The role of intragemmular osmotic pressure in cell division and hatching of gemmules of the fresh-water sponge Spongilla lacustris (Porifera)

Summary The gemmule coat of Spongilla lacustris is histologically single-layered in the gemmules studied in this work. This single layer is comparable to the classically described internal chitinous membrane of Leveaux (1939). It has been found to contain collagen with an axial period in electron micrographs of about 120 Å and is bounded internally by a thin dense layer which is separate from the internal gemmular cells, and which may be chitinous.Gemmules of this sponge studied during March to June of 1973 respond to 230 mOsmolar solutions of small molecules by: 1. undergoing no change, in which case the substances are freely permeable to the gemmule coat and cells; 2. displaying shrinkage of the cell mass, in which case the substances are permeable to the coat but relatively impermeable to the cells; 3. displaying folding of the coat and cell mass shrinkage because the substances are relatively impermeable to both the coat and the cells; and 4. displaying complete collapse of the gemmule due to impermeability to the coat. The lipid solubility of a substance is directly related to its ability to penetrate the coat. Further, molecular size and charge are also of apparent importance.Substances which penetrate the coat and remain osmotically active (are not metabolized) inhibit hatching. Low concentrations of sodium chloride (23 mOsmolar) have been demonstrated to reversibly inhibit hatching. Higher concentrations cause irreversible damage at 20° C but have little effect at 4° C, indicating that damage is related to the metabolic level of the cells. Once hatching is stimulated by increased temperature the cells become progressively less sensitive to an increase in osmotically active substances.Inhibition of gemmule hatching can theoretically occur by: 1. an addition of solutes to the gemmular fluid, or 2. through an increase in concentration of intragemmular solutes by water withdrawal.Our results raise the question of whether the inhibition of hatching by gemmulostasine, reported by Rasmont (1965) and Rozenfeld (1970, 1971), is due to an osmotic effect rather than to a specific physiological one.Based upon the results reported here and on the work of Zeuthen (1939) and Schmidt (1970) we propose a tight coupling between the intragemmular osmotic pressure and the triggering of hatching (cell division). Any substance which increases intragemmular osmotic pressure to a large enough extent will inhibit hatching. Furthermore, it can be hypothesized that hatching is normally triggered by a decrease in osmotic pressure due to water movement into the gemmule, the movement of solutes out of the gemmule, or to a combination of these.This work was supported by a grant from the National Science Foundation (GB-37775) to T. L. S.     

Correlation of cyclic GMP and cyclic AMP immunofluorescence with cytochemical patterns during dormancy release and development from gemmules in Spongilla lacustris L. (Porifera: Spongillidae)

The spongillid freshwater sponges asexually produce an encapsulated dormant stage, the gemmule. With release from dormancy, internal, yolk-laden, binucleate thesocytes differentiate into histoblasts or archeocytes. The histoblasts emerging first from the gemmule form the initial pinacoderm of the hatching sponge. Immunohistochemistry was employed to examine the distribution of cyclic GMP (cGMP) and cyclic AMP (cAMP) following dormancy release and during gemmule germination and hatching in the freshwater sponge, Spongilla lacustris L. Cyclic nucleotide fluorescence patterns were analyzed in relation to the distribution of cytochemically demonstrable macromolecular constituents and intracellular organelles. Twenty-four hours following temperature-activated release from dormancy, cGMP fluorescence levels are elevated in thesocytes at the gemmule periphery prior to histoblast formation. The cAMP fluorescence in the gemmule also occurs first in those thesocytes differentiating into histoblasts. Cytochemical patterns in germinating gemmules are comparable with those described by Ruthmann ('65) and Tessenow ('69). However, cytochemically demonstrable events of cytodifferentiation follow the earlier appearance of cGMP and cAMP in the histoblast precursors by approximately 12 hours. In addition, cGMP appears to be associated with the membranes of cytoplasmic organelles, possibly lysosomes or lipid inclusions, in the region of vitelline platelets and with symbiotic algae. cAMP is located primarily on the membranes of the vitelline platelets and on membranes of vacuoles involved in forming the spicular skeleton These observations suggest that cGMP and cAMP are involved in the mobilization of nutrient reserves and in ion transport during dormancy release and development from gemmules in freshwater sponges.     

Calcium and the release from dormancy of freshwater sponge gemmules.

Divalent cations (Zn, Mn, Ba, Sr) inhibit the development of dormant gemmules of the freshwater sponge Spongilla lacustris. This inhibition is overcome by calcium which can be interpreted to mean that this divalent ion is essential for germination (cell division) in this system. Inhibitory divalent cations have different effective concentrations which indicate differing binding affinities for sites which may normally bind calcium. Ethylene glycol bis(β-aminoethyl ether)N,N-tetraacetic acid does not effect gemmule development at 15°C but stimulates it at 4°C, indicating that a dislocation of endogenous calcium stimulates release from dormancy. Magnesium will only partially substitute for calcium in overcoming divalent cation inhibition implying a different specificity for this ion in gemule development. Calcium is also indicated as being essential for hatching (cell motility) in this system.     

Cost of oviposition site selection in a water strider Aquarius paludum insularis: Egg mortality increases with oviposition depth

Females generally avoid selecting sites for oviposition which have a high predation risk to increase offspring survival. Previous studies have focused on costs to ovipositing females. However, although offspring may also incur costs by being oviposited at low predation risk sites, no studies have focused on costs to offspring. Such costs to offspring were examined by using Aquarius paludum insularis, females of which avoid eggs parasitism by ovipositing at deep sites. Deep sites are safe from egg parasitism but may be unsuitable for hatching due to environmental factors. We examined the costs to offspring at deep sites by comparing the hatching rate, the duration to hatching and the proportion of drowned larvae between eggs that were set at three levels of water depth (0 cm, 25 cm and 50 cm depth). While the hatching rate at 50 cm was lower than that at 0 cm, the rate at 25 cm did not differ from that at 0 cm. Duration to hatching and the proportion of drowned larvae did not differ between the three depths. It is suggested that the declining survival rate of A. paludum eggs was due to increased water pressure at greater depth. Such a cost may exist in other species and such an observation may aid in understanding oviposition site selection.     

Effect of hatching time on time to first feed intake,organ development,enzymatic activity and growth in broiler chicks hatched on-farm

The conventional commercial hatcheries used today do not allow the newly hatched chicks to consume feed or water. Combined with natural variation in hatching time, this can lead to early hatched chicks being feed-deprived for up to 72 h before being unloaded at the rearing site. This study investigated the effects of hatching time on time to first feed intake and development of organs, digestive enzymes and productivity in terms of growth and feed conversion ratio in chicks hatched on-farm. Chicks were divided into three hatching groups (early, mid-term and late), and assessed over a full production cycle of 34 days. The results revealed that chicks remain inactive for a considerable amount of time before engaging in eating-related activities. Eating activity of 5% (i.e. when 5% of birds in each hatching group were eating or standing close to the feeder) was recorded at an average biological age (BA) of 25.4 h and a proportion of 50% birds with full crop was reached at an average BA of 30.6 h. Considering that the hatching window was 35 h in this study, the average chick probably did not benefit from access to feed and water immediately post-hatch in this case. At hatch, mid-term hatchlings had a heavier small intestine (30.1 g/kg bw) than both early (26.4 g/kg bw) and late (26.0 g/kg bw) hatchlings. Relative length of the small intestine was shorter in late hatchlings (735 cm/kg bw) than in mid-term (849 cm/kg bw) and early (831 cm/kg bw) hatchlings. However, the relative weight of the bursa fabricii was greater in mid-term (1.30 g/kg bw) than in early hatchlings (1.01 g/kg bw). At hatch, late hatchlings were heavier than early and mid-term hatchlings (P < 0.05), but by 3 days of age early hatchlings were heavier than mid-term and late hatchlings (P < 0.01). The only effect persisting throughout the study was a difference in the relative weight of the small intestine, where late hatchlings had heavier intestines than early hatchlings (P < 0.05). Thus, while there were differences between hatching groups, this study showed that the hatchlings seemed capable of compensating for these as they grew.     

Vergleichende rasterelektronenmikroskopische Darstellung der Gemmulaschalen von Ephydatia fluviatilis,E. muelleri und Spongilla fragilis (Porifera)

Zusammenfassung Die Gemmulaschalen der Süßwasserschwämme besitzen eine arttypische Oberflächenstruktur, die in der vorliegenden Arbeit bei drei Spongillidenarten rasterelektronenmikroskopisch dargestellt ist. Anhand angeschnittener, aus dem Einbettungsmittel herausgelöster Gemmulaschalen wird die Schaleninnenstruktur rasterelektronenmikroskopisch untersucht. Das mit dieser Methode (Weissenfels 1982a) gewonnene Bildmaterial liefert Informationen zur Architektur der Gemmulaschalen und zur Entstehung der sog. Kästchenschicht in den Gemmulaschalen von Spongilla fragilis.

---

Comparative scanning-electron-microscope study of the gemmule shells of Ephydatia fluviatilis, Ephydatia muelleri and Spongilla fragilis (Porifera)

Summary The gemmule shells of fresh-water sponges have a species-specific surface structure, described here for three spongillid species by reference to scanning electron micrographs. The internal structure of the shell is revealed in scanning electron micrographs of sectioned shells released from the embedding medium. Pictures obtained by this method (Weissenfels 1982a) provide information about the architecture of the gemmule shells and the development of the so-called compartmented layer in the gemmule shells of Spongilla fragilis.

     

Hatching of freshwater sponge gemmules after low temperature exposure: Ephydatia mülleri (Porifera: Spongillidae)

1. 1.|Gemmules of Ephydatia mülleri can withstand exposure to temperatures down to −80°C for 63 days without loss of hatchability.

2. 2.|Hatching is slowed following exposure to temperatures below −27°C.

3. 3.|There is a slight but significant relationship between gemmule size and the time to hatch.

4. 4.|This species can withstand long-term exposure to winter air temperatures occurring within its known geographic range.

The influence of an eucaryotic intranuclear cell parasite on the production of gemmules inEphydatia fluviatilis (Porifera,Spongillidae)

Summary A prerequisite for the production of gemmules is the presence of intact archaeocytes and trophocytes, which give rise to the thesocytes with which the gemmule is eventually filled. The coat enclosing the gemmule requires spongioblasts for its formation and incorporates amphidisk spicules, which develop in amphidiskoblasts. The cell parasite, the development of which is described here, infects mainly archaeocytes but also spongioblasts and amphidiskoblasts. Even a moderate infection results in significant malformation of the gemmule covering. In the thesocyte nucleus, the parasite can survive the resting phase of the gemmule. After the gemmule has hatched, the parasite, again in the virulent form, is present in the young, developing sponge. The parasite may be a microsporidian of the primitive type, close to the genusMetchnikovella, which typically occurs in gregarines.Abbreviations for the microscopic procedures PhM phase-contrast microscopy - TEM transmission electron microscopy - SEM scanning electron microscopy     

Dormancy of Heterodera glycines in Missouri

A 2-year study was conducted in field microplots to determine the relative importance of soybean phenology and soil temperature on induction of dormancy in Heterodera glycines in Missouri. Four near-isogenic soybean lines differing for maturity date were planted in microplots infested with a race 5 isolate of H. glycines. Soil temperature was monitored at a depth of 15 cm. Eggs of H. glycines, extracted from cysts collected monthly from each microplot, were used in hatching tests and bioassays to determine dormancy. Egg hatching and second-stage juvenile (J2) infectivity rates decreased sharply from their highest levels in midsummer (July-August) to a low level by October of each year and remained low (< 10% hatching and < 0.2 J2/cm root) until May or June of the following year. The patterns of numbers of females and eggs in the bioassays were similar. The decreases were not related to soil temperature and did not differ consistently among soybean isolines. The monophasic changes in all nematode responses with peak midsummer rates suggest that H. glycines produces one primary generation per year in central Missouri. Changes in hatching rates and the timing of minimum and maximum rates suggested that H. glycines eggs exhibit more than one type of dormancy.     

Constitutive but no Triops-induced differences in bet-hedging strategies for hatching in Daphnia

Since cladocerans from the genus Daphnia are known to have evolved several inducible defenses (morphological and life history shifts) against the notostracan predator Triops, we investigated whether hatching was also altered in response to Triops. We tested whether dormant eggs of Daphnia magna are able to detect Triops cancriformis kairomones in the water as a signal of predation pressure and alter their hatching response accordingly to avoid predation. We predicted that, in the presence of Triops kairomones, hatching fractions might be reduced (postponing hatching to a next growing season) and/or that hatching might peak earlier (increasing chances to reproduce before Triops becomes predatory). We also tested whether this response depended on the origin of the population. Ephippia from three D. magna populations, originating from one permanent lake and two temporary pond systems, were exposed to Triops kairomone and control treatments. We observed significant population differences in hatching patterns, both in terms of the fraction of eggs that hatch as well as the timing of hatching, with evidence for within-season bet-hedging through delayed hatching in the populations inhabiting temporary habitats. However, no indication was found that the populations also adjust their hatching pattern to the presence of Triops kairomones.     

Influence of Herbicide Application to Soybeans on Soybean Cyst Nematode Egg Hatching

The hatching of Heterodera glycines eggs in soybean root exudates collected after postemergence application of three herbicides, and the hatching potential of H. glycines eggs from females feeding on herbicide-treated plants, were measured in vitro. Hatching in all root exudate solutions (RES) was greater than in deionized water but less than in 0.003 M ZnSO₄ solution. Filtering RES with a 0.22-μm-filter increased H. glycines hatching in RES. Application of acifluorfen, bentazon, and lactofen to foliage of soybean plants inhibited hatching of H. glycines eggs from the same plants. Hatching in RES from the different herbicide-treated soybeans was similar. Application of crop oil concentrate and non-ionic surfactant adjuvant to foliage did not affect hatching of H. glycines eggs from soybean plants.     

Temperature,salinity tolerance,and buoyancy during early development and starvation of Clyde and North Sea herring,cod, and flounder larvae

Tolerance limits, at which 50% of larvae could survive high temperature and low salinity for 24 h, were determined for the yolk-sac larvae of Clyde and North Sea herring (Clupea harengus L.), cod (Gadus morhua L.) and flounder (Platichthys flesus L.) during early development and starvation. Clyde and North Sea herring, cod and flounder from hatching to the end of the yolk-sac stage, could withstand 21–23.5 °C, 20.5–23 °C, 15.5–18 °C and 21.5–24°C, respectively. The temperature tolerance was reduced by about 3.5–4 °C for Clyde herring and cod, 4–4.5 °C for North Sea herring and 8–8.5 °C for flounder when the larvae reached the point-of-no-return (PNR, when 50% of larvae, although still alive, are no longer strong enough to feed). The lowest salinity tolerance between hatching and the end of yolk-sac stage was 1–1.5‰ for Clyde and North Sea herring, 2–3‰ for cod and 0–1‰ for flounder. In no instance was there a loss of tolerance to low salinity during starvation. In fact, tolerance improved somewhat until the larvae became moribund. At hatching Clyde and North Sea herring larvae were negatively buoyant with a sinking rate of 0.35–0.4cm · s⁻¹ which steadily decreased until the larvae became moribund. Cod and flounder larvae, however, were positively buoyant at hatching but became progressively less buoyant and, by the end of the yolk-sac stage they were negatively buoyant with a sinking rate of 0.06–0.07 cm · s⁻¹. This sinking rate then decreased slightly until the PNR stage. The low salinity tolerance of all three species varied in a similar fashion to buoyancy.     

Syphacia muris: Water permeability of eggs and its effect on hatching

As a result of a previous study, it appeared that hatching of eggs of Syphacia muris is activated by the application of heat (37 °C) or cysteine or trypsin but that these are not the essential stimuli. In the present study it has been established that exposure of eggs prior to hatching for several hours to 37 °C or cysteine or trypsin, or for 3 days to 22 °C, accelerated hatching. Pretreatment with 37 °C or cysteine or trypsin also increased permeability of the eggshell to water; however, it did not induce the operculum to open. The operculum opened only if the eggs, after pretreatment, were immersed in water. The larvae could leave the opened eggs only in water and not in any other medium such as paraffin oil. These data made it possible to distinguish between three stages in the hatching process. During Stage 1, the eggshell becomes permeable to water. This can be induced by dissolving the proteins of the eggshell in a trypsin solution or by stimulating the larvae with temperature or cysteine. The permeability of the eggshell is essential to successful hatching. In Stage 2, which occurs only in the presence of water, the larvae dissolve the chitinous seal between the operculum and the eggshell. In Stage 3 the larvae probably increase their size by water absorption and leave the eggs. In the discussion it has been proposed that all nematodes, both those hatching in the intestine and the species hatching in the open, could well have an identical hatching mechanism to the one observed in Syphacia muris.     

Antigenic characterization of chick erythrocytes and erythropoietic precursors: identification of several definitive populations during embryogenesis.

During ontogenesis of the chick, three normocyte populations can be resolved on the basis of their membrane antigens. Embryonic erythrocytes bear an embryonic antigen (E₁) which is not present on adult red cells. Conversely an adult antigen (A) is detected only on adult red cells. A third population bearing simultaneously both antigens develops transiently during the first month after hatching. These normocyte antigens were investigated at the level of erythrocytic stem cell identified by in vivo and in vitro assays. The antigens can be revealed only on erythrocytic precursors CFU-cE giving rise to erythrocytic clones in vitro in presence of avian erythropoietin. Three CFU-cE populations were defined therefrom. In marrow, all these populations are present in the embryo but only CFU-cE bearing A antigen subsist after hatching.     

A calibration method to generate seasonal hatching profiles for the fiddler crabs Uca pugnax (Smith, 1870) and Uca minax (LeConte, 1855) (Decapoda : Brachyura)

A statistical method for generating seasonal egg hatching profiles is applied to the brachyuran crabs Uca pugnax (Smith) and U. minax (LeConte) in New Jersey. Calibration experiments quantified the time course of egg development, using serial egg sampling at 1- to 2- day intervals from marked ovigerous females maintained in cages in the field. Egg stage was ranked from 1 to 10, based on morphological changes during development. Equations for predicting the number of days remaining until hatching from egg developmental stage were obtained from the calibration experiments, using stepwise polynomial regression. To cover the reproductive season, three consecutive calibration experiments using 15 or more females were run for U. pugnax; two for U. minax. Significant seasonal differences in the time course of egg development were detected. Weekly collections of females for each species were made; the date of larval release for each ovigerous female was predicted from the proximate calibration equation, yielding weekly hatching profiles. Weekly hatching profiles were summed to obtain seasonal hatching profiles. The average number of broods produced per female over the reproductive season was 1.9 for U. pugnax and 1.6 for U. minax. Hatching peaks for both species were associated with spring tides. The merits of this and other methods used to estimate daily variation in egg hatching of crabs are discussed.     

Early life history timings in marbled rockcod (Notothenia rossii) fingerlings from the South Shetland Islands as revealed by otolith microincrement

Although it has been reported that Notothenia rossii elsewhere hatches in spring, our daily increment back-counting from the capture date in otoliths of fingerlings caught in Potter Cove, South Shetland Islands, in the 2000s, showed two main periods of larval hatching, one in summer (February–March) and another in winter (July). In concordance, the simultaneous presence of two cohorts born the same year was identified in the age/length frequency distribution of fish sampled in spring 2010, which belonged to biological ages 0+ and 1+ and hatched, respectively, in summer and winter–spring. Maximum and minimum ages of pelagic blue-phase and demersal brown-phase fingerlings were, respectively, 227 and 240 days, indicating a demersal settlement after about 8 months from hatching. The estimated growth rate was 0.23–0.33 mm/day, equivalent to that of South Georgia fingerlings and higher than those of other nototheniids of similar size range. Based on early life events associated with the hatching periods, two types of life cycles are hypothesised for South Shetland fingerlings. The pelagic blue-phase fingerlings (6.5–7.6 cm TL, age group 0+) hatched in July (winter cohort), entering in Potter Cove in February–March. The brown-phase fingerlings (6.3–10.6 cm, mostly of age group 0+) hatched in February–March (summer cohort) and were collected in the cove in spring (the smaller specimens) or in summer (the larger ones). Finally, early juveniles (10.7–15.5 cm, age group 1+) hatched in winter, mainly in July (winter cohort), entering in the cove the following year to spend the second winter inshore.     

Larval and early juvenile development of Lithodes santolla (Molina, 1782) (Decapoda: Anomura: Lithodidae) reared at different temperatures in the laboratory

The southern king crab, Lithodes santolla Molina, is distributed in cold-temperate and subantarctic waters ranging from the southeastern Pacific island of Chiloé (Chile) and the deep Atlantic waters off Uruguay, south to the Beagle Channel (Tierra del Fuego, Argentina/Chile). Recent investigations have shown that its complete larval development from hatching to metamorphosis, comprising three zoeal stages and a megalopa, is fully lecithotrophic, i.e. independent of food. In the present study, larvae were individually reared in the laboratory at seven constant temperatures ranging from 1 to 18 °C, and rates of survival and development through successive larval and early juvenile stages were monitored throughout a period of 1 year. The highest temperature (18 °C) caused complete mortality within 1 week; only a single individual moulted under this condition, 2 days after hatching, to the second zoeal stage, while all other larvae died later in the zoea I stage. At the coldest condition (1 °C), 71% of the larvae reached the zoea III stage, but none of these moulted successfully to a megalopa. A temperature of 3 °C allowed for some survival to the megalopa stage (17-33% in larvae obtained from two different females), but only a single individual passed successfully, 129 days after hatching, through metamorphosis to the first juvenile crab instar. At all other experimental conditions (6, 9, 12 and 15 °C), survival through metamorphosis varied among temperatures and two hatches from 29% to 90% without showing a consistent trend. The time of nonfeeding development from hatching to metamorphosis lasted, on average, from 19 days at 15 °C to 65 days at 6 °C. The relationship between the time of development through individual larval or juvenile stages (D) and temperature (T) was described as a power function (D=aT^b, or log[D]=log[a]blog[T]). The same model was also used to describe the temperature dependence of cumulative periods of development from hatching to later larval or juvenile stages. One year after hatching, the 7th (6 °C) to 9th (15 °C) crab instar was reached. Under natural temperature conditions in the region of origin of our material (Beagle Channel, Argentina), L. santolla should reach metamorphosis in October-December, i.e. ca. 2 months after hatching (taking place in winter and early spring). Within 1 year from hatching, the crabs should grow approximately to juvenile instars VII-VIII. Our results indicate that the early life-history stages of L. santolla tolerate moderate cold stress as well as planktonic food-limitation in winter, implying that this species is well adapted to subantarctic environments with low temperatures and a short seasonal plankton production.     

Role of cAMP in the release from dormancy of freshwater sponge gemmules.

The role of 3′5′-cyclic AMP (cAMP) in the release from dormancy of gemmules from the freshwater sponge Spongilla lacustris was investigated. During the first 2 hr of germination a significant decrease in the gemmule cAMP content was observed. In the presence of amino-phylline, at concentrations which inhibit the gemmule-cAMP-phosphodiesterase, the cAMP content did not decrease and germination was arrested at a stage prior to nuclear separation and cell division. The findings suggest that inhibition of cell division by cAMP participates in the control of dormancy.     

Acoustic communication in a king penguin colony: importance of bird location within the colony and of the body position of the listener

This study focuses on the propagation of the display call used for individual recognition between penguin partners. Transmission of acoustic information in a noisy environment such as a king penguin colony is very difficult. Conditions of propagation were examined for two areas of the colony (hatching and courtship areas) and reception at three heights from the ground (10, 45 and 90 cm). Signal modification was assessed in terms of attenuation of signal, amplitude modulation and spectral content. The acoustic recognition of the mate, which is decisive for breeding success, took place in the hatching area where signal degradation was less great for all parameters studied. When the receiver was located 10 cm above the ground, degradation of the signal was much more pronounced than when it was located 45 or 90 cm above ground. The characteristic incubating attitude of the king penguin (i.e. standing with the head at 45 cm above the ground) enables it to receive the main part of the signal in spite of the noisy environment. Accepted: 19 October 1998     

Life-cycles of lotic populations of Spongilla lacustris and Eunapius fragilis (Porifera: Spongillidae)

SUMMARY. The life-cycles of green and white morphs of the freshwater sponge Spongilla lacustris were examined in the light of past evidence that zoochlorellae may augment their sponge host's nutrition. Field collections from a lotic population of S. lacustris were supplemented by laboratory experiments on gemmule hatching and gemmule size. Both white and green S. lacustris produced sperm for a 6-week period in 1976 starting in the middle of May. Out of thirty white and thirty green sponges examined during this period, twenty white and ten green sponges contained sperm. Sperm production in both morphs was limited primarily to the basal 3.18mm of sponge tissue, and the density of sperm packets in the two morphs was the same. Out of 180 white and green sponges examined in 1976, only four eggs, no embryos, and no larvae were observed. White sponges gemmulated a week or two earlier, and produced smaller gemmules which were more uniform in size than those of green sponges. White and green gemmules hatched synchronously in the spring. In 1977 one female and numerous male specimens of S. lacustris , and numerous females but no males of another sponge, Eunapius fragilis , were found. The life-cycles are discussed in the light of other recent studies on freshwater sponges.