Interannual variation in life-cycle characteristics of the veined squid (Loligo forbesi) in Scottish (UK) waters

2005 ◽  
Vol 18 (4) ◽  
pp. 327-340 ◽  
Author(s):  
Graham J. Pierce ◽  
Alain F. Zuur ◽  
Jennifer M. Smith ◽  
M. Begoña Santos ◽  
Nick Bailey ◽  
...  
Author(s):  
N. A. Holme

The distinguishing features of the common squid of British waters, Loligo forbesi, are summarized, and contrasted with those of L. vulgaris. The life-cycle and growth of L. forbesi are described, based on samples from trawl catches off Plymouth. This species seems to be an annual - young squid first appear in the trawl in late May, when their length is about 10 or 11 cm. Subsequent growth is rapid, and the males reach 30 cm and the females 25 cm by November. Spawning takes place mainly in December-January, but may continue into the spring. Neither sex survives beyond a single spawning season. Hatching of the spawn probably takes 30–40 days, and if the young squid taken in the trawl in late May hatched in the early part of the same year, a growth rate of about 25 mm/month would be required. Known growth rates for other species of Loligo are about 20 mm/month, so that indicated for L. forbesi does not seem to be impossibly high. The life-cycle is summarized in Fig. 8. There is also a summer spawning population, which grows to a rather smaller size at maturity, and which also seems to be annual.During the summer L. forbesi ranges throughout the English Channel and southern North Sea, particularly in inshore areas. In October the squid migrate farther offshore and tend to occupy the western part of the Channel.Values for total weight of squid/2 h trawl are given, on a monthly basis, for 1966–9. The largest quantities are usually taken in October and November, the highest single figure being 30.54 kg/2 h trawl, in November 1967.


Author(s):  
A. Kong-Lum ◽  
G.J. Pierce ◽  
C. Yau

The timing of spawning and recruitment in the squid Loligo forbesi in Scottish waters is described on the basis of data from three sources: monthly samples of squid caught by commercial trawls (1986–1988), egg masses found by fishermen (1987–1991), and statistical data on animals caught by research trawls (1978–1987).Spawning females were present in samples from December to June, with peak spawning occurring in March. Most records of egg masses were from these months, but eggs were also found in August and September. These results suggest that there is an extended spawning season.Small squid (≤100 mm dorsal mantle length) were rarely present in commercial samples, but were recorded in research samples almost all year round. Thus there appears to be more or less continuous recruitment into the catchable population.The results of the present study are consistent with published data from other parts of the geographic range in that there is a regular seasonal peak in spawning, and spawning adults disappear from the population in summer. Further interpretation of the life-cycle of this species is not justified on the basis of current knowledge, and more information is needed on migrations, geographical variation, and lifespan in Loligo forbesi.


Author(s):  
C. Lordan ◽  
J. Casey

Records of the squid (Loligo forbesi) egg masses which were incidentally caught in demersal trawls at three offshore sites are presented. These sites were at water depths of 135, 302 and 507 m. This represents the deepest ever record of spawning in a loliginid squid species. There has been speculation in the literature about offshore spawning in L. forbesi but it has not previously been recorded and may have important implications for the life cycle.


Author(s):  
Betty Ruth Jones ◽  
Steve Chi-Tang Pan

INTRODUCTION: Schistosomiasis has been described as “one of the most devastating diseases of mankind, second only to malaria in its deleterious effects on the social and economic development of populations in many warm areas of the world.” The disease is worldwide and is probably spreading faster and becoming more intense than the overall research efforts designed to provide the basis for countering it. Moreover, there are indications that the development of water resources and the demands for increasing cultivation and food in developing countries may prevent adequate control of the disease and thus the number of infections are increasing.Our knowledge of the basic biology of the parasites causing the disease is far from adequate. Such knowledge is essential if we are to develop a rational approach to the effective control of human schistosomiasis. The miracidium is the first infective stage in the complex life cycle of schistosomes. The future of the entire life cycle depends on the capacity and ability of this organism to locate and enter a suitable snail host for further development, Little is known about the nervous system of the miracidium of Schistosoma mansoni and of other trematodes. Studies indicate that miracidia contain a well developed and complex nervous system that may aid the larvae in locating and entering a susceptible snail host (Wilson, 1970; Brooker, 1972; Chernin, 1974; Pan, 1980; Mehlhorn, 1988; and Jones, 1987-1988).


Author(s):  
Randolph W. Taylor ◽  
Henrie Treadwell

The plasma membrane of the Slime Mold, Physarum polycephalum, process unique morphological distinctions at different stages of the life cycle. Investigations of the plasma membrane of P. polycephalum, particularly, the arrangements of the intramembranous particles has provided useful information concerning possible changes occurring in higher organisms. In this report Freeze-fracture-etched techniques were used to investigate 3 hours post-fusion of the macroplasmodia stage of the P. polycephalum plasma membrane.Microplasmodia of Physarum polycephalum (M3C), axenically maintained, were collected in mid-expotential growth phase by centrifugation. Aliquots of microplasmodia were spread in 3 cm circles with a wide mouth pipette onto sterile filter paper which was supported on a wire screen contained in a petri dish. The cells were starved for 2 hrs at 24°C. After starvation, the cells were feed semidefined medium supplemented with hemin and incubated at 24°C. Three hours after incubation, samples were collected randomly from the petri plates, placed in plancettes and frozen with a propane-nitrogen jet freezer.


1994 ◽  
Vol 11 (1) ◽  
pp. 47-56
Author(s):  
Virginia C. Day ◽  
Zachary F. Lansdowne ◽  
Richard A Moynihan ◽  
John A. Vitkevich

1978 ◽  
Vol 23 (2) ◽  
pp. 85-86
Author(s):  
BERTRAM J. COHLER
Keyword(s):  

1978 ◽  
Vol 23 (9) ◽  
pp. 697-697
Author(s):  
ALVIN G. BURSTEIN

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