Quantifying 25 years of disease‐caused declines in Tasmanian devil populations: host density drives spatial pathogen spread

2021 ◽  
Vol 24 (5) ◽  
pp. 958-969
Author(s):  
Calum X. Cunningham ◽  
Sebastien Comte ◽  
Hamish McCallum ◽  
David G. Hamilton ◽  
Rodrigo Hamede ◽  
...  
Keyword(s):  
Host Density ◽  
Tasmanian Devil

scholarly journals Disease and the dynamics of extinction

2012 ◽  
Vol 367 (1604) ◽  
pp. 2828-2839 ◽  
Author(s):  
Hamish McCallum
Keyword(s):  
Infectious Diseases ◽  
Disease Transmission ◽  
Management Strategies ◽  
Host Density ◽  
Habitat Destruction ◽  
Broad Host Range ◽  
Tasmanian Devil ◽  
Management Options ◽  
Reservoir Species ◽  
Devil Facial Tumour Disease

Invading infectious diseases can, in theory, lead to the extinction of host populations, particularly if reservoir species are present or if disease transmission is frequency-dependent. The number of historic or prehistoric extinctions that can unequivocally be attributed to infectious disease is relatively small, but gathering firm evidence in retrospect is extremely difficult. Amphibian chytridiomycosis and Tasmanian devil facial tumour disease (DFTD) are two very different infectious diseases that are currently threatening to cause extinctions in Australia. These provide an unusual opportunity to investigate the processes of disease-induced extinction and possible management strategies. Both diseases are apparently recent in origin. Tasmanian DFTD is entirely host-specific but potentially able to cause extinction because transmission depends weakly, if at all, on host density. Amphibian chytridiomycosis has a broad host range but is highly pathogenic only to some populations of some species. At present, both diseases can only be managed by attempting to isolate individuals or populations from disease. Management options to accelerate the process of evolution of host resistance or tolerance are being investigated in both cases. Anthropogenic changes including movement of diseases and hosts, habitat destruction and fragmentation and climate change are likely to increase emerging disease threats to biodiversity and it is critical to further develop strategies to manage these threats.

Natural parasitism of eggs of yellow stem borer, Scirpophaga incertulas Walker (Lepidoptera: Crambidae) in rice ecosystem at Tiruchirappalli, Tamil Nadu

ENTOMON ◽  
2020 ◽  
Vol 45 (3) ◽  
pp. 181-188
Author(s):  
T. Sharmitha ◽  
C. Gailce Leo Justin ◽  
S. Sheeba Joyce Roseleen ◽  
P. Yasodha
Keyword(s):  
Field Study ◽  
Tamil Nadu ◽  
Host Density ◽  
Stem Borer ◽  
Scirpophaga Incertulas ◽  
Egg Masses ◽  
Yellow Stem Borer ◽  
Rice Ecosystem ◽  
Natural Parasitism

Three species of parasitoids viz., Telenomus dignus Gahan, Trichogramma japonicum, Ishii and Tetrastichus schoenobii Ferriere were recorded from the egg masses of rice yellow stem borer, Scirpophaga incertulas (Walker) in a field study. The extent of parasitism was high during Rabi (43.33 – 93.33 %) and low during Kharif (0 - 40.00 %). Parasitism by T. dignus was maximum in October (50.00 %), T. japonicum, in November (23.08 %) and T. schoenobii in February (55.55 %). dignus and T. schoenobii in combination parasitized maximum number of egg masses (41.82 %). Multiple parasitism by the three species was high in December (8.33 %) and January (7.14%). Parasitic potential was maximum, when T. schoenobii alone parasitised the egg masses followed by T. dignus and T. schoenobii in combination. Host density in the field influenced the extent of parasitism.

scholarly journals No evidence of inbreeding depression in a Tasmanian devil insurance population despite significant variation in inbreeding

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Rebecca Gooley ◽  
Carolyn J. Hogg ◽  
Katherine Belov ◽  
Catherine E. Grueber
Keyword(s):  
Inbreeding Depression ◽  
Significant Variation ◽  
Tasmanian Devil

scholarly journals Host density predicts the probability of parasitism by avian brood parasites

2019 ◽  
Vol 374 (1769) ◽  
pp. 20180204 ◽  
Author(s):  
Iliana Medina ◽  
Naomi E. Langmore
Keyword(s):  
Spatial Distribution ◽  
Reproductive Success ◽  
Host Species ◽  
Field Data ◽  
Host Density ◽  
Brood Parasites ◽  
Parasitism Rates ◽  
Analyse Data ◽  
First Time ◽  
Determining Factor

The spatial distribution of hosts can be a determining factor in the reproductive success of parasites. Highly aggregated hosts may offer more opportunities for reproduction but can have better defences than isolated hosts. Here we connect macro- and micro-evolutionary processes to understand the link between host density and parasitism, using avian brood parasites as a model system. We analyse data across more than 200 host species using phylogenetic comparative analyses and quantify parasitism rate and host reproductive success in relation to spatial distribution using field data collected on one host species over 6 years. Our comparative analysis reveals that hosts occurring at intermediate densities are more likely to be parasitized than colonial or widely dispersed hosts. Correspondingly, our intraspecific field data show that individuals living at moderate densities experience higher parasitism rates than individuals at either low or high densities. Moreover, we show for the first time that the effect of host density on host reproductive success varies according to the intensity of parasitism; hosts have greater reproductive success when living at high densities if parasitism rates are high, but fare better at low densities when parasitism rates are low. We provide the first evidence of the trade-off between host density and parasitism at both macro- and micro-evolutionary scales in brood parasites. This article is part of the theme issue ‘The coevolutionary biology of brood parasitism: from mechanism to pattern’.

scholarly journals Low major histocompatibility complex diversity in the Tasmanian devil predates European settlement and may explain susceptibility to disease epidemics

2013 ◽  
Vol 9 (1) ◽  
pp. 20120900 ◽  
Author(s):  
Katrina Morris ◽  
Jeremy J. Austin ◽  
Katherine Belov
Keyword(s):  
Major Histocompatibility Complex ◽  
Tasmanian Devil ◽  
Major Histocompatibility ◽  
European Settlement ◽  
Low Genetic Diversity ◽  
Histocompatibility Complex ◽  
Devil Facial Tumour Disease ◽  
History Of ◽  
Mhc Diversity ◽  
Disease Epidemics

The Tasmanian devil ( Sarcophilus harrisii ) is at risk of extinction owing to the emergence of a contagious cancer known as devil facial tumour disease (DFTD). The emergence and spread of DFTD has been linked to low genetic diversity in the major histocompatibility complex (MHC). We examined MHC diversity in historical and ancient devils to determine whether loss of diversity is recent or predates European settlement in Australia. Our results reveal no additional diversity in historical Tasmanian samples. Mainland devils had common modern variants plus six new variants that are highly similar to existing alleles. We conclude that low MHC diversity has been a feature of devil populations since at least the Mid-Holocene and could explain their tumultuous history of population crashes.

BIOLOGY OF TACHINAEPHAGUS ZEALANDICUS (HYMENOPTERA: ENCYRTIDAE), PARASITOID OF SYNANTHROPIC DIPTERA

1974 ◽  
Vol 106 (8) ◽  
pp. 785-800 ◽  
Author(s):  
G. S. Olton ◽  
E. F. Legner
Keyword(s):  
Life History ◽  
Developmental Stages ◽  
Average Length ◽  
Host Density ◽  
Adult Emergence ◽  
Reproductive Period ◽  
Laboratory Studies ◽  
Pupal Parasitoid ◽  
History Of ◽  
Parasitoid Development

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.

Effect of Host Density on Parasitism

1935 ◽  
Vol 28 (6) ◽  
pp. 898-900 ◽  
Author(s):  
S. E. Flander
Keyword(s):  
Host Density

Parasite infection and host dynamics in a naturally fluctuating rodent population

2012 ◽  
Vol 90 (9) ◽  
pp. 1149-1160 ◽  
Author(s):  
J.C. Winternitz ◽  
M.J. Yabsley ◽  
S.M. Altizer
Keyword(s):  
Population Density ◽  
Experimental Studies ◽  
Host Density ◽  
Positive Association ◽  
Population Cycles ◽  
Host Population ◽  
Reproductive Status ◽  
Vole Cycles ◽  
Host Infection ◽  
The Impact

Parasites can both influence and be affected by host population dynamics, and a growing number of case studies support a role for parasites in causing or amplifying host population cycles. In this study, we examined individual and population predictors of gastrointestinal parasitism on wild cyclic montane voles ( Microtus montanus (Peale, 1848)) to determine if evidence was consistent with theory implicating parasites in population cycles. We sampled three sites in central Colorado for the duration of a multiannual cycle and recorded the prevalence and intensity of directly transmitted Eimeria Schneider, 1875 and indirectly transmitted cestodes from a total of 267 voles. We found significant associations between host infection status, individual traits (sex, age, and reproductive status) and population variables (site, trapping period, and population density), including a positive association between host density and cestode prevalence, and a negative association between host density and Eimeria prevalence. Both cestode and Eimeria intensity correlated positively with host age, reproductive status, and population density, but neither parasite was associated with poorer host condition. Our findings suggest that parasites are common in this natural host, but determining their potential to influence montane vole cycles requires future experimental studies and long-term monitoring to determine the fitness consequences of infection and the impact of parasite removal on host dynamics.

Risk factors associated with Enteromyxum scophthalmi (Myxozoa) infection in cultured turbot, Scophthalmus maximus (L.)

Parasitology ◽  
2006 ◽  
Vol 133 (4) ◽  
pp. 433-442 ◽  
Author(s):  
M. I. QUIROGA ◽  
M. J. REDONDO ◽  
A. SITJÀ-BOBADILLA ◽  
O. PALENZUELA ◽  
A. RIAZA ◽  
...  
Keyword(s):  
Risk Factors ◽  
Distribution Pattern ◽  
Control Strategies ◽  
Host Density ◽  
Scophthalmus Maximus ◽  
Fish Distribution ◽  
Fish Mortality ◽  
Infection Prevalence ◽  
Western Spain ◽  
Turbot Scophthalmus Maximus

An epidemiological cohort study of Enteromyxum scophthalmi in cultured turbot was performed on a farm in North Western Spain. Four different ongrowing stocks (A, B, C, D) were monitored monthly until market size. Fish from stocks C and D were divided into 2 subgroups, receiving filtered (CF and DF) or unfiltered (CUF and DUF) water. The lack of water filtration was positively associated with infection prevalence, as all fish kept in filtered water remained uninfected. Parasite abundance varied seasonally (P<0·05) in stock B and subgroup CUF. Infection was also associated (P<0·05) with host weight, and the highest prevalences and intensities were detected in 101–200 g and 201–300 g fish. Distribution pattern of E. scophthalmi in subgroups CUF and DUF had a variance higher than the mean, indicating overdispersion. The minimum period necessary for the first detection of the parasite and for the appearance of disease symptoms and mortality, varied depending on the stock and introduction date, although a long pre-patent period was always observed. Several factors, such as host density, parasite recruitment and parasite-induced fish mortality can contribute to the observed distribution pattern. Risk factors found to be associated with E. scophthalmi infection, including water quality and accumulation of infective stages in the culture tanks, should be considered when designing control strategies to prevent the introduction and spread of infective stages in the facilities.

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