Sampling Strategies and Life History of Non-Insectan Freshwater Invertebrates

1979 ◽  
Vol 36 (3) ◽  
pp. 311-318 ◽  
Author(s):  
D. F. Malley ◽  
J. B. Reynolds

Life history of benthic freshwater invertebrates, excluding insects, may influence a number of features of sampling programs, such as the environment sampled, sampling technique or equipment used, frequency and timing of sampling, and mesh sizes of nets or sieves. Consideration of the life history should increase the effectiveness of the program and, in the extreme, may allow one to recognize artifacts that would otherwise lead to incorrect conclusions.Aspects of life history that influence sampling programs are (1) direct or indirect embryonic development and the extent to which young are sampled simultaneously with adults during the breeding season, (2) times of year when various developmental stages are present, (3) differences in size between various life stages necessitating use of more than one sampling method during the year, (4) change in habitat due to migrations or assumption of a pelagic, parasitic, or aerial existence for part of the life cycle, (5) change in mobility over the life cycle, (6) sex differences in size or behavior, and (7) adaptations to adverse conditions. Examples of ways in which life history affects sampling are based on the literature and on original data on the opposum shrimp, Mysis relicta, and the crayfish, Orconectes virilis.We recommend that quantitative studies of benthic invertebrate communities be started with a pilot study employing at least two complementary sampling techniques and sufficiently frequent sampling times to allow the development of a reliable strategy for the objective. Key words: life history, sampling, benthic invertebrates, Crustacea, Mysis relicta, Orconectes virilis

1985 ◽  
Vol 6 (2) ◽  
pp. 193-197 ◽  
Author(s):  
T. O. Ezulike ◽  
J. A. Odebiyi

AbstractThe life history of Amblyseius fustis (Pritchard and Baker) was studied in the laboratory at a fluctuating temperature and relative humidity ranging from 24.4 to 28.0°C and 55.5 to 75.6%, respectively. The developmental stages consist of egg, larva, protonymph, deutonymph and adult. The life cycle, from egg to adult of both male and female was about 8 days, while longevity was about 19.2 days. Mated female laid an average of 18.8 eggs. There was no significant difference in the longevity and fecundity of predators fed on different life stages of the host. The proportion of male to female in the progeny of mated females was 1:4.A. fustis has a shorter developmental period and lives longer than its prey, but the latter is more fecund (26.9 eggs/♀) and has a higher proportion of females in its progeny (1:4.8). The shorter developmental period and the longer life span of the predator are likely to offset the higher fecundity of the prey.


1974 ◽  
Vol 106 (8) ◽  
pp. 785-800 ◽  
Author(s):  
G. S. Olton ◽  
E. F. Legner

AbstractThe synonymy, distribution, host range, and life history of the gregarious larval–pupal parasitoid Tachinaephagus zealandicus Ashmead, is discussed. Laboratory studies of its biology were conducted at 25° ± 2 °C using Musca domestica L. as host. Its developmental stages are described. Under laboratory conditions its life cycle lasted 23–27 days. Parasitoid development accelerated with higher average densities per host. Single standardized hosts produced 3–18 adult parasitoids. Mated females provided with hosts lived 50.4–67.2 h. The average length of the reproductive period and number of hosts parasitized were independent of host density; however, the average number of eggs deposited per host increased at lower host densities. Adult emergence displayed circadian rhythmicity independent of photoperiod over 3+ days.


Author(s):  
J. B. Brown-Gilpin

The wide variety of reproductive patterns and behaviour in the many species of Nereidae already studied clearly justifies further research. But the life history of Nereis fucata (Savigny) is not only of interest from the comparative point of view. Its commensal habit (it occurs within shells occupied by hermit crabs) immediately gives it a special importance. This alone warrants a detailed study, particularly as no commensal polychaete has yet been reared through to metamorphosis and settlement on its host (Davenport, 1955; Davenport & Hickok, 1957). The numerous interesting problems which arise, and the experimental methods needed to study them, are, however, beyond the range of a paper on nereid development. It is therefore proposed to confine the present account to the reproduction and development up to the time when the larvae settle on the bottom. The complete life cycle, the mechanism of host-adoption, and related topics, will be reported in later papers.


1953 ◽  
Vol 31 (4) ◽  
pp. 351-373 ◽  
Author(s):  
Liang-Yu Wu

A cause of swimmer's itch in the lower Ottawa River is Trichobilharzia cameroni sp. nov. Its life cycle has been completed experimentally in laboratory-bred snails and in canaries and ducks, and the various stages are described. The eggs are spindle-shaped. The sporocysts are colorless and tubular. Mother sporocysts become mature in about a week. The younger daughter sporocyst is provided with spines on the anterior end and becomes mature in about three weeks. The development in the snail requires from 28 to 35 days. A few cercariae were found to live for up to 14 days at 50 °C., although their life at 16° to 18 °C. was about four days. Cercariae kept at room temperature for 60 to 72 hr. were found infective. The adults become mature in canaries and pass eggs in about 12 to 14 days. Physa gyrina is the species of snail naturally infected. It was found in one case giving off cercariae for five months after being kept in the laboratory. Domestic ducks were found to become infected until they were at least four months old, with the parasites developing to maturity in due course; no experiments were made with older ducks. Furthermore, miracidia were still recovered from the faeces four months after the duck had been experimentally infected, and it is suggested that migratory birds are the source of the local infection.


2013 ◽  
Vol 88 (2) ◽  
pp. 230-236 ◽  
Author(s):  
R. Brinesh ◽  
K.P. Janardanan

AbstractThe life-cycle stages of Pleurogenoides malampuzhensis sp. nov. infecting the Indian bullfrog Hoplobatrachus tigerinus (Daudin) and the skipper frog Euphlyctiscyanophlyctis (Schneider) occurring in irrigation canals and paddy fields in Malampuzha, which forms part of the district of Palakkad, Kerala, are described. The species is described, its systematic position discussed and compared with the related species, P. gastroporus (Luhe, 1901) and P. orientalis (Srivastava, 1934). The life-cycle stages, from cercaria to egg-producing adult, were successfully established in the laboratory. Virgulate xiphidiocercariae emerged from the snail Digoniostoma pulchella (Benson). Metacercariae are found in muscle tissues of dragonfly nymphs and become infective to the frogs within 22 days. The pre-patent period is 20 days. Growth and development of both metacercariae and adults are described.


1975 ◽  
Vol 53 (7) ◽  
pp. 942-952 ◽  
Author(s):  
T. Amaratunga ◽  
S. Corey

A 17-month field study showed that Mysis stenolepis in Passamaquoddy Bay, New Brunswick lives for about 1 year. Young are released in shallow water early in spring and grow rapidly during the summer. In the fall, young adults migrate to deeper water where they reach sexual maturity. Transfer of sperm lakes place during winter in deeper regions of the Bay. soon after which the males die. Females survive and in spring migrate to shallow waters to release young after which they die. Females breed once and carry an average of 157 young per brood. Developmental stages of the postmarsupial young are described and discussed.


During a short stay at Plymouth, in 1889, I was engaged in studying certain points in the anatomy of Cirripedia; finding, however, that a knowledge of the embryology was necessary in order to arrive at a complete understanding of the adult structure, I became wishful to investigate the life-history of some one member of the group. This I had an opportunity of doing at Naples, where I was appointed to occupy the Cambridge University Table at the Zoological Station for a period of six months, subsequently increased to nine. I here succeeded in obtaining a practically complete series of stages of Balanus perforatus , Bruguiere, as well as many stages in other members of the group. Though a number of able observers have occupied themselves with the embryology of Cirripedes, yet, owing to lack of opportunity, and to the difficulty of obtaining complete series of developmental stages, as well' as to the inherent difficulties in the subject, much remained to be done in this line. Willemoes-Suhm alone, with the advantages afforded by his position during the Challenger Expedition, has hitherto obtained a complete series of stages of any one form, but he failed to trace the history of the earlier stages, and in the later, limited himself to the appearance of fresh and spirit specimens, as seen without cutting sections. In fact the method of sections has been little applied to the development of Cirripedes, and not at all to the earlier stages. There is, therefore, little apology needed for an account embracing the results obtained by the employment of some of the more modern methods of embryological study.


1952 ◽  
Vol 84 (10) ◽  
pp. 316-321 ◽  
Author(s):  
R. W. Stark

General.—The purpose of this paper is to analyse a sampling method devised to assess larval populations in an outbreak of the lodgepole needle miner, Recurvaria milleri Busck (Busck 1914, Hopping 1945).The problem of developing an adequate sampling method is intimately concerned with the life-history of the insect, the region of the outbreak and the nature of the forest stand in which the outbreak occurs. In sampling most defoliator populations the problem is made more difficult by external feeding and wandering habits, hence it is usually done in some relatively inactive stage at a fixed time. de Gryse (1934) describes the problems inherent in sampling these insects. The needle miner, however, is fixed in its location for most of its life-cycle and is therefore readily obtainable for study. The problem here is reduced to a statistical one, that of obtaining an acceptable sample i.e. within suitable error limits with due regard for existing variables.


1957 ◽  
Vol 35 (6) ◽  
pp. 641-689 ◽  
Author(s):  
Gordon K. Sweatman

Chorioptic mange mites have been reared in vitro on epidermal debris. The life history of the mite has been observed, and each stage in the cycle described. Mites from the cow, horse, goat, sheep, and llama have been shown to be identical biologically and morphologically, and the specific names of equi, caprae, and ovis have been synonymized with C. bovis. The in vitro life cycle has been completed on epidermal debris from a variety of wild Cervidae, Bovidae, and Equidae, as well as on material from several breeds of domestic cattle, horses, sheep, and goats. From these and other data, three additional species or subspecies of Chorioptes were synonymized also with C. bovis. Only one other species, namely C. texanus, remains in the genus.


1972 ◽  
Vol 50 (2) ◽  
pp. 201-204 ◽  
Author(s):  
Doris N. Jensen

The life cycle of the brachylaemid trematode Scaphiostomum pancreaticum McIntosh, 1934, was completed experimentally in the laboratory. Eggs were obtained from trematodes removed from naturally infected Tamias striatus. Eggs are mature when laid and hatch naturally only after ingestion by a snail. In vitro hatching and subsequent examination of the miracidium was accomplished in snail gastric juice. Sporocysts developed in Anguispira alternata and cercarial emergence began 129 days after infection. Metacercariae developed in the kidney of A. alternata, Triodopsis albolabris, and Haplotrema concavum and were infective to the chipmunk after 5 months, and ovigerous adults were obtained in 30 days. This is the first description of the life cycle of a member of this genus.


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