Oviposition and development of the immature stages of Tomicus minor (Coleoptera, Scolytidae)

1 This paper describes the construction process of the brood gallery of Tomicus minor and its total length as well as the length of each arm, the fertile part where the female lays her eggs and also, the infertile part. >2 The presence of the parents during the process and their position in the brood gallery (arms or mating chamber) is studied and how it influences the number of eggs laid. Both the first brood galleries and those burrowed by the repenetrating females were observed. 3 The development and duration of the immature stages of the insect in the 3-year study period, from laying to the emergence of the young beetles from the F₁ generation, were also studied.     

The mating and reproductive biology of the freshwater planktonic calanoid copepod Eudiaptomus gracilis

1. Quantitative aspects of the mating and reproductive biology of the freshwater planktonic calanoid copepod Eudiaptomus gracilis, including duration and frequency of mating, duration of various phases of the oviducal cycle, egg production rate and adult longevity were studied under laboratory conditions. One set of copepods was fed the alga Chlamydomonas reinhardtii whose density was adjusted to 2 × 10⁵ cells mL^?1 (about 10 mg C L^?1), another set was fed a mixed diet consisting of natural plankton (copepod nauplii, small rotifers and large algae) in the size range of 50–150 μm (dry mass approximately 90 mg L^?1). 2. The entire mating process, from the grasping of the female by the male’s right geniculate antennule to the separation of the pair, lasted about 2 min. Spermatophore placement started at about 30 s to 1 min after mating began and took approximately 1 min. Immediately after the spermatophore had been fixed in the female’s genital segment, the pair separated. 3. The total oviducal cycle, including the gravid phase where the female carried ripe oocytes and the non‐gravid phase where the female did not carry ripe oocytes, lasted about 5–6 days. The non‐gravid phase was particularly long; it was longer than the gravid phase and constituted 62–72% of the total cycle. 4. Mating and spermatophore placement usually occurred with gravid females although occasionally (in 30 of 200 observations) spermatophores were attached in the genital segment of non‐gravid females. Generally two to four, but up to seven, spermatophores were observed at a female’s genital segment at the same time. 5. Clutch size, rate of egg production and adult longevity depended on food. When fed on C. reinhardtii, females carried 7–8 eggs clutch^?1, produced a mean of 1.3 clutches and lived 14 days on average. When fed natural mixed food, females carried 10 eggs clutch^?1, produced 5.6 clutches and lived 37 days on average. 6. Removal of males after the first clutch resulted in no further egg production. Re‐mating is necessary in E. gracilis for continuous clutch production and the production of fertile eggs. 7. Mating duration is comparatively short and the non‐gravid phase comparatively long in E. gracilis. This could be an adaption to the life in the pelagic zone of the lake, where fish predators are present. Fish select ovigerous females, pairs in copula and, probably, females with ripe oocytes which make them conspicuous. Thus, a short mating duration and a prolonged period without conspicuous oocytes, can be advantageous.     

The Nesting Behavior of Dawson's Burrowing Bee, Amegilla dawsoni (Hymenoptera: Anthophorini), and the Production of Offspring of Different Sizes

Females of Dawson's burrowing bees have a well-defined brood cell cycle involving cell construction, waxing, provisioning, egg laying, and cell capping. In one study population, nesting bees built smaller brood cells for offspring of lower weight and larger ones for heavier offspring, demonstrating their ability to anticipate the desired size of an offspring at the outset of a brood cell cycle. Furthermore, individual females varied the number of provisioning trips made per brood cell cycle by a factor of two or more, apparently exercising control over the amount of brood provisions supplied to an offspring. The size distribution of emerging males at two widely separated locations in 1997 was nearly identical to that recorded in 1995. These findings suggest that the production of small males (minors) is the result of active female control rather than the product of food shortages that force females to undersupply some brood cells. Female foraging decisions resulted in a bimodal distribution of weights of mature dormant larvae at one site in 1997. However, the times required to complete brood cell cycles at this site were not distributed bimodally. This result stemmed in part from daily variation among females in the duration of their provisioning trips as well as from seasonal variation in provisioning trip times. When provisioning trips lasted longer, females tended to make fewer trips per brood cell cycle, and so were presumably more likely to produce minor sons. As a result, the weight of an offspring was not tightly linked to the time investment required to produce it, making it difficult to compare the relative costs of minors and majors in terms of maternal time investments.     

Biology of <Emphasis Type="Italic">Dermacentor silvarum</Emphasis> (Acari: Ixodidae) under laboratory conditions

The minimum life cycle of Dermacentor silvarum Olenev had a mean duration of 87.5 days (range 74–102 days) under laboratory conditions [(27±1 °C), 70% RH, 6 L: 18 D]. The mean time in (days) for the different stages of its cycle was as follows: incubation period of eggs was 15.3 days; prefeeding, feeding and premoulting periods of larvae and nymphs averaged 5.5, 4.0 and 7.3 days, and 5.2, 5.0 and 14.6 days, respectively; prefeeding, feeding, preoviposition and oviposition periods of female adults lasted for 7.8, 4.5, 4.3 and 14.0 days, respectively. There existed a highly significant correlation between engorged body weight of females and egg masses laid (r = 0.9877, p<0.001). The reproductive efficiency index (REI) and reproductive fitness index (RFI) in females were 11.09 and 9.58, respectively. No relationship between nymphal engorged body weight and resultant sexes was observed. Delayed feeding and non-oviposition (in June and July) existed in females, and low temperature (−10 °C) treatment for 45 days could terminate oviposition diapause. However, the egg masses laid by post-diapause females were significantly smaller than those laid by females engorged in March, April and May.     

Seasonal growth and reproduction in a highly fecund brachyuran crab, Metopograpsus messor (Forskal) (Grapsidae)

The annual cycle of a Metopograpsus population (Muzhupilangad estuary) had three distinct periods: (1) growth-reproduction (January–May), when crabs were involved in moult and reproduction; (2) inactive period (June–July), and (3) reproductive period (August–December). Usually, spawning was immediately followed by another vitellogenic cycle, paralleled by the embryogenesis of prehatch eggs in the brood. Moulting was seemingly an annual event. In the programming of moult and reproduction, the species deviated from the common brachyuran pattern, inasmuch as the postmoult females engaged in active vitellogenesis. The synchrony in the stages of maturation and spawning, and the precision with which the physiological events are programmed, make this highly fecund species an ideal model for an integrated study of the physiology of growth and reproduction.     

Gonad morphology,oocyte development and spawning cycle of the calanoid copepod <Emphasis Type="Italic">Acartia clausi</Emphasis>

Information on gonad morphology and its relation to basic reproductive parameters such as clutch size and spawning frequency is lacking for Acartia clausi, a dominant calanoid copepod of the North Sea. To fill this gap, females of this species were sampled at Helgoland Roads from mid March to late May 2001. Gonad structure and oogenesis were studied using a combination of histology and whole-body-analysis. In addition, clutch size and spawning frequency were determined in incubation experiments, during which individual females were monitored at short intervals for 8 and 12 h, respectively. The histological analysis revealed that the ovary of A. clausi is w-shaped with two distinct tips pointing posteriorly. It is slightly different from that of other Acartia species and of other copepod taxa. From the ovary, two anterior diverticula extend into the head region, and two posterior diverticula extend to the genital opening in the abdomen. Developing oocytes change in shape and size, and in the appearance of the nucleus and the ooplasm. Based on these morphological characteristics, different oocyte development stages (OS) were identified. Mitotically dividing oogonia and young oocytes (OS 0) were restricted to the ovary, whereas vitellogenic oocytes (OS 1–4) were present in the diverticula. The development stage of the oocytes increased with distance to the ovary in both, anterior and posterior diverticula. Most advanced oocytes were situated ventrally, and their number varied between 1 and 18, at a median of 4. All oocyte development stages co-occur indicating that oogenesis in A. clausi is a continuous process. These morphological features reflect the reproductive traits of this species. In accordance with the low numbers of mature oocytes in the gonads, females usually produced small clutches of one to five eggs. Clutches were released throughout the entire observation period at intervals of 90 min (median) resulting in mean egg production rates of 18–28 eggs female⁻¹ day⁻¹.     

Oviposition behavior and progeny allocation of the polyembryonic waspCopidosoma floridanum (Hymenoptera: Encyrtidae)

Oviposition behavior was used to determine the primary clutch size and sex ratio of the polyembryonic wasp Copidosoma floridanumAshmead (Hymenoptera: Encyrtidae) parasitizing Pseudoplusia includens(Walker) (Lepidoptera: Noctuidae). The laying of a female egg was associated with a pause in abdominal contractions during oviposition, while the laying of a male egg was associated with uninterrupted abdominal contractions. Although unmated females produced only male broods, they also displayed male and female egg oviposition movements. Wasps always laid a primary clutch of one or two eggs. For mated females if only one egg was laid, the emerging secondary clutch was all male or female, but if two eggs were laid a mixed brood of males and females was almost always produced. The secondary clutch of single sex broods was usually between 1000 and 1200 individuals, but the secondary clutch of mixed broods averaged 1143 females and 49 males. Thus, the primary sex ratio for mixed broods was 0.5 (frequency males), but the secondary sex ratio was 0.042. Manipulation of the sequence of male and female egg oviposition or of the primary clutch did not produce major alterations in the secondary clutch size or sex ratio.     

Change in offspring sex ratio over a very short season in Lincoln's Sparrows: the potential role of bill development

ABSTRACT The sex ratios of offspring are targets of natural selection that can affect parental energy expenditure and fitness, adult sex ratios, and population dynamics. Parents may manipulate offspring sex ratios based on sex differences in their offsprings' potential for reproductive success. In Lincoln's Sparrows (Melospiza lincolnii), male bill shape is associated with the quality of songs, and song quality predicts female preferences in a reproductive context. Males and females that hatch later relative to brood mates or later in the breeding season tend to develop bill shapes that are, for males, associated with low‐quality song. Because females do not sing and do not experience this selection pressure, we predicted that the sex of offspring produced late relative to their brood mates or relative to the season should be biased toward females. Using a molecular technique to sex nestlings, we found no effects of hatching order or any interaction between date of clutch initiation (season) and hatching order on offspring sex. However, we found a seasonal decline in the proportion of male offspring, from approximately 0.8 at the beginning to 0.4 at the end of a clutch initiation season only 19 d in duration. To our knowledge, this is the shortest period over which the offspring sex ratio has been shown to change in a bird population. Moreover, these findings are consistent with the hypothesis that sex differences in the potential attractiveness of offspring ultimately influence offspring sex ratios.     

Consequences of chronic infections with three different avian malaria lineages on reproductive performance of Lesser Kestrels (Falco naumanni)

We studied the consequences of chronic infections by three different lineages of avian malaria, two Plasmodium (RTSR1, LK6) and one Haemoproteus (LK2), on reproductive performance of Lesser Kestrels (Falco naumanni). Malaria infections in male and female parents had no effect on clutch size, hatching success or nesting success. However, when only successful nests were considered, we found that males parasitized by LK6 raised a lower number of fledglings, suggesting that the level of parental effort by males may be limited by this particular lineage of Plasmodium. This effect was not evident in females, probably due to the higher investment of males during the chick rearing period in this species. Overall, we have found that chronic stages of specific malaria lineages have certain negative consequences on host reproductive performance, highlighting the importance of considering genetic differences among malaria parasites to study their consequences on natural bird populations.     

Observations on the female reproductive cycles of captive Asian yellow pond turtles (Mauremys mutica) with radiography and ultrasonography

The annual reproductive cycle of 27 female Mauremys mutica was observed by radiography and ultrasonography from April 2006 to August 2007. Radiography was used to monitor clutch size and ultrasonography was used to monitor changes in the ovarian follicles. The follicles started to enlarge in September and became preovulatory in January. The mean maximum follicle diameter of ovulation was 18.30±1.44 mm, and ovulation occurred from March through August. Eggs were laid between April and August. Turtles entered latent period in early August and the maximum follicular size was at a low of 13.22±2.36 mm in late September. The vitellogenesis of the next reproductive cycle began in October. The 24 adult females laid 56 clutches containing a total of 227 eggs. Average clutch size was 4.05 eggs (range 1–8) and there were 2.33 clutches (range 1–4) per female. Egg shell images were first observed on the sixth or seventh day after ovulation. The oviductal period averaged 6.9 weeks (range 2–16 weeks) on the first clutch, 3.4 weeks (range 2–8 weeks) on the second, and 2.75 weeks (range 2–6 weeks) for the third. Radiography and ultrasonography are non‐invasive and convenient methods to evaluate the reproductive cycle of female M. mutica. They should be applicable to other turtles and should greatly enhance knowledge of reproductive physiology. Zoo Biol 29:50–58, 2010. © 2009 Wiley‐Liss, Inc.