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<br />/ <br /> <br />/.-~ <br /> <br />~ <br /> <br />r <br /> <br />animals (3, 19) are also considered prerequisites of a successful <br />translocation. <br />We found thar several rfaaors were associated with success of <br />translocarions (fable 1). Native game species were more likely to be . <br />successfully tranSlocated than werethrc:atened. endangered. or <br />sensitive species. Increased habitat quality was associared with <br />greater success. Translocations into the core of species historical <br />ranges were more successful than were those on the periphery of or <br />outside historical ranges. Herbivores were more likc:ly to be success- <br />full)' translocated than either carnivores or omnivores. Trans!oca- <br />tions intQ areas with potential competitori of similar life fann were <br />less successful than rrans1ocations into areas \\ithout competitors or <br />areas, with a congeneri~ potential competitor. Early breeders with <br />large clutches were slightly more likely to be successfully translocat- <br />ed than were species that bred late and had small clutches. <br />Translocations of exclusively wild-caught animals were more <br />likely to succeed than were those of exclusively captive-reared <br />animals (fable 1). Among translocations of exclusively wild-caughr <br />animals, success depended (P:S 0.10) on whether the source popu- <br />lation density was. high (779ft success, " = 109), medium (78%, <br />II = 37), or low (37%, " = 8). Success ohranslocations of wild:- <br />caught animals was also associated (P s 0.10) with whether the <br />source population was increasing (83% success, " = 93), stable <br />(63%, n = 49), or declining (44%,,, = 9). Successful translocations <br />released more animals than unsu(:cessful translo-::ations (160 com- <br />pared to 54, respecrively;P = 0.024). <br />Our resullts are consistent with analyses of naturally invading or <br />COlOnizin~' pc:cies that show (i) larger founde:r populations ,are more <br />successful ( ,21), (ii) that habitat suitability is important (21), and <br />(iii) incr ed number and size of clutches enhances successful <br />invasion (2f)' Our data also support the h}'J>Othesis that herbivores <br /> <br /> <br />Table 1. perentage success ofintcnrional introductions or reintroductions <br />(tr3llslocatio s) of narive birds and mammals 10 the wild in AUstralia, <br />C3Ilada, Ha '3ii, New Zc.1bnd, and the United States between 1m and <br />1986, Data . ere obtained from a survey conducted in 1987 (15), The data <br />include 134 ~ransJocations ofbirds and 64 translocations of mamnuls_ For ;ill <br />\'ariables list~d, ,twu statistically signiliant (P :S 0.10),implyingtnJC, <br />, dilTen:ncesiq the percentages of suCccssful tt;iiU\ocations among the catego- <br />ries. Anim~that first give binh at age 1 or kss with average clutch sizcof <br />three or mor~ are considered arly brccdcrs with large clutches; all othcrsare <br />late brcc:dersiwith small clutches. <br /> <br />Variabk <br /> <br />T cans- Succcss <br />locations <br />(II) (%) <br />80 44 <br />118 86 <br />63 84 <br />98 69 <br />32 38 <br />133 76 <br />54 48 <br />163 75 <br />34 38 <br />40 48 <br />145 77 <br />13 38 <br />102 7S <br />96 62 <br />39 72 <br />48 52 <br />105 75 <br /> <br /> <br />T1uC'atened, ~ndangered, or ~nsitive species <br />:-:ati\'e gamei <br />Rdeasc: area Ihabitat <br />Excellent i <br />Good . <br />_Fair or pobr <br />Location of tdcase <br />" Core of h~toric range <br />, Periphery pr outside <br />Wild-caught i <br />Captive-rear+t <br />Adult food Habit <br />Cami~'bre l <br />,H~rblvorci'"v: <br />_Omnivorei <br />Early brccdct, laric clutch <br />Late breederl small clutch <br />Potential corhpctitors <br />Congeneri~ <br />Similar i <br />Neither i <br />I <br />i <br /> <br />I <br /> <br />478 <br /> <br />are more successful invaders than carnivores (17) and the conclusion <br />that, for birds, morphologically similar speCies have a greater <br />depressing effect on successful invaSi9n than do congeneric species <br />(~. , <br />We found no consistent association oftraI1slocation success with <br />number of releases, habitat i~provcment, whether the release was <br />hard (no food and shelter provided on site) or soft,immediate: or <br />delayed release on site, or average physical condition of animals at <br />release. We were un.able to directly evaluate genetic he:terogeneity. <br />sex and age composition, o~ specific rearing and handling proce- <br />dures for released animals because of inadequate response: to survey <br />questions. <br /> <br />Evalua~g Alternative Strategies' <br /> <br />Analyscs of individual factors associated with translocation suc- <br />cess dci not adequately reflect the multivariate' nature of actUal <br />translocations. To overcome this problem, we used stepwise logistic <br />regression (24, 25) to develop preliminary predicti\'e' equations for <br />estimating the success of trans locations (Table 2). An cxpandeddata <br />set or independent sample would probably rield diffen:nnegression <br />coefficients and estimates of success than we report. As a result, <br />extrapolation to conditions much diffe:rent than those represented <br />by our data and applications to individual species are discouraged. <br />The: coefficients from Table 2 can be used to plot predicted succesS <br />of different kinds' of translocations as a function of continuous <br />\'ariable:s such as the: number released, We: prescnt an example for a <br />threatene:d,endangered,or sensitive bird (Fig. 1). <br />This exercise (Fig, 1) illustrates that the increase in success <br />associated with releasing larger numbers of organisms' quickly <br />becomes asymptotic. Releases larger than 80 to 120 birds do little: to <br />increase: the chances that a translocation will be successful for this <br />particular set of conditions. The asymptotic property is consistent <br />across other classifications of the data but the inflection point ,.aries_ <br />For large nati\'e game m:lmmals the asymptote is reached at releases <br />of 20 to 40 animals with aconcurrentlv higher prediC:i:ed,sllccess.,' <br />The as}'mptoricproPerty of thca'ssociation of 'translocation <br />success and number released (Fig. 1) is consistent with theoretical <br />predictions (13) and analytical treaune:ncs (26) to'lat suggest a <br />threshold population size below which extinction is li~e1y, primarily' <br />due to chance ~ents affecting birth and death of in4ividuals;,The <br />, existence of the inflection (Fig. 1) is also consistent with the <br />prediction ofathrcshold density below whichpopuJationsocial, <br />inte:ractions and mating succc.sSare disrupted (27), again Ie:ading to <br />diminished population viability. <br />The coefficients from Table 2 and relationships presented in Fig. 1 <br />can be used to asse:ss alternative strategics-Suppose: 300 threatened <br />and endangered birds are available for a translocation program and <br />they must be released during a 3-year time frame:.-Funher suppose <br />that two pote:ntial translocation are:aSare available within the core of <br />the species historical range. If the goa,1 of the: translocation is to <br />'establish at least one geographically disjunct population to reduce <br />the risk of catastrophic loss of the species, how should the birds be <br />distributed betwee:n the two potential translocation areas to mini- <br />mize the: probability that botlltranslocations will f~il? <br />If both releasearcas havc-cxcellent, habitat quality, and the: are:as <br />arc inde:pendent,the answer-is obvious. The birds should be divided <br />betwe:en the: areas. The coefficients from Table 2 allow us to estimate <br />the probability that a single: release of 300 birds will fail (1.0 minus <br />probability of success) is 0.257. Two rele:asc:s of 150 birds~a~h have <br />individual probabilities of failure of 0,312. The probability, that <br />both will fail is 0.312 X 0.312 = 0.097; substantial gain is achieved <br />by splitting the birds between areas. <br /> <br />c::rn=l'\J'rJ:' vnT ?A( <br /> <br />