A testate amoeba from a forest fen in Wakefield, Quebec. The specimen was air-dried and imaged in a scanning electron microscope at the Canadian Museum of Nature.
The image shows two features that differentiate Galeripora from its cousin Arcella: 1) an organic coating on the outer ventral surface of the shell, obscuring the hexagonal units out of which it is composed; and 2) small pores encircling the aperture.
Likely a Leptopharynx costatus with zoochlorellae.
Like other microthoracids, it is equipped with extrusomes. When exploded, these have four arms at the tip (a character of the family Microthoracidae, per Omar & Foissner, 2012, link below). The last two images show discharged extrusomes.
I looked at two specimens closely (the first is shown in images 1-3, the second in images 4 and 5). Both were a bit over 50 μm in length, and resemble those of L. bromeliophilus (as recorded in Omar & Foissner, 2011, link below).
A ciliate with a curious flagellum-like process at its anterior. This structure is not a true flagellum. It does not move independently, but simply dangles from the ciliate's mouth as it swims around. Its purpose is not known. In other respects, Ileonema closely resembles Trachelophyllum. Like members of that genus it is enveloped by a coat of ornate epicortical scales, visible only in the scanning electron microscope. (See Foissner's monograph on Terrestrial and Semiterrestrial Ciliates from Venezuela and Galápagos, pp. 50ff)
Ileonema dispar is the type species of the genus, which was erected in 1884 by Alfred C. Stokes. In 1922, Penard described a similar species under the name I. simplex. I think there reason to believe that I. dispar and I. simplex are the same species, viewed in different conditions. Penard observed only one specimen, although he was able to watch it for a couple of hours. Stokes found I. dispar "in abundance", and describes it as having a variable shape: "Its changes of form are...quite constant as it rests among the algal threads and lengthens the entire body into a club-shaped creature searching for food, or contracts into an egg-shape with a short, narrow neck." However, he only illustrates one specimen (a rather pudgy one!), and it is this illustration that was reproduced in Kahl, with a short description (Kahl does not seem to have found the organism himself). Stokes also observed that his Ileonema is nearly identical in overall appearance to Trachelophyllum apiculatum: a telling comment, since the latter is usually quite slender, like Penard's simplex.
Stokes describes the "flagellum" as follows: "entire flagellum one-half the length of the body, the basal half thick, obliquely grooved and presenting a twisted or cord-like appearance, slightly tapering yet suddenly constricted at the beginning of the finely filamentous distal one-half."
The "flagella" of my critters are generally shaped much as Stokes describes: quite thick at the proximal end, finely filamentous at the distal. Seeing them at low magnification, it's easy to see how he might have misinterpreted the flagellum as being twisted, or ropelike. In my observations, the flagella of some individuals, at certain levels of illumination, appear to be quite uniform from base to tip.
The Ileonema in my population are also extremely contractile, ranging in shape from plumply ovoid to gracefully attenuated and vermiform. After they've eaten, they become almost unrecognizable!
Water sample taken from the stagnate edge of a freshwater lake was taken on 2023-06-09 using a turkey baster.
See Martin Kreutz's page:
https://realmicrolife.com/dexiotrichides-centralis/
Aspidiophorus paradoxus is the largest Aspidiophorus species with about 300µm length.
Fig. 1: Dorsal scales.
The entire animal is covered with relatively large rhombic peduncle scales.
Fig. 2: Cross section
In cross-section, the structure of the peduncle scales can be clearly seen: the scales sit with a small basal plate on the cuticle of the animal, from which a thin, hollow peduncle rises. At the end of the peduncle sits a rhombic terminal plate, with a central keel. At the posterior end of the animal, the terminal plates of the last row of scales are enlarged.
The pharynx of the animal is terminally swollen, and the head is weakly five-lobed with two separate pairs of palpal tufts.
Fig. 3: Ventral view.
Ventrally, the strong hypostomion behind the mouth opening is striking. The two ciliated bands split at the head, but the inner branches do not unite in the population I examined. The base of the toes does not bear scales, the adhesive tubes
measure about 50% to 70% of the toe length and taper to a point.
Let's take a closer look at the scales:
Fig. 4: Back scales
In the scales on the back, the rhombic shape of the end plates can be seen most clearly. Less conspicuous - but typical for the species - is the middle keel of the scales.
Fig. 5: Cross section of scales
In cross section the complex geometry of the peduncle scales becomes clear - base plate, peduncle and end plate form a very flexible and stable carapace. The additional cavity under the outer scales acts like a "crumple zone" and further increases the protective effect.
Fig. 6: Cross-section of scale stems.
The stems of the scales consist of hollow tubes that ensure maximum stability with minimum material input - a fascinating example of evolutionary optimization.
The abdomen of the animals is not completely covered with petiolar scales. Rather, they end in the anal region and are joined by simple small, rounded keel scales that are not an obstruction to feces.
Fig. 7: Scaling of the abdomen.
At the furca base some (according to literature 4) spines protrude into the toe cutout.
The head is almost completely covered with slightly smaller peduncle scales:
Fig. 8: Head scales
Cephalion and pleurae are quite small and inconspicuous.
According to literature A. paradoxus has three teeth in the pharynx:
Fig. 9: Mouth armament.
In the animals I examined, only a curved stylet brace was found, the tip of which protrudes into the lumen of the pharynx and probably serves to open algal cells that are conveyed past it. It is possible that the literature reference to "three teeth" is merely based on a microscopic artifact, as the entire clasp may not be in the focal plane as a whole.
Mag. 400x
For reference images see http://www.digicodes.info/Micrasterias_muricata.html. This taxon has been observed in 2 nearby waterbodies: https://www.inaturalist.org/observations/132612551 and https://www.inaturalist.org/observations/105465282.
Mag. 400x
Filled with Zoochlorellae, like Acanthocystis turfacea and A. pernardi, both found locally. However. this specimen is very different in that it is covered with loose, elliptical scales (5-10µ in length). I do not see any spine-scales. The long axipodea are very granular and are, occasionally, piled high from the base with elliptical scales (40-50µ high!). The elliptical scales form a disorganizes, 10µ thick layer enveloping the entire protoplasm. The best candidate (by my eye) for an ID, at Siemensma's Microworld, is Raphidocystis ambigua https://arcella.nl/raphidocystis-ambigua/. A 2nd possibility is R. symmetrica https://arcella.nl/raphidocystis-symmetrica/, but the current specimen is much larger than those recorded by Siemensma. No reference to Zoochrorella is made in describing either taxon. I could not find a match among the Acanthocystis.
Prorocentrum species from the intertidal benthos of marine estuary Acabonac Harbor at Louse Point. I'm thinking this is Prorocentrum lima. Does anyone have any better insight as to species? The cells measure 49 um in length. The GIFs and three stills are from one of the few motile cells I have found. The remaining photos are from numerous non-motile cells. In many cells you can see the central pyrenoid with its ring-like starch sheath, the large posterior nucleus, and in some cells the anterior pusule- a system of membrane vesicles, tubules, and sacs connected with the flagellar canal by a permanent opening which is thought to play a role in osmoregulation and nutrient uptake.
"Species of the genus Prorocentrum C.G.Ehrenberg are recurrently reported from tropical and temperate waters, where they occur in benthic, epibenthic and planktonic habitats. Approximately 70 species of Prorocentrum are known, with Prorocentrum micans C.G.Ehrenberg as the type, of which around 30 species are associated with sediments and live epiphytically on macroalgal surfaces, floating detritus and corals. Morphologically, prorocentroid dinoflagellates are quite distinct compared to other dinoflagellates. They have two larger thecal plates separated by a sagittal suture and tiny platelets in the periflagellar area. They are also devoid of the typical dinoflagellate cingulum and sulcus but possess two typical dinoflagellate flagella arising from the flagellar pore. The taxonomy of Prorocentrum is based mainly on criteria such as cell shape and size, thecal plate surface morphology (ornamentation and pore patterns), intercalary band morphology and the architectural details of the periflagellar area (number of platelets, spines, collars and protrusions). Ultrastructural features such as the presence of trichocysts and mucocysts and the presence or organization of pyrenoids in the plastids have also been used for taxonomic descriptions" (1).
"Several Prorocentrum species, namely P. lima (Ehrenberg) Stein; P. cordatum (Ostenfeld) Dodge (as P. minimum (Pavillard) Schiller); P. borbonicum Ten-Hage, Turquet, Quod, Puiseux-Dao and Couté; P. concavum Fukuyo; P. leve Faust, Kibler, Vandersea, Tester and Litaker; P. rhathymum A.R. Loeblich III, Sherley and Schmidt; P. hoffmannianum Faust emend. Fraga (also P. maculosum Faust); and P. caipirignum Fraga, Menezes and Nascimento have been shown to produce complex toxic molecules such as okadaic acid (OA); dinophysistoxin (DTX)-1, -2, -4 and -5c; borbotoxins; and prorocentrolides. OA and/or its analogues are complex lipid- and water- soluble polyether molecules that have been associated with diarrhetic shellfish poisoning (DSP) in humans due to the consumption of contaminated clams, crabs and mussels" (1).
Mag. 400
The interesting thing here is that this rotund ciliate has swallowed Peridinium-like, freshwater dinoflagellate; this is the large brownish mass... in the 2nd image, the girdle of dinoflagellate is readily visible.
Holophtrya-species with symbiotic zoochlorellae. More on this here:
https://www.plingfactory.de/Science/Atlas/KennkartenProtista/01e-protista/e-Ciliata/e-source/Holophrya%20ovum.html
found as epibionts on a copepod.
More on this here:
http://www.plingfactory.de/Science/Atlas/KennkartenProtista/01e-protista/e-Ciliata/e-source/Trichodina%20domerguei%20megamicronuleata.html
very colourful ciliate due to digestion of cyanobacteria. More on this here:
https://www.plingfactory.de/Science/Atlas/KennkartenProtista/01e-protista/e-Ciliata/e-source/Nassula%20ornata.html