisk.


Key to families and marine genera of Heteromastigida.
1. Two flagella nearly equal in size Family Bodonidæ
  One main and 2 accessory flagella Family Trimastigidæ
Family Bodonidæ:  
1. Body very plastic, almost amœboid Genus *Bodo
  Body not plastic; with large anterior cavity, holding flagella Genus *Oxyrrhis
Family Trimastigidæ:  
1. With an undulatory membrane between accessory flagella Genus Trimastix
  Without such membrane; flagella contained in a ventral groove while at rest Genus Costia
* Presence at Woods Hole indicated by asterisk.


Key to marine genera of Polymastigida.
1. Body flattened; ends rounded; sides hollowed; often with wing-like processes; cross section S-shaped Genus Trepomonas
2. Body pyriform; one large asymmetrical groove; 4 flagella Genus Tetramitus
3. Body spherical; many flagella equally distributed Genus Multicilia


Key to families and marine genera of Euglenida.
1. With deeply-insunk pharynx; no mouth 2
  With pharynx and distinct mouth Family Peranemidæ
2 Body plastic; usually with chromatophores and eye-spot Family Euglenidæ
  Body plastic; no chromatophores; no eye-spot Family Astastidæ
Family Euglenidæ:  
  Body Euglena-like, inclosed in shell with round opening for exit of flagellum Genus Trachelomonas
Family Astastidæ:  
  Body with one flagellum Genus *Astasia
Family Peranemidæ:  
1. Body striped; plastic; two diverse flagella Genus Heteronema
2. Body striped; not plastic; posterior flagellum longer than the other Genus *Anisonema
3. Body striped; not plastic; with rod-like organ in pharynx Genus Entosiphon
* Presence at Woods Hole indicated by asterisk.