Myxosoma microspora n. sp. (Myxosporidia: Protozoa) parasitic in the gills of Mugil cephalus L.

A new histozoic species of myxosporidian, Myxosoma microspora n.sp., infecting the gill filaments of Mugil cephalus is described. Cysts measuring 0.5–1.0 mm in diameter were found attached to the gill filaments. Spherical or slightly oval, spores 4.8–5.2 μm in diameter, were present and possessed a thin outer mucous envelope which appeared as small conical protuberances at the ends of the equatorial axis. Polar capsules were pyriform in shape, equal in size and measured 1.6–2.0 × 1.0–1.2 μm; the polar filaments were 22–28 μm in length. There was a bean-shaped sporoplasm measuring 3.5 × 1.5 μm. No iodine vacuole was detected when the parasite was stained with Lugol's iodine.     

Winter Ciliates in a British Columbian Fjord: Six New Species and an Analysis of Ciliate Putative Prey

ABSTRACT. This work provides the first study of North Pacific planktonic ciliates by quantitative protargol staining. Triplicate water bottle samples were collected at a depth of 2 m (above the shallow pycnocline) at six stations in Indian Arm, British Columbia, on February 15, 1990, and February 26, 1991. Thirty-six ciliate species were observed. Six new species are described from protargolstained specimens: Strombidium lynni n. sp., Strombidium taylori n. sp., Strombidium basimorphum n. sp., Slrombidiurn ventropinnum n. sp., Strobilidium undinum n. sp., and Urotricha cyrtonucleata n. sp.
Ciliate abundance varied significantly (ANOVA, α= 0.05) between sampling sites, ranging from 550 to 6,800 cells/liter in 1990 and from 1,800 to 7,900 cells/liter in 1991. Biomass also varied significantly (ANOVA, α= 0.05) ranging from 3.7 × 10⁵ to 3.3 × 10⁶ pg carbon/liter in 1990 and 3.04 × 10⁶− 6.97 × 10⁶ pg carbon/liter in 1991. Putative prey were enumerated in three size fractions (1.5–5 μm, 5–10 μm and 10–25 μm). The source of variation in ciliate abundance and biomass was not identified. Parameters of salinity, temperature, putative prey, chlorophyll a and pycnocline depth did not significantly correlate with ciliate biomass or abundance (α= 0.05).     

Aggregata dobelli N. Sp. and Aggregata millerorum N. Sp. (Apicomplexa: Aggregatidae) from Two Species of Octopus (Mollusca: Octopodidae) from the Eastern North Pacific Ocean

ABSTRACT. Gamogony and sporogony of two new species of Aggregata (Apicomplexa: Aggregatidae) commonly were observed during histopathological examination of the digestive tracts of octopuses from the National Aquarium in Baltimore. North Pacific giant octopus, Octopus dofleini martini Pickford 1964, from British Columbia and Washington state were infected with Aggregata dobelli n. sp. Sporocysts were smooth-surfaced, dark-staining, subspherical to subovoid, typically 18–31 μ m long by 15–27 μ m wide, and contained 9–22 sporozoites, 18–23 μ m long. California two-spotted octopus, Octopus bimaculoides Pickford and McConnaughey 1949, from California were infected with Aggregata millerorum n. sp. Sporocysts were smooth-surfaced, dark-staining, and subspherical to subovoid, 12–20 μ m long by 11–17 μ m wide, and contained 8–10 sporozoites, 18–31 μ m long. Both species infected the noncuticularized spiral caecum and intestine; A. millerorum n. sp. also infected the cuticularized esophagus and crop. Both parasites were present in the submucosa, muscularis, and serosa. Our observations of Aggregata infections in cuticularized regions of the gut and in the muscularis and serosa appear to be novel. Associated pathologic features included hypertrophy of invaded cells, edema, inflammation, and ulceration.     

Eimeria zapi sp. n. from the Meadow Jumping Mouse, Zapus hudsonius Zimmerman in Southwestern Michigan

SYNOPSIS Four of 5 meadow jumping mice ( Zapus hudsonius ) captured had in their feces a previously undescribed species of Eimeria which is named Eimeria zapi sp. n. The sporulated oocysts measured 21.7 (19.5–24.0) × 20.3 (17.5–23.0) μm. The single-layered oocyst wall was 1.5 μm thick, rough, pitted and appeared clear-to-amber. Usually 2 polar granules could be seen. An oocyst residuum was not observed. Each sporocyst averaged 16.0 (12.5–18.0) × 9.7 (7.5–11.5) μm. A substiedal body was present. The sporocyst residuum consisted of a membrane-enclosed packet of 15 to 20 granules. This is the first species of Eimeria to be described from the genus Zapus.     

Newly discovered linkages between the cortical (pellicular) ridges of Opalina

Samples of Opalina ranarum have been prepared for electron microscopy by ultra-rapid cryofixation followed by substitution fixation in a solvent containing tannic acid. This technique has made it possible to see that very thin linkages exist between the pleated ridges that form the surface of the cell. Between any two adjacent cortical ridges, the linkages, which are approximately 0.1 μm long, occur as a single row, 0.1 μm below the free edge, with an impressively regular spacing of 0.1 μm. The cortical ridges of the Opalinids are spaced with remarkable uniformity, even when thrown into undulating patterns. The linkages described here will inevitably stabilize the complex architecture of the cortex. Other possible functions are discussed.     

A unique surface pattern and micropylar apparatus in the eggs of Luciocephalus sp. (Perciformes, Luciocephalidae)

A hitherto undescribed Luciocephalus species was bred in captivity for the first time. The male mouthbrooders spawned about 80 slightly pear-shaped eggs with a diameter varying from 2-2 to 3-4 mm. The enveloping zona radiata measured 15 μm in thickness. In the SEM the outer surface of the zona radiata showed a pattern which is unique among all teleosts studied to date. Many of the numerous, virtually parallel ridges extended from the vegetal to the animal pole. There they spiralled towards the micropyle and terminated in its pit. The role of such a surface pattern as a sperm guidance system was discussed.     

Phytoplankton and pelagic primary productivity in Øvre Heimdalsvatn

A phytoplankton investigation was carried out in the subalpine, low-productive Norwegian lake Øvre Heimdalsvatn in 1969–70 and 1972. This paper describes the temporal and spatial distribution of the standing stock of phytoplankton, and phytoplankton primary productivity. The annual average primary productivity in 1972 was 4.0–4.9 mg C m⁻³ d⁻¹; the annual average standing stock varied from 120 mg m⁻³ (freshweight) in 1969–70, to 250 mg m⁻³ in 1972. Phytoplankton species composition and size distribution is discussed. Throughout the year the phytoplankton is dominated by small (ultraplankton) species; μ-algae (< 5 μm) showed cell concentrations up to 15 mill. cells 1⁻¹. The dominating group was chrysophytes; cryptophytes, dinoflagellates or green algae were at times abundant. A phytoplankton monthly budget and a diagram showing annual average carbon flow through the standing stock of phytoplankton are presented; the phytoplankton dynamics in Øvre Heimdalsvatn is compared to that of other low-productive lakes.     

Sphaerospora epinepheli N. Sp. (Myxosporea: Sphaerosporidae) Observed in Grouper (Epinephelus malabaricus)

Sphaerospora epinepheli n. sp. is described from grouper, Epinephelus malabaricus , in cage-cultured and wild fish collected from both coastal lines of southern Thailand. Subspherical to spherical spores and mono- or disporous pseudoplasmodia were observed in the lumen of kidney tubules. Pseudoplasmodia were round to elongate, size range 15.6–22.9 μm (length) × 8.4–21.6 μm (width). Spores were 7.8–10.0 μm (length) × 12.3–14.5 μm (thickness), and 7.0–9.5 μm (width) with two spherical polar capsules of equal size measuring 2.9–4.4 μm in diameter and containing polar filaments with six or seven windings. Two uninucleate sporoplasms showed iodine vacuoles. Blood stages, similar to C-blood protozoans observed from freshwater fish in Europe, were found from peripheral blood smears of grouper. Ultrastructural studies of blood stages showed a similar structure to unidentified mobile protozoans from the blood of carp. Electron dense bodies were observed in the cytoplasm of the primary cell blood stages. Infected proximal-tubular epithelial cells showed highly vacuolated cytoplasm and pycnotic nuclei.     

Cutaneous taste buds in cod

The distribution of cutaneous taste buds was determined quantitatively in larvae, juveniles and young adults of cod, using scanning electron microscopy. Changes in these distributions associated with development were followed in laboratory reared fish. Taste buds were first seen on the snout and lips of cod at a total length of 8 mm, and on the barbel at a length of 22 mm. The highest taste bud densities were seen at a length of around 90 mm, and subsequently declined on the barbel and pelvic fins with further growth. In these late 0-group fish, mean taste bud densities over much of the head, e.g. throat, dentary and sides of the snout were <100 mm⁻². On the tip of the snout and the lips, mean densities were in the region of 350–400 mm⁻², while on projecting parts of the fish, especially the barbel, anterior naris flap and extremities of the fins, spot densities occasionally exceeded 1000 mm⁻² at some sites. Mean taste bud diameter increased rapidly from 2.23μ± 0.35 μm (S.D.) at a length of 22 mm to 7.19 ± 0.23 μm at 90 mm length, with a much slower increase to about 8 μm associated with a further doubling in body length. These changes indicate a phase of rapid proliferation and growth in size of cutaneous taste buds in the period preceding the adoption of a benthic habit in their first summer. The presence of high taste bud densities on the barbel and pelvic fins in particular appears to correlate with the known feeding behaviour of cod.     

Eimeria procyonis sp. n., an Isospora sp., and a Redescription of E. nuttalli Yakimoff and Matikaschwili, 1932 (Protozoa: Eimeriidae) from the American Raccoon (Procyon lotor)

SYNOPSIS. Thirty-two of 48 raccoons examined were infected with a previously undescribed species of Eimeria which is herein named E. procyonis. Of the 32 infected animals, 10 also harbored E. nuttalli and 1 had Isospora sp. oocysts.
The ellipsoid to ovoid oocysts of E. procyonis measured 23.4 × 18.0 (16–29 × 13–24) μm; its sporocysts measured 12.1 × 9.3 (11.5–15 × 7–10) μm, each containing a slightly flattened substiedal body. The sporocyst residuum consisted of numerous scattered granules each ∼1 μm in diameter. The oocyst wall was double-layered. The outer layer appeared rough and pitted, measuring 1.5 μm, except at the micropyle where it was 1 μm thick.
The oocysts of the Isospora sp. measured 16.8 × 13.7 (16–18.5 × 12.5–15.5) μm. The wall consisted of a single layer ∼0.5 μm thick. The sporocysts measured 11.2 × 9.1 (9.5–11.5 × 8–10) μm, and each contained 4 elongate sporozoites. The oocysts of E. nuttalli measured 17.5 × 13.6 (12-21 × 11-15) μm, with a smooth single-layered wall approximately 0.7 μm thick. The sporocysts measured 12.2 × 7.1 (9-13 × 5.5–11) μm. Each sporocyst had a thin, dark, Stieda body and the sporocyst residuum consisted of many fine granules.     

Pollen morphology and its systematic implications for the genera<Emphasis Type="Italic">Keiskea</Emphasis> miq. and<Emphasis Type="Italic">Collinsonia</Emphasis> L. (Elsholtzieae-Lamiaceae)

The pollen morphology of six species ofKeiskea and three representative taxa ofCollinsonia was studied in detail using LM, SEM, and TEM. In both genera, pollen grains are monad, hexa-colpate, and mostly medium in size [P = 28.0 to 37.0 μm, E = 24.3 to 30.7 μm (Keiskea); P = 30.0 to 45.0 μm, E = 26.0 to 39.0 μm (Collinsonia)]. Polar outlines are of circular or ellipsoid form. Shapes range from primarily oblate-spheroidal to prolate-spheroidal to subprolate, and rarely prolate in the equatorial view. Their exine, including the inline characters, are clearly distinct from each other:Keiskea, well-developed bi-reticulate, often forming large lumina by supratectal ridges, unbranched columellae, one-third to one-half of the total exine thickness; versusCollinsonia, mostly perforate without supratectal ridges or a faint/very weak bi-reticulate appearance without supratectal ridges, seemingly branched columellae, ca. two-thirds of the total exine thickness. As demonstrated by these current data, the pollen morphology of the two genera is well distinguished, easily supporting the separation ofKeiskea fromCollinsonia.     

A fibre-optic scalar irradiance microsensor: application for spectral light measurements in sediments

Abstract The manufacturing of a new spherical fibre-optic microsensor is described. The microsensor measures scalar irradiance, i.e. the spherically integrated light at a point in space. The light collector of the probe was a 70-μm diffusing sphere cast on the tip of a 125-μm wide optical fibre tapered down to 15–20 μm diametre. The microsensor had an isotropic (±10%) response from −160° to +160° over the whole spectral range from 400–900 nm in air as well as in water. The microsensor was coupled to a sensitive spectroradiometre and the spectral distribution of scalar irradiance in sediments was measured at 100 μm spatial resolution. Light was available for photosynthesis near the sediment surface at a higher intensity and a different spectral composition than could be expected from the illumination. By the combination of oxygen microelectrodes and the present fibre-optic microsensor it is now possible to study the depth distribution of microbenthic photosynthesis in relation to the available photosynthetically active radiation at ≤ 100 μ m resolution.     

Light and Electron Microscopy of the Spore of Myxobolus heckelii n. sp. (Myxozoa), Parasite from the Brazilian Fish Centromochlus heckelii (Teleostei, Auchenipteridae)

ABSTRACT. A myxosporean parasitizing the gill filaments of the freshwater teleost fish Centromochlus heckelii collected in the Tocantins River (Lower Amazonian Region, Brazil) is described using light and electron microscopy. This parasite produces spherical to ellipsoidal cyst-like plasmodia up to 250 μm in diameter, with a thick wall strengthened by several stratified juxtaposed crossed collagen layers, whose thickness varies according to the number of the layers. Several compressed fibroblasts are observed among the collagen fibrils. Deposits of spherical dense material are scattered at the internal periphery of the cysts. Plasmodia and different developmental stages, including immature and mature spores, filled the central region of the cysts. The spore body is ellipsoidal in valvar view and biconvex in sutural view. It is formed by two equal-sized and symmetric valves measuring 12.7 μm long (12.2–13.1) ( n =50), 6.6 μm wide (6.3–6.9) ( n =25), and 4.0 μm (3.7–4.4) ( n =20) thick. A thin layer formed by fine and anastomosed microfibrils is observed at the spore surface. Two equal, elongated pyriform polar capsules measure 2.9 μm (2.7–3.3) × 1.7 μm (1.4–2.0) ( n =25), each containing four or five oblique polar filament coils. The binucleated sporoplasm contains numerous spherical sporoplasmosomes, glycogen particles, and a large vacuole with fine granular matrix. Based on the morphological and ultrastructural differences and specificity of the host, we describe this isolate as a new myxosporidian, Myxobolus heckelii n. sp. (Myxozoa, Myxosporea).     

KINETIC ANALYSIS OF ENTIRE OOGENESIS IN XENOPUS LAEVIS

In our breeding conditions (without artificial hormonal stimulation) two years after metamorphosis are necessary for a Xenopus laevis female to produce mature oocytes. Four periods of different growth rates can be distinguished into this first wave of oogenesis: 1) oocytes reach 120 μm in diameter (early stage I according to D umont (5)) in a few weeks after metamorphosis; 2) growth slows down and the size of 250–300 μm (late stage I) is obtained 6–7 months later; 3) a rapid growth resumes during vitellogenesis (stages II, III and IV) and a 1,000–1,100 μm diameter is reached in 2–3 months; 4) the last period spans for a year and the oocyte grows up to 1,200 μm. This phase covers many physiological changes and it should be critical to size carefully the oocytes for biochemical investigations and comparisons.
At last most of the oocytes in a young female do not proceed through this entire oogenesis, they are stopped at the end of the second growth phase (about 250 μm in diameter).     

Fiber development in preanthesis cotton ovules

A tissue culture method was developed to investigate the production of cotton (Gossypium hirsutum L. cv. Texas Marker-1) fibers in vitro. Ovules were excised from 3, 5, 7 and 9 days preanthesis ovaries and placed on an agar-solidified, modified Murashige and Skoog medium containing 2.3 μ M kinetin and 0.45 μ M –2,4–dichlo-rophenoxyacetic acid or 2.3 μ M kinetin and 10.7 μ M naphthaleneacetic acid. Ovules formed fibers and callus tissue. Fibers formed in vitro were up to 10 mm long, 10–22 μ wide and the cell wall was 1–3 μ M thick. Callus tissue cells were subcultured for over 25 weeks and their degree of elongation was monitored. The ability of ovule-derived cells to direct expansion in a longitudinal direction diminished, while lateral expansion increased with time in culture.     

Eimeria tarentolae n. sp. from the Moorish Gecko, Tarentola mauritanica

ABSTRACT. A new species of Eimeria from the Moorish gecko, Tarentola mauritanica , of Minorca, Spain, is described. Oocysts of Eimeria tarentolae are ellipsoidal and measure 17.8 (17.6–18.7) μm by 13.5 (12.9–14.0) μm. Micropyle, oocyst residuum, and polar granule are absent. Each oocyst contains four spherical to slightly subspherical sporocysts 6.8 (6.4–7.0) μm in diameter. A sporocyst residuum is present, while a Stieda body is lacking. Sporulation is completed within 24–32 h at 21 ± 2°C.     

AGGREGATIONS OF MATURE MALE SPERM WHALES ON THE GALÁPAGOS ISLANDS BREEDING GROUND

The distribution and behavior of mature (12.3–16.3 m) male sperm whales ( Physeter macrocephalus ) were studied on the Galápagos Islands breeding ground from April to June 1995. In contrast to previous research seasons when males were observed only in close spatial and temporal proximity to mixed schools of females and immature animals, in 1995 males were sighted in loose aggregations, separated by hours to days from our vessel's encounters with mixed schools. Only one of ten identified males was observed in spatial proximity to a mixed school.
Aggregations consisted of two to four (minimum estimates) mature males travelling within a range of a few kilometers and were characterized by consistency of heading among individuals. Aggregations moved over time. During encounters, one to three males were observed at the surface at the same time, with interindividual distances of less than 1,000 m. Synchrony of heading was apparent between spatial associates, and its extent appeared to be related to interindividual distance. Clustering (two or more individuals within 100 m) was observed on only two occasions. No agonistic behaviors were seen.
Functions of mature male aggregation on a breeding ground remain unclear. Possible explanations for our observations are local prey abundance, or some form of sociality mediated over spatial scales of hundreds to thousands of meters.     

Molecular Phylogeny and Surface Morphology of Marine Archigregarines (Apicomplexa), Selenidium spp., Filipodium phascolosomae n. sp., and Platyproteum n. g. and comb. from North-Eastern Pacific Peanut Worms (Sipuncula)

ABSTRACT. The trophozoites of two novel archigregarines, Selenidium pisinnus n. sp. and Filipodium phascolosomae n. sp., were described from the sipunculid Phascolosoma agassizii . The trophozoites of S. pisinnus n. sp. were relatively small (64–100 μm long and 9–25 μm wide), had rounded ends, and had about 21 epicytic folds per side. The trophozoites of F. phascolosomae n. sp. were highly irregular in shape and possessed hair-like surface projections. The trophozoites of this species were 85–142 μm long and 40–72 μm wide and possessed a distinct longitudinal ridge that extended from the mucron to the posterior end of the cell. In addition to the small subunit (SSU) rDNA sequences of these two species, we also characterized the surface morphology and SSU rDNA sequence of Selenidium orientale , isolated from the sipunculid Themiste pyroides . Molecular phylogenetic analyses demonstrated that S. pisinnus n. sp. and S. orientale formed a strongly supported clade within other Selenidium and archigregarine-like environmental sequences. Filipodium phascolosomae n. sp. formed the nearest sister lineage to the dynamic, tape-like gregarine Selenidium vivax . Overall, these data enabled us to reassess the molecular systematics of archigregarines within sipunculid hosts and make the following revisions: (1) Filipodium was transferred from the Lecudinidae (eugregarines) to the Selenidiidae (archigregarines), and (2) Platyproteum n. g. was established for Platyproteum vivax n. comb. (ex. S. vivax ) in order to account for the highly divergent morphological features and better resolved phylogenetic position of this lineage.     

Eimeria sinaitae n. sp. (Apicomplexa: Eimeriidae) from the Rock Agama (Agama sinaita) in Saudi Arabia

Eimeria sinaitae n. sp. is described from the gall bladder of Agama sinaita from Wasie, Saudi Arabia. Sporulated oocysts are elongate-ellipsoid 34.4 times 22.0 (29.0–40.0 times 17.4–24.5) μm. Oocyst wall is smooth, greenish yellow, 1.2 (1.0–1.4) μm thick, and two-layered. Micropyle, polar granule, and oocyst residuum are absent. Sporocysts are ellipsoid 11.4 times 7.6 (9.8–15.0 times 6.7–9.0) μm. Sporocyst residuum is present. The sporocysts lack a Stieda body. Sporozoites are crescent-shaped, blunt at one end and tapered at the other. Eimeria species from Agamidae are compared.