What can parasites do? According to Kathleen McAuliffe’s book This is Your Brain on Parasites, they can affect human thinking and behavior, and thus change us into obedient machines.
The effects of application of an artificial honeydew mixture of glucose, fructose and trehalose (GFT), honey and Bemisia tabaci nymph-extract as kairomonal sources in enhancing the foraging efficiency and performance of Eretmocerus sp. near furuhashii on cucumber plants were studied. Experiments were conducted in small greenhouses (4×3×3 m) using life table methods. Life table data indicated that the total mortality in B. tabaci immature cohorts in all treatments was in the order of fourth instar > first instar > second = third > egg > pupa cohorts. The tested kairomonal materials had a significant effect on the rate of parasitism (p > 0.0415) with 13.23, 9.04 and 10.54% higher than that of control in artificial honeydew of GFT, nymph-extract and honey treatments, respectively. B. tabaci egg/adult survival ratio was also significantly affected (p > 0.0001) by the tested kairomonal sources being lowest (22.91%) in nymph-extract treatment. Moreover, the tested kairomonal materials arrested significantly more parasitoids to colonize the treated plants comparing to control. Apparently, the tested materials were significantly effective in attracting the parasitoids up to 3 days after applications then significant difference was not found between treatments.
Over half of all organisms living on Earth today are parasites, and there are hardly any species which are free from them. How can the “wild immunology” approach help us understand them better?
The highest infestation by phoronts (resting stages) of Apostoma ciliates forms 1, 2, is restricted to the 3-th and 4-th pairs of E. superba thoracic limbs. They occur mostly on meropodites of endopodite and plumose setae of exopodite. The trophonts (trophic stage) of those Apostoma are present in large numbers in krill's tissue. The life cycle of those histophagous Apostoma include also free-living stage - tomit. Swarm formed by krill seems to be a reason for the common and extensive infestation by protozoans.
Parasitic isopods (Aega antarclica and Gnathia calva) were discovered on fishes collected during Polish expeditions to the Atlantic sector of the Southern Ocean. Pranizae of G.calva infected 14.5% of Nololhenia corriceps neglecta and 16% of Notothenia rossi marmorata. The infestation rates are probably underestimated.
In total, 8511 amphipods of 12 species caught in Admiralty Bay were examined for the presence of acanthocephalans using them as intermediate hosts. Only 27 specimens of eight species were infected (total prevalence 0.32%). Acanthellae and cystacanths of four species using fishes as either definitive or paratenic hosts were found. Normally, single parasites occurred; in one case two acanthocephalans were present in one specimen of Bovallia gigantea. This host species was the most strongly infected, with the prevalence 3.41%. Six other amphipod species were infected with the prevalence 0.08-0.66%. One of two Jassa ingens examined was also infected. Over 50% of acanthocephalans belonged to one echinorhynchid species maturing in fishes, Aspersentis megarhynchus, which occurred in five host species of four amphipod families, B. gigantea, Gondogeneia antarctica, J. ingens, Hippomedon kergueleni and Orchomenella rotundi-frons. Two polymorphid species maturing in seals, Corynosoma hamanni and C. pseudohamanni, were found in a single host species each, Prostebbingia brevicornis and Cheirimedon femoratus, respectively. Three parasite species mentioned occurred exclusively in sublittoral host species, at the depth 0-30 m. The third polymorphid species, C. bullosum, was the only species occurring in the amphipod, Waldeckia obesa, living in the deeper water (infected specimen was caught at the depth 60 m), but was found also in B. gigantea. Differences between infections of Amphipoda and fishes with echinorhynchids and polymorphids are discussed.
The two bathydraconid species, Gymnodraco acuticeps and Cygnodraco mawsoni, caught in the Ross Sea (Antarctic summer 2002) were examined for internal parasites. All specimens (four G. acuticeps and one C. mawsoni) were infected. G. acuticeps harboured larval Cestoda (bilocular tetraphyllidean cercoids, diphyllobothriid plerocercoids) and Nematoda (Contracaecum spp.), acanthocephalan cystacanths and adult helminths (three species of Digenea and one species of Nematoda). Two specimens of C. mawsoni (including data from one additional specimen examined earlier) were infected by larval Cestoda (bilocular cercoid) and Nematoda (Contracaecum spp.) and adult helminths (three species of Digenea and one species of Nematoda). The present data are compared and discussed with the relevant literature data.
Trematomus newnesi (Nototheniidae), a bentho-pelagic fish, caught off Adélie Land (eastern Antarctic) was examined for the presence of internal parasitic worms. These fishes were infected with 11 species and larval forms of parasites: Digenea (Macvicaria pennelli, Neolebouria terranovaensis, Genolinea bowersi, and Elytrophalloides oatesi), larval Cestoda (two forms of tetraphyllidean metacestodes, bilocular form and trilocular form, and diphyllobothriid plerocercoids), Acanthocephala (Metacanthocephalus campbelli, M. johnstoni) and larval Nematoda (Contracaecum osculatum, C. radiatum). Larval cestodes were the dominant parasites, whereas acanthocephalans were relatively rare. Five species and larval forms were recorded also in fish caught in the Davis Sea. A check list of parasites of T. newnesi recorded in the eastern- and western Antarctic comprises 21 species and larval forms. Probably, T. newnesi plays an important role in life cycles of parasitic worms in the Antarctic.
In total, 18 species and larval forms of endoparasitic worms were found in 19 newly examined notothenioid fishes of three species, Trematomus hansom, Notothenia coriiceps and Chionodraco hamatus, caught off Adelie Land. One digenean species, Neolepidapedon trema-tomi, was recorded in this area for the first time. A total list of endoparasitic worms prepared by Zdzitowiecki etal. (1998) increased from 20 to 21 species and larval forms and concerns 11 determined and one determined species of Digenea (the most diverse group), three larval forms of Cestoda, three species (one identified only to genus) of Acanthocephala, two species (one in the larval stage) and one larval form of Nematoda. All these species and forms, with the exception of the indetcrmined digenean, occur also in the deep Antarctica, in the Ross Sea and/or in the Weddell Sea. The prevalence and relative density of infection with each parasite in three host species is given based on summarized previous and new data.
The infections of four fish species, Trematomus newnesi, T. bernacchii, Lindbergichthys nudifrons and Harpagifer antarcticus with parasitic worms, in the coastal zone off the Vernadsky Station (Argentine Islands, West Antarctica) are described. Data on infections are compared with previous results from Admiralty Bay at the South Shetland Islands. Indices of infection are for each host-parasite relationship. In total, 16 taxa of parasites were recorded: 6 digeneans, 3 larval cestodes, 4 (adult and cystacanth) acanthocephalans, and 3 (adult and larval) nematodes. Fifteen of them have been previously recorded in Notothenia coriiceps from this area. Hence, the number of parasitic taxa recorded in this region increased from 21 to 22. Either the digenean Macvicaria georgiana or acanthocephalan Corynosoma pseudohamanni were dominants in different hosts. Trematomus bernacchii was the most strongly infected, especially with M. georgiana (prevalence 100%, mean abundance 113.7). The infection parameters of the majority of parasites were lower at the Vernadsky Station than in the Admiralty Bay, especially for host-parasite relations with larval cestodes and nematodes. The presently reported study have confirmed that the southern range of distribution of two acanthocephalans, Aspersentis megarhynchus and Corynosoma hamanni extends south to the area near the Argentine Islands.
For the last few decades there have been reports not only of the occurrence of new invasive species of European water-courses, but also their increasing expansion. One of such species is the Amur sleeper (Perccottus glenii). The present work contains assessment of age and length distribution, condition as well as growth rate and analysis of the parasite fauna of theAmur sleeper from the waters of the Vistula River tributary in its middle course (the Habdziński Canal). During the catch performed in 2017 and 2019, the total of 177 Amur sleepers were recorded in the studied watercourse and a statistically significant sex structure disproportion was observed. Among the specimens caught in 2017 dominant were fishes with lengths of 50.1–60.1 mm whereas in 2019 the majority of the Amur sleeper specimens measured 30.1–50.0 mm.Six age groups were recorded among the caught fish with a clear prevalence of specimens aged 1+ (70.06%). The most frequently recorded parasite of P. glenii was non-quantifiable Trichodina rostrata ciliate for which the Amur sleeper from the Polish waters appeared to be a new host. Moreover, the presence of an acanthocephalan Acanthocephalus lucii, not recorded in Poland in this host before, was observed in the chyme. Also, accidental presence of larvae of the Opisthioglyphe ranae tre-madote, which is a parasite typical of amphibians, was also recorded. Despite unfavourable habitat conditions and in-creased volumes of biogenic substances in the waters of the Habdziński Canal, the Amur sleeper found convenient condi-tions to reside in this small watercourse.
A new attack against the Kirchhoff-Law-Johnson-Noise (KLJN) secure key distribution system is studied with unknown parasitic DC-voltage sources at both Alice’s and Bob’s ends. This paper is the generalization of our earlier investigation with a single-end parasitic source. Under the assumption that Eve does not know the values of the parasitic sources, a new attack, utilizing the current generated by the parasitic dc-voltage sources, is introduced. The attack is mathematically analyzed and demonstrated by computer simulations. Simple defense methods against the attack are shown. The earlier defense method based solely on the comparison of current/voltage data at Alice’s and Bob’s terminals is useless here since the wire currents and voltages are equal at both ends. However, the more expensive version of the earlier defense method, which is based on in-situ system simulation and comparison with measurements, works efficiently.