Filippova N A, Musatov S A
Parazitologiia. 1996 May-Jun;30(3):205-15.
The aim of the article is to estimate geographic variation of Ixodes persulcatus adults as a whole. Intraspecific variation of the females and males of Ixodes persulcatus Schulze, 1930 has been studied in eight geographical localities ("populations") of its distribution range (fig. 1.). The distance between western and eastern localities is more than 8700 km, between northern and southern ones it is approximately 2900 km. Twenty five to thirty specimens of each sex were studied in each geographical locality. The following eleven characters were used (fig. 2, 3): length of scutum (conscutum), width of scutum (conscutum), length of anal ring, width of anal ring, length of spiracular plate, width of spiracular plate, length of gnathosoma, width of gnathosoma, length of II-III articles of palps, length of hypostome, length of tarsus 1. The multidimensional scaling method by means of software package SYSTAT was used for estimation of relationships between populations on the basis of morphometrical data. The differences between the populations were revealed only from absolute sizes of organs, whereas their proportions (i. e. shape) were constant in all geographical localities. Fig. 4, 1 shows that females from localities G (Primorski Territory) and C (Tien Shan Mountains) occupy extreme positions. Fig. 4, 2 shows that males from localities G (Primorski Territory) and D (SW Altai Mountains) on the one hand and A, B (European) on the other one occupy extreme positions. Locality C (Tien Shan Mountains) is similar to F (Western Sayan Mountains) and to European (A, B) whereas females of locality C differ from A, B and F. Taking into account the partial discrepancy of relationships between populations in sexes we have united the data on corresponding characters of both sexes in the aggregate data base (fig. 4, 3). This was possible owing to the multidimensional scaling method. Fig. 4, 3 shows isolated position of the population G (Primorski Territory), specimens of which are the largest in sizes. The populations D (SW Altai Mountains) and H (Sakhalin Island) are morphometrically most similar to the population G. The population C (Tien-Shan Mountains) is represented of the smallest specimens. The European populations (A and B) are closer to C. The largest sizes are typical of the populations G and D associated with relict Tertiary landscapes of Primorski Territory and SW Altai with which areas of ecological optimum of I. persulcatus coincide. The smallest sizes are observed in the European populations (A, B) near the north-western boundary of the distribution range of the species, as well as in the Alpine population of Tien-Shan Mountains, near the upper vertical boundary of the distribution range (2000-3000 m above sea level). Climatic conditions of the habitat in these areas are similar to those of the northwestern part of the distribution range of I. persulcatus.
本文的目的是整体评估全沟硬蜱成虫的地理变异。对1930年全沟硬蜱舒尔茨的雌蜱和雄蜱的种内变异,在其分布范围内的八个地理区域(“种群”)进行了研究(图1)。西部和东部区域之间的距离超过8700公里,北部和南部区域之间约为2900公里。在每个地理区域研究了25至30个每种性别的标本。使用了以下11个特征(图2、3):盾板长度(盾板)、盾板宽度(盾板)、肛环长度、肛环宽度、气门板长度、气门板宽度、颚体长度、颚体宽度、须肢II - III节长度、下咽长度、跗节1长度。借助SYSTAT软件包的多维标度法,根据形态测量数据评估种群之间的关系。种群之间的差异仅体现在器官的绝对大小上,而它们的比例(即形状)在所有地理区域都是恒定的。图4.1显示,来自区域G(滨海边疆区)和C(天山山脉)的雌蜱占据极端位置。图4.2显示,一方面来自区域G(滨海边疆区)和D(阿尔泰山脉西南部)的雄蜱,另一方面来自A、B(欧洲)的雄蜱占据极端位置。区域C(天山山脉)与F(西萨彦岭)和欧洲(A、B)相似,而区域C的雌蜱与A、B和F不同。考虑到两性种群之间关系的部分差异,我们将两性相应特征的数据合并到汇总数据库中(图4.3)。这借助多维标度法得以实现。图4.3显示了区域G(滨海边疆区)种群的孤立位置,该区域的标本尺寸最大。种群D(阿尔泰山脉西南部)和H(萨哈林岛)在形态测量上与种群G最相似。种群C(天山山脉)的标本最小。欧洲种群(A和B)与C更接近。最大尺寸是与滨海边疆区和阿尔泰山脉西南部的第三纪残遗景观相关的种群G和D的典型特征,全沟硬蜱的生态最适区域与这些地区重合。最小尺寸出现在该物种分布范围西北边界附近的欧洲种群(A、B),以及分布范围垂直上限(海拔2000 - 3000米)附近的天山山脉高山种群。这些地区栖息地的气候条件与全沟硬蜱分布范围西北部的气候条件相似。