The Work Speaks—Part 7: Leaky Sink

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggeration, misrepresentations, errors, and obvious bias. In Part 6 of this series, I critiqued Christopher Lepczyk’s paper Landowners and cat predation across rural-to-urban landscapes, published in 2003. Here, I’m going to examine two studies conducted by Philip J. Baker and various collaborators.

The Studies
In the first study, Baker et al. distributed questionnaires to 3,494 households across a 4.2 km2 area of northwest Bristol (UK), and used responses to estimate cat ownership and predation levels (via prey returned home). [2] This work served as a pilot study for the subsequent study.

The second study, conducted August 2005–July 2006, was also conducted in Bristol. Added to the original 4.2 km2 site were nine 1 km2 sites. The researchers used very similar sampling methods, but, based on results of their pilot study, had somewhat more specific objectives:

  1. To quantify cat density
  2. To quantify the various species of birds killed by cats.
  3. To estimate the impact of cat predation by species and site.
  4. To determine whether the predation observed was compensatory or additive. [3]

Sources and Sinks
Among the authors’ conclusions from the pilot study was that, at least for three of the ten bird species surveyed:

“…it is possible that cat predation was significantly affecting levels of recruitment and creating a dispersal sink for more productive neighboring areas.” [2]

Dispersal sinks or habitat sinks, are patches of low-quality habitat that are unable to sustain a population of a particular species were it not for immigration from higher quality habitat patches—called sources—nearby. So, what Baker et al. are suggesting is that predation by cats may be extensive enough to deplete populations of certain bird species at their study site, such that at least some of the birds observed there were immigrants from nearby habitat.

But the authors also point out that, “despite occurring at very high densities, the summed effects on prey populations appeared unlikely to affect population size for the majority of prey species.” [2] And even for House sparrows, which were among the three species of concern (and, apparently, in decline throughout the UK’s urban areas), Baker et al. note that their “numbers appear to be stable in Bristol as a whole.”

So, is the area a habitat sink or not?

A cursory look at the theory and empirical measurement of source-sink dynamics reveals great complexity. Variations across time and geography must be taken into account—the ebb and flow of local populations might easily be overlooked or misunderstood by applying a short time horizon (i.e., 12 months) and arbitrary boundaries (i.e., those that define the study site). Annual rainfall, for example, can dramatically influence yearly population levels on a local scale. And it’s been shown that source-sink dynamics can occur over distances of 60–80 km. [4] In fact, the determination of sinks and sources in the field can be problematic enough that sources sometimes appear to be sinks and vice-versa. [5]

Given the complex nature of source-sink dynamics, the suggestion by Baker et al. that cat predation may be creating a habitat sink seems rather premature. Such assertions—despite the requisite disclaimers (the authors note only that “it is possible”)—tend to attract attention and gain traction. Longcore et al., for example, cited the pilot study in their 2009 essay, “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return.” [6]

Of greater interest to me, though, are the assumptions Baker et al. used to estimate the impact of cat predation.

Counting Cats and Counting Birds
In both studies, the authors quantified the impact of cat predation on bird populations by comparing different levels of predation with different bird densities. Their maximum impacts, for example, assumed that all cats were hunters—despite the fact that 51–74% of the cats included in the two studies brought home no prey at all—and that bird productivity was zero (i.e., no young birds survive to adulthood). As the authors admit:

“This was clearly not realistic, as the estimated maximum numbers of birds killed typically exceeded breeding density and productivity combined, such that the prey populations studied would probably have gone extinct rapidly at a local level or acted as a major sink for birds immigrating from neighbouring areas.” [3]

But how realistic are their other estimates?

A detailed examination of a single species at a one site (taken from the second study, for which such information is available) illustrates some flaws. I looked at House sparrows for the 1 km2 site designated as ST5277. Here, 18 participants reported that their 22 cats returned a total of 30 prey items, nine of which were birds (two of them “unidentified”). Of the birds returned home, two were House sparrows.

When it comes to estimating impacts, though, Baker et al. use figures of 332–1,245 House sparrows killed by the cats of ST5277. The maximum, we already know, is “not realistic,” but even the minimum seems awfully high. So, where are these birds coming from?

To start with, two adjustments have to be made to the original predation figure. First, the two unidentified birds are “distributed” across the categories of bird species that were identified. Then, we have to account for participant drop-out; not all of the 22 cats were surveyed for the entire year of the study. Now we’re up to an average of 8.7 House sparrows brought home annually by the cats at this site.

But of course there are more than 22 cats at ST5277. Baker et al. estimate that there are 314 of them (although we know very little about the factors that affect their hunting ability and success—for example, their access to the outdoors, age, etc.). We also know that only seven of the 22 cats included in the study brought home prey. In other words, 32% of the cats surveyed were documented hunters. Based on these numbers, then, we can estimate the yearly predation rate of House sparrows at ST5277 to be roughly 125—well short of the minimum proposed by Baker et al. (and just a quarter of their intermediate rate).

There are some minor differences between their method for estimating predation rates and mine. For the most part, though, the “missing” sparrows can be found in the authors’ use of a correction factor (3.3) proposed by Kays and DeWan to account for prey killed but not returned home. [7] Undoubtedly, cats fail to bring home all the prey they catch (though they also undoubtedly bring home prey they didn’t kill), but there is good reason to doubt Kays and DeWan’s “correction.” Among the flaws in their analysis were small, dissimilar samples of cats, and a failure to account for highly skewed data sets.

So, even setting aside the complexities of source-sink dynamics, these inflated predation rates, combined with the fact that “the estimates of breeding density presented in this manuscript should be regarded as minima,” [3] raise serious doubts about whether the site is in fact a habitat sink (or, if so, to what extent).

Compensatory and Additive Predation
As I’ve discussed previously, even accurately predicted levels of predation can be deceptive. There’s compensatory predation (in which prey would have died even in the absence of a particular predator, due to illness, starvation, other predators, etc.) and additive predation (in which healthy prey are killed). It’s the difference between, as Beckerman et al. put it, the “doomed surplus hypothesis” and the “hapless survivor hypothesis.” [8]

When it comes to relating predation to population levels, it’s critical to understand the difference, and know the extent to which each type is occurring.

To get at this critical issue, Baker et al. compared the physical attributes (e.g., muscle mass score, mean fat score, etc.) of 86 birds killed by collisions (e.g., with cars, windows, etc.) to those of 48 birds killed by cats. Although the authors point out, “the relationship between body mass and quality (i.e., likelihood of long-term survival and therefore reproductive potential) in passerines is complex,” they nevertheless conclude that the birds killed by cats “were likely to have had poor long-term survival prospects.” [3] (An earlier study comparing spleen mass arrived at essentially the same conclusion: that birds killed by cats “often have a poor health status.” [9])

Still, Baker et al. express caution about their findings:

“The distinction between compensatory and additive mortality does, however, become increasingly redundant as the number of birds killed in a given area increases: where large numbers of prey are killed, predators would probably be killing a combination of individuals with poor and good long-term survival chances. The predation rates estimated in this study would suggest that this was likely to have been the case for some species on some sites.”

But their inflated predation rates and low estimates of breeding density combine to diminish the apparent level of compensatory predation. Were these estimates adjusted to better reflect the conditions at the site, the “redundancy” the authors refer to would be reduced considerably.

*     *     *

It’s not clear why Longcore et al. cited the pilot study their essay, but left out any mention of the much larger subsequent study. Perhaps it was just a matter of timing—“Cats About Town” was published in August of 2008, while “Critical Assessment” was published in August of 2009. A year is not much time in the world of scientific journals, and it’s possible that the two manuscripts more or less crossed in the mail. On the other hand, the pilot study fits more neatly into the argument put forward by Longcore et al.—an argument that doesn’t even recognize the distinction between compensatory and additive predation.

Of course, Baker et al. did themselves no favors, either. By using inflated predation rates—the result of some peculiar, unjustified assumptions—they virtually buried the most important findings of their study.

References
1. Lepczyk, C.A., Mertig, A.G., and Liu, J., “Landowners and cat predation across rural-to-urban landscapes.” Biological Conservation. 2003. 115(2): p. 191-201.

2. Baker, P.J., et al., “Impact of predation by domestic cats Felis catus in an urban area.” Mammal Review. 2005. 35(3/4): p. 302-312.

3. Baker, P.J., et al., “Cats about town: is predation by free-ranging pet cats Felis catus likely to affect urban bird populations? Ibis. 2008. 150: p. 86-99.

4. Tittler, R., Fahrig, L., and Villard, M.-A., “Evidence of Large-Scale Source-Sink Dynamics and Long-Distance Dispersal among Wood Thrush Populations.” Ecology. 2006. 87(12): p. 3029-3036.

5. Runge, J.P., Runge, M.C., and Nichols, J.D., “The Role of Local Populations within a Landscape Context: Defining and Classifying Sources and Sinks.” The American Naturalist. 2006. 167(6): p. 925-938.

6. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

7. Kays, R.W. and DeWan, A.A., “Ecological impact of inside/outside house cats around a suburban nature preserve.” Animal Conservation. 2004. 7(3): p. 273-283.

8. Beckerman, A.P., Boots, M., and Gaston, K.J., “Urban bird declines and the fear of cats.” Animal Conservation. 2007. 10(3): p. 320-325.

9. Møller, A.P. and Erritzøe, J., “Predation against birds with low immunocompetence.” Oecologia. 2000. 122(4): p. 500-504.

The Work Speaks—Part 6: Pain by Numbers

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggeration, misrepresentations, errors, and obvious bias. In Part 5 of this series, I critiqued Cole Hawkins’ 1998 PhD dissertation. Here, I’m going to untangle some of Lepczyk’s own PhD work: Landowners and cat predation across rural-to-urban landscapes, published in 2003.

The Study
In this study, surveys were distributed across three southeastern Michigan landscapes (rural, suburban, and urban) corresponding to established breeding bird survey (BBS) routes. [2] Among the survey questions:

“If you or members of your household own cats that are allowed access to the outside, approximately how many dead or injured birds a week do all the cats bring in during the spring and summer months (April through August) (0, 1, 2–3, 4–5, 6–7, 8–9, 10–15, 16–20, more than 20)?”

Based on 968 surveys returned from 1654 private landowners (a decent response rate of 58.5%), Lepczyk et al. conclude:

“Across the three landscapes there were ~800 to ~3100 cats, which kill between ~16,000 and ~47,000 birds during the breeding season, resulting in a minimum of ~1 bird killed/km/day.”

Increasing Uncertainty
How do Lepczyk and his collaborators arrive at these figures? It’s not entirely clear, actually. Despite numerous attempts, I’ve been unable to follow all of their calculations. However, using their data, I developed my own estimate: 1,119 outdoor cats, 511 of which were reported to be successful hunters.

Using this figure, I then summed across all three landscapes the birds killed or injured, plus those killed or injured by non-respondents’ hunting cats (based on the ratio of hunters to outdoor cats owned by respondents, or about 50%). The resulting estimate is 15,856 birds killed over the 22-week breeding season—close to the low estimate suggested by Lepczyk et al., but just a third of their maximum.

So, why the discrepancy?

One reason is that, at least for some of their estimates, Lepczyk et al. assumed that every landowner who didn’t respond to the survey owned outdoor cats. This, despite their survey results, which indicated that only about one-third of landowners fell into this category.

But the authors go further, generating predation estimates based on pure speculation, specifically that “non-respondents have 150% the number of outdoor cats as respondents.” [2] It should be noted that Lepczyk et al. also ran another scenario in which non-respondents had half the outdoor cats as did respondents—but, again, in both cases they assume that every non-respondent owned outdoor cats.

As a result of this approach, the authors end up in some strange territory: the estimated number of cats owned by non-respondents (based on the assumptions described above) far exceeds the number owned by respondents—by more than a two-to-one margin, in some cases. If the greatest impacts are going to be attributable to non-respondents, then what’s the point of doing the survey in the first place? There are accepted methods by which one can manage uncertainty—statistical analysis, confidence intervals, and the like. What Lepczyk et al. have done serves just one purpose: to inflate apparent predation rates.

Skewed Distributions
In addition to the flaws described above, there are some fundamental errors in the way the authors handle their data. Like so many others, Lepczyk et al. ignore the fact that their data is not normally distributed:

  1. Lepczyk et al. use the average number of birds killed/cat to calculate the total number of bids killed for each of the three landscapes. As I discussed previously), this is a highly positively skewed distribution—using a simple average, therefore, greatly overestimates the cats’ impact (by as much as a factor of two).
  2. A similar error is made when the authors use an average to describe the number of outdoor cats owned by each landowner. Again, because this is a skewed distribution, their use of a simple average exaggerates the extent of predation.
  3. The two inflated figures described in (1) and (2) are multiplied together, further inflating estimated predation rates.

Barratt has suggested that “median numbers of prey estimated or observed to be caught per year are approximately half the mean values, and are a better representation of the average predation by house cats based on these data.” [3] Accounting for the first point alone, then, my estimate is reduced to 8,000 birds killed over the 22-week breeding season.

Accounting for the second point is somewhat trickier. For one thing, we don’t know what constitutes an outdoor cat here—the survey simply asked respondents if they owned cats “that are allowed access to the outdoors.” [2] However, we do know the results of a 2003 survey, which indicated that nearly half of the cats with outdoor access were outside for two or fewer hours a day. And 29% were outdoors for less than an hour each day. [4] Although these figures almost certainly reflect owners in urban and suburban landscapes more than those in rural landscapes, it’s clear that a simple yes-or-no question on the subject is insufficient. Indeed, such a question will invariably overestimate the number of “outdoor cats”—which in turn overestimates predation rates.

This, coupled with the error inherent in using a simple average, pushes predation estimates lower. And the third point reduces those estimates further still. Taken together, these corrections could put my estimate closer to 4,000 birds. More important, the upper estimate proposed by Lepczyk et al.—47,000 birds—could easily be 10 times too high.

The Small Print
Despite their inflated figures, Lepczyk et al. suggest—rather absurdly, in light of the substantial flaws described above—that perhaps their estimates are actually too conservative:

“One caveat to our study is that landowners may have underestimated the number of cats they allow access to the outside. Such a result was found in a similar study of landowners in Wisconsin (Coleman and Temple, 1993).” [1] (Note: After reviewing “Rural Residents’ Free-Ranging Domestic Cats: A Survey,” [5] I’ve found no evidence of such a result.)

“… we found that a very common volunteered response among landowners that had no outdoor cats was that either their neighbors owned outdoor cats or that feral cats were present in the vicinity of their land… [suggesting] that at least some landowners under reported or chose not to report the number of outdoor cats they owned.”

But what about their reports of birds brought home killed or injured—how trustworthy were those? After all, the survey (mailed during the first week of October) asked respondents to recall the number of birds their cat(s) brought home April through August. Surely, there was a lot of guesswork involved. In fact, David Barratt found this kind of guesswork to overestimate predation rates. In a study published five years prior to “Landowners and Cat Predation,” Barratt concluded, “predicted rates of predation greater than about ten prey per year generally over-estimated predation observed.” [3]

The two studies cannot be compared directly for a number of reasons, but by way of comparison, the average predation rate used by Lepczyk et al. is approximately 31 birds/cat for the 22-week breeding season. Using Barratt’s work, in which the “heaviest” six continuous months correspond to about 58% of yearly prey totals, [6] I converted this to a yearly rate of 53 birds/cat/year. Barratt has shown that the actual predation rate, at this level, is less than half the rate predicted by cat owners. In other words, predictions of 50 birds/year generally correspond to catches closer to 25 birds/year.

While Lepczyk et al. emphasize the potential for under-estimating predation levels, they never consider the risk of over-estimating these levels—or their most obvious potential source of error: landowners’ recollections of birds killed. The authors question respondents’ reports of outdoor cats, but accept without question their reports of birds injured or killed over the previous six-month period. And, as Barratt indicated, such reports can be inflated by a factor of two or more!

Something else I find troubling comes, of all places, from the Acknowledgements section. Among those thanked “for helpful and constructive reviews” are American Bird Conservancy (ABC) president George Fenwick and Linda Winter, director of ABC’s Cats Indoors! campaign. It’s not clear how Fenwick and Winter contributed to the final paper, but their involvement on any level raises questions about possible bias. Certainly, Winter has credibility issues when it comes to “research” about the impact of free-roaming cats on birds, as I’ve already described (see also pp. 18–24 of TNR Past present and future: A history of the trap-neuter-return movement [7]).

*     *     *

The same year Lepczyk’s paper was published, the American Veterinary Medicine Association held an Animal Welfare Forum “devoted to the management of abandoned and feral cats.” [8] In attendance were more than 200 veterinarians, animal control officials, wildlife conservationists, and animal advocates—each with a different perspective on feral cats in general and TNR in particular.

In welcoming this diverse group, then-President-Elect Bonnie Beaver recognized the range of contentious issues before them:

“Feral cats evoke hot debates about ecological issues, individual cat welfare, human responsibilities, intercat disease transmission, humaneness, zoonosis control, and management and dissolution of unowned cats.” [8]

Amidst the “hot debate,” though, Beaver was optimistic:

“We will not always agree, but we will come away with increased knowledge and a renewed commitment to work for the welfare of all the animals with which we share the earth” [8]

While I tend to share Beaver’s optimism, I think the debate is hurt—if not derailed entirely—by the publication of research aimed not at increasing our collective knowledge, but rather at supporting a particular position. Like Cole Hawkins’ dissertation, “Landowners and Cat Predation” is, at best, an interesting pilot study for subsequent work. And yet, it’s widely—and uncritically—cited in the feral cat/TNR literature. Longcore et al., for example, refer to it as “evidence [indicating] that cats can play an important role in fluctuations of bird populations,” [9] despite the fact that Lepczyk et al. don’t actually address the issue of bird populations at all. More recently, Dauphiné and Cooper use the inflated predation rate suggested by Lepczyk et al. (along with rates proposed by other researchers) to arrive at their “billion birds” figure. [10]

The method employed in “Landowners and Cat Predation”—asking owners of cats to recall the number and species of birds over the previous six-month period—invites overestimation from the very outset. Lepczyk et al. then inflate these numbers through both careless (e.g., using averages to describe skewed data) and deliberate (e.g., assuming all non-respondents owned cats—perhaps 50% more than respondents did) means. Rather than getting us any closer to the truth about cat predation, this study only obscured it further.

Worse, it’s been packaged and sold—and subsequently “bought”—as rigorous science, thereby giving it an undeserved legitimacy. Such efforts are impediments to knowledge and understanding—and therefore, to progress.

References
1. Lepczyk, C.A., et al., “What Conservation Biologists Can Do to Counter Trap-Neuter-Return: Response to Longcore et al.” Conservation Biology. 2010. 24(2): p. 627-629.

2. Lepczyk, C.A., Mertig, A.G., and Liu, J., “Landowners and cat predation across rural-to-urban landscapes.” Biological Conservation. 2003. 115(2): p. 191-201.

3. Barratt, D.G., “Predation by house cats, Felis catus (L.), in Canberra, Australia. II. Factors affecting the amount of prey caught and estimates of the impact on wildlife.” Wildlife Research. 1998. 25(5): p. 475–487.

4. Clancy, E.A., Moore, A.S., and Bertone, E.R., “Evaluation of cat and owner characteristics and their relationships to outdoor access of owned cats.” Journal of the American Veterinary Medical Association. 2003. 222(11): p. 1541-1545.

5. Coleman, J.S. and Temple, S.A., “Rural Residents’ Free-Ranging Domestic Cats: A Survey.” Wildlife Society Bulletin. 1993. 21(4): p. 381–390.

6. Barratt, D.G., “Predation by House Cats, Felis catus (L.), in Canberra, Australia. I. Prey Composition and Preference.” Wildlife Research. 1997. 24(3): p. 263–277.

7. Berkeley, E.P., TNR Past present and future: A history of the trap-neuter-return movement. 2004, Bethesda, MD: Alley Cat Allies.

8. Kuehn, B.M. and Kahler, S.C. The Cat Debate. JAVMA Online 2004 November 27, 2009 [accessed 2009 December 24].  http://www.avma.org/onlnews/javma/jan04/040115a.asp.

9. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

10. Dauphiné, N. and Cooper, R.J., Impacts of Free-ranging Domestic Cats (Felis catus) on birds in the United States: A review of recent research with conservation and management recommendations, in Fourth International Partners in Flight Conference: Tundra to Tropics. 2010. p. 205–219.

The Work Speaks—Part 5: Jumping to Conclusions

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggeration, misrepresentations, errors, and obvious bias. In Part 4 of this series, I discussed how feral cat/TNR researchers often misuse averages to characterize skewed distributions, and how that error overestimates the impact of free-roaming cats on wildlife.

For the next few posts, I’m going to critique three of the studies most often cited by these researchers, starting with Cole Hawkins’ 1998 PhD dissertation, Impact of a subsidized exotic predator on native biota: Effect of house cats (Felis catus) on California birds and rodents. I mentioned Hawkins’ dissertation previously, but only briefly. Here, I’ll take a closer look, paying particular attention to how he gets from his results to his rather dubious conclusions.

The Study
Hawkins’ two-year study was conducted in Alameda County, CA, spread across two adjacent parks. He started by designating a “cat area” (where, nearby, free-roaming cats were being fed) and a “no-cat area” (where no cats were being fed), and then designated “rodent grids” (nine locations used for trapping and counting rodents) and walking transects (from which bird surveys were conducted) in each area. Hawkins then compared the number of birds and rodents detected in the two areas.

Among Hawkins’ conclusions:

“The differences observed in this study were the results of the cat’s predatory behavior.” [2] (It should be noted that Hawkins tempered this assertion in his 1999 article summarizing the work: “The differences observed in this study may have been due to the cats’ predatory behavior.” [3] (italics mine))

And this:

“The presence of cats in this study area already has caused a shift in the composition of the rodent community; it is possible that a shift in the larger biotic community could follow.”

And, finally:

“It is not prudent to manage for wildlife and allow cat feeding in the same parks.”

Unfair Comparisons
But Hawkins’ findings are insufficient to supports such claims; indeed, his methodology doesn’t allow for them. Hawkins has no idea what the cat area was like prior to his arrival; he merely assumes the populations of birds and rodents would have been identical to those found at the no-cat area, and makes his comparisons accordingly. In fact, there are a number of factors that indicate that the two areas are not as comparable as Hawkins suggests:

  • The cat area was almost a peninsula, with a lake on one side and a residential area (within 0.5 km) on the other. The no-cat area, on the other hand, was located largely in the interior of the parks.
  • Hawkins notes that there were more people in the cat area (of­ten twice as many as were observed at the no-cat area), but dismisses the possibility that their presence may have influenced the numbers of birds and rodents he observed there.
  • The habitat along the 2.2 km transects from which bird counts were conducted varied considerably between the two areas. Compared to the no-cat area, the cat area had 31% less chaparral, 183% more trees, 52% less grass, and 240% more “modified” habitat (it’s not clear what Hawkins means by “modified,” but I assume it refers to habitat that reflects significant human impact).
  • Finally, the presence of pesticides may have played a role. According to a 2002 report (the earliest I was able to find) from the East Bay Regional Park District, “The focus of Lake Chabot’s weed control efforts are vegetation reduction within the two-acre overflow parking lot, picnic sites and firebreaks around park buildings, corp. yard, service yard, and the Lake Chabot classroom.” [4] And it’s clear from Hawkins’ 1999 article that the cat area did include picnic sites: “…over half of the cat scat in this study was collected under and around picnic tables.” [3] Now, Hawkins’ fieldwork was done in 1995 and 1996, but if there was any pesticide use during the study period, it may have affected the results—especially if the pesti­cide was distributed differently across the two areas.

Cats and Birds
“Almost twice as many birds were seen on the no-cat transect as on the cat transect,” writes Hawkins. But it’s not quite as simple as that—the details reveal a rather complex, often uneven count over the course of the study. Nevertheless—and despite the differences between the two areas—Hawkins’ only explanation is the cats. This is especially true for ground-feeders:

The preference of ground feeding birds for the no-cat treatment was striking; for ex­ample, California quail were seen almost daily in the no-cat area, whereas they were never seen in the cat area.

What’s more striking to me is the fact that five of the nine ground-feeding species included in the study showed no preference for either area. But Hawkins scarcely acknowledges the point, and doesn’t even hint at an explanation. “Birds that were known to nest on or near the ground or in shrubs and vines ≤ 1.5 m in height” also showed no preference between the two areas (though no nest counts were conducted).

The picture painted by Hawkins is that bird species absent from the cat area represent species killed off by the cats. But it’s generally accepted that cats are opportunistic hunters, catching whatever prey is readily available and easily caught. [5–8] Fitzgerald and Turner, for ex­ample, argue that “domestic cats (both house and feral ones) are best described as generalist resident preda­tors, exploiting a wide range of prey, and able to switch readily from one prey to another.” [9] So, how is it that some species were present at the cat site while others were not? Again, Hawkins offers no explanation.

In fact, it’s clear from Hawkins’ study that the cats aren’t much of threat at all to the birds—even vulnerable ground-feeding and ground-nesting species—in the cat area. Of the 120 scat samples found by searching the cat area, “65% were found to contain rodent hair and 4% feathers.” [2] This finding comes toward the end of the study, when the cat population was at its greatest—and still, only 4% contained feathers. And this could easily represent one cat and one bird.

One final point about the birds: Hawkins suggests (without explanation) that the olive-sided flycatcher, American robin, and Stellar’s jay—all of which showed no preference for either the no-cat area or the cat area—may have been responding to a “specialized habitat.” Could it be that the birds not seen in the cat area were also responding to a specialized habitat—by “migrating” to a place with less human activity (e.g., the no-cat area), for example? Once again, Hawkins has no comment.

Cats and Rodents
The fact that scats indicated rodents were predated to a greater extent than birds is hardly surprising [5, 6, 9, 10], but it should be noted the 65% figure represents the frequency of occurrence, and not a predation rate (a topic I address in greater detail here).

Hawkins’ analysis didn’t reveal whether the rodent hair was that of deer mice, harvest mice (both of which were found less often in the cat area than in the no-cat area), house mice (found more often in the cat area), or California voles (which showed no preference for either area). In any case, it’s not clear that the cats were responsible for the presence or absence of any of these rodent species. Again, the selective dietary habits suggested by Hawkins simply don’t fit with the domestic cat’s profile as a “generalist resident predator.”

Two additional points that might explain the differences Hawkins observed concern the habitat of the cat area. First, there’s the nearby lake and residences—potential sources of pollution that could affect nearby plant and animal life. Secondly, there’s the issue of possible pesticide use mentioned previously. As I say, it’s largely conjecture on my part; at the same time, though, it’s easy to imagine its potential impact on small mammals (and ground-feeding birds, for that matter).

Finally, Hawkins suggests that certain bird species were responding to specialized habitat—perhaps the rodents were simply doing the same.

Cats
Hawkins used track plates (baited devices that detect the presence of mammals by way of preserved “footprints”) for “estimating a relative cat presence index,” but found only one cat track in 200 track plate nights. And, “in 560 days of exposure, no scat was found in any of the sand boxes.” [2] Now, the cats were seen at feeding stations and on the rodent grids of the cat area—as many as 26 during a one-week period toward the end of the study. But clearly, they were not where Hawkins was expecting them to be. If, after two years at the study site, Hawkins was unable to get a better handle on the presence of the cats, how can he be so sure of their behavior when it comes to predation?

If, as Hawkins argues, the differences observed between the two areas are a result of the cats’ predatory behavior, then one would expect the number of birds and rodents to decrease as the number of cats increases. Yet, Hawkins’ findings don’t bear this out.

And then there are the unanswered questions about the cats—for example:

  • Where did these cats come from—were they illegally dumped, the result of nearby residents’ unsterilized cats breeding? Did they belong to the residents?
  • Were the cats sterilized? (Their increasing numbers would suggest that they weren’t.)
  • Were these cats part of a managed TNR colony? (Local newspaper reports indicate a long-standing battle between TNR advocates and opponents. [11–13])

Considering the central role these cats played in Hawkins’ two-year study, he knew surprisingly little about their behavior—including various factors that surely had an impact on his findings.

*     *     *

In their recent comment, Lepczyk et al. suggest that conservation biologists and wildlife ecologists “look to the evolutionary biology community” [1] for an example of how to influence policy. For feral cat/TNR opponents interested in shaping policy, it seems Hawkins’ study has become quite popular. [14–17] Actually, Nico Dauphiné and Robert J. Cooper take its already-tenuous claims one step further, citing Hawkins’ work (actually a 2004 conference paper that summarizes his dissertation [18]) as evidence that “the continuous predation pressure exerted by exotic predators in exponentially high densities can and has resulted in numerous local extinctions of continental land birds.” [8]

But is Hawkins’ methodology one that evolutionary biologists would advocate—or even recognize? Not likely.

Hawkins draws conclusions—infers important causal relationships—without any evidence of what “pre-treatment” conditions were like. And ignores entirely his own findings when they contradict his conclusions. Rather than beginning his inquiry with questions to answer, it seems Hawkins had his answer from the outset. At best, his work is an interesting pilot study—generating research questions for a more rigorous, less biased investigation.

References
1. Lepczyk, C.A., et al., “What Conservation Biologists Can Do to Counter Trap-Neuter-Return: Response to Longcore et al.” Conservation Biology. 2010. 24(2): p. 627-629.

2. Hawkins, C.C., Impact of a subsidized exotic predator on native biota: Effect of house cats (Felis catus) on California birds and rodents. 1998, Texas A&M University.

3. Hawkins, C.C., Grant, W.E., and Longnecker, M.T., “Effects of Subsidized House Cats on California Birds and Rodents.” Transactions of the Western Section of the Wildlife Society. 1999. 35: p. 29–33.

4. Brownfield, N.T., 2002 Annual Analysis of Pesticide Use East Bay Regional Park District. 2003, East Bay Regional Park District. www.ebparks.org/files/stew_pest_report_02.pdf

5. Barratt, D.G., “Predation by house cats, Felis catus (L.), in Canberra, Australia. II. Factors affecting the amount of prey caught and estimates of the impact on wildlife.” Wildlife Research. 1998. 25(5): p. 475–487.

6. Fitzgerald, B.M., Diet of domestic cats and their impact on prey populations, in The Domestic cat: The biology of its behaviour, D.C. Turner and P.P.G. Bateson, Editors. 1988, Cambridge University Press: Cambridge; New York. p. 123–147.

7. Lepczyk, C.A., Mertig, A.G., and Liu, J., “Landowners and cat predation across rural-to-urban landscapes.” Biological Conservation. 2003. 115(2): p. 191-201.

8. Dauphiné, N. and Cooper, R.J., Impacts of Free-ranging Domestic Cats (Felis catus) on birds in the United States: A review of recent research with conservation and management recommendations, in Fourth International Partners in Flight Conference: Tundra to Tropics. 2010. p. 205–219.

9. Fitzgerald, B.M. and Turner, D.C., Hunting Behaviour of domestic cats and their impact on prey populations, in The Domestic Cat: The biology of its behaviour, D.C. Turner and P.P.G. Bateson, Editors. 2000, Cambridge University Press: Cambridge, U.K.; New York. p. 151–175.

10. Woods, M., McDonald, R.A., and Harris, S., “Predation of wildlife by domestic cats Felis catus in Great Britain.” Mammal Review. 2003. 33(2): p. 174-188.

11. Chui, G., Stray Cats Live Harsh Lives in Area Parks, in San Jose Mercury News. 1985. p. 1

12. Bogue, G., Those Poor Cats Need a Human Assist, in Contra Costa Times. 1997: Walnut Creek, CA. p. A02

13. n.a., Spring controversy: What to do with feral cats?, in San Mateo Daily Journal, The (CA). 2001.

14. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

15. ABC, Domestic Cat Predation on Birds and Other Wildlife. n.d., American Bird Conservancy: The Plains, VA. www.abcbirds.org/abcprograms/policy/cats/materials/predation.pdf

16. Winter, L. and Wallace, G.E., Impacts of Feral and Free-Ranging Cats on Bird Species of Conservation Concern, G.E. Wallace, Editor. 2006, American Bird Conservancy. www.abcbirds.org/newsandreports/NFWF.pdf

17. Ash, S.J. and Adams, C.E., “Public Preferences for Free-Ranging Domestic Cat (Felis catus) Management Options.” Wildlife Society Bulletin. 2003. 31(2): p. 334–339.

18. Hawkins, C.C., Grant, W.E., and Longnecker, M.T. Effect of house cats, being fed in parks, on California birds and rodents. in Proceedings Of The 4th International Symposium On Urban Wildlife Conservation. 2004. Tucson, AZ: University of Arizona. http://cals.arizona.edu/pubs/adjunct/snr0704/snr07042l.pdf

The Work Speaks—Part 4: Mean Spirited

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggeration, misrepresentations, errors, and obvious bias. In Part 3 of this series, I discussed the distinction between compensatory and additive predation. Here, I’ll focus on how feral cat/TNR researchers often misuse averages to characterize skewed distributions, and how that error overestimates the impact of free-roaming cats on wildlife.

Something’s Askew
When a data set is skewed, it is inappropriate to use the mean, or average, as a measure of central tendency. The mean should be used only when the data set can be considered normal—the familiar bell curve. As Woods et al put it:

“the simple average number of animals brought home is not a useful measure of central tendency because of the skewed frequency distribution of the numbers of prey items brought home…” [2]

Studies of cat predation routinely reveal a positively skewed distribution; a few cats are responsible for many kills, while many of the cats kill few, if any, prey. So when researchers use the mean to calculate the total number of prey killed by cats in a particular area, they overestimate the cats’ impact.

How common is this? Very [see, for example, 3-9]. Of the many cat predation studies I’ve read, only a few [2, 10, 11] properly account for the skewed nature of this distribution. And others [12-17] often take these inflated figures at face value—as evidence of the impact cats have on wildlife. Published repeatedly, the erroneous estimates take on an undeserved legitimacy.

The proper method for handling skewed distributions involves data transformations, the details of which I won’t go into here. The important point is this: in the case of a positively skewed distribution, the back-transformed mean will always be less than the simple mean of the same data set.

Big Deal
Depending on the particular distribution, the difference between the simple mean and the back-transformed mean can be considerable. Let’s use the 2003 study by Woods et al. [2] to illustrate. In the case of mammals killed and returned home by pet cats, the back-transformed mean was 28.3% less than the simple mean. Or, put another way, the simple mean would have overestimated the number of mammals killed by 39.5%. Similarly, when all prey items were totaled (as depicted in the illustration above), the simple mean would have overestimated the total number off all prey (mammals, birds, herpetofauna, and “others”) by 46.9%.

On the other hand, the figures for birds appear to break the rule mentioned above. In this case, the back-transformed mean (4.1) is actually a bit higher than the simple mean (4.0). How can this be? In order to log-transform the data set, Woods et al. had to first eliminate all the instances where cats returned home no prey—you can’t take the logarithm of 0. So, they were actually working with two data sets. Now, the second data set—which includes only those cats that returned at least one prey item—is also highly positively skewed. As a point of reference, its simple mean was approximately 5.6 birds/cat, which, compared to the back-transformed mean, is an overestimation of 37.5%.

By now, it should be apparent that log-transformed means have another important advantage over simple means: because you have to eliminate those zeros from the data set, you are forced to focus only on the cats that returned prey home—which, of course, is the whole point of such studies! And in the case of this study, Woods et al. found that 20–30% of cats brought home either no birds or no mammals. And 8.6% of the cats brought home no prey at all over the course of the study.

Transforming a data set (and then back-transforming its mean) is simpler than it sounds, but Barratt offers a useful alternative, rule-of-thumb method (one echoed by Fitzgerald and Turner [18]):

“…median numbers of prey estimated or observed to be caught per year are approximately half the mean values, and are a better representation of the average predation by house cats based on these data.” [10]

So, whereas Dauphiné and Cooper (and others) suggest increasing such estimates by factors of two and three (“predation rates measured through prey returns may represent one half to less than one third of what pet cats actually kill…” [14]), they should, in fact, be reducing them by half.

Cat Ownership
There are other instances in which simple averages are used to describe similarly skewed distributions—with similar results. That is, they overestimate a particular characteristic—and not in the cats’ favor.

Cat ownership, for example, is not a normal distribution. Many people own one or two cats; a few people own many cats. This is precisely what Lepczyk et al. found in their 2003 study:

“The total number of free-ranging cats across all landscapes was 656, ranging from 1 to 30 per landowner…” [6]

In fact, about 113 (I’m estimating from the histogram printed in the report) of those landowners owned just one cat apiece. About 70 of them owned two cats. Only one—maybe two—owned 30 cats. And yet, Lepczyk et al. calculate an average of 2.59 cats/landowner (i.e., 656 cats/253 landowners who allow their cats outdoors), thereby substantially overestimating cat ownership—and, in turn, predation rates (which calculations are based upon the average number of cats/landowner).

Lepczyk et al. are not the only ones to make this mistake; several other researchers have done the same. [4, 5, 7-9]

Outdoor Access
The amount of time cats spend outdoors is also highly positively skewed, as is apparent from the 2003 survey conducted by Clancy, Moore, and Bertone. [19] Their work showed that nearly half of the cats with outdoor access were outside for two or fewer hours a day. And 29% were outdoors for less than an hour each day.

Among those researchers to overlook the skewed nature of this distribution are Kays and DeWan, who calculate an average of 8.35 hours/day. This greatly overestimates potential predation, and leads them to conclude—erroneously—that the actual number of prey killed by cats was “3.3 times greater than the rate estimated from prey brought home,” [9] as was discussed previously.

Compound Errors
Clearly, these errors are substantial—in some cases, doubling the apparent impact of cats on wildlife. Of course the errors are even more significant when one inflated figure is multiplied by another—as when Lepczyk et al. [6] multiply the average number of prey items returned by the average number of outdoor cats per owner. The resulting predation figures may well be four times greater than they should be! (Actually, there are additional problems with the authors’ predation estimates, which I’ll address in a future post).

*     *     *

The fact that such a fundamental mistake—one a student couldn’t get away with in a basic statistics course—is made so often is shocking. The fact that such errors slip past journal reviewers is inexcusable.

References
1. Lepczyk, C.A., et al., “What Conservation Biologists Can Do to Counter Trap-Neuter-Return: Response to Longcore et al.” Conservation Biology. 2010. 24(2): p. 627-629.

2. Woods, M., McDonald, R.A., and Harris, S., “Predation of wildlife by domestic cats Felis catus in Great Britain.” Mammal Review. 2003. 33(2): p. 174-188.

3. Coleman, J.S. and Temple, S.A., On the Prowl, in Wisconsin Natural Resources. 1996, Wisconsin Department of Natural Resources: Madison, WI. p. 4–8. http://dnr.wi.gov/wnrmag/html/stories/1996/dec96/cats.htm

4. Baker, P.J., et al., “Impact of predation by domestic cats Felis catus in an urban area.” Mammal Review. 2005. 35(3/4): p. 302-312.

5. Baker, P.J., et al., “Cats about town: is predation by free-ranging pet cats Felis catus likely to affect urban bird populations? Ibis. 2008. 150: p. 86-99.

6. Lepczyk, C.A., Mertig, A.G., and Liu, J., “Landowners and cat predation across rural-to-urban landscapes.” Biological Conservation. 2003. 115(2): p. 191-201.

7. Crooks, K.R., et al., “Exploratory Use of Track and Camera Surveys of Mammalian Carnivores in the Peloncillo and Chiricahua Mountains of Southeastern Arizona.” The Southwestern Naturalist. 2009. 53(4): p. 510-517.

8. van Heezik, Y., et al., “Do domestic cats impose an unsustainable harvest on urban bird populations? Biological Conservation. 143(1): p. 121-130.

9. Kays, R.W. and DeWan, A.A., “Ecological impact of inside/outside house cats around a suburban nature preserve.” Animal Conservation. 2004. 7(3): p. 273-283.

10. Barratt, D.G., “Predation by house cats, Felis catus (L.), in Canberra, Australia. II. Factors affecting the amount of prey caught and estimates of the impact on wildlife.” Wildlife Research. 1998. 25(5): p. 475–487.

11. Barratt, D.G., “Predation by House Cats, Felis catus (L.), in Canberra, Australia. I. Prey Composition and Preference.” Wildlife Research. 1997. 24(3): p. 263–277.

12. May, R.M., “Control of feline delinquency.” Nature. 1988. 332(March): p. 392-393.

13. Jessup, D.A., “The welfare of feral cats and wildlife.” Journal of the American Veterinary Medical Association. 2004. 225(9): p. 1377-1383.

14. Dauphiné, N. and Cooper, R.J., Impacts of Free-ranging Domestic Cats (Felis catus) on birds in the United States: A review of recent research with conservation and management recommendations, in Fourth International Partners in Flight Conference: Tundra to Tropics. 2010. p. 205–219

15. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

16. Winter, L., “Trap-neuter-release programs: the reality and the impacts.” Journal of the American Veterinary Medical Association. 2004. 225(9): p. 1369-1376.

17. Clarke, A.L. and Pacin, T., “Domestic cat “colonies” in natural areas: a growing species threat.” Natural Areas Journal. 2002. 22: p. 154–159.

18. Fitzgerald, B.M. and Turner, D.C., Hunting Behaviour of domestic cats and their impact on prey populations, in The Domestic Cat: The biology of its behaviour, D.C. Turner and P.P.G. Bateson, Editors. 2000, Cambridge University Press: Cambridge, U.K.; New York. p. 151–175.

19. Clancy, E.A., Moore, A.S., and Bertone, E.R., “Evaluation of cat and owner characteristics and their relationships to outdoor access of owned cats.” Journal of the American Veterinary Medical Association. 2003. 222(11): p. 1541-1545.

Available: Resources

As some of you may have noticed, I’ve added a new tab to the Vox Felina site. Resources is where you’ll find printer-friendly documents adapted from Vox Felina content.

The first, “Reassessment: A Closer Look at ‘Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return,’” is a brief review of the essay “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” by Travis Longcore, Catherine Rich, and Lauren M. Sullivan. It’s based on a four-part series of posts from May. Download PDF

The Work Speaks—Part 3: Predatory Blending?

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggeration, misrepresentations, errors, and obvious bias. In a previous post, I presented examples of researchers drawing big conclusions from small sample sizes. Here, I’ll discuss the important distinction between compensatory and additive predation—a point too often left out of the feral cat/TNR discussion.

Sins of Omission
Focusing on the number of prey injured or killed by cats, without also recognizing that there are different types of predation, implies that each and every bird, mammal, reptile, etc. is destined to be part of its species’ breeding population. Of course, that’s not at all how things work out in the natural world—with or without predation by cats.

And yet, numerous studies [2-10], reviews [11], and other published papers [12-14] fail to acknowledge the critical difference between compensatory predation (in which prey would have died even in the absence of a particular predator, due to illness, starvation, other predators, etc.) and additive predation (in which healthy prey are killed). It’s the difference between, as Beckerman et al. put it, the “doomed surplus hypothesis” and the “hapless survivor hypothesis.” [15]

This is a critical point when it comes to connecting predation rates (from cats or any other predator) to population impacts. The more additive the predation, the greater the potential impact on population numbers. Purely compensatory predation, on the other hand, is less likely to affect overall populations. Of course, the connection is seldom so simple and direct, and a number of factors (e.g., habitat area and type, base population numbers, etc.) influence the ultimate outcome—making it quite difficult to tease out specific causal relationships. Nevertheless, if we want to better understand the impact of free-roaming cats on wildlife, we cannot ignore the distinction between—and inherent implications of—these two types of predation.

Honorable Mentions
Although Churcher and Lawton failed to mention the distinction between compensatory and additive predation in their now-classic “English village” study [4], Churcher later suggested that their findings were largely in the compensatory category: “If the cats weren’t there, something else would be killing the sparrows or otherwise preventing them from breeding.” [16]

Woods et al. don’t address the topic directly, but warn against drawing direct connections between predation numbers and potential effects on population dynamics:

“Our estimates of the total numbers of animals brought home by cats throughout Britain should be treated with requisite caution and these figures do not equate to an assessment of the impact of cats on wildlife populations.” [3]

Unfortunately, other researchers have used this study to make exactly that connection. In “Critical Assessment,” for example, Longcore et al. cite Woods et al. (along with Lepczyk et al. 2003, the subject of a future post) when they write, “evidence indicates that cats can play an important role in fluctuations of bird populations.” [11]

Under-Compensating?
In their 2008 study, Baker et al. found that “birds killed by cats in this study had significantly lower fat and pectoral muscle mass scores than those killed by collisions,” [17] suggesting that they may have been among the “doomed surplus” portion of the population. Similar results were reported eight years earlier by Møller and Erritzøe, who found that “small passerine birds falling prey to cats had spleens that were significantly smaller than those of conspecifics that died for other reasons,” concluding ultimately that the birds killed by cats “often have a poor health status.” [18]

But Baker et al. express caution about their findings:

“…the distinction between compensatory and additive mortality does… become increasingly redundant as the number of birds killed in a given area increases: where large numbers of prey are killed, predators would probably be killing a combination of individuals with poor and good long-term survival chances.”

Whatever their concerns, it must be noted that Baker et al. inflated their predation numbers by a factor of 3.3 on the basis of Kays and DeWan’s dubious conclusions [9] (which I discussed in some detail previously). Doing so raises considerable doubts about any level of “redundancy,” as well the authors’ suggestion that cat predation in the area might be “creating a dispersal sink for more productive neighboring areas.” [19] (Such “sinks” can occur when predation outstrips local prey populations, requiring that prey be “recruited” from surrounding areas.)

Implications
Given all the work that’s been done on cat predation, one might expect the subject of compensatory predation to be addressed more fully and more often. By omitting this important issue from the feral cat/TNR discussion, researchers portray a situation both simpler and harsher (in terms of what it implies about the impact of free-roaming cats) than reality suggests. Whether or not such omissions are intentional, I cannot say. I do, however, find it curious—what’s included compared to what’s left out, and by whom.

References
1. Lepczyk, C.A., et al., “What Conservation Biologists Can Do to Counter Trap-Neuter-Return: Response to Longcore et al.” Conservation Biology. 2010. 24(2): p. 627-629.

2. Coleman, J.S. and Temple, S.A., On the Prowl, in Wisconsin Natural Resources. 1996, Wisconsin Department of Natural Resources: Madison, WI. p. 4–8. http://dnr.wi.gov/wnrmag/html/stories/1996/dec96/cats.htm

3. Woods, M., McDonald, R.A., and Harris, S., “Predation of wildlife by domestic cats Felis catus in Great Britain.” Mammal Review. 2003. 33(2): p. 174-188.

4. Churcher, P.B. and Lawton, J.H., “Predation by domestic cats in an English village.” Journal of Zoology. 1987. 212(3): p. 439-455.

5. Coleman, J.S. and Temple, S.A., “Rural Residents’ Free-Ranging Domestic Cats: A Survey.” Wildlife Society Bulletin. 1993. 21(4): p. 381–390.

6. Coleman, J.S. and Temple, S.A., Effects of Free-Ranging Cats on Wildlife: A Progress Report, in Fourth Eastern Wildlife Damaage Control Conference. 1989: University of Nebraska—Lincoln. p. 8–12. http://digitalcommons.unl.edu/ewdcc4/7

7. Hawkins, C.C., Impact of a subsidized exotic predator on native biota: Effect of house cats (Felis catus) on California birds and rodents. 1998. PhD Dissertation, Texas A&M University.

8. Hawkins, C.C., Grant, W.E., and Longnecker, M.T., “Effects of Subsidized House Cats on California Birds and Rodents.” Transactions of the Western Section of the Wildlife Society. 1999. 35: p. 29–33.

9. Kays, R.W. and DeWan, A.A., “Ecological impact of inside/outside house cats around a suburban nature preserve.” Animal Conservation. 2004. 7(3): p. 273-283.

10. Lepczyk, C.A., Mertig, A.G., and Liu, J., “Landowners and cat predation across rural-to-urban landscapes.” Biological Conservation. 2003. 115(2): p. 191-201.

11. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

12. Dauphiné, N. and Cooper, R.J., Impacts of Free-ranging Domestic Cats (Felis catus) on birds in the United States: A review of recent research with conservation and management recommendations, in Fourth International Partners in Flight Conference: Tundra to Tropics. 2010. p. 205–219

13. Coleman, J.S., Temple, S.A., and Craven, S.R., Cats and Wildlife: A Conservation Dilemma. 1997, University of Wisconsin, Wildlife Extension. http://forestandwildlifeecology.wisc.edu/wl_extension/catfly3.htm

14. Andersen, M.C., Martin, B.J., and Roemer, G.W., “Use of matrix population models to estimate the efficacy of euthanasia versus trap-neuter-return for management of free-roaming cats.” Journal of the American Veterinary Medical Association. 2004. 225(12): p. 1871-1876.

15. Beckerman, A.P., Boots, M., and Gaston, K.J., “Urban bird declines and the fear of cats.” Animal Conservation. 2007. 10(3): p. 320-325.

16. n.a., What the Cat Dragged In, in Catnip. 1995, Tufts University School of Veterinary Medicine: Boston, MA. p. 4–6

17. Baker, P.J., et al., “Cats about town: is predation by free-ranging pet cats Felis catus likely to affect urban bird populations? Ibis. 2008. 150: p. 86-99.

18. Møller, A.P. and Erritzøe, J., “Predation against birds with low immunocompetence.” Oecologia. 2000. 122(4): p. 500-504.

Feeding Bans: Policy Hungry for Science

A recent news item from Alley Cat Allies reports “a disturbing and increasing trend of feeding ban proposals as a way to ‘eradicate’ cats from their outdoor homes.” Among the reasons cited for opposing such bans:

  • Cats don’t magically disappear when you stop feeding them—there’s an abundance of garbage available (from households, restaurants, supermarkets, etc.) as an alternative food source. Wherever you find people—and their trash—you’ll also find cats.
  • TNR requires regular feeding schedules. No feeding means no TNR—and no sterilization means more cats, not fewer.
  • Punishing concerned citizens is bad policy, and bad for communities.

I’d like to add one more: The concerns that prompt such proposals are, more than likely, based on erroneous, exaggerated, and/or misleading claims—all made in the name of science.

I’ll bet if I contacted officials in Brookhaven, NY, Wheaton, IL, and Benzie County, MI (communities listed in the Alley Cat Allies story), they’d tell me all about the numerous “threats” posed by free-roaming cats—wildlife killed and injured, rabies, toxoplasmosis, etc. And if pressed, they would almost certainly produce the Travis Longcore/Urban Wildlands Group article from Conservation Biology, some reference to the Wisconsin Study, a clipping of the L.A. Times story from January, or some comparable (read: dubious) bit of “evidence.”

Which is precisely what Longcore et al. are pushing for:

Conservation scientists and advocates must properly identify the environmental implications of feral cat management and actively engage this issue to bring scientific information to the attention of policy makers. [1]

I’ve got nothing against scientists getting involved with policy making—on the contrary, I think we need more of it. But from what I’ve seen, too many scientists involved in feral cat/TNR research are putting the cart before the horse. They’re shaping public policy before properly identifying any environmental implications. Too much interest in active engagement, not enough interest in active science.

References
1. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

The Work Speaks—Part 2: Sample-Minded Research

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggeration, misrepresentations, errors, and obvious bias. In my previous post, I presented examples of researchers “reinterpreting” the work of others to better fit their own arguments. For the next few posts, I’ll focus on some of the major flaws in the feral cat/TNR research itself—beginning with the reliance, by some, on small sample sizes.

Size Does Matter
There are all kinds of reasons for small sample sizes, perhaps the most common being limited resources (e.g., time, funding, etc.). And they are often a fact of life in real-world research, where investigators have less control over conditions than they might in a laboratory environment. Studies employing small sample sizes are not without value; indeed, they often serve as useful pilot studies for future, more comprehensive, work. They do become problematic, though, when broad conclusions are drawn from their results. Below are three (among many!) examples of such studies.

Impressive Estimates
In “Free-Ranging Domestic Cat Predation on Native Vertebrates in Rural and Urban Virginia,” [2] published in 1992, the authors estimated that the state’s 1,048,704 cats were killing between 3,146,112 and 26,217,600 songbirds each year. “This number,” they note, “is certainly inaccurate to some degree, although the estimates are impressive.” [2] Impressive? I suppose. Maybe incredible is more fitting—since the study from which they were derived included exactly five cats, four “urban” and one “rural.”

Mitchell and Beck acknowledged “the limitations of extrapolation to large areas from relatively small data sets such as ours,” suggesting that their work was intended to provoke future “careful and detailed studies that can reveal truer estimates of the impact of this introduced species.” Hawkins [3] and Dauphiné and Cooper [4], however, seem to take them at their word, regardless of any disclaimers.

Many Cats, Multiple Seasons
In a recent study on Catalina Island, the researchers “examined the home-range behavior and movements of sterilized and intact radiocollared feral cats living in the interior” [5] of the island. Although Guttilla and Stapp concede that “sample sizes, especially for males, were relatively low” despite having “tracked many cats across multiple seasons,” they nevertheless come to some rather dramatic conclusions. Among them: “sterilization likely would not reduce the impact of feral cats on native prey.” [5]

So what do the authors mean by many and multiple? Actually, there were just 27 cats in the study (of an estimated 614–732 on the island). “Four cats were tracked during all four seasons, 9 cats were tracked for three consecutive seasons, 4 cats were tracked for 2 consecutive seasons, and the remaining cats were tracked for 1 season.” [5] And these numbers were effectively cut in half, because the researchers were comparing sterilized and non-sterilized cats. At best, this is a pilot study—though it’s already morphed into something more substantial in the mainstream media.

Myth vs. Math
In their 2004 study, “Ecological Impact of Inside/Outside House Cats Around a Suburban Nature Preserve,” Kays and DeWan observed hunting cats, concluding that their kill rate (13%) is “3.3 times greater than the rate estimated from prey brought home.” [6] Not surprisingly, this figure has been used as an instant multiplier (much in the same way William George’s work has been misused) for researchers interested in “correcting” (inflating?) prey numbers. [4, 7-11]

But this ratio, 3.3, hinges on the hunting behaviors of just 24 cats—12 that returned prey home, and another 12 (11 pets and 1 feral) that were observed hunting for a total of 181 hours (anywhere from 4.8–46.5 hours per cat). It’s interesting to note that the cat observed the most (46.5 hours) was only a year old—the youngest of the 12 observed, and likely the most active hunter. This factor alone could have had a significant influence on the outcome of the study.

Also, as several studies have shown [7,8,12,13], the distribution of prey catches tends to be highly skewed (many cats catch few/no prey, while a few catch a lot). In other words, the distribution is not the familiar bell curve at all—making it inappropriate to use a simple average for calculating estimations (a topic I’ll address in detail later). What’s more, with only 12 cats being monitored, how can we be sure their behaviors accurately represent any real distribution at all?

But the key to their calculation is the average time spent outdoors. This, too, tends to be a highly skewed distribution [14, 15], although—curiously—Kays and DeWan’s data suggest otherwise. By way of example, a 2003 survey conducted by Clancy, Moore, and Bertone [15] revealed that nearly half of the cats with outdoor access were outside for two or fewer hours a day. And 29% were outdoors for less than an hour each day. A survey conducted by the American Bird Conservancy revealed similar behavior, reporting that “35% keep their cats indoors all of the time” and “31% keep them indoors mostly with some outside access.” [14]

Kays and DeWan’s average of 8.35 hours/day, then, seems rather out of line with other studies. This, in addition to a number of unknowns (e.g., influence of time of day/night on hunting success, actual time spent hunting by each cat, etc.) raises serious questions about their conclusions.

By way of comparison, using an average of 2.5 hours/day (which is not out of line with the surveys described above) would yield a ratio of 1:1. In other words, no difference between predation rates predicted by actual hunting observation and those predicted by way of prey returned home. Which is not to say that I agree with Kays and DeWan’s underlying methods—we don’t know the possible effects of seasonal variation, for example, or differences in habitat. I’m only pointing out how sensitive this one factor—with its enormous consequences—is to the amount of time cats actually spend outdoors (and, just to introduce one more complication: I’d be very surprised if the amount of outdoor time cats spend hunting is normally distributed; it, too, is probably skewed).

Ironically, while the authors express disappointment that “biologists have rarely sampled both cat and prey populations in such a way that direct effects on prey populations can be shown,” [6] they seem to have had no misgivings about how their work—suffering from its own sampling issues—might be used to misrepresent those same effects.

*     *     *

Next, I’ll discuss the difference between compensatory and additive predation, and how that affects predictions of feral cat impacts on wildlife.

References
1. Lepczyk, C.A., et al., “What Conservation Biologists Can Do to Counter Trap-Neuter-Return: Response to Longcore et al.” Conservation Biology. 2010. 24(2): p. 627-629.

2. Mitchell, J.C. and Beck, R.A., “Free-Ranging Domestic Cat Predation on Native Vertebrates in Rural and Urban Virginia.” Virginia Journal of Science. 1992. 43(1B): p. 197–207.

3. Hawkins, C.C., Impact of a subsidized exotic predator on native biota: Effect of house cats (Felis catus) on California birds and rodents. 1998. PhD Dissertation, Texas A&M University.

4. Dauphiné, N. and Cooper, R.J., Impacts of Free-ranging Domestic Cats (Felis catus) on birds in the United States: A review of recent research with conservation and management recommendations, in Fourth International Partners in Flight Conference: Tundra to Tropics. 2010. p. 205–219

5. Guttilla, D.A. and Stapp, P., “Effects of sterilization on movements of feral cats at a wildland-urban interface.” Journal of Mammalogy. 2010. 91(2): p. 482-489.

6. Kays, R.W. and DeWan, A.A., “Ecological impact of inside/outside house cats around a suburban nature preserve.” Animal Conservation. 2004. 7(3): p. 273-283.

7. Baker, P.J., et al., “Impact of predation by domestic cats Felis catus in an urban area.” Mammal Review. 2005. 35(3/4): p. 302-312.

8. Baker, P.J., et al., “Cats about town: is predation by free-ranging pet cats Felis catus likely to affect urban bird populations? Ibis. 2008. 150: p. 86-99.

9. van Heezik, Y., et al., “Do domestic cats impose an unsustainable harvest on urban bird populations? Biological Conservation. 143(1): p. 121-130.

10. Nelson, S.H., Evans, A.D., and Bradbury, R.B., “The efficacy of collar-mounted devices in reducing the rate of predation of wildlife by domestic cats.” Applied Animal Behaviour Science. 2005. 94(3-4): p. 273-285.

11. MacLean, M.M., et al., “The usefulness of sensitivity analysis for predicting the effects of cat predation on the population dynamics of their avian prey.” Ibis. 2008. 150(Suppl. 1): p. 100-113.

12. Churcher, P.B. and Lawton, J.H., “Predation by domestic cats in an English village.” Journal of Zoology. 1987. 212(3): p. 439-455.

13. Woods, M., McDonald, R.A., and Harris, S., “Predation of wildlife by domestic cats Felis catus in Great Britain.” Mammal Review. 2003. 33(2): p. 174-188.

14.  ABC, Human Attitudes and Behavior Regarding Cats. 1997, American Bird Conservancy: Washington, DC. http://www.abcbirds.org/abcprograms/policy/cats/materials/attitude.pdf

15. Clancy, E.A., Moore, A.S., and Bertone, E.R., “Evaluation of cat and owner characteristics and their relationships to outdoor access of owned cats.” Journal of the American Veterinary Medical Association. 2003. 222(11): p. 1541-1545.

The Work Speaks—Part 1: Lost in Translation

In April, Conservation Biology published a comment authored by Christopher A. Lepczyk, Nico Dauphiné, David M. Bird, Sheila Conant, Robert J. Cooper, David C. Duffy, Pamela Jo Hatley, Peter P. Marra, Elizabeth Stone, and Stanley A. Temple. In it, the authors “applaud the recent essay by Longcore et al. (2009) in raising the awareness about trap-neuter-return (TNR) to the conservation community,” [1] and puzzle at the lack of TNR opposition among the larger scientific community:

“…it may be that conservation biologists and wildlife ecologists believe the issue of feral cats has already been studied enough and that the work speaks for itself, suggesting that no further research is needed.”

In fact, “the work”—taken as a whole—is neither as rigorous nor as conclusive as Lepczyk et al. suggest. And far too much of it is plagued by exaggerations, misrepresentations, errors, and obvious bias. For the next few posts, I’m going to present a sampling of its more serious flaws, beginning with how some researchers “reinterpret” work of others to suit their own purposes.

Tell It Like It Is
Studies of cat predation frequently cite the work of William G. George, who, in 1974, published a paper documenting his meticulous observations of the hunting behavior of three cats on his southern Illinois farm. “The results,” wrote George, “established a basis for examining the possibility that cat predation may result in depleted winter populations of microtine rodents and other prey of Red-tailed Hawks, Marsh Hawks, and American Kestrels.” [2]

Thirty years later, David A. Jessup interpreted things rather differently, giving George’s work an additional—and unwarranted—degree of certainty. Gone are the doubts that George expressed—first, regarding the impact of cat predation on rodent and other prey populations; second, regarding the relationship between these populations and the raptors that feed on them. For Jessup—who offers no additional evidence—it’s all very straightforward: “Feral cats also indirectly kill native predators by removing their food base.” [3]

More recently, Guttilla and Stapp seem to prefer Jessup’s take: “Human-subsidized cats… can spill over into less densely populated wildland areas where they reduce prey for native predators (George 1974).” [4]

If any additional work has been done on the subject (surely there are more cats in the area these days; how are the voles and raptors faring?), it seems to have gone unnoticed. Instead, Jessup, Guttilla, and Stapp (and others, too, no doubt) have simply rewritten George’s conclusion to suit their own purposes. Perhaps their version makes for a better story, but it’s rather poor science.

Credit Where Little/None Is Due
When the Lancet recently retracted a 1998 paper linking vaccinations to autism in children—“research” that sparked the ongoing backlash against vaccinations—it was headline news. The move prompted this criticism from one member of the British Parliament: “The Lancet article should never have been published, and its peer review system failed. The article should now be expunged from the academic record…”

At the risk of drawing too many parallels between the two papers, I think the same can be said for Coleman and Temple’s infamous “Wisconsin Study.” (On the other hand, it does serve a useful purpose as a red flag.) Actually, as Goldstein et al. point out, Coleman and Temple’s paper was never peer-reviewed (not necessarily a deal-breaker in my book, but such publications do warrant additional scrutiny), but achieved its mythical status by being cited ad nauseam in peer-reviewed journals, as well as the mainstream media.

Does anybody actually believe the numbers suggested by Coleman and Temple? Stanley Temple (one of the co-authors of the recent anti-feral cat/TNR comment in Conservation Biology) himself admitted their published figures “aren’t actual data; that was just our projection to show how bad it might be.” [5]

I don’t think Longcore et al. [6] or the editors at Conservation Biology put much stock in the Wisconsin Study—so why continue to publish “projections” that have been so thoroughly discredited? Because doing so strengthens their case, at least among those who don’t know any better—especially people outside the scientific community, including many journalists, policy makers, judges, and the general public.

In their recent comment, Lepczyk et al. suggest that conservation biologists and wildlife ecologists “look to the evolutionary biology community” [1] for an example of how to influence policy:

“When local policies or regulations are put forth that promote the teaching of creationism or intelligent design, the evolutionary biologists have responded in force from across the nation and world.” [1]

Let’s set aside for the moment all the baggage associated with their analogy. My question is this: Is the evolutionary biology community still publishing bogus “projections” from 13 years ago? I doubt it.

Check Your Premises
In their recent paper (available for download via the American Bird Conservancy (ABC) website), Dauphiné and Cooper arrive at their absurd figure of “117–157 million free-ranging cats in the United States,” [7] in part, by way of Jessup’s “estimated 60 to 100 million feral and abandoned cats in the United States.” [3]

So where does Jessup’s figure come from? We have no idea—there’s no citation. And Jessup is no authority on the subject—having conducted no studies or reviews of studies that quantify the feral cat population. What’s more, his “estimation” is among the highest figures published. Yet this is the shaky foundation upon which Dauphiné and Cooper attempt to build their subsequent argument.

The authors then add to the (dubious) number of feral cats the proportion of pet cats allowed outdoors. They refer to a 2004 paper by Linda Winter, director of ABC’s Cats Indoors! campaign, in which it was reported, “A 1997 nationwide random telephone survey indicated that 66% of cat owners let their cats outdoors some or all of the time.” [8]

That’s an interesting way to put it—Winter makes it sound like two-thirds of pet cats are essentially outdoor cats. But the surveycommissioned by ABC!—actually indicates that “35% keep their cats indoors all of the time” and “31% keep them indoors mostly with some outside access.” [9] The difference in wording is subtle, and hampered by imprecision—it all comes down to the meaning of some.

Winter’s 2004 paper implies that there are twice as many outdoor pet cats as was indicated in the original survey—an interpretation Dauphiné and Cooper seem to embrace. Had they looked further—and to a less biased source—they might have been able to get a better handle on the degree of outdoor access. For example: a 2003 survey conducted by Clancy, Moore, and Bertone [10] revealing that nearly half of the cats with outdoor access were outside for two or fewer hours a day. And 29% were outdoors for less than an hour each day.

Do these “part-timers” have the same impact on wildlife as feral cats? Dauphiné and Cooper would have us believe they do.

[Note: For a closer look at the flaws in Dauphiné and Cooper’s paper, download “One Billion Birds,” by Laurie D. Goldstein.]

The lesson? Credible research begins with a solid foundation; a weak foundation—one plagued with unsubstantiated claims—on the other hand, leads to pseudoscience.

Or worse. ABC’s Senior Policy Advisor, Steve Holmer, cited Dauphiné and Cooper’s bogus numbers when he spoke to the Los Angeles Times about his organization’s involvement with the legal battle against TNR. It’s like the Wisconsin Study all over again.

When All Else Fails, Look It Up
Though this would seem to be utterly obvious, it apparently bears repeating: Don’t cite work you haven’t actually read.

Isn’t this emphasized in all graduate (indeed, undergraduate, too) programs? What grad student isn’t, at one time or another, tempted to take the easy way out—ride the coattails of somebody else who’s (presumably) done the real work? In addition to the ethical implications, such shortcuts tend to invite more immediate troubles, too. Again, George’s work (described above) provides an excellent case study. Below are some examples of how his work has been referenced in the cat predation literature:

“It is very unlikely that cats bring home all of the prey that they capture. What proportion they bring home has been little studied. George (1974) on a farm in Illinois USA found that three house cats, all adequately fed, brought home about 50% of the prey that they killed.” [11]

“George found that about 50% of prey were indeed brought home, with the other 50% being eaten, scavenged by other animals or simply not found.” [12]

“These approximations are probably underestimates, assuming that cats do not bring back all the prey that they kill.” [13]

Trouble is, George never said these things; what he said was:

“… the cats never ate or deposited prey where caught but instead carried it into a ‘delivery area,’ consisting of the house and lawn. The exclusive use of this delivery area was verified in 18 to 70 mammal captures per cat, as witnessed between early 1967 and 1971.” [2]

In 2000, Fitzgerald and Turner pointed out the fact that George’s work was being misrepresented, noting that the erroneous 50% figure “has been reported widely, though it is unfounded.” [14] Nevertheless, the myth persists—even in 2010.

“In Illinois, George (1974) found that only about half of animals killed by cats were provided to their owners, and in upstate New York, Kays and DeWan (2004) found that observed cat predation rates were 3.3 times higher than predation rates measured through prey returns to owners. Thus, predation rates measured through prey returns may represent one half to less than one third of what pet cats actually kill…” [7]

As Dauphiné and Cooper demonstrate, the “reinterpreted” version of George’s work makes for a very convenient multiplier—suddenly, every kill reported is doubled (or tripled, if Kays and DeWan are to be believed—and they’re not, but that’s a topic for another post). Never mind the fact that it has no basis in actual fact.

Getting a copy of George’s study isn’t difficult, especially with the inter-library loan services available today. To reference it—to use George’s work so that your own appears more credible—without ever having actually read it, is simply inexcusable. But citing it blindly suggests more than laziness—it points to a certain coziness that has no place in scientific discourse. Too much Kool-Aid drinking, and not enough honest research.

*     *     *

Scientists can (and do) look at identical results and come to very different conclusions. But misinterpreting, misrepresenting, or dismissing the conclusions of others, is something else altogether. As the above examples (and there are many, many more!) illustrate, this happens far too often in the feral cat/TNR literature. And if we can’t believe what researchers are saying about the work of others, why would we believe what they say about their own work?

Next, I’ll focus on some of the major flaws in the feral cat/TNR literature—beginning with small sample sizes

References
1. Lepczyk, C.A., et al., “What Conservation Biologists Can Do to Counter Trap-Neuter-Return: Response to Longcore et al.” Conservation Biology. 2010. 24(2): p. 627-629.

2. George, W., “Domestic cats as predators and factors in winter shortages of raptor prey.” The Wilson Bulletin. 1974. 86(4): p. 384–396.

3. Jessup, D.A., “The welfare of feral cats and wildlife.” Journal of the American Veterinary Medical Association. 2004. 225(9): p. 1377-1383.

4. Guttilla, D.A. and Stapp, P., “Effects of sterilization on movements of feral cats at a wildland-urban interface.” Journal of Mammalogy. 2010. 91(2): p. 482-489.

5. Elliott, J., The Accused, in The Sonoma County Independent. 1994. p. 1, 10

6. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

7. Dauphiné, N. and Cooper, R.J., Impacts of Free-ranging Domestic Cats (Felis catus) on birds in the United States: A review of recent research with conservation and management recommendations, in Fourth International Partners in Flight Conference: Tundra to Tropics. 2010. p. 205–219

8. Winter, L., “Trap-neuter-release programs: the reality and the impacts.” Journal of the American Veterinary Medical Association. 2004. 225(9): p. 1369-1376.

9. ABC, Human Attitudes and Behavior Regarding Cats. 1997, American Bird Conservancy: Washington, DC. http://www.abcbirds.org/abcprograms/policy/cats/materials/attitude.pdf

10. Clancy, E.A., Moore, A.S., and Bertone, E.R., “Evaluation of cat and owner characteristics and their relationships to outdoor access of owned cats.” Journal of the American Veterinary Medical Association. 2003. 222(11): p. 1541-1545.

11. Churcher, P.B. and Lawton, J.H., “Predation by domestic cats in an English village.” Journal of Zoology. 1987. 212(3): p. 439-455.

12. May, R.M., “Control of feline delinquency.” Nature. 1988. 332(March): p. 392-393.

13. Crooks, K.R. and Soule, M.E., “Mesopredator release and avifaunal extinctions in a fragmented system.” Nature. 1999. 400(6744): p. 563.

14. Fitzgerald, B.M. and Turner, D.C., Hunting Behaviour of domestic cats and their impact on prey populations, in The Domestic Cat: The biology of its behaviour, D.C. Turner and P.P.G. Bateson, Editors. 2000, Cambridge University Press: Cambridge, U.K.; New York. p. 151–175.

A Critical Assessment of “Critical Assessment”—Part 4

The fourth in a series of posts that breaks down my critique of the essay “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894) by Travis Longcore, Catherine Rich, and Lauren M. Sullivan.

In the past few posts, I’ve addressed their claims regarding the numbers of birds killed by cats, and alleged wildlife impacts. Now I’d like to focus on some of their claims regarding TNR. While I agree with the authors that there is a need for additional research into the effectiveness and impact (environmental and otherwise) of TNR, I’m not sure any subsequent findings would satisfy the standards—some of which border on the absurd—suggested by Longcore et al.

Adoptions
To begin with, the authors challenge the efficacy of TNR, noting—correctly—for example, that where TNR has proven effective at reducing the size of colonies, success has been “derive[d] in part from intensive efforts to remove cats for adoption as part of the TNR program.” [1] Shouldn’t this appeal to Longcore and the Urban Wildlands Group? Adoptions lead to fewer free-roaming cats, right?

It’s unclear how a successful adoption program lessens the efficacy of TNR; indeed, such efforts are integral to any TNR program. For Longcore et al., however, it’s as if adoptions constitute cheating.

Researchers vs. Volunteers
Another of their assertions, that “programs implemented by researchers are likely to be much more thorough than programs implemented exclusively by volunteers,” [1] could be applied to virtually any conservation effort. Of course the results will be better when the experts are involved directly!

Indeed, while compiling data for the Atlas of Breeding Birds of Maryland and the District of Columbia, researchers found Cooper’s Hawk (Accipiter cooperii) in 46% of the areas surveyed, while volunteers reported only a 14% occurrence of this “secretive species that requires special effort.” [2] Here, the experts “performed” more than three times better than well-meaning volunteers with less experience and/or training. Should we discontinue all efforts that include volunteers, then? Or shut down these programs until the volunteers perform as well as experts? Obviously not.

Anecdotes of Success
Longcore et al. criticize supporters of TNR for their “anecdotes of success” and “assertions of colony declines often… supported only by reference to Web sites.” [1] By calling the data “anecdotal,” the authors dismiss it out of hand. So, what measures of success would be acceptable?

In general, caretakers of feral colonies—as providers of food, water, shelter, and, often, healthcare—know their cats quite well. Yet, Longcore et al. suggest that their reports are not to be trusted—trusted to a lesser degree, in fact, than the reports generated by members of the public recruited to watch and listen for birds. Breeding Bird Surveys “annually engage tens of thousands of participants,” and these efforts are now beginning to leverage the power of the Internet via Web-based programs such as eBird. [3] All of which sounds very anecdotal. So, do the authors question the validity of this work as well?

Prevailing Conditions
Citing a 2006 study from Rome, [4] Longcore et al. chose to focus not on TNR’s rather remarkable success, but on its greatest challenge: “Ten years of TNR in Rome showed a 16–32% decrease in population size across 103 colonies but concluded that TNR was ‘a waste of time, energy, and money’ if abandonment of owned cats could not be stopped.” [1] It must be recognized that TNR is part of a larger mission that includes adoptions (as mentioned above), sterilization of owned cats, and the burgeoning no-kill movement (which may reduce the number of abandoned cats).

In any case, what rescue/conservation work isn’t “a waste of time, energy, and money” when considered in the harsh light of what the authors call “prevailing conditions”? We could, for example, say the same about efforts to save songbirds faced with the elimination and fragmentation of habitat, increased levels of pollution, and the like (indeed, endangered and threatened species are, by definition, the victims of prevailing conditions). Or, to take a very timely example, the work being done to save the wildlife affected by millions of gallons of oil spilling into the Gulf of Mexico even as I write this.

The fact that such efforts are uphill battles may say something about their underlying moral imperative—but very little about their efficacy.

*     *     *

Common Ground
Essentially, the argument put forth by Longcore et al. in this part of their essay boils down to these three points:

  • TNR can and does work, though not always as well as one would like.
  • Adoptions are critical, as is training and rigorous tracking.
  • Abandonment of pet cats—which is, in any case, illegal—should be stopped.

So, how is this any different than what TNR advocates are promoting? Here at least, we would seem to have some common ground. Apparently, what’s really at issue is not how success is defined, but by whom:

For many TNR advocates, success is not defined by elimination of feral cats in an area, but rather by the welfare of the cats… conservation scientists and wildlife veterinarians measure success of a feral cat management program by the decline and elimination of free-roaming cats. [1]

All of which leaves me wondering: How much time have the authors spent with people who practice TNR? Of course practitioners are interested in the welfare of the cats—just as any animal lover is interested in the welfare of the animals they enjoy. But they’re also thrilled when “kitten season” comes and goes without any new arrivals in their colonies.

More common ground? It would seem so—but if that’s the case, one is left to wonder why the Urban Wildlands Group sued the City of Los Angeles to put an end to publicly supported TNR. (Or at least I am left to wonder, as Longcore has not responded to my inquiries.) One thing that does seem certain: more cats are reproducing as a result of the injunction. And no doubt more are dying, too. Hard to imagine the wildlife and environment being any better off, either. There are lots of losers here—where are the winners?

References
1. Longcore, T., Rich, C., and Sullivan, L.M., “Critical Assessment of Claims Regarding Management of Feral Cats by Trap–Neuter–Return.” Conservation Biology. 2009. 23(4): p. 887–894.

2. Robbins, C.S. and Blom, E.A.T., Atlas of the breeding birds of Maryland and the District of Columbia. Pitt series in nature and natural history. 1996.

3. Sullivan, B.L., et al., “eBird: A citizen-based bird observation network in the biological sciences.” Biological Conservation. 2009. 142(10): p. 2282-2292.

4. Natoli, E., et al., “Management of feral domestic cats in the urban environment of Rome (Italy).” Preventive Veterinary Medicine. 2006. 77(3-4): p. 180-185.

A Critical Assessment of “Critical Assessment”—Part 3

The third in a series of posts that breaks down my critique of the essay “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894) by Travis Longcore, Catherine Rich, and Lauren M. Sullivan.

As I’ve suggested previously, much of the “evidence” that Longcore et al. cite regarding cat predation is rather weak. The links between predation and declining wildlife populations (especially birds) are, not surprisingly, no better. According to Longcore et al., “Comparative field studies and population measurements illustrate the adverse effects of feral and free roaming cats on birds and other wildlife.” Let’s take a closer look at some of these studies…

In canyons in San Diego native bird diversity declined significantly with density of domestic cats (Crooks & Soulé 1999). —Longcore et al.

  • Longcore fail to mention the density of people here—the study site was a “moderately sized fragment (~20 ha) [approximately 49 acres] bordered by 100 residences.” [1]
  • It’s also not clear how sites such as this one, which the authors describe as, “undeveloped steep-sided canyons… habitat islands in an urban sea,” correspond to the environment overall. Don’t forget: when Longcore and the Urban Wildlands Group sued the City of Los Angeles last year, it was to put a stop to publicly supported TNR throughout the city.

In a comparative study in Alameda County, California, a site with a colony of feral cats had significantly fewer resident birds, fewer migrant birds, and fewer breeding birds than a control site without cats (Hawkins 1998). Ground-foraging species, notably California Quail (Calipepla californica) and California Thrashers (Toxostoma redivivum), were present at the control site but never observed at the site with cats. Native rodent density was drastically reduced at the site with cats, whereas exotic house mice (Mus musculus) were more common (Hawkins 1998). —Longcore et al.

Hawkins’ dissertation [2] is so problematic—and cited frequently enough as “evidence” of the impact of cats on wildlife—that it warrants a post of its own. Here, I’ll touch on just a few issues.

  • Hawkins describes the “cat” and “no-cat” sites as being similar enough that a valid A-B comparison is appropriate. But a closer look at the study suggests otherwise. Much of the cat site bordered the park’s lake and marina, not far from a number of picnic sites. Hawkins notes that there were more people in the cat area, but doesn’t even admit to the possibility that their presence may have influenced the numbers of birds and rodents he observed there.
  • In addition, the presence of pesticides may have played a role. According to a 2002 report (the earliest I was able to find) from the East Bay Regional Park District, “The focus of Lake Chabot’s weed control efforts are vegetation reduction within the two-acre overflow parking lot, picnic sites and firebreaks around park buildings, corp. yard, service yard, and the Lake Chabot classroom.” [3] Now, Hawkins’ fieldwork was done in 1995 and 1996, but if there was any pesticide use going on during the study period, it may have affected the results—especially if the pesticide was distributed differently across the two sites.
  • Hawkins writes, “The preference of ground feeding birds for the no-cat treatment was striking; for example, California quail were seen almost daily in the no-cat area, whereas they were never seen in the cat area.” What’s more striking to me, though, is the fact that five of the nine ground-feeding species included in the study showed no preference for the cat or no-cat area—a point Hawkins downplays, and Longcore et al. ignore entirely.
  • Finally, it’s not clear how this study constitutes an experiment at all. Hawkins chose two sites, one where cats were being fed, and another (approximately two miles away) where cats were not being fed. We have no idea what the cat area was actually like prior to the cats being fed there—Hawkins merely assumes the populations of birds and rodents would have been identical to those found at the no-cat site. We also have no idea what effect the feeding had—what if the cats were present but had to fend for themselves? And we don’t know if the cats were sterilized, or what impact that might have had on the study. In other words, Hawkins doesn’t actually know enough about what’s going on at the two sites to conclude, as he does, that “it is not prudent to manage for wildlife and allow cat feeding in the same parks.”

In Bristol, United Kingdom Baker et al. (2005) calculated that the predation rates by cats on 3 bird species in an urban area is high relative to annual productivity, which led the authors to suggest that the area under study may be a habitat sink. —Longcore et al.

  • Also, Longcore et al. fail to mention that Baker et al. concede an important point: “collectively, despite [cats] occurring at very high densities, the summed effects on prey populations appeared unlikely to affect population size for the majority of prey species.”
  • In addition, a subsequent study (also conducted in Bristol) involving two of the authors, suggests that much of the predation observed was compensatory rather than additive. That is, many of these birds would have, for one reason or another, died anyhow, whether the cats were present or not. Specifically, the authors found that “birds killed by cats in this study had significantly lower fat and pectoral muscle mass scores than those killed by collisions.” [6] Baker at al. are cautious about these findings, suggesting, “the distinction between compensatory and additive mortality does… become increasingly redundant as the number of birds killed in a given area increases: where large numbers of prey are killed, predators would probably be killing a combination of individuals with poor and good long-term survival chances.” But once again, their estimates of birds killed by cats are inflated by a factor of 3.3, as described above—thereby raising doubts about any level of “redundancy.”
  • Another study to investigate compensatory vs. additive predation was more conclusive. Møller and Erritzøe compared the average spleen mass of birds killed by cats to that of birds killed in collisions with windows found that, “small passerine birds falling prey to cats had spleens that were significantly smaller than those of conspecifics that died for other reasons,” concluding that the birds killed by cats “often have a poor health status.” [7] In other words, the birds killed by cats were among the population least likely to survive anyhow.

Clearly, this is a complex—not to mention contentious—issue. But Longcore et al. make it out to be remarkably straightforward. The “adverse effects of feral and free roaming cats on birds and other wildlife,” they seem to suggest, are widely accepted common knowledge.

*     *     *

Then, too, there are those—and there are many—who have disputed the broad-brush claims about the impact of cat predation on wildlife. Consider, for example, the following studies:

  • Biologist C.J. Mead, reviewing the deaths of “ringed” (banded) birds reported by the public, suggests that cats may be responsible for 6.2–31.3% of bird deaths. “Overall,” writes Mead, “it is clear that cat predation is a significant cause of death for most of the species examined.” But the relationship between bird deaths and population declines is complex. In fact, Mead concludes that “there is no clear evidence of cats threatening to harm the overall population level of any particular species… Indeed, cats have been kept as pets for many years and hundreds of generations of birds breeding in suburban and rural areas have had to contend with their predatory intentions.” [8]
  • Mike Fitzgerald and Dennis Turner come to essentially the same conclusion. (Their contribution to The Domestic Cat: The Biology of its Behaviour is a must-read for anybody interested in the subject.) “We consider that we do not have enough information yet to attempt to estimate on average how many birds a cat kills each year,” write Fitzgerald and Turner. “And there are few, if any studies apart from island ones that actually demonstrate that cats have reduced bird populations.” [9]
  • Martin, Twigg, and Robinson conclude more broadly, “it is not possible to make any inferences concerning the real impact of feral cats on prey populations from dietary studies.” [10]

Given the scope of their essay, perhaps it’s understandable that Longcore et al. were unable to cover each aspect of this rather broad topic in a comprehensive manner. Nevertheless, the amount of research into cat predation and declining bird populations—a critical piece of the puzzle, to be sure—that was omitted, glossed over, and/or misrepresented suggests a clear agenda. Read carefully, their essay comes across as not as scientific discourse, but as fodder for a marketing campaign. (And, given the number of wildlife conservation/bird advocacy groups that have posted it on their websites—not to mention the L.A. Superior court decision—it’s been effective.)

*     *     *

Many proponents of TNR will acknowledge that the practice is not appropriate for all environments. Crooks and Soulé’s work in San Diego’s canyon country (cited previously), writes Ellen Perry Berkeley, “suggests to even the most ardent TNR advocate that such a landscape might not be the best place for TNR… The world is a complicated place.” [11] Gary J. Patronek, the former Director of the Center for Animals and Public Policy at the Cummings School of Veterinary Medicine at Tufts University, and one of the founders of the Hoarding of Animals Research Consortium, goes further: “the release of cats into an environment where they would impact endangered or threatened species, or even into wildlife preserves or refuges, is inexcusable.” [12]

This, I worry, is a slippery slope. Given the current nature of the cat debate, how long would it be before every alley, Dumpster, and abandoned property is deemed a wildlife preserve? And, given the number of endangered and threatened species—and their wide range—would there be any environment left for cats? Nevertheless, Patronek’s larger point is an important one:

I do not believe that this is being advocated by cat protectors who see urban, managed colonies as an imperfect but still preferable alternative to the euthanasia of healthy animals. Abandoned pet cats whose own habitat has been reduced to colonies, and the wild species endangered by clear-cutting or beachfront development, are casualties of the same callous disregard for the lives of animals. I see little justification for shifting the role of cats to that of scapegoat.

For Longcore and the Urban Wildlands Group (and others, too, of course), though, there’s simply no place for TNR anywhere. But there’s something even more troubling with their argument: they’re asking the wrong questions. As Patronek puts it so eloquently:

If the real objection to managed colonies is that it is unethical to put cats in a situation where they could potentially kill any wild creature, then the ethical issue should be debated on its own merits without burdening the discussion with highly speculative numerical estimates for either wildlife mortality or cat predation. Whittling down guesses or extrapolations from limited observations by a factor of 10 or even 100 does not make these estimates any more credible, and the fact that they are the best available data is not sufficient to justify their use when the consequence may be extermination for cats… What I find inconsistent in an otherwise scientific debate about biodiversity is how indictment of cats has been pursued almost in spite of the evidence, and without regard to the differential effects of cats in carefully selected, managed colonies, versus that of free-roaming pets, owned farm cats, or truly feral animals. Assessment of well-being for any is an imprecise and contentious process at best. Additional research is clearly needed concerning the welfare of these cats.

In a future post, I’ll get into the ways Longcore et al. would have us measure the success of TNR.

References
1. Crooks, K.R. and Soule, M.E., “Mesopredator release and avifaunal extinctions in a fragmented system.” Nature. 1999. 400(6744): p. 563.

2. Hawkins, C.C., Impact of a subsidized exotic predator on native biota: Effect of house cats (Felis catus) on California birds and rodents. 1998, Texas A&M University.

3. Brownfield, N.T., 2002 Annual Analysis of Pesticide Use East Bay Regional Park District. 2003, East Bay Regional Park District.

4. Baker, P.J., et al., “Impact of predation by domestic cats Felis catus in an urban area.” Mammal Review. 2005. 35(3/4): p. 302-312.

5. Kays, R.W. and DeWan, A.A., “Ecological impact of inside/outside house cats around a suburban nature preserve.” Animal Conservation. 2004. 7(3): p. 273-283.

6. Baker, P.J., et al., “Cats about town: is predation by free-ranging pet cats Felis catus likely to affect urban bird populations? Ibis. 2008. 150: p. 86-99.

7. Møller, A.P. and Erritzøe, J., “Predation against birds with low immunocompetence.” Oecologia. 2000. 122(4): p. 500-504.

8. Mead, C.J., “Ringed birds killed by cats.” Mammal Review. 1982. 12(4): p. 183-186.

9. Fitzgerald, B.M. and Turner, D.C., Hunting Behaviour of domestic cats and their impact on prey populations, in The Domestic Cat: The biology of its behaviour, D.C. Turner and P.P.G. Bateson, Editors. 2000, Cambridge University Press. p. 151–175.

10. Martin, G.R., Twigg, L.E., and Robinson, D.J., “Comparison of the Diet of Feral Cats From Rural and Pastoral Western Australia.” Wildlife Research. 1996. 23(4): p. 475-484.

11. Berkeley, E.P., TNR Past present and future: A history of the trap-neuter-return movement. 2004, Bethesda, MD: Alley Cat Allies.

12. Patronek, G.J., “Letter to Editor.” Journal of the American Veterinary Medical Association. 1996. 209(10): p. 1686–1687.

A Critical Assessment of “Critical Assessment”—Part 2

The second in a series of posts that breaks down my critique of the essay “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894) by Travis Longcore, Catherine Rich, and Lauren M. Sullivan.

Like so many others interested in blaming cats for declining bird populations, Longcore et al. refer to a 1996 article in Wisconsin Natural Resources magazine [1], in which the authors estimate that 8–219 million birds are killed annually by “free-ranging rural cats” in the state. More than any other work, the “Wisconsin Study” (which is actually a series of articles, the first being published in 1993 [2]) has been used as “evidence” against advocates for free-roaming cats in general, and TNR in particular.

In my previous post, I referred only briefly to Coleman and Temple’s work; in fact, careful scrutiny is in order. Among the study’s more notable flaws:

  • Its “estimate that 23 percent of [cats’] diet consists of birds” is well above the 7–10.5% figure suggested by Fitzgerald, [3] one of the world’s foremost experts on the subject (for a detailed account, see Ellen Perry Berkeley’s 2004 book, TNR Past present and future: A history of the trap-neuter-return movement [4]). In fact, Coleman and Temple cite Fitzgerald’s work, making the error all the more egregious.
  • Coleman and Temple assume that all cats hunt; in fact, it has been suggested that only 35–56% of cats are hunters. [5,6]
  • Their figures for cat density, too, have been challenged. [7]

For a more complete critique of the Wisconsin Study, download the 2003 report by Laurie D. Goldstein, Christine L. O’Keefe, and Heidi L. Bickel at Stray Pet Advocacy.

Now 14 years old, the Wisconsin Study has achieved mythical status—but not in a good way. I suppose it’s because the numbers are so impressive. Forget the fact that they’re essentially fictitious—they’re simply too tempting for people who see cats as the primary reason for declining bird populations. James Tantillo, a Lecturer in the Department of Natural Resources at Cornell University’s College of Agriculture and Life Sciences, is right on the money when he refers to Coleman and Temple’s estimate as an example of a “‘mutant statistic’ whose origins and genesis have been greatly lost to the people who cite it.” [8]

*     *     *

Among those who cite it are, of course, Longcore et al. But they failed to cite an important follow-up comment by one of the authors of the Wisconsin Study. In a 1994 interview, an “exasperated” Temple told The Sonoma County Independent:

The media has had a field day with this since we started. Those figures were from our proposal. They aren’t actual data; that was just our projection to show how bad it might be. [9]

More than the media, however, it’s been the wildlife conservationists and bird advocates who have had a field day with the Wisconsin Study. Here are just a few examples:

  • The American Bird Conservancy refers to the study in its brochure Domestic Cat Predation on Birds and Other Wildlife. But ABC goes one step further, pointing out that Coleman and Temple’s estimate was for rural cats, and that “suburban and urban cats add to that toll.” [10]
  • The U.S. Fish and Wildlife Service cites the study’s “intermediate” estimate of 39 million birds in its Migratory Bird Mortality Fact Sheet.
  • A recent article in Audubon Magazine suggests “cats were annually knocking off somewhere in the neighborhood of 8 million birds just in rural Wisconsin.” [11] To the magazine’s credit, they used Coleman and Temple’s low estimate (a surprise given the overall tone of the piece). Still, none of the numbers from the Wisconsin Study are scientifically sound (indeed, one can make a strong argument that none of the work constitutes actual research).

For Longcore et al. to cite the Wisconsin Study without even a mention of its numerous flaws, or the rather public admission by one of its authors that their estimates “aren’t actual data,” casts serious doubt on the entire paper. Either they didn’t know how flimsy Coleman and Temple’s work was, or they knew and ignored the facts. Neither approach makes for good science, of course.

*     *     *

Estimating the number of birds killed by cats is difficult enough; demonstrating that their predation is the cause of declining bird populations is an even greater challenge. Nevertheless, Longcore et al. suggest the evidence is both plentiful and compelling. I’ll lay out an argument to the contrary in my next post

References
1. Coleman, J. S., & Temple, S. A. (1996). On the Prowl. Wisconsin Natural Resources, 20, 4–8. http://www.dnr.state.wi.us/wnrmag/html/stories/1996/dec96/cats.htm

2. Coleman, J. S., & Temple, S. A. (1993). Rural Residents’ Free-Ranging Domestic Cats: A Survey. Wildlife Society Bulletin, 21(4), 381–390.

3. Fitzgerald, B. M. (1988). Diet of domestic cats and their impact on prey populations. In D. C. Turner & P. P. G. Bateson (Eds.), The Domestic cat: The biology of its behaviour (1st ed., pp. 123–147). Cambridge; New York: Cambridge University Press.

4. Berkeley, E. P. (2004). TNR Past present and future: A history of the trap-neuter-return movement. Bethesda, MD: Alley Cat Allies.

5. Baker, P. J., Molony, S. E., Stone, E., Cuthill, I. C., & Harris, S. (2008). Cats about town: is predation by free-ranging pet cats Felis catus likely to affect urban bird populations? Ibis, 150, 86-99.

6. Goldstein, L. D., O’Keefe, C. L., & Bickel, H. L. (2003). Addressing “The Wisconsin Study.” http://www.straypetadvocacy.org/html/wisconsin_study.html

7. Clifton, M. (2003). Where cats belong—and where they don’t. Animal People http://www.animalpeoplenews.org/03/6/wherecatsBelong6.03.html

8. Tantillo, J. A. (2006). Killing Cats and Killing Birds: Philosophical issues pertaining to feral cats. In J. R. August (Ed.), Consultations in Feline Internal Medicine Volume 5 (5th ed., pp. 701–708). St. Louis, MO: Elsevier Saunders.

9. Elliott, J. (1994, March 3–16). The Accused. The Sonoma County Independent, pp. 1, 10.

10. American Bird Conservancy (undated). Domestic Cat Predation on Birds and Other Wildlife. The Plains, VA. www.abcbirds.org/abcprograms/policy/cats/materials/predation.pdf

11. Williams, T. (2009). Felines Fatale. Audubon Magazine. http://www.audubonmagazine.org/incite/incite0909.html

A Critical Assessment of “Critical Assessment”—Part 1

The first in a series of posts that breaks down my critique of the essay “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894) by Travis Longcore, Catherine Rich, and Lauren M. Sullivan.

How many birds are killed by cats? It’s a fair question. And if Longcore et al. are to be believed, we actually have a pretty good handle on this issue:

Feral and free-roaming cats are efficient predators, and their abundance results in substantial annual mortality of wildlife. Churcher and Lawton (1987) concluded that cats were responsible for 30% of the mortality of House Sparrows (Passer domesticus) in an English village. May (1988) extrapolated their results to an estimated 100 million birds and small mammals killed per year in England. Although this extrapolation is often criticized for the limited geographic scope and number of cats studied, Woods et al. (2003) confirmed and refined this result with a larger sample size and geographic area that included England, Scotland, and Wales. From a survey of cat owners that documented prey returned by 696 cats, Woods et al. (2003) estimated that the 9 million cats in Britain kill at least 52–63 million mammals, 25–29 million birds, and 4–6 million reptiles each summer. In North America Coleman and Temple (1996) developed estimates of cat densities in Wisconsin and associated mortality of 8–217 million birds per year.

The relationship between cat predation and bird populations is highly complex, and our understanding quite limited—something Longcore et al. only hint at. It doesn’t help matters that results of small, isolated studies are often extrapolated from rural to urban environments, from one region to another, and so forth. In 1995, Churcher himself cautioned against making such leaps: “I’d be very wary about extrapolating our results even for the rest of Britain, let alone America,” he told Catnip, a newsletter published by the Cummings School of Veterinary Medicine at Tufts University.

Actually, Churcher went much further: “I don’t really go along with the idea of cats being a threat to wildlife. If the cats weren’t there, something else would be killing the sparrows or otherwise preventing them from breeding.” [1] Although Longcore et al. seem eager to cite Churcher and Lawton’s now-classic work as “evidence” of the damage cats can do, they make no mention of Churcher’s later comments (just one of many examples of their tendency to “cherry pick” from the literature only the bits and pieces that fit neatly into their argument).

But back to the number of birds killed by cats. Many of the studies on the subject—including those cited by Longcore et al.—are quite flawed. Among the numerous issues that call into question their estimates are assumptions regarding the number of cats that actually hunt, the number of cats allowed outdoors, the number of cats that live in a particular area, and so forth. And then, of course, there are the risks inherent in estimating population numbers and characteristics based on a small sample size.

(In fact, Woods et al. go to some lengths to emphasize the limitations of their study, conceding, for example, that they “may have focused on predatory cats.” [2] This is just one of many reasons the authors cite for requesting that their work be treated “with requisite caution”—a request apparently ignored by Longcore et al.)

By referring uncritically to such studies, Longcore et al. give far greater importance to this work than is warranted. Repeating—and therefore reinforcing—figures known to be erroneous and/or misleading is simply irresponsible.

The fact that the “English village” study and “Wisconsin Study” have been so thoroughly discredited (see, for example, the comments of Nathan Winograd, director of the No Kill Advocacy Center, and a report by Laurie D. Goldstein, Christine L. O’Keefe, and Heidi L. Bickel) raises some unsettling questions about their inclusion in a paper billed as a “critical assessment.” For example: Are the authors interested enough in rigorous scientific inquiry to look beyond “the usual suspects” in their assessment of the key issues?

One might also wonder: Given the important literature that Longcore et al. choose to overlook, ignore, or dismiss (to be addressed in detail in future posts), what is their motivation for writing the essay in the first place? Actually, this question was answered in January, two months after the paper’s publication, when L.A. Superior Court Judge Thomas McKnew decided in favor of an injunction against publicly supported TNR in Los Angeles (LASC BS115483). The Urban Wildlands Group (for which Longcore serves as Science Director, and Rich as Executive Officer) was the lead petitioner in the case.

If “Critical Assessment” is any indication, the case had much more to do with politics, PR, and marketing than with science.

References
1. n.a. (1995). What the Cat Dragged In. Catnip, 4–6.

2. Woods, M., Mcdonald, R. A., & Harris, S. (2003). Predation of wildlife by domestic cats Felis catus in Great Britain. Mammal Review, 33(2), 174-188.

Works cited in “Critical Assessment” excerpt:

• Churcher, P. B., & Lawton, J. H. (1987). Predation by domestic cats in an English village. Journal of Zoology, 212(3), 439-455.
• Coleman, J. S., & Temple, S. A. (1996). On the Prowl. Wisconsin Natural Resources, 20, 4–8.
• May, R. M. (1988). Control of feline delinquency. Nature, 332, 392-393.

The Things People Say (or Don’t)—Part 1

Wildlife/bird advocates opposed to TNR are eager to talk to the press, so why won’t they reply to my e-mail?

Just about the time I was writing my response to “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894), its lead author, Travis Longcore, began showing up in the news. The Urban Wildlands Group, for which Longcore serves as science director, was the lead petitioner in the case that would eventually lead to an injunction against publicly supported TNR in Los Angeles.

Given the obvious bias and overall tone of Longcore’s paper, I was hardly surprised to read what he told the press. There’s this, for example, from an interview with Southern California Public Radio:

“Feral cats are documented predators of native wildlife,” said Travis Longcore, science director for the Urban Wildlands Group. “We do not support release of this non-native predator into our open spaces and neighborhoods, where they kill birds and other wildlife.”

Hardly the stuff of controversy, at least at first glance. Who can argue with the fact that cats kills birds and other wildlife? That’s what predators—including cats and a number of other species, too, of course—do. Nobody’s debating that. What impact this predation has on birds and wildlife is another matter altogether—one Longcore doesn’t address here. (I’ll be addressing this issue repeatedly in future posts, starting with a critique of Longcore’s essay in Conservation Biology).

What’s more interesting is Longcore’s reference to cats as “non-native” and wildlife as “native.” It’s a recurring theme in the feral cat debate: native is inherently good; non-native is inherently bad (even worse is invasive non-native, another term often used to demonize cats). Never mind the fact that the cats are here because we brought them here, or the hypocrisy of the native/non-native argument. We routinely protect non-native species from native predators—consider, for example, the current controversy over livestock and wolves. Again, a topic to delve into more deeply in the future.

A week later, Longcore was quoted in the Los Angeles Times:

“It’s ugly; it’s gotten very vicious,” said Travis Longcore of the Urban Wildlands Group, one of the organizations that sued the city on behalf of the birds. “It’s not like we’ve got a vendetta here. This is a real environmental issue, a real public health issue.”

No vendetta? Maybe not, but Longcore’s essay in Conservation Biology has an agenda that takes priority over the science (hardly surprising in retrospect—given the timing of its publication, it must have been written while Longcore was preparing for the L.A. case). His apparent concern for the environment and public health strike me as largely disingenuous.

Also from the Times:

Those cats, Longcore said, often are diseased. And when colonies are fed, the practice often attracts more cats, either from around the neighborhood or because people dump new cats.

Let’s set aside for the moment Longcore’s assertion about colonies attracting cats, feral or dumped (I’ll get to that in another post). What about his suggestion that “these cats are often diseased”? In his own paper, Longcore acknowledges a rate of only 5–12% overall for feline leukemia virus (FeLV) and/or feline immunodeficiency virus (FIV). In the largest of the studies he cites, more than 12,000 cats were tested for FeLV and FIV, revealing an overall rate of infection of 5.2%, which, noted the researchers, “is similar to results previously reported for feral cats and for pet cats.” [1]

What about rabies? According to the Centers for Disease Control and Prevention, “approximately 1% of cats… tested for rabies were found positive” in 2008, the last year for which statistics are available.

It’s difficult to see how these rates of infection would lead anybody to suggest that free-roaming cats are “often diseased.” And I don’t expect to get any clarification from Longcore. While he seems eager to talk to mainstream media, which accepts his claims at face value (and passes them along as accurate to the public), he has yet to respond to my e-mail inquires.

I realize that taking issue with Longcore’s comments will no doubt strike some people as nitpicking. But such statements—which put PR before science—only impede any honest discussion of the issues.

References
[1] Wallace, J. L., & Levy, J. K. (2006). Population characteristics of feral cats admitted to seven trap-neuter-return programs in the United States. Journal of Feline Medicine & Surgery, 8, 279–284.

Nibbling at the Margins—Part 2

In December 2009, my critique of “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894) was rejected by outgoing editor Gary Meffe. Frustrated that Meffe was willing to publish something he considered “nibbling at the margins” topic-wise, but then reject a thoughtful critique of it, I appealed—noting, among other things:

  1. Longcore et al. were very “careful” about the studies they selected, and even the particular claims within the studies cited (this despite the fact that they criticize TNR advocates for their “reference to selected peer reviewed studies”). The authors make no attempt to explain their rationale for this obvious cherry picking.
  2. Although I was, as Meffe suggests, “critiquing the overall literature in the area and pointing out its complexities, problems, and uncertainties,” it was only to put the original essay into context. Meffe’s comment ignores the larger issue: Longcore et al. were essentially breathing new life into flawed studies by citing them uncritically. And here, Conservation Biology is also implicated (which might help explain Meffe’s decision to reject my commentary), a point I made to Meffe:

Conservation Biology is, according to the journal’s website, “the most influential and frequently cited journal in its field.” I’m afraid that by publishing the essay submitted by Longcore et al., Conservation Biology has effectively given its “stamp of approval,” thereby burying more deeply the complexities of the subject and its body of literature. No wonder bird advocacy groups have embraced the paper, including PDFs on their websites—here, it would seem, is additional “proof” of the damage cats are doing to bird populations!

In the end, Meffe didn’t budge. And neither did current editor Erica Fleishman, who seemed to have little patience for the subject. What Meffe found to be too broad, Fleishman read as a “fairly personal critique,” adding, “…we aim for objective presentation of facts that may provide evidence contrary to a previous publication rather than (what comes across as) a more pointed rejoinder to authors and the journal.”

At this point, it seemed clear that I was getting nowhere. Nevertheless, I appealed, explaining what I intended to include in my paper:

… regarding “a more comprehensive piece,” what I’m proposing is a detailed review of the literature regarding cat predation on birds, the scope of which includes—but also goes well beyond—the material covered in the essay by Longcore et al.

Once again, my appeal fell on deaf ears, eliciting this response—obviously intended to put an end to the discussion—from Fleishman:

Thanks for the detailed explanation. I think it would be best to pursue publication of your review in a different journal. Good luck and again thank you for considering Conservation Biology.

Perhaps I will follow her advice and submit a similar proposal to another journal. For now, though, it’s all going right here. Indeed, many of the next several posts will draw on the main points I made in my first letter to Conservation Biology.

Nibbling at the Margins—Part 1

Since I first became involved with the Great Kitty Rescue, I’d begun slowly compiling journal articles and news stories related to feral cat management, and in particular, TNR. As a newcomer to the world of cat rescue, I was struggling to sift through the many claims made—on both sides of this highly controversial issue—regarding its efficacy and potential impact.

When I came across the essay “Critical Assessment of Claims Regarding Management of Feral Cats by Trap-Neuter-Return” (Conservation Biology, Volume 23, No. 4, 887–894). I thought I’d struck gold. Here, I naively assumed, was what I’d been looking for, all neatly complied in a single document (complete with an extensive list of references, allowing me to chase down all of the original research as well). As it turned out, the discovery of this essay proved to be a turning point—but not in the way that I expected. Instead of answering my questions, this paper (the details of which will be the focus of many future posts) raised many more. This “critical assessment,” authored by Travis Longcore, Catherine Rich, and Lauren M. Sullivan—with its glaring omissions, numerous misrepresentations, and obvious bias—revealed for me the ugly side of the feral cat/TNR debate.

So I did what any writer in my position would do: I wrote a letter to the editor.

I was then invited by outgoing editor Gary Meffe (who had been at the helm when the original essay was published) to submit a letter for possible publication in the journal. The letter, suggested Meffe, was “to be substantive and shed more light than heat. In other words, if it is simply a difference of opinion it will not be suitable. I always look for letters to be substantive critiques of a paper.”

Which, I maintain, is precisely what I delivered. Meffe, however, disagreed, and—to his credit—explained in detail his reasoning:

I am not saying it is unimportant to conservation, but it is a fairly narrow and specialized topic. Publication of the Longcore et al. paper was nibbling at the margins to begin with, but I and the reviewers felt that it had enough relevance and interest for us to publish it. I am reluctant to further engage the topic in the journal in great detail, so any responses to it need to be very focused and address specific errors in the paper. Your critique gets into assessment of the broader literature on the subject and its use by Longcore et al. I don’t think this is the format to do that. You are really critiquing the overall literature in the area and pointing out its complexities, problems, and uncertainties; one could do that for almost any topic in conservation and probably for many papers that are published. If this cat TNR literature really is problematic then it calls for a much more comprehensive critical assessment in a thorough review paper. Thus, if you would like to prepare a comprehensive review paper on cat TNR that thoroughly examines the literature and its complexities and problems, then perhaps that could be of interest to this journal.

Not the response I was hoping for, obviously—but I’d already invested too much to give up so easily. Perhaps my next letter would be more successful…