Feeding by the newly described heterotrophic dinoflagellate Stoeckeria changwonensis: A comparison with other species in the family Pfiesteriaceae

The feeding ecology of the newly described heterotrophic dinoflagellate Stoeckeria changwonensis was explored. The feeding behavior of S. changwonensis, and the kinds of prey species that it feeds on were investigated with several different types of microscopes and high-resolution video-microscopy. Additionally, the growth and ingestion rates of S. changwonensis as a function of prey concentration for perch (Lateolabrax japonicus) blood cells, the raphidophyte Heterosigma akashiwo, the cryptophytes Rhodomonas salina and Teleaulax sp., and the phototrophic dinoflagellate Amphidinium carterae prey were measured. S. changwonensis feeds on prey through a peduncle, after anchoring the prey by using a tow filament. This type of feeding behavior is similar to that of Stoeckeria algicida, Pfiesteria piscicida, and Luciella masanensis in the family Pfiesteriaceae; however, S. changwonensis feeds on various kinds of prey species different from those of the other heterotrophic dinoflagellates. S. changwonensis ingested perch blood cells and diverse algal species, in particular, the large thecate dinoflagellate Lingulodinium polyedrum which are not eaten by the other peduncle feeders. H. akashiwo and the perch blood cells supported positive growth of S. changwonensis, but R. salina, Teleaulax sp., and A. carterae which support positive growth of P. piscicida and L. masanensis did not support positive growth of S. changwonensis. With increasing mean prey concentration the growth rates for S. changwonensis on H. akashiwo and the perch blood cells increased rapidly and then slowly or became saturated. The maximum growth rates of S. changwonensis on H. akashiwo and the perch blood cells were 0.376 and 0.354 d⁻¹, respectively. Further, the maximum ingestion rates of S. changwonensis on H. akashiwo and the perch blood cells were 0.35 ng C predator⁻¹ d⁻¹ (3.5 cells predator⁻¹ d⁻¹) and 0.27 ng C predator⁻¹ d⁻¹ (29 cells predator⁻¹ d⁻¹), respectively. These maximum growth and ingestion rates of S. changwonensis on H. akashiwo, the perch blood cells, R. salina, Teleaulax sp., and A. carterae differed considerably from those of S. algicida, P. piscicida, and L. masanensis on the same prey species. Thus, the feeding behavior of S. changwonensis may differ from that of other species in the family Pfiesteriaceae.     

Population dynamics ofHeloniopsis orientalis C. Tanaka (Liliaceae) in natural forests — Annual life cycle

Annual changes in the leaves and reproductive organs ofHeloniopsis orientalis C. Tanaka (Liliaceae), a perennial evergreen herb, were studied from 1991 to 1997 in two areas of South Korea, Namhansanseong and Maranggol. The period for active growth in the leaves was from mid-March to early June. Average leaf angle was 70° in early June, decreasing to 50° in late October. From December until June of each following year, leaf angle was maintained a 0° to horizontal. The specific leaf area (SLA) value was 185 cm².g^-1 early in the growing season, increasing to 332 cm²g^-1 in early June. By the end of October, SLA had decreased to 159 cm²g^-1, after which it increased again from March to June. Because the SLA curve had two peaks, it was inferred thatH. orientalis possesses two means for survival: 1) an anti-freezing mechanism by which its leaves thicken during the winter, and 2) a reallocation of energy from old leaves to new leaves or to reproductive organs.H. orientalis flowered in a semi-enclosed state in late March. Blooming out of the bract, the front of the flower faced the ground. Growth of the peduncle ended in early June, at which point it was 60 cm long. At that time, the fruit was oriented so that the seeds were dispersed upward. Therefore one can see thatH. orientalis has two physiological features that enhance long-distance seed dispersal — a rather long peduncle relative to overall plant size and an upward seed-dispersal mechanism. In the Namhansanseong area, energy from the roots and old leaves was translocated to new leaves early in the growing season (from late March to early May). However, after mid-May, energy was re-translocated from new leaves to the roots. Moreover, the leaves on flowering plants grew more slowly than on non-flowering plants because energy was translocation to the reproductive organs. Therefore, new leaf growth depended on energy stores of the roots and the biomass of old leaves early in the growing season.     

Bud regeneration from inflorescence explants for rapid propagation of geophytes in vitro

Bulbs, corms and other subterranean storage organs are commonly used as explant source material for the establishment of geophytes in vitro. The inflorescence stalk was found to be a good alternative source of explants to overcome explant contamination originating from underground storage organs. Inflorescence explants of Allium, Dichelostemma, Eucrosia, Gladiolus, Haemanthus, Hyacinthus, Narcissus, Nerine and Ornithogalum were used to establish cultures in vitro. The regeneration potential of the inflorescence was compared with regeneration from bulb twin scales or from apical buds isolated from corms. Gladiolus (Iridaceae) explants isolated from the floral stem just below the expanding florets, still enclosed in the bracts, were highly regenerative in the presence of naphthalene acetic acid (NAA) and kinetin. In the presence of 2,4-dichlorophenoxyacetic acid and benzyl aminopurine (BA) in the medium, explants isolated from the tissue at the junction between the peduncle and the pedicels of a young Nerine (Amaryllidaceae) inflorescence regenerated several buds. The scapes of young unemerged inflorescences taken from sprouting bulbs of Narcissus (Amaryllidaceae), following a 15 °C storage treatment, regenerated buds in the presence of NAA, BA, elevated phosphate and adenine sulfate in the medium. The number of buds regenerated depended on the location on the scape from which the explant was isolated, and on the duration of the 15°C treatment. In Allium (Alliaceae), capitulum tissue between the flower pedicels regenerated buds. Explants excised from the peduncle, as well as the pedicel-peduncle junction of Dichelostemma (Alliaceae), Ornithogalum, Hyacinthus (Hyacinthaceae) and Eucrosia (Amaryllidaceae) regenerated several buds in each type of explant. In the case of Haemanthus (Amaryllidaceae), pedicel-peduncle junction explants regenerated buds only when excised from inner whorl florets. Propagation protocols and the potential use of expediently isolated inflorescence explants for efficient micropropagation of geophytes are discussed. Received: 1 September 1999 / Revision received: 13 December 1999 / Accepted: 13 December 1999     

A histological description of shortspine thornyhead,Sebastolobus alascanus,ovaries: structures associated with the production of gelatinous egg masses

The ovarian structure of the shortspine thornyhead,Sebastolobus alascanus (Scorpaeniformes), which is similar to the ovarian structure previously described only for the pigmy lion fish,Dendrochirus brachypterus (Scorpaeniformes), is specialized for the production and expulsion of pelagic gelatinous egg masses. The germinative tissue and oocytes ofS. alascanus encircle a mass of spongy stroma that is located within the center of the ovary. The stroma is attached to the ovary wall only at the anterior end of each ovarian lobe; hence, the ovarian lumen surrounds the stroma, germinative tissue, and oocytes. Secondary oocyte development takes place on the ends of vascularized peduncles that are protrusions of the ovarian stroma. A gelatinous material is simultaneously secreted into the ovarian lumen by a single row of specialized cells that line the ovary wall. Eggs detach from peduncles and ovulate into the gelatinous material.     

Isolation, purification and characterization of silk protein sericin from cocoon peduncles of tropical tasar silkworm, Antheraea mylitta

A high molecular weight water-soluble glue protein, sericin was identified in the cocoon peduncle (a strong thread connecting the cocoons to the branches of the tree with a ring) of the tropical tasar silkworm, Antheraea mylitta. The sericin was isolated by 8 M urea containing 1% sodium dodecyl sulfate and β-mercaptoethenol (2%) or by 1% sodium chloride. The protein was purified by gel filtration chromatography. In SDS-PAGE, a single band of approximately 200 kDa was detected both in non-reducing and reducing conditions. Amino acid analysis showed that the protein is enriched in glycine and serine. There is a slight difference observed in amino acid composition between the sericin from cocoon peduncle and cocoon of A. mylitta. Secondary structure estimation by circular dichroism spectrometry showed 36.7% β-sheets, 52.7% random coils, 10.6% turns and no helices.