Open Access

Life history traits of the Chinese minnow Rhynchocypris oxycephalus in the upper branch of Yangtze River, China

Zoological Studies201453:36

DOI: 10.1186/s40555-014-0036-0

Received: 28 February 2014

Accepted: 13 June 2014

Published: 1 July 2014



Study of the life history traits of any species plays an essential role for understanding their relationship with the surrounding environment and scientific management. The Chinese minnow Rhynchocypris oxycephalus, an ecologically and economically important species which was widely distributed in East Asia, is currently diminishing. In the present study, we depicted the main life history traits of R. oxycephalus for the first time.


A total of 442 individuals were collected from April 2012 to March 2013, with total length (TL) ranging from 32.2 to 158.0 mm. The otolith (lapillus) was proved suitable for age determination. Moreover, the results from marginal increment ratio (MIR) analyses demonstrated its unusual growth pattern: two pairs of opaque and transparent bands were formed each year, which might provide some implications for the age determination of other species. The maximum age for females (4 years) was higher than for males (3 years), while 1- and 2-year-old individuals dominated the population. Both females and males reached maturity at 1 year, and the TL at first maturity was 78.8 mm for females and 60.3 mm for males. Obvious sexual dimorphism was observed as females growing faster and larger than males after maturity. As a multiple spawner, R. oxycephalus releases batches of eggs from April to August. The fecundity of R. oxycephalus was higher, and the size of eggs was larger than that of its closely related species.


R. oxycephalus is a short-lived, fast-growing, highly fecund, and early-maturing species; therefore, even a short recovery time after overexploitation or disturbance would be of great use for their restoration. Some life history traits of R. oxycephalus demonstrate obvious differences with its closely related species, indicating that latitude and local environment conditions are important selective forces for this species.


Annuli Otolith Age determination Growth pattern Reproduction


The Rhynchocypris minnows are typical small cold water fish, mainly distributed in Asia (Chen [1998]). The Chinese minnow Rhynchocypris oxycephalus (Sauvage et Dabry, 1874) is an endemic species of East Asia, widely distributed from southern China to most parts of the Korean Peninsula and western Japan (Chen [1998]; Park et al. [2001]; Ito et al. [2002]; Sakai et al. [2006]; Bogutskaya et al. [2008]; Takai et al. [2012]). In China, R. oxycephalus is mainly distributed in well-oxygenated montane stream headwaters of Yangtze River Basin (Chen [1998]; Zhang and Chen [1997]), at the southern-distribution boundary of Rhynchocypris minnows. In its inhabited streams, R. oxycephalus often has a large population, acting as the dominant species and playing a crucial role in maintaining the balance of stream ecosystem. Besides, as an important component of local fishery, R. oxycephalus also has economic importance. However, with the development of agriculture and industry, most river ecosystems are experiencing severe ecological degradation in China (Chen [2005]), making the fish habitats more vulnerable. As indicated by Maxent models, 78.1% of the most suitable habitats for R. oxycephalus would disappear by 2080, and most range contractions would occur in southeastern China (Yu et al. [2012]). Worsened by overfishing and water pollution, the population of R. oxycephalus is diminishing in recent years.

The life history traits of fish display geographical variations, which are considered as responses to local environment (Vinyoles et al. [2010]; Grabowska et al. [2012]), and explaining those variations is a central objective of evolutionary biology. Latitude is one of the most important factors that influence several life history traits of freshwater fish (Blanck and Lamouroux [2007]). Compared with its closely related species (Rhynchocypris, Phoxinus, and Chrosomus minnows), R. oxycephalus in China is distributed in the lowest latitude regions. The life history traits of many populations of Rhynchocypris, Phoxinus, and Chrosomus minnows have been reported (Starnes and Starnes [1981]; Mills and Eloranta [1985]; Mills [1987], [1988]; Hamed et al. [2008]; Wang et al. [2012]). However, for R. oxycephalus, this information is very limited. There have been only a few publications about its reproductive characteristics and distributions (Xiong [1984]; Chen [1998]; Yu et al. [2012]). Knowing the life history traits of this species may contribute to better understanding of the influence latitude has on the life history traits of freshwater fish. In addition, it is also indispensable for their effective conservation and scientific management, for fundamental links existing between the individual life history and increasing rate of population (Hutchings [2002]; Foster and Vincent [2004]; Jia and Chen [2011]). Both theoretical and empirical analyses showed that certain life history traits made the species more vulnerable to anthropogenic threats (Jennings et al. [1999]; Sadovy [2001]; Denney et al. [2002]; Foster and Vincent [2004]).

The objectives of the current study were to (1) present the key life history traits of R. oxycephalus under natural conditions, including its age, growth development, and reproduction, to provide essential information for their effective protection and scientific management and (2) compare those traits with its closely related species for better understanding of the influences of latitude and local environment on the stream fish community.


Study area

This study was carried out in the Laohegou Stream (E 104° 40′, N 32° 31′), a montane stream located in the upper Yangtze River drainage, south of China (Figure 1). This stream, with an elevation span of 763 to 1,948 m, drains a surface area of 110 km2 over its 52-km length. It has a typical subtropical monsoon climate, characterized by rainfall mainly occurring in spring and summer. The mean water temperature ranges from 3.78°C (in December) to 19.8°C (in August), and annual mean water temperature is 11.04°C. Its 20-km upper reaches and surrounding areas have been established as the Laohegou Social Welfare Reserve, within which a large amount of R. oxycephalus is distributed.
Figure 1

Location of the Laohegou Stream and sampling sites.

Sample collection and procedures

From April 2012 to March 2013, 442 individuals were collected by electrofishing at monthly intervals (samplings of January and February 2013 were prevented by bad weather) from four sampling sites (Figure 1). The specimens were individually measured for total length (TL, 0.1 mm), standard length (SL, 0.1 mm), and weighted body weight (BW, 0.01 g) and dissected. Gonad of each specimen was weighted (gonad weight, GW, 0.01 g), inspected to determine the sex, and classified into six maturity stages (I-VI) based on the visual traits including profile, size, color, and vascularization, following Yin ([1993]). Somatic weight (SW, 0.01 g) of each specimen has also been recorded. Scales, vertebrae, opercula, dorsal fin spine, and three couples of otolith (asteriscus, lapillus, and sagitta) of each specimen were extracted to determine the age. All processed specimens and mature ovaries at stage IV were preserved in 8% neutralized formaldehyde solution. Besides, eight environmental variables were recorded during each sampling: longitude, latitude, elevation, dissolved oxygen, wetted width, water depth, water temperature, and current velocity.


To determine age, every aging material was prepared following Chen et al. ([2002]). We chose the lapillus for age determination after analyzing and comparing the materials above. For the lapillus, respective distance from the nucleus to the edge (radius, R) and to the distal edge of each opaque band (r) along the reading zone was measured to the nearest 1 μm. The periodicity of annulus formation was determined by monthly changes of marginal increment ratio (MIR), using the following equation: MIR = (R − r n ) / (r n  − r n−1), where r n is the distance between the nucleus and the outer margin of the last opaque mark (Casselman [1987]). Age estimation was performed independently by two readers without information of size. Samples with identical readings were used in further age and growth analysis. Ages were also verified using length frequency distribution. Identification of the first annulus in lapillus was confirmed by comparing the total length back-calculated from the first annual to the first peak of total length distribution (Mills [1987]).


The relationship between TL and BW was described by the exponential equation: BW = a TL b , where a is the intercept and b is the slope of the regression curve. Difference between sexes for the TL-BW relationship (LWR) was tested using analysis of covariance (ANCOVA) (Sokal and Rohlf [1995]). The relative condition factor (K N) was used to describe seasonal fluctuations of fish plumpness (Le Cren [1951]), which was calculated as K N = SW/PW, where PW is the predicted somatic weight at its total length by the TL-SW relationship, and SW is the measured somatic weight. To back-calculate the TL at age, the relationship between TL and radius was described by linear regression: TL = a + bR, where R is the radius of lapillus, and a and b are both constants. TL at age was obtained using the Fraser-Lee equation (Duncan [1980]): TL n  = a + (TL − a)r n / R, where TL is the measured total length, TL n is the back-calculated total length (BCL) at age n, a is the intercept in TL-R linear function, and r n is the distance between core and the n th annulus. The von Bertalanffy growth formula (VBGF) (von Bertalanffy [1938]) was used to describe the growth curve that fitted to back-calculated data: TL t  = L [1 − e −k(tt 0)], where TL t is the predicted TL at age t (year), L is the theoretical maximum TL, k is the growth rate parameter (year−1) describing the rate that fish reach L , and t 0 is theoretical initial age (year) when TL is zero. All those parameters were estimated by the least square method. Back-calculation of the VBGF was fitted to males and females, respectively. The growth performance index (φ′) was calculated as φ′ = 2log10 L  + log10 k (Munro and Pauly [1983]). The growth inflexion age t i (year) was calculated as t i = (lnb) / k + t 0 (Yin [1993]), where b is the one in the equation of BW-TL, and k and t 0 were estimated from the VBGF.


To calculate the TL at first maturation (TLm, TL at 50% maturity), the proportion of mature individuals per 5-mm TL intervals was fitted to a logistic function Pi = 100(1 + e−(a + b TL))−1, where Pi is the proportion of mature individuals in TL class i, and a and b are both constants. The TLm was calculated as TLm = −ab −1 (King [1995]). To describe the reproductive effort and gonadal annual cycle, the monthly gonado-somatic index (GSI) was calculated (Yin [1993]): GSI = 100(GW/SW), where GW is gonad weight and SW is somatic weight. The annual fecundity (F) was estimated as the total number of ripening and ripe oocytes from mature ovaries before spawning (Yin [1993]), and relative fecundity (RF) was calculated as (Bagenal [1978]) RF = F/SW. To analyze size frequency distribution of egg diameter in ripened gonads, the diameters of 80 to 100 randomly sampled oocytes were measured during breeding season. Sex ratio was calculated, and its difference from 1:1 was tested by χ 2 test (Zar [1999]). The present study was carried out following permission issued from the Hubei Province Association for Laboratory Animal Sciences.



The sectioned lapillus showed clear nucleus and alternating opaque and translucent bands under transmitted light (Figure 2). Monthly variations of MIR showed double cyclical trend of increment within 1 year (Figure 3). In April and August, the mean MIR decreased while the range of MIR increased, indicating that the opaque band was completed and a new translucent band began to form. Most lapilli taken from specimens in the first peak of total length frequency distribution (70 to 90 mm) (Figure 4) were forming (36.8%) or just formed (46.6%) their first opaque band. Thus, we considered the first opaque band as their first annulus. We concluded that the lapillus formed one pair of opaque and translucent bands in its first year and then two pairs every year. Consequently, R. oxycephalus in this study was aged as follows: individuals with none or one just-formed opaque band were in age 1 group, individuals with one or two opaque bands or having its third opaque band just formed were in age 2 group, individuals with three or four opaque bands or having its fifth opaque band just formed were in age 3 group, and so on for other individuals. The percent agreement among two readers was 94.1%, and the coefficient of variation (CV) was 9.5%.
Figure 2

The appearance of a cross section of a 4-year-old R. oxycephalus lapillus under transmitted light. N, nucleus; TB, translucent band; OB, opaque band. Solid circles show annuli, and the longest arrow shows the direction of measurement.

Figure 3

Monthly variations of marginal increment ratio of R. oxycephalus lapillus. Solid circles and the line indicate the mean MIR.

Figure 4

Total length distributions of R. oxycephalus .

For all collected individuals, 153 were identified as females (52.9 to 158 mm, TL), 258 males (46.8 to 123.6 mm, TL), and 31 juveniles (32.2 to 84.3 mm, TL) too young for sex identification. The sex ratio (females/males) was 1:1.69, which is significantly different from 1:1 (χ 2  = 26.4, df = 1, P < 0.05). Using the sectioned otolith, 416 specimens were successfully aged, and three age groups for males and four age groups for females were observed. Individuals of age 1 (63.7%) and age 2 (25.5%) groups dominated the population; only 2.7% males were in age 3 group and 5.2% females in age 4 group.


The TL-BW equations were as follows: BW = 1.3 × 10−5TL2.9298 (r 2 = 0.9578, n = 258, P < 0.05) for males and BW = 4.9 × 10−6TL3.1543 (r 2 = 0.9665, n = 153, P < 0.05) for females. These equations were significantly different between sexes (ANCOVA, df = 409, P < 0.05). The value of K N showed two peaks, in March and August, throughout the year. The females and males presented similar fluctuating patterns of K N (Figure 5). The relationship between TL and R was calculated as TL = 33.907 + 129.1R (r 2 = 0.8357, n = 140, P < 0.05) for females and TL = 44.46 + 93.1R (r 2 = 0.6702, n = 210, P < 0.05) for males. The difference between the two equations was significant (ANCOVA, df = 348, P < 0.05). The back-calculated TLs at ages (TLs at 3 years for males and at 4 years for females were acquired by measuring the full age individuals) are presented in Table 1. The body size of males was slightly larger than that of females at age 1 year (t test, df = 154, P < 0.05) but was smaller at age 2 years (t test, df = 81, P < 0.05) and age 3 years (t test, df = 18, P < 0.05). The length and weight at age for females were described by the VBGF (Figure 6) as TL = 220.56[1 − e−0.251(t + 0.80)] and BW = 120.89[1 − e−0.251(t + 0.80)]3.1543. The VBGF for males was not calculated as their age structure was too simple. Based on L and k values in VBGF, the growth performance index (φ′) was 4.09 years and the growth inflexion (t i) was 3.78 years for females. The relationship between TL and SL was described by SL = 0.8279TL − 0.3439 (r 2 = 0.9963, n = 422, P < 0.05).
Figure 5

Monthly variations of relative condition factor ( K N ) with its respective SD.

Table 1

Back-calculated total length at age of R. oxycephalus

Age (years)




80.11 ± 7.06 (n = 81)

82.75 ± 4.76 (n = 75)


111.21 ± 9.87 (n = 54)

98.92 ± 6.45 (n = 29)


135.81 ± 8.15 (n = 15)

110.42 ± 1.42 (n = 5)


154.5 ± 2.89 (n = 4)


Mean ± SD (n = number of individuals measured).

Figure 6

Growth curves of total length in VBGF derived from the back-calculated data.


Both females and males reached 50% maturity at 1 year. The TLm was 60.3 mm for males and 78.8 mm for females (Figure 7). Among sampled mature individuals, the minimum TLs were 53.6 and 60.0 mm for males and females, respectively. The monthly variations of GSI presented similar seasonal patterns for females and males (Figure 8). In August, only 9.8% individuals have mature gonad at stage V, and no mature gonad was found in September. Therefore, the breeding season for R. oxycephalus in the Laohegou Stream was carried out from April to August.
Figure 7

The percentage contributions of mature R. oxycephalus in each sequential 5-mm total length intervals.

Figure 8

Monthly variations of gonado-somatic index with its respective SD.

The ripened ovaries of R. oxycephalus contained groups of oocytes of different sizes, especially at the beginning of the spawning season (Figure 9). In April, ripened oocytes (opaque) constituted about 50% of all oocytes in ripened ovaries (Figure 9A), and ripening oocytes (semi-transparent) constituted about 35%; from late June to August, the ripened oocytes constituted about 85% of all oocytes in ripened ovaries, while few ripening oocytes were found (Figure 9D,E). It can be concluded that the R. oxycephalus is a multiple spawner that releases at least two groups of oocytes during breeding season.
Figure 9

Size-frequency distributions of egg diameter in ripened gonads of R. oxycephalus during breeding season. (A) 4 April, (B) 25 May, (C) 23 June, (D) 26 July, and (E) 15 August.

In April and May, 27 mature ovaries (at gonadal stage IV) were collected to estimate the annual fecundity (F). The mean F of R. oxycephalus was 2,457 oocytes, ranging from 751 (TL at 78.1 mm) to 5,189 (TL at 154.2 mm).The fecundity was correlated with TL, specified by F = 0.1848TL2.0073 (r 2 = 0.7319, n = 27, P < 0.05). Mean relative fecundity was 150 oocytes/g, ranging from 88 oocytes/g to 220 oocytes/g.


Otolith growth pattern

Otolith is one of the most frequently used aging structures (Campana [2001]; Campana and Thorrold [2001]). Its sequence of increment is interrupted by checks or discontinuities that mark the occurrence of stressful periods in the life of the fish (Pannella [1974], [1980]; Campana [1983]; Chen et al. [2002]). For riverine fishes, the formation of increments and discontinuities of otolith is mainly influenced by water temperature, water level, and reproductive activity (Welcomme [1979]; Mills [1987]). In our study, the monthly variations of MIR showed that the otolith of R. oxycephalus formed two translucent discontinuous bands during May to early July and September to February, and two opaque incremental bands during March to April and late July to August, separately. We speculated that the first discontinuity (formed during May to July) was mainly caused by the reproductive activity, while the second one (formed during September to February) was mainly caused by the low water temperature and decreased water level. Due to energetic trade-off between somatic growth and reproduction, increasing reproductive effort can lead to decreasing somatic growth rate (Kozlowski [1996]; Joanna et al. [2011]). During breeding season, the feeding rate of R. oxycephalus decreased (unpublished data) while the reproductive effort sharply increased, which, as a result, would put stress on somatic growth. Results from our survey indicated that the rainfall in Laohegou Stream drainage mainly occurred from April to early September, and the water level and the abundance of bait shrunk sharply since mid-September. Along with increasing GSI, large amount of energy would be devoted to the development of gonad. Therefore, the stress of somatic growth of R. oxycephalus increased since then. This provides a possible explanation to why the winter in Laohegou Stream drainage began in November, but the forming of the second discontinuity on otolith began in September. The monthly variations of K N, a useful index for assessing the condition of fish independent of fish size (Baigun et al. [2009]; Llompart et al. [2013]), coincided with our speculation. The K N of R. oxycephalus showed two peak values in March and August, just when the two opaque bands were forming; when the two translucent bands were forming, the value of K N was low. Mills ([1987]) suggested that two translucent bands formed on the otolith of Phoxinus phoxinus during summer and winter in southern England; a similar growth pattern was also suggested for the vertebrae of sharks (Pratt and Casey [1983]; Branstetter and Musick [1994]; Natanson et al. [2002]).


R. oxycephalus in our study presented larger maximum observed TL and faster growth rate than most of its closely related species (Table 2), especially in the early life stage (Figure 10). Results from BCL showed that a large part of individuals had already attained 50% of the maximum observed TL by age 1 year (Figure 6). The fast growth in the early life stage is a common life history trait adopted by fish living in fluctuating environments like Laohegou Stream (Herrera and Fernandezdelgado [1994]; Aparicio and de Sostoa [1998]; Ribeiro et al. [2000]; Vinyoles et al. [2010]), as a bigger body attributes to survive their first harsh season (Baras and Philippart [1999]; Duponchelle et al. [2007]), i.e., winter. As proved, the growth rate of fish usually varies along the latitudinal gradient (Heibo et al. [2005]; Blanck and Lamouroux [2007]). The fast growth of R. oxycephalus in this study might relate to its lowest latitude distribution. TL distribution and BCL at each age indicated that females grow faster than males and dominated the larger size groups. Larger body could induce females to contribute more energy to reproduction and producing more offspring (Parker [1992]), which is significant for the R. oxycephalus to maintain its population in the fluctuating environment. The WLR of R. oxycephalus was similar to that of its closely related species (Table 2).
Table 2

Length-weight relationship parameters of R. oxycephalus and closely related species







Length range (mm)

r 2


R. oxycephalus

Laohegou Stream

32° 31′ N, 104° 40′ E


1.3 × 10−5 (♂)


46.8 to 123.6 (TL)


Present study


4.9 × 10−6 (♀)


52.9 to 158.1 (TL)


R. lagowskii

Suifen River

43° 20′ N, 130° 20′ E


3.67 × 10−5


24 to 138 (SL)


Wang et al. ([2012])

R. percnurus

Suifen River

43° 20′ N, 130° 20′ E


7.91 × 10−5


32 to 88(SL)


Wang et al. ([2012])

C. cumberlandensis

Young's Creek

37° 15′ N, 76° 43′ W


1.88 × 10−5 (♂)


20 to 67.5 (SL)


Starnes and Starnes ([1981])


1.86 × 10−5 (♀)




P. phoxinus

Atares River

42° 45′ N, 0° 14′ W


9.1 × 10−6


31.0 to 74.0 (TL)


Leunda et al. ([2006])

P. phoxinus

Middle Gallego

42° 32 N′, 0° 19′ W


5.4 × 10−6


50.0 to 94.0(TL)


Leunda et al. ([2006])

P. phoxinus

Larraun River

42° 57′ N to 1° 50′ W


4.2 × 10−6


22.0 to 84.0 (TL)


Oscoz et al. ([2005])

P. phoxinus




1.07 × 10−5




Oscoz et al. ([2005])

Figure 10

Mean standard length at age for R. oxycephalus and closely related species. (a) R. oxycephalus in Laohegou Stream (32° 30′ N, 104° 38′ E), (b) R. lagowski in Suifen River (43° 20′ to 44° 40′ N, 130° 20′ to 132° 30′ E), (c) R. percnurus in Suifen River (43° 20′ to 44° 40′ N, 130° 20′ to 132° 30′ E), (d) C. tennesseensis in Tennessee stream (36° 34′ N, 82° 26′ W), (e) P. phoxinus in Frome River (50° 19′ N, 2° 20′ W), (f) P. phoxinus in Utsjoki River (69° 38′ N, 27° 04′ E).


The logistic model indicated that 50% sexual maturity of R. oxycephalus occurred at 1 year when they reached an SL of 64.9 mm for females and 49.6 mm for males. The age at maturity of its closely related species showed gradual changes along the latitudinal gradient, from 1 to 2 years and up to 6 years, while their SLs at maturity were similar (Table 3). Commonly, the age at maturity would be affected by environmental determinants of growth; populations in lower latitude regions often need less time to reach size for maturation (Clarke et al. [2007]). The size and age at sexual maturity are important life history traits, which have profound influence on other life history characteristics such as ultimate body size, mortality, and reproductive success (Stearns [1992]; Bernardo [1993]; Roff [2002]; Barthel et al. [2008]). For example, early maturity has side effect on longevity, somatic growth, and fecundity (Heino et al. [2002]). The results from the back-calculation of the only four full 4-year aged individuals showed that their SLs at 1 year were 53.53, 56.78, 57.2, and 57.61 mm, respectively, and their mean SLs at each age were 56.3 mm (1 year), 89.4 mm (2 years), and 120.2 mm (3 years). Those results indicated that none of these four individuals reached maturity at 1 year and their mean growth rate after 1 year was higher than the average of the whole population. So we speculated that early maturity has side effect on the longevity and somatic growth of R. oxycephalus.
Table 3

Reproduction parameters of R. oxycephalus and closely related species




Ripe egg diameter

SLmfor female

SLmfor male

Mature age

Spawn season






(mean ± SD)

R. oxycephalus

Laohegou Stream

32° 31′ N, 104° 40′ E





April to August

2,457 ± 1,056

C. tennesseensis

Tennessee Streama

36° 34′ N, 82° 26′ W





April to July

556 ± 46

C. cumberlandensis

Young's Creekb

37° 15′ N, 76° 43′ W

0.82 to 1.36




April to July


R. lagowskii

Suifen Riverc

43° 20′ N, 130° 20′ E






2,142 ± 467

R. percnurus

Suifen Riverc

43° 20′ N, 130° 20′ E






2,567 ± 303

P. phoxinus

Frome Riverd

50° 19′ N, 2° 20' W





April to August


P. phoxinus

Lake Konnevesie

62° 36′ N, 26° 31′ E





May to July

632.6 ± 112

P. phoxinus

Utsjoki Riverf

69° 41′ N ,27° 06′ E





April to August


aHamed et al. ([2008]); bStarnes and Starnes ([1981]); cWang et al. ([2012]); dMills ([1987]); eMills and Eloranta ([1985]); fMills ([1988]).

Our study showed that in Laohegou Stream, R. oxycephalus spawned from April to mid-August, which was similar with P. phoxinus in Frome River and Utsjoki River (Mills [1987], [1988]). For Chrosomus tennesseensis in Tennessee Stream and Chrosomus cumberlandensis in Young's Creek, spawning occurred from April to July (Starnes and Starnes [1981]; Hamed et al. [2008]). P. phoxinus in Konnevesi Lake showed delayed and shortened spawning period, from May to July (Mills and Eloranta [1985]). Spawning at an appropriate time plays a crucial role for successful reproduction of fish (Lowe-McConnell [1987]; Wootton [1990]). For fishes living in fluctuating waters, the spawning season often coincides with local annual flood (Welcomme [1979]; Goulding [1980]), because flood brings abundant organics from the terrestrial ecosystem into the river ecosystem, increasing the food availability and providing more suitable breeding habitats (Goulding [1980]; Lowe-McConnell [1987]; Alkins-Koo [2000]). The spawning season of R. oxycephalus in Laohegou Stream was almost simultaneous with local main rainfall period (from April to early September).

The size frequency distribution of oocytes during the spawning season indicated that R. oxycephalus produced batches of oocytes at different times. Repeated spawning over a long breeding period could help avoid a very high density of juveniles at one time, making better use of the diets and thus improving the survival rate of juveniles (Cambray and Bruton [1984]; Burt et al. [1988]; Vinyoles et al. [2010]). This is an important life history trait especially for the fish living in fluctuating environments since it contributes to the recruitment of the populations (Nikolsky [1963]). Commonly, the fecundity was postitively associated with body size (Wootton [1990]). The R. oxycephalus in Laohegou Stream presented the highest fecundity and the largest oocyte among its closely related species that have been reported (Table 3). This is possibly attributable to its large body size. It is well known that larvae hatched from larger oocytes tend to survive better (Ware [1975]; Mann and Mills [1979]). Early maturity, added by long breeding period and high GSI, indicated a high reproductive effort of R. oxycephalus.


In conclusion, R. oxycephalus is a short-lived, fast-growing, early-maturing, and highly fecund species. Therefore, even a short recovery time after overexploitation or disturbance would be of great use for their restoration. Many life history traits of R. oxycephalus are typical traits for species inhabiting fluctuating waters, indicating its great fitness to local environment. Compared with its closely related species that are distributed in higher latitude regions, R. oxycephalus grows faster and matures earlier, which may be responses to lower latitude distribution and local environmental conditions.



analysis of covariance:


back-calculated total length:


body weight:


coefficient of variation:


annual fecundity:


gonado-somatic index:


gonad weight:


total length-body weight relationship:


marginal increment ratio:


predicted somatic weight:




relative fecundity:


standard length:


somatic weight:


total length:


TL at 50% maturity:


von Bertalanffy growth formula:



This study received financial support from the State Key Program of the National Natural Science Foundation of China (grant no. 41030208), the Sichuan Nature Conservation Foundation (SNCF), and The Nature Conservancy (TNC). We thank Ms. Juan Lei, Mr. Xing-Gui Cai, Mr. Xiang-Hui Chen, and Mr. Peng Zhao for their assistance in sample collection and procedure. We also thank Dr. Wen Xiong, Mr. Juan Tao, Mr. ABM Khaldun, and Ms. Helen for their constructive comments on earlier versions of this manuscript.

Authors’ Affiliations

Laboratory of Biological Invasion and Adaptive Evolution, Institute of Hydrobiology, Chinese Academy of Sciences
University of Chinese Academy of Sciences
School of Life Sciences, Peking University


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