Laboratory studies of factors affecting egg hatch of triops longicaudatus (LeConte) (Notostraca : Triopsidae)

Egg hatch was greatest (78.33%) for eggs not previously desiccated. A reduction in numbers hatched occurred as the relative humidity at which they were dried decreased. Some eggs hatched (0.67–79.33%) at pH levels of 3.10–10.01 with the highest hatch at pH 5.60. Water temperature greatly affected egg hatch. No hatch occurred until temperatures were above 14°C. A constant 29°C significantly inhibited hatching. Egg hatch increased 13.00 to 43.42% as salinity decreased from 2200 to 9.24 micromhos/cm. As little as 13 mm of flooded soil covering the eggs prevented them from hatching for 14 days. Eighteen percent hatch resulted when soil and eggs were redistributed to a 1 mm soil layer. Egg samples from the same parent, even though treated similarly, often hatched at greatly varying rates and only rarely was hatching 100% within a replication.     

Embryonic development, larval growth and life cycle of Coenagrion puella (Odonata: Zygoptera) from an Austrian pond

SUMMARY. 1. Newly-laid eggs of Coenagrion puella (L.) from a pond near Herzogenburg (Lower Austria) were kept at constant water temperatures (range c .3.5°C to c .28°C)in the laboratory. Hatching success varied with temperature; no eggs hatched below 12°C and nearly all hatched at c .l6°C. Hatching time decreased with increasing temperature and the relationship between the two variables within the range 12–28 °C was well described by a power law. The length of the hatching period was less than 12 days. Hatching times estimated from the power-law equations and those obtained in the field experiments were similar. Therefore both the hatching time and the length of the hatching period in the field could be estimated from the laboratory data for the range 12–28°C.
2. The maximum number of instars from egg to imago was 11; the average body length increment (mm) per moult was proportionately constant at c .26% and Dyar's rule was applicable. The interval between moults decreased with increasing temperature up to the seventh instar and the relationship between the two variables within the range 12–28°C was well described by a power law. The moulting interval for instars 8–11 ranged from 23 to 48 days and was relatively independent of temperature. No moulting occurred at temperatures below 12°C.
3. Larval growth was logistic in the laboratory and variations in mean logistic growth rate (range 0–2.5% length day⁻¹) were related to mean temperature with no growth at temperatures <12°C. Larval growth rates in pond experiments were similar to those estimated from laboratory data, and therefore the regression equations obtained from the laboratory experiments are probably applicable to larval growth in the field.
4. Information on the life cycle of C. puella is briefly reviewed and it is concluded that C. puella from the pond near Herzogenburg has an univoltine life cycle.     

Oviposition cycle in the oviparous fish Xenopoecilus sarasinorum

To clarify the reproduction of the oviparous teleost Xenopoecilus sarasinorum, changes in oocyte composition and oviposition cycle were investigated. After release, a batch of spawned eggs hung from the urogenital pore by attaching filaments (36.3+/-0.8 in number, n=31; about 4.3-7.8 mm in length, 5-8 microm in diameter) on the chorion (egg envelope) in the vegetal pole region. Females accommodated a cluster of fertilized eggs in a belly concavity until the embryos hatched. Hatching of embryos took place from 18-19 days after oviposition (25 degrees C). Between 0-2 days following hatching, the attaching filaments disappeared from the urogenital pore. Between 3 and 4 days following hatching, most of the females spawned again. The growth of oocytes proceeded slowly throughout the period when the egg cluster was carried in the belly, and no ovulation occurred during this period. If the current brood was accidentally lost, the day of the next oviposition was sooner. This might imply that carrying embryos in the belly affects endocrine activity, as in viviparous reproduction.     

Reproductive behaviour and early development of the Drysdale hardyhead, Craterocephalus sp. nov. (Pisces: Atherinidae), from the Alligator Rivers System, Northern Territory, Australia

Craterocephalus sp. nov. showed sexual dimorphism in body shape during the breeding season. Pairing occurred during daylight with a single release of eggs amongst submerged vegetation between sunrise and the early afternoon on the same day. The eggs were demersal, adhesive, spherical (0.87–0.96 mm diameter) and had 12 adhesive filaments (0.5–1.5 mm long) at the animal pole. Approximately 24 oil droplets (0.02–0.08 mm diameter) persisted throughout egg and larval development. Hatching occurred 155–160 h after spawning at 25–27° C.
The yolk-sac larvae were 3.85–3.95 mm notochord length at hatching and began feeding at the surface after absorption of the yolk (3–12 h after hatching). All fin rays were developed in 9.4 mm standard length fry, which moved from midwater to feed on the substrate. Aquarium reared fish first spawned at 30 mm s.L. when 165 days of age.
Features of Craterocephalus reproduction, as they relate to a specific survival strategy, are briefly discussed.     

Desiccation and egg viability of the ragwort flea beetle,Longitarsus flavicornis (Coleoptera: Chrysomelidae)

A study was conducted to investigate the effect of desiccation on the survival of eggs of Longitarsus flavicornis. Eclosion of L. flavicornis eggs in laboratory trials decreased with increasing desiccation time between 0 days (93% hatching) and 42 days (no egg hatching) at 50±2% relative humidity and 23±2°C. Probit analysis indicated that 25, 50 and 99% mortality of L. flavicornis eggs occurred after 5.7, 9.3 and 50.4 days desiccation, respectively. Egg development varied between a minimum of 8 days at 7 days desiccation to a maximum of 15 days at 28 days desiccation. Hatching span did not differ between treatments with all eggs hatching within 12 days of each other. A relative humidity of 88–100% was measured under ragwort rosettes in non-drought field conditions. This would be expected to facilitate successful egg eclosion. However, the occurrence of summer drought could be detrimental to egg survival.     

Lifetime egg production and egg mortality in the damselflyPyrrhosoma nymphula (Sulzer) (Zygoptera: Coenagrionidae)

Artificial oviposition sites were used to estimate egg deposition rates in the field. Females laid an average of 10.76 eggs/minute with a mean duration of 22.81 minutes, giving an average clutch size of 245 eggs. Since one mating corresponded to one clutch of eggs, lifetime mating success was used as a measure of the number of clutches produced. Mean lifetime clutch production was 5.91 clutches per female, equating to 1447 eggs per female per lifetime. Eggs were hatched in the laboratory at temperatures comparable with those in the field. Hatching was highly synchronised and the overall hatching success was 75.1%. Causes of egg mortality in the laboratory were limited to infertility and unhatchability. Since no other sources of egg mortality could be found at the study site, this value was a good reflection of hatching success in the field. Lifetime egg production and hatching success were used to estimate the number of viable offspring produced per female, giving a higher order estimate of reproductive success than has previously been published for a zygopteran.     

An individual-based model for predicting the emergence period of sea trout fry in a Lake District stream

The objective of this study was to predict interannual fluctuations in the emergence period of sea trout fry, using models developed from field data for 70 excavated redds, and laboratory data on egg and alevin development at 30 constant temperatures (range 1·5–10·5° C with 100 naturally fertilized eggs at each temperature). Egg weight and numbers per redd both increased with female length; a power function described the relationship. Early spawners were the largest females laying the largest and most numerous eggs, whilst late spawners were the smallest females laying the smallest and least numerous eggs; middle spawners being intermediate between these two extremes. Mean values for egg weight and numbers of eggs per redd were obtained for these three groups. Hatching and emergence times in the laboratory decreased with increasing temperature. Of five models tested for hatching time, the best fit was provided by a three-parameter hyperbolic model which formed the asis of the individual-based model used to predict egg hatching and fry emergence. Model development was described in detail and the final equations predicted the times taken for 5, 50 and 95% of the fry to emerge, and hence the period over which 90% of the fry emerged. Analogous models were obtained for egg hatching. All models were excellent fits to the laboratory data. Hatching times for eggs kept in perforated boxes in the stream were almost identical to those kept at similar mean temperatures in the laboratory. Model predictions of fry emergence times were validated by field data for 8 years (1967–1971, 1974, 1975, 1980). The chief objective was therefore fulfilled, and predictions for the 30-year study (1967–1996) revealed a large variation in the timing of emergence (extremes: 11 March–4 April 1989, 15–20 May 1979). Most of the variation in median emergence date was due to variations in water temperature, with spawning dates as a secondary factor; the latter, however, had a greater effect on the length of the emergence period.     

Egg production, hatching rates, and abbreviated larval development of Campylonotus vagans Bate, 1888 (Crustacea: Decapoda: Caridea), in subantarctic waters

Early life history patterns were studied in the caridean shrimp, Campylonotus vagans Bate, 1888, from the subantarctic Beagle Channel (Tierra del Fuego). As a consequence of very large egg size (minimum 1.4 mm), fecundity was low, ranging from 83 to 608 eggs per female (carapace length [CL] 11-22.5 mm). Egg size increased continuously throughout embryonic development, reaching prior to hatching about 175% of the initial diameter. Due to low daily numbers of larval release, hatching of an egg batch lasted for about 2-3 weeks. The complete larval and early juvenile development was studied in laboratory cultures fed with Artemia sp. nauplii. At 7.0±0.5 °C, development from hatching to metamorphosis lasted for about 6 weeks. It comprised invariably two large zoeal stages and one decapodid, with mean stage durations of 12, 17, and 15 days, respectively. Larvae maintained without food survived on average for 18 days (maximum: 29 days), but did not reach the moult to the zoea II stage. Size increments at ecdysis were low in all larval stages (2.1-3.9%), indicating partial utilisation of internal energy reserves. A clearly higher increment (14%) was observed in the moult from the first to the second juvenile stage. Low fecundity, large size of eggs and larvae, an abbreviated mode of larval development, high larval survival rates during absence of food, demersal behaviour of the early life history stages, and an extended hatching period with low daily release rates are interpreted as adaptations to conditions typically prevailing in subantarctic regions, namely low temperatures (causing long durations of development) in combination with a pronounced seasonality in plankton production (i.e., short periods of food availability).     

Declining egg viability explains higher hatching failure in a suburban population of the threatened Florida scrub‐jay Aphelocoma coerulescens

Hatching failure occurs in approximately 10% of all avian eggs, but varies both within and among species. This reduction in viable offspring can have significant fitness consequences for breeding parents; therefore, it is important to understand which factors influence variation in hatching failure among populations. Previous research suggests that hatching failure is higher in a suburban than in a wildland population in the Florida scrub‐jay. From 2003 to 2007, we performed two experiments to examine whether increased hatching failure in the suburbs resulted from 1) increased length of off‐bouts during incubation (predation risk hypothesis, 2003–2004) or 2) increased exposure to ambient temperature during laying (egg viability hypothesis, 2005–2007). Hatching failure was higher for females that took fewer off‐bouts, but the length of those off‐bouts did not influence hatching failure. Thus, nest predation risk does not appear to explain higher hatching failure in the suburbs. Alternatively, hatching failure increased with increasing exposure of eggs to ambient conditions during the laying period. First‐laid eggs in the suburbs had the greatest pre‐incubation exposure to ambient temperature and the greatest rate of hatching failure, consistent with the egg viability hypothesis. Urbanization influences hatching failure through a series of complex interactions. Access to predictable food sources advances mean laying date in suburban scrub‐jays, leading to larger clutch sizes. Because scrub‐jays begin incubation with the ultimate egg, first‐laid eggs in the suburbs may be exposed to ambient temperatures for longer periods, thus reducing their viability.     

First confirmed complete incubation of a flapper skate (Dipturus intermedius) egg in captivity

An egg of the critically endangered flapper skate Dipturus intermedius was successfully incubated to hatching in captivity in what is believed to be a first for the species. Water conditions (temperature, salinity, flow rate) were recorded, with mean water temperatures ranging from a monthly mean of 8.3 ± 1.2 to 13.2 ± 0.3°C and salinity from a monthly mean of 30.5 ± 1.2 to 36.6 ± 2.3 ppt. Hatching occurred after 534 days, suggesting that flapper skate eggs take c. 5700 growing degree-days to incubate to hatching. The egg's prolonged embryonic development raises concerns about flapper skate eggs' vulnerability to anthropogenic disturbance.     

1. A CENSUS AND STUDY OF BIRDS IN ALBANY OPEN THORNBUSHVELD

Williams, A. J. &; Cooper, J. 1983. The Crowned Cormorant: breeding biology, diet, and offspring reduction strategy. Ostrich 54:213-219.

Crowned Cormorants Phalacrocorax coronatus were studied at Dassen and Marcus Islands. The most frequent clutch was three eggs. Egg size varied within clutches with first-laid eggs being largest and heaviest and subsequent eggs progressively smaller and lighter, The mean laying interval was 2,2 days, the mean laying-to-hatching interval was 23,0 days, and the hatching interval was one day. The normal incubation period was 22.4 days. The weight of hatchings was related to the position of the originating egg in the laying sequence. Chicks were fed within 24 h of hatching. Chick development is described over the first 35 days. One chick could fly at 35 days. Hatching success was 48,2%. Hatching success was greatest in second-laid eggs, least in last-laid eggs. The mean number of chicks hatched at a nest was two. Mean diving time was 23,5 s. Most food was fish, particularly klipfish Clinidae and pipefish Syngnathus, 60–160 mm long. The number of offspring produced can be related to food availability by interaction of difference in egg size, hatching asynchrony, and the preferential feeding by adults of the strongest-begging chick. There is a trend towards producing two chicks, normally those from the first two eggs to be laid.     

Hatching success, delay of emergence and hatchling biometry of the spur-thighed tortoise, Testudo graeca, in south-western Spain

Hatching success, egg incubation, emergence and hatchling characteristics were assessed for 44 naturally incubating nests of Testudo graeca in south-western Spain. Nest predation rate was 4.5% and overall hatching success was 82.4%. Incubation periods ranged from 78 to 114 days, and hatchlings delayed emergence from the nest from one to 23 days. Emergences occurred from mid August to late September, and were not correlated with nesting dates, but earlier laid nests had longer incubation times, which was probably owing to lower temperatures experienced by clutches laid at the beginning of the nesting season. Variance of hatchling body size and mass was high and was mainly influenced by the gravid female. Mean straight carapace length was 34.14mm, and mean body mass 10.8g. Hatchlings from clutches laid last in the nesting season had significantly better physical condition. Hatchling mass was positively correlated with egg mass, and both variables were positively correlated with emergence date. Both better physical condition and relatively late emergence may confer advantages to hatchlings in the face of unfavourable environmental conditions in autumn.     

Early ontogeny of Galeichthys feliceps from the south east coast of South Africa

The early development of Galeichthys feliceps (Valenciennes, 1840) was investigated using a combination of incubator-reared embryos and embryos removed from the buccal cavities of wild-caught parents. The eggs were 15·7 mm in diameter and the average brood size was 49. Hatching occurred at an advanced developmental state after approximately 75–80 days, when branchial and fin differentiation were complete. Exogenous feeding began within the adult buccal cavity shortly after hatching. The young were released as juveniles after approximately 140 days, at a total length of 54 mm.     

Zur fortpflanzungsbiologie von mesostoma ehrenbergii (Focke, 1836) (Turbellaria)

1. At temperature levels from 10 to 25°C animals from resting eggs produce subitaneous eggs independent on temperature. In contrast animals from subitaneous eggs produce subitaneous eggs dependent on temperature. At a high rate subitaneous eggs are only formed at temperature levels above 20°C.
2. Below 10°C no development occurs in the juveniles. At temperatures of 30/22°C (24.7°C) the first subitaneous eggs are formed after 6–9 days, at 14/9°C (10.7°C) they are formed after 34 days. At different temperature levels the developmental rate of the young is from 10.5 to 42 days. One generation extends over 16.5 (30/22°C) to 75 days (14/9°C). The average egg production is 10–20 subitaneous eggs or 30–60 resting eggs. The maximum egg production of one individual is 50 subitaneous eggs or 84 resting eggs. 50% of the animals have just formed resting eggs, before the juveniles are hatched. Resting eggs in the first egg-batch are formed 6–20 days later than subitaneous eggs. The duration of life is between 65 (30/22°C) and 140 days (19/13°C).
3. Young worms in resting eggs have a dormance period of at least 15–30 days.

At room temperatures (20°C) no juvenile in resting eggs hatches from water. By combining room and refrigerator (3.5°C) temperatures the hatching rate increases to a maximum of 85%. To reach a hatching rate of 50–65% the influence of low temperatures must be at least 30 days. At room temperatures 60% of the young in resting eggs hatch from mud covered with water. Combining high and low temperatures the hatching success is between 67 and 81%, where the highest percentage of the young may hatch at room temperature. Up to 90 days low temperatures cause a maximum hatching rate of 79%. It decreases to approximately 30% after 180 days. At high temperatures resting eggs preserved in 100% moist mud, survive for two months. By adding a period of low temperatures the hatching rate increases to a maximum of 52%. Low temperatures are survived for more than 6 months. Up to 30 days preservation at 3.5°C causes a maximum hatching rate of 61%, up to 12o days it decreases to 30%. At room temperature the young in resting eggs are not resistant against air-dried mud (30–40% rel. air moisture). Combining high and low temperatures air-dried mud is endured 1 month (hatching rate 5–14%). Preservation of 30–120 days at 3.5°C and 70% rel. air moisture result in a hatching rate of 43–61%. li]4. In the open air in Middle-Europe there occur 5–6 generations of M. ehrenbergii per life-cycle. The first generation hatches from resting eggs in May, where the production of subitaneous eggs is independent on temperature. All other generations up to October hatch from subitaneous eggs. The egg-production of those worms is dependent on environmental factors. In summer subitaneous egg production prevails, in autumn resting egg production. The abundance during the life-cycle is dependent on the number of animals which produce subitaneous eggs. Resting eggs are predestinated to endure periods of dryness and cold. The life-cycles of the species M. lingua and M. productum are different from those of M. ehrenbergii in length and in the number of generations. In both species 7 generations occur over 8 to 8.5 respectively 5.5 months. M. nigrirostrum only forms resting eggs. The life-cycle consists of one generation from February/March to May/June.     

长江口沿岸碎波带刀鲚仔稚鱼的日龄组成与生长

实验研究了长江口沿岸碎波带刀鲚仔稚鱼的日龄组成、孵化期、早期生长率和滞留时间。从2007年5-10月在长江口沿岸碎波带采集的刀鲚仔稚鱼中,共选取594尾(体长范围为3.0-30.5mm),划分发育阶段,并取矢耳石进行日龄分析。仔稚鱼日龄范围为7-34d,以13-18d日龄比例较高,占总数的50.1%;仔稚鱼体长(L,mm)与日龄(D,days)呈显著直线关系:L=0.73D+5.09,R2=0.74;孵化期为5月23日至10月4日,高峰期集中在5月末至8月上旬,且早期个体在孵化后7d左右开始进入到碎波带,在碎波带滞留约23d。       

The life history of Chirocephalus kerkyrensis Pesta (Crustacea: Anostraca) in temporary waters of Circeo National Park (Latium,Italy)

The life cycle of Chirocephalus kerkyrensis, a typicalspecies of the Mediterranean plain forest, was studied in thefield during 1990/91 and 1991/92.Temperature, and its variation, was the major factor affectinglife history. Marked, sudden temperature fluctuations resultedin depressed growth and longevity. Fertility was positivelycorrelated (P<0.001) with female body length. Nodecline in egg production was observed at the end of life, incontrast to other species. Hatching was observed after a longdrought followed by alternating wet and dry phases. Laboratorytests on hatching gave contrasting results and showed thatdrying is not obligatory. Cysts stored in 100% relativehumidity gave higher numbers of nauplii after a shorter timethan dried ones, at all temperatures tested.     

Interspecific and intraspecific variations in egg hatching for British populations of the stoneflies Siphonoperla torrentium and Chloroperia tripunctata (Plecoptera: Chloroperiidae)

SUMMARY 1. The objective was to compare variations in egg hatching between the two species (interspecific variations) and between populations of the same species (intraspecific variations). There were significant interspecific, but not intraspecific, differences in female size, adult life-span, egg production, hatching success, incubation periods and hatching periods.
2. The optimum temperature for hatching success within the range 3.8–22.1°C in the laboratory and the range over which at least 50% of the eggs hatched were lower for Chloroperia tripunctata (Scopoli) (8.5°C, 4.2–17.3°C) than for Siphonoperla torrentium (Pictet) (12.8°C, 6.1–19.4°C). Few eggs hatched at 22.r°C.
3. The relationship between incubation period (d days) and water temperature (T°C) was given by: d=1219/T^1.368 for S. torrentium , d=253/T^0.459 for C. tripunctata . Both equations successfully predicted incubation periods for eggs placed in a stream. The period over which eggs hatched was much longer for C. tripunctata than for S. torrentium at all temperatures.
4. The shorter incubation period (at r>5.6°C) and shorter hatching period for S. torrentium ensure that larvae of this species are already growing when eggs of C. tripunctata start to hatch, but the prolonged hatching period of the latter species ensures a long period of larval recruitment to the population. These differences in egg hatching may reduce competition between the two closely-related species.     

Early warning of egg hatching in pea moth (Cydia nigricana)

Female pea moths (Cydia nigricana) kept at 23 ^oC began to lay eggs 2–3 days after emergence, lived for 16–21 days and laid on average 71 eggs. Individuals kept in field cages lived for slightly longer and laid on average 91 eggs. About 85% of eggs were laid during the first 11 days of the oviposition period, usually in the late afternoon and early evening. The relationship between the rate of egg development and temperature was defined. The estimated developmental zero was 9-4 ^oC at constant temperatures and 8-5 ^oC at fluctuating temperatures. Above 28 ^oC mortality increased and above 31 ^oC development was apparently retarded. Development at constant temperatures took 6–16% longer than at fluctuating temperatures with the same mean. Estimates of hatching dates in the field made from temperature data recorded at several sites in and near a pea crop, and 8 km distant, were usually within a day of the observed date. In warm weather, estimated and observed dates usually coincided; in cooler weather hatching was 2–3 days later than expected. Hatching dates predicted from temperature data after only 80% of development had occurred were correct on 28 out of 36 occasions. An example is given to show how the method could be used eventually with a sex attractant trapping system to provide early warning of first hatching and spraying dates.     

Effects of embryonic responses to clutch mates on egg hatching patterns of Pentatomidae (Heteroptera)

Stink bugs and shield bugs of the family Pentatomidae (Heteroptera) generally produce a clutch of densely deposited eggs. In a few species of this family, embryos hatch in response to some form of cues associated with the preceding hatching to synchronize egg hatching with clutch mates. The aim of the present study is to obtain a family‐wide understanding of the extent to which the hatching response to clutch mates accelerates hatching within egg clutches. Accordingly, the hatching patterns in intact egg clutches and eggs individually detached from egg clutches are compared in eight species among different genera. In Halyomorpha halys, hatching is significantly and highly synchronized by the effect of the hatching response: when eggs are not attached to each other, the hatching rate is only 3.8% at 15 min and exceeds 95% at 200 min. By contrast, when eggs are attached to each other, the hatching rate reaches more than 95% at 15 min. Hatching is also significantly synchronized by the hatching response in Nezara viridula (which shows relatively high hatching synchronization) and in Piezodorus hybneri and Plautia stali (both of which show milder hatching synchronization). Synchronization of hatching is not found to be promoted by a hatching response in Aelia fieberi, Dolycoris baccarum, Eurydema rugosum or Palomena angulosa. These findings reveal that the hatching response varies depending on the species in Pentatomidae, with a wide spectrum of effects on the hatching patterns of the egg clutches.     

Assessment of egg quality and realised fecundity of whiting Merlangius merlangus L. in captivity

Potential predictors of egg quality were assessed in whiting Merlangius merlangus L. permitted to spawn in a tank from which eggs were collected. These included fertilisation rate, the proportion of viable buoyant eggs, egg diameter, and egg wet and dry weights; all were influenced by temporal effects and were negatively correlated with days from start of spawning. The spawning period was protracted, from February to June. Mean daily egg production per female was 2.74 ± 2.43 g and 2338 ± 2075 eggs, equivalent to 14.6 ± 13.1 g kg^?1 day^?1 female^?1. Egg diameter was 1.21 ± 0.04 mm, egg wet weight 1.20 ± 0.21 mg, dry weight 0.10 ± 0.02 mg, and mean fertilisation rate and hatching rates were 76.8 and 73.3%, respectively. The incubation period ranged from 72 to 80 degree days and was dependent on temperature (x) and described by the equation y = 25.92 e^?0.1219x. Realised fecundity was also assessed to determine if this gave a more accurate measure of reproductive potential, and this was compared with potential fecundity estimated from predictive regressions on fish length from fisheries data. Realised egg production of 20 females of 185 g mean weight and 256 mm fork length was 4 444 360 (95% CL 4 093 961–4 743 018), similar to predicted seasonal egg production based on gravimetric fecundity measurements of wild caught fish.