Gemmulation, Gemmule Hatching, and Sexual Reproduction in Fresh-Water Sponges II. Life Cycle Events in Young, Larva-Produced Sponges of Spongilla lacustris and an Unidentified Species

1974 ◽  
Vol 93 (1) ◽  
pp. 39 ◽  
Author(s):  
Tracy L. Simpson ◽  
John J. Gilbert
2018 ◽  
Vol 24 (2) ◽  
Author(s):  
R.R. DANDAWATE

Present paper deals with study of cestode parasites of genus Circumoncobothrium from fresh water fish Clarius batracus at Savitri river, (Dapoli) for the percentages of infection occurance during summer season,minimum during winter and tolarate during rainy season.The parasite mainly infected the intestine of host and fed on nutrients from digested food. It completed its life cycle in the intestine of host. By camparing different characters of it to identify that the species is new


Author(s):  
Ekaterina A. Volkova

Identification of Spirogyra species is based on the morphology of the fertile specimens. This work provides characteristics of growth and the time of reproduction of Spirogyra decimina var. juergensii in Lake Baikal and describes sexual reproduction and conditions for germination of new filaments of this species isolated from the lake.


2004 ◽  
Vol 1 (2) ◽  
pp. 200-206
Author(s):  
Baghdad Science Journal

Thi s study included the effect of chronic exposure of di fferent concentrations of Nan on the biology of fresh water zroDplonk ton species Moina 41.112' ( Cladcxe'ra The concentrations used for chronic exposure were 03, 0.75. 1 960 to investigate iI effects on the life cycle and la lables of this species after exposure period and the range of this exposure effects on the rate of expectation for further life, also the effect of salinity on reproduotive parameters was studied which included average of total number of eggs and young produced, volume clutch's (6.95. indiclutch for control group , 14.516 indi clutch for 0.596a ,3_65 ind./ clutch for (175 5(.. and 03 Ind} cruel] for 1960) and number of Clutch's (5.5 clutch/ female for control group, 1.7 clutch/ funEoc for 0.5.9(z.z, 1:2 dutch?' female for 0,75960 and 0,1 oluchi female for 196.) which howed a reduction_ But had no effects on the time 10 tarsi clutch produced. Time of surviving ( 12.9 day for control g.roup. 63 day for 0.5%0, 15_2 day for 0.75%.0 and 4.6 day for I 9f,), average final length and average of daily length, growth increasing were studied_ In addition to the studying the orient of salinity on the number of moults which showed a reduction. in its number.


Genetics ◽  
1992 ◽  
Vol 132 (4) ◽  
pp. 1195-1198 ◽  
Author(s):  
D B Goldstein

Abstract The life cycle of eukaryotic, sexual species is divided into haploid and diploid phases. In multicellular animals and seed plants, the diploid phase is dominant, and the haploid phase is reduced to one, or a very few cells, which are dependent on the diploid form. In other eukaryotic species, however, the haploid phase may dominate or the phases may be equally developed. Even though an alternation between haploid and diploid forms is fundamental to sexual reproduction in eukaryotes, relatively little is known about the evolutionary forces that influence the dominance of haploidy or diploidy. An obvious genetic factor that might result in selection for a dominant diploid phase is heterozygote advantage, since only the diploid phase can be heterozygous. In this paper, I analyze a model designed to determine whether heterozygote advantage could lead to the evolution of a dominant diploid phase. The main result is that heterozygote advantage can lead to an increase in the dominance of the diploid phase, but only if the diploid phase is already sufficiently dominant. Because the diploid phase is unlikely to be increased in organisms that are primarily haploid, I conclude that heterozygote advantage is not a sufficient explanation of the dominance of the diploid phase in higher plants and animals.


2020 ◽  
Vol 42 (4) ◽  
pp. 403-410 ◽  
Author(s):  
Haruka Takagi ◽  
Atsushi Kurasawa ◽  
Katsunori Kimoto

Abstract Gamete release has been frequently observed in laboratory cultures of various species of planktonic foraminifera. Those observations have been taken as evidence that these organisms produce new generations exclusively by sexual reproduction. We report here the first observation of asexual reproduction in Globigerinita uvula, a small, microperforate foraminifera. The asexual phase was associated with the release of ca. 110 offspring, all of which hosted symbiotic algae that must have been passed on directly from the parent. This event was also the first observation of vertical transmission of symbionts in planktonic foraminifera. Although the trigger of the observed asexual reproduction and its frequency in nature remain unknown, our observation indicates that among the planktonic foraminifera, at least G. uvula has not abandoned the asexual phase of its life cycle.


1987 ◽  
Vol 22 (4) ◽  
pp. 243-251 ◽  
Author(s):  
Tomoyoshi YOSHINAGA ◽  
Kazuo OGAWA ◽  
Hisatsugu WAKABAYASHI

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