scholarly journals The life histories and population dynamics of monogenean gill parasites of Trachurus trachurus (L.)

Author(s):  
J. Llewellyn

Gastrocotyle trachuri and Pseudaxine trachuri infect young Trachurus trachurus at Plymouth as soon as the 3- or 4-month-old adolescent fishes descend to the sea bottom in October. The parasites normally mature in 3 or 4 months, but, exceptionally, in about 1 month, and the life-span is normally no longer than 1 year. Trachurus specimens at the beginning of their second year pick up a largely new infection of parasites.G. trachuri and P. trachuri are much less frequent on 2- and 3-year-old specimens of Trachurus and probably occur only very rarely on still older fishes, the limiting factor being not an age-immunity but a post-spawning migration of the host from the concentration of free-living infective stages of the parasites in coastal waters.The parasites have adapted themselves to a seasonal change in the feeding habits of Trachurus by ceasing to produce larvae in anticipation of the summer disappearance of scad from the sea bottom in pursuit of pelagic food-organisms.

1986 ◽  
Vol 64 (7) ◽  
pp. 1375-1384 ◽  
Author(s):  
Martin L. Adamson

A hypothetical phylogeny of life-history patterns in zooparasitic nematodes is presented. It is suggested that the course of evolution of life histories has been strongly influenced by conditions under which parasitism arose; two factors appear particularly important, namely the primitive mode of transmission and the feeding habits of the ancestral populations. Two transmission modes were available at the outset: active penetration (usually cutaneous) and passive oral contamination. Only groups that arose using the former mode developed tissue parasitism and heteroxeneity. With percutaneous transmission, nematodes were forced to respond and adapt to the tissue environment from the beginnings of parasitism, and the penetrating habit probably facilitated experimentation with intermediate hosts. The Enoplida and Tylenchia arose from stylet-bearing predaceous or plant-parasitic fluid feeders adapted to feed on tissues. Cutaneous penetration was probably the primitive transmission mode and these groups were tissue dwelling at the outset. Zooparasitic Rhabditia and Diplogasteria are derived from free-living particulate feeders and the earliest parasitic forms probably fed on the intestinal microflora of the host; tissue parasitism arose secondarily and only in lineages that primitively used penetrative transmission.


Paleobiology ◽  
1988 ◽  
Vol 14 (3) ◽  
pp. 272-286 ◽  
Author(s):  
Takashi Okamoto

Nipponites, a Late Cretaceous nostoceratid ammonite, shows a peculiar meandering shell growth in the middle-late stage. Assuming neutral buoyancy, and a constant aperture angle relative to the sea bottom, meandering growth of this ammonite was modeled by computer simulation. In this model, the meandering shell growth is controlled by regulation of life orientation. The remarkable similarity in the coiling modes and rib obliquity patterns between the computer-simulated and actual specimens strongly suggests a free living mode of life in Nipponites with an approximately neutral buoyancy. The simulation also suggests that morphological saltation from a simple helicoid form like Eubostrychoceras japonicum to a meandering shell form like Nipponites occurred abruptly without any intermediate form by minor change of the upper and lower limits of growth direction.


2008 ◽  
Vol 41 (1) ◽  
pp. 32-38 ◽  
Author(s):  
Sung-Hoi Huh ◽  
Ki-Mun Nam ◽  
Hyun-Gi Choo ◽  
Gun-Wook Baeck

2016 ◽  
Vol 49 (5) ◽  
pp. 635-641
Author(s):  
Jae-Mook Jeong ◽  
Kang-Seok Hwang ◽  
Se-hyun Song ◽  
Hee-yong Kim ◽  
Jeong-Ho Park ◽  
...  

Zoosymposia ◽  
2021 ◽  
Vol 20 ◽  
Author(s):  
LIANA JOHANN ◽  
GUILHERME LIBERATO DA SILVA

The family Tydeidae consists of small, free-living, soft-bodied mites with a diversity of feeding habits, including phytophages, pollen feeders and even predators, but the majority are scavengers or fungivores. Approximately 330 species in 30 genera have been described from throughout the world, but only a few species (<1% of all species) have been studied for their life history. This review provides a survey of their life history with a focus on their lifespan.


2021 ◽  
pp. 185-215
Author(s):  
Nabil Majdi ◽  
Tom Moens ◽  
Walter Traunspurger

Abstract This chapter provides overview of the feeding habits and food sources of aquatic nematodes. The environmental constraints on feeding, food recognition, and feeding selectivity are also addressed, together with the complex, indirect trophic interactions between nematodes and their microbial prey. To raise awareness of the inherent methodological and/or interpretational problems in studies of nematode feeding ecology, the chapter ends with a brief look at the methods that have been adapted to quantify feeding rates in nematodes.


1991 ◽  
Vol 48 (3) ◽  
pp. 363-371 ◽  
Author(s):  
T. Haug ◽  
A. B. Kroyer ◽  
K. T. Nilssen ◽  
K. I. Ugland ◽  
P. E. Aspholm

2015 ◽  
Vol 66 (8) ◽  
pp. 701 ◽  
Author(s):  
Siew Wen Lee ◽  
Choon Weng Lee ◽  
Chui Wei Bong ◽  
Kumaran Narayanan ◽  
Edmund Ui-Hang Sim

We investigated the dynamics of attached and free-living bacterial abundance over a period of 18 months in tropical coastal waters of Malaysia. We measured the abundance at both oligotrophic coastal water (Port Dickson) and eutrophic estuary (Klang), and hypothesised that attached bacteria are predominant in eutrophic waters. We found that bacterial abundance was higher at Klang than Port Dickson (Student’s t-test: t=4.87, d.f.=19, P<0.001). Attached bacteria also formed a large fraction of the total bacteria at Klang (75% ±13s.d.) relative to Port Dickson (56% ±22), and showed preference for chlorophyll-a-based particles rather than total suspended solids. The bacterial community structure was clearly different between the two stations but was similar between the attached and free-living bacterial population. Our results showed the importance of attached bacteria in eutrophic water where they could play a major role in carbon and nutrient cycling.


mBio ◽  
2013 ◽  
Vol 4 (4) ◽  
Author(s):  
Haiwei Luo ◽  
Miklós Csűros ◽  
Austin L. Hughes ◽  
Mary Ann Moran

ABSTRACT Marine bacteria in the Roseobacter and SAR11 lineages successfully exploit the ocean habitat, together accounting for ~40% of bacteria in surface waters, yet have divergent life histories that exemplify patch-adapted versus free-living ecological roles. Here, we use a phylogenetic birth-and-death model to understand how genome content supporting different life history strategies evolved in these related alphaproteobacterial taxa, showing that the streamlined genomes of free-living SAR11 were gradually downsized from a common ancestral genome only slightly larger than the extant members (~2,000 genes), while the larger and variably sized genomes of roseobacters evolved along dynamic pathways from a sizeable common ancestor (~8,000 genes). Genome changes in the SAR11 lineage occurred gradually over ~800 million years, whereas Roseobacter genomes underwent more substantial modifications, including major periods of expansion, over ~260 million years. The timing of the first Roseobacter genome expansion was coincident with the predicted radiation of modern marine eukaryotic phytoplankton of sufficient size to create nutrient-enriched microzones and is consistent with present-day ecological associations between these microbial groups. We suggest that diversification of red-lineage phytoplankton is an important driver of divergent life history strategies among the heterotrophic bacterioplankton taxa that dominate the present-day ocean. IMPORTANCE One-half of global primary production occurs in the oceans, and more than half of this is processed by heterotrophic bacterioplankton through the marine microbial food web. The diversity of life history strategies that characterize different bacterioplankton taxa is an important subject, since the locations and mechanisms whereby bacteria interact with seawater organic matter has effects on microbial growth rates, metabolic pathways, and growth efficiencies, and these in turn affect rates of carbon mineralization to the atmosphere and sequestration into the deep sea. Understanding the evolutionary origins of the ecological strategies that underlie biochemical interactions of bacteria with the ocean system, and which scale up to affect globally important biogeochemical processes, will improve understanding of how microbial diversity is maintained and enable useful predictions about microbial response in the future ocean.


1985 ◽  
Vol 63 (10) ◽  
pp. 2313-2322 ◽  
Author(s):  
Premysl Hamr ◽  
Michael Berrill

The life histories of the crayfish Cambarus robustus and Cambarus bartoni were studied in the Kawartha Lakes region of southern Ontario. There were marked differences in their breeding and molting cycles compared with the familiar pattern of the Orconectes species of this region. Egg extrusion occurred later (July in C. robustus, June in C. bartoni), and juveniles therefore did not become free living until late summer or early fall. With little growing time in their first summer, they measured only 5–10 mm in carapace length (CPL) before growth ceased for the winter. At the end of their second summer the still immature crayfish measured 17–26 mm CPL in C. robustus and 13–20 mm CPL in C. bartoni. Maturity was therefore not attained until the end of the third summer, when most C. robustus matured at 34–45 mm CPL and C. bartoni at 25–30 mm CPL. The majority of individuals apparently reproduced for the first time during their fourth summer; a few apparently survived into another summer, reaching carapace lengths greater than 50 mm in C. robustus and 30 mm in C. bartoni. In males of both species, form 1 and form 2 occur throughout the summer. Although lacking the synchrony of Orconectes species, breeding and molting activities are still confined to the period between April and October. The timing of the life-history events observed in these two Cambarus species may be adaptations to seasonal stresses of the swift water environments that these species inhabit as well as to the relative harshness of the northern temperate climate.


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