Journal of Medical Entomology Impact Factor & Information

Publisher: Bernice Pauahi Bishop Museum. Dept. of Entomology, Entomological Society of America

Journal description

Journal of Medical Entomology is published bimonthly in January, March, May, July, September, and November. The editorial board comprises one representative each from Sections A, B, C, E, and F and five representatives from section D. The journal currently has three coeditors. The journal publishes reports on all phases of medical entomology and medical acarology, including the systematics and biology of insects, acarines, and other arthropods of public health and veterinary significance. In addition to full-length research articles, the journal publishes Book Review, Forum, Short Communications and Rapid Communications. Published by the Entomological Society of America.

Current impact factor: 1.82

Impact Factor Rankings

2015 Impact Factor Available summer 2015
2013 / 2014 Impact Factor 1.815
2012 Impact Factor 1.857
2011 Impact Factor 1.762
2010 Impact Factor 1.925
2009 Impact Factor 1.921
2008 Impact Factor 1.967
2007 Impact Factor 1.864
2006 Impact Factor 1.95
2005 Impact Factor 1.489
2004 Impact Factor 1.609
2003 Impact Factor 1.394
2002 Impact Factor 1.137
2001 Impact Factor 0.949
2000 Impact Factor 1.051
1999 Impact Factor 1.011
1998 Impact Factor 1.074
1997 Impact Factor 1.066
1996 Impact Factor 1.067
1995 Impact Factor 1.09
1994 Impact Factor 1.134
1993 Impact Factor 0.821
1992 Impact Factor 0.785

Impact factor over time

Impact factor
Year

Additional details

5-year impact 2.27
Cited half-life 9.60
Immediacy index 0.27
Eigenfactor 0.01
Article influence 0.60
Website Journal of Medical Entomology website
Other titles Journal of medical entomology
ISSN 0022-2585
OCLC 1783323
Material type Periodical, Internet resource
Document type Journal / Magazine / Newspaper, Internet Resource

Publisher details

Entomological Society of America

  • Pre-print
    • Author cannot archive a pre-print version
  • Post-print
    • Author cannot archive a post-print version
  • Restrictions
    • 12 months embargo
  • Conditions
    • On one of an author's personal web site or institutional repository only
    • Publisher's version/PDF (Open Access PDF) can be used for a fee
    • Author's version
    • Publisher copyright and source must be acknowledged
    • Set statement to accompany article, 'This article is the copyright property of the Entomological Society of America and may not be used for any commercial or other private purpose without specific written permission of the Entomological Society of America'
  • Classification
    ​ white

Publications in this journal

  • Journal of Medical Entomology 08/2015; DOI:10.1093/jme/tjv110
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    ABSTRACT: A new species of sand fly, which we describe as Lutzomyia (Trichophoromyia) nautaensis n. sp., was collected in the northern Peruvian Amazon Basin. In this region of Peru, cutaneous leishmaniasis is transmitted primarily by anthropophilic sand flies; however, zoophilic sand flies of the subgenus Trichophoromyia may also be incriminated in disease transmission. Detection of Leishmania spp. in Lutzomyia auraensis Mangabeira captured in the southern Peruvian Amazon indicates the potential of this and other zoophilic sand flies for human disease transmission, particularly in areas undergoing urban development. Herein, we describe Lutzomyia (Trichophoromyia) nautaensis n. sp., and report new records of sand flies in Peru.
    Journal of Medical Entomology 07/2015; 52(4). DOI:10.1093/jme/tjv057
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    ABSTRACT: The outbreak of disease caused by chikungunya virus (CHIKV) in 2006 and the recent spread of this virus to the Americas in 2013 indicate the potential for this virus to spread and cause significant disease. However, there are currently no accurate and reliable field-usable, diagnostic methods to provide critical, real-time information for early detection of CHIKV within the vector populations in order to implement appropriate vector control and personal protective measures. In this article, we report the ability of an immuno-chromatographic assay developed by VecTOR Test Systems Inc. to detect CHIKV in a pool of female Aedes mosquitoes containing a single CHIKV-infected mosquito. The CHIKV dipstick assay was simple to use, did not require a cold chain, and provided clear results within 1 h. It was highly specific and did not cross-react with samples spiked with a variety of other alpha, bunya, and flaviviruses. The CHIKV assay can provide real-time critical information on the presence of CHIKV in mosquitoes to public health personnel. Results from this assay will allow a rapid threat assessment and the focusing of vector control measures in high-risk areas.
    Journal of Medical Entomology 07/2015; DOI:10.1093/jme/tjv047
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    ABSTRACT: Since its emergence in North America, West Nile virus (WNV) has had a large impact on equines, humans, and wild bird communities, yet gaps remain in our understanding of how the virus persists at temperate latitudes when winter temperatures preclude virus replication and host-seeking activity by mosquito vectors. Bird-to-bird transmission at large communal American Crow roosts could provide one mechanism for WNV persistence. Herein, we describe seasonal patterns of crow and Culex mosquito abundance, WNV infection rates, and the prevalence of WNV-positive fecal samples at a winter crow roost to test the hypothesis that bird-to-bird transmission allows WNV to persist at winter crow roosts. Samples were collected from large winter crow roosts in the Sacramento Valley of California from January 2013 until August 2014, encompassing two overwintering roost periods. West Nile virus RNA was detected in local crow carcasses in both summer [13/18 (72% WNV positive)] and winter [18/44 (41% WNV positive)] 2013-2014. Winter infections were unlikely to have arisen by recent bites from infected mosquitoes because Culex host-seeking activity was very low in winter and all Culex mosquitoes collected during winter months tested negative for WNV. Opportunities existed for fecal-oral transfer at the overwintering roost: most carcasses that tested positive for WNV had detectable viral RNA in both kidney and cloacal swabs, suggesting that infected crows were shedding virus in their feces, and >50% of crows at the roost were stained with feces by mid-winter. Moreover, 2.3% of fecal samples collected in late summer, when mosquitoes were active, tested positive for WNV RNA. Nevertheless, none of the 1,119 feces collected from three roosts over two winters contained detectable WNV RNA. This study provided evidence of WNV infection in overwintering American crows without mosquito vector activity, but did not elucidate a mechanism of WNV transmission during winter.
    Journal of Medical Entomology 07/2015; 52(4). DOI:10.1093/jme/tjv040
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    ABSTRACT: The principal vectors of chikungunya and dengue viruses typically oviposit in water-filled artificial and natural containers, including tree holes. Despite the risk these and similar tree hole-inhabiting mosquitoes present to global public health, surprisingly few studies have been conducted to determine an efficient method of applying larvicides specifically to tree holes. The Stihl SR 450, a backpack sprayer commonly utilized during military and civilian vector control operations, may be suitable for controlling larval tree-hole mosquitoes, as it is capable of delivering broadcast applications of granular and liquid dispersible formulations of Bacillus thuringiensis var. israelensis (Bti) to a large area relatively quickly. We compared the application effectiveness of two granular (AllPro Sustain MGB and VectoBac GR) and two liquid (Aquabac XT and VectoBac WDG) formulations of Bti in containers placed on bare ground, placed beneath vegetative cover, and hung 1.5 or 3 m above the ground to simulate tree holes. Aedes aegypti (L.) larval mortality and Bti droplet and granule density data (when appropriate) were recorded for each formulation. Overall, granular formulations of Bti resulted in higher mortality rates in the simulated tree-hole habitats, whereas applications of granular and liquid formulations resulted in similar levels of larval mortality in containers placed on the ground in the open and beneath vegetation.
    Journal of Medical Entomology 07/2015; 52(4). DOI:10.1093/jme/tjv043
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    ABSTRACT: We conducted field trials to evaluate the ability of a garlic juice-based product to control or suppress nymphal activity of the blacklegged tick, Ixodes scapularis Say, at residential properties in Connecticut in 2009, 2010, and 2011. The product was applied at a rate of 0.2 g AI/m2. Percent control of nymphal densities achieved by the spray treatment at 6, 11, and 18 d postspray for the 3 yr was 37.0, 59.0, and 47.4%, respectively. Differences between nymphal densities were greatest during the first post-spray sampling period. While garlic may require multiple applications for the suppression of tick activity, this product could provide a minimal-risk option for the short-term control of nymphal I. scapularis in the residential landscape.
    Journal of Medical Entomology 07/2015; 52(4). DOI:10.1093/jme/tjv044
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    ABSTRACT: The etiological agents responsible for Lyme disease (Borrelia burgdorferi), human granulocytic anaplasmosis (Anaplasma phagocytophilum), and babesiosis (Babesia microti) are primarily transmitted by the blacklegged tick, Ixodes scapularis Say. Despite Pennsylvania having in recent years reported the highest number of Lyme disease cases in the United States, relatively little is known regarding the geographic distribution of the vector and its pathogens in the state. Previous attempts at climate-based predictive modeling of I. scapularis occurrence have not coincided with the high human incidence rates in parts of the state. To elucidate the distribution and pathogen infection rates of I. scapularis, we collected and tested 1,855 adult ticks statewide from 2012 to 2014. The presence of I. scapularis and B. burgdorferi was confirmed from all 67 Pennsylvania counties. Analyses were performed on 1,363 ticks collected in the fall of 2013 to avoid temporal bias across years. Infection rates were highest for B. burgdorferi (47.4%), followed by Ba. microti (3.5%) and A. phagocytophilum (3.3%). Coinfections included B. burgdorferi + Ba. microti (2.0%), B. burgdorferi + A. phagocytophilum (1.5%) and one tick positive for A. phagocytophilum + Ba. microti. Infection rates for B. burgdorferi were lower in the western region of the state. Our findings substantiate that Lyme disease risk is high throughout Pennsylvania.
    Journal of Medical Entomology 07/2015; 52(4). DOI:10.1093/jme/tjv037
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    ABSTRACT: Re-examination of Dermacentor taiwanensis Sugimoto, 1935 specimens in the United States National Tick Collection revealed that two morphologically distinct Dermacentor species were identified under this name. One of them corresponds to Sugimoto’s description of D. taiwanensis , while another species is identical to Schulze’s Dermacentor bellulus (Schulze, 1935). The latter species has not been considered valid by recent workers. D. bellulus is reinstated here as a valid species and all its stages are redescribed. The adults of D. taiwanensis are also redescribed, and its immature stages are described for the first time. Males and females of D. bellulus can be distinguished from those of D. taiwanensis by the shape of the conscutum and scutum, color pattern, genital structures, size of the palpi and cornua, and the spurs of coxa I. Nymphs of D. bellulus can be distinguished from those of D. taiwanensis by the shape of the scutum, basis capituli, and the hypostomal dentition. Larvae of D. bellulus can be differentiated from those of D. taiwanensis by the shape of the basis capituli, and the degree of development of the auriculae and spur on palpal segment III ventrally. D. bellulus has been recorded from China, Japan, Nepal, Taiwan, and Vietnam; adults have been collected from wild boars, bears, panda, dog, and human; the immature stages are known from rodents, hares, ferret-badger, and bamboo-partridge. D. taiwanensis is found in China, Taiwan, and Vietnam; adults have been collected from wild boars; the immature stages are known from rodents, hares, mustelids, and domestic dog.
    Journal of Medical Entomology 07/2015; 52:573-595. DOI:10.1093/jme/tjv034